Stockholm, Sweden
Sat 03 16:00
S10.2
Molecular response of the growth plate to inflammatory cytokines
Stockholm, Sweden
London, United Kingdom
Glasgow, United Kingdom
Madrid, Spain
Pittsburgh, USA
Fri 02 15:30
S6.3
Rotterdam, The Netherlands
Sat 03 09:35
FC7.3
IGF-I levels, complex formation and igf-bioactivity in growth hormone treated children with Prader-Willi syndrome
Rotterdam, The Netherlands
Linköping, Sweden
Bethesda, USA
Salt, Spain
Sat 03 12:50
FC10.3
Sao Paulo, Brazil
Ljubljana, Slovenia
Paris, France)
Stockholm, Sweden
Fri 02 10:05
FC4.6
Positive association between height and cancer in the Swedish population
Stockholm, Sweden
Oxford, UK
Milan, Italy
Tübingen, Germany
Sat 03 13:10
FC-LB-5
Paternally inherited IGF2 mutation results in intrauterine and postnatal growth retardation
Tübingen, Germany
Rome, Italy
Paris, France
Gothenburg, Sweden
Modena, Italy
Sat 03 12:30
FC12.1
Evaluation of cardiovascular risk in childhood: data from a survey of dyslipidaemic children
Modena, Italy
Erlangen, Germany
Toulouse, France
Victoria, Australia
Girona, Spain
Girona, Spain
San Paolo, Brazil
Vancouver, Canada
Athens, Greece
Cambridge, UK
Madrid, Spain
Paris, France
Rome, Italy
Prague, Czech Republic
London, UK
Munich, Germany
Thu 01 08:40
WG4.2
Los Angeles, USA
Sat 03 17:45
PL6
The complex relationship between the GH/IGF axis and aging and longevity – the interface with diet and mitochondrial peptides
Los Angeles, USA
Brussels, Belgium
Fri 02 09:15
FC3.1
RNA-based MAFA over-expression is sufficient to drive human pancreatic duct-derived cells toward a -cell-like phenotype
Brussels, Belgium
Rome, Italy
Sat 03 13:10
FC14.5
Rotterdam, The Netherlands
Thu 01 08:30
WG3.2
DSD in Indonesia: the course of psychological development in late identified patients
Rotterdam, The Netherlands
Birmingham, UK
Sheffield, UK
Glasgow, United Kingdom
Thu 01 10:00
WG6.4
Management of middle ear and hearing problems in Turner's syndrome - how can we do better?
Glasgow, United Kingdom
Brussels, Belgium
Thu 01 09:00
WG5.3
Restoration of fertility in cancer adolescents after chemotherapy
Brussels, Belgium
Fribourg, Switzerland
Tennessee, USA
Fri 02 14:45
SS1.3
Gothenburg, Sweden
Naples, Italy
Nancy, France
Bern, Switzerland
Bologna, Italy
Vienna, Austria
Vienna, Austria
Fri 02 15:20
SS1.6
Pro-Con debate - Arguments in favour of screening survivors at risk with palpation of the neck
Vienna, Austria
Copenhagen, Denmark
Sat 03 13:20
FC14.6
An evaluation of glandular breast tissue development and volume by MRI in 121 healthy peripubertal girls
Copenhagen, Denmark
London, UK
Katowice, Poland
Sat 03 12:50
FC12.3
Los Angeles, USA
Birmingham, UK
Sat 03 13:00
FC11.4
Idiopathic multiple pituitary hormone deficiency (IMPHD): radiological and perinatal factors
Birmingham, UK
California, USA
Bialystok, Poland
Uppsala, Sweden
Bondy, France
Copenhagen, Denmark
Sat 03 13:00
FC14.4
Genetic variation of AMH signaling affects AMH and inhibin B levels in healthy peripubertal girls
Copenhagen, Denmark
Manchester, UK
Sat 03 09:15
FC9.1
Paris, France
Nes Ziona, Israel
Exeter, UK
Madrid, Spain
Cambridge, UK
Fri 02
NP1.2
Beer Sheva, Israel
(Geneva, Switzerland)
Haifa, Isreal)
Linz, Austria
Amsterdam, The Netherlands
Sat 03 13:10
FC10.5
Lack of association between transient hypothyroxinaemia of prematurity and neurodevelopmental and behavioral outcomes in young adulthood
Amsterdam, The Netherlands
Kiel, Germany
Sat 03 09:15
FC6.1
Correlation of AR expression and AR transcriptional activity in cultured human genital fibroblasts
Kiel, Germany
London, UK
Florida, USA
London, UK
Doha, Qatar
Madrid, Spain
Sat 03 13:20
FC13.6
TRIAC treatment of allan-herndon-dudley syndrome (AHDS) due to defects in thyroid hormone transporter MCT8
Madrid, Spain
Cincinnati, USA
Cincinnati, USA
Enschede, The Netherlands
Patras, Greece
Manchester, UK
Nijmegen, The Netherlands
Fri 02 09:25
FC5.2
MEN1 syndrome because of combined germline and somatic mosaicism, with important consequences for relatives
Nijmegen, The Netherlands
Leipzig, Germany
Manitoba, Canada
Berlin, Germany
Umea, Sweden
Berlin, Germany
Stockholm, Sweden
Barcelona, Spain
Fri 02 10:45
PL3
Inchon, Republic of Korea
Sat 03 10:05
FC8.6
Metabolic effects of ADP355, protein-based adiponectin receptor agonist, on mice with high-fat diet induced fatty liver disease
Inchon, Republic of Korea
Leipzig, Germany
Philadelphia, USA
Fri 02 09:25
FC2.2
Identification of mutations in TBX1 and AIRE in isolated hypoparathyroidism patients
Philadelphia, USA
Örebro, Sweden
Philadelphia, USA
Sat 03 15:30
S10.1
Molecular mechanisms of growth plate adaptation during undernutrition
Philadelphia, USA
St. Louis, USA
Helsinki, Finland
Helsinki, Finland
Sat 03
YB3.3
Moscow, Russia
Bern, Switzerland
Sat 03 09:35
FC6.3
Establishing the role of the steroid backdoor pathway for androgen biosynthesis in the human ovary
Bern, Switzerland
New South Wales, Australia
Sat 03 12:50
FC11.3
Next generation sequencing: towards a new clinical frontier in the diagnosis and management of pituitary tumours
New South Wales, Australia
Paris, France
London, UK
Bern, Switzerland
Fri 02 09:45
FC4.4
Modulation of GH-1 splicing as potential strategy to rescue growth hormone deficiency type II
Bern, Switzerland
Michigan, USA
Edinburgh, UK
Madrid, Spain
Munich, Germany
Manchester, UK
London, UK
New York, USA
Petah Tikva, Israel
Stockholm, Sweden
Cambridge, United Kingdom
Boston, USA
Cambridge, UK
Bern, Switzerland
Sat 03 13:00
FC10.4
Boston, USA
London, UK
Copenhagen, Denmark
Sat 03 15:30
S8.1
Disentangling disease and drug signatures in the human gut microbiome
Copenhagen, Denmark
Barcelona, Spain
Thu 01 09:40
WG4.3
Israel
Leiderdorp, The Netherlands
Thu 01 08:05
WG6.1
Incidental prenatal diagnosis of Turner Syndrome, perspectives of parents and professionals
Leiderdorp, The Netherlands
Tel Aviv, Israel
Lausanne, Switzerland
Paris, France
Rome, Italy
Leuven, Belgium
Berlin, Germany
Helsinki, Finland
Fri 02 15:30
S7.3
Modeling GnRH deficiency with the use of human pluripotent cells
Helsinki, Finland
Datteln, Germany
Colorado, USA
Gainesville, USA
Fri 02 15:35
SS1.6
Pro - Con Debate: Arguments in favour of screening survivors at risk with thyroid ultrasound
Gainesville, USA
Minneapolis, USA
Seattle, USA
Sat 03 09:35
FC8.3
Paris, France
Toronto, Canada
Kuopio, Finland
Fri 02 09:55
FC4.5
Michigan, USA
Rotterdam, The Netherlands
Thu 01 10:30
WG6.5
Report on the progress and difficulties on transdermal Estradiol supplementation in Europe
Rotterdam, The Netherlands
Prague, Czech Republic
New York, USA
Hamilton, Canada
Fri 02 14:30
S5.1
Paris, France
Stockholm, Sweden
Bad Nauheim, Germany
Fri 02
NP1.1
Prague, Czech Republic
Greece
Basel, Switzerland
Lyon, France
Toulouse, France
Fri 02
MTE6.1
Sat 03
MTE6.2
St Louis, USA
Fri 02 12:15
PL4
Moscow, Russia
Ormskirk, UK
Santiago, Chile
Paris, France
Germany
Stockholm, Sweden
Sat 03 13:00
FC-LB-4
Long-term cognitive effects of antenatal dexamethasone treatment in Swedish adolescents with and without CAH
Stockholm, Sweden
Glasgow, UK
Sat 03 16:30
S10.3
Athens, Greece
Fri 02 09:55
FC3.5
C-peptide levels and glycemic control in children, adolescents and young adults with type 1 diabetes (TID)
Athens, Greece
Lausanne, Switzerland
Sat 03 12:30
FC14.1
KLB, encoding the co-receptor for FGF21, is mutated in congenital hypogonadotropic hypogonadism
Lausanne, Switzerland
Ankara, Turkey
Fri 02 10:05
FC3.6
First report of nationwide incidence and prevalence of type 1 diabetes among children in Turkey
Ankara, Turkey
London, UK
Sat 03 13:20
FC11.6
Osaka, Japan
Hangzhou, China
Sat 03 12:30
FC10.1
Effect of sonic hedgehog signalling on regulation the expression of 11β-HSD2 in the placenta
Hangzhou, China
Adrenals and HPA Axis
Diabetes and Insulin
Hypoglycaemia
Perinatal and Neonatal Endocrinology
Puberty and Neuroendocrinology
Bone, Growth Plate and Mineral Metabolism
Thyroid
Gonads and Gynaecology
Turner Syndrome
Miscellaneous
Autoimmune Endocrine Disease
Endocrine Oncology
Pituitary
Fat Metabolism, Obesity
Sex Differentiation
GH and IGF Treatment
Growth
Programming/Epigenetics
GH and IGF Physiology
P1-1
Evaluation of Glucose Metabolism and Cardiovascular Risk Factors and Hyperandrogenemia in Prepubertal Girls with Premature Pubarche
Digdem Bezen, Filiz Tutunculer, Emine Dilek, Didem Ag Seleci, Hakan Erbas
Evaluation of Glucose Metabolism and Cardiovascular Risk Factors and Hyperandrogenemia in Prepubertal Girls with Premature Pubarche
Digdem Bezen, Filiz Tutunculer, Emine Dilek, Didem Ag Seleci, Hakan Erbas
P1-10
Use of a Cord Blood F-Dex Monocyte Binding Assay to Study the Glucocorticoid Receptor in Neonates
Arun Kashyap, Javier Aisenberg, Steven Ghanny
Use of a Cord Blood F-Dex Monocyte Binding Assay to Study the Glucocorticoid Receptor in Neonates
Arun Kashyap, Javier Aisenberg, Steven Ghanny
P1-11
Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with a Reversible Cardiomyopathy Caused by a Novel CYP11B1 Mutation: Report of Three Cases
Mohammad Ahmad Awwad Alqahtani, Ayed A Shati, Minjing Zou, Ali M Alsuheel, Abdullah A Alhayani, Saleh M Al-Qahtani, Hessa M Gilban, Brain F Meyer, Yufei Shi
Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with a Reversible Cardiomyopathy Caused by a Novel CYP11B1 Mutation: Report of Three Cases
Mohammad Ahmad Awwad Alqahtani, Ayed A Shati, Minjing Zou, Ali M Alsuheel, Abdullah A Alhayani, Saleh M Al-Qahtani, Hessa M Gilban, Brain F Meyer, Yufei Shi
P1-144
Primary Adrenal Insufficiency in children
without congenital adrenal hyperplasia:
Molecular and clinical characterization of a nationwide cohort
Tulay Guran, Federica Buonocore, Nurcin Saka, Mehmet Nuri Ozbek, Zehra Aycan, Abdullah Bereket, Firdevs Bas, Sukran Darcan, Aysun Bideci, Serap Turan, Ayla Guven, Omer Tarim, Sebahat Yilmaz Agladioglu, Zeynep Atay, Samim Ozen, Korcan Demir, Aysehan Akinci, Banu Kucukemre Aydin, Muammer Buyukinan, Bilgin Yuksel, Metin Yildiz, Teoman Akcay, Cengiz Kara, Tolga Ozgen, Gonul Catli, Emregul Isik, Semih Bolu, Bayram Ozhan, Fatih Gurbuz, Ahmet Ucar, Huseyin Demirbilek, Zehra Yavas Abali, Esra Doger, Erdal Eren, Merih Berberoglu, Bulent Hacihamdioglu, John C. Achermann
Primary Adrenal Insufficiency in children
without congenital adrenal hyperplasia:
Molecular and clinical characterization of a nationwide cohort
Tulay Guran, Federica Buonocore, Nurcin Saka, Mehmet Nuri Ozbek, Zehra Aycan, Abdullah Bereket, Firdevs Bas, Sukran Darcan, Aysun Bideci, Serap Turan, Ayla Guven, Omer Tarim, Sebahat Yilmaz Agladioglu, Zeynep Atay, Samim Ozen, Korcan Demir, Aysehan Akinci, Banu Kucukemre Aydin, Muammer Buyukinan, Bilgin Yuksel, Metin Yildiz, Teoman Akcay, Cengiz Kara, Tolga Ozgen, Gonul Catli, Emregul Isik, Semih Bolu, Bayram Ozhan, Fatih Gurbuz, Ahmet Ucar, Huseyin Demirbilek, Zehra Yavas Abali, Esra Doger, Erdal Eren, Merih Berberoglu, Bulent Hacihamdioglu, John C. Achermann
P1-145
Clinical follow-up of the first SF-1 deficient female patient
Karine Gerster, Anna Biason-Lauber, Eugen J. Schoenle
Clinical follow-up of the first SF-1 deficient female patient
Karine Gerster, Anna Biason-Lauber, Eugen J. Schoenle
P1-2
ONTOGENY OF THE SYNCHRONIZATION BETWEEN ADRENAL CLOCK GENES, ADRENAL STEROIDOGENESIS-RELATED GENES AND THE CIRCADIAN RHYTHM OF THE HPA AXIS IN RATS
Silvia Ruiz, Clarissa Martins, Margaret Castro, Sonir Antonini, Edson Martinez, Ayrton Moreira
ONTOGENY OF THE SYNCHRONIZATION BETWEEN ADRENAL CLOCK GENES, ADRENAL STEROIDOGENESIS-RELATED GENES AND THE CIRCADIAN RHYTHM OF THE HPA AXIS IN RATS
Silvia Ruiz, Clarissa Martins, Margaret Castro, Sonir Antonini, Edson Martinez, Ayrton Moreira
P1-3
Are heterozygous carriers of CYP21A2 less vulnerable to psychological stress?
Anna Nordenström, Agnieszka Butwicka, Henrik Falhammar, Angelica Lindén Hirschberg, Catharina Almqvist, Agneta Nordenskjöld, Louise Frisén
Are heterozygous carriers of CYP21A2 less vulnerable to psychological stress?
Anna Nordenström, Agnieszka Butwicka, Henrik Falhammar, Angelica Lindén Hirschberg, Catharina Almqvist, Agneta Nordenskjöld, Louise Frisén
P1-4
Effect of CYP17A1 inhibitors orteronel and galeterone on adrenal androgen biosynthesis.
Sameer S. Udhane, Amit V. Pandey
Effect of CYP17A1 inhibitors orteronel and galeterone on adrenal androgen biosynthesis.
Sameer S. Udhane, Amit V. Pandey
P1-5
Genetic heterogeneity in triple A syndrome – discrimination of the classic syndrome from two triple A-like syndromes
Angela Huebner, Felix Reschke, Ingo Kurth, Susann Kutzner, Eda Utine, Filiz Hazan, Dana Landgraf, Christian A. Hübner, Katrin Koehler
Genetic heterogeneity in triple A syndrome – discrimination of the classic syndrome from two triple A-like syndromes
Angela Huebner, Felix Reschke, Ingo Kurth, Susann Kutzner, Eda Utine, Filiz Hazan, Dana Landgraf, Christian A. Hübner, Katrin Koehler
P1-6
Genetic diagnosis of congenital primary adrenal insufficiency by Massive Parallel Sequencing (MPS).
Florence Roucher Boulez, Delphine Mallet Motak, Mad-Helenie Guerrin Elsensohn, Claire Bardel, Pascal Roy, Yves Morel
Genetic diagnosis of congenital primary adrenal insufficiency by Massive Parallel Sequencing (MPS).
Florence Roucher Boulez, Delphine Mallet Motak, Mad-Helenie Guerrin Elsensohn, Claire Bardel, Pascal Roy, Yves Morel
P1-7
Carriers of 21- Hydroxylase Deficiency Demonstrate Increased Psychological Vulnerability to Stress
Georgia Koltsida, Ioanna Farakla, Aikaterini Papanikolaou, Gerasimos Kolaitis, Emilia Mantzou, Evangelia Charmandari
Carriers of 21- Hydroxylase Deficiency Demonstrate Increased Psychological Vulnerability to Stress
Georgia Koltsida, Ioanna Farakla, Aikaterini Papanikolaou, Gerasimos Kolaitis, Emilia Mantzou, Evangelia Charmandari
P1-8
CORTISOL – CORTISONE RATIO AND METALLOPROTEINASE-9 EMERGING AS RISK FACTORS ASSOCIATED WITH PEDIATRICS HIPERTENSION
Alejandro Martinez-Aguayo, Carmen Campino, Rene Baudrand, Cristian Carvajal, Constanza Pinochet, Hernan Garcia, Rodrigo Bancalari, Alejandra Tapia, Lorena Garcia, Carolina Loureiro, Carolina Mendoza, Andrea Vecchiola, Carolina Valdivia, Cristobal Fuente, Carlos Lagos, Francisca Grob, Sandra Solari, Fidel Allende, Alexis Kalergis, Carlos Fardella
CORTISOL – CORTISONE RATIO AND METALLOPROTEINASE-9 EMERGING AS RISK FACTORS ASSOCIATED WITH PEDIATRICS HIPERTENSION
Alejandro Martinez-Aguayo, Carmen Campino, Rene Baudrand, Cristian Carvajal, Constanza Pinochet, Hernan Garcia, Rodrigo Bancalari, Alejandra Tapia, Lorena Garcia, Carolina Loureiro, Carolina Mendoza, Andrea Vecchiola, Carolina Valdivia, Cristobal Fuente, Carlos Lagos, Francisca Grob, Sandra Solari, Fidel Allende, Alexis Kalergis, Carlos Fardella
P1-9
Founder Effect and the Clinical and Molecular Characteristics in a Cohort of Classical and Non-Classical Congenital Lipoid Adrenal Hyperplasia (CLAH) due to StAR Mutations
Abdulsalam Abu-Libdeh, Ariella Weinberg Shokrun, Ephrat Levy-Lahad, Osnat Admoni, Yardena Tenenbaum-Rakover, David Zangen
Founder Effect and the Clinical and Molecular Characteristics in a Cohort of Classical and Non-Classical Congenital Lipoid Adrenal Hyperplasia (CLAH) due to StAR Mutations
Abdulsalam Abu-Libdeh, Ariella Weinberg Shokrun, Ephrat Levy-Lahad, Osnat Admoni, Yardena Tenenbaum-Rakover, David Zangen
P2-166
Late diagnosis of adrenal insufficiency caused by novel compound heterozygous mutations in POMC.
Elena Frolova, Irina Shirokova, Svetlana Karpova, Anna Kolodkina, Nina Makretskaya, Anatoly Tiulpakov
Late diagnosis of adrenal insufficiency caused by novel compound heterozygous mutations in POMC.
Elena Frolova, Irina Shirokova, Svetlana Karpova, Anna Kolodkina, Nina Makretskaya, Anatoly Tiulpakov
P2-167
Hyponatraemia secondary to exudative eczema
Irene Pilar Fernandez Viseras, Michal Ajzensztejn
Hyponatraemia secondary to exudative eczema
Irene Pilar Fernandez Viseras, Michal Ajzensztejn
P2-168
The Natural Mutant Receptor hGRαT556I Causes Primary Generalized Glucocorticoid Resistance Through Decreased Affinity for the Ligand and Impaired Interaction with the GRIP1 Coactivator
Nicolas C. Nicolaides, Eirini Skyrla, Dimitrios Vlachakis, Anna-Maria G. Psarra, Amalia Sertedaki, Sophia Kossida, Evangelia Charmandari
The Natural Mutant Receptor hGRαT556I Causes Primary Generalized Glucocorticoid Resistance Through Decreased Affinity for the Ligand and Impaired Interaction with the GRIP1 Coactivator
Nicolas C. Nicolaides, Eirini Skyrla, Dimitrios Vlachakis, Anna-Maria G. Psarra, Amalia Sertedaki, Sophia Kossida, Evangelia Charmandari
P2-169
References values under Synacthen® test for 6 steroids in serum by LC-MS/MS
marie Souillot, ingrid Plotton, chantal Rigaud, veronique Tardy, severine Ruet, yves Morel
References values under Synacthen® test for 6 steroids in serum by LC-MS/MS
marie Souillot, ingrid Plotton, chantal Rigaud, veronique Tardy, severine Ruet, yves Morel
P2-170
Usefulness of salivary cortisol levels in secondary adrenal insufficiency in pediatric population
Raquel Corripio, Jacobo Pérez, Ariadna Borràs, Laura Capdevila, Judith Sánchez, Josefa Rivera
Usefulness of salivary cortisol levels in secondary adrenal insufficiency in pediatric population
Raquel Corripio, Jacobo Pérez, Ariadna Borràs, Laura Capdevila, Judith Sánchez, Josefa Rivera
P2-171
Acute adrenal failure in a term newborn with congenital cytomegalovirus infection: case description and review of the literature
Lucia Marseglia, Tommaso Alterio, Lauretta Manti, Tommaso Aversa, Maria Rosa Calafiore, Eloisa Gitto, Malgorzata Wasniewska
Acute adrenal failure in a term newborn with congenital cytomegalovirus infection: case description and review of the literature
Lucia Marseglia, Tommaso Alterio, Lauretta Manti, Tommaso Aversa, Maria Rosa Calafiore, Eloisa Gitto, Malgorzata Wasniewska
P2-172
Resveratrol disrupts steroidogenesis in human fetal adrenals
Iuliia Savchuk, Olle Söder, Konstantin Svechnikov
Resveratrol disrupts steroidogenesis in human fetal adrenals
Iuliia Savchuk, Olle Söder, Konstantin Svechnikov
P2-173
Normal Ranges of Basal and Glucagon-Stimulated Free Cortisol in Children
Anita Schachter Davidov, Ori Eyal, Anat Becker Anat, Asaf Oren, Naftali Stern, Rona Limor, Naomi Weintrob
Normal Ranges of Basal and Glucagon-Stimulated Free Cortisol in Children
Anita Schachter Davidov, Ori Eyal, Anat Becker Anat, Asaf Oren, Naftali Stern, Rona Limor, Naomi Weintrob
P2-174
CLINICAL, BIOCHEMICAL AND MOLECULAR CHARACTERISTICS OF THE PATIENTS WITH NONCLASSICAL CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY IN CROATIA
Miroslav Dumic, Nevena Krnic, Vesna Kusec, Zorana Grubic, Katarina Stingl, Tony Yuen, Katja Dumic Kubat, Veselin Skrabic, Maria I. New
CLINICAL, BIOCHEMICAL AND MOLECULAR CHARACTERISTICS OF THE PATIENTS WITH NONCLASSICAL CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY IN CROATIA
Miroslav Dumic, Nevena Krnic, Vesna Kusec, Zorana Grubic, Katarina Stingl, Tony Yuen, Katja Dumic Kubat, Veselin Skrabic, Maria I. New
P2-175
Abnormal circadian blood pressure profile in patients with congenital adrenal hyperplasia without overt hypertension
Dominika Janus, Malgorzata Wojcik, Katarzyna Tyrawa, Jerzy Starzyk
Abnormal circadian blood pressure profile in patients with congenital adrenal hyperplasia without overt hypertension
Dominika Janus, Malgorzata Wojcik, Katarzyna Tyrawa, Jerzy Starzyk
P2-176
Triple A syndrome - the second most common cause of chronic adrenal insufficiency in North Africa?
Kahina Mohammedi, Asmahane Ladjouze, Ammar Tebaibia, Leila Kedji, Abdelmajid Maoudj, Karima Berkouk, Manoubia Bensmina, Souhila Amoura, Mohamed El Amine Boudjella, Abdennour Laraba
Triple A syndrome - the second most common cause of chronic adrenal insufficiency in North Africa?
Kahina Mohammedi, Asmahane Ladjouze, Ammar Tebaibia, Leila Kedji, Abdelmajid Maoudj, Karima Berkouk, Manoubia Bensmina, Souhila Amoura, Mohamed El Amine Boudjella, Abdennour Laraba
P2-179
Primary adrenal insufficiency: About a pediatric series
imen nardine, nora soumeya fedala, boubker derghoum, leyla ahmed ali, ali el mahdi haddam, djamila meskine, farida chentli
Primary adrenal insufficiency: About a pediatric series
imen nardine, nora soumeya fedala, boubker derghoum, leyla ahmed ali, ali el mahdi haddam, djamila meskine, farida chentli
P2-180
High-dose Hook Effect in 17- Hydroxyprogesterone Assay in 21-hydroxylase deficiency
Mesut Parlak, Doga Turkkahraman, Ayse Eda Parlak, Hamit Yasar Ellidag
High-dose Hook Effect in 17- Hydroxyprogesterone Assay in 21-hydroxylase deficiency
Mesut Parlak, Doga Turkkahraman, Ayse Eda Parlak, Hamit Yasar Ellidag
P2-181
Baseline cortisol concentrations predict positively and negatively anti- and pro- oxidation, respectively that are measured following an acute aerobic exercise bout in pre- and early pubertal normal-weight and obese boys.
George Paltoglou, Maria Papagianni, Ioannis G. Fatouros, Aimilia Mantzou, Athanasios Jamurtas, Alexandra Avloniti, Charikleia Stefanaki, Christina Kanaka-Gantenbein, George P. Chrousos, George Mastorakos
Baseline cortisol concentrations predict positively and negatively anti- and pro- oxidation, respectively that are measured following an acute aerobic exercise bout in pre- and early pubertal normal-weight and obese boys.
George Paltoglou, Maria Papagianni, Ioannis G. Fatouros, Aimilia Mantzou, Athanasios Jamurtas, Alexandra Avloniti, Charikleia Stefanaki, Christina Kanaka-Gantenbein, George P. Chrousos, George Mastorakos
P2-182
Insulin sensitivity and adipocytokynes in children with Classical Congenital Adrenal Hyperplasia
Nicola Improda, Manuela Cerbone, Andrea Esposito, Flavia Barbieri, Raffaella Di Mase, Donatella Capalbo, Mariacarolina Salerno
Insulin sensitivity and adipocytokynes in children with Classical Congenital Adrenal Hyperplasia
Nicola Improda, Manuela Cerbone, Andrea Esposito, Flavia Barbieri, Raffaella Di Mase, Donatella Capalbo, Mariacarolina Salerno
P2-183
24-hour urinary free cortisol as a screening test for Cushing’s syndrome in children.
Lucy Shapiro, Shezan Elahi, Joe Baliey, Les Perry, Lee Martin, Ashley Grossman, Scott Akker, John Monson, William Drake, Martin Savage, Helen Storr
24-hour urinary free cortisol as a screening test for Cushing’s syndrome in children.
Lucy Shapiro, Shezan Elahi, Joe Baliey, Les Perry, Lee Martin, Ashley Grossman, Scott Akker, John Monson, William Drake, Martin Savage, Helen Storr
P2-184
Familial Hyporeninemic Hyperkalemia and Hypertension (Pseudohypoaldosteronism Type II) in Infancy and Childhood.
Aaron Hanukoglu, Shira London, Rafael Halevi, Yardena Tenenbaum-Rakover
Familial Hyporeninemic Hyperkalemia and Hypertension (Pseudohypoaldosteronism Type II) in Infancy and Childhood.
Aaron Hanukoglu, Shira London, Rafael Halevi, Yardena Tenenbaum-Rakover
P2-185
Severe craniosynostosis syndrome associated to salt wasting congenital adrenal hyperplasia
Luciana Amorim Beltrão, Elisa Cordeiro Apolinario, Liana Capelo Costa, Yve Lozovei, Simone Martins Castro, Rafael Fabiano Machado Rosa, Cristiane Kopacek
Severe craniosynostosis syndrome associated to salt wasting congenital adrenal hyperplasia
Luciana Amorim Beltrão, Elisa Cordeiro Apolinario, Liana Capelo Costa, Yve Lozovei, Simone Martins Castro, Rafael Fabiano Machado Rosa, Cristiane Kopacek
P2-186
TESTICULAR ADRENAL CELL REST TUMORS ARE NOT ASSOCIATED WITH 21 HYDROXYLASE MUTATIONS OR THERAPY COMPLIANCE IN BOYS WITH CLASSIC FORM OF CAH
Mirjana Kocova, Vesna Janevska, Violeta Anastasovska, Elena Sukarova-Angelovska
TESTICULAR ADRENAL CELL REST TUMORS ARE NOT ASSOCIATED WITH 21 HYDROXYLASE MUTATIONS OR THERAPY COMPLIANCE IN BOYS WITH CLASSIC FORM OF CAH
Mirjana Kocova, Vesna Janevska, Violeta Anastasovska, Elena Sukarova-Angelovska
P2-187
A large family with a novel mutation in the SCNN1A gene causing a mild and transient form of autosomal recessive Pseudohypoaldosteronism type 1 (PHA1)
Alexandra Efthymiadou, Amalia Sertedaki, George Chrousos, Dionisios Chrysis
A large family with a novel mutation in the SCNN1A gene causing a mild and transient form of autosomal recessive Pseudohypoaldosteronism type 1 (PHA1)
Alexandra Efthymiadou, Amalia Sertedaki, George Chrousos, Dionisios Chrysis
P2-188
Phosphoglucomutase -1 deficiency presented as adrenal insufficiency
Neta Loewenthal, Ruti Parvari, Alon Haim, Judy Tavashi, Eli Hetshkovits
Phosphoglucomutase -1 deficiency presented as adrenal insufficiency
Neta Loewenthal, Ruti Parvari, Alon Haim, Judy Tavashi, Eli Hetshkovits
P2-189
The etiological spectrum of congenital adrenal hyperplasia based on molecular genetic analyses
Jin-Ho Choi, Ja Hye Kim, Eungu Kang, Ja Hyang Cho, Gu-Hwan Kim, Han-Wook Yoo
The etiological spectrum of congenital adrenal hyperplasia based on molecular genetic analyses
Jin-Ho Choi, Ja Hye Kim, Eungu Kang, Ja Hyang Cho, Gu-Hwan Kim, Han-Wook Yoo
P2-190
Higher serum DHEAS concentration is associated with lower plasma LDL cholesterol concentration in children
Aino Mäntyselkä, Jarmo Jääskeläinen, Virpi Lindi, Timo Lakka
Higher serum DHEAS concentration is associated with lower plasma LDL cholesterol concentration in children
Aino Mäntyselkä, Jarmo Jääskeläinen, Virpi Lindi, Timo Lakka
P2-191
Central adrenal insufficiency is not a common feature in CHARGE syndrome
Gianni Bocca, Monica Wong, Conny van Ravenswaaij-Arts
Central adrenal insufficiency is not a common feature in CHARGE syndrome
Gianni Bocca, Monica Wong, Conny van Ravenswaaij-Arts
P2-192
Baseline adrenal function by measurement of long term cortisol levels in scalp hair of asthmatic children using inhaled corticosteroids equals healthy controls.
Maria Smit, Ed van Leer, Gerard Noppe, Yolanda de Rijke, Jurriaan Hoekx, Erica van den Akker
Baseline adrenal function by measurement of long term cortisol levels in scalp hair of asthmatic children using inhaled corticosteroids equals healthy controls.
Maria Smit, Ed van Leer, Gerard Noppe, Yolanda de Rijke, Jurriaan Hoekx, Erica van den Akker
P2-193
Adrenal function in children born small for gestational age
Indre Petraitiene, Rasa Verkauskiene
Adrenal function in children born small for gestational age
Indre Petraitiene, Rasa Verkauskiene
P2-194
Cushing's syndrome in children and adolescents : About a pediatric serie
aicha houatia, soumeya nora fedala, ali el mahdi haddam, djamila meskine, farida chentli
Cushing's syndrome in children and adolescents : About a pediatric serie
aicha houatia, soumeya nora fedala, ali el mahdi haddam, djamila meskine, farida chentli
P2-195
Serum cortisol and cortisone ratio as sensitive tool to identify subjects with severe or partial 11β-hydroxysteroid dehydrogenase type 2 deficiency
Cristian Carvajal, Virginia Iturrieta, Carmen Campino, Carolina Valdivia, Jaime Lizama, Fidel Allende, Sandra Solari, René Baudrand, Carlos Lagos, Andrea Vecchiola, Alejandro Martínez-Aguayo, Hernán García, Carlos Fardella
Serum cortisol and cortisone ratio as sensitive tool to identify subjects with severe or partial 11β-hydroxysteroid dehydrogenase type 2 deficiency
Cristian Carvajal, Virginia Iturrieta, Carmen Campino, Carolina Valdivia, Jaime Lizama, Fidel Allende, Sandra Solari, René Baudrand, Carlos Lagos, Andrea Vecchiola, Alejandro Martínez-Aguayo, Hernán García, Carlos Fardella
P2-196
The role of de Nurse practitioner in optimizing care for Children with Congenital Adrenal Hyperplasia
Viviane van de Crommert, Janiëlle van Alfen-van der Velden, Annelieke van der Linde, Kees Noordam, Hedi Claahsen-van der Grinten
The role of de Nurse practitioner in optimizing care for Children with Congenital Adrenal Hyperplasia
Viviane van de Crommert, Janiëlle van Alfen-van der Velden, Annelieke van der Linde, Kees Noordam, Hedi Claahsen-van der Grinten
P2-197
Evaluation of medical treatment in the first 2 years of life with a new Dutch national longitudinal registry for children with congenital adrenal hyperplasia (CAH)
Annelieke van der Linde, Erica van den Akker, Willy Bakker- van Waarde, Sabine Hannema, Gea Hoorweg-Nijman, Hetty van de Kamp, Daniel Klink, Roelof Odink, Saartje Straetemans, Paul van Trotsenburg, Paul Verkerk, Hedi Claahsen-van der Grinten
Evaluation of medical treatment in the first 2 years of life with a new Dutch national longitudinal registry for children with congenital adrenal hyperplasia (CAH)
Annelieke van der Linde, Erica van den Akker, Willy Bakker- van Waarde, Sabine Hannema, Gea Hoorweg-Nijman, Hetty van de Kamp, Daniel Klink, Roelof Odink, Saartje Straetemans, Paul van Trotsenburg, Paul Verkerk, Hedi Claahsen-van der Grinten
P2-198
Incidence of nonclassical 21-hydroxylase deficiency in Russian population as estimated by the carrier frequency of V281L mutation
Tatiana Anosova, Anatoly Tiulpakov
Incidence of nonclassical 21-hydroxylase deficiency in Russian population as estimated by the carrier frequency of V281L mutation
Tatiana Anosova, Anatoly Tiulpakov
P2-199
CARDIO-METABOLIC RISK FACTORS IN CHILDREN AND ADOLESCENTS WITH CLASSICAL 21-HYDROXYLASE DEFICIENCY
Kansuda Ariyawatkul, Supatporn Tepmongkol, Taninee Sahakitrungruang
CARDIO-METABOLIC RISK FACTORS IN CHILDREN AND ADOLESCENTS WITH CLASSICAL 21-HYDROXYLASE DEFICIENCY
Kansuda Ariyawatkul, Supatporn Tepmongkol, Taninee Sahakitrungruang
P2-200
A novel mutation (c.delG209) in the proopiomelanocortin (POMC) gene in a child with early-onset obesity
Semra Cetinkaya, Tulay Guran, Erdal Kurnaz, Meliksah Keskin, Elif Sagsak, Senay Savas Erdeve, Federica Buonocore, Zehra Aycan
A novel mutation (c.delG209) in the proopiomelanocortin (POMC) gene in a child with early-onset obesity
Semra Cetinkaya, Tulay Guran, Erdal Kurnaz, Meliksah Keskin, Elif Sagsak, Senay Savas Erdeve, Federica Buonocore, Zehra Aycan
P2-201
IMPROVED LINEAR GROWTH IN PATIENTS WITH CLASSICAL CONGENITAL ADRENAL HYPERPLASIA.
Silvia Roma, Carla Bizzarri, Giuseppe Scirè, Gian Luigi Spadoni, Marco Cappa, Chiara Maggioli
IMPROVED LINEAR GROWTH IN PATIENTS WITH CLASSICAL CONGENITAL ADRENAL HYPERPLASIA.
Silvia Roma, Carla Bizzarri, Giuseppe Scirè, Gian Luigi Spadoni, Marco Cappa, Chiara Maggioli
P3-581
New mutation causing systemic Pseudohypoaldosteronism
Stefania Pedicelli, Paola Cambiaso, Maria-Christina Zennaro, Giusy Ferro, Stefano Cianfarani, Marco Cappa
New mutation causing systemic Pseudohypoaldosteronism
Stefania Pedicelli, Paola Cambiaso, Maria-Christina Zennaro, Giusy Ferro, Stefano Cianfarani, Marco Cappa
P3-582
Rapid Molecular Diagnosis of CAH by Strip Hybridization Assay in DEMPU
Fatma El-Mougy, Mona Hafez, Sahar Abdel Atty, Amany Ibrahim, Hend Mehawed, Noha Musa, Sherif Ekladious, Marwa Elsharkawy, Mona Abdullatif, Alaa Afif, Heba El Baz
Rapid Molecular Diagnosis of CAH by Strip Hybridization Assay in DEMPU
Fatma El-Mougy, Mona Hafez, Sahar Abdel Atty, Amany Ibrahim, Hend Mehawed, Noha Musa, Sherif Ekladious, Marwa Elsharkawy, Mona Abdullatif, Alaa Afif, Heba El Baz
P3-583
Insufficient mineralocorticoid replacement as a predictor factor for the TART in boys with congenital adrenal hyperplasia
Igor Chugunov, Maria Kareva, Elizaveta Orlova, Elvira Kuznecova
Insufficient mineralocorticoid replacement as a predictor factor for the TART in boys with congenital adrenal hyperplasia
Igor Chugunov, Maria Kareva, Elizaveta Orlova, Elvira Kuznecova
P3-584
CYP11B1 Gene Mutations in Patients with Congenital Adrenal Hyperplasia in Turkey
FIRDEVS BAS, BERRIN ERGUN-LONGMIRE, NURCIN SAKA, GUVEN TOKSOY, OYA UYGUNER, SUKRAN POYRAZOGLU, SHAUN AHMED, EDWARD COBB, UMUT ALTUNOGLU, RUVEYDE BUNDAK, FEYZA DARENDELILER, HULYA GUNOZ, MARIA I NEW, ROBERT WILSON
CYP11B1 Gene Mutations in Patients with Congenital Adrenal Hyperplasia in Turkey
FIRDEVS BAS, BERRIN ERGUN-LONGMIRE, NURCIN SAKA, GUVEN TOKSOY, OYA UYGUNER, SUKRAN POYRAZOGLU, SHAUN AHMED, EDWARD COBB, UMUT ALTUNOGLU, RUVEYDE BUNDAK, FEYZA DARENDELILER, HULYA GUNOZ, MARIA I NEW, ROBERT WILSON
P3-585
Living with adrenal hyperplasia for children in primary school between 6 and 11 years.
Educational innovation and design of a learning tool for therapeutic education
Catherine PIENKOWSKI, Audrey CARTAULT, Adelaide DURAND, Zeina AJALTOUNI, Béatrice JOURET, Maithé TAUBER
Living with adrenal hyperplasia for children in primary school between 6 and 11 years.
Educational innovation and design of a learning tool for therapeutic education
Catherine PIENKOWSKI, Audrey CARTAULT, Adelaide DURAND, Zeina AJALTOUNI, Béatrice JOURET, Maithé TAUBER
P3-586
Longitudinal changes during prepubertal years in visceral fat and steroid hormones - SGA versus AGA children
Carina Ankarberg-Lindgren, Mats X Andersson, Ann-Katrine Karlsson, Jovanna Dahlgren
Longitudinal changes during prepubertal years in visceral fat and steroid hormones - SGA versus AGA children
Carina Ankarberg-Lindgren, Mats X Andersson, Ann-Katrine Karlsson, Jovanna Dahlgren
P3-587
ADRENAL ATROPHY SECONDARY TO INAPPROPRIATE ORAL ADMINISTRATION OF EXOGENOUS STEROID PRESENTING WITH HYPERCALCEMIA
Ayla Güven, Suna Kılınç, Didem Helvacıoğlu, L.İhsan Kuru
ADRENAL ATROPHY SECONDARY TO INAPPROPRIATE ORAL ADMINISTRATION OF EXOGENOUS STEROID PRESENTING WITH HYPERCALCEMIA
Ayla Güven, Suna Kılınç, Didem Helvacıoğlu, L.İhsan Kuru
P3-588
CASE REPORT: HYPOTHYROIDISM AND ACTH-DEFICIENCY CAUSED BY TBX 19 MUTATION:
COINCIDENCE OR PATHOGENETIC CORRELATION?
Esther Schulz, Halit Ilker Akkurt, Chris Mühlhausen, René Santer, Maik Welzel, Paul Martin Holterhus
CASE REPORT: HYPOTHYROIDISM AND ACTH-DEFICIENCY CAUSED BY TBX 19 MUTATION:
COINCIDENCE OR PATHOGENETIC CORRELATION?
Esther Schulz, Halit Ilker Akkurt, Chris Mühlhausen, René Santer, Maik Welzel, Paul Martin Holterhus
P3-589
Deletion Mapping in Xp21 for a family With Complex Glycerol Kinase Deficiency Using Array-based comparative genomic hybridization
Zhangqian Zheng, Feihong Luo, Bingbing Wu, Miaoying Zhang
Deletion Mapping in Xp21 for a family With Complex Glycerol Kinase Deficiency Using Array-based comparative genomic hybridization
Zhangqian Zheng, Feihong Luo, Bingbing Wu, Miaoying Zhang
P3-590
Characterization of Ovarian Adrenal Rest Tumors in Children and Adolescent Females with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency
Zhe Su, Yanhong Li, Huamei Ma, Minlian Du
Characterization of Ovarian Adrenal Rest Tumors in Children and Adolescent Females with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency
Zhe Su, Yanhong Li, Huamei Ma, Minlian Du
P3-591
Pseudohypoaldosteronism – Subtle presentations with critical electrolyte imbalances Experiences from one hospital
Caroline Ponmani, Kostas Karampoulos, Morgan Keane, Sylevester Gomes, Aber Eaqub, Kausik Banerjee
Pseudohypoaldosteronism – Subtle presentations with critical electrolyte imbalances Experiences from one hospital
Caroline Ponmani, Kostas Karampoulos, Morgan Keane, Sylevester Gomes, Aber Eaqub, Kausik Banerjee
P3-592
Atypical prednisone-metabolism: Pharmacological studies in a boy with classical adrenal hyperplasia and suspected malcompliance
Melanie Hess, Adrian Derungs, Urs W. Zumsteg, Gabor Szinnai
Atypical prednisone-metabolism: Pharmacological studies in a boy with classical adrenal hyperplasia and suspected malcompliance
Melanie Hess, Adrian Derungs, Urs W. Zumsteg, Gabor Szinnai
P3-593
CYP21A2 gene mutations analysis in 21 Chinese patients with salt-wasting form of congenital adrenal hyperplasia
Hui Yao, Luhong Yang, Xiaoli Huang, Xiaohong Chen
CYP21A2 gene mutations analysis in 21 Chinese patients with salt-wasting form of congenital adrenal hyperplasia
Hui Yao, Luhong Yang, Xiaoli Huang, Xiaohong Chen
P3-594
X-Linked Adrenoleucodystrophy (X-ALD) presenting as Addison’s disease in childhood: a case report.
Antonella Meloni, Mauro Congia, Maria Rosaria Casini, Silvia Ibba, Marco Bonomi, Maria Cristina Rosatelli
X-Linked Adrenoleucodystrophy (X-ALD) presenting as Addison’s disease in childhood: a case report.
Antonella Meloni, Mauro Congia, Maria Rosaria Casini, Silvia Ibba, Marco Bonomi, Maria Cristina Rosatelli
P3-595
Three Siblings with Corticosterone Methyloxidase Deficiency Type 2 due to c.1175T>C mutation + a Novel c.788T>A Mutation in CYP11B2 gene
Bahar Ozcabi, Olcay Evliyaoglu, Oya Ercan, Feride Tahmiscioglu Bucak, Amra Adrovic, Serdar Ceylaner
Three Siblings with Corticosterone Methyloxidase Deficiency Type 2 due to c.1175T>C mutation + a Novel c.788T>A Mutation in CYP11B2 gene
Bahar Ozcabi, Olcay Evliyaoglu, Oya Ercan, Feride Tahmiscioglu Bucak, Amra Adrovic, Serdar Ceylaner
P3-597
Generalized glucocorticoid resistance in an adolescent girl with severe hyperandrogenia without mutations in NR3C1 gene.
Nadezhda Makazan, Elizaveta Orlova, Maria Kareva
Generalized glucocorticoid resistance in an adolescent girl with severe hyperandrogenia without mutations in NR3C1 gene.
Nadezhda Makazan, Elizaveta Orlova, Maria Kareva
P3-598
Remission with Cabergolin with Recurrent hypercortisolism after pituitary surgery in Cushing’s Disease
Samim Ozen, Nurhan Ozcan, Ilkin Majidov, Tuncer Turhan, Celal Cinar, Damla Goksen, Sukran Darcan
Remission with Cabergolin with Recurrent hypercortisolism after pituitary surgery in Cushing’s Disease
Samim Ozen, Nurhan Ozcan, Ilkin Majidov, Tuncer Turhan, Celal Cinar, Damla Goksen, Sukran Darcan
P3-599
Phaeochromocytoma in placental mesenchymal dysplasia: who should we screen and for how long?
Mary White, George McGillivray, Sue White, Margaret Zacharin
Phaeochromocytoma in placental mesenchymal dysplasia: who should we screen and for how long?
Mary White, George McGillivray, Sue White, Margaret Zacharin
P3-600
A DOUBLE DOSE OF TRIPLES
V.SRI NAGESH, Y. MURALIDHAR REDDY, PRAJNYA RANGANATH, SHAGUN AGGARWAL, VIKRANT REDDY
A DOUBLE DOSE OF TRIPLES
V.SRI NAGESH, Y. MURALIDHAR REDDY, PRAJNYA RANGANATH, SHAGUN AGGARWAL, VIKRANT REDDY
P3-601
Central cortisol deficiency (isolated ACTH deficiency)in a child.
Fawzia Alyafei, Ashraf Soliman
Central cortisol deficiency (isolated ACTH deficiency)in a child.
Fawzia Alyafei, Ashraf Soliman
P3-602
THE FIRST CASE OF PRIMARY GENERALIZED GLUCOCORTICOID RESISTANCE IN SERBIA IN AN 8 YEAR OLD BOY WITH G679S MUTATION OF THE NR3C1 GENE
Katarina Mitrovic, Rade Vukovic, Tatjana Milenkovic, Sladjana Todorovic, Ljiljana Plavsic, Dragan Zdravkovic
THE FIRST CASE OF PRIMARY GENERALIZED GLUCOCORTICOID RESISTANCE IN SERBIA IN AN 8 YEAR OLD BOY WITH G679S MUTATION OF THE NR3C1 GENE
Katarina Mitrovic, Rade Vukovic, Tatjana Milenkovic, Sladjana Todorovic, Ljiljana Plavsic, Dragan Zdravkovic
P3-603
A CASE OF PHEOCHROMOCYTOMA DIAGNOSED AS ADRENAL INCIDENTALOMA
Dogus Vuralli, Pinar Isik Agras, Esra Tapci, Yildiz Bilge Dallar
A CASE OF PHEOCHROMOCYTOMA DIAGNOSED AS ADRENAL INCIDENTALOMA
Dogus Vuralli, Pinar Isik Agras, Esra Tapci, Yildiz Bilge Dallar
P3-604
Severe high blood pressure with renal failure in a neglected case of 11β-hydroxylase deficient congenital adrenal hyperplasia (11β-OH CAH)
Alina Daniela Belceanu, Mihaela Munteanu, Mariana Florea, Maria-Christina Ungureanu, George Zmau, Mirela Puiu, Ioana Armasu, Voichita Mogos, Carmen Vulpoi
Severe high blood pressure with renal failure in a neglected case of 11β-hydroxylase deficient congenital adrenal hyperplasia (11β-OH CAH)
Alina Daniela Belceanu, Mihaela Munteanu, Mariana Florea, Maria-Christina Ungureanu, George Zmau, Mirela Puiu, Ioana Armasu, Voichita Mogos, Carmen Vulpoi
P3-605
Delayed diagnosis of salt wasting congenital adrenal hyperplasia, without complications of cortisol deficiency: a case report
Karijn Pijnenburg-Kleizen, Kees Noordam, Barto Otten, Hedi Claahsen-van der Grinten
Delayed diagnosis of salt wasting congenital adrenal hyperplasia, without complications of cortisol deficiency: a case report
Karijn Pijnenburg-Kleizen, Kees Noordam, Barto Otten, Hedi Claahsen-van der Grinten
P3-606
Familial Hyperaldosteronism Type I in an infant without hypertension: how important could be the early treatment with hydrocortisone?
Alejandro Martinez-Aguayo, Carolina Mendoza, Carolina Loureiro, Carmen Campino, Cristian Carvajal, Rene Baudrand, Hana Rumie, Rodrigo Bancalari, Hernan Garcia, Andrea Vecchiola, Carolina Valdivia, Carlos Fardella
Familial Hyperaldosteronism Type I in an infant without hypertension: how important could be the early treatment with hydrocortisone?
Alejandro Martinez-Aguayo, Carolina Mendoza, Carolina Loureiro, Carmen Campino, Cristian Carvajal, Rene Baudrand, Hana Rumie, Rodrigo Bancalari, Hernan Garcia, Andrea Vecchiola, Carolina Valdivia, Carlos Fardella
P3-607
HOMOZYGOSITY FOR A MUTATION IN THE CYP11B2 GENE AND GH DEFICIENCY IN A CHILD WITH SEVERE GROWTH DELAY
Maria Cristina Maggio, Beatrice Vergara, Caterina Salvo, Paolo Porcelli, Carmelo Fabiano, Giovanni Corsello
HOMOZYGOSITY FOR A MUTATION IN THE CYP11B2 GENE AND GH DEFICIENCY IN A CHILD WITH SEVERE GROWTH DELAY
Maria Cristina Maggio, Beatrice Vergara, Caterina Salvo, Paolo Porcelli, Carmelo Fabiano, Giovanni Corsello
P3-608
A PROSPECTIVE EVALUATION OF ANTHROPOMETRIC AND METABOLIC PROFILE IN PREMATURE ADRENARCHE PATIENTS
gülcan seymen karabulut, murat imal, filiz mine çizmecioğlu, sukru hatun
A PROSPECTIVE EVALUATION OF ANTHROPOMETRIC AND METABOLIC PROFILE IN PREMATURE ADRENARCHE PATIENTS
gülcan seymen karabulut, murat imal, filiz mine çizmecioğlu, sukru hatun
P3-609
The prevalence of сongenital adrenal hyperplasia due to 21-hydroxylase deficiency among children 0-18 years old in Ukraine
Nataliya Zelinska, Nataliya Pogadayeva, Evgenia Globa, Irina Shevchenko
The prevalence of сongenital adrenal hyperplasia due to 21-hydroxylase deficiency among children 0-18 years old in Ukraine
Nataliya Zelinska, Nataliya Pogadayeva, Evgenia Globa, Irina Shevchenko
P3-610
Development of a patient with severe pseudohypoaldosteronism due to mutation in the alpha subunit of ENaC
Erwin Lankes, Heiko Krude, Dirk Schnabel
Development of a patient with severe pseudohypoaldosteronism due to mutation in the alpha subunit of ENaC
Erwin Lankes, Heiko Krude, Dirk Schnabel
P3-611
Methodological considerations into the approach for genetic diagnostics of CAH in a girl with SW form and relatively higher needs of mineralcorticoids
Ganka Dineva, Iva Stoeva, Andrey Kirov, Albena Todorova, Daniel Iliev, Narcis Kaleva, L. Grozdanova
Methodological considerations into the approach for genetic diagnostics of CAH in a girl with SW form and relatively higher needs of mineralcorticoids
Ganka Dineva, Iva Stoeva, Andrey Kirov, Albena Todorova, Daniel Iliev, Narcis Kaleva, L. Grozdanova
P3-612
11β-hydroxylase deficiency: Twenty years follow-up
Ayla Güven, Didem Helvacioglu, Suna Kilinç
11β-hydroxylase deficiency: Twenty years follow-up
Ayla Güven, Didem Helvacioglu, Suna Kilinç
P3-613
Near-final height outcome of congenital adrenal hyperplasia (CAH) due to classic 21-hydroxylase deficiency(21OHD) in 55 Chinese patients
Juan Lin, Huamei Ma, Yanhong LI, Minlian DU, Hongshan CHEN, Qiuli CHEN, Jun ZHANG
Near-final height outcome of congenital adrenal hyperplasia (CAH) due to classic 21-hydroxylase deficiency(21OHD) in 55 Chinese patients
Juan Lin, Huamei Ma, Yanhong LI, Minlian DU, Hongshan CHEN, Qiuli CHEN, Jun ZHANG
P3-614
Late diagnosis of childhood adrenal insufficiency and hypogonadotropic hypogonadism due to DAX 1 gene mutation
Maria Karantza, Sotirios Bogris, George Chrousos, Amalia Sertedaki
Late diagnosis of childhood adrenal insufficiency and hypogonadotropic hypogonadism due to DAX 1 gene mutation
Maria Karantza, Sotirios Bogris, George Chrousos, Amalia Sertedaki
P3-615
Paraaortical paragangliomas as incidental findings in a female adolescent.
Konstantina Mouzaki, Eleni Kotanidou, Maria Ioannidou, Evangelia Karaiskou, Ioannis Kyrgios, Georgios Arsos, Ioannis Tsitouridis, Ioannis Efstratiou, Maria Eboriadou-Petikopoulou, Assimina Galli-Tsinopoulou
Paraaortical paragangliomas as incidental findings in a female adolescent.
Konstantina Mouzaki, Eleni Kotanidou, Maria Ioannidou, Evangelia Karaiskou, Ioannis Kyrgios, Georgios Arsos, Ioannis Tsitouridis, Ioannis Efstratiou, Maria Eboriadou-Petikopoulou, Assimina Galli-Tsinopoulou
P3-616
Nephrotic syndrome developing in a girl with classic 21-hydroxylase deficiency---first report
Huamei MA, Juan LIN, Jun ZHANG, Yanhong LI, Qiuli CHEN, Hongshan CHEN, Minlian DU
Nephrotic syndrome developing in a girl with classic 21-hydroxylase deficiency---first report
Huamei MA, Juan LIN, Jun ZHANG, Yanhong LI, Qiuli CHEN, Hongshan CHEN, Minlian DU
P3-617
Conservative treatment allows substantial improvement of neonatal Cushing syndrome in McCune Albright syndrome, a 2 year follow-up.
Nancy, HG van Nieuwaal, Roderick, HJ Houwen, Hedi, L Claahsen - van der Grinten, Annemarie, A Verrijn Stuart
Conservative treatment allows substantial improvement of neonatal Cushing syndrome in McCune Albright syndrome, a 2 year follow-up.
Nancy, HG van Nieuwaal, Roderick, HJ Houwen, Hedi, L Claahsen - van der Grinten, Annemarie, A Verrijn Stuart
P3-618
A CYP21A2 gene mutation in patients with congenital adrenal hyperplasia:
Molecular genetics report from Saudi Arabia
Sarar Mohamed, Suzan El-Kholy, Nasir Al-Juryyan, Abdulrahman M. Al-Nemri, Khaled K. Abu-Amero
A CYP21A2 gene mutation in patients with congenital adrenal hyperplasia:
Molecular genetics report from Saudi Arabia
Sarar Mohamed, Suzan El-Kholy, Nasir Al-Juryyan, Abdulrahman M. Al-Nemri, Khaled K. Abu-Amero
P3-619
Adrenal cortex dysfunction as a consequence of chronic therapies other than oral steroid therapy – cases presentation.
Izabela Rogozinska, Krystyna Grela
Adrenal cortex dysfunction as a consequence of chronic therapies other than oral steroid therapy – cases presentation.
Izabela Rogozinska, Krystyna Grela
P3-620
A RARE CAUSE OF HYPERTENSION: PSEUDOPHEOCHROMOCYTOMA
Nihal Hatipoglu, Ulku Gul, Deniz Okdemir, Leyla Akin, Mustafa Kendirci, Selim Kurtoglu
A RARE CAUSE OF HYPERTENSION: PSEUDOPHEOCHROMOCYTOMA
Nihal Hatipoglu, Ulku Gul, Deniz Okdemir, Leyla Akin, Mustafa Kendirci, Selim Kurtoglu
P3-621
A Case of X-Linked Adrenal Hypoplasia Congenita; Adrenal Hypoplasia Congenita, Glycerol Kinase Deficiency and Duchenne Muscular Dystrophy
Bilgin Yuksel, Eda Mengen, Gül Cirkin Seker, Fatih Gurbuz, Ali Kemal Topaloglu
A Case of X-Linked Adrenal Hypoplasia Congenita; Adrenal Hypoplasia Congenita, Glycerol Kinase Deficiency and Duchenne Muscular Dystrophy
Bilgin Yuksel, Eda Mengen, Gül Cirkin Seker, Fatih Gurbuz, Ali Kemal Topaloglu
P3-622
Prenatal treatment of Congenital Adrenal Hyperplasia (CAH): A survey of Paediatric Endocrinologist.
Ethical group of Sociedad Española de Endocrinología Pediátrica (SEEP)
Maria J. Chueca Guindulain, Isolina Riaño-Galán, Elisabeth Blarduni Cardón, Mª Victoria Borras Pérez, Lidia Castro Feijóo, Ignacio Diez Lopez, Mª Angeles Donoso Sanz, Gertrudis Martí Aromir, Mª Teresa Muñoz Calvo, Pilar Terradas Mercader
Prenatal treatment of Congenital Adrenal Hyperplasia (CAH): A survey of Paediatric Endocrinologist.
Ethical group of Sociedad Española de Endocrinología Pediátrica (SEEP)
Maria J. Chueca Guindulain, Isolina Riaño-Galán, Elisabeth Blarduni Cardón, Mª Victoria Borras Pérez, Lidia Castro Feijóo, Ignacio Diez Lopez, Mª Angeles Donoso Sanz, Gertrudis Martí Aromir, Mª Teresa Muñoz Calvo, Pilar Terradas Mercader
P3-623
A case of ACTH resistance with generalized hyperpigmentation at birth
Takako Sasasaki, Amano Naoko, Satoshi Narumi, Tomonobu Hasegawa, Mai Tomita, Okada jyunichirou, Yatsuga Shuichi, Yasutoshi Koga
A case of ACTH resistance with generalized hyperpigmentation at birth
Takako Sasasaki, Amano Naoko, Satoshi Narumi, Tomonobu Hasegawa, Mai Tomita, Okada jyunichirou, Yatsuga Shuichi, Yasutoshi Koga
P3-624
Clinical and genotypic characterization of simple virilizing forms of congenital adrenal hyperplasia
Rita Cardoso, Susana Pacheco, Joana Serra Caetano, Isabel Dinis, Alice Mirante
Clinical and genotypic characterization of simple virilizing forms of congenital adrenal hyperplasia
Rita Cardoso, Susana Pacheco, Joana Serra Caetano, Isabel Dinis, Alice Mirante
P3-625
‛Reexpansion’ of testicular tissue after testis-sparing surgery in an adolescent
Yasar Sen, Emine Ayca Cimbek, Sevil Ari Yuca, Ilhan Ciftci, Fuat Bugrul
‛Reexpansion’ of testicular tissue after testis-sparing surgery in an adolescent
Yasar Sen, Emine Ayca Cimbek, Sevil Ari Yuca, Ilhan Ciftci, Fuat Bugrul
P3-626
Exogenous Cushing’s syndrome due to misuse of topical corticosteroid therapy
Maria Korpal- Szczyrska, Malgorzata Mysliwiec
Exogenous Cushing’s syndrome due to misuse of topical corticosteroid therapy
Maria Korpal- Szczyrska, Malgorzata Mysliwiec
P3-627
Familial Glucocorticoid Deficiency – A case report
Navoda Atapattu, Sureka Mohomad, Shammi Rathnasiri, Asoka Padmakanthi Wijesuriya
Familial Glucocorticoid Deficiency – A case report
Navoda Atapattu, Sureka Mohomad, Shammi Rathnasiri, Asoka Padmakanthi Wijesuriya
LBP-1259
Adrenal Steroid Precursors Accumulating in Congenital Adrenal Hyperplasia lead to Transactivation of the Glucocorticoid Receptor
Karijn Pijnenburg-Kleizen, Manon Engels, Christiaan Mooij, Aliesha Griffin, Nils Krone, Paul Span, Antonius van Herwaarden, Fred Sweep, Hedi Claahsen-van der Grinten
Adrenal Steroid Precursors Accumulating in Congenital Adrenal Hyperplasia lead to Transactivation of the Glucocorticoid Receptor
Karijn Pijnenburg-Kleizen, Manon Engels, Christiaan Mooij, Aliesha Griffin, Nils Krone, Paul Span, Antonius van Herwaarden, Fred Sweep, Hedi Claahsen-van der Grinten
P1-100
Atypical features in patients with Leprechaunism suggesting a wide clinical spectrum of disease
Harshini Katugampola, Nicola Improda, Pratik Shah, Hannah Gordon, Rakesh Amin, Catherine J Peters, Robert K Semple, Mehul T Dattani
Atypical features in patients with Leprechaunism suggesting a wide clinical spectrum of disease
Harshini Katugampola, Nicola Improda, Pratik Shah, Hannah Gordon, Rakesh Amin, Catherine J Peters, Robert K Semple, Mehul T Dattani
P1-102
The role of HNF1B in human pancreas development and diabetes
Ranna El Khairi, Andrew Hattersley, Ludovic Vallier
The role of HNF1B in human pancreas development and diabetes
Ranna El Khairi, Andrew Hattersley, Ludovic Vallier
P1-23
Safety and efficacy of treatment with long-acting lanreotide autogel® in early infancy in patients with congenital hyperinsulinism
Heike Corda, Thomas Meissner, Sebastian Kummer, Alena Welters, Norbert Teig
Safety and efficacy of treatment with long-acting lanreotide autogel® in early infancy in patients with congenital hyperinsulinism
Heike Corda, Thomas Meissner, Sebastian Kummer, Alena Welters, Norbert Teig
P1-24
The influence of miR-125b in pancreatic β-cell apoptosis
Bei Han, Ziyang Zhu, Wei Gu, Shining Ni, Ruixue Yang, Xing Shi, Xuewen Yuan, Wentao Gao
The influence of miR-125b in pancreatic β-cell apoptosis
Bei Han, Ziyang Zhu, Wei Gu, Shining Ni, Ruixue Yang, Xing Shi, Xuewen Yuan, Wentao Gao
P1-25
Lower Bone Mineral Density in type 1 Diabetes Mellitus (T1DM) is probably associated with Wnt/β-catenin pathway downregulation through increased Dickkopf-1 levels
Kyriaki Karavanaki, Charalampos Tsentidis, Lydia Kossiva, Antonios Marmarinos, Artemis Doulgeraki, Dimitrios Gourgiotis
Lower Bone Mineral Density in type 1 Diabetes Mellitus (T1DM) is probably associated with Wnt/β-catenin pathway downregulation through increased Dickkopf-1 levels
Kyriaki Karavanaki, Charalampos Tsentidis, Lydia Kossiva, Antonios Marmarinos, Artemis Doulgeraki, Dimitrios Gourgiotis
P1-26
Human Placenta-Derived Mesenchymal Stem Cells: a novel protocol for pancreatic differentiation.
Viviana Dora Patianna, Bernard Okere, Barbara Predieri, Patrizia Bruzzi, Lorenzo Iughetti
Human Placenta-Derived Mesenchymal Stem Cells: a novel protocol for pancreatic differentiation.
Viviana Dora Patianna, Bernard Okere, Barbara Predieri, Patrizia Bruzzi, Lorenzo Iughetti
P1-27
Activation of insulin signaling in gastrocnemius after central leptin infusion is associated with an increase in proliferation and muscle fiber size
Vicente Barrios, Emma Burgos-Ramos, Sandra Canelles, Amaia Rodríguez, Javier Gómez-Ambrosi, Julie A. Chowen, Gema Frühbeck, Jesús Argente
Activation of insulin signaling in gastrocnemius after central leptin infusion is associated with an increase in proliferation and muscle fiber size
Vicente Barrios, Emma Burgos-Ramos, Sandra Canelles, Amaia Rodríguez, Javier Gómez-Ambrosi, Julie A. Chowen, Gema Frühbeck, Jesús Argente
P1-28
Clinical characterisation of a novel RFX6 mutation- a rare cause of neonatal diabetes syndrome
Moira Cheung, Simon Chapman, Katie Hunt, Erin Makin, Ann Hickey, Jonathan Hind, Sian Ellard, Charles Buchanan, Ritika Kapoor
Clinical characterisation of a novel RFX6 mutation- a rare cause of neonatal diabetes syndrome
Moira Cheung, Simon Chapman, Katie Hunt, Erin Makin, Ann Hickey, Jonathan Hind, Sian Ellard, Charles Buchanan, Ritika Kapoor
P1-29
Is reduced heart rate variability associated with arterial stiffness in youth with childhood-onset type 1 diabetes mellitus?
Hwa Young Kim, Hae Woon Jung, Gyung Min Lee, So Youn Kim, Kyung A Jeong, Keun Hee Choi, Jieun Lee, Young Ah Lee, Choong Ho Shin, Sei Won Yang
Is reduced heart rate variability associated with arterial stiffness in youth with childhood-onset type 1 diabetes mellitus?
Hwa Young Kim, Hae Woon Jung, Gyung Min Lee, So Youn Kim, Kyung A Jeong, Keun Hee Choi, Jieun Lee, Young Ah Lee, Choong Ho Shin, Sei Won Yang
P1-30
A NOVEL MUTATION IN THE ABCC8 GENE CAUSING A VARIABLE PHENOTYPE OF IMPAIRED GLUCOSE METABOLISM IN THE SAME FAMILY
Evelina Maines, Khalid Hussain, Sarah E. Flanagan, Sian Ellard, Claudia Piona, Grazia Grazia Morandi, Sarah Dal Ben, Paolo Cavarzere, Franco Franco Antoniazzi, Rossella Gaudino
A NOVEL MUTATION IN THE ABCC8 GENE CAUSING A VARIABLE PHENOTYPE OF IMPAIRED GLUCOSE METABOLISM IN THE SAME FAMILY
Evelina Maines, Khalid Hussain, Sarah E. Flanagan, Sian Ellard, Claudia Piona, Grazia Grazia Morandi, Sarah Dal Ben, Paolo Cavarzere, Franco Franco Antoniazzi, Rossella Gaudino
P1-31
Type 1 Diabetes Onset: a story of innate and adaptive immune cells?
Ana Laura Fitas, Catarina Martins, Anabela Alonso, Glória Nunes, Rosa Pina, Daniela Amaral, Sigurd Lenzen, Lurdes Lopes, Luis Miguel Borrego, Catarina Limbert
Type 1 Diabetes Onset: a story of innate and adaptive immune cells?
Ana Laura Fitas, Catarina Martins, Anabela Alonso, Glória Nunes, Rosa Pina, Daniela Amaral, Sigurd Lenzen, Lurdes Lopes, Luis Miguel Borrego, Catarina Limbert
P1-32
Etiological diagnosis of diabetes in Italian diabetic children and adolescents
Maurizio Delvecchio, Giuseppina Salzano, Enza Mozzillo, Giulio Frontino, Ippolita Patrizia Patera, Sonia Toni, Ivana Rabbone, Valentino Cherubini, Stefano Tumini, Giuseppe D'Annunzio, Lorenzo Iughetti, Giulio Maltoni, Vittoria Cauvin, Marco Marigliano, Fabrizio Barbetti
Etiological diagnosis of diabetes in Italian diabetic children and adolescents
Maurizio Delvecchio, Giuseppina Salzano, Enza Mozzillo, Giulio Frontino, Ippolita Patrizia Patera, Sonia Toni, Ivana Rabbone, Valentino Cherubini, Stefano Tumini, Giuseppe D'Annunzio, Lorenzo Iughetti, Giulio Maltoni, Vittoria Cauvin, Marco Marigliano, Fabrizio Barbetti
P1-33
Improved genetic testing for monogenic diabetes in the Swiss population by targeted next generation sequencing
Mirjam Dirlewanger, Jean-Louis Blouin, Philippe Klee, Montserrat Castellsague-Perolini, Céline Girardin, Federico Santoni, Valérie Schwitzgebel
Improved genetic testing for monogenic diabetes in the Swiss population by targeted next generation sequencing
Mirjam Dirlewanger, Jean-Louis Blouin, Philippe Klee, Montserrat Castellsague-Perolini, Céline Girardin, Federico Santoni, Valérie Schwitzgebel
P1-34
Low bone mineral density is associated to poor glycemic control and increased dickkopf-1 (DKK-1) serum levels in children and adolescents with type 1 diabetes
Maria Felicia Faienza, Maurizio Delvecchio, Anna Fusillo, Antonella Lonero, Clara Zecchino, Angelo Acquafredda, Laura Piacente, Maria Grano, Luciano Cavallo, Giacomina Brunetti
Low bone mineral density is associated to poor glycemic control and increased dickkopf-1 (DKK-1) serum levels in children and adolescents with type 1 diabetes
Maria Felicia Faienza, Maurizio Delvecchio, Anna Fusillo, Antonella Lonero, Clara Zecchino, Angelo Acquafredda, Laura Piacente, Maria Grano, Luciano Cavallo, Giacomina Brunetti
P1-35
Effect of 6 months therapy with Metreleptin in an African American boy with Congenital generalized lipodystrophy.
Svetlana Ten, Amrit Bhangoo, Divya Khurana, Mark Flyer, Abhimanyu Garg
Effect of 6 months therapy with Metreleptin in an African American boy with Congenital generalized lipodystrophy.
Svetlana Ten, Amrit Bhangoo, Divya Khurana, Mark Flyer, Abhimanyu Garg
P1-36
Somatic paternal UPD on chromosome 11p15 in focal form of congenital hyperinsulinism (CHI) causes monoallelic expression of mutant ABCC8 and KCNJ11
Ina Dallmann, Silke Vogelgesang, Winfried Barthlen, Emine Varol, Wolfgang Mohnike, Susann Empting, Klaus Mohnike, Martin Zenker, Ilse Wieland
Somatic paternal UPD on chromosome 11p15 in focal form of congenital hyperinsulinism (CHI) causes monoallelic expression of mutant ABCC8 and KCNJ11
Ina Dallmann, Silke Vogelgesang, Winfried Barthlen, Emine Varol, Wolfgang Mohnike, Susann Empting, Klaus Mohnike, Martin Zenker, Ilse Wieland
P1-37
Hyperthyroidism in 276 Children and Adolescents with Type 1 Diabetes from Germany and Austria
Axel Dost, Tilman R. Rohrer, Elke Fröhlich-Reiterer, Esther Bollow, Beate Karges, Andreas Böckmann, Johannes Hamann, Reinhard W. Holl
Hyperthyroidism in 276 Children and Adolescents with Type 1 Diabetes from Germany and Austria
Axel Dost, Tilman R. Rohrer, Elke Fröhlich-Reiterer, Esther Bollow, Beate Karges, Andreas Böckmann, Johannes Hamann, Reinhard W. Holl
P1-38
METABOLIC SYNDROME FREQUENCY IN LONGITUDINALLY FOLLOWED CHILDREN WITH PREMATURE ADRENARCHE DURING PUBERTAL AGES
Gamze Kaya, Sükran Poyrazoglu, Oguz Bulent Erol, Seha Saygili, Mine Sükür, Firdevs Bas, Ruveyde Bundak, Feyza Darendeliler
METABOLIC SYNDROME FREQUENCY IN LONGITUDINALLY FOLLOWED CHILDREN WITH PREMATURE ADRENARCHE DURING PUBERTAL AGES
Gamze Kaya, Sükran Poyrazoglu, Oguz Bulent Erol, Seha Saygili, Mine Sükür, Firdevs Bas, Ruveyde Bundak, Feyza Darendeliler
P1-39
EVALUATION OF ABILITY OF URINARY PODOCALYXIN, NEPHRIN AND LIVER TYPE FATTY ACID BINDING PROTEIN FOR EARLY DIAGNOSIS IN RENAL INJURY IN ADOLESCENTS WITH TYPE 1 DIABETES
seniha kiremitci yilmaz, fatma taneli, arzu oran, gülgün yilmaz ovali, betül ersoy
EVALUATION OF ABILITY OF URINARY PODOCALYXIN, NEPHRIN AND LIVER TYPE FATTY ACID BINDING PROTEIN FOR EARLY DIAGNOSIS IN RENAL INJURY IN ADOLESCENTS WITH TYPE 1 DIABETES
seniha kiremitci yilmaz, fatma taneli, arzu oran, gülgün yilmaz ovali, betül ersoy
P1-40
Efficacy and safety of a fixed combination of insulin degludec/ insulin aspart in children and adolescents with type 1 diabetes
Tadej Battelino, Larry Deeb, Panagiota Diamantopoulou Reiter, Tina Maria Greve, Georgeanna Klingensmith, Miriana Kocova, Margarita Kovarenko, Naim Shehadeh
Efficacy and safety of a fixed combination of insulin degludec/ insulin aspart in children and adolescents with type 1 diabetes
Tadej Battelino, Larry Deeb, Panagiota Diamantopoulou Reiter, Tina Maria Greve, Georgeanna Klingensmith, Miriana Kocova, Margarita Kovarenko, Naim Shehadeh
P1-41
Current care and outcomes for children and young people with diabetes in England and Wales: Results from the National Paediatric Diabetes Audit
Naomi Holman, Fiona Campbell, Justin Warner
Current care and outcomes for children and young people with diabetes in England and Wales: Results from the National Paediatric Diabetes Audit
Naomi Holman, Fiona Campbell, Justin Warner
P1-42
Dynamics perceptions of their own health in the process of learning self-control adolescents with type 1 diabetes mellitus
Olena Budreiko, Olena Kirilova, Sergey Tsylyuryk, Svitlana Chumak
Dynamics perceptions of their own health in the process of learning self-control adolescents with type 1 diabetes mellitus
Olena Budreiko, Olena Kirilova, Sergey Tsylyuryk, Svitlana Chumak
P1-43
Evaluation of median nerve in children with type1 diabetes using ultrasonographic imaging and
electrophysiology
Nancy Elbarbary, Abeer Maghawry, Rana ElHilaly, Rania Refaat
Evaluation of median nerve in children with type1 diabetes using ultrasonographic imaging and
electrophysiology
Nancy Elbarbary, Abeer Maghawry, Rana ElHilaly, Rania Refaat
P1-44
Is metabolic control affected by military service in young adults with type 1 diabetes?
Avivit Brener, Eran Mel, Shlomit Shalitin, Liora Lazar, Liat de Vries, Ariel Tenebaum, Tal Oron, Moshe Philip, Yael Lebenthal
Is metabolic control affected by military service in young adults with type 1 diabetes?
Avivit Brener, Eran Mel, Shlomit Shalitin, Liora Lazar, Liat de Vries, Ariel Tenebaum, Tal Oron, Moshe Philip, Yael Lebenthal
P1-46
Trends in insulin therapy in 50,861 children and adolescents with type 1 diabetes from Austria and Germany between 2000 and 2014
Barbara Bohn, Susanna Wiegand, Sebastian Kummer, Ulrike Menzel, Olga Kordonouri, Claudia Böttcher, Elke Fröhlich-Reiterer, Reinhard W. Holl
Trends in insulin therapy in 50,861 children and adolescents with type 1 diabetes from Austria and Germany between 2000 and 2014
Barbara Bohn, Susanna Wiegand, Sebastian Kummer, Ulrike Menzel, Olga Kordonouri, Claudia Böttcher, Elke Fröhlich-Reiterer, Reinhard W. Holl
P1-47
RELATIVE HYPOALDOSTERONISM IN A PATIENT WITH WOLCOTT-RALLISON SYNDROME
Ahmet Ucar, Yusuf Aydemir, Ayse Dogan, Ebru Tuncez
RELATIVE HYPOALDOSTERONISM IN A PATIENT WITH WOLCOTT-RALLISON SYNDROME
Ahmet Ucar, Yusuf Aydemir, Ayse Dogan, Ebru Tuncez
P1-48
Structured Education Programmes for Children with Type 1 Diabetes – A Systematic Review
Anbezhil Subbarayan
Structured Education Programmes for Children with Type 1 Diabetes – A Systematic Review
Anbezhil Subbarayan
P2-243
Dyslipidemia in Children with Diabetes
Pei Kwee Lim, Rashida Vasanwala, Tuck Seng Cheng, Ngee Lek, Yuen Ching Angela Hui, Soo Ting Lim, Fabian Yap
Dyslipidemia in Children with Diabetes
Pei Kwee Lim, Rashida Vasanwala, Tuck Seng Cheng, Ngee Lek, Yuen Ching Angela Hui, Soo Ting Lim, Fabian Yap
P2-244
Diabetes mellitus and hypoparathyroidism in a girl with mitochondrial disease
Gonul Buyukyilmaz, Nazli Gonc, Goknur Haliloglu, Beril Talim, Alev Ozon, Ayfer Alikasifoglu, Nurgun Kandemir
Diabetes mellitus and hypoparathyroidism in a girl with mitochondrial disease
Gonul Buyukyilmaz, Nazli Gonc, Goknur Haliloglu, Beril Talim, Alev Ozon, Ayfer Alikasifoglu, Nurgun Kandemir
P2-245
Association of ghrelin levels and insulin resistance in small for gestational age rats
wangkai liu, zhenyu shen, minlian du, siqi zhuang, huamei ma
Association of ghrelin levels and insulin resistance in small for gestational age rats
wangkai liu, zhenyu shen, minlian du, siqi zhuang, huamei ma
P2-247
A case of Donohue Syndrome : New Genetic Mutation and added phenotypic characteristics
Fawzia Alyafei, Mahmoud Zyoid, , Ashraf Soliman, Anas Abdulkayoum, Rawia Jarir, Bader Kurdi, Laila Mahmoud
A case of Donohue Syndrome : New Genetic Mutation and added phenotypic characteristics
Fawzia Alyafei, Mahmoud Zyoid, , Ashraf Soliman, Anas Abdulkayoum, Rawia Jarir, Bader Kurdi, Laila Mahmoud
P2-248
Genetic analysis and follow-up of 23 neonatal diabetes mellitus patients in China
Cao bingyan, Gong chunxiu, Wu di, Lu chaoxia, Liu Fang, Liu Xiaojing, Zhang Ying-xian, Gu Yi, Qi Zhan, Li Xiaoqiao, Liu Min, Li Wenjing, Su Chang, Liang Xuejun, Feng Mei
Genetic analysis and follow-up of 23 neonatal diabetes mellitus patients in China
Cao bingyan, Gong chunxiu, Wu di, Lu chaoxia, Liu Fang, Liu Xiaojing, Zhang Ying-xian, Gu Yi, Qi Zhan, Li Xiaoqiao, Liu Min, Li Wenjing, Su Chang, Liang Xuejun, Feng Mei
P2-249
Level of knowledge about type I diabetes mellitus among nurses employed at endocrinological dispensaries
Akmaral Tashmanova
Level of knowledge about type I diabetes mellitus among nurses employed at endocrinological dispensaries
Akmaral Tashmanova
P2-250
Recombinant human insulin-like growth factor-1 treatment in patients with insulin receptor mutations resulting in Donohue syndrome: a 10-year experience in a tertiary centre.
Nicola Improda, Harshini Katugampola, Pratik Shah, Hannah Gordon, Rakesh Amin, Catherine J Peters, Robert K Semple, Mehul T Dattani
Recombinant human insulin-like growth factor-1 treatment in patients with insulin receptor mutations resulting in Donohue syndrome: a 10-year experience in a tertiary centre.
Nicola Improda, Harshini Katugampola, Pratik Shah, Hannah Gordon, Rakesh Amin, Catherine J Peters, Robert K Semple, Mehul T Dattani
P2-251
Sick day rule: Survey of parents of children with Type 1 diabetes (experience and Knowledge)
Juliana Chizomam Agwu, S May Ng, J DREW, J EDGE, M KERSHAW, N WRIGHT, C GARDNER
Sick day rule: Survey of parents of children with Type 1 diabetes (experience and Knowledge)
Juliana Chizomam Agwu, S May Ng, J DREW, J EDGE, M KERSHAW, N WRIGHT, C GARDNER
P2-252
Brachial Flow Mediated Dilation and its Relation to Osteoprotegerin in Type 1 Diabetes Mellitus
Eman Sherief, Omneyia Youssef, Karim Abd El-Tawab, Hoda Ez-elarab, Moaz Ibrahim, Nermine Amr
Brachial Flow Mediated Dilation and its Relation to Osteoprotegerin in Type 1 Diabetes Mellitus
Eman Sherief, Omneyia Youssef, Karim Abd El-Tawab, Hoda Ez-elarab, Moaz Ibrahim, Nermine Amr
P2-253
Value of the intrarenal arterial resistivity indices and different renal biomarkers for early identification of diabetic nephropathy in type 1 diabetic patients.
Ahmed Battah, Soha Abd El Dayem, Abo El Magd El Bohy, Amal El Shohaby, Nagwa Abd Allah
Value of the intrarenal arterial resistivity indices and different renal biomarkers for early identification of diabetic nephropathy in type 1 diabetic patients.
Ahmed Battah, Soha Abd El Dayem, Abo El Magd El Bohy, Amal El Shohaby, Nagwa Abd Allah
P2-254
Can we rely on finger stick haemoglobin A1c?
Comparison of levels assayed by DCA 2000 with IFCC reference method in a pediatric cohort
Gianluca Tornese, Nadia Milic, Laura Spetti, Daniela Gembrini, Carmen Loganes, Maria Chiara Pellegrin, Lucia Radillo, Oriano Radillo, Elena Faleschini, Alessandro Ventura
Can we rely on finger stick haemoglobin A1c?
Comparison of levels assayed by DCA 2000 with IFCC reference method in a pediatric cohort
Gianluca Tornese, Nadia Milic, Laura Spetti, Daniela Gembrini, Carmen Loganes, Maria Chiara Pellegrin, Lucia Radillo, Oriano Radillo, Elena Faleschini, Alessandro Ventura
P2-255
Significant impact of nocturnal melatonin secretion on obesity-related metabolic disorders in children and adolescents
Johanna Overberg, Peter Kühnen, Andrea Ernert, Heiko Krude, Susanna Wiegand
Significant impact of nocturnal melatonin secretion on obesity-related metabolic disorders in children and adolescents
Johanna Overberg, Peter Kühnen, Andrea Ernert, Heiko Krude, Susanna Wiegand
P2-256
Exposure to phthalates and phenols in relation to gestational blood glucose homeostasis
Benjamin G. Fisher, Hanne Frederiksen, Anna-Maria Andersson, Anders Juul, A Thankamony, Kenneth K. Ong, David B. Dunger, Ieuan A. Hughes
Exposure to phthalates and phenols in relation to gestational blood glucose homeostasis
Benjamin G. Fisher, Hanne Frederiksen, Anna-Maria Andersson, Anders Juul, A Thankamony, Kenneth K. Ong, David B. Dunger, Ieuan A. Hughes
P2-257
Developing a targeted, mobile-health technology (e-book) to promote self-care during diabetes transition
Andrew Dwyer, Samaita Unal, Severine Emmanouilidis, Marie-Paule Aquarone-Vaucher, Silvia Pichard, Teresa Gyuriga, Joelle Korpes, Francois Jornayvaz, Elena Gonzalez-Rodriguez, Eglantine Elowe-Gruau, Sophie Stoppa, Anne Zanchi-Delacretaz, Jardena Puder, Francesca Amati, Therese Bouthors, Franziska Phan-Hug, Nelly Pitteloud, Michael Hauschild
Developing a targeted, mobile-health technology (e-book) to promote self-care during diabetes transition
Andrew Dwyer, Samaita Unal, Severine Emmanouilidis, Marie-Paule Aquarone-Vaucher, Silvia Pichard, Teresa Gyuriga, Joelle Korpes, Francois Jornayvaz, Elena Gonzalez-Rodriguez, Eglantine Elowe-Gruau, Sophie Stoppa, Anne Zanchi-Delacretaz, Jardena Puder, Francesca Amati, Therese Bouthors, Franziska Phan-Hug, Nelly Pitteloud, Michael Hauschild
P2-258
CARDIAC AUTONOMIC NEUROPATHY IS HIGHLY PREDICTIVE FOR SURVIVAL IN CHILDREN WITH MAURIAC SYNDROME
Margarita Arshinkova, Olga Slavcheva, Maia Konstantinova
CARDIAC AUTONOMIC NEUROPATHY IS HIGHLY PREDICTIVE FOR SURVIVAL IN CHILDREN WITH MAURIAC SYNDROME
Margarita Arshinkova, Olga Slavcheva, Maia Konstantinova
P2-259
Predictors of Cystic Fibrosis-Related Diabetes (CFRD) in Patients with CF and Pancreatic Insufficiency
Joseph Meyerovitch, Rony Be'eri Berkowiz, Meir Mei-Zahav, Hannah Blau, Huda Mussaffi-Georgy
Predictors of Cystic Fibrosis-Related Diabetes (CFRD) in Patients with CF and Pancreatic Insufficiency
Joseph Meyerovitch, Rony Be'eri Berkowiz, Meir Mei-Zahav, Hannah Blau, Huda Mussaffi-Georgy
P2-260
Adherence to diabetes care in children and adolescents with Type 1 Diabetes Mellitus in Spain: Results from the CHRYSTAL Study.
Juan Pedro López Siguero, Luis Alberto Vázquez, Renata Villoro, Dingfeng Jiang, María Merino, Jesús Reviriego, Magaly Perez-Nieves
Adherence to diabetes care in children and adolescents with Type 1 Diabetes Mellitus in Spain: Results from the CHRYSTAL Study.
Juan Pedro López Siguero, Luis Alberto Vázquez, Renata Villoro, Dingfeng Jiang, María Merino, Jesús Reviriego, Magaly Perez-Nieves
P2-261
Gaining from patient experience on a local level: The introduction of annual questionnaires for children and teenagers with diabetes
Emily Cottrell, Manju Chandwani, Frances Hanson, James Wong
Gaining from patient experience on a local level: The introduction of annual questionnaires for children and teenagers with diabetes
Emily Cottrell, Manju Chandwani, Frances Hanson, James Wong
P2-262
Factitious administration of analogue insulin to a 2 year old child
Nehal Thanawala, Sarah Cheney, Gwen Wark, Mario Thevis, A Thomas, V Tziaferi, James Greening
Factitious administration of analogue insulin to a 2 year old child
Nehal Thanawala, Sarah Cheney, Gwen Wark, Mario Thevis, A Thomas, V Tziaferi, James Greening
P2-263
Insulin Sensitivity in Adolescents with Gender Dysphoria during Puberty Suppressing Therapy with GnRH Agonists
Sebastian Schagen, Henriette Delemarre-van de Waal, Sabine Hannema
Insulin Sensitivity in Adolescents with Gender Dysphoria during Puberty Suppressing Therapy with GnRH Agonists
Sebastian Schagen, Henriette Delemarre-van de Waal, Sabine Hannema
P2-264
Ethnic variation in the correlation of waist circumference to daily insulin requirement in children with type 1 diabetes
Suma Uday, Shaun Gorman, Richard Feltbower, Mathew Mathai
Ethnic variation in the correlation of waist circumference to daily insulin requirement in children with type 1 diabetes
Suma Uday, Shaun Gorman, Richard Feltbower, Mathew Mathai
P2-265
IMPORTANCE OF THROMBOCYTE VOLUME PARAMETERS IN TYPE I DIABETES MELLITUS PATIENTS WITH AND WITHOUT CLINICAL FINDINGS OF DIABETIC KETOACIDOSIS
Dogus Vuralli, Hatice Tatar Aksoy, Arzu Yilmaz, Ozlem Engiz, Yildiz Bilge Dallar
IMPORTANCE OF THROMBOCYTE VOLUME PARAMETERS IN TYPE I DIABETES MELLITUS PATIENTS WITH AND WITHOUT CLINICAL FINDINGS OF DIABETIC KETOACIDOSIS
Dogus Vuralli, Hatice Tatar Aksoy, Arzu Yilmaz, Ozlem Engiz, Yildiz Bilge Dallar
P2-266
Increased Arterial Wall Stiffness in Children with Type 1 Diabetes and Poor Metabolic Control: An Early Marker of Vascular Complications?
Barbora Obermannova, Lenka Petruzelkova, Terezie Sulakova, Zdenek Sumnik
Increased Arterial Wall Stiffness in Children with Type 1 Diabetes and Poor Metabolic Control: An Early Marker of Vascular Complications?
Barbora Obermannova, Lenka Petruzelkova, Terezie Sulakova, Zdenek Sumnik
P2-267
Glycaemic dysregulation in transfusion dependent thalassaemia patient in a children’s hospital
SONG HAI LIM, WILKINS LIM, THIAN LIAN SOO
Glycaemic dysregulation in transfusion dependent thalassaemia patient in a children’s hospital
SONG HAI LIM, WILKINS LIM, THIAN LIAN SOO
P2-268
MODY-GCK and MODY-HNF1A in children and adolescents in Russian population
Elena Sechko, Lubov Zilberman, Olga Ivanova, Tamara Kuraeva, Valentina Peterkova
MODY-GCK and MODY-HNF1A in children and adolescents in Russian population
Elena Sechko, Lubov Zilberman, Olga Ivanova, Tamara Kuraeva, Valentina Peterkova
P2-269
Clinical and hormonal profile in Mini-puberty of daughters born after pregnancies with diabetes: preliminary report
Joel Riquelme, Daniela Martínez, Teresa Sir-Petermann, Claudio Villarroel, Ethel Codner
Clinical and hormonal profile in Mini-puberty of daughters born after pregnancies with diabetes: preliminary report
Joel Riquelme, Daniela Martínez, Teresa Sir-Petermann, Claudio Villarroel, Ethel Codner
P2-270
Growth and Endocrinopathy in Wolfram Syndrome: the experience of a nationally commissioned specialist clinic.
Melanie Kershaw, Susan Gleeson, Denise Williams, Rajat Gupta, John Ainsworth, Archana Kulkarni, Liam McCarthy, Lesley MacPherson, Rachel Bates, Marie McGee, Timothy G Barrett
Growth and Endocrinopathy in Wolfram Syndrome: the experience of a nationally commissioned specialist clinic.
Melanie Kershaw, Susan Gleeson, Denise Williams, Rajat Gupta, John Ainsworth, Archana Kulkarni, Liam McCarthy, Lesley MacPherson, Rachel Bates, Marie McGee, Timothy G Barrett
P2-271
Evaluation of a Novel Tool to Adjust Insulin Boluses based on Continuous Glucose Monitoring Trend Arrows and Insulin Sensitivity (Trend Arrow Adjustment Tool©) in Children and Youth with Type 1 Diabetes using Insulin Pump Therapy
Emmeline Heffernan, Margaret Lawson, Brenda Bradley, Jennilea Courtney, Christine Richardson
Evaluation of a Novel Tool to Adjust Insulin Boluses based on Continuous Glucose Monitoring Trend Arrows and Insulin Sensitivity (Trend Arrow Adjustment Tool©) in Children and Youth with Type 1 Diabetes using Insulin Pump Therapy
Emmeline Heffernan, Margaret Lawson, Brenda Bradley, Jennilea Courtney, Christine Richardson
P2-272
Circulating GLP-1 in infants born small-for-gestational-age: breast-feeding versus formula-feeding
Marta Díaz, Judit Bassols, Giorgia Sebastiani, Abel López-Bermejo, Lourdes Ibáñez, Francis de Zegher
Circulating GLP-1 in infants born small-for-gestational-age: breast-feeding versus formula-feeding
Marta Díaz, Judit Bassols, Giorgia Sebastiani, Abel López-Bermejo, Lourdes Ibáñez, Francis de Zegher
P2-273
Utility of estimated glucose disposal rate and fat mass percentage for predicting metabolic syndrome in children and adolescents with type 1 diabetes
Ozlem Koken, Cengiz Kara, Gulay Can Yilmaz, Murat Aydin
Utility of estimated glucose disposal rate and fat mass percentage for predicting metabolic syndrome in children and adolescents with type 1 diabetes
Ozlem Koken, Cengiz Kara, Gulay Can Yilmaz, Murat Aydin
P2-274
Friedreich’s Ataxia presenting with Diabetes Mellitus in an adolescent
Serpil Bas, Saygin Abali, Zeynep Atay, Ziya Gurbanov, Dilsad Turkdogan, Serap Turan, Abdullah Bereket
Friedreich’s Ataxia presenting with Diabetes Mellitus in an adolescent
Serpil Bas, Saygin Abali, Zeynep Atay, Ziya Gurbanov, Dilsad Turkdogan, Serap Turan, Abdullah Bereket
P2-275
DO PANCREATIC FUNCTIONS PREDICT CARDIAC AND LIVER IRON LOADING IN TRANSFUSION-DEPENDENT BETA THALASSEMIA MAJOR PATIENTS USING CARDIOVASCULAR AND LIVER T2-STAR (T2*)MAGNETIC RESONANCE ?
Galila Mokhtar, Wafaa Ibrahim, Nancy Elbarbary, Randa Matter, Ahmed Ibrahim, Safa Sayed
DO PANCREATIC FUNCTIONS PREDICT CARDIAC AND LIVER IRON LOADING IN TRANSFUSION-DEPENDENT BETA THALASSEMIA MAJOR PATIENTS USING CARDIOVASCULAR AND LIVER T2-STAR (T2*)MAGNETIC RESONANCE ?
Galila Mokhtar, Wafaa Ibrahim, Nancy Elbarbary, Randa Matter, Ahmed Ibrahim, Safa Sayed
P2-276
Determinants of outcome of children with type 1 diabetes in Cameroon.
Loveline Niba, Benedikt Aulinger, Wilfred Mbacham, Klaus Parhofer
Determinants of outcome of children with type 1 diabetes in Cameroon.
Loveline Niba, Benedikt Aulinger, Wilfred Mbacham, Klaus Parhofer
P2-277
Psychosocial Screening in children with Type 1 Diabetes in Ireland
Elena Hennessy, Patricia Gallagher, Triona Butler, Norma O’Toole, Susan M O’Connell, Stephen MP O’Riordan
Psychosocial Screening in children with Type 1 Diabetes in Ireland
Elena Hennessy, Patricia Gallagher, Triona Butler, Norma O’Toole, Susan M O’Connell, Stephen MP O’Riordan
P2-278
Neonatal Diabetes –Experience from a single center in Sri Lanka
Navoda Atapattu, Vasundara Vithanage, Kirikankanange Shamya Harshini de Silva, Daham Haresha de Silva, Mala Mangalika Jayathilaka, Andrew T Hattersley, Sian Ellard, Sarah E. Flanagan, J.A.L Houghton, Khalid Hussain
Neonatal Diabetes –Experience from a single center in Sri Lanka
Navoda Atapattu, Vasundara Vithanage, Kirikankanange Shamya Harshini de Silva, Daham Haresha de Silva, Mala Mangalika Jayathilaka, Andrew T Hattersley, Sian Ellard, Sarah E. Flanagan, J.A.L Houghton, Khalid Hussain
P2-279
Dive: a serious game for diabetes therapeutic education in children
Cecile Godot, Nadine Lepage, Isabelle Jourdon, Marie-Eve Schmidt, Pierre Maccini, Michel Polak, Jacques Beltrand
Dive: a serious game for diabetes therapeutic education in children
Cecile Godot, Nadine Lepage, Isabelle Jourdon, Marie-Eve Schmidt, Pierre Maccini, Michel Polak, Jacques Beltrand
P2-280
GLUCOSE AND INSULIN RESPONSE AT STANDARD ORAL GLUCOSE LOAD AND FOLLOWED SUBMAXIMAL TREADMILL TEST IN OBESE ADOLESCENTS
Tetyana Chaychenko, Olena Rybka
GLUCOSE AND INSULIN RESPONSE AT STANDARD ORAL GLUCOSE LOAD AND FOLLOWED SUBMAXIMAL TREADMILL TEST IN OBESE ADOLESCENTS
Tetyana Chaychenko, Olena Rybka
P2-281
Insulin Dynamics and Biochemical Markers for Predicting Impaired Glucose Tolerance in Thai Obese Youth
Sirapassorn Tirabanchasak, Sukumarn Siripunthana, Vichit Supornsilchai, Suttipong Wacharasindhu, Taninee Sahakitrungruang
Insulin Dynamics and Biochemical Markers for Predicting Impaired Glucose Tolerance in Thai Obese Youth
Sirapassorn Tirabanchasak, Sukumarn Siripunthana, Vichit Supornsilchai, Suttipong Wacharasindhu, Taninee Sahakitrungruang
P2-282
Total-Body Irradiation is a major risk factor for young adult onset diabetes mellitus and hyperlipidemia in childhood cancer survivors after hematopoietic stem cell transplantation.
Ryuichi Nakagawa, Atsumi Tsuji, Yuki Aoki, Keisuke Nakajima, Akito Sutani, Yuichi Miyakawa, Kei Takasawa, Daisuke Tomizawa, Masatoshi Takagi, Kenichi Kashimada, Tomohiro Morio
Total-Body Irradiation is a major risk factor for young adult onset diabetes mellitus and hyperlipidemia in childhood cancer survivors after hematopoietic stem cell transplantation.
Ryuichi Nakagawa, Atsumi Tsuji, Yuki Aoki, Keisuke Nakajima, Akito Sutani, Yuichi Miyakawa, Kei Takasawa, Daisuke Tomizawa, Masatoshi Takagi, Kenichi Kashimada, Tomohiro Morio
P2-283
Variables in Diabetic Children and Adolescents associated with High, Acceptable and Low range of Glycosylated Haemoglobin (HbA1c) in a DGH setting – An Analysis
Karthi Manoharan, Sharon Lim
Variables in Diabetic Children and Adolescents associated with High, Acceptable and Low range of Glycosylated Haemoglobin (HbA1c) in a DGH setting – An Analysis
Karthi Manoharan, Sharon Lim
P2-284
In-patient care for children with type 1 diabetes- a regional audit in the Yorkshire and Humber region in the north of England.
Suma Uday, Nadia Amin, Fiona Campbell, James Yong
In-patient care for children with type 1 diabetes- a regional audit in the Yorkshire and Humber region in the north of England.
Suma Uday, Nadia Amin, Fiona Campbell, James Yong
P2-285
Implementation of Effective Transition from Paediatric to Adult Diabetes Care: Epidemiological and clinical characteristics. A pioneering experience in North Africa.
ESSADDAM Leïla, TURKI Zinet, FITOURI Zohra, BEN SLAMA Claude, MATOUSSI Nadia, BEN BECHER Saayda
Implementation of Effective Transition from Paediatric to Adult Diabetes Care: Epidemiological and clinical characteristics. A pioneering experience in North Africa.
ESSADDAM Leïla, TURKI Zinet, FITOURI Zohra, BEN SLAMA Claude, MATOUSSI Nadia, BEN BECHER Saayda
P2-286
Assessment of Ventricular Function by Tissue Doppler Echocardiography in Children and Adolescents with Type 1 Diabetes Mellitus
Shereen Abdelghaffar, Nermeen Salah, Mona Attia, Mona Hafez, Mona Mamdouh, Abeer Atef, Fatma Elmougy, Sahar Abdelaty, Amany Ibrahim, Hend Mehawed, Noha Musa, Noha Arafa, Marwa Farouk, Mohamed Ismail, Faten Abdelaziz, Aya Fattouh, Eman Hussein, Isis Ghali
Assessment of Ventricular Function by Tissue Doppler Echocardiography in Children and Adolescents with Type 1 Diabetes Mellitus
Shereen Abdelghaffar, Nermeen Salah, Mona Attia, Mona Hafez, Mona Mamdouh, Abeer Atef, Fatma Elmougy, Sahar Abdelaty, Amany Ibrahim, Hend Mehawed, Noha Musa, Noha Arafa, Marwa Farouk, Mohamed Ismail, Faten Abdelaziz, Aya Fattouh, Eman Hussein, Isis Ghali
P2-287
Incidence of Type 1 Diabetes among Korean Children and Adolescents in 2012-2013: Analysis of Data from the Nationwide Registry of Korea
Jae Hyun Kim, Young Ah Lee, Sei Won Yang, Choong Ho Shin
Incidence of Type 1 Diabetes among Korean Children and Adolescents in 2012-2013: Analysis of Data from the Nationwide Registry of Korea
Jae Hyun Kim, Young Ah Lee, Sei Won Yang, Choong Ho Shin
P2-288
Functional condition of the kidneys (K/DOQI , 2002) by ACE gene I/D polymorphism in children and adolescents with type I diabetes mellitus
Gulnara Rakhimova, Akida Sadikova, Nasiba Alimova
Functional condition of the kidneys (K/DOQI , 2002) by ACE gene I/D polymorphism in children and adolescents with type I diabetes mellitus
Gulnara Rakhimova, Akida Sadikova, Nasiba Alimova
P2-289
LONGITUDINAL STUDY OF IRISH CHILDREN AND ADOLESCENTS ON CONTINUOUS SUBCUTANEOUS INSULIN INFUSION (CSII)
Mary-Ellen Bohane, Niamh McGrath, Aoife Carroll, Dympna Devenney, Ciara McDonnell, Nuala Murphy
LONGITUDINAL STUDY OF IRISH CHILDREN AND ADOLESCENTS ON CONTINUOUS SUBCUTANEOUS INSULIN INFUSION (CSII)
Mary-Ellen Bohane, Niamh McGrath, Aoife Carroll, Dympna Devenney, Ciara McDonnell, Nuala Murphy
P2-290
C peptide variation after the diagnosis of type 1 diabetes in pediatric age
Joana Correia, Catarina Mendes, Marina Pinheiro, Clara Preto, Helena Cardoso, Maria João Oliveira, Teresa Borges
C peptide variation after the diagnosis of type 1 diabetes in pediatric age
Joana Correia, Catarina Mendes, Marina Pinheiro, Clara Preto, Helena Cardoso, Maria João Oliveira, Teresa Borges
P2-291
Metformin Utilization Patterns in Pediatric Population aged 10-19 years in the US: 2009-2013
Tongtong Wang, Ann Marie McNeill, Yong Chen, Ravi Shankar
Metformin Utilization Patterns in Pediatric Population aged 10-19 years in the US: 2009-2013
Tongtong Wang, Ann Marie McNeill, Yong Chen, Ravi Shankar
P2-292
Incidence of Type 1 Diabetes in Children Under 15 years old in Navarre (Spain) Between 1980 and 2014
Sada Zarikian, María Chueca, Sara Berrade, Elisabet Burillo, Koldo Cambra, Arkaitz Galbete, LLuis Forga, Mirentxu Oyarzabal
Incidence of Type 1 Diabetes in Children Under 15 years old in Navarre (Spain) Between 1980 and 2014
Sada Zarikian, María Chueca, Sara Berrade, Elisabet Burillo, Koldo Cambra, Arkaitz Galbete, LLuis Forga, Mirentxu Oyarzabal
P2-293
QUALITY OF LIFE IN ADOLESCENT WITH TYPE 1 DIABETES (T1D) AND ITS RELATIONSHIP WITH METABOLIC CONTROL
E. Aranzazu Garza Espi, Gracia Maria Lou Frances, Elena Corella Aznar, Marta Ferrer Lozano
QUALITY OF LIFE IN ADOLESCENT WITH TYPE 1 DIABETES (T1D) AND ITS RELATIONSHIP WITH METABOLIC CONTROL
E. Aranzazu Garza Espi, Gracia Maria Lou Frances, Elena Corella Aznar, Marta Ferrer Lozano
P2-294
The prevalence of different subtypes of maturity-onset diabetes of the young in Russian Federation as defined by targeted next-generation sequencing
Natalya Zubkova, Olesya Gioeva, Yulia Tichonovich, Vasily Petrov, Evgeny Vasilyev, Oleg Malievsky, Alexey Kiyaev, Alexey Timofeev, Anatoly Tiulpakov
The prevalence of different subtypes of maturity-onset diabetes of the young in Russian Federation as defined by targeted next-generation sequencing
Natalya Zubkova, Olesya Gioeva, Yulia Tichonovich, Vasily Petrov, Evgeny Vasilyev, Oleg Malievsky, Alexey Kiyaev, Alexey Timofeev, Anatoly Tiulpakov
P2-295
Sirolimus therapy in infants with congenital hyperinsulinism after near total pancreatectomy
keun Hee Choi, Hye Rim Chung
Sirolimus therapy in infants with congenital hyperinsulinism after near total pancreatectomy
keun Hee Choi, Hye Rim Chung
P2-296
Children born from mothers with gestational diabetes mellitus are at higher risk of metabolic derangement
Reiko Horikawa, Naoko Arata, Yasuhiro Naiki
Children born from mothers with gestational diabetes mellitus are at higher risk of metabolic derangement
Reiko Horikawa, Naoko Arata, Yasuhiro Naiki
P2-297
GH promotes mRNA expression and secretion of progranulin in 3T3-L1 cells.
Guo Song, Chen Hongshan, Zhang Jun, Du Minlian, Ma Huamei, Li Yanhong, Chen Qiuli, Peng Yangshui
GH promotes mRNA expression and secretion of progranulin in 3T3-L1 cells.
Guo Song, Chen Hongshan, Zhang Jun, Du Minlian, Ma Huamei, Li Yanhong, Chen Qiuli, Peng Yangshui
P2-299
Improving glycaemic control at diagnosis of type 1 diabetes: insulin dosing depending on degree of ketonaemia at presentation
Sarah Kiff, Kathryn Noyes, Ailish Nimmo, Louise Bath
Improving glycaemic control at diagnosis of type 1 diabetes: insulin dosing depending on degree of ketonaemia at presentation
Sarah Kiff, Kathryn Noyes, Ailish Nimmo, Louise Bath
P2-300
Non-immune diabetes mellitus and neurodegeneration: two distinct cases of Wolfram syndrome.
Annelies Lemay, Margje Sinnema, Marieke den Brinker, Hilde Dotremont, Annick France, Raoul Rooman, Saartje Straetemans
Non-immune diabetes mellitus and neurodegeneration: two distinct cases of Wolfram syndrome.
Annelies Lemay, Margje Sinnema, Marieke den Brinker, Hilde Dotremont, Annick France, Raoul Rooman, Saartje Straetemans
P2-301
EVALUATION OF CONTINUOUS GLUCOSE MONITORING IN CYSTIC FIBROSIS PATIENTS
Laura Bilbao, María Clemente, Laura Costas, Silvia Gartner, Milagros Losada, Eulàlia Armengol, Diego Yeste, Antonio Carrascosa
EVALUATION OF CONTINUOUS GLUCOSE MONITORING IN CYSTIC FIBROSIS PATIENTS
Laura Bilbao, María Clemente, Laura Costas, Silvia Gartner, Milagros Losada, Eulàlia Armengol, Diego Yeste, Antonio Carrascosa
P2-302
The Impact of Diurnal Glycemic Variability on the Cardiovascular System
in Children with Type 1 Diabetes Mellitus
Oleg Dianov, Sergey Gnusaev, Ekaterina Lavrova
The Impact of Diurnal Glycemic Variability on the Cardiovascular System
in Children with Type 1 Diabetes Mellitus
Oleg Dianov, Sergey Gnusaev, Ekaterina Lavrova
P3-686
A rare reason of hyperinsulinism: Münchausen Syndrome by Proxy
EDIZ YESILKAYA, ONUR AKIN, ERKAN SARI, ENES MACIT, CAGDAS AKAR, HUSAMETTIN GUN
A rare reason of hyperinsulinism: Münchausen Syndrome by Proxy
EDIZ YESILKAYA, ONUR AKIN, ERKAN SARI, ENES MACIT, CAGDAS AKAR, HUSAMETTIN GUN
P3-687
Correlation of vitamin D levels with glycemic control, total daily insulin dose, BMI and ethnicity in pediatric patients with type 1 diabetes mellitus.
Monica Bianco, Ramon Durazo, Ramon Durazo-Arvizu, Carla Minutti
Correlation of vitamin D levels with glycemic control, total daily insulin dose, BMI and ethnicity in pediatric patients with type 1 diabetes mellitus.
Monica Bianco, Ramon Durazo, Ramon Durazo-Arvizu, Carla Minutti
P3-688
Management of children with Type 1 diabetes during illness (sick days): Is there a need for national consensus guideline?
Astha Soni, Chizo Agwu, Neil Wright, Chris Moudiotis, Melanie Kershaw, Julie Edge, Josephine Drew, Sze May Ng
Management of children with Type 1 diabetes during illness (sick days): Is there a need for national consensus guideline?
Astha Soni, Chizo Agwu, Neil Wright, Chris Moudiotis, Melanie Kershaw, Julie Edge, Josephine Drew, Sze May Ng
P3-689
Incretin secretion was not impaired in obese Korean children and adolescents with type 2 diabetes
SO HYUN PARK, JAE HONG KIM, MIN HO JUNG, SIN HEE KIM, GYUNG SUN CHO, MOON BAE AHN, WON GYUNG CHO, IN A JUNG, YEON JIN JEON, BYUNG KYU SUH
Incretin secretion was not impaired in obese Korean children and adolescents with type 2 diabetes
SO HYUN PARK, JAE HONG KIM, MIN HO JUNG, SIN HEE KIM, GYUNG SUN CHO, MOON BAE AHN, WON GYUNG CHO, IN A JUNG, YEON JIN JEON, BYUNG KYU SUH
P3-690
NEONATAL DIABETES MELLITUS: CLINICAL FEATURE AND OUTCOME
Bich Ngoc Can Thi, Dung Vu Chi, Thao Bui Phuong, Khanh Nguyen Ngoc, Maria Craig, Sian Ellard, Hoan Nguyen Thi
NEONATAL DIABETES MELLITUS: CLINICAL FEATURE AND OUTCOME
Bich Ngoc Can Thi, Dung Vu Chi, Thao Bui Phuong, Khanh Nguyen Ngoc, Maria Craig, Sian Ellard, Hoan Nguyen Thi
P3-691
Acute kidney injury as a severe complication of diabetic ketoacidosis
Alagusutha Jeyaraman, Eric Finlay, Verghese Mathew, Sanjay Gupta
Acute kidney injury as a severe complication of diabetic ketoacidosis
Alagusutha Jeyaraman, Eric Finlay, Verghese Mathew, Sanjay Gupta
P3-692
Body mass index in children and young people with Type 1 diabetes in England and Wales
Naomi Holman, Fiona Campbell, Justin Warner
Body mass index in children and young people with Type 1 diabetes in England and Wales
Naomi Holman, Fiona Campbell, Justin Warner
P3-693
Blood versus urine ketone monitoring in a pediatric cohort of patients with type 1 diabetes: a crossover study
Line Goffinet, Thierry Barrea, Valérie Vandooren, Philippe Lysy
Blood versus urine ketone monitoring in a pediatric cohort of patients with type 1 diabetes: a crossover study
Line Goffinet, Thierry Barrea, Valérie Vandooren, Philippe Lysy
P3-694
ELASTARGENE 3C HELPS TO IMPROVE GLYCATED HAEMOGLOBIN IN CHILDREN AND ADOLESCENTS WITH TYPE 1 DIABETES USING INSULIN PUMP THERAPY.
Andrea Scaramuzza, Matteo Ferrari, Maddalena Macedoni, Laura De Angelis, Francesca Redaelli, Alessandra De Palma, Gian Vincenzo Zuccotti
ELASTARGENE 3C HELPS TO IMPROVE GLYCATED HAEMOGLOBIN IN CHILDREN AND ADOLESCENTS WITH TYPE 1 DIABETES USING INSULIN PUMP THERAPY.
Andrea Scaramuzza, Matteo Ferrari, Maddalena Macedoni, Laura De Angelis, Francesca Redaelli, Alessandra De Palma, Gian Vincenzo Zuccotti
P3-695
Intraosseous infusion: sometimes the only way to treat severe diabetic ketoacidosis
Francesco Gallo, Pietro Conte, Francesco La Torre, Maria Alba Calò, Fulvio Moramarco
Intraosseous infusion: sometimes the only way to treat severe diabetic ketoacidosis
Francesco Gallo, Pietro Conte, Francesco La Torre, Maria Alba Calò, Fulvio Moramarco
P3-696
Influence of hypoglycemic episodes on attention and behavioral abnormalities in diabetic children
Michael Wurm, Vera Niebuhr, Kristiane Hallermann, Alexandra Krause, Natascha van der Werf-Grohmann, Karl Otfried Schwab
Influence of hypoglycemic episodes on attention and behavioral abnormalities in diabetic children
Michael Wurm, Vera Niebuhr, Kristiane Hallermann, Alexandra Krause, Natascha van der Werf-Grohmann, Karl Otfried Schwab
P3-697
Recurrent ketosis after prolonged exercise in type 1 diabetes – the need for glycogen replacement strategies. Case report
Mirjam van Albada, Willie Bakker - van Waarde
Recurrent ketosis after prolonged exercise in type 1 diabetes – the need for glycogen replacement strategies. Case report
Mirjam van Albada, Willie Bakker - van Waarde
P3-698
Adherence to Diabetic Ketoacidosis Management Protocol: A Paediatric Center Experience
Daphné Cloutier, Joanie Barbe, Isabelle Bouchard, Julie Gagné, Macha Bourdages
Adherence to Diabetic Ketoacidosis Management Protocol: A Paediatric Center Experience
Daphné Cloutier, Joanie Barbe, Isabelle Bouchard, Julie Gagné, Macha Bourdages
P3-699
Continuous intersticial glucose monitoring in early detection of glucose tolerance abnormalities in adolescents with cystic fibrosis.
Jacobo Perez, Raquel Corripio, David Belver, Oscar Asensio, Montserrat Bosque, Josefa Rivera
Continuous intersticial glucose monitoring in early detection of glucose tolerance abnormalities in adolescents with cystic fibrosis.
Jacobo Perez, Raquel Corripio, David Belver, Oscar Asensio, Montserrat Bosque, Josefa Rivera
P3-700
Health Related Quality of Life in children and adolescents with Type 1 Diabetes Mellitus in Spain: Results from the CHRYSTAL Study.
Luis Alberto Vázquez, Juan Pedro López Siguero, Renata Villoro, Dingfeng Jiang, María Merino, Jesús Reviriego, Magaly Perez-Nieves
Health Related Quality of Life in children and adolescents with Type 1 Diabetes Mellitus in Spain: Results from the CHRYSTAL Study.
Luis Alberto Vázquez, Juan Pedro López Siguero, Renata Villoro, Dingfeng Jiang, María Merino, Jesús Reviriego, Magaly Perez-Nieves
P3-701
HBA1C RATHER THAN BMI, LIFESTYLE AND ADHERENCE TO MEDITERRANEAN DIET IS THE MAJOR DETERMINANT OF TRIGLYCERIDE/HDL CHOLESTEROL RATIO IN ADOLESCENTS WITH TYPE-1 DIABETES (T1D)
Silvia Poluzzi, Stefano Zucchini, Giulio Maltoni, Maximiliano Zioutas, Claudia Balsamo, Antonio Maria Morselli-Labate, Elena Nardi, Laura Mazzanti
HBA1C RATHER THAN BMI, LIFESTYLE AND ADHERENCE TO MEDITERRANEAN DIET IS THE MAJOR DETERMINANT OF TRIGLYCERIDE/HDL CHOLESTEROL RATIO IN ADOLESCENTS WITH TYPE-1 DIABETES (T1D)
Silvia Poluzzi, Stefano Zucchini, Giulio Maltoni, Maximiliano Zioutas, Claudia Balsamo, Antonio Maria Morselli-Labate, Elena Nardi, Laura Mazzanti
P3-702
Non-HDL cholesterol in diabetic children: Treatment recommendations considering glycemic control, BMI, age, gender, and generally accepted cut points
Karl Otfried Schwab, Juergen Doerfer, Andreas Hungele, Nicole Scheuing, Andreas Krebs, Axel Dost, Tilman R. Rohrer, Sabine Hofer, Reinhard W. Holl
Non-HDL cholesterol in diabetic children: Treatment recommendations considering glycemic control, BMI, age, gender, and generally accepted cut points
Karl Otfried Schwab, Juergen Doerfer, Andreas Hungele, Nicole Scheuing, Andreas Krebs, Axel Dost, Tilman R. Rohrer, Sabine Hofer, Reinhard W. Holl
P3-703
A 1 year follow up study to evaluate efficacy and compliance of continuous glucose monitoring (CGM) in children with Type 1 Diabetes Mellitus (T1DM)
Astha Soni, Marisa Clemente, Sze May Ng
A 1 year follow up study to evaluate efficacy and compliance of continuous glucose monitoring (CGM) in children with Type 1 Diabetes Mellitus (T1DM)
Astha Soni, Marisa Clemente, Sze May Ng
P3-704
Diabetic ketoacidosis treatment: experience from a pediatric tertiary centre (2004-2014)
Joana Serra-Caetano, Lia Gata, Alexandra Dinis, Rita Cardoso, Isabel Dinis, Alice Mirante
Diabetic ketoacidosis treatment: experience from a pediatric tertiary centre (2004-2014)
Joana Serra-Caetano, Lia Gata, Alexandra Dinis, Rita Cardoso, Isabel Dinis, Alice Mirante
P3-705
Treatment of dyslipidemia in children and adolescents with diabetes mellitus type 1
M.M.H. Borgerink, M.A. van Albada, G. Venema, W.M. Bakker-van Waarde
Treatment of dyslipidemia in children and adolescents with diabetes mellitus type 1
M.M.H. Borgerink, M.A. van Albada, G. Venema, W.M. Bakker-van Waarde
P3-706
Hearing changes in children and adolescents with type 1 diabetes mellitus
Young-Jun Rhie, Joon Woo Baek, Hyo-Kyoung Nam, Kee-Hyoung Lee
Hearing changes in children and adolescents with type 1 diabetes mellitus
Young-Jun Rhie, Joon Woo Baek, Hyo-Kyoung Nam, Kee-Hyoung Lee
P3-707
A novel genetic mutation in a Turkish family with GCK-MODY
S.Ahmet Ucakturk, Figen Gunindi, Fatma Demirel, Selin Elmaogullari, Eda Mengen, Bilgin Yuksel
A novel genetic mutation in a Turkish family with GCK-MODY
S.Ahmet Ucakturk, Figen Gunindi, Fatma Demirel, Selin Elmaogullari, Eda Mengen, Bilgin Yuksel
P3-708
INCIDENCE AND RISK FACTORS OF DIABETIC NEPHROPATHY IN CHILDREN AND ADOLESCENTS AS PER REPUBLIC OF UZBEKISTAN NATIONAL REGISTER
Gulnara Rakhimova, Nasiba Alimova
INCIDENCE AND RISK FACTORS OF DIABETIC NEPHROPATHY IN CHILDREN AND ADOLESCENTS AS PER REPUBLIC OF UZBEKISTAN NATIONAL REGISTER
Gulnara Rakhimova, Nasiba Alimova
P3-709
Elevated HbA1c and cardiometabolic risk factors in Korean children and adolescents: Data from the Korean National Health and Nutrition Examination Survey, 2011-2012
Jieun Lee, Jae Hyun Kim
Elevated HbA1c and cardiometabolic risk factors in Korean children and adolescents: Data from the Korean National Health and Nutrition Examination Survey, 2011-2012
Jieun Lee, Jae Hyun Kim
P3-710
How approprıate are the lenghts of syringe needles used for subcutaneous injections to the children at school age
Sultan Kaba, Murat Doğan, Keziban Bulan, Alpaslan Yavuz, Aydın Bora, Muazzez Didin, İlyas Dündar, Nihat Demir
How approprıate are the lenghts of syringe needles used for subcutaneous injections to the children at school age
Sultan Kaba, Murat Doğan, Keziban Bulan, Alpaslan Yavuz, Aydın Bora, Muazzez Didin, İlyas Dündar, Nihat Demir
P3-711
Heterogeneous Presentation of Paediatric Hyperglycaemic Hyperosmolar State – A case series
Zainaba Mohamed, Tabitha Randell, Prem Sundaram, James Greening, Louise Denvir, Pooja Sachdev
Heterogeneous Presentation of Paediatric Hyperglycaemic Hyperosmolar State – A case series
Zainaba Mohamed, Tabitha Randell, Prem Sundaram, James Greening, Louise Denvir, Pooja Sachdev
P3-712
A NOVEL COMPOUND HETEROZYGOUS MUTATION IN AN ADOLESCENT WITH INSULIN-DEPENDENT DIABETES: A CASE REPORT OF WOLFRAM SYNDROME
Giulio Maltoni, Vilma Mantovani, Stefano Zucchini, Carlotta Pia Cristalli, Raffaella Minardi, Laura Mazzanti
A NOVEL COMPOUND HETEROZYGOUS MUTATION IN AN ADOLESCENT WITH INSULIN-DEPENDENT DIABETES: A CASE REPORT OF WOLFRAM SYNDROME
Giulio Maltoni, Vilma Mantovani, Stefano Zucchini, Carlotta Pia Cristalli, Raffaella Minardi, Laura Mazzanti
P3-713
Sirolimus therapy in an infant with Persistent Hyperinsulinemic Hypoglycemia
Yvonne Yijuan Lim, Andrew Anjian Sng, Khalid Hussain, Kah-Yin Loke
Sirolimus therapy in an infant with Persistent Hyperinsulinemic Hypoglycemia
Yvonne Yijuan Lim, Andrew Anjian Sng, Khalid Hussain, Kah-Yin Loke
P3-714
Permanent Neonatal Diabetes Mellitus in Beckwith Wiedemann Syndrome: An unusual co-occurrence.
Dipesalema Joel, Seeletso Nchingane, Motlalekgomo Matsheng-Samuel, Loeto Mazhani
Permanent Neonatal Diabetes Mellitus in Beckwith Wiedemann Syndrome: An unusual co-occurrence.
Dipesalema Joel, Seeletso Nchingane, Motlalekgomo Matsheng-Samuel, Loeto Mazhani
P3-715
Prevalence of vascular complications in children with type 1 diabetes in Ireland
Triona Butler, Elena Hennessy, Patricia Gallagher, Norma O’Toole, Susan M O'Connell, Stephen MP O'Riordan
Prevalence of vascular complications in children with type 1 diabetes in Ireland
Triona Butler, Elena Hennessy, Patricia Gallagher, Norma O’Toole, Susan M O'Connell, Stephen MP O'Riordan
P3-716
Hyperglycaemia during Chemotherapy for Acute Lymphoblastic Leukaemia among Taiwanese Children
Meng-Che Tsai, Jainn-Shiu Chen
Hyperglycaemia during Chemotherapy for Acute Lymphoblastic Leukaemia among Taiwanese Children
Meng-Che Tsai, Jainn-Shiu Chen
P3-718
Effect of Reward-Based Motivation on Metabolic Control in Children and Adolescents with Type 1 Diabetes Mellitus
Cemil Kocyigit, Gonul Catli, Sule Penbe Can, Bumin Nuri Dundar
Effect of Reward-Based Motivation on Metabolic Control in Children and Adolescents with Type 1 Diabetes Mellitus
Cemil Kocyigit, Gonul Catli, Sule Penbe Can, Bumin Nuri Dundar
P3-719
Fanconi-Bickel syndrome due to a Novel SLC2A2 Mutation Presenting with Transient Neonatal Diabetes
Selin Elmaogullari, Fatma Demirel, Derya Tepe, Nida Dincel, Meltem Tayfun, Seyit Ahmet Ucakturk, Fatih Gurbuz, Houghton Jayne
Fanconi-Bickel syndrome due to a Novel SLC2A2 Mutation Presenting with Transient Neonatal Diabetes
Selin Elmaogullari, Fatma Demirel, Derya Tepe, Nida Dincel, Meltem Tayfun, Seyit Ahmet Ucakturk, Fatih Gurbuz, Houghton Jayne
P3-720
Cardiovascular autonomic neuropathy and early atherosclerosis in adolescent type 1 diabetic patient
Ahmed Battah, Soha Abd El Dayem, Abo El Magd El Bohy, Nagwa Abd Allah
Cardiovascular autonomic neuropathy and early atherosclerosis in adolescent type 1 diabetic patient
Ahmed Battah, Soha Abd El Dayem, Abo El Magd El Bohy, Nagwa Abd Allah
P3-721
GAD antibodies negative type 1 diabetes and Dravet syndrome
Sara Ciccone, Romana Marini, Lucia Fusco, Alessandra Terracciano, Riccardo Schiaffini, Marco Cappa
GAD antibodies negative type 1 diabetes and Dravet syndrome
Sara Ciccone, Romana Marini, Lucia Fusco, Alessandra Terracciano, Riccardo Schiaffini, Marco Cappa
P3-722
Social risk assessment in children with type 1 diabetes mellitus to plan medical and social care
Anna Karpushkina, Valentina Peterkova, Natalia Vartapetova, Elena Dedyukina, Alla Philimonova, Evgenia Mikhailova, Oleg Malievsky, Yulia Samoylova, Elena Bashnina, Elena Khramova, Oleg Shvabsky, Maria Pankratova, Mikhail Starovoitov
Social risk assessment in children with type 1 diabetes mellitus to plan medical and social care
Anna Karpushkina, Valentina Peterkova, Natalia Vartapetova, Elena Dedyukina, Alla Philimonova, Evgenia Mikhailova, Oleg Malievsky, Yulia Samoylova, Elena Bashnina, Elena Khramova, Oleg Shvabsky, Maria Pankratova, Mikhail Starovoitov
P3-723
The investigation of frequency of diabetic ketoacidosis in children with new-onset diabetes mellitus type 1.
Goar Okminyan, Lubov Samsonova, Elena Kiseleva, Oleg Latyshev, Evgenia Evsukova, Irina Kolomina, Elvira Kasatkina
The investigation of frequency of diabetic ketoacidosis in children with new-onset diabetes mellitus type 1.
Goar Okminyan, Lubov Samsonova, Elena Kiseleva, Oleg Latyshev, Evgenia Evsukova, Irina Kolomina, Elvira Kasatkina
P3-724
Study of Adiponectin Level in Diabetic Adolescent Girls in Relation to Glycemic Control and Complication of Diabetes
Soha Abd El Dayem, Hayam K. Nazif, Mona Abd El Kader, Maha El-Tawil, Ahmed Battah
Study of Adiponectin Level in Diabetic Adolescent Girls in Relation to Glycemic Control and Complication of Diabetes
Soha Abd El Dayem, Hayam K. Nazif, Mona Abd El Kader, Maha El-Tawil, Ahmed Battah
P3-725
Frequent and prolonged daytime hypoglycemia in diabetic children detected by continuous glucose monitoring (cgms): a problem of hypoglycemia unawareness?
Sara Bachmann, Kerstin Metzger, Melanie Hess, Urs Zumsteg
Frequent and prolonged daytime hypoglycemia in diabetic children detected by continuous glucose monitoring (cgms): a problem of hypoglycemia unawareness?
Sara Bachmann, Kerstin Metzger, Melanie Hess, Urs Zumsteg
P3-726
NEONATAL DIABETES MELLITUS DUE TO INSULIN GENE MUTATION
Bich Ngoc Can Thi, Dung Vu Chi, Thao Bui Phuong, Khanh Nguyen Ngoc, Maria Craig, Sian Ellard, Hoan Nguyen Thi
NEONATAL DIABETES MELLITUS DUE TO INSULIN GENE MUTATION
Bich Ngoc Can Thi, Dung Vu Chi, Thao Bui Phuong, Khanh Nguyen Ngoc, Maria Craig, Sian Ellard, Hoan Nguyen Thi
P3-727
SINGLE CENTRE EXPERIENCE OF NEONATAL DIABETES
V. SRI NAGESH, ANDREW HATTERSLEY, SIAN ELLARD, BIPIN KUMAR SETHI, RAVISHANKAR KANITHI, RAVI KUMAR NALLI, JAYANT KELWADE, HARSH PAREKH
SINGLE CENTRE EXPERIENCE OF NEONATAL DIABETES
V. SRI NAGESH, ANDREW HATTERSLEY, SIAN ELLARD, BIPIN KUMAR SETHI, RAVISHANKAR KANITHI, RAVI KUMAR NALLI, JAYANT KELWADE, HARSH PAREKH
P3-728
Assessment of the effect of the diagnosis of T1DM in the nutritional habits of unaffected family members
Avgi Karaiskou, Panagiota Triantafyllou, Athanasios Christoforidis
Assessment of the effect of the diagnosis of T1DM in the nutritional habits of unaffected family members
Avgi Karaiskou, Panagiota Triantafyllou, Athanasios Christoforidis
P3-729
LIFESTYLE AND METABOLIC CONTROL IN ADOLESCENTS WITH TYPE 1 DIABETES (T1D)
Gracia M. Lou-Francés, Aranzazu Garza-Espí, Elena Corella-Aznar, Marta Ferrer-Lozano
LIFESTYLE AND METABOLIC CONTROL IN ADOLESCENTS WITH TYPE 1 DIABETES (T1D)
Gracia M. Lou-Francés, Aranzazu Garza-Espí, Elena Corella-Aznar, Marta Ferrer-Lozano
P3-730
β cells’ functional exhaustion at Type 1 Diabetes onset may lead to early microvascular complications
Nektaria Papadopoulou, Catherine Dacou-Voutetakis, George Chrousos, Christina Kanaka-Gantenbein
β cells’ functional exhaustion at Type 1 Diabetes onset may lead to early microvascular complications
Nektaria Papadopoulou, Catherine Dacou-Voutetakis, George Chrousos, Christina Kanaka-Gantenbein
P3-731
Influence of pancreatic autoinmunity in the onset and progression of diabetes in pediatric population
Yoko Oyakawa, María Martín-Frías, Rosa Yelmo, Milagros Alonso, Belén Roldán, Raquel Barrio
Influence of pancreatic autoinmunity in the onset and progression of diabetes in pediatric population
Yoko Oyakawa, María Martín-Frías, Rosa Yelmo, Milagros Alonso, Belén Roldán, Raquel Barrio
P3-732
Severe insulin resistance and dyslipidaemia with unremarkable fat distribution in an adolescent girl due to mutation in the PPARG gene (Familial partial lipodystrophy type 3)
Carsten Döing, Sebastian Kummer, David Savage, Burak Salgin, Robert Sample, Ertan Mayatepek, Thomas Meissner
Severe insulin resistance and dyslipidaemia with unremarkable fat distribution in an adolescent girl due to mutation in the PPARG gene (Familial partial lipodystrophy type 3)
Carsten Döing, Sebastian Kummer, David Savage, Burak Salgin, Robert Sample, Ertan Mayatepek, Thomas Meissner
P3-733
Use of Smartphone, a Cellular Glucometer and Social Media App in the Management of Type 1 DM in the Adolescent Population: The Future of Diabetes Care
Rachel Rothenberg, Mary Zetelski, Jennifer Sivitz, Genna Klein, Amy Chartoff, JoAnn Pearson, Janet Post, Aviva Cohen, Javier Aisenberg, Steven Ghanny
Use of Smartphone, a Cellular Glucometer and Social Media App in the Management of Type 1 DM in the Adolescent Population: The Future of Diabetes Care
Rachel Rothenberg, Mary Zetelski, Jennifer Sivitz, Genna Klein, Amy Chartoff, JoAnn Pearson, Janet Post, Aviva Cohen, Javier Aisenberg, Steven Ghanny
P3-735
Cardiovascular risk factors in children and adolescents with type 1diabetes
Carla Ferreira, Helena Ferreira, Filipa Correia, Carla Meireles
Cardiovascular risk factors in children and adolescents with type 1diabetes
Carla Ferreira, Helena Ferreira, Filipa Correia, Carla Meireles
P3-736
Megaloblastic anemia and diabetes in a young girl
Anissa Messaaoui, Sylvie Tenoutasse, Harry Dorchy
Megaloblastic anemia and diabetes in a young girl
Anissa Messaaoui, Sylvie Tenoutasse, Harry Dorchy
P3-737
Audit assessing glycaemic control in children aged less than 16 years with Type 1 diabetes in Malta over the period 2013 – 2014.
Nancy Formosa, John Torpiano
Audit assessing glycaemic control in children aged less than 16 years with Type 1 diabetes in Malta over the period 2013 – 2014.
Nancy Formosa, John Torpiano
P3-738
Prestarium pharmacogenetic efficacy in predicting diabetic nephropathy in children and adolescents
Gulnara Rakhimova, Akida Sadikova
Prestarium pharmacogenetic efficacy in predicting diabetic nephropathy in children and adolescents
Gulnara Rakhimova, Akida Sadikova
P3-739
Assessment of Quality of life in adolescents with type 1 diabetes; A pilot study
Mona Hassan, Noha Musa, Rehab Abdel Hay, Ashgan Fathy
Assessment of Quality of life in adolescents with type 1 diabetes; A pilot study
Mona Hassan, Noha Musa, Rehab Abdel Hay, Ashgan Fathy
P3-740
MODY3 early identification and diagnosis
Lyubov Zilberman, Elena Sechko, Svetlana Sapunova, Olga Ivanova, Tamara Kuraeva
MODY3 early identification and diagnosis
Lyubov Zilberman, Elena Sechko, Svetlana Sapunova, Olga Ivanova, Tamara Kuraeva
P3-741
Low fT3 syndrome due to metabolic acidosis/ketoacidosis in Type 1 diabetes mellitus (type 1 DM)
Irina Demikhova, Susanne Bechtold Dalla Pozza, Claudia Weissenbacher, Carmen Sydlik, Julia Roeb, Heinrich Schmidt
Low fT3 syndrome due to metabolic acidosis/ketoacidosis in Type 1 diabetes mellitus (type 1 DM)
Irina Demikhova, Susanne Bechtold Dalla Pozza, Claudia Weissenbacher, Carmen Sydlik, Julia Roeb, Heinrich Schmidt
P3-742
Coping styles of adolescents with type 1 diabetes and their parents: Association with metabolic control and disease duration.
Feneli Karachaliou, Chrysa Drosatou, B Kandyla, Eirini Sakou, Antonia Mavri, Artemis Tsitsika, Kyriaki Karavanaki
Coping styles of adolescents with type 1 diabetes and their parents: Association with metabolic control and disease duration.
Feneli Karachaliou, Chrysa Drosatou, B Kandyla, Eirini Sakou, Antonia Mavri, Artemis Tsitsika, Kyriaki Karavanaki
P3-743
Examination of Diabetes Nurse Educator Guided Diabetes Care Team in Pediatric Type 1 Diabetes
Eman Alshehri
Examination of Diabetes Nurse Educator Guided Diabetes Care Team in Pediatric Type 1 Diabetes
Eman Alshehri
P3-744
Transition during adolescence, is there room to improve?
Sinead Glackin, Sinead Molloy, Orla Neylon
Transition during adolescence, is there room to improve?
Sinead Glackin, Sinead Molloy, Orla Neylon
P3-745
Vitamin D status in Egyptian children with T1D and the role of Vitamin D replacement on glycemic control
Mona Hafez, Mona Hassan, Sahar Sharaf, Noha Musa, Sally Sameh
Vitamin D status in Egyptian children with T1D and the role of Vitamin D replacement on glycemic control
Mona Hafez, Mona Hassan, Sahar Sharaf, Noha Musa, Sally Sameh
P3-746
RESIDUAL C-PEPTIDE IN PAEDIATRIC PATIENTS WITH TIPE 1 DIABETES
Maria Martin-Frias, Yoko P Oyakawa, Milagros Alonso, Belen Roldan, M Angeles Alvarez, Raquel Barrio
RESIDUAL C-PEPTIDE IN PAEDIATRIC PATIENTS WITH TIPE 1 DIABETES
Maria Martin-Frias, Yoko P Oyakawa, Milagros Alonso, Belen Roldan, M Angeles Alvarez, Raquel Barrio
P3-747
A novel nonsense mutation in the WFS1 gene causes the wolfram syndrome
shahab noorian, shahram savad, davood mohamadshahi
A novel nonsense mutation in the WFS1 gene causes the wolfram syndrome
shahab noorian, shahram savad, davood mohamadshahi
P3-748
Health Literacy of Caregivers of Children with Type 1 Diabetes: A Pilot Study on Impact on Glycemic Control in an Arabic-speaking Population
Dalia Al-Abdulrazzaq, Muneera Alhaddad, Amani Al-fadhli, Amna Alyousef, Abeer Altararwa, Maria Mahdi, Nabeela Zanati, Majedah AbdulRasoul, Abdulla Altaiar, Azza Shaltout
Health Literacy of Caregivers of Children with Type 1 Diabetes: A Pilot Study on Impact on Glycemic Control in an Arabic-speaking Population
Dalia Al-Abdulrazzaq, Muneera Alhaddad, Amani Al-fadhli, Amna Alyousef, Abeer Altararwa, Maria Mahdi, Nabeela Zanati, Majedah AbdulRasoul, Abdulla Altaiar, Azza Shaltout
P3-749
Achievement of therapy targets in children and adolescents with type 1 diabetes mellitus at the “Diabetes School”.
Gulnora Rakhimova, Said Ismailov, Akmaral Tashmanova, Nasiba Alimova
Achievement of therapy targets in children and adolescents with type 1 diabetes mellitus at the “Diabetes School”.
Gulnora Rakhimova, Said Ismailov, Akmaral Tashmanova, Nasiba Alimova
P3-750
Oral glucose tolerance test as a routine tool to discriminate high risk individuals of type 2 diabetes in child obesity
Thomas Kintis, Staffan Mårild, Jovanna Dahlgren
Oral glucose tolerance test as a routine tool to discriminate high risk individuals of type 2 diabetes in child obesity
Thomas Kintis, Staffan Mårild, Jovanna Dahlgren
P3-751
FASTING THE HOLY MONTH OF RAMADAN IN OLDER CHILDREN AND ADOLESCENCE WITH TYPE 1 DIABETES IN KUWAIT
kholoud Mohamed, Dalia Al-Abdulrazzaq, Eman El Busairi, Faisal Al Shawaf, Majedah Abdul-Rasoul
FASTING THE HOLY MONTH OF RAMADAN IN OLDER CHILDREN AND ADOLESCENCE WITH TYPE 1 DIABETES IN KUWAIT
kholoud Mohamed, Dalia Al-Abdulrazzaq, Eman El Busairi, Faisal Al Shawaf, Majedah Abdul-Rasoul
P3-752
The long-term insulin management with premixed insulin in neonates and infants with diabetes
Hakan Doneray, Muhammet Oktay Yalcinoz
The long-term insulin management with premixed insulin in neonates and infants with diabetes
Hakan Doneray, Muhammet Oktay Yalcinoz
P3-753
Gestational Diabetes mellitus: How well-established are the AWMF guidelines and which of the cord blood parameters suggest an experienced gestational diabetes ?
Alexandra Krause, Karl Otfried Schwab, Roland Hentschel
Gestational Diabetes mellitus: How well-established are the AWMF guidelines and which of the cord blood parameters suggest an experienced gestational diabetes ?
Alexandra Krause, Karl Otfried Schwab, Roland Hentschel
P3-754
Thyroid function and prevalence of celiac disease in children with T1D in Lithuanian pediatric population
Ingrida Stankute, Rimante Dobrovolskiene, Edita Jasinskiene, Giedre Mockeviciene, Brone Urbonaite, Dalia Marciulionyte, Nijole Jurgeviciene, Valerie Schwitzgebel
Thyroid function and prevalence of celiac disease in children with T1D in Lithuanian pediatric population
Ingrida Stankute, Rimante Dobrovolskiene, Edita Jasinskiene, Giedre Mockeviciene, Brone Urbonaite, Dalia Marciulionyte, Nijole Jurgeviciene, Valerie Schwitzgebel
P3-755
Severe hypertriglyceridemia in a child with severe diabetic ketoacidosis
Gülay Karagüzel, Recep Polat, Gülay Kaya, Semra Atasoy Yilmaz
Severe hypertriglyceridemia in a child with severe diabetic ketoacidosis
Gülay Karagüzel, Recep Polat, Gülay Kaya, Semra Atasoy Yilmaz
P3-756
Factors Related to Progression to Macroalbuminuria in Type 1 Diabetic Children with microalbuminuria
keun Hee Choi, Hwa Young Kim, Hae Woon Jung, Gyung Min Lee, Kyung A Jung, So Youn Kim, Young Ah Lee, Hye Rim Chung, Choong Ho Shin, Sei Won Yang
Factors Related to Progression to Macroalbuminuria in Type 1 Diabetic Children with microalbuminuria
keun Hee Choi, Hwa Young Kim, Hae Woon Jung, Gyung Min Lee, Kyung A Jung, So Youn Kim, Young Ah Lee, Hye Rim Chung, Choong Ho Shin, Sei Won Yang
P3-757
ACUTE PAINFUL NEUROPATHY IN A TEENAGER WITH TYPE 1 DIABETES (T1D) AND EATING DISORDERS
Maria Louraki, Marina Katsalouli, Dimitra Kallinikou, Christina Kanaka-Gantenbein, Betina Kandyla, Eirini Sakkou, Kyriaki Karavanaki
ACUTE PAINFUL NEUROPATHY IN A TEENAGER WITH TYPE 1 DIABETES (T1D) AND EATING DISORDERS
Maria Louraki, Marina Katsalouli, Dimitra Kallinikou, Christina Kanaka-Gantenbein, Betina Kandyla, Eirini Sakkou, Kyriaki Karavanaki
P3-758
A Case of Tacrolimus Related Posttranslated Diabetes Mellitus(PTDM)
Mehmet Keskin, Murat Karaoglan, Mehtap Akbalik Kara, Mithat Buyukcelik, Ozlem Keskin
A Case of Tacrolimus Related Posttranslated Diabetes Mellitus(PTDM)
Mehmet Keskin, Murat Karaoglan, Mehtap Akbalik Kara, Mithat Buyukcelik, Ozlem Keskin
P3-759
Short-term use of continuous glucose monitoring system in pediatric patients with type 1 diabetes mellitus and correlation with short-term improvement in glycemic control
Monica Bianco, Teresa Alesia, Ramon Durazo-Arvizu, Carla Minutti
Short-term use of continuous glucose monitoring system in pediatric patients with type 1 diabetes mellitus and correlation with short-term improvement in glycemic control
Monica Bianco, Teresa Alesia, Ramon Durazo-Arvizu, Carla Minutti
P3-760
Neonatal diabetes - the great masquerader Experiences from one hospital
Caroline Ponmani, Jeremy Allgrove, Evelien Gevers, Morgan Keane, Kausik Banerjee, Rachel Besser
Neonatal diabetes - the great masquerader Experiences from one hospital
Caroline Ponmani, Jeremy Allgrove, Evelien Gevers, Morgan Keane, Kausik Banerjee, Rachel Besser
P3-761
DAILY SUBCUTANEOUS INSULIN REQUIREMENTS OF CHILDREN WITH TYPE 1 DIABETES AFTER DIABETIC KETOACIDOSIS TREATMENT
Ihsan Esen, Selcuk Dogan
DAILY SUBCUTANEOUS INSULIN REQUIREMENTS OF CHILDREN WITH TYPE 1 DIABETES AFTER DIABETIC KETOACIDOSIS TREATMENT
Ihsan Esen, Selcuk Dogan
P3-762
METABOLIC CONTROL AND GLYCEMIC VARIABILITY IN PEDIATRIC PATIENTS WITH TYPE 1 DIABETES IN MULTIPLE DAILY INJECTIONS THERAPY USING AUTOMATED BOLUS CALCULATOR GLUCOMETER
Marta Murillo-Vallés, Federico Vazquez-San Miguel, María Martinez-Barahona, Joan Bel-Comós
METABOLIC CONTROL AND GLYCEMIC VARIABILITY IN PEDIATRIC PATIENTS WITH TYPE 1 DIABETES IN MULTIPLE DAILY INJECTIONS THERAPY USING AUTOMATED BOLUS CALCULATOR GLUCOMETER
Marta Murillo-Vallés, Federico Vazquez-San Miguel, María Martinez-Barahona, Joan Bel-Comós
P3-763
Maturity onset diabetes of the young: just think about it
Anissa Messaaoui, Sylvie Tenoutasse, Harry Dorchy
Maturity onset diabetes of the young: just think about it
Anissa Messaaoui, Sylvie Tenoutasse, Harry Dorchy
P3-764
THE ROLE OF KCNJ11 GENE IN NEONATAL DIABETES
Soha Abd El Dayem, Shereen Shawky, Mona Abd El Kader, Solaf Kamel, Rania Hassan Khalifa, Dalia El Lebedy, Dina Ahmed
THE ROLE OF KCNJ11 GENE IN NEONATAL DIABETES
Soha Abd El Dayem, Shereen Shawky, Mona Abd El Kader, Solaf Kamel, Rania Hassan Khalifa, Dalia El Lebedy, Dina Ahmed
P3-765
A case of DEND (developmental delay, epilepsy, and neonatal diabetes) syndrome with heterozygous KCNJ11 mutation successfully treated with sulfonylurea therapy
Ja Hye Kim, Ja Hyang Cho, Eungu Kang, Jin-Ho Choi, Gu-Hwan Kim, Han Wook Yoo
A case of DEND (developmental delay, epilepsy, and neonatal diabetes) syndrome with heterozygous KCNJ11 mutation successfully treated with sulfonylurea therapy
Ja Hye Kim, Ja Hyang Cho, Eungu Kang, Jin-Ho Choi, Gu-Hwan Kim, Han Wook Yoo
P3-766
TWO PERMANENT NEONATAL DIABETES MELLITUS CASES DUE TO MUTATION IN ABCC8 GENES IN VIET NAM: CLINICAL FEATURES AND LONG – TERM OUTCOME IN TREATING BY SULFONYLUREA (2008-2014)
Phuong Khanh Nguyen, Thoai Loan Huynh
TWO PERMANENT NEONATAL DIABETES MELLITUS CASES DUE TO MUTATION IN ABCC8 GENES IN VIET NAM: CLINICAL FEATURES AND LONG – TERM OUTCOME IN TREATING BY SULFONYLUREA (2008-2014)
Phuong Khanh Nguyen, Thoai Loan Huynh
P3-767
Type 1 diabetes in pediatric patients: demographic and clinical characterization
Helena Ferreira, Carla Ferreira, Filipa Correia, Carla Meireles
Type 1 diabetes in pediatric patients: demographic and clinical characterization
Helena Ferreira, Carla Ferreira, Filipa Correia, Carla Meireles
P3-769
Cutaneous Manifestations among Type 1 Diabetic Patients in DEMPU
Randa Youssef, Amany Ibrahim, Iman Amin, Amany Abd El naser
Cutaneous Manifestations among Type 1 Diabetic Patients in DEMPU
Randa Youssef, Amany Ibrahim, Iman Amin, Amany Abd El naser
P3-770
Particularités du diabete chez les enfants dont l'age de révélation est avant 5ans
Mazari wafaa, bouriche khadidja, senouci djawida, zerga yasmine, chiali snaa, bendeddouche salih
Particularités du diabete chez les enfants dont l'age de révélation est avant 5ans
Mazari wafaa, bouriche khadidja, senouci djawida, zerga yasmine, chiali snaa, bendeddouche salih
P3-771
Evaluation Of Boluses Delivered By Insulin Pump In TYPE1 Diabetes Mellitus Pediatric Patients
Snijezana Hasanbegovic
Evaluation Of Boluses Delivered By Insulin Pump In TYPE1 Diabetes Mellitus Pediatric Patients
Snijezana Hasanbegovic
P3-772
Insulin therapy in the pediatric age –group.
Hanna Mikhno, Anzhalika Solntsava, Natalia Volkova
Insulin therapy in the pediatric age –group.
Hanna Mikhno, Anzhalika Solntsava, Natalia Volkova
P3-773
MAURIAC SYNDROME, A RARE COMPLICATION OF TYPE 1 DIABETES MELLITUS
María José Rivero-Martín, M. Pilar Pérez-Segura, María José Alcázar-Villar, David Montes-Bentura, M. Eugenia Oros Milian
MAURIAC SYNDROME, A RARE COMPLICATION OF TYPE 1 DIABETES MELLITUS
María José Rivero-Martín, M. Pilar Pérez-Segura, María José Alcázar-Villar, David Montes-Bentura, M. Eugenia Oros Milian
P3-774
Is autoimmunity on the increase in type 1 Diabetes Mellitus?
Presentation of multiple auto-immune disorders at diagnosis of type 1 Diabetes Mellitus
Diluxshy Elangaratnam, Sadhanandham Punniyakodi, Vijith Puthi
Is autoimmunity on the increase in type 1 Diabetes Mellitus?
Presentation of multiple auto-immune disorders at diagnosis of type 1 Diabetes Mellitus
Diluxshy Elangaratnam, Sadhanandham Punniyakodi, Vijith Puthi
P3-775
Type 1 diabetes mellitus and precocios puberty : rare association
Mimouna Bessahraoui, Radia Rezak, Sidi mohamed Azzouz
Type 1 diabetes mellitus and precocios puberty : rare association
Mimouna Bessahraoui, Radia Rezak, Sidi mohamed Azzouz
P3-776
SCHOOL AGED PRESENTATION OF DIABETES MELLITUS TYPE 1 WITH REPEAT HYPERGLYCEMIA, POSITIVE PANCREATIC AUTOIMMUNITY AND RELATED GENETIC RISKS
Ana Dolores Alcalde, Magdalena Hawkins, Julia Yebra, Alfredo Tagarro, Alfonso Cañete
SCHOOL AGED PRESENTATION OF DIABETES MELLITUS TYPE 1 WITH REPEAT HYPERGLYCEMIA, POSITIVE PANCREATIC AUTOIMMUNITY AND RELATED GENETIC RISKS
Ana Dolores Alcalde, Magdalena Hawkins, Julia Yebra, Alfredo Tagarro, Alfonso Cañete
P3-777
Clinical changes observed AFTER SYSTEM IMPLEMENTATION OF JUNIORSTAR systems in children with Dm1a
Ignacio Diez-Lopez, Ainhoa Sarasua-Miranda, Isabel Lorente-Blazquez
Clinical changes observed AFTER SYSTEM IMPLEMENTATION OF JUNIORSTAR systems in children with Dm1a
Ignacio Diez-Lopez, Ainhoa Sarasua-Miranda, Isabel Lorente-Blazquez
P3-778
Metabolic control in children in northern Spain DM1A with deficit of vitamin D
Ignacio Diez-Lopez, Ainhoa Sarasua-Miranda, Isabel Lorente-Blazquez
Metabolic control in children in northern Spain DM1A with deficit of vitamin D
Ignacio Diez-Lopez, Ainhoa Sarasua-Miranda, Isabel Lorente-Blazquez
P3-779
Effects of Educational Interventions for Children and Adolescents with Type I Diabetes Mellitus
Abeer Atef, Mona Attia, Amany Ibrahim, Shaimaa Ibrahim, Wafaa Dowidar, Sameh Tawfik
Effects of Educational Interventions for Children and Adolescents with Type I Diabetes Mellitus
Abeer Atef, Mona Attia, Amany Ibrahim, Shaimaa Ibrahim, Wafaa Dowidar, Sameh Tawfik
LBP-1269
Reduced Humanin Levels In Children With Type-1 Diabetes Mellitus
Maria Isabel Hernandez, Junxiang Wan, Carolina Valdes, Alejandra Avila, Ethel Codner, Pinchas Cohen
Reduced Humanin Levels In Children With Type-1 Diabetes Mellitus
Maria Isabel Hernandez, Junxiang Wan, Carolina Valdes, Alejandra Avila, Ethel Codner, Pinchas Cohen
P1-103
Molecular Characterization of a Novel Non-Stop KCNJ11 Mutation Associated with a Dual Focal and Diffuse Hyperinsulinaemic Hypoglycaemia Phenotype
Ved Bhushan Arya, Qadeer Aziz, Sarah E. Flanagan, Sian Ellard, Andrew Tinker, Khalid Hussain
Molecular Characterization of a Novel Non-Stop KCNJ11 Mutation Associated with a Dual Focal and Diffuse Hyperinsulinaemic Hypoglycaemia Phenotype
Ved Bhushan Arya, Qadeer Aziz, Sarah E. Flanagan, Sian Ellard, Andrew Tinker, Khalid Hussain
P1-104
Diazoxide Responsive Congenital Hyperinsulinism in a Patient with Dual Genetic Aetiology (HNF4A and ABCC8 mutation)
Dinesh Giri, Sarah E. Flanagan, Julie Park, Sian Ellard, Mo Didi, Senthil Sennaippan
Diazoxide Responsive Congenital Hyperinsulinism in a Patient with Dual Genetic Aetiology (HNF4A and ABCC8 mutation)
Dinesh Giri, Sarah E. Flanagan, Julie Park, Sian Ellard, Mo Didi, Senthil Sennaippan
P1-105
Fluoxetine induced Hypoglycemia in a patient with Congenital Hyperinsulinism on Lanreotide Therapy
Dinesh Giri, Zoe Yung, Kelly Stirrup, Mo Didi, Senthil Seniappan
Fluoxetine induced Hypoglycemia in a patient with Congenital Hyperinsulinism on Lanreotide Therapy
Dinesh Giri, Zoe Yung, Kelly Stirrup, Mo Didi, Senthil Seniappan
P1-106
Influence of nocturnal glycemia on ventricular repolarization and heart rate variability in prepubertal children with type 1 diabetes.
Marie-Béatrice Saade, Aurélien Pecquet, Patrick Pladys, Alain Beuchée, Fabienne Pelé, Sylvie Nivot, Marc de Kerdanet
Influence of nocturnal glycemia on ventricular repolarization and heart rate variability in prepubertal children with type 1 diabetes.
Marie-Béatrice Saade, Aurélien Pecquet, Patrick Pladys, Alain Beuchée, Fabienne Pelé, Sylvie Nivot, Marc de Kerdanet
P2-485
Is Bedside Monitoring of Blood Beta-hydroxybutyrate Levels Reliable in the Management of Hypoglycaemia in Children?
Supriya Phanse, Catherine Collingwood, Hussain Alsaffar, Mohammed Didi, Senthil Senniappan
Is Bedside Monitoring of Blood Beta-hydroxybutyrate Levels Reliable in the Management of Hypoglycaemia in Children?
Supriya Phanse, Catherine Collingwood, Hussain Alsaffar, Mohammed Didi, Senthil Senniappan
P2-486
Transient Hyperinsulinaemic Hypoglycaemia in Association with a Novel ABCC8 Mutation: Expanding the Clinical Phenotypes
Ved Bhushan Arya, Qadeer Aziz, Zainaba Mohamed, Sarah E. Flanagan, Sian Ellard, Sarah Ehtisham, Andrew Tinker, Khalid Hussain
Transient Hyperinsulinaemic Hypoglycaemia in Association with a Novel ABCC8 Mutation: Expanding the Clinical Phenotypes
Ved Bhushan Arya, Qadeer Aziz, Zainaba Mohamed, Sarah E. Flanagan, Sian Ellard, Sarah Ehtisham, Andrew Tinker, Khalid Hussain
P2-487
Congenital hyperinsulinism in Ukraine
Eugenia Globa, Nataliya Zelinska, Sarah Flanagan, Sian Ellard, Henrik Christesen
Congenital hyperinsulinism in Ukraine
Eugenia Globa, Nataliya Zelinska, Sarah Flanagan, Sian Ellard, Henrik Christesen
P2-488
Unexplained altered states of consciousness in a girl
Stefanie Graf, Karine Gerster, Sabine Kroiss, Daniel Konrad, Eugen Schönle
Unexplained altered states of consciousness in a girl
Stefanie Graf, Karine Gerster, Sabine Kroiss, Daniel Konrad, Eugen Schönle
P2-489
The Effectiveness of Sirolimus in a Newborn with Hyperinsulinemic Hypoglycemia
Belma Haliloglu, Heybet Tuzun, Sarah Flanagan, Avni Kaya, Muhittin Celik
The Effectiveness of Sirolimus in a Newborn with Hyperinsulinemic Hypoglycemia
Belma Haliloglu, Heybet Tuzun, Sarah Flanagan, Avni Kaya, Muhittin Celik
P2-490
CONGENITAL HYPERINSULINISM CAUSED BY A COMBINATION OF NOVEL HETEROZYGOUS ABCC8 AND KCNJ11 MUTATIONS
Klara Rozenkova, Azizun Nessa, Barbora Obermannova, Lenka Dusatkova, Petra Dusatkova, Zdenek Sumnik, Jan Lebl, Khalid Hussain, Stepanka Pruhova
CONGENITAL HYPERINSULINISM CAUSED BY A COMBINATION OF NOVEL HETEROZYGOUS ABCC8 AND KCNJ11 MUTATIONS
Klara Rozenkova, Azizun Nessa, Barbora Obermannova, Lenka Dusatkova, Petra Dusatkova, Zdenek Sumnik, Jan Lebl, Khalid Hussain, Stepanka Pruhova
P2-491
FUNCTIONAL ANALYSIS OF NOVEL ABCC8 MUTATIONS FOUND IN CZECH PATIENTS WITH CONGENITAL HYPERINSULINISM
Klara Rozenkova, Petra Dusatkova, Lenka Dusatkova, Azizun Nessa, Barbora Obermannova, Jitka Kytnarova, Zdenek Sumnik, Jan Lebl, Khalid Hussain, Stepanka Pruhova
FUNCTIONAL ANALYSIS OF NOVEL ABCC8 MUTATIONS FOUND IN CZECH PATIENTS WITH CONGENITAL HYPERINSULINISM
Klara Rozenkova, Petra Dusatkova, Lenka Dusatkova, Azizun Nessa, Barbora Obermannova, Jitka Kytnarova, Zdenek Sumnik, Jan Lebl, Khalid Hussain, Stepanka Pruhova
P2-492
Syndromic hypoketotic, hypoinsulinemic hypoglycaemia due to a mosaic activating phosphatidylinositol 3-kinase (PI3K) mutation
Sebastian Kummer, Sarah M Leiter, Alena Welters, Ines Barroso, Thomas Meissner, Robert K Semple
Syndromic hypoketotic, hypoinsulinemic hypoglycaemia due to a mosaic activating phosphatidylinositol 3-kinase (PI3K) mutation
Sebastian Kummer, Sarah M Leiter, Alena Welters, Ines Barroso, Thomas Meissner, Robert K Semple
P2-493
Long Acting Somatostatin Analogue (Lanreotide) therapy in Congenital Hyperinsulinism - Pharmacokinetics and long term follow-up study
Pratik Shah, Sofia Rahman, Sharon McElroy, Clare Gilbert, Kate Morgan, Louise Hinchey, Syeda Alam, Senthil Senniappan, Roberta Button, Rebecca Margetts, Hannah Levy, Carles Morte Marti, Carles Celma Lezcano, Emma Bascompta Santacreu, Rakesh Amin, Khalid Hussain
Long Acting Somatostatin Analogue (Lanreotide) therapy in Congenital Hyperinsulinism - Pharmacokinetics and long term follow-up study
Pratik Shah, Sofia Rahman, Sharon McElroy, Clare Gilbert, Kate Morgan, Louise Hinchey, Syeda Alam, Senthil Senniappan, Roberta Button, Rebecca Margetts, Hannah Levy, Carles Morte Marti, Carles Celma Lezcano, Emma Bascompta Santacreu, Rakesh Amin, Khalid Hussain
P2-494
Congenital Hyperinsulinism in association with Poland Syndrome and Chromosome 10p11-p13 duplication
Dinesh Giri, Rachel Hart, Kamal Weerasinghe, Mo Didi, Senthil Senniappan
Congenital Hyperinsulinism in association with Poland Syndrome and Chromosome 10p11-p13 duplication
Dinesh Giri, Rachel Hart, Kamal Weerasinghe, Mo Didi, Senthil Senniappan
P2-495
Rapid Biochemical Evaluation Aids Timely Management of Congenital Hyperinsulinism
Georgia Swain, Julie Park, Kelly Stirrup, Zoe Yung, Senthil Senniappan, Mohammed Didi
Rapid Biochemical Evaluation Aids Timely Management of Congenital Hyperinsulinism
Georgia Swain, Julie Park, Kelly Stirrup, Zoe Yung, Senthil Senniappan, Mohammed Didi
P3-1058
Cystic encephalomalacia and infantile spasm as a complication of transient and mild hyperinsulinemic hypoglycemia
Ahmet Anik, Ayse Anik, Tolga Unuvar, Ayse Fahriye Tosun, Siar Dursun, Abdullah Baris Akcan, Yasemin Durum, Munevver Kaynak Turkmen
Cystic encephalomalacia and infantile spasm as a complication of transient and mild hyperinsulinemic hypoglycemia
Ahmet Anik, Ayse Anik, Tolga Unuvar, Ayse Fahriye Tosun, Siar Dursun, Abdullah Baris Akcan, Yasemin Durum, Munevver Kaynak Turkmen
P3-1059
HYPERGLYCEMIA PRECEDED BY NEONATAL HYPERINSULINEMIC HYPOGLYCEMIA IN INFANTS WITH NOVEL HNF1A MUTATIONS
Jana Malikova, Barbora Obermannova, Klara Rozenkova, Lenka Dusatkova, Petra Dusatkova, Lise Bjørkhaug, Ingvild Aukrust, Jan Lebl, Stepanka Pruhova
HYPERGLYCEMIA PRECEDED BY NEONATAL HYPERINSULINEMIC HYPOGLYCEMIA IN INFANTS WITH NOVEL HNF1A MUTATIONS
Jana Malikova, Barbora Obermannova, Klara Rozenkova, Lenka Dusatkova, Petra Dusatkova, Lise Bjørkhaug, Ingvild Aukrust, Jan Lebl, Stepanka Pruhova
P3-1060
Transient congenital hyperinsulinism and renal Fanconi syndrome
Corinna Melanie Brichta, Martin Pohl, Ekkehart Lausch, Jürgen Kohlhase, Natascha van der Werf-Grohmann, Michael Wurm, Alexandra Krause, Karl Otfried Schwab
Transient congenital hyperinsulinism and renal Fanconi syndrome
Corinna Melanie Brichta, Martin Pohl, Ekkehart Lausch, Jürgen Kohlhase, Natascha van der Werf-Grohmann, Michael Wurm, Alexandra Krause, Karl Otfried Schwab
P3-1061
Clinical characteristics and molecular analysis of Turkish patients with congenital hyperinsulinism: A Single-Center Experience with 15 cases
Sebahat Yilmaz Agladioglu, Zehra Aycan, Semra Cetinkaya, Senay Savas Erdeve, Elif Sagsak, Meliksah Keskin, Erdal Kurnaz, Sarah E Flanagan, Sian Ellard, Khalid Hussain
Clinical characteristics and molecular analysis of Turkish patients with congenital hyperinsulinism: A Single-Center Experience with 15 cases
Sebahat Yilmaz Agladioglu, Zehra Aycan, Semra Cetinkaya, Senay Savas Erdeve, Elif Sagsak, Meliksah Keskin, Erdal Kurnaz, Sarah E Flanagan, Sian Ellard, Khalid Hussain
P3-1062
Congenital Hyperinsulinemic Hypoglycemia of Infancy, Renal Fanconi Syndrome and Hepatopathy due to a Mutation in the HNF4A Gene
Alejandro Vargas Pieck, María Clemente León, Ariana Campos Martorell, Luis Castaño González, Gema Ariceta Iraola, Antonio Carrascosa Lezcano
Congenital Hyperinsulinemic Hypoglycemia of Infancy, Renal Fanconi Syndrome and Hepatopathy due to a Mutation in the HNF4A Gene
Alejandro Vargas Pieck, María Clemente León, Ariana Campos Martorell, Luis Castaño González, Gema Ariceta Iraola, Antonio Carrascosa Lezcano
P3-1063
Genotype-phenotype associations in 90 children with congenital hyperinsulinism
Maria Melikyan, Henrik Christesen, Elena Petryakina, Anatoly Tulpakov, Julia Tihonovich, Alexey Stepanov, Maria Kareva, Sarah Flanagan, Sian Ellard, Klaus Brusgaard, Valentina Peterkova, Khalid Hussain
Genotype-phenotype associations in 90 children with congenital hyperinsulinism
Maria Melikyan, Henrik Christesen, Elena Petryakina, Anatoly Tulpakov, Julia Tihonovich, Alexey Stepanov, Maria Kareva, Sarah Flanagan, Sian Ellard, Klaus Brusgaard, Valentina Peterkova, Khalid Hussain
P3-1064
Comparison of diagnostic value of blood glucose meter with laboratory method in neonatal hypoglycemia
Robabeh Ghergherehchi, Manizheh Mostafa Gharehbaghi, Nazanin Hazhir
Comparison of diagnostic value of blood glucose meter with laboratory method in neonatal hypoglycemia
Robabeh Ghergherehchi, Manizheh Mostafa Gharehbaghi, Nazanin Hazhir
P3-1065
Glycogen-Storage Disease Type VI in a girl presenting with Recurrent Ketotic Hypoglycaemia but no Hepatomegaly
Victoria Price, Mohammed Didi, Andrew Morris, Senthil Senniappan
Glycogen-Storage Disease Type VI in a girl presenting with Recurrent Ketotic Hypoglycaemia but no Hepatomegaly
Victoria Price, Mohammed Didi, Andrew Morris, Senthil Senniappan
P3-1066
Congenital hyperinsulinism in a newborn with a novel paternally inherited heterozygous mutation ( p.E1517G ) in the ABCC8 gene
Nancy Elbarbary, Sian Ellard, Khalid Hussain
Congenital hyperinsulinism in a newborn with a novel paternally inherited heterozygous mutation ( p.E1517G ) in the ABCC8 gene
Nancy Elbarbary, Sian Ellard, Khalid Hussain
P3-1067
Discontinuation of Diazoxide therapy in children with Hyperinsulinaemic Hypoglycaemia with no identified genetic aetiology. A long-term follow-up study.
Mouza AlYahyaei, Pratik Shah, Maria Guemes, Clare Gilbert, Kate Morgan, Sarah Flanagan, Sian Ellard, Khalid Hussain
Discontinuation of Diazoxide therapy in children with Hyperinsulinaemic Hypoglycaemia with no identified genetic aetiology. A long-term follow-up study.
Mouza AlYahyaei, Pratik Shah, Maria Guemes, Clare Gilbert, Kate Morgan, Sarah Flanagan, Sian Ellard, Khalid Hussain
P3-1068
Pancreatic hormones in children with hyperinsulinaemic hypoglycaemia
Maria Güemes, Clare Gilbert, Kate Morgan, Sofia Rahman, Khalid Hussain
Pancreatic hormones in children with hyperinsulinaemic hypoglycaemia
Maria Güemes, Clare Gilbert, Kate Morgan, Sofia Rahman, Khalid Hussain
P3-1069
Experience based on 193 18-F-DOPA PET CTs in patients with congenital hyperinsulinism: Pearls and pitfalls in imaging diagnostics in patients with CHI
Peter Kühnen, Vikas Prasad, Winfried Brenner, Wolfgang Mohnike, Oliver Blankenstein
Experience based on 193 18-F-DOPA PET CTs in patients with congenital hyperinsulinism: Pearls and pitfalls in imaging diagnostics in patients with CHI
Peter Kühnen, Vikas Prasad, Winfried Brenner, Wolfgang Mohnike, Oliver Blankenstein
P3-1071
A case of mild congenital hyperinsulinemia presenting with developmental delay, complicated by diazoxide-induced transient neutropenia
Yuki Abe, Yoshimi Nishizaki, Seiichi Sato
A case of mild congenital hyperinsulinemia presenting with developmental delay, complicated by diazoxide-induced transient neutropenia
Yuki Abe, Yoshimi Nishizaki, Seiichi Sato
P3-1072
Failure of Sirolimus response on three more cases with a diffuse type of Congenital hyperinsulinism
Angham al Mutair, Rana Al BALWI, Ahlam al Otaibi, Mohsen Atawi
Failure of Sirolimus response on three more cases with a diffuse type of Congenital hyperinsulinism
Angham al Mutair, Rana Al BALWI, Ahlam al Otaibi, Mohsen Atawi
P3-1073
Auxological characteristics of persistent hyperinsulinemic hypoglycemia at birth
Hironori Shibata, Mamiko Yamada, Tomohiro Ishii, Yohei Matsuzaki, Kazushige Ikeda, Yuka Nagashima, Masaki Takagi, Yukihiro Hasegawa, Tomonobu Hasegawa
Auxological characteristics of persistent hyperinsulinemic hypoglycemia at birth
Hironori Shibata, Mamiko Yamada, Tomohiro Ishii, Yohei Matsuzaki, Kazushige Ikeda, Yuka Nagashima, Masaki Takagi, Yukihiro Hasegawa, Tomonobu Hasegawa
P3-1074
Congenital hyperinsulinism in siblings – case report.
Agnieszka Brandt, Marta Buraczewska, Małgorzata Myśliwiec
Congenital hyperinsulinism in siblings – case report.
Agnieszka Brandt, Marta Buraczewska, Małgorzata Myśliwiec
P3-1075
GENETIC CAUSES OF CONGENITAL HYPERINSULINISM IN SLOVAKIA
Juraj Staník, Lucia Valentínová, Martina Škopková, Monika Rosoľanková, Daniela Staníková, Ľubica Tichá, Daniela Gašperíková, Iwar Klimeš
GENETIC CAUSES OF CONGENITAL HYPERINSULINISM IN SLOVAKIA
Juraj Staník, Lucia Valentínová, Martina Škopková, Monika Rosoľanková, Daniela Staníková, Ľubica Tichá, Daniela Gašperíková, Iwar Klimeš
P3-1076
Hyperinsulinism secondary to congenital portosystemic shunt in a neonate
Yong Hee Hong, Dong Hoon Lee, Sung Shin Kim
Hyperinsulinism secondary to congenital portosystemic shunt in a neonate
Yong Hee Hong, Dong Hoon Lee, Sung Shin Kim
P3-1077
Clinical presentation of a patient with a novel homozygous mutation in the TRPM6 gene.
Ayça ALTINCIK, Karl Peter SCHLINGMANN
Clinical presentation of a patient with a novel homozygous mutation in the TRPM6 gene.
Ayça ALTINCIK, Karl Peter SCHLINGMANN
P3-1078
Long acting somatostatin analogs in the management of congenital hyperinsulinism in cases with poor compliance to conventional therapy
Huseyin Demirbilek, Kahraman Oncel, Mehmet Nuri Ozbek, Ahmet Deniz, Birsen Baysal, Ved Bhushan Arya, Sarah E. Flanagan, Sian Ellard, Khalid Hussain
Long acting somatostatin analogs in the management of congenital hyperinsulinism in cases with poor compliance to conventional therapy
Huseyin Demirbilek, Kahraman Oncel, Mehmet Nuri Ozbek, Ahmet Deniz, Birsen Baysal, Ved Bhushan Arya, Sarah E. Flanagan, Sian Ellard, Khalid Hussain
P3-1079
Isolated Postprandial Hyperinsulinaemic Hypoglycaemia
Maria Güemes, Maria Melikyan, Senthil Senniappan, Khalid Hussain
Isolated Postprandial Hyperinsulinaemic Hypoglycaemia
Maria Güemes, Maria Melikyan, Senthil Senniappan, Khalid Hussain
P3-1080
Severe Congenital Hyperinsulinism in a Neonate Homozygous for Two Novel Missense Mutations in the KCNJ11 Gene
Alev Ozon, Ayfer Alikasifoglu, Sian Ellard, Sarah Flanagan, Nazli Gonc, Diclehan Orhan, Saniye Ekinci, Nurgun Kandemir
Severe Congenital Hyperinsulinism in a Neonate Homozygous for Two Novel Missense Mutations in the KCNJ11 Gene
Alev Ozon, Ayfer Alikasifoglu, Sian Ellard, Sarah Flanagan, Nazli Gonc, Diclehan Orhan, Saniye Ekinci, Nurgun Kandemir
P3-1081
Congenital glucose-galactose malabsorption in a male infant
Nevenka Slaveska, Marina Krstevska-Konstantinova
Congenital glucose-galactose malabsorption in a male infant
Nevenka Slaveska, Marina Krstevska-Konstantinova
P3-1082
PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY EVALUATION - IS HYNIC TOC AN ALTERNATIVE TO 18F DOPA?
GOKUL RAMANATHAN, ASHWATH DURAISWAMY
PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY EVALUATION - IS HYNIC TOC AN ALTERNATIVE TO 18F DOPA?
GOKUL RAMANATHAN, ASHWATH DURAISWAMY
LBP-1258
A Distinct Population of Islet Cells Defines Diffuse Congenital Hyperinsulinism in Infancy but Not Other Forms of the Disease
Bing Han, Melanie Newbould, Gauri Batra, Edmund Cheesman, Ross Craigie, Zainab Mohammad, Lindsey Rigby, Raja Padidela, Mars Skae, Aleksandr Mironov, Tobias Starborg, Karl Kadler, Karen Cosgrove, Indraneel Banerjee, Mark Dunne
A Distinct Population of Islet Cells Defines Diffuse Congenital Hyperinsulinism in Infancy but Not Other Forms of the Disease
Bing Han, Melanie Newbould, Gauri Batra, Edmund Cheesman, Ross Craigie, Zainab Mohammad, Lindsey Rigby, Raja Padidela, Mars Skae, Aleksandr Mironov, Tobias Starborg, Karl Kadler, Karen Cosgrove, Indraneel Banerjee, Mark Dunne
P1-107
CHANGES IN SERUM PROTEIN EXPRESSION IN SMALL-FOR-GESTATIONAL-AGE NEWBORN INFANTS AT DIFFERENT GESTATIONAL AGES
Ramón Cañete, María Dolores Ruiz-González, María Dolores Cañete, José Luis Gómez-Chaparro, Nieves Abril-Díaz, Juan Luis López-Barea
CHANGES IN SERUM PROTEIN EXPRESSION IN SMALL-FOR-GESTATIONAL-AGE NEWBORN INFANTS AT DIFFERENT GESTATIONAL AGES
Ramón Cañete, María Dolores Ruiz-González, María Dolores Cañete, José Luis Gómez-Chaparro, Nieves Abril-Díaz, Juan Luis López-Barea
P1-108
Liver ER stress and Intrauterine growth retardation in rats
Annalisa Deodati, Josepmaria Argemi, Antonella Puglianiello, Daniela Germani, Roberto Ferrero, Tomas Aragon, Stefano Cianfarani
Liver ER stress and Intrauterine growth retardation in rats
Annalisa Deodati, Josepmaria Argemi, Antonella Puglianiello, Daniela Germani, Roberto Ferrero, Tomas Aragon, Stefano Cianfarani
P1-109
Continuous subcutaneous infusion of recombinant LH and FSH during early infancy promotes testicular descent in congenital hypogonadotropic hypogonadism.
Anne Sophie LAMBERT, Philippe Lucchini, Claire Bouvattier, Pierre Bougnères
Continuous subcutaneous infusion of recombinant LH and FSH during early infancy promotes testicular descent in congenital hypogonadotropic hypogonadism.
Anne Sophie LAMBERT, Philippe Lucchini, Claire Bouvattier, Pierre Bougnères
P1-110
Neonatal screening program for Central Congenital Hypothyroidism
Debora Braslavsky, Laura Prieto, Ana Keselman, Laura Gruñeiro de Papendieck, Rosa Enacan, Virginia Mendez, Ignacio Bergadá, Ana Chiesa
Neonatal screening program for Central Congenital Hypothyroidism
Debora Braslavsky, Laura Prieto, Ana Keselman, Laura Gruñeiro de Papendieck, Rosa Enacan, Virginia Mendez, Ignacio Bergadá, Ana Chiesa
P2-496
Serial 3-dimensional ultrasonographic evaluation of foetal adrenal volumes in the 2nd and 3rd trimester of pregnancy characterises human adrenal development in utero.
Nerma Baftic, Harshini Katugampola, Muriel Meso, Rebecca Allen, Shemoon Marleen, Shezan Elahi, Joe Aquilina, Leo Dunkel, Helen Storr
Serial 3-dimensional ultrasonographic evaluation of foetal adrenal volumes in the 2nd and 3rd trimester of pregnancy characterises human adrenal development in utero.
Nerma Baftic, Harshini Katugampola, Muriel Meso, Rebecca Allen, Shemoon Marleen, Shezan Elahi, Joe Aquilina, Leo Dunkel, Helen Storr
P2-497
Genetic variation in the FSH signalling pathway affects female reproductive hormones during infancy
Louise S. Henriksen, Casper P. Hagen, Maria Assens, Kristian Almstrup, Katharina M. Main
Genetic variation in the FSH signalling pathway affects female reproductive hormones during infancy
Louise S. Henriksen, Casper P. Hagen, Maria Assens, Kristian Almstrup, Katharina M. Main
P2-498
Longitudinal comparison of inhibin B and AMH levels and testicular volumes between preterm and full-term infant boys
Tanja Kuiri-Hänninen, Raija Seuri, Erja Tyrväinen, Leo Dunkel, Ulla Sankilampi
Longitudinal comparison of inhibin B and AMH levels and testicular volumes between preterm and full-term infant boys
Tanja Kuiri-Hänninen, Raija Seuri, Erja Tyrväinen, Leo Dunkel, Ulla Sankilampi
P2-499
Postnatal catch-down growth is not associated with disturbances in metabolic parameters in large-for-gestational-age infants at the age of eight years
Julia Peters, Joachim Woelfle, Susanne Joergens, Peter Bartmann, Bettina Gohlke
Postnatal catch-down growth is not associated with disturbances in metabolic parameters in large-for-gestational-age infants at the age of eight years
Julia Peters, Joachim Woelfle, Susanne Joergens, Peter Bartmann, Bettina Gohlke
P2-500
Birth incidence of Prader-Willi syndrome in France
Céline Bar, Gwenaelle Diene, Catherine Molinas, Charlotte Casper, Maithé Tauber
Birth incidence of Prader-Willi syndrome in France
Céline Bar, Gwenaelle Diene, Catherine Molinas, Charlotte Casper, Maithé Tauber
P2-501
Variation of Environmental Chemicals Measured in Serum During Pregnancy
Maria Assens, Hanne Frederiksen, Anders Juul, Katharina Main
Variation of Environmental Chemicals Measured in Serum During Pregnancy
Maria Assens, Hanne Frederiksen, Anders Juul, Katharina Main
P2-502
Auxological parameters, endocrine growth factors and insulin resistance from birth to 12 months of life in children born small for gestational age (SGA)
Laura Guazzarotti, Silvia Mauri, Federica Occhipinti, Mariangela Petruzzi, Micol Sonnino, Andrea Angela Tenconi, Laura Pogliani, Gian Vincenzo Zuccotti
Auxological parameters, endocrine growth factors and insulin resistance from birth to 12 months of life in children born small for gestational age (SGA)
Laura Guazzarotti, Silvia Mauri, Federica Occhipinti, Mariangela Petruzzi, Micol Sonnino, Andrea Angela Tenconi, Laura Pogliani, Gian Vincenzo Zuccotti
P2-503
SERUM FETUIN-A LEVEL FOR DIAGNOSIS HEPATIC STEATOSIS IN CHILDEREN WITH TYPE 1 DIABETES MELLITUS
Selim Kurtoglu, Murat Dogan, Nihal Hatipoglu, Sebahattin Muhtaroglu, Selim Doganay, Ulku Gul, Ferhan Elmali
SERUM FETUIN-A LEVEL FOR DIAGNOSIS HEPATIC STEATOSIS IN CHILDEREN WITH TYPE 1 DIABETES MELLITUS
Selim Kurtoglu, Murat Dogan, Nihal Hatipoglu, Sebahattin Muhtaroglu, Selim Doganay, Ulku Gul, Ferhan Elmali
P2-504
Association of Dll4 levels and VEGFR-1, VEGFR-2 in mice model of oxygen-induced retinopathy
wangkai liu, yihua su, siqi zhuang, xiaoyu li, yijuan li
Association of Dll4 levels and VEGFR-1, VEGFR-2 in mice model of oxygen-induced retinopathy
wangkai liu, yihua su, siqi zhuang, xiaoyu li, yijuan li
P2-505
EVALUATION OF THYROID FUNCTION IN PRETERM NEWBORNS OF 24-30 WEEKS OF GESTATION
CAMPOS-MARTORELL ARIADNA, CLEMENTE MARIA, YESTE DIEGO, CASTILLO FELIX, NARVAEZ KARLA MARIA, CARRASCOSA ANTONIO
EVALUATION OF THYROID FUNCTION IN PRETERM NEWBORNS OF 24-30 WEEKS OF GESTATION
CAMPOS-MARTORELL ARIADNA, CLEMENTE MARIA, YESTE DIEGO, CASTILLO FELIX, NARVAEZ KARLA MARIA, CARRASCOSA ANTONIO
P2-506
The gonads condition in 1 – 3 month boys with unilateral cryptorchidism
Nadezda Raygorodskaya, Nina Bolotova
The gonads condition in 1 – 3 month boys with unilateral cryptorchidism
Nadezda Raygorodskaya, Nina Bolotova
P3-1070
Severe neonatal hypoglycemia in the newborn despite prenatal diagnosed cerebral midline malformations – A review of three cases
Felix Reschke, Gita Gemulla, Monika Flury, Sebastian Brenner, Heike Schuetzle, Heidrun Gurth, Gabriele Hahn, Heike Taut, Jack Glajzer, Hans-Christian Gottschalk, Angela Hübner
Severe neonatal hypoglycemia in the newborn despite prenatal diagnosed cerebral midline malformations – A review of three cases
Felix Reschke, Gita Gemulla, Monika Flury, Sebastian Brenner, Heike Schuetzle, Heidrun Gurth, Gabriele Hahn, Heike Taut, Jack Glajzer, Hans-Christian Gottschalk, Angela Hübner
P3-1083
Cholestatic hepatopathy and hypoglycaemic seizures as primary manifestation of hypocortisolism in infancy
Peter Saupp, Michael Fried, Carsten Bergmann, Thomas Meissner, Sebastian Kummer
Cholestatic hepatopathy and hypoglycaemic seizures as primary manifestation of hypocortisolism in infancy
Peter Saupp, Michael Fried, Carsten Bergmann, Thomas Meissner, Sebastian Kummer
P3-1084
Plasma Kisspeptin Levels of Infants Breast Growth in Neonatal Period
Avni Kaya, Zerrin Orbak, Harun Polat, Atilla Çayir, Abdullah Erdil, Hakan Döneray
Plasma Kisspeptin Levels of Infants Breast Growth in Neonatal Period
Avni Kaya, Zerrin Orbak, Harun Polat, Atilla Çayir, Abdullah Erdil, Hakan Döneray
P3-1085
Circadian variation in cortisol concentration in mother’s milk.
Bibian van der Voorn, Annemieke Heijboer, Marita de Waard, Hester Verheijen, Joost Rotteveel, Martijn Finken
Circadian variation in cortisol concentration in mother’s milk.
Bibian van der Voorn, Annemieke Heijboer, Marita de Waard, Hester Verheijen, Joost Rotteveel, Martijn Finken
P3-1086
Usefulness of ultrasonography for detecting adrenal hemorrhage in neonates with relative adrenal insufficiency
Kyung A Jeong, Hwa Young Kim, Hae Woon Jung, So Youn Kim, Keun Hee Choi, Gyung Min Lee, Young Ah Lee, Choong Ho Shin, Sei Won Yang
Usefulness of ultrasonography for detecting adrenal hemorrhage in neonates with relative adrenal insufficiency
Kyung A Jeong, Hwa Young Kim, Hae Woon Jung, So Youn Kim, Keun Hee Choi, Gyung Min Lee, Young Ah Lee, Choong Ho Shin, Sei Won Yang
P3-1087
Differences in leptin levels between newborns with and without Intrauterine Growth Restriction born in the Hospital Gineco Obstétrico “Isidro Ayora” of Quito-Ecuador. Year 2013-2014.
Maria Elisa Acosta De la Vega, Marco Antonio Pino, William Daniel Acosta Naranjo, Alfredo Naranjo
Differences in leptin levels between newborns with and without Intrauterine Growth Restriction born in the Hospital Gineco Obstétrico “Isidro Ayora” of Quito-Ecuador. Year 2013-2014.
Maria Elisa Acosta De la Vega, Marco Antonio Pino, William Daniel Acosta Naranjo, Alfredo Naranjo
P3-1088
Leptin and Neuropeptide Y Levels in Newborns
Avni Kaya, Zerrin Orbak, Ismail Polat, Harun Polat, Musa Gümüsdere
Leptin and Neuropeptide Y Levels in Newborns
Avni Kaya, Zerrin Orbak, Ismail Polat, Harun Polat, Musa Gümüsdere
P3-1089
CORD BLOOD AND MATERNAL SERUM INSULIN-LIKE GROWTH FACTOR-I,II(IGF-I,II) , INSULIN-LIKE GROWTH FACTOR BINDING PROTEIN-3 (IGFBP-3) LEVELS IN OVERWEIGHT PREGNANTS
Aysehan Akinci, Önder Celik, Ibrahim Ozerol
CORD BLOOD AND MATERNAL SERUM INSULIN-LIKE GROWTH FACTOR-I,II(IGF-I,II) , INSULIN-LIKE GROWTH FACTOR BINDING PROTEIN-3 (IGFBP-3) LEVELS IN OVERWEIGHT PREGNANTS
Aysehan Akinci, Önder Celik, Ibrahim Ozerol
P3-1090
Crystal formation in the meibomian glands as diagnostic proof of pseudohypoaldosteronism type I
Natascha van der Werf-Grohmann, Ekkehart Lausch, Michael Wurm, Cecil Kannan, Hans Fuchs, Ute Spiekerkötter, Karl Otfried Schwab
Crystal formation in the meibomian glands as diagnostic proof of pseudohypoaldosteronism type I
Natascha van der Werf-Grohmann, Ekkehart Lausch, Michael Wurm, Cecil Kannan, Hans Fuchs, Ute Spiekerkötter, Karl Otfried Schwab
P3-1091
TRANSIENT NEONATAL HYPOPARATHYROIDISM SECONDARY TO AN UNKNOWN MATERNAL PARATHYROID ADENOMA
PEREZ MARIA TERESA, LABRA REGINA, LLORENTE ANA
TRANSIENT NEONATAL HYPOPARATHYROIDISM SECONDARY TO AN UNKNOWN MATERNAL PARATHYROID ADENOMA
PEREZ MARIA TERESA, LABRA REGINA, LLORENTE ANA
P3-1092
Relations of birth chest circumference to blood serum Insulin-like Growth Factor-I in the newborn free of life-threatening disease: possible role of birth body weight in addition to respiratory supportive treatment.
Cesare Terzi, Werner F. Blum, Gabriele Tridenti, Andrea Cerioli, Marco Riani, Elena Chesi, Sergio Bernasconi, Gian Luigi Dé Angelis, Cristiana Magnani, Raffaele Virdis, Giacomo Banchini
Relations of birth chest circumference to blood serum Insulin-like Growth Factor-I in the newborn free of life-threatening disease: possible role of birth body weight in addition to respiratory supportive treatment.
Cesare Terzi, Werner F. Blum, Gabriele Tridenti, Andrea Cerioli, Marco Riani, Elena Chesi, Sergio Bernasconi, Gian Luigi Dé Angelis, Cristiana Magnani, Raffaele Virdis, Giacomo Banchini
P3-1093
Relations of birth chest circumference to blood serum Insulin-like Growth Factor Binding Protein-3 in the newborn free of life-threatening disease: relevance of birth body weight and of blood serum Insulin-like Growth Factor-I beyond respiratory supportive treatment.
Cesare Terzi, Raffaele Virdis, Gabriele Tridenti, Lidia Garavelli, Andrea Cerioli, Marco Riani, Sergio Bernasconi, Gian Luigi Dé Angelis, Cristiana Magnani, Werner F. Blum, Giacomo Banchini
Relations of birth chest circumference to blood serum Insulin-like Growth Factor Binding Protein-3 in the newborn free of life-threatening disease: relevance of birth body weight and of blood serum Insulin-like Growth Factor-I beyond respiratory supportive treatment.
Cesare Terzi, Raffaele Virdis, Gabriele Tridenti, Lidia Garavelli, Andrea Cerioli, Marco Riani, Sergio Bernasconi, Gian Luigi Dé Angelis, Cristiana Magnani, Werner F. Blum, Giacomo Banchini
P3-1094
EPIPEG-PREMEB proyect. Clinical situation before 12 mouths go on a SGA population
Ainhoa Sarasua-Miranda, Ignacio Diez-Lopez, Marta del Hoyo-Moracho, Isabel Lorente-Blazquez, Raquel Gomez de Segura, Dorleta Perez-Campos, Maria Teresa Macarulla-Arenaza, Victor Manuel Rodriguez-Rivera
EPIPEG-PREMEB proyect. Clinical situation before 12 mouths go on a SGA population
Ainhoa Sarasua-Miranda, Ignacio Diez-Lopez, Marta del Hoyo-Moracho, Isabel Lorente-Blazquez, Raquel Gomez de Segura, Dorleta Perez-Campos, Maria Teresa Macarulla-Arenaza, Victor Manuel Rodriguez-Rivera
P3-1095
McCune-Allbright syndrome in a male newborn with hyperthiroydism
María Esperanza Rueda Valencia, Olga Pérez Rodríguez, Diego López de Lara, Esther Vaquero Sosa, María Isabel Armadá Maresca, Enrique Criado Vega
McCune-Allbright syndrome in a male newborn with hyperthiroydism
María Esperanza Rueda Valencia, Olga Pérez Rodríguez, Diego López de Lara, Esther Vaquero Sosa, María Isabel Armadá Maresca, Enrique Criado Vega
P3-1096
Role of Notch1-Dll4 signaling pathway in mice model of oxygen-induced retinopathy
wangkai liu, yihua su, siqi zhuang, xiaoyu li, yijuan li
Role of Notch1-Dll4 signaling pathway in mice model of oxygen-induced retinopathy
wangkai liu, yihua su, siqi zhuang, xiaoyu li, yijuan li
P3-1097
Experience in insulin pump therapy in the treatment of neonatal diabetes.
Tlif Asiet, Chernyak Irina, Shtoda Irina, Golovenko Irina, Kondratyeva Elena
Experience in insulin pump therapy in the treatment of neonatal diabetes.
Tlif Asiet, Chernyak Irina, Shtoda Irina, Golovenko Irina, Kondratyeva Elena
P3-1098
Case Presentation; A Neonate Presenting to a District General Hospital with Isolated Cranial Diabetes Insipidus Evolving to Partial Hypopituitarism
Gemma Keelty, Kamal Weerasinghe, John Gregory
Case Presentation; A Neonate Presenting to a District General Hospital with Isolated Cranial Diabetes Insipidus Evolving to Partial Hypopituitarism
Gemma Keelty, Kamal Weerasinghe, John Gregory
P3-1169
Large goiter in a patient with congenital hypothyroidism.
Anna Bolmasova, Maria Melikyan, Marina Narogan, Yulia Podurovskaya
Large goiter in a patient with congenital hypothyroidism.
Anna Bolmasova, Maria Melikyan, Marina Narogan, Yulia Podurovskaya
P1-111
Serum Neurokinin B level can be used to differentiate central precocious puberty from premature thelarche.
Mesut Parlak, Doga Turkkahraman, Hamit Yasar Ellidag, Ayse Eda Parlak
Serum Neurokinin B level can be used to differentiate central precocious puberty from premature thelarche.
Mesut Parlak, Doga Turkkahraman, Hamit Yasar Ellidag, Ayse Eda Parlak
P1-112
Etiological spectrum and clinical characteristics of 129 children with gonadotropin independent precocious puberty: A nationwide cohort study
Zeynep Atay, Ediz Yeşilkaya, Senay Savas Erdeve, Leyla Akin, Erdal Eren, Esra Döger, Zehra Aycan, Zehra Yavaş Abali, Ayşehan Akinci, Zeynep Şiklar, Samim Özen, Cengiz Kara, Meltem Tayfun, Filiz Tutunculer, Gülcan Seymen Karabulut, Gülay Karagüzel, Halil Sağlam, Aysun Bideci, Selim Kurtoğlu, Abdullah Bereket, Serap Turan, Erkan Sari, Semra Çetinkaya, Tülay Güran, Turkish Peropheral Puberty Research Group
Etiological spectrum and clinical characteristics of 129 children with gonadotropin independent precocious puberty: A nationwide cohort study
Zeynep Atay, Ediz Yeşilkaya, Senay Savas Erdeve, Leyla Akin, Erdal Eren, Esra Döger, Zehra Aycan, Zehra Yavaş Abali, Ayşehan Akinci, Zeynep Şiklar, Samim Özen, Cengiz Kara, Meltem Tayfun, Filiz Tutunculer, Gülcan Seymen Karabulut, Gülay Karagüzel, Halil Sağlam, Aysun Bideci, Selim Kurtoğlu, Abdullah Bereket, Serap Turan, Erkan Sari, Semra Çetinkaya, Tülay Güran, Turkish Peropheral Puberty Research Group
P1-113
Relevance of astrocytic signals for GnRH-neuronal function
Johanna Ernst, Hanna Moeller, Manuel Pfeifer, Sabine Heger
Relevance of astrocytic signals for GnRH-neuronal function
Johanna Ernst, Hanna Moeller, Manuel Pfeifer, Sabine Heger
P1-114
Screening of mutations in idiopathic hypogonadotropic hypogonadism using a targeted next-generation sequencing approach
Anna Kolodkina, Maria Kareva, Natalia Kalinchenko, Nadezhda Raygorodskaya, Oleg Malievsky, Olga Fidelina, Evgeny Vasilyev, Vasily Petrov, Maria Naumova, Anatoly Tiulpakov
Screening of mutations in idiopathic hypogonadotropic hypogonadism using a targeted next-generation sequencing approach
Anna Kolodkina, Maria Kareva, Natalia Kalinchenko, Nadezhda Raygorodskaya, Oleg Malievsky, Olga Fidelina, Evgeny Vasilyev, Vasily Petrov, Maria Naumova, Anatoly Tiulpakov
P1-115
Clinical guidance on 17β-Estradiol and LH serum levels in girls with Premature Thelarche based on clinical outcome of 129 girls aged up to 4 year with premature thelarche in West Sweden.
Martin Österbrand, Kerstin Alvin, Hans Fors, Ensio Norjavaara
Clinical guidance on 17β-Estradiol and LH serum levels in girls with Premature Thelarche based on clinical outcome of 129 girls aged up to 4 year with premature thelarche in West Sweden.
Martin Österbrand, Kerstin Alvin, Hans Fors, Ensio Norjavaara
P1-116
FSHB/FSHR genetic variants alter serum FSH levels and prepubertal ovarian follicular growth in healthy girls
Alexander S. Busch, Casper P. Hagen, Kristian Almstrup, Katharina M. Main, Anders Juul
FSHB/FSHR genetic variants alter serum FSH levels and prepubertal ovarian follicular growth in healthy girls
Alexander S. Busch, Casper P. Hagen, Kristian Almstrup, Katharina M. Main, Anders Juul
P1-117
Transient breast budding in healthy girls is a frequent phenomenon: Description of pubertal progression and associations to gonadotropins, estradiol and FSHB/FSHR genetic polymorphisms
Marie Lindhardt Johansen, Casper P. Hagen, Mikkel G. Mieritz, Jørgen Holm Petersen, Anders Juul
Transient breast budding in healthy girls is a frequent phenomenon: Description of pubertal progression and associations to gonadotropins, estradiol and FSHB/FSHR genetic polymorphisms
Marie Lindhardt Johansen, Casper P. Hagen, Mikkel G. Mieritz, Jørgen Holm Petersen, Anders Juul
P1-118
Specific hypothalamic activation pattern by mGlu5 receptor blockade in vivo during pubertal development in female mice
Ioana Inta, Roberto de Angelis, Katja Lankisch, Christof Dormann, Natascha Pfeiffer, Ulrich Boehm, Peter Gass, Markus Bettendorf
Specific hypothalamic activation pattern by mGlu5 receptor blockade in vivo during pubertal development in female mice
Ioana Inta, Roberto de Angelis, Katja Lankisch, Christof Dormann, Natascha Pfeiffer, Ulrich Boehm, Peter Gass, Markus Bettendorf
P1-119
Lipid profiles in gender dysphoric adolescents treated with GnRH agonists alone and in combination with cross-sex hormones
Sebastian Schagen, Henriette Delemarre-van de Waal, Sabine Hannema
Lipid profiles in gender dysphoric adolescents treated with GnRH agonists alone and in combination with cross-sex hormones
Sebastian Schagen, Henriette Delemarre-van de Waal, Sabine Hannema
P1-120
A novel LHX4 mutation is associated with hypogonadotropic hypogonadism, not combined pituitary hormone deficiency
Masaki Takagi, Takashi Daitsu, Chikahiko Numakura, Takeshi Sato, Satoshi Narumi, Tomonobu Hasegawa
A novel LHX4 mutation is associated with hypogonadotropic hypogonadism, not combined pituitary hormone deficiency
Masaki Takagi, Takashi Daitsu, Chikahiko Numakura, Takeshi Sato, Satoshi Narumi, Tomonobu Hasegawa
P1-121
A missense mutation in MKRN3 in a Danish girl with central precocious puberty and her brother with early puberty
Johanna Känsäkoski, Taneli Raivio, Anders Juul, Johanna Tommiska
A missense mutation in MKRN3 in a Danish girl with central precocious puberty and her brother with early puberty
Johanna Känsäkoski, Taneli Raivio, Anders Juul, Johanna Tommiska
P1-136
The Eap1 promoter is differentially methylated at the onset of puberty in normal weight and obese female rats
Hanna Moeller, Sabine Heger
The Eap1 promoter is differentially methylated at the onset of puberty in normal weight and obese female rats
Hanna Moeller, Sabine Heger
P2-523
Copy Number Variants in Patients with Congenital Hypopituitarism Associated with Complex Phenotypes
Fernanda A Correa, Marcela M Franca, Ana P M Canton, Aline P Otto, Everlayny F Costalonga, Vinicius N Brito, Luciani R Carvalho, Silvia Costa, Ivo J P Arnhold, Alexander A L Jorge, Carla Rosenberg, Berenice B Mendonca
Copy Number Variants in Patients with Congenital Hypopituitarism Associated with Complex Phenotypes
Fernanda A Correa, Marcela M Franca, Ana P M Canton, Aline P Otto, Everlayny F Costalonga, Vinicius N Brito, Luciani R Carvalho, Silvia Costa, Ivo J P Arnhold, Alexander A L Jorge, Carla Rosenberg, Berenice B Mendonca
P2-524
Pulsatile GnRH is superior to hCG in therapeutic efficacy in adolescent boys with hypogonadotropic hypogonadodism
Chunxiu Gong, Ying Liu, Miao Qin, Di Wu, Xiaoling Wang
Pulsatile GnRH is superior to hCG in therapeutic efficacy in adolescent boys with hypogonadotropic hypogonadodism
Chunxiu Gong, Ying Liu, Miao Qin, Di Wu, Xiaoling Wang
P2-525
The lack of MKRN3 gene mutations in patients with idiopathic sporadic GnRH-dependent precocious puberty
Beata Wikiera, Karolina Pesz, Elzbieta Petriczko, Julita Nocon-Bohusz, Ewa Urbanowicz, Mieczyslaw Walczak, Maria Sasiadek, Anna Noczynska
The lack of MKRN3 gene mutations in patients with idiopathic sporadic GnRH-dependent precocious puberty
Beata Wikiera, Karolina Pesz, Elzbieta Petriczko, Julita Nocon-Bohusz, Ewa Urbanowicz, Mieczyslaw Walczak, Maria Sasiadek, Anna Noczynska
P2-526
Serum AMH levels are lower in healthy boys who develop pubertal gynaecomastia
Mikkel G. Mieritz, Casper P. Hagen, Kristian Almstrup, Jørgen H. Petersen, Lars L Râket, Stefan H. Sommer, Anders Juul
Serum AMH levels are lower in healthy boys who develop pubertal gynaecomastia
Mikkel G. Mieritz, Casper P. Hagen, Kristian Almstrup, Jørgen H. Petersen, Lars L Râket, Stefan H. Sommer, Anders Juul
P2-527
Evaluation of final height in girls taking GnRH analogue: Should the age limit for precocious puberty be changed?
Dogus Vuralli, Yildiz Bilge Dallar, Esra Tapci, Ozlem Engiz, Enver Simsek
Evaluation of final height in girls taking GnRH analogue: Should the age limit for precocious puberty be changed?
Dogus Vuralli, Yildiz Bilge Dallar, Esra Tapci, Ozlem Engiz, Enver Simsek
P2-528
Correlation of clinical phenotype and genotype of Prader-Willi syndrome (PWS) and the deletion of paternal MKRN3 allele in PWS patients with central precocious puberty
Ja Hyang Cho, Eungu Kang, Jin-Ho Choi, Gu-Hwan Kim, Eul-Ju Seo, Han-Wook Yoo
Correlation of clinical phenotype and genotype of Prader-Willi syndrome (PWS) and the deletion of paternal MKRN3 allele in PWS patients with central precocious puberty
Ja Hyang Cho, Eungu Kang, Jin-Ho Choi, Gu-Hwan Kim, Eul-Ju Seo, Han-Wook Yoo
P2-529
Doppler evaluation of the uterine artery for the diagnosis and follow-up of patients with precocious puberty
Jeannette Linares, Anibal Espinoza, Joel Riquelme, Alejandra Avila, Fernando Cassorla
Doppler evaluation of the uterine artery for the diagnosis and follow-up of patients with precocious puberty
Jeannette Linares, Anibal Espinoza, Joel Riquelme, Alejandra Avila, Fernando Cassorla
P2-530
Nephrogenic Diabetes Insipidus with partial response to ddAVP caused by a novel AVPR2 splice site mutation
Marie Helene Schernthaner-Reiter, David Adams, Ola Nilsson, Giampaolo Trivellin, Mary Scott Ramnitz, Margarita Raygada, Gretchen Golas, Fabio R. Faucz, Kavitha Dileepan, Maya B. Lodish, Paul R. Lee, Thomas C. Markello, Cynthia J. Tifft, William A. Gahl, Constantine A. Stratakis
Nephrogenic Diabetes Insipidus with partial response to ddAVP caused by a novel AVPR2 splice site mutation
Marie Helene Schernthaner-Reiter, David Adams, Ola Nilsson, Giampaolo Trivellin, Mary Scott Ramnitz, Margarita Raygada, Gretchen Golas, Fabio R. Faucz, Kavitha Dileepan, Maya B. Lodish, Paul R. Lee, Thomas C. Markello, Cynthia J. Tifft, William A. Gahl, Constantine A. Stratakis
P2-531
Regional Brain Volume and Luteinizing Hormone in Girls with Idiopathic Central Precocious Puberty
Eun Young Kim, Shin Eui Park, Min Sun Kim
Regional Brain Volume and Luteinizing Hormone in Girls with Idiopathic Central Precocious Puberty
Eun Young Kim, Shin Eui Park, Min Sun Kim
P2-532
Determination of final height in girls with precocious puberty. Which is the most accurate method?
Daniela Quiroga, Constanza Pinochet, Jaime Cerda, Andreina Cattani, Hernan Garcia
Determination of final height in girls with precocious puberty. Which is the most accurate method?
Daniela Quiroga, Constanza Pinochet, Jaime Cerda, Andreina Cattani, Hernan Garcia
P2-533
The relationship between steriod receptors and Aromatase in the Mouse Brain
Bertan Yilmaz, Hong Zhao, David Brooks, Veysel Fenkci, Gonca Yenicesu, Erkut Attar, Serdar Bulun
The relationship between steriod receptors and Aromatase in the Mouse Brain
Bertan Yilmaz, Hong Zhao, David Brooks, Veysel Fenkci, Gonca Yenicesu, Erkut Attar, Serdar Bulun
P2-534
Evaluation of body proportions in children with precocious or delayed puberty
Anaëlle Wagner, Franziska Phan-Hug, Sophie Stoppa-Vaucher, Eglantine Elowe-Gruau, Andrew Dwyer, Silvia Pichard, Nelly Pitteloud, Michael Hauschild
Evaluation of body proportions in children with precocious or delayed puberty
Anaëlle Wagner, Franziska Phan-Hug, Sophie Stoppa-Vaucher, Eglantine Elowe-Gruau, Andrew Dwyer, Silvia Pichard, Nelly Pitteloud, Michael Hauschild
P2-535
GH Deficiency with Advanced Bone Age: GHRH Receptor mutation detected by exome sequencing associated to non-classical congenital adrenal hyperplasia (CAH)
Fernanda de Azevedo Correa, Marcela M França, Qing Fang, Qianyi Ma, Tania A Bachega, Berenice B Mendonca, Alexander L Jorge, Luciani R Carvalho, Sally A Camper, Ivo J P Arnhold
GH Deficiency with Advanced Bone Age: GHRH Receptor mutation detected by exome sequencing associated to non-classical congenital adrenal hyperplasia (CAH)
Fernanda de Azevedo Correa, Marcela M França, Qing Fang, Qianyi Ma, Tania A Bachega, Berenice B Mendonca, Alexander L Jorge, Luciani R Carvalho, Sally A Camper, Ivo J P Arnhold
P2-540
A case of familial central precocious puberty caused by a novel mutation in the makorin RING finger protein 3 gene.
Anna Grandone, Grazia Cantelmi, Pierluigi Marzuillo, Grazia Cirillo, Caterina Luongo, Flora Micillo, Emanuele Miraglia del Giudice, Laura Perrone
A case of familial central precocious puberty caused by a novel mutation in the makorin RING finger protein 3 gene.
Anna Grandone, Grazia Cantelmi, Pierluigi Marzuillo, Grazia Cirillo, Caterina Luongo, Flora Micillo, Emanuele Miraglia del Giudice, Laura Perrone
P2-541
Distribution of Mutations in Genes Known to be Associated with Idiopathic Hypogonadotropic Hypogonadism in a Large Familial Cohort.
L. Damla Kotan, Eda Mengen, Fatih Gurbuz, Elif Ozsu, Selma Tunc, Yilmaz Kor, Esra P. Cakir, Ayhan Abaci, Korcan Demir, Teoman Akcay, Birgul Kirel, Sibel T. Kinik, Samim Ozen, Ahmet Ucakturk, Aysun Bideci, Erdem Durmaz, Kursad Unluhizarci, Ihsan Turan, Bilgin Yuksel, A. Kemal Topaloglu
Distribution of Mutations in Genes Known to be Associated with Idiopathic Hypogonadotropic Hypogonadism in a Large Familial Cohort.
L. Damla Kotan, Eda Mengen, Fatih Gurbuz, Elif Ozsu, Selma Tunc, Yilmaz Kor, Esra P. Cakir, Ayhan Abaci, Korcan Demir, Teoman Akcay, Birgul Kirel, Sibel T. Kinik, Samim Ozen, Ahmet Ucakturk, Aysun Bideci, Erdem Durmaz, Kursad Unluhizarci, Ihsan Turan, Bilgin Yuksel, A. Kemal Topaloglu
P2-542
Gonadotropin-releasing hormone agonist analog (tripotorelin) stimulation test in evaluation of pituitary -testicular function in boys
Xiuzhi Lin, Huamei Ma, Yanhong Li, Minlian Du, Hongshan Chen, Qiuli Chen, Jun Zhang
Gonadotropin-releasing hormone agonist analog (tripotorelin) stimulation test in evaluation of pituitary -testicular function in boys
Xiuzhi Lin, Huamei Ma, Yanhong Li, Minlian Du, Hongshan Chen, Qiuli Chen, Jun Zhang
P2-543
The Endocrine Response to a Gonadotropin Releasing Hormone (GnRH) Test: Establishing a Reference Interval in Healthy Girls below 6 Years of Age
Esben Vestergaard, Mia Sømod, Kostas Kamperis, Karin Kastberg, Søren Rittig, Kurt Kristensen, Niels Birkebæk
The Endocrine Response to a Gonadotropin Releasing Hormone (GnRH) Test: Establishing a Reference Interval in Healthy Girls below 6 Years of Age
Esben Vestergaard, Mia Sømod, Kostas Kamperis, Karin Kastberg, Søren Rittig, Kurt Kristensen, Niels Birkebæk
P2-544
Increasing body mass index is associated with lower luteinizing hormone levels in girls with central precocious puberty at the early pubertal stage.
Hae Sang Lee, Eun Young Kim, Jin Soon Hwang
Increasing body mass index is associated with lower luteinizing hormone levels in girls with central precocious puberty at the early pubertal stage.
Hae Sang Lee, Eun Young Kim, Jin Soon Hwang
P2-545
Change of Growth Pattern and Bone Mineral Density in Ovariectomized Female Rats According to Estrogen Dosage
Byung Ho Kang, Mun Suk Park, You Jung Yang, Sung Jig Lim, Kye Shik Shim
Change of Growth Pattern and Bone Mineral Density in Ovariectomized Female Rats According to Estrogen Dosage
Byung Ho Kang, Mun Suk Park, You Jung Yang, Sung Jig Lim, Kye Shik Shim
P2-546
Gynecomastia with precocious onset in Peutz-Jeghers Syndrome: managing the aromatase overexpression
Joana Simões-Pereira, Ana Filipa Marques, Catarina Limbert, Lurdes Lopes
Gynecomastia with precocious onset in Peutz-Jeghers Syndrome: managing the aromatase overexpression
Joana Simões-Pereira, Ana Filipa Marques, Catarina Limbert, Lurdes Lopes
P3-1130
CLINICAL FEATURES AND PUBERTAL TIMING IN GIRLS WITH PREMATURE ADRENARCHE
Sevinc Celik, Heves Kirmizibekmez, Rahime Gul Yesiltepe Mutlu, Feyza Yildiz
CLINICAL FEATURES AND PUBERTAL TIMING IN GIRLS WITH PREMATURE ADRENARCHE
Sevinc Celik, Heves Kirmizibekmez, Rahime Gul Yesiltepe Mutlu, Feyza Yildiz
P3-1131
Growth Outcomes in Childhood Craniopharyngioma: A Longitudinal Assessment of 21 Cases at a Single Centre
Maria Michaelidou, Laura Losa, Ashraf Ederies, Helen Spoudeas
Growth Outcomes in Childhood Craniopharyngioma: A Longitudinal Assessment of 21 Cases at a Single Centre
Maria Michaelidou, Laura Losa, Ashraf Ederies, Helen Spoudeas
P3-1132
Effects of GnRH agonists and antagonists on Danazol-induced precocious puberty rat
Aram Yang, Rimm Huh, Jinsup Kim, Sung Yoon Cho, Dong-Kyu Jin
Effects of GnRH agonists and antagonists on Danazol-induced precocious puberty rat
Aram Yang, Rimm Huh, Jinsup Kim, Sung Yoon Cho, Dong-Kyu Jin
P3-1133
Clinical Characteristics of Girls with Atypical Precocious Puberty
Laura Mawer, Ruben Willemsen
Clinical Characteristics of Girls with Atypical Precocious Puberty
Laura Mawer, Ruben Willemsen
P3-1134
Paraphilic compulsion secondary to dopamine replacement therapy and successful treatment with gonadotropin-releasing hormone (GnRH) analogues
Anna Brewka, Tamsin Owen, Jean-Pierre Lin, Michal Ajzensztejn
Paraphilic compulsion secondary to dopamine replacement therapy and successful treatment with gonadotropin-releasing hormone (GnRH) analogues
Anna Brewka, Tamsin Owen, Jean-Pierre Lin, Michal Ajzensztejn
P3-1135
Cardiovascular disease risk factors in girls with isolated premature pubarche.
THAMY BRUNO NASCIMENTO, TUAMI VANESSA WERLE, DEISI MARIA VARGAS
Cardiovascular disease risk factors in girls with isolated premature pubarche.
THAMY BRUNO NASCIMENTO, TUAMI VANESSA WERLE, DEISI MARIA VARGAS
P3-1136
Menstruation Pattern in Idiopathic Central Precocious Puberty (ICPP) Girls after Discontinuing Gonadotropin-Releasing Hormone Agonist (GnRHa) Therapy
Rapeepun Chai-udom, Suttipong Wacharasindhu, Tassawan Rungruxsirivorn
Menstruation Pattern in Idiopathic Central Precocious Puberty (ICPP) Girls after Discontinuing Gonadotropin-Releasing Hormone Agonist (GnRHa) Therapy
Rapeepun Chai-udom, Suttipong Wacharasindhu, Tassawan Rungruxsirivorn
P3-1137
Age of menarche and near final height after long-term use of gonadotropin-releasing hormone agonist or combined with growth hormone in idiopathic central precocious girls
YunHee Gyon, Yeong Ju Yun, Heon-Seok Han, Yong-Dae Kim, Jae-Hong Yu
Age of menarche and near final height after long-term use of gonadotropin-releasing hormone agonist or combined with growth hormone in idiopathic central precocious girls
YunHee Gyon, Yeong Ju Yun, Heon-Seok Han, Yong-Dae Kim, Jae-Hong Yu
P3-1138
Psychosocial changes after GnRH agonist treatment in girls with idiopathic central precocious puberty
Seung Yang, Young Suk Shim, Min Jae Kang, Yeon Joung Oh, Il Tae Hwang
Psychosocial changes after GnRH agonist treatment in girls with idiopathic central precocious puberty
Seung Yang, Young Suk Shim, Min Jae Kang, Yeon Joung Oh, Il Tae Hwang
P3-1139
Multicenter study of early screening and prevention of Prader-Willi Syndrome
WEI LU, LI XI, RUO-QIAN CHENG, XIAO-JING LI, MIAO-YING ZHANG, ZHANG-QIAN ZHENG, RONG YE, ZHU-HUI ZHAO, SHUI-XIAN SHEN, FEI-HONG LUO
Multicenter study of early screening and prevention of Prader-Willi Syndrome
WEI LU, LI XI, RUO-QIAN CHENG, XIAO-JING LI, MIAO-YING ZHANG, ZHANG-QIAN ZHENG, RONG YE, ZHU-HUI ZHAO, SHUI-XIAN SHEN, FEI-HONG LUO
P3-1140
A novel GLUT-1 mutation in a patient with apparently normal cerebrospinal fluid glucose level
Ala Üstyol, Mehmet Ali Duman, Halil Ugur Hatipoglu, Murat Elevli, Hatice Nilgün Selçuk Duru
A novel GLUT-1 mutation in a patient with apparently normal cerebrospinal fluid glucose level
Ala Üstyol, Mehmet Ali Duman, Halil Ugur Hatipoglu, Murat Elevli, Hatice Nilgün Selçuk Duru
P3-1141
Does treatment with gonadotropin releasing hormone (GnRH) analogues affect BMI in children with precocious or early puberty?
Madhavi Madhusudhana, Linda Willingham, Sanjay Gupta, Verghese Matthew
Does treatment with gonadotropin releasing hormone (GnRH) analogues affect BMI in children with precocious or early puberty?
Madhavi Madhusudhana, Linda Willingham, Sanjay Gupta, Verghese Matthew
P3-1142
Qualitative assessment of precocious puberty-related UCC(User Created Contents) on YouTube
Hyo-Kyoung Nam, Soo Min Bang, Joon Woo Baek, Young-Jun Rhie, Kee-Hyoung Lee
Qualitative assessment of precocious puberty-related UCC(User Created Contents) on YouTube
Hyo-Kyoung Nam, Soo Min Bang, Joon Woo Baek, Young-Jun Rhie, Kee-Hyoung Lee
P3-1143
Premature adrenarche is associated to precocious thelarche but not to precocious gonadarche or pubarche in Chilean adolescents
Ana Pereira, Camila Corvalan, Veronica Mericq
Premature adrenarche is associated to precocious thelarche but not to precocious gonadarche or pubarche in Chilean adolescents
Ana Pereira, Camila Corvalan, Veronica Mericq
P3-1144
Central precocious puberty in cerebral palsy.
Patrizia Bruzzi, Maria Francesca Messina, Alessandra Bartoli, Laura Lucaccioni, Barbara Predieri, Filippo De Luca, Lorenzo Iughetti
Central precocious puberty in cerebral palsy.
Patrizia Bruzzi, Maria Francesca Messina, Alessandra Bartoli, Laura Lucaccioni, Barbara Predieri, Filippo De Luca, Lorenzo Iughetti
P3-1145
Changes in body mass index during gonadoropin-releasing hormone agonist treatment in girls with idiopathic central precocious puberty and early pubety.
Hae Sang Lee, Hwal Rim Jeong, Eun Young Kim, Jin Soon Hwang
Changes in body mass index during gonadoropin-releasing hormone agonist treatment in girls with idiopathic central precocious puberty and early pubety.
Hae Sang Lee, Hwal Rim Jeong, Eun Young Kim, Jin Soon Hwang
P3-1146
An Elevated Tumor Marker and Adrenarche in a Child using Lavender Oil - a case report
Susan Lathrop
An Elevated Tumor Marker and Adrenarche in a Child using Lavender Oil - a case report
Susan Lathrop
P3-1147
Persistent isolated cyclical vaginal bleeding (premature menarche) not associated with GnRH pubertal response or endometrial echo should be considered for examination under general anaesthesia (EUA)
Swathi Upadrasta, Lauren Watson, Anuja Natarajan, Sze May Ng
Persistent isolated cyclical vaginal bleeding (premature menarche) not associated with GnRH pubertal response or endometrial echo should be considered for examination under general anaesthesia (EUA)
Swathi Upadrasta, Lauren Watson, Anuja Natarajan, Sze May Ng
P3-1148
Endocrine Dysfunction in Hypothalamic Hamartoma Depends on Presentation (endocrine or epileptogenic), Radiological Characteristics and Surgery
Elisabetta Caredda, Robert Wilkinson, Ash Ederies, Nicola Improda, Sophia Varadkar, Helen Cross, Martin Tisdall, Helen A Spoudeas
Endocrine Dysfunction in Hypothalamic Hamartoma Depends on Presentation (endocrine or epileptogenic), Radiological Characteristics and Surgery
Elisabetta Caredda, Robert Wilkinson, Ash Ederies, Nicola Improda, Sophia Varadkar, Helen Cross, Martin Tisdall, Helen A Spoudeas
P3-1149
Idiopathic central precocious puberty – treatment criteria
Joana Serra-Caetano, Rita Coutinho, Maria Miguel Almiro, Daniela Guelho, Rosa Dantas, Rita Cardoso, Isabel Dinis, Alice Mirante
Idiopathic central precocious puberty – treatment criteria
Joana Serra-Caetano, Rita Coutinho, Maria Miguel Almiro, Daniela Guelho, Rosa Dantas, Rita Cardoso, Isabel Dinis, Alice Mirante
P3-1150
Physiological dose reverse rhythm testosterone treatment abolishes the development of permanent gynaecomastia in adolescent boys with 47,XXY Klinefelter syndrome
Gary Butler
Physiological dose reverse rhythm testosterone treatment abolishes the development of permanent gynaecomastia in adolescent boys with 47,XXY Klinefelter syndrome
Gary Butler
P3-1151
Urinary bisphenol A and its relation with kisspeptin in girls with idiopathic central puberty precocious and premature telarche
Ilker Tolga Ozgen, Emel Torun, Bilge Bayraktar-Tanyeri, Erdem Durmaz, Yasar Cesur
Urinary bisphenol A and its relation with kisspeptin in girls with idiopathic central puberty precocious and premature telarche
Ilker Tolga Ozgen, Emel Torun, Bilge Bayraktar-Tanyeri, Erdem Durmaz, Yasar Cesur
P31152
Prevalence of parental consanguinity in children with precocious puberty and kisspeptin gene polymorphisms
Mahin Hashemipour, Silva Hovsepian, Ali Mazaheri, Mansour Salehi
Prevalence of parental consanguinity in children with precocious puberty and kisspeptin gene polymorphisms
Mahin Hashemipour, Silva Hovsepian, Ali Mazaheri, Mansour Salehi
P3-1153
EFFECTS OF NUTRITION AND VITAMIN D DEFICIENCY ON CENTRAL PUBERTY PRECOCIOUS
Hatice Asli Bayraktar, Heves Kirmizibekmez, Eda Koksal
EFFECTS OF NUTRITION AND VITAMIN D DEFICIENCY ON CENTRAL PUBERTY PRECOCIOUS
Hatice Asli Bayraktar, Heves Kirmizibekmez, Eda Koksal
P3-1154
The relationships between serum vitamin D level and precocious puberty in Korean girls
Se Young Kim, Yeoloon Woo
The relationships between serum vitamin D level and precocious puberty in Korean girls
Se Young Kim, Yeoloon Woo
P3-1155
Familial precocious puberty: clinical characteristics and GnRH agonist response
Hwalrim Jeong, Eun Byul Kwon, Hae Sang Lee, Jung Sub Lim, Jin Soon Hwang
Familial precocious puberty: clinical characteristics and GnRH agonist response
Hwalrim Jeong, Eun Byul Kwon, Hae Sang Lee, Jung Sub Lim, Jin Soon Hwang
P3-1158
Evaluation of the effect of two different GnRH-agonist therapies on the anthropometric measurements in girls with idiopathic central precocious puberty (ICPP)
Ayla Güven
Evaluation of the effect of two different GnRH-agonist therapies on the anthropometric measurements in girls with idiopathic central precocious puberty (ICPP)
Ayla Güven
P3-1159
Testotoxicosis: be careful to predict the final height!
Letícia Guimarães de Souza, Paula de Magalhães Velasco Bastos, Claudia Teixeira Cabido Pinheiro, Leandra Steinmetz, Louise Cominato, Vaê Dichtchekenian, Thais Della Manna, Hilton Kuperman, Hamilton de Cabral MEnezes Filho, Durval Damiani
Testotoxicosis: be careful to predict the final height!
Letícia Guimarães de Souza, Paula de Magalhães Velasco Bastos, Claudia Teixeira Cabido Pinheiro, Leandra Steinmetz, Louise Cominato, Vaê Dichtchekenian, Thais Della Manna, Hilton Kuperman, Hamilton de Cabral MEnezes Filho, Durval Damiani
P3-1160
Central precocious puberty presented due to late started treatment for familial testotoxicosis
yilmaz kor, erdem durmaz, derya bulus, serdar ceylaner
Central precocious puberty presented due to late started treatment for familial testotoxicosis
yilmaz kor, erdem durmaz, derya bulus, serdar ceylaner
P3-1161
A Practical and integrative approach to differantial diagnosis between preoccious puberty and premature telarch:
Newly proposed clinical and laboratory finding-based diagnostic scoring in preoccious puberty and premature telarch:
Murat Karaoglan, Mehmet Keskin, Ayhan Ozkur, Ozlem Keskin
A Practical and integrative approach to differantial diagnosis between preoccious puberty and premature telarch:
Newly proposed clinical and laboratory finding-based diagnostic scoring in preoccious puberty and premature telarch:
Murat Karaoglan, Mehmet Keskin, Ayhan Ozkur, Ozlem Keskin
P3-1162
Delayed puberty in girl : clinical and etiologic study
ali el mahdi haddam, soumeya nora fedala, farida chentli, djamila meskine
Delayed puberty in girl : clinical and etiologic study
ali el mahdi haddam, soumeya nora fedala, farida chentli, djamila meskine
P3-1163
Pubertal development anticipation
Elisa Guidoni, Michela Franceschini, Cristina Mucaria, Renato Scarinci, Giovanna Municchi
Pubertal development anticipation
Elisa Guidoni, Michela Franceschini, Cristina Mucaria, Renato Scarinci, Giovanna Municchi
P3-1164
The Relationship between Xenoestrogens exposure and early puberty among young females living in Jeddah, Saudi Arabia.
Nouf Alnwsany, Abdulmoein Al-Agha
The Relationship between Xenoestrogens exposure and early puberty among young females living in Jeddah, Saudi Arabia.
Nouf Alnwsany, Abdulmoein Al-Agha
P3-1165
ONE YEAR FOLLOW-UP OF CHILDREN WITH ASYMPTOMATIC PRECOCIOUS PUBERTY: CLINICAL AND LABORATORY CHARACTERISTICS
Kyung-Mi JANG, Eun-Mi CHO, Cheol-Woo KO
ONE YEAR FOLLOW-UP OF CHILDREN WITH ASYMPTOMATIC PRECOCIOUS PUBERTY: CLINICAL AND LABORATORY CHARACTERISTICS
Kyung-Mi JANG, Eun-Mi CHO, Cheol-Woo KO
P3-1166
Functional MRI of a Female Teenager of Prada-Willi Syndrome Complicated with Mosaic Turner Syndrome
Wei Wang, Juan Li, Ying Sun, Hui You, Chao Ma, Hongmei Song, Weigang Zhao
Functional MRI of a Female Teenager of Prada-Willi Syndrome Complicated with Mosaic Turner Syndrome
Wei Wang, Juan Li, Ying Sun, Hui You, Chao Ma, Hongmei Song, Weigang Zhao
P3-1167
In a Severe Precocious Puberty Case Who Treated With Frequent
Leuprolid Acetate Injections, a Rare Adverse Effect: Streile Abscess
Mehmet Keskin, Murat Karaoglan, Korcan Demir, Ozlem Keskin
In a Severe Precocious Puberty Case Who Treated With Frequent
Leuprolid Acetate Injections, a Rare Adverse Effect: Streile Abscess
Mehmet Keskin, Murat Karaoglan, Korcan Demir, Ozlem Keskin
P3-1168
Endocrinopathies in a 17-years-old girl with Diamond-Blackfan anemia and transfusion-associated iron overload
Elena Ilyina, Ludmila Papusha, Natalya Smetanina, Alexey Gvozdev
Endocrinopathies in a 17-years-old girl with Diamond-Blackfan anemia and transfusion-associated iron overload
Elena Ilyina, Ludmila Papusha, Natalya Smetanina, Alexey Gvozdev
P1-12
GENETIC DIAGNOSIS USING WHOLE EXOME ANALYSIS IN TWO CASES WITH MALIGN INFANTILE OSTEOPETROSIS
Korcan Demir, Özlem Nalbantoğlu, Kadri Karaer, Hüseyin Anıl Korkmaz, Melek Yıldız, Selma Tunç, Behzat Özkan
GENETIC DIAGNOSIS USING WHOLE EXOME ANALYSIS IN TWO CASES WITH MALIGN INFANTILE OSTEOPETROSIS
Korcan Demir, Özlem Nalbantoğlu, Kadri Karaer, Hüseyin Anıl Korkmaz, Melek Yıldız, Selma Tunç, Behzat Özkan
P1-13
Osteogenesis imperfecta - a pilot trial on treatment with the RANKL-antibody Denosumab
Heike Hoyer-Kuhn, Christian Netzer, Barbara Hero, Eckhard Schoenau, Oliver Semler
Osteogenesis imperfecta - a pilot trial on treatment with the RANKL-antibody Denosumab
Heike Hoyer-Kuhn, Christian Netzer, Barbara Hero, Eckhard Schoenau, Oliver Semler
P1-14
No secular trend in vitamin D levels over the past 30 years in Swedish children
Björn Andersson, Kerstin Albertsson-Wikland, Diana Swolin-Eide, Per Magnusson
No secular trend in vitamin D levels over the past 30 years in Swedish children
Björn Andersson, Kerstin Albertsson-Wikland, Diana Swolin-Eide, Per Magnusson
P1-15
Lithium chloride prevents glucocorticoid-induced growth failure in cultured fetal rat metatarsal bones
Ondrej Soucek, Farasat Zaman, Lars Sävendahl
Lithium chloride prevents glucocorticoid-induced growth failure in cultured fetal rat metatarsal bones
Ondrej Soucek, Farasat Zaman, Lars Sävendahl
P1-152
Noonan syndrome-causing SHP2 mutant inhibits murine growth plate chondrogenesis and bone development: role of Ras/MAPK hyperactivation
Armelle Yart, Mylène Tajan, Florence Capilla, Nicolas Beton, Jean-Luc Davignon, Maithé Tauber, Jean-Pierre Salles, Thomas Edouard
Noonan syndrome-causing SHP2 mutant inhibits murine growth plate chondrogenesis and bone development: role of Ras/MAPK hyperactivation
Armelle Yart, Mylène Tajan, Florence Capilla, Nicolas Beton, Jean-Luc Davignon, Maithé Tauber, Jean-Pierre Salles, Thomas Edouard
P1-153
Relationship between Vitamin D and Brainstem Auditory Evoked Potentials (BAEPs)
Murat Doğan, İlyas Aydın, Keziban Aslı Bala, Sultan Kaba, Özlem Gülpınar
Relationship between Vitamin D and Brainstem Auditory Evoked Potentials (BAEPs)
Murat Doğan, İlyas Aydın, Keziban Aslı Bala, Sultan Kaba, Özlem Gülpınar
P1-154
Novel Compound Heterozygous BMP1 variants associated with Osteogenesis Imperfecta
Aram Yang, Rimm Huh, Jinsup Kim, Sung Yoon Cho, Dong-Kyu Jin
Novel Compound Heterozygous BMP1 variants associated with Osteogenesis Imperfecta
Aram Yang, Rimm Huh, Jinsup Kim, Sung Yoon Cho, Dong-Kyu Jin
P1-16
Diverse presentations of hypophosphatasia in pediatric patients: a review of the case literature
Eileen K Sawyer, Karen Anderson
Diverse presentations of hypophosphatasia in pediatric patients: a review of the case literature
Eileen K Sawyer, Karen Anderson
P1-17
Humanin prevents undesired apoptosis of chondrocytes without interfering with the anti-inflammatory effect of Dexamethasone in a model of arthritis
Bettina Sederquist, Cecilia Aulin, Farasat Zaman, Lars Sävendahl
Humanin prevents undesired apoptosis of chondrocytes without interfering with the anti-inflammatory effect of Dexamethasone in a model of arthritis
Bettina Sederquist, Cecilia Aulin, Farasat Zaman, Lars Sävendahl
P1-18
RESPONSE TO VITAMIN D REPLACEMENT IS DETERMINED BY BODY SURFACE AREA IN CHILDREN WITH VITAMIN D DEFICIENCY
In Hyuk Chung, Yu Sun Kang, Eun-Gyong Yoo
RESPONSE TO VITAMIN D REPLACEMENT IS DETERMINED BY BODY SURFACE AREA IN CHILDREN WITH VITAMIN D DEFICIENCY
In Hyuk Chung, Yu Sun Kang, Eun-Gyong Yoo
P1-19
Bone-Muscle Unit Assessment With pQCT In Children With Inflammatory Bowel Disease Following Treatment With Infliximab
Mabrouka Altowati, UMM-IE-SALMA Malik, Sheila Shepherd, Paraic Mcgrogan, Richard Russell, Faisal Ahmed, S. C. Wong
Bone-Muscle Unit Assessment With pQCT In Children With Inflammatory Bowel Disease Following Treatment With Infliximab
Mabrouka Altowati, UMM-IE-SALMA Malik, Sheila Shepherd, Paraic Mcgrogan, Richard Russell, Faisal Ahmed, S. C. Wong
P1-20
24 hydroxylase polymorphism as a possible contributor to the increased 1, 25(OH)2D in African Americans
Thomas O Carpenter, David EC Cole, Laleh Ardeshirpour, Shadab Salehpour
24 hydroxylase polymorphism as a possible contributor to the increased 1, 25(OH)2D in African Americans
Thomas O Carpenter, David EC Cole, Laleh Ardeshirpour, Shadab Salehpour
P1-21
Effects of inorganic phosphate and FGF23 on C2C12 myoblast cells
Adalbert Raimann, Alexander Dangl, Susanne Greber-Platzer, Monika Egerbacher, Gabriele Haeusler
Effects of inorganic phosphate and FGF23 on C2C12 myoblast cells
Adalbert Raimann, Alexander Dangl, Susanne Greber-Platzer, Monika Egerbacher, Gabriele Haeusler
P1-22
EVALUATION OF BONE MINERAL DENSITY AND MICROARCHITECTURAL PARAMETERS BY DXA AND HR-pQCT IN 36 X-LINKED HYPOPHOSPHATEMIC RICKETS PATIENTS FROM A SINGLE-CENTER STUDY
Guido de Paula Colares Neto, Rosa Maria Rodrigues Pereira, Jackeline Couto Alvarenga, Liliam Takayama, Mariana Ferreira de Assis Funari, Regina Matsunaga Martin
EVALUATION OF BONE MINERAL DENSITY AND MICROARCHITECTURAL PARAMETERS BY DXA AND HR-pQCT IN 36 X-LINKED HYPOPHOSPHATEMIC RICKETS PATIENTS FROM A SINGLE-CENTER STUDY
Guido de Paula Colares Neto, Rosa Maria Rodrigues Pereira, Jackeline Couto Alvarenga, Liliam Takayama, Mariana Ferreira de Assis Funari, Regina Matsunaga Martin
P2-204
Children With Coeliac Disease On Gluten Free Diet Have Normal Bone Mass, Geometry And Muscle Mass
M Mackinder, S C Wong, M Tsiountsioura, S Shepherd, E Buchanan, C Edwards, S F Ahmed, K Gerasimidis
Children With Coeliac Disease On Gluten Free Diet Have Normal Bone Mass, Geometry And Muscle Mass
M Mackinder, S C Wong, M Tsiountsioura, S Shepherd, E Buchanan, C Edwards, S F Ahmed, K Gerasimidis
P2-205
Mechanism of bone disease in Prader-Willi syndrome
Maria Felicia Faienza, Giacomina Brunetti, Graziano Grugni, Antonino Crinò, Sarah Bocchini, Angela Oranger, Isabella Gigante, Laura Piacente, Annamaria Ventura, Silvia Colucci, Maria Grano, Luciano Cavallo, Maurizio Delvecchio
Mechanism of bone disease in Prader-Willi syndrome
Maria Felicia Faienza, Giacomina Brunetti, Graziano Grugni, Antonino Crinò, Sarah Bocchini, Angela Oranger, Isabella Gigante, Laura Piacente, Annamaria Ventura, Silvia Colucci, Maria Grano, Luciano Cavallo, Maurizio Delvecchio
P2-206
Hereditary vitamin D-resistant rickets (HVDRR): Report of four cases with successful use of intermittent intravenous calcium via peripheral route
Saygin Abali, Mayuko Tamura, Zeynep Atay, Pinar Isguven, Tulay Guran, Belma Haliloglu, Serpil Bas, Tsuyoshi Isojima, Serap Turan, Sachiko Kitanaka, Abdullah Bereket
Hereditary vitamin D-resistant rickets (HVDRR): Report of four cases with successful use of intermittent intravenous calcium via peripheral route
Saygin Abali, Mayuko Tamura, Zeynep Atay, Pinar Isguven, Tulay Guran, Belma Haliloglu, Serpil Bas, Tsuyoshi Isojima, Serap Turan, Sachiko Kitanaka, Abdullah Bereket
P2-207
A novel PRKAR1A gene mutation with mild brachydactyly
Hiroko Yagi, Masaki Takagi, Toshikastu Mistui, Tomonobu Hasegawa, Yukihiro Hasegawa
A novel PRKAR1A gene mutation with mild brachydactyly
Hiroko Yagi, Masaki Takagi, Toshikastu Mistui, Tomonobu Hasegawa, Yukihiro Hasegawa
P2-208
Bone mineral density in children and adolescents with vertical HIV infection.
Deisi Maria Vargas, Daniela Oliveira Prust, Jose Carlos Galvão
Bone mineral density in children and adolescents with vertical HIV infection.
Deisi Maria Vargas, Daniela Oliveira Prust, Jose Carlos Galvão
P2-209
Sclerostin and its associations with energy metabolism in children and adolescents
Anna Wedrychowicz, Jerzy Starzyk
Sclerostin and its associations with energy metabolism in children and adolescents
Anna Wedrychowicz, Jerzy Starzyk
P2-210
Genetic and epigenetic alterations at the GNAS locus and clinical consequences in Pseudohypoparathyroidism: a new healthcare pathway
Federica Giachero, Francesca M. Elli, Marta Baricco, Patrizia Matarazzo, Giovanna Mantovani, Luisa de Sanctis
Genetic and epigenetic alterations at the GNAS locus and clinical consequences in Pseudohypoparathyroidism: a new healthcare pathway
Federica Giachero, Francesca M. Elli, Marta Baricco, Patrizia Matarazzo, Giovanna Mantovani, Luisa de Sanctis
P2-211
Fibrous cortical defects and non-ossifying fibromas in patients with precocious puberty
Bang Won Lee, Kyung-Sue Shin
Fibrous cortical defects and non-ossifying fibromas in patients with precocious puberty
Bang Won Lee, Kyung-Sue Shin
P2-212
The effect of high dose oral 17ß estradiol on bone mineralization and body composition in young women with Turner syndrome - a 5 year randomized controlled clinical trial
Line Cleemann, Kirsten Holm, Hanne Kobbernagel, Bent Kristensen, Sven Olaf Skouby, Andreas Emil Kryger Jensen, Claus Gravholt
The effect of high dose oral 17ß estradiol on bone mineralization and body composition in young women with Turner syndrome - a 5 year randomized controlled clinical trial
Line Cleemann, Kirsten Holm, Hanne Kobbernagel, Bent Kristensen, Sven Olaf Skouby, Andreas Emil Kryger Jensen, Claus Gravholt
P2-213
Comparison of cost benefits and efficacy of Zoledronic acid and Pamidronate in the treatment of Osteogenesis Imperfecta in children.
Vrinda Saraff, Jaskiran Sahota, Nicola Crabtree, Nick Shaw, Wolfgang Högler
Comparison of cost benefits and efficacy of Zoledronic acid and Pamidronate in the treatment of Osteogenesis Imperfecta in children.
Vrinda Saraff, Jaskiran Sahota, Nicola Crabtree, Nick Shaw, Wolfgang Högler
P2-214
TmP/GFR is a useful marker in making a clinical diagnosis of X-linked hypophosphatemic rickets caused by the PHEX gene mutation
Ryojun Takeda, Kentaro Miyai, Masaki Takagi, Masahiro Goto, Daisuke Ariyasu, Masako Izawa, Junko Igaki, Eri Suzuki, Yoshie Nakamura, Yukihiro Hasegawa
TmP/GFR is a useful marker in making a clinical diagnosis of X-linked hypophosphatemic rickets caused by the PHEX gene mutation
Ryojun Takeda, Kentaro Miyai, Masaki Takagi, Masahiro Goto, Daisuke Ariyasu, Masako Izawa, Junko Igaki, Eri Suzuki, Yoshie Nakamura, Yukihiro Hasegawa
P2-215
Whole body vibration training improves physical function and increases bone and muscle mass in youngsters with mild cerebral palsy
Silmara Gusso, Patricia Colle, Jose G B Derraik, Janene Biggs, Craig Munns, Wayne Cutfield, Paul Hofman
Whole body vibration training improves physical function and increases bone and muscle mass in youngsters with mild cerebral palsy
Silmara Gusso, Patricia Colle, Jose G B Derraik, Janene Biggs, Craig Munns, Wayne Cutfield, Paul Hofman
P2-217
The spectrum of molecular defects in 64 patients with hypophosphatemic rickets identified by targeted next-generation sequencing.
Kristina Kulikova, Anna Kolodkina, Evgeny Vasilyev, Vasily Petrov, Fedor Gofman, Anatoly Horkin, Vladimir Kenis, Michael Petrov, Anatoly Tiulpakov
The spectrum of molecular defects in 64 patients with hypophosphatemic rickets identified by targeted next-generation sequencing.
Kristina Kulikova, Anna Kolodkina, Evgeny Vasilyev, Vasily Petrov, Fedor Gofman, Anatoly Horkin, Vladimir Kenis, Michael Petrov, Anatoly Tiulpakov
P2-218
NEPHROCALCINOSIS AND NEPHROLITHIASIS IN 36 X-LINKED HYPOPHOSPHATEMIC RICKETS PATIENTS: DIAGNOSTIC IMAGING AND EVALUATION OF RISK FACTORS IN A SINGLE-CENTER STUDY
Guido de Paula Colares Neto, Fernando Ide Yamauchi, Ronaldo Hueb Baroni, Igor Fontenele, Andrea Cavalanti Gomes, Maria Cristina Chammas, Regina Matsunaga
NEPHROCALCINOSIS AND NEPHROLITHIASIS IN 36 X-LINKED HYPOPHOSPHATEMIC RICKETS PATIENTS: DIAGNOSTIC IMAGING AND EVALUATION OF RISK FACTORS IN A SINGLE-CENTER STUDY
Guido de Paula Colares Neto, Fernando Ide Yamauchi, Ronaldo Hueb Baroni, Igor Fontenele, Andrea Cavalanti Gomes, Maria Cristina Chammas, Regina Matsunaga
P2-219
Early increase of the bone formation marker PINP is in a higher degree related to growth response compared to bone mineralization in GH treated prepubertal children
Ralph Decker, Björn Andersson, Diana Swolin-Eide, Per Magnusson, Berit Kriström, Kerstin Albertsson-Wikland
Early increase of the bone formation marker PINP is in a higher degree related to growth response compared to bone mineralization in GH treated prepubertal children
Ralph Decker, Björn Andersson, Diana Swolin-Eide, Per Magnusson, Berit Kriström, Kerstin Albertsson-Wikland
P2-220
Genotype and phenotype characteristics in 22 patients with Vitamin D Dependent Rickets
Type I (VDDR1)
Sophia Tahir, Huseyin Demirbilek, Mehmet Nuri Ozbek, Riza Taner Baran, Sibel Tanriverdi, Khalid Hussain
Genotype and phenotype characteristics in 22 patients with Vitamin D Dependent Rickets
Type I (VDDR1)
Sophia Tahir, Huseyin Demirbilek, Mehmet Nuri Ozbek, Riza Taner Baran, Sibel Tanriverdi, Khalid Hussain
P2-221
Evidence of a link between resting energy expenditure and bone remodelling, glucose homeostasis and adipokine variations in adolescent girls with anorexia nervosa
Laurent Maimoun, Sebastien Guillaume, Patrick Lefbvre, Pascal Philibert, Helena Bertet, Marie-Christine Picot, Laura Gaspari, Françoise Paris, Maude Sennec, Anne-Marie Dupuys, Philippe Courtet, Eric Thomas, Denis Mariano-Goulart, Jacques Bringer, Eric Renard, Charles Sultan
Evidence of a link between resting energy expenditure and bone remodelling, glucose homeostasis and adipokine variations in adolescent girls with anorexia nervosa
Laurent Maimoun, Sebastien Guillaume, Patrick Lefbvre, Pascal Philibert, Helena Bertet, Marie-Christine Picot, Laura Gaspari, Françoise Paris, Maude Sennec, Anne-Marie Dupuys, Philippe Courtet, Eric Thomas, Denis Mariano-Goulart, Jacques Bringer, Eric Renard, Charles Sultan
P2-222
Bone density, HIV infection and antiretroviral treatment: a 10-year follow-up in young patients
Stefano Mora, Katia Maruca, Alessandro Ambrosi, Maria Puzzovio, Paola Erba, Pilar Nannini, Annarita Benincaso, Silvia Capelli, Vania Giacomet
Bone density, HIV infection and antiretroviral treatment: a 10-year follow-up in young patients
Stefano Mora, Katia Maruca, Alessandro Ambrosi, Maria Puzzovio, Paola Erba, Pilar Nannini, Annarita Benincaso, Silvia Capelli, Vania Giacomet
P2-223
Refractory Hypercalcaemia of Malignancy: Responsiveness to Denosumab and Zoledronate
Dinesh Giri, Renuka Ramakrishnan, James Hayden, Lynda Brook, Urmi Das, M.Zulf Mughal, Peter Selby, Poonam Dharmaraj, Senthil Senniappan
Refractory Hypercalcaemia of Malignancy: Responsiveness to Denosumab and Zoledronate
Dinesh Giri, Renuka Ramakrishnan, James Hayden, Lynda Brook, Urmi Das, M.Zulf Mughal, Peter Selby, Poonam Dharmaraj, Senthil Senniappan
P2-224
Fractures In Boys With Duchenne Muscular Dystrophy And Their Relationship To Age
Shuko Joseph, Marina Di Marco, Iain Horrocks, S Faisal Ahmed, S C Wong
Fractures In Boys With Duchenne Muscular Dystrophy And Their Relationship To Age
Shuko Joseph, Marina Di Marco, Iain Horrocks, S Faisal Ahmed, S C Wong
P2-225
Early Detection of Increased Bone Turnover among Children and Adolescents with Type 1 Diabetes Mellitus
Amina Abdel Wahab, Sonia El Sharkawy, Fadia Attia, Mona Amin
Early Detection of Increased Bone Turnover among Children and Adolescents with Type 1 Diabetes Mellitus
Amina Abdel Wahab, Sonia El Sharkawy, Fadia Attia, Mona Amin
P2-226
Association between oxidative stress and bone turnover markers in the obese children
Pawel Matusik, Magdalena Olszanecka-Glinianowicz, Jerzy Chudek, Ewa Malecka-Tendera
Association between oxidative stress and bone turnover markers in the obese children
Pawel Matusik, Magdalena Olszanecka-Glinianowicz, Jerzy Chudek, Ewa Malecka-Tendera
P2-227
Longitudinal bone development in patients with classical congenital adrenal hyperplasia: data using peripheral quantitative computed tomography
Susanne Bechtold, Leyla Duman, Claudia Weissenbacher, Julia Roeb, Robert Dalla Pozza, Heinrich Schmidt
Longitudinal bone development in patients with classical congenital adrenal hyperplasia: data using peripheral quantitative computed tomography
Susanne Bechtold, Leyla Duman, Claudia Weissenbacher, Julia Roeb, Robert Dalla Pozza, Heinrich Schmidt
P2-228
Online Survey to Characterize the Burden of Illness in Children with X-linked Hypophosphatemia (XLH)
Agnes Linglart MD, PhD, Melita Dvorak-Ewell, PhD, Ayla Marshall, Javier San Martin, MD, Alison Skrinar, PhD
Online Survey to Characterize the Burden of Illness in Children with X-linked Hypophosphatemia (XLH)
Agnes Linglart MD, PhD, Melita Dvorak-Ewell, PhD, Ayla Marshall, Javier San Martin, MD, Alison Skrinar, PhD
P2-229
Comparison of the response to bisphosphonate treatment between acute lymphoblastic leukaemia and osteogenesis imperfecta type I
Suma Uday, Anitha Kumaran, Nimasari Ginige, Sophia Sakka, Vrinda Saraff, J Sahota, Nicola Crabtree, Nick Shaw, Wolfgang Högler
Comparison of the response to bisphosphonate treatment between acute lymphoblastic leukaemia and osteogenesis imperfecta type I
Suma Uday, Anitha Kumaran, Nimasari Ginige, Sophia Sakka, Vrinda Saraff, J Sahota, Nicola Crabtree, Nick Shaw, Wolfgang Högler
P2-230
The relationship between serum 25-hydroxyvitamin D and parathyroid hormone in children
Hae Soon Kim, Jung In Kang, Ye Jin Han
The relationship between serum 25-hydroxyvitamin D and parathyroid hormone in children
Hae Soon Kim, Jung In Kang, Ye Jin Han
P2-231
Cinacalcet treatment in girls with hereditary vitamin D resistant rickets
Erkan Sari, Firat Ozkececi, Onur Akin, Ahmet Bolat, Ediz Yesilkaya
Cinacalcet treatment in girls with hereditary vitamin D resistant rickets
Erkan Sari, Firat Ozkececi, Onur Akin, Ahmet Bolat, Ediz Yesilkaya
P2-232
Regulation of bone growth via ligand-specific activation of estrogen receptor alpha
Maryam Iravani, Marie Lagerquist, Claes Ohlsson, Lars Savendahl
Regulation of bone growth via ligand-specific activation of estrogen receptor alpha
Maryam Iravani, Marie Lagerquist, Claes Ohlsson, Lars Savendahl
P2-233
Teriparatide (rhPTH) therapy in a boy with Hypoparathyroidism-Deafness-Renal dysplasia (HDR) syndrome due to GATA3 mutation
Dinesh Giri, Senthil Senniappan, Poonam Dharmaraj, Lynne Hatchard, Renuka Ramakrishnan
Teriparatide (rhPTH) therapy in a boy with Hypoparathyroidism-Deafness-Renal dysplasia (HDR) syndrome due to GATA3 mutation
Dinesh Giri, Senthil Senniappan, Poonam Dharmaraj, Lynne Hatchard, Renuka Ramakrishnan
P2-234
Variable degree of hormonal resistance in patients with Progressive Osseous Heteroplasia
Kentaro Miyai, Noriko Nishina, Masaki Takagi, Masahiro Goto, Yukihiro Hasegawa
Variable degree of hormonal resistance in patients with Progressive Osseous Heteroplasia
Kentaro Miyai, Noriko Nishina, Masaki Takagi, Masahiro Goto, Yukihiro Hasegawa
P2-235
Assessment of foramen magnum in early infancy is efficient for patients with achondroplasia
Chisumi Sogi, Miki Kamimura, Akiko Hakoda, Junko Kanno, Ikuma Fujiwara, Shigeo Kure
Assessment of foramen magnum in early infancy is efficient for patients with achondroplasia
Chisumi Sogi, Miki Kamimura, Akiko Hakoda, Junko Kanno, Ikuma Fujiwara, Shigeo Kure
P2-236
Body composition measures on different DEXA scanners are not the same
Udo Meinhardt, Fabienne Witassek, Christiane Fritz, Urs Eiholzer
Body composition measures on different DEXA scanners are not the same
Udo Meinhardt, Fabienne Witassek, Christiane Fritz, Urs Eiholzer
P2-237
Intrauterine growth restriction, gestational age, steroidal prophylaxis and breastfeeding influence bone mass in prepubertal children
Annalisa Calcagno, Giovanna Pala, Anna Elsa Maria Allegri, Flavia Napoli, Nadia Fratangeli, Maria Grazia Calevo, Mohamad Maghnie, Natascia Di Iorgi
Intrauterine growth restriction, gestational age, steroidal prophylaxis and breastfeeding influence bone mass in prepubertal children
Annalisa Calcagno, Giovanna Pala, Anna Elsa Maria Allegri, Flavia Napoli, Nadia Fratangeli, Maria Grazia Calevo, Mohamad Maghnie, Natascia Di Iorgi
P2-238
Can vitamin D deficiency cause prolongation in visual evoked potentials?
Murat Doğan, İlyas Aydin, Sultan Kaba, Keziban Aslı Bala, Özlem Gülpınar
Can vitamin D deficiency cause prolongation in visual evoked potentials?
Murat Doğan, İlyas Aydin, Sultan Kaba, Keziban Aslı Bala, Özlem Gülpınar
P2-239
Novel CYP27B1 Gene Mutations in Children with Vitamin D-Dependent Rickets Type 1A
Korcan Demir, Walaa E Kattan, Minjing Zou, Erdem Durmaz, Huda BinEssa, Ozlem Nalbantoglu, Roua A.Al-Rijjal, Brian Meyer, Behzat Ozkan, Yufei Shi
Novel CYP27B1 Gene Mutations in Children with Vitamin D-Dependent Rickets Type 1A
Korcan Demir, Walaa E Kattan, Minjing Zou, Erdem Durmaz, Huda BinEssa, Ozlem Nalbantoglu, Roua A.Al-Rijjal, Brian Meyer, Behzat Ozkan, Yufei Shi
P2-240
Size-corrected bone mineral density is not affected by haematopoietic stem cell transplantation and total body irradiation (HSCT/TBI) in leukaemia survivors
Christina Wei, Ruth Elson, Rachel Cox, Karin Bradley, John Barton, Michael Stevens, Elizabeth Crowne
Size-corrected bone mineral density is not affected by haematopoietic stem cell transplantation and total body irradiation (HSCT/TBI) in leukaemia survivors
Christina Wei, Ruth Elson, Rachel Cox, Karin Bradley, John Barton, Michael Stevens, Elizabeth Crowne
P2-241
Quantitative Sonometeric Bone Age (SBA) as a Function of Height and BMI
Alina German, Nira Koren-Morag, Shmuel Levin, Ze'ev Hochberg
Quantitative Sonometeric Bone Age (SBA) as a Function of Height and BMI
Alina German, Nira Koren-Morag, Shmuel Levin, Ze'ev Hochberg
P3-639
Is serum serotonin involved in the bone loss of young females with anorexia nervosa ?
Laurent Maimoun, Sebastien Guillaume, Patrick Lefebvre, Pascal Philibert, Helena Bertet, Marie-Christine Picot, Laura Gaspari, Françoise Paris, Denis Mariano-Goulart, Eric Renard, Charles Sultan
Is serum serotonin involved in the bone loss of young females with anorexia nervosa ?
Laurent Maimoun, Sebastien Guillaume, Patrick Lefebvre, Pascal Philibert, Helena Bertet, Marie-Christine Picot, Laura Gaspari, Françoise Paris, Denis Mariano-Goulart, Eric Renard, Charles Sultan
P3-640
Cranial MR Spectrometry Findings of Patients Aged 10-15 years with Diagnosis of Rickets
Murat Doğan, İlyas Aydin, Keziban Aslı Bala, Sultan Kaba, Özlem Gulpinar
Cranial MR Spectrometry Findings of Patients Aged 10-15 years with Diagnosis of Rickets
Murat Doğan, İlyas Aydin, Keziban Aslı Bala, Sultan Kaba, Özlem Gulpinar
P3-641
Evaluation of bone geometry, quality and bone markers in children with type 1 diabetes
Silvia Longhi, Roberto Franceschi, Vittoria Cauvin, Giuseppe Gallo, Fiorenzo Lupi, Petra Reinstadler, Giorgio Radetti
Evaluation of bone geometry, quality and bone markers in children with type 1 diabetes
Silvia Longhi, Roberto Franceschi, Vittoria Cauvin, Giuseppe Gallo, Fiorenzo Lupi, Petra Reinstadler, Giorgio Radetti
P3-642
Comparison of treatment alternatives for hypercalcemia due to vitamin D intoxication in children
Korcan Demir, Hakan Döneray, Ediz Yesilkaya, Cengiz Kara, Zeynep Atay, Semra Çetinkaya, Atilla Çayir, Ahmet Anik, Erdal Eren, Fatma Demirel, Gülay Can Yilmaz, Ayca Torel Ergur, Mustafa Kendirci, Zehra Aycan, Abdullah Bereket, Murat Aydin, Zerrin Orbak, Behzat Özkan
Comparison of treatment alternatives for hypercalcemia due to vitamin D intoxication in children
Korcan Demir, Hakan Döneray, Ediz Yesilkaya, Cengiz Kara, Zeynep Atay, Semra Çetinkaya, Atilla Çayir, Ahmet Anik, Erdal Eren, Fatma Demirel, Gülay Can Yilmaz, Ayca Torel Ergur, Mustafa Kendirci, Zehra Aycan, Abdullah Bereket, Murat Aydin, Zerrin Orbak, Behzat Özkan
P3-643
Influence of birth weight and total body less head bone mineral contents in 10-18 Korean adolescents: Results from the Korea National Health and Nutrition Examination Surveys (KNHANES) 2008 - 2010.
Won Kyoung Cho, Yoonji Lee, Moonbae Ahn, Yeon Jin Jeon,, In Ah Jung, Shin Hee Kim, So Hyun Park, Min Ho Jung, Byung-Kyu Suh
Influence of birth weight and total body less head bone mineral contents in 10-18 Korean adolescents: Results from the Korea National Health and Nutrition Examination Surveys (KNHANES) 2008 - 2010.
Won Kyoung Cho, Yoonji Lee, Moonbae Ahn, Yeon Jin Jeon,, In Ah Jung, Shin Hee Kim, So Hyun Park, Min Ho Jung, Byung-Kyu Suh
P3-644
Clinical and molecular characterization of patients with pseudohypoparathyroidism
Eungu Kang, Yoon-Myung Kim, Ja Hyang Cho, Gu-Hwan Kim, Jin-Ho Choi, Han-Wook Yoo
Clinical and molecular characterization of patients with pseudohypoparathyroidism
Eungu Kang, Yoon-Myung Kim, Ja Hyang Cho, Gu-Hwan Kim, Jin-Ho Choi, Han-Wook Yoo
P3-645
Long term effects of bisphosphonate treatment in a case with infantile onset severe form of juvenile Paget’s disease
E. Nazli Gonc, Z. Alev Ozon, Gonul Buyukyilmaz, Ayfer Alikasifoglu, Ozlem Simsek, Nurgun Kandemir
Long term effects of bisphosphonate treatment in a case with infantile onset severe form of juvenile Paget’s disease
E. Nazli Gonc, Z. Alev Ozon, Gonul Buyukyilmaz, Ayfer Alikasifoglu, Ozlem Simsek, Nurgun Kandemir
P3-646
Diagnosis and management of Gorham-Stout disease: a protocol proposal
Natascia Di Iorgi, Elisabetta Godano, Alberto Di Mascio, Nadia Vercellino, Flavia Napoli, Pietro Dalmonte, Mohamad Maghnie
Diagnosis and management of Gorham-Stout disease: a protocol proposal
Natascia Di Iorgi, Elisabetta Godano, Alberto Di Mascio, Nadia Vercellino, Flavia Napoli, Pietro Dalmonte, Mohamad Maghnie
P3-647
Vitamin D dependent rickets type 1A with genetic analysis in 3 Chinese children
Wenjing Li, Chunxiu Gong, Liya Wei
Vitamin D dependent rickets type 1A with genetic analysis in 3 Chinese children
Wenjing Li, Chunxiu Gong, Liya Wei
P3-648
A novel mutation in CYP24A1 gene in an infant with severe hypercalcemia and unique neurological presentation
Yael Levy-Shraga, Orit Pinhas-Hamiel, Dganit Dinour, Dalit Modan-Moses
A novel mutation in CYP24A1 gene in an infant with severe hypercalcemia and unique neurological presentation
Yael Levy-Shraga, Orit Pinhas-Hamiel, Dganit Dinour, Dalit Modan-Moses
P3-649
CONTINUOUS 1-34 rhPTH THERAPY IN A GIRL WITH A PTH-GENE DEFECT
Diana-Alexandra Ertl, Adalbert Raimann, Gabriele Haeusler
CONTINUOUS 1-34 rhPTH THERAPY IN A GIRL WITH A PTH-GENE DEFECT
Diana-Alexandra Ertl, Adalbert Raimann, Gabriele Haeusler
P3-650
PREVALENCE OF VITAMIN D DEFICIENCY IN SICKLE CELL ANEMIC CHILDREN IN JOS, NIGERIA
Ibrahim I Abok, Rensom Mukuwhana, Katja Konrad, Selina Okolo
PREVALENCE OF VITAMIN D DEFICIENCY IN SICKLE CELL ANEMIC CHILDREN IN JOS, NIGERIA
Ibrahim I Abok, Rensom Mukuwhana, Katja Konrad, Selina Okolo
P3-651
VITAMIN D LEVEL AND VITAMIN D RECEPTOR DNA IN CHILDREN WITH DIABETES MELLITUS STUDYING SEQUENCE ANALYSE AND POLIMORPHISM
Murat Doğan, Muazzez Didin, Keziban Bala, Sultan Kaba
VITAMIN D LEVEL AND VITAMIN D RECEPTOR DNA IN CHILDREN WITH DIABETES MELLITUS STUDYING SEQUENCE ANALYSE AND POLIMORPHISM
Murat Doğan, Muazzez Didin, Keziban Bala, Sultan Kaba
P3-652
Endocrine function, vitamin D and bone mass status in β-thalassemia major.
Ayça ALTINCIK, Mehmet AKIN
Endocrine function, vitamin D and bone mass status in β-thalassemia major.
Ayça ALTINCIK, Mehmet AKIN
P3-653
LATE SEQUEL OF MENINGOCOCCEMIA: PRESENTING AS SKELETAL DYSPLASIA
gülcan seymen karabulut, aysegül büte yüksel, yasemin alanay, sukru hatun
LATE SEQUEL OF MENINGOCOCCEMIA: PRESENTING AS SKELETAL DYSPLASIA
gülcan seymen karabulut, aysegül büte yüksel, yasemin alanay, sukru hatun
P3-654
LRP5 mutation in a boy with osteopetrosis and normal stature despite low IGF-I levels
Soraya Milani, Wilson Araujo da Silva Jr, Greice De Molfetta, Dalila Zanette, Thiago Hirose, Bruna Garcia, Raphael Liberatore Jr, Francisco Albuquerque de Paula, Carlos Martinelli Jr
LRP5 mutation in a boy with osteopetrosis and normal stature despite low IGF-I levels
Soraya Milani, Wilson Araujo da Silva Jr, Greice De Molfetta, Dalila Zanette, Thiago Hirose, Bruna Garcia, Raphael Liberatore Jr, Francisco Albuquerque de Paula, Carlos Martinelli Jr
P3-655
A longitudinal, prospective, long-term registry of patients with hypophosphatasia
Agnès Linglart, Wolfgang Högler, Craig Langman, Etienne Mornet, Keiichi Ozono, Cheryl Rockman-Greenberg, Lothar Seefried, Camille Bedrosian, Kenji P Fujita, Alex Cole, Priya Kishnani
A longitudinal, prospective, long-term registry of patients with hypophosphatasia
Agnès Linglart, Wolfgang Högler, Craig Langman, Etienne Mornet, Keiichi Ozono, Cheryl Rockman-Greenberg, Lothar Seefried, Camille Bedrosian, Kenji P Fujita, Alex Cole, Priya Kishnani
P3-656
Retrospective Evaluation of Patients Diagnosed as Nutritional Rickets: A Single Center Study
Meryem Karaca, Semra Çağlar Çetinkaya, Melikşah Keskin, Zehra Aycan
Retrospective Evaluation of Patients Diagnosed as Nutritional Rickets: A Single Center Study
Meryem Karaca, Semra Çağlar Çetinkaya, Melikşah Keskin, Zehra Aycan
P3-657
Discrepancy in bone age rating using Tanner-Whitehouse rating and automated bone age determination in a child who was later diagnosed with metaphyseal dysplasia.
Niels Birkebæk, Michel Hellfritzsch
Discrepancy in bone age rating using Tanner-Whitehouse rating and automated bone age determination in a child who was later diagnosed with metaphyseal dysplasia.
Niels Birkebæk, Michel Hellfritzsch
P3-658
VITAMIN LEVELS IN PREGNANT WOMEN AND IN CORD BLOOD IN NEWBORN IN OUR AREA. PRELIMINARY RESULTS.
Maria Ruiz del Campo, Yolanda Ruiz del Prado, Yoana Yerro Chocarro, Jose Julian Revorio Gonzalez
VITAMIN LEVELS IN PREGNANT WOMEN AND IN CORD BLOOD IN NEWBORN IN OUR AREA. PRELIMINARY RESULTS.
Maria Ruiz del Campo, Yolanda Ruiz del Prado, Yoana Yerro Chocarro, Jose Julian Revorio Gonzalez
P3-659
Vitamin D status in Romanian children 0-18 years – should we be more careful regarding supplementation?
Adela Chirita-Emandi, Maria Puiu
Vitamin D status in Romanian children 0-18 years – should we be more careful regarding supplementation?
Adela Chirita-Emandi, Maria Puiu
P3-660
4 years follow up for 25OHD and iPTH in Vitamin D substituted patients with Diabetes mellitus 1 (DM1): an unicentric prospective study
Claudia Weissenbacher, Julia Roeb, Carmen Sydlik, Susanne Bechtold Dalla Pozza, Michael Marx, Heinrich Schmidt
4 years follow up for 25OHD and iPTH in Vitamin D substituted patients with Diabetes mellitus 1 (DM1): an unicentric prospective study
Claudia Weissenbacher, Julia Roeb, Carmen Sydlik, Susanne Bechtold Dalla Pozza, Michael Marx, Heinrich Schmidt
P3-661
Bone Mineral Density in Prader-Willi females during the transition phase
Graziano Grugni, Danilo Fintini, Giuliana Mazzilli, Sarah Bocchini, Alessandro Sartorio, Antonino Crinò
Bone Mineral Density in Prader-Willi females during the transition phase
Graziano Grugni, Danilo Fintini, Giuliana Mazzilli, Sarah Bocchini, Alessandro Sartorio, Antonino Crinò
P3-662
Seasonal differences in plasma 25-OH vitamin D concentrations in cord blood
Sandra Ortigosa Gómez, Cristina Manzano Varo, Oscar Garcia Algar, Antonio Mur Sierra, Roser Ferrer Costa, Antonio Carrascosa Lezcano, Diego Yeste Fernández
Seasonal differences in plasma 25-OH vitamin D concentrations in cord blood
Sandra Ortigosa Gómez, Cristina Manzano Varo, Oscar Garcia Algar, Antonio Mur Sierra, Roser Ferrer Costa, Antonio Carrascosa Lezcano, Diego Yeste Fernández
P3-663
Spondyloenchondrodysplasia with immune dysregulation and without neurological involvement: Report of two siblings with ACP5 gene mutation.
Ayla Guven, Ayse Nurcan Cebeci, Yanick Crow
Spondyloenchondrodysplasia with immune dysregulation and without neurological involvement: Report of two siblings with ACP5 gene mutation.
Ayla Guven, Ayse Nurcan Cebeci, Yanick Crow
P3-664
Short stature in Osteogenesis Imperfecta is not caused by deficiencies in IGF1 or IGF-BP3
Oliver Semler, Heike Hoyer-Kuhn, Gabriel Allo, Eckhard Schoenau
Short stature in Osteogenesis Imperfecta is not caused by deficiencies in IGF1 or IGF-BP3
Oliver Semler, Heike Hoyer-Kuhn, Gabriel Allo, Eckhard Schoenau
P3-665
Vitamin D Status in Children in the Western Part of Turkey
bayram özhan, havva evrengül, sebahat yilmaz agladioglu, sükrü umit yasar, süleyman demir
Vitamin D Status in Children in the Western Part of Turkey
bayram özhan, havva evrengül, sebahat yilmaz agladioglu, sükrü umit yasar, süleyman demir
P3-666
PARATHYROID ADENOMA SHOULD BE CONSIDERED IN THE MANAGEMENT OF HYPOPHOSPHATEMIC RICKETS
Deniz Okdemir, Ulku Gul, Leyla Akin, Nihal Hatipoglu, Mustafa Kendirci, Selim Kurtoglu
PARATHYROID ADENOMA SHOULD BE CONSIDERED IN THE MANAGEMENT OF HYPOPHOSPHATEMIC RICKETS
Deniz Okdemir, Ulku Gul, Leyla Akin, Nihal Hatipoglu, Mustafa Kendirci, Selim Kurtoglu
P3-667
NEUROLOGICAL CLINIC DELAYS THE DIAGNOSIS OF PSEUDOHYPOPARATHYROIDISM
PEREZ MARIA TERESA, LABRA REGINA, GARCIA ZOA, LLORENTE ANA
NEUROLOGICAL CLINIC DELAYS THE DIAGNOSIS OF PSEUDOHYPOPARATHYROIDISM
PEREZ MARIA TERESA, LABRA REGINA, GARCIA ZOA, LLORENTE ANA
P3-668
TREATMENT OF LIFE THREATENING HYPERCALCEMIA IN TWO INFANTS
Didem Helvacioglu, Suna Kilinc, Ayla Guven
TREATMENT OF LIFE THREATENING HYPERCALCEMIA IN TWO INFANTS
Didem Helvacioglu, Suna Kilinc, Ayla Guven
P3-669
Comparison of the levels of vitamin D in children in northern Spain (domestic or foreign)
Ainhoa Sarasua-Miranda, Ignacio Diez-Lopez, Isabel Lorente-Blazquez
Comparison of the levels of vitamin D in children in northern Spain (domestic or foreign)
Ainhoa Sarasua-Miranda, Ignacio Diez-Lopez, Isabel Lorente-Blazquez
P3-670
A cause of severe hypercalcemia: Overdose or hypersensitivity to vitamin D?
Zerrin Orbak, Remziye Seda Yesilcibik, Bahri Unal
A cause of severe hypercalcemia: Overdose or hypersensitivity to vitamin D?
Zerrin Orbak, Remziye Seda Yesilcibik, Bahri Unal
P3-671
How are we using bisphosphonates in children with secondary osteoporosis in a tertiary centre?
Victoria Price, Lynne Hatchard, Renuka Ramakrishnan, Senthil Senniappan, Poonam Dharmaraj
How are we using bisphosphonates in children with secondary osteoporosis in a tertiary centre?
Victoria Price, Lynne Hatchard, Renuka Ramakrishnan, Senthil Senniappan, Poonam Dharmaraj
P3-672
PSEUDOHYPOPARATHYROIDISM (PHP): clinical heterogeneity illustrated by 3 different cases.
Annelies Lemay, Marieke den Brinker, Hilde Dotremont, Berten Ceulemans, Annick France
PSEUDOHYPOPARATHYROIDISM (PHP): clinical heterogeneity illustrated by 3 different cases.
Annelies Lemay, Marieke den Brinker, Hilde Dotremont, Berten Ceulemans, Annick France
P3-673
Successful treatment of severe hypercalcemia in an infant with Williams syndrome using a single infusion of pamidronate followed by low calcium diet.
Rasha Odeh, Jumana Albaramki, Abeer Alassaf
Successful treatment of severe hypercalcemia in an infant with Williams syndrome using a single infusion of pamidronate followed by low calcium diet.
Rasha Odeh, Jumana Albaramki, Abeer Alassaf
P3-674
25-Hydroxy Vitamin D levels in patients with chronic diseases on corticosteroid treatment
Desislava Yordanova, Elissaveta Stefanova, Krasimira Kazakova, Zdravka Todorova, Mihaela Dimitrova
25-Hydroxy Vitamin D levels in patients with chronic diseases on corticosteroid treatment
Desislava Yordanova, Elissaveta Stefanova, Krasimira Kazakova, Zdravka Todorova, Mihaela Dimitrova
P3-675
PSEUDOHYPOPARATHYROIDISM TYPE 1b, A RARE DIAGNOSIS IN ADOLESCENTS
ELPIDA-ATHINA VLACHOPAPADOPOULOU, EIRINI DIKAIAKOU, KYRIAKI KARAVANAKI, ELLI ANAGNOSTOU, MARIA-ELENI TSITOURA, MARIZA TSOLIA, DEBORAH J.G. MACKAY, STEPHANOS MICHALACOS
PSEUDOHYPOPARATHYROIDISM TYPE 1b, A RARE DIAGNOSIS IN ADOLESCENTS
ELPIDA-ATHINA VLACHOPAPADOPOULOU, EIRINI DIKAIAKOU, KYRIAKI KARAVANAKI, ELLI ANAGNOSTOU, MARIA-ELENI TSITOURA, MARIZA TSOLIA, DEBORAH J.G. MACKAY, STEPHANOS MICHALACOS
P3-676
What Lies Beneath: An enigma of missed opportunities and Calcium problem
Dalia Hammouche, Anjum Rafiq, Vijith Puthi
What Lies Beneath: An enigma of missed opportunities and Calcium problem
Dalia Hammouche, Anjum Rafiq, Vijith Puthi
P3-677
A novel homozygous 6 nucleotide deletion in GLUT2 gene in a Fanconi–Bickel syndrome family
farzaneh abbasi, rowshanak abbasi, Soudeh Ghafouri-Fard
A novel homozygous 6 nucleotide deletion in GLUT2 gene in a Fanconi–Bickel syndrome family
farzaneh abbasi, rowshanak abbasi, Soudeh Ghafouri-Fard
P3-678
Final Heigh(FH) in a patient with Fanconi Syndrome(FS) and Growth Hormone Deficiency(GHD) treated with Growth Hormone
Maria Cláudia Schmitt-Lobe, Leticia Salm, Lais Dadan
Final Heigh(FH) in a patient with Fanconi Syndrome(FS) and Growth Hormone Deficiency(GHD) treated with Growth Hormone
Maria Cláudia Schmitt-Lobe, Leticia Salm, Lais Dadan
P3-680
Oral alendronate treatment in children and adolescents with osteoporosis
Atilla Buyukgebiz, Ece Bober, Ayhan Abaci
Oral alendronate treatment in children and adolescents with osteoporosis
Atilla Buyukgebiz, Ece Bober, Ayhan Abaci
P3-681
A case of vitamin D deficient rickets showing resistance to the treatment of active vitamin D: Severe calcium deficiency cause vitamin D resistance.
Hiroyuki Tanaka, Kosei Hasegawa, Moe Takatsuka, Chika Okahara, Yoshie Noguchi, Tsutomu Takata, Kazuo Ogura
A case of vitamin D deficient rickets showing resistance to the treatment of active vitamin D: Severe calcium deficiency cause vitamin D resistance.
Hiroyuki Tanaka, Kosei Hasegawa, Moe Takatsuka, Chika Okahara, Yoshie Noguchi, Tsutomu Takata, Kazuo Ogura
P3-682
Metadiaphyseal dysplasia associated with confirmed GH deficiency - family report
Ioana Armasu, Elena Braha, Iulia Crumpei, Ioana Vasiliu, Adina Manolachie, Mirela Puiu, Irina Zetu, Voichita Mogos, Carmen Vulpoi
Metadiaphyseal dysplasia associated with confirmed GH deficiency - family report
Ioana Armasu, Elena Braha, Iulia Crumpei, Ioana Vasiliu, Adina Manolachie, Mirela Puiu, Irina Zetu, Voichita Mogos, Carmen Vulpoi
P3-683
Hypocalcemia by parathyroid dysfunction in children and adolescents
ali el mahdi haddam, soumeya nora fedala, farida chentli, djamila meskine
Hypocalcemia by parathyroid dysfunction in children and adolescents
ali el mahdi haddam, soumeya nora fedala, farida chentli, djamila meskine
P3-684
VDR Gene Analysis Results of Four Patients With Hereditary1,25-Dihydroxyvitamin D
Resistant Rickets
Esra Deniz PAPATYA ÇAKIR, Özgür ALDEMİR, SeyitAhmet UCAKTÜRK, Erdal EREN, Samim OZEN
VDR Gene Analysis Results of Four Patients With Hereditary1,25-Dihydroxyvitamin D
Resistant Rickets
Esra Deniz PAPATYA ÇAKIR, Özgür ALDEMİR, SeyitAhmet UCAKTÜRK, Erdal EREN, Samim OZEN
P3-685
NUTRITIONAL RICKETS IN A BOTTLE-FED TWO MONTHS OLD BABY
María Magdalena Hawkins Solís, Ana Dolores Alcalde de Alvaré, Julia Yebra Yebra, Araceli García Pose, Ana Sancho Martínez
NUTRITIONAL RICKETS IN A BOTTLE-FED TWO MONTHS OLD BABY
María Magdalena Hawkins Solís, Ana Dolores Alcalde de Alvaré, Julia Yebra Yebra, Araceli García Pose, Ana Sancho Martínez
LBP-1266
Determining the effects of race, skin colour and genotype on the response to vitamin D therapy.
Jaya Sujatha Gopal Kothandapani, Lucy Evans, Jennifer Walsh, Richard Eastell, Nick Bishop
Determining the effects of race, skin colour and genotype on the response to vitamin D therapy.
Jaya Sujatha Gopal Kothandapani, Lucy Evans, Jennifer Walsh, Richard Eastell, Nick Bishop
P1-122
Congenital hypothyroidism in twin couples and triplets
Antonella Olivieri, Giovanna Weber, Alessandra Cassio, Pietro Costa, Francesca Calaciura, Emanuela Medda, Maria Cristina Vigone, Tiziana De Filippis, Giulia Gelmini, Federica Marelli, Valeria Di Russo, Luca Persani
Congenital hypothyroidism in twin couples and triplets
Antonella Olivieri, Giovanna Weber, Alessandra Cassio, Pietro Costa, Francesca Calaciura, Emanuela Medda, Maria Cristina Vigone, Tiziana De Filippis, Giulia Gelmini, Federica Marelli, Valeria Di Russo, Luca Persani
P1-123
Th17 cells in children with Graves’ disease during methimazole treatment
Maria Klatka, Ewelina Grywalska, Jacek Rolinski
Th17 cells in children with Graves’ disease during methimazole treatment
Maria Klatka, Ewelina Grywalska, Jacek Rolinski
P1-124
Thyrocytes are particularly well protected against oxidative stress induced by H2O2
Chiraz Ghaddhab, Emmanuel Van Den Eeckhaute, Olivier Hancisse, Natacha Driessens, Jacques-Emile Dumont, Françoise Miot, Bernard Corvilain
Thyrocytes are particularly well protected against oxidative stress induced by H2O2
Chiraz Ghaddhab, Emmanuel Van Den Eeckhaute, Olivier Hancisse, Natacha Driessens, Jacques-Emile Dumont, Françoise Miot, Bernard Corvilain
P1-125
Thyrocyte is particularly well protected against oxidative stress induced by H2O2
Chiraz Ghaddhab, Emmanuel Van Den Eeckhaute, Olivier Hancisse, Natacha Driessens, Soetkin Versteyhe, Françoise Miot, Jacques-Emile Dumont, Bernard Corvilain
Thyrocyte is particularly well protected against oxidative stress induced by H2O2
Chiraz Ghaddhab, Emmanuel Van Den Eeckhaute, Olivier Hancisse, Natacha Driessens, Soetkin Versteyhe, Françoise Miot, Jacques-Emile Dumont, Bernard Corvilain
P1-126
Characteristics and Outcome of Neonates with Congenital Hypothyroidism Born after In Vitro Fertilisation (IVF)
Vassiliki Giogli, Christina Kanaka-Gantenbein, Jessica-Debora Arditi, Dimitris Platis, George Chouliaras, Chrysoula Kourkouti, Ioanna Kosteria, Anna Gika, Alexandra Iliadi, George Chrousos, Panagiotis Girginoudis, Antonis Voutetakis
Characteristics and Outcome of Neonates with Congenital Hypothyroidism Born after In Vitro Fertilisation (IVF)
Vassiliki Giogli, Christina Kanaka-Gantenbein, Jessica-Debora Arditi, Dimitris Platis, George Chouliaras, Chrysoula Kourkouti, Ioanna Kosteria, Anna Gika, Alexandra Iliadi, George Chrousos, Panagiotis Girginoudis, Antonis Voutetakis
P1-127
Transient vs. Permanent Congenital Hypothyroidism: The Use of Baseline Characteristics and Long-term Data Can Help Formulate a Practical Prognostic Algorithm
Vassiliki Giogli, Christina Kanaka-Gantenbein, George Chouliaras, Jessica-Debora Arditi, Anna Gika, Alexandra Iliadi, Dimitris Platis, Eleni Magdalini Kyritsi, Petros Karkalousos, George-Albert Karikas, Chrysanthi Mengreli, George Chrousos, Panagiotis Girginoudis, Antonis Voutetakis
Transient vs. Permanent Congenital Hypothyroidism: The Use of Baseline Characteristics and Long-term Data Can Help Formulate a Practical Prognostic Algorithm
Vassiliki Giogli, Christina Kanaka-Gantenbein, George Chouliaras, Jessica-Debora Arditi, Anna Gika, Alexandra Iliadi, Dimitris Platis, Eleni Magdalini Kyritsi, Petros Karkalousos, George-Albert Karikas, Chrysanthi Mengreli, George Chrousos, Panagiotis Girginoudis, Antonis Voutetakis
P1-128
Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor Alpha Mutations
Korcan Demir, Anja van Gucht, Muammer Büyükinan, Gönül Catli, Yavuz Ayhan, Veysel Nijat Bas, Bumin Nuri Dündar, Behzat Ozkan, Marcel E. Meima, W. Edward Visser, Robin P. Peeters, Theo J. Visser
Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor Alpha Mutations
Korcan Demir, Anja van Gucht, Muammer Büyükinan, Gönül Catli, Yavuz Ayhan, Veysel Nijat Bas, Bumin Nuri Dündar, Behzat Ozkan, Marcel E. Meima, W. Edward Visser, Robin P. Peeters, Theo J. Visser
P1-129
Intelligence and behaviour in children and adolescents with Hashimoto´s thyroiditis
Claudia Boettcher, Burkhard Brosig, Henriette Windhaus, Stefan A. Wudy, Andreas Hahn
Intelligence and behaviour in children and adolescents with Hashimoto´s thyroiditis
Claudia Boettcher, Burkhard Brosig, Henriette Windhaus, Stefan A. Wudy, Andreas Hahn
P1-130
Brain-lung-thyroid syndrome - update on the clinical spectrum of a heterogeneous disorder
Nina Lenherr, Jean-Marc Vuissoz, Karl Heinimann, Gabor Szinnai
Brain-lung-thyroid syndrome - update on the clinical spectrum of a heterogeneous disorder
Nina Lenherr, Jean-Marc Vuissoz, Karl Heinimann, Gabor Szinnai
P1-131
Increased Detection Rate of Paired Box Domain Gene Mutations by Application of Multiplex Ligation-Dependent Probe Amplification Analysis in Patients with Primary Congenital Hypothyroidism and Thyroid Dysgenesis
Malgorzata Kumorowicz-Czoch, Pia Hermanns, Anna Madetko-Talowska, Joahim Pohlenz
Increased Detection Rate of Paired Box Domain Gene Mutations by Application of Multiplex Ligation-Dependent Probe Amplification Analysis in Patients with Primary Congenital Hypothyroidism and Thyroid Dysgenesis
Malgorzata Kumorowicz-Czoch, Pia Hermanns, Anna Madetko-Talowska, Joahim Pohlenz
P1-132
A severe hyperthyroidism in an infant revealed a familial nonautoimmune hyperthyroidism with novel heterozygous thyrotropin receptor gene mutation.
Isabelle OLIVER PETIT, Frédérique SAVAGNER, Thomas EDOUARD, Philippe CARON
A severe hyperthyroidism in an infant revealed a familial nonautoimmune hyperthyroidism with novel heterozygous thyrotropin receptor gene mutation.
Isabelle OLIVER PETIT, Frédérique SAVAGNER, Thomas EDOUARD, Philippe CARON
P1-162
Congenital Hypothyroidism: Reduction in the Female to Male Ratio Following the Decrease of the TSH Cut-off Point Used for Neonatal Screening
Antonis Voutetakis, Vassiliki Giogli, Dimitris Platis, Anna Gika, Alexandra Iliadi, Chrysanthi Mengreli, George Chrousos, Christina Kanaka-Gantenbein, Panagiotis Girginoudis
Congenital Hypothyroidism: Reduction in the Female to Male Ratio Following the Decrease of the TSH Cut-off Point Used for Neonatal Screening
Antonis Voutetakis, Vassiliki Giogli, Dimitris Platis, Anna Gika, Alexandra Iliadi, Chrysanthi Mengreli, George Chrousos, Christina Kanaka-Gantenbein, Panagiotis Girginoudis
P1-163
Pediatric Thyroid Nodule Score (PTNS): Derivation and Validation of a Predictive Score for Thyroid Nodule Assessment in Children
Danielle van der Kaay, Jonathan Wasserman, Nadia Akseer, Michael Roskies, Frederique la Liberte, Lily Nguyen, Pramod Puligandla
Pediatric Thyroid Nodule Score (PTNS): Derivation and Validation of a Predictive Score for Thyroid Nodule Assessment in Children
Danielle van der Kaay, Jonathan Wasserman, Nadia Akseer, Michael Roskies, Frederique la Liberte, Lily Nguyen, Pramod Puligandla
P1-164
Practical application of elastography in the diagnosis of thyroid nodules in children.
Hanna Borysewicz-Sanczyk, Beata Sawicka, Janusz Dzieciol, Katarzyna Drzewek, Magdalena Oleksinska, Klaudyna Noiszewska, Artur Bossowski
Practical application of elastography in the diagnosis of thyroid nodules in children.
Hanna Borysewicz-Sanczyk, Beata Sawicka, Janusz Dzieciol, Katarzyna Drzewek, Magdalena Oleksinska, Klaudyna Noiszewska, Artur Bossowski
P2-552
Even in the era of congenital hypothyroidism screening mild and subclinical sensorineural hearing loss remains a relatively common complication of severe congenital hypothyroidism
Rocco Bruno, Tommaso Aversa, Mariaausilia Catena, Mariella Valenzise, Maria Francesca Messina, Filippo De Luca, Malgorzata Wasniewska
Even in the era of congenital hypothyroidism screening mild and subclinical sensorineural hearing loss remains a relatively common complication of severe congenital hypothyroidism
Rocco Bruno, Tommaso Aversa, Mariaausilia Catena, Mariella Valenzise, Maria Francesca Messina, Filippo De Luca, Malgorzata Wasniewska
P2-553
Efficacy of supplemental Liothyronine for patients with congenital hypothyroidism and pituitary resistance to thyroid hormone
Laura Paone, Abby F Fleisch, Henry Feldman, Marco Cappa, Rosalind Brown, Ari J Wassner
Efficacy of supplemental Liothyronine for patients with congenital hypothyroidism and pituitary resistance to thyroid hormone
Laura Paone, Abby F Fleisch, Henry Feldman, Marco Cappa, Rosalind Brown, Ari J Wassner
P2-554
Hypoceruloplasminemia as a marker of severe hypothyroidism
Mariella Valenzise, Concetta Sferlazzas, Federica Porcaro, Maria Francesca Messina, Malgorzata Wasniewska, Maurizio Cinquegrani, Filippo De Luca
Hypoceruloplasminemia as a marker of severe hypothyroidism
Mariella Valenzise, Concetta Sferlazzas, Federica Porcaro, Maria Francesca Messina, Malgorzata Wasniewska, Maurizio Cinquegrani, Filippo De Luca
P2-555
PITUITARY RESISTANCE TO EXOGENOUS LEVOTHYROXINE IN HUMANS
Nerea Lacamara, Arancha Escribano, Julio Guerrero-Fernandez, Ana Coral Barreda, Isabel Gonzalez-Casado, Jose Carlos Moreno
PITUITARY RESISTANCE TO EXOGENOUS LEVOTHYROXINE IN HUMANS
Nerea Lacamara, Arancha Escribano, Julio Guerrero-Fernandez, Ana Coral Barreda, Isabel Gonzalez-Casado, Jose Carlos Moreno
P2-556
Novel PAX8 Mutations in Zhuang Chinese with congenital hypothyroidism
Chunyun Fu, Rongyu Chen, Yun Chen
Novel PAX8 Mutations in Zhuang Chinese with congenital hypothyroidism
Chunyun Fu, Rongyu Chen, Yun Chen
P2-557
Potentially excessive levothyroxine doses in cases of congenital hypothyroidism with eutopic thyroid gland
Hidetoshi Satoh, Keisuke Nagasaki, Youhei Ogawa, Akihiko Saitoh
Potentially excessive levothyroxine doses in cases of congenital hypothyroidism with eutopic thyroid gland
Hidetoshi Satoh, Keisuke Nagasaki, Youhei Ogawa, Akihiko Saitoh
P2-558
Objective versus subjective measurement of thyroid volume by ultrasound in infants referred with TSH elevation on newborn screening
Chourouk Mansour, Yasmine Ouarezki, Jeremy Jones, Morag Attaie, Emily Stenhouse, Joachim Pohlenz, Malcolm Donaldson
Objective versus subjective measurement of thyroid volume by ultrasound in infants referred with TSH elevation on newborn screening
Chourouk Mansour, Yasmine Ouarezki, Jeremy Jones, Morag Attaie, Emily Stenhouse, Joachim Pohlenz, Malcolm Donaldson
P2-559
Central or Primary Hypothyroidism? How to Differentiate in Patients with low T4 but mildly elevated TSH levels
Serap Turan, Ziya Gurbanov, Serpil Bas, Saygin Abali, Zeynep Atay, Abdullah Bereket
Central or Primary Hypothyroidism? How to Differentiate in Patients with low T4 but mildly elevated TSH levels
Serap Turan, Ziya Gurbanov, Serpil Bas, Saygin Abali, Zeynep Atay, Abdullah Bereket
P2-560
A rare adverse effect of methimazole: Serum sickness
Emine DEMET AKBAS, Aysun BIDECI, Onur AKIN, Ozge YUCE, Esra DOGER, Arzu BAKIRTAS, Orhun CAMURDAN, Peyami CINAZ
A rare adverse effect of methimazole: Serum sickness
Emine DEMET AKBAS, Aysun BIDECI, Onur AKIN, Ozge YUCE, Esra DOGER, Arzu BAKIRTAS, Orhun CAMURDAN, Peyami CINAZ
P2-561
Analysis of chosen polymorphisms rs5742909 C/T - CTLA4, rs7522061 C/T – FCRL3, rs7138803 A/G - FAIM2 in pathogenesis of autoimmune thyroid diseases in children.
Ewa Jakubowska, Joanna Goscik, Natalia Wawrusiewicz-Kurylonek, Anna Bossowska, Adam Kretowski, Artur Bossowski
Analysis of chosen polymorphisms rs5742909 C/T - CTLA4, rs7522061 C/T – FCRL3, rs7138803 A/G - FAIM2 in pathogenesis of autoimmune thyroid diseases in children.
Ewa Jakubowska, Joanna Goscik, Natalia Wawrusiewicz-Kurylonek, Anna Bossowska, Adam Kretowski, Artur Bossowski
P2-562
THYROID DYSFUNCTION IS ASOCIATED WITH BIOCHEMICAL MARKERS OF NON ALCOHOLIC FATTY LIVER DISEASE (NAFLD) IN PEDIATRIC POPULATION
Carolina Loureiro, Alejandro Martínez, Carmen Campino, Paulina Correa, Carolina Mendoza, Diego Carrillo, Marlene Aglony, Rodrigo Bancalari, Cristian Carvajal, Carlos Fardella, Hernan García, Francisca Grob
THYROID DYSFUNCTION IS ASOCIATED WITH BIOCHEMICAL MARKERS OF NON ALCOHOLIC FATTY LIVER DISEASE (NAFLD) IN PEDIATRIC POPULATION
Carolina Loureiro, Alejandro Martínez, Carmen Campino, Paulina Correa, Carolina Mendoza, Diego Carrillo, Marlene Aglony, Rodrigo Bancalari, Cristian Carvajal, Carlos Fardella, Hernan García, Francisca Grob
P2-563
Nonautoimmune neonatal hyperthyroidism due to A633G mutation in the thyrotropin receptor gene
In Ah Jung, Won Kyoung Cho, Yeon Jin Jeon, Hyo Jin Chae, Myung Shin Kim, Byung Kyu Suh
Nonautoimmune neonatal hyperthyroidism due to A633G mutation in the thyrotropin receptor gene
In Ah Jung, Won Kyoung Cho, Yeon Jin Jeon, Hyo Jin Chae, Myung Shin Kim, Byung Kyu Suh
P2-564
Are children with Congenital Primary HypoThyroidism (CPHT) overtreated?
Claire SECHTER, Francis VASSEUR, Maryse CARTIGNY-MACIEJEWSKI, Iva GUEORGUIEVA, Chantal STUCKENS, Jacques WEILL
Are children with Congenital Primary HypoThyroidism (CPHT) overtreated?
Claire SECHTER, Francis VASSEUR, Maryse CARTIGNY-MACIEJEWSKI, Iva GUEORGUIEVA, Chantal STUCKENS, Jacques WEILL
P2-565
Metamorphic thyroid autoimmunity in Down Syndrome: from Hashimoto’s thyroiditis to Graves’ disease and beyond
Tommaso Aversa, Mariella Valenzise, Mariacarolina Salerno, Andrea Corrias, Lorenzo Iughetti, Giorgio Radetti, Filippo De Luca, Malgorzata Wasniewska
Metamorphic thyroid autoimmunity in Down Syndrome: from Hashimoto’s thyroiditis to Graves’ disease and beyond
Tommaso Aversa, Mariella Valenzise, Mariacarolina Salerno, Andrea Corrias, Lorenzo Iughetti, Giorgio Radetti, Filippo De Luca, Malgorzata Wasniewska
P2-566
Analysis of B regulatory cells with phenotype CD19+CD24hiCD27+IL-10+ and CD19+IL-10+ in the peripheral blood of children with Graves’ disease and Hashimoto’s thyroiditis
Artur Bossowski, Kamil Grubczak, Paulina Singh, Urszula Radzikowska, Milena Dabrowska, Beata Sawicka, Anna Bossowska, Marcin Moniuszko
Analysis of B regulatory cells with phenotype CD19+CD24hiCD27+IL-10+ and CD19+IL-10+ in the peripheral blood of children with Graves’ disease and Hashimoto’s thyroiditis
Artur Bossowski, Kamil Grubczak, Paulina Singh, Urszula Radzikowska, Milena Dabrowska, Beata Sawicka, Anna Bossowska, Marcin Moniuszko
P2-567
Case Report: Resistance of Thyroid Hormone due to a novel Thyroid Hormone Receptor β-Gene Mutation
Meltem Tayfun, Selin Elmaogullari, Ahmet Yesilyurt, Fatma Demirel
Case Report: Resistance of Thyroid Hormone due to a novel Thyroid Hormone Receptor β-Gene Mutation
Meltem Tayfun, Selin Elmaogullari, Ahmet Yesilyurt, Fatma Demirel
P2-568
Levothyroxine Replacement in Primary Congenital Hypothyroidism: The Higher The Initial Dose The Higher The Rate of Overtreatment
Hale Tuhan, Ayhan Abaci, Gizem Cicek, Ahmet Anik, Gonul Catli, Korcan Demir, Ece Bober
Levothyroxine Replacement in Primary Congenital Hypothyroidism: The Higher The Initial Dose The Higher The Rate of Overtreatment
Hale Tuhan, Ayhan Abaci, Gizem Cicek, Ahmet Anik, Gonul Catli, Korcan Demir, Ece Bober
P2-569
PARENTING STRESS PROFILE AND CHILDREN BEHAVIOUR IN PATIENTS WITH CONGENITAL HYPOTHYROIDISM
Maria Cristina Maggio, Ettore Piro, Alessandra Alongi, Rita Riticella, Giuseppe Salvo, Giovanni Corsello
PARENTING STRESS PROFILE AND CHILDREN BEHAVIOUR IN PATIENTS WITH CONGENITAL HYPOTHYROIDISM
Maria Cristina Maggio, Ettore Piro, Alessandra Alongi, Rita Riticella, Giuseppe Salvo, Giovanni Corsello
P2-570
GOITROUS HYPOTHYROIDISM OF PUBERTAL ONSET CAUSED BY A NOVEL MUTATION IN DEHAL1 GENE.
Esther Schulz, Ainhoa Iglesias, Halit Ilker Akkurt, Knut Helmke, José Carlos Moreno
GOITROUS HYPOTHYROIDISM OF PUBERTAL ONSET CAUSED BY A NOVEL MUTATION IN DEHAL1 GENE.
Esther Schulz, Ainhoa Iglesias, Halit Ilker Akkurt, Knut Helmke, José Carlos Moreno
P2-571
Mutation screening of the TSH receptor gene in a cohort of 192 China patients with congenital hypothyroidism
Chunyun Fu, Yun Chen
Mutation screening of the TSH receptor gene in a cohort of 192 China patients with congenital hypothyroidism
Chunyun Fu, Yun Chen
P2-572
Mutational analysis of TSH receptor and the clinical characteristics of congenital hypothyroidism
Jeesuk Yu, Seung Ho Lee, Kyudong Han
Mutational analysis of TSH receptor and the clinical characteristics of congenital hypothyroidism
Jeesuk Yu, Seung Ho Lee, Kyudong Han
P2-573
Characteristics of delayed TSH elevation in neonatal intensive care unit (NICU) newborns
Amnon Zung, Arie Yehieli, Shlomo Almashanu
Characteristics of delayed TSH elevation in neonatal intensive care unit (NICU) newborns
Amnon Zung, Arie Yehieli, Shlomo Almashanu
P2-574
Three year follow-up of children with abnormal newborn screening results for congenital hypothyroidism: Who needs treatment and who needs permanent treatment?
Min Jae Kang, Young Suk Shim, Yeon Joung Oh, Hye Rim Chung, Seung Yang, Il Tae Hwang
Three year follow-up of children with abnormal newborn screening results for congenital hypothyroidism: Who needs treatment and who needs permanent treatment?
Min Jae Kang, Young Suk Shim, Yeon Joung Oh, Hye Rim Chung, Seung Yang, Il Tae Hwang
P2-575
Attention Deficit (AD) and Sluggish Cognitive Tempo (SCT) symptoms in Congenital Hypothyroidism (CH): results from a case-control study.
Annalisa Esposito, Ida D'Acunzo, Raffaella Di Mase, Ennio Del Giudice, Mateu Servera, Mariacarolina Salerno
Attention Deficit (AD) and Sluggish Cognitive Tempo (SCT) symptoms in Congenital Hypothyroidism (CH): results from a case-control study.
Annalisa Esposito, Ida D'Acunzo, Raffaella Di Mase, Ennio Del Giudice, Mateu Servera, Mariacarolina Salerno
P2-576
Relationship between cord blood phthalates and maternal and neonatal thyroid functions
Serkan Ozsoylu, Leyla Akin, Tamer Gunes, Mustafa Kendirci, Figen Narin, Selim Kurtoglu
Relationship between cord blood phthalates and maternal and neonatal thyroid functions
Serkan Ozsoylu, Leyla Akin, Tamer Gunes, Mustafa Kendirci, Figen Narin, Selim Kurtoglu
P2-577
Osteoprotegerin and free T4 levels in subclinical hypothyroidism of childhood
Aristeidis Giannakopoulos, Elena Katsantoni, Alexandra Efthymiadou, Dimitra Kritikou, Dionisios Chrysis
Osteoprotegerin and free T4 levels in subclinical hypothyroidism of childhood
Aristeidis Giannakopoulos, Elena Katsantoni, Alexandra Efthymiadou, Dimitra Kritikou, Dionisios Chrysis
P2-578
Cryptorchidism is commonly observed in Allan Herndon Dudley syndrome
Noriyuki Namba, Satoshi Takakuwa, Hirofumi Nakayama, Keiko Yamamoto, Makoto Fujiwara, Yasuhisa Ohata, Taichi Kitaoka, Takuo Kubota, Keiichi Ozono
Cryptorchidism is commonly observed in Allan Herndon Dudley syndrome
Noriyuki Namba, Satoshi Takakuwa, Hirofumi Nakayama, Keiko Yamamoto, Makoto Fujiwara, Yasuhisa Ohata, Taichi Kitaoka, Takuo Kubota, Keiichi Ozono
P2-579
Co-existence of Thyroid Nodule and Thyroid Cancer in Children and Adolescents with Hashimoto Thyroiditis; A Single-Center Study
Melikşah Keskin, Şenay Savas-Erdeve, Zehra Aycan
Co-existence of Thyroid Nodule and Thyroid Cancer in Children and Adolescents with Hashimoto Thyroiditis; A Single-Center Study
Melikşah Keskin, Şenay Savas-Erdeve, Zehra Aycan
P2-580
The diagnostic, treatment and follow-up features of childhood thyroid malignancies-A preliminary report
Aysun Bideci, Ediz Yesilkaya, Merih Berberoglu, Zeynep Siklar, Sukran Darcan, Samim Ozen, Serpil Bas, Esra Doger, Erdal Eren, Serap Turan, Aysehan Akinci, Fatma Demirel, Enver Simsek, Semra Cetinkaya, Iffet Bircan, Murat Aydin, Ece Bober, Erkan Sari, Nihal Hatipoglu, Meltem Tayfun, Halil Saglam, Mehmet Nuri Ozbek, Ruken Yildirim, Bumin Dundar, Atilla Cayir, Engin Alagoz, Erman Atas
The diagnostic, treatment and follow-up features of childhood thyroid malignancies-A preliminary report
Aysun Bideci, Ediz Yesilkaya, Merih Berberoglu, Zeynep Siklar, Sukran Darcan, Samim Ozen, Serpil Bas, Esra Doger, Erdal Eren, Serap Turan, Aysehan Akinci, Fatma Demirel, Enver Simsek, Semra Cetinkaya, Iffet Bircan, Murat Aydin, Ece Bober, Erkan Sari, Nihal Hatipoglu, Meltem Tayfun, Halil Saglam, Mehmet Nuri Ozbek, Ruken Yildirim, Bumin Dundar, Atilla Cayir, Engin Alagoz, Erman Atas
P3-1170
TOPICAL IODINE INDUCED THYROTOXICOSIS IN A NEWBORN WITH GIANT OMPHALOCELE
Sonali Malhotra, Shilpa Kumta, Roja Motaghedi
TOPICAL IODINE INDUCED THYROTOXICOSIS IN A NEWBORN WITH GIANT OMPHALOCELE
Sonali Malhotra, Shilpa Kumta, Roja Motaghedi
P3-1171
A familial case of congenital hypothyroidism (CH) due to a mutation in the thyroglobulin (TG) gene detected by Next Generation Sequencing (NGS)
Maria Cristina Vigone, Elena Peroni, Gaia Vincenzi, Giulia Gelmini, Tiziana de Filippis, Fulvio Sileo, Luca Persani, Giovanna Weber
A familial case of congenital hypothyroidism (CH) due to a mutation in the thyroglobulin (TG) gene detected by Next Generation Sequencing (NGS)
Maria Cristina Vigone, Elena Peroni, Gaia Vincenzi, Giulia Gelmini, Tiziana de Filippis, Fulvio Sileo, Luca Persani, Giovanna Weber
P3-1172
Central hypothyroidism and growth hormone deficiency in a boy with Williams-Beuren Syndrome
Sara Ciccone, Adriana Fumarola, Stefania Bigoni, Valentina Bonifacci, Elisa Maria Gabriella Marrella, Barbara Buldrini, Cristina Host
Central hypothyroidism and growth hormone deficiency in a boy with Williams-Beuren Syndrome
Sara Ciccone, Adriana Fumarola, Stefania Bigoni, Valentina Bonifacci, Elisa Maria Gabriella Marrella, Barbara Buldrini, Cristina Host
P3-1173
Avoidable thiamazole-induced omphalomesenteric duct remnants -20-year retrospective study in our hospital-
Hiroyuki Shinohara, Koji Komori, Seiichi Hirobe, Yukihiro Hasegawa
Avoidable thiamazole-induced omphalomesenteric duct remnants -20-year retrospective study in our hospital-
Hiroyuki Shinohara, Koji Komori, Seiichi Hirobe, Yukihiro Hasegawa
P3-1174
The impact on families of receiving a diagnosis of congenital hypothyroidism
Sabah Alvi, Julia Priestley, Amanda Whitehead, Jenny Walker, Talat Mushtaq
The impact on families of receiving a diagnosis of congenital hypothyroidism
Sabah Alvi, Julia Priestley, Amanda Whitehead, Jenny Walker, Talat Mushtaq
P3-1175
Final height in Italian patients with congenital hypothyroidism detected by neonatal screening: an observational study over 20 years
Maurizio Delvecchio, Mariacarolina Salerno, Maria Cristina Vigone, Malgorzata Wasniewska, Rosa Lapolla, Pietro Pio Popolo, Giulia Maria Tronconi, Raffaella Di Mase, Filippo De Luca, Luciano Cavallo, Giovanna Weber, Maria Felicia Faienza
Final height in Italian patients with congenital hypothyroidism detected by neonatal screening: an observational study over 20 years
Maurizio Delvecchio, Mariacarolina Salerno, Maria Cristina Vigone, Malgorzata Wasniewska, Rosa Lapolla, Pietro Pio Popolo, Giulia Maria Tronconi, Raffaella Di Mase, Filippo De Luca, Luciano Cavallo, Giovanna Weber, Maria Felicia Faienza
P3-1176
Graves´ disease in childhood and adolescence: clinical manifestations, adverse effects, and predictive factors for response to antithyroid drugs
Noelia Vanesa Dujovne, Gustavo Dratler, Fabián Pitoia, Laura Felipe, Victor Ayarzabal, Ianina Soria, Malena Berger, Alicia Belgorosky, Viviana Herzovich
Graves´ disease in childhood and adolescence: clinical manifestations, adverse effects, and predictive factors for response to antithyroid drugs
Noelia Vanesa Dujovne, Gustavo Dratler, Fabián Pitoia, Laura Felipe, Victor Ayarzabal, Ianina Soria, Malena Berger, Alicia Belgorosky, Viviana Herzovich
P3-1177
The correlation between TSH levels and BMI percentiles in hypothyroid children who are chemically euthyroid on levothyroxine treatment
Asma Shaoba, Carla Minutti
The correlation between TSH levels and BMI percentiles in hypothyroid children who are chemically euthyroid on levothyroxine treatment
Asma Shaoba, Carla Minutti
P3-1178
Short Stature with lipodystrophy: reminder of a forgotten syndrome
Rakesh Kumar, Robin Rifkin, Sarah Ehtisham
Short Stature with lipodystrophy: reminder of a forgotten syndrome
Rakesh Kumar, Robin Rifkin, Sarah Ehtisham
P3-1179
Plasma visfatin level and its association with apolipoproteins A1 and B in hypothyroid children
Elham Hashemi Dehkordi, Noushin Rostampour, Karamali Kasiri, Mohammad Moafi, Mohammad Esmail Aramesh, Mahin Hashemipour
Plasma visfatin level and its association with apolipoproteins A1 and B in hypothyroid children
Elham Hashemi Dehkordi, Noushin Rostampour, Karamali Kasiri, Mohammad Moafi, Mohammad Esmail Aramesh, Mahin Hashemipour
P3-1180
Outcome of thyrotoxicosis in childhood and adolescence in a geographically define area;a 24-year experience
Mariam Kourime, Sheena McGowan, Mabrouka Al-Towati, Faisal Ahmed, Graham Stewart, Scott Williamson, Ian Hunter, Malcolm Donaldson
Outcome of thyrotoxicosis in childhood and adolescence in a geographically define area;a 24-year experience
Mariam Kourime, Sheena McGowan, Mabrouka Al-Towati, Faisal Ahmed, Graham Stewart, Scott Williamson, Ian Hunter, Malcolm Donaldson
P3-1181
Early discrimination between transient and permanent congenital hypothyroidism in children with eutopic gland
Maria Francesca Messina, Tommaso Aversa, Giuseppina Salzano, Giuseppina Zirilli, Concetta Sferlazzas, Filippo De Luca, Fortunato Lombardo
Early discrimination between transient and permanent congenital hypothyroidism in children with eutopic gland
Maria Francesca Messina, Tommaso Aversa, Giuseppina Salzano, Giuseppina Zirilli, Concetta Sferlazzas, Filippo De Luca, Fortunato Lombardo
P3-1182
The role of early thyroid imaging in children with congenital hypothyroidism
Tal Oron, Yael Lebenthal, Shimon Ben-Yishai, Ariel Tenenbaum, Michal Yackobovitch-Gavan, Moshe Phillip, Liora Lazar
The role of early thyroid imaging in children with congenital hypothyroidism
Tal Oron, Yael Lebenthal, Shimon Ben-Yishai, Ariel Tenenbaum, Michal Yackobovitch-Gavan, Moshe Phillip, Liora Lazar
P3-1183
EFFECT OF MARIJUANA USE ON THYROID FUNCTION AND AUTO IMMUNITY
Sonali Malhotra, Peter Homel, Roja Motaghedi
EFFECT OF MARIJUANA USE ON THYROID FUNCTION AND AUTO IMMUNITY
Sonali Malhotra, Peter Homel, Roja Motaghedi
P3-1184
pediatric thyroid disease: About a series of 48 cases
hakima abaes, ali el mahdi haddam, soumeya nora fedala, djamila meskine, farida chentli
pediatric thyroid disease: About a series of 48 cases
hakima abaes, ali el mahdi haddam, soumeya nora fedala, djamila meskine, farida chentli
P3-1185
Neonatal hyperthyroidism with craniolacunia
Junko Igaki, Fumitaka Inoue, Tohru Fujiu, Shinitsu Hatakeyama
Neonatal hyperthyroidism with craniolacunia
Junko Igaki, Fumitaka Inoue, Tohru Fujiu, Shinitsu Hatakeyama
P3-1186
Is transient hypothyroidism in preterm infants true?
Amparo González Vergaz, Beatriz García Cuartero, Rosa Sánchez Dehesa, Veronica Sánchez Escudero, ersilia González Carrasco
Is transient hypothyroidism in preterm infants true?
Amparo González Vergaz, Beatriz García Cuartero, Rosa Sánchez Dehesa, Veronica Sánchez Escudero, ersilia González Carrasco
P3-1187
The benefits of preterm neonate development by early replacement therapy with L-thyroxine – longitudinal prospective study
Iwona Ben-Skowronek, Magdalena Wisniowiecka
The benefits of preterm neonate development by early replacement therapy with L-thyroxine – longitudinal prospective study
Iwona Ben-Skowronek, Magdalena Wisniowiecka
P3-1188
INTRATHYROIDAL ECTOPIC THYMIC TISSUE MIMICING A THYROID NODULE: A REPORT OF THREE PEDIATRIC CASES
Gülay Karagüzel, Serpil Kaya, Ilker Eyupoglu, Havvanur Turgutalp, Aysenur Okten
INTRATHYROIDAL ECTOPIC THYMIC TISSUE MIMICING A THYROID NODULE: A REPORT OF THREE PEDIATRIC CASES
Gülay Karagüzel, Serpil Kaya, Ilker Eyupoglu, Havvanur Turgutalp, Aysenur Okten
P3-1189
Simultaneous occurrence of thyroid storm, diabetic ketoacidosis, and multiple cerebral infarction in a 16-year-old girl
Byoungho Noh, Sang-Won Cho, So-Eun Park, Sung Yeon Ahn
Simultaneous occurrence of thyroid storm, diabetic ketoacidosis, and multiple cerebral infarction in a 16-year-old girl
Byoungho Noh, Sang-Won Cho, So-Eun Park, Sung Yeon Ahn
P3-1190
Two Cousins with Allen-Herndon-Dudley Syndrome: A Novel Mutation on MCT8 Gene
Gul Yesiltepe Mutlu, Heves Kirmizibekmez, Elaine C. Lima de Souza, Sukru Hatun, Theo J. Visser
Two Cousins with Allen-Herndon-Dudley Syndrome: A Novel Mutation on MCT8 Gene
Gul Yesiltepe Mutlu, Heves Kirmizibekmez, Elaine C. Lima de Souza, Sukru Hatun, Theo J. Visser
P3-1191
Audit of Thyroid Carcinoma in children, adolescents and adults
Wei Li Cindy Ho, Margaret Zacharin
Audit of Thyroid Carcinoma in children, adolescents and adults
Wei Li Cindy Ho, Margaret Zacharin
P3-1192
The Comparing of Thyroid Volumes Between Healthy and Obese Children in Respect of Anthropometric , Biochemical, Metabolic Parameters
Mehmet Keskin, Murat Karaoglan, Onur Balci, Ayhan Ozkur, Ozlem Keskin
The Comparing of Thyroid Volumes Between Healthy and Obese Children in Respect of Anthropometric , Biochemical, Metabolic Parameters
Mehmet Keskin, Murat Karaoglan, Onur Balci, Ayhan Ozkur, Ozlem Keskin
P3-1193
NKX2-1 p.Asp266Argfs142X de novo mutation in a girl with congenital hypothyroidism (CH): phenotypic description
Iva Stoeva, Anne Thorwarth, Boris Stoilov, Heiko Krude
NKX2-1 p.Asp266Argfs142X de novo mutation in a girl with congenital hypothyroidism (CH): phenotypic description
Iva Stoeva, Anne Thorwarth, Boris Stoilov, Heiko Krude
P3-1194
Development and risk factors of thyroid dysfunction in patients with positive TPO antibodies
C. Nicolas Gomez, J. McNeilly, A. Mason, SF. Ahmed, SC. Wong, G. Shaikh
Development and risk factors of thyroid dysfunction in patients with positive TPO antibodies
C. Nicolas Gomez, J. McNeilly, A. Mason, SF. Ahmed, SC. Wong, G. Shaikh
P3-1195
The evaluation of CD8+CD122+ T cells in children with autoimmune thyroiditis.
Anna Kucharska, Anna Stelmaszczyk- Emmel, Katarzyna Popko, Beata Pyrzak, Katarzyna Kadziela
The evaluation of CD8+CD122+ T cells in children with autoimmune thyroiditis.
Anna Kucharska, Anna Stelmaszczyk- Emmel, Katarzyna Popko, Beata Pyrzak, Katarzyna Kadziela
P3-1196
Hoffmann syndrome in a boy with severe acquired primary hypothyroidism.
Lucia Garzón Lorenzo, Jaime Cruz Rojo, Cristina Martínez del Pozo, Noemí Núñez Enamorado, Jaime Sánchez del Pozo
Hoffmann syndrome in a boy with severe acquired primary hypothyroidism.
Lucia Garzón Lorenzo, Jaime Cruz Rojo, Cristina Martínez del Pozo, Noemí Núñez Enamorado, Jaime Sánchez del Pozo
P3-1197
Congenital Hypothyroidism incidence and dysgenesis or dyshormonogenesis prevalence in a large infants cohort from south of France.
Isabelle Oliver Petit, Emilie Lobinet, Isabelle Gennero, Thomas Edouard, Audrey Cartault, Maithé Tauber
Congenital Hypothyroidism incidence and dysgenesis or dyshormonogenesis prevalence in a large infants cohort from south of France.
Isabelle Oliver Petit, Emilie Lobinet, Isabelle Gennero, Thomas Edouard, Audrey Cartault, Maithé Tauber
P3-1198
Thyroid function in a large group of obese children: causes and consequences
Fiorenzo Lupi, Giorgio Radetti, Silvia Longhi, Graziano Grugni, Nicoletta Marazzi, Antonio Fanolla, Alessandrio Sartorio
Thyroid function in a large group of obese children: causes and consequences
Fiorenzo Lupi, Giorgio Radetti, Silvia Longhi, Graziano Grugni, Nicoletta Marazzi, Antonio Fanolla, Alessandrio Sartorio
P3-1199
THYROID NODULES IN CHILDREN AND ADOLESCENTS
GEMA GRAU BOLADO, MAITE PEREZ DE CIRIZA CORDEU, ANDREA CEREZO AGUIRRE, JAVIER NUÑEZ RODRIGUEZ, AMAIA VELA SOJO, AMAIA RODRIGUEZ ESTEVEZ, ITXASO RICA ECHEVARRIA, CONCEPCION FERNANDEZ RAMOS
THYROID NODULES IN CHILDREN AND ADOLESCENTS
GEMA GRAU BOLADO, MAITE PEREZ DE CIRIZA CORDEU, ANDREA CEREZO AGUIRRE, JAVIER NUÑEZ RODRIGUEZ, AMAIA VELA SOJO, AMAIA RODRIGUEZ ESTEVEZ, ITXASO RICA ECHEVARRIA, CONCEPCION FERNANDEZ RAMOS
P3-1200
Trisomy 21 and thyroid dysfunction: About 50 pediatric cases
ali el mahdi haddam, soumeya nora fedala, farida chentli, djamila meskine
Trisomy 21 and thyroid dysfunction: About 50 pediatric cases
ali el mahdi haddam, soumeya nora fedala, farida chentli, djamila meskine
P3-1201
NKX2-1 (TTF-1) Germline mutations are not a frequent cause of congenital hypothyroidism due to dysgenesis
Aidy Gonzalez Nunez, Ariadna Gonzalez del Angel, Miguel Angel Alcantara Ortigoza, Victor Martinez Cruz
NKX2-1 (TTF-1) Germline mutations are not a frequent cause of congenital hypothyroidism due to dysgenesis
Aidy Gonzalez Nunez, Ariadna Gonzalez del Angel, Miguel Angel Alcantara Ortigoza, Victor Martinez Cruz
P3-1202
A Curious Case of Thyrotoxic Crisis and Lower Extremity Weakness in a 15 year-old Female with Graves Disease
Magdalena Dumin, Khalid Afzal, Carol Macmillan, Dorit Koren
A Curious Case of Thyrotoxic Crisis and Lower Extremity Weakness in a 15 year-old Female with Graves Disease
Magdalena Dumin, Khalid Afzal, Carol Macmillan, Dorit Koren
P3-1203
Newborns of Mothers with Graves’Disease – survey of 14 years
Rita Cardoso, Mónica Jerónimo, Joana Serra Caetano, Isabel Dinis, Alice Mirante
Newborns of Mothers with Graves’Disease – survey of 14 years
Rita Cardoso, Mónica Jerónimo, Joana Serra Caetano, Isabel Dinis, Alice Mirante
P3-1204
Use of liothyronine in a case of consumptive hypothyroidism caused by hepatic hemangiomas
Shinji Higuchi, Masaki Takagi, Masahiro Goto, Yukihiro Hasegawa
Use of liothyronine in a case of consumptive hypothyroidism caused by hepatic hemangiomas
Shinji Higuchi, Masaki Takagi, Masahiro Goto, Yukihiro Hasegawa
P3-1205
Subclinical hypothyroidism in children and adolescents – a 5-year single-center follow-up study
Aneta Gawlik, Kamila Such, Aleksandra Dejner, Agnieszka Zachurzok, Aleksandra Antosz, Ewa Malecka-Tendera
Subclinical hypothyroidism in children and adolescents – a 5-year single-center follow-up study
Aneta Gawlik, Kamila Such, Aleksandra Dejner, Agnieszka Zachurzok, Aleksandra Antosz, Ewa Malecka-Tendera
P3-1206
The difference between cord and filter paper TSH level in congenital hypothyroidism screening programme
Fahad Aljuraibah, Ali Alothaim, Wafa Aleyaid, Angham Almutair
The difference between cord and filter paper TSH level in congenital hypothyroidism screening programme
Fahad Aljuraibah, Ali Alothaim, Wafa Aleyaid, Angham Almutair
P3-1207
Neonatal hyperthyrotropinemia - watchful waiting versus treatment
Experiences from a tertiary centre
Caroline Ponmani, Catherine Peters, Shirley Langham
Neonatal hyperthyrotropinemia - watchful waiting versus treatment
Experiences from a tertiary centre
Caroline Ponmani, Catherine Peters, Shirley Langham
P3-1208
Congenital central hypothyroidism due to a homozygous mutation in the TSHB gene – just think about it!
Monika Flury, Andrea Naeke, Nataliya Di Donato, Gabriele Hahn, Angela Huebner
Congenital central hypothyroidism due to a homozygous mutation in the TSHB gene – just think about it!
Monika Flury, Andrea Naeke, Nataliya Di Donato, Gabriele Hahn, Angela Huebner
P3-1209
A Case of Acute Suppurative Thyroiditis with Piriform Sinus Fistula treated with Chemocauterization using Trichloroacetic acid
Kyung lae Son, Heung sik Kim
A Case of Acute Suppurative Thyroiditis with Piriform Sinus Fistula treated with Chemocauterization using Trichloroacetic acid
Kyung lae Son, Heung sik Kim
P3-1210
Thyroid dysfunction in children with trisomy 21: when subclinical hypothyroidism should be treated?
Elena Sukarova-Angelovska, Mirjana Kocova, Tatjana Zorcec
Thyroid dysfunction in children with trisomy 21: when subclinical hypothyroidism should be treated?
Elena Sukarova-Angelovska, Mirjana Kocova, Tatjana Zorcec
P3-1211
Rectal diluted levothyroxine for the treatment of neonatal hypothyroidism: an alternative route of administration
Marina Ybarra, Claudia Pinheiro, Nuvarte Setian, Durval Damiani, Vae Dichtcekennian
Rectal diluted levothyroxine for the treatment of neonatal hypothyroidism: an alternative route of administration
Marina Ybarra, Claudia Pinheiro, Nuvarte Setian, Durval Damiani, Vae Dichtcekennian
P3-1212
Goiter in childhood and adolescence; clinical course and associated factors for thyroid autoimmunity or isolated nonautoimmune hyperthyrotropinemia
So Youn Kim, Hae Woon Jung, Kyung A Jeong, Keun Hee Choi, Gyung Min Lee, Hwa Young Kim, Young Ah Lee, Choong Ho Shin, Sei Won Yang
Goiter in childhood and adolescence; clinical course and associated factors for thyroid autoimmunity or isolated nonautoimmune hyperthyrotropinemia
So Youn Kim, Hae Woon Jung, Kyung A Jeong, Keun Hee Choi, Gyung Min Lee, Hwa Young Kim, Young Ah Lee, Choong Ho Shin, Sei Won Yang
P3-1213
HYPERTHYROIDISM IN CHILDREN AND ADOLESCENTS:CAUSES, WHEN AND HOW TO TREAT. A TUNISIAN EXPERIENCE
ESSADDAM Leïla, KALLALI Wafa, GUEDRI Rahma, FITOURI Zohra, MATOUSSI Nadia, BEN BECHER Saayda
HYPERTHYROIDISM IN CHILDREN AND ADOLESCENTS:CAUSES, WHEN AND HOW TO TREAT. A TUNISIAN EXPERIENCE
ESSADDAM Leïla, KALLALI Wafa, GUEDRI Rahma, FITOURI Zohra, MATOUSSI Nadia, BEN BECHER Saayda
P3-1214
Massive pericardial effusion and short stature caused by autoimmune hypothyroidism in 9-yr old dyspneic girl
Heon-Seok Han, Jae-Hong Yu, YunHee Gyon
Massive pericardial effusion and short stature caused by autoimmune hypothyroidism in 9-yr old dyspneic girl
Heon-Seok Han, Jae-Hong Yu, YunHee Gyon
P3-1215
Prevalence of goiter and thyroid nodule and analysis of the association between anthropometric measurements and thyroid volume in children
Sultan Kaba, Murat Doğan, Keziban Bulan, Aydın Bora, Alpaslan Yavuz, Muazzez Didin, İlyas Dündar
Prevalence of goiter and thyroid nodule and analysis of the association between anthropometric measurements and thyroid volume in children
Sultan Kaba, Murat Doğan, Keziban Bulan, Aydın Bora, Alpaslan Yavuz, Muazzez Didin, İlyas Dündar
P3-1217
Subclinical hypothyroidism in children and adolescents : About a study of 25 cases
soumeya nora fedala, ali el mahdi haddam, leyla ahmed ali, djamila meskine, farida chentli
Subclinical hypothyroidism in children and adolescents : About a study of 25 cases
soumeya nora fedala, ali el mahdi haddam, leyla ahmed ali, djamila meskine, farida chentli
P3-1218
Effects of Subclinically Hypothyroidism on Hemorheological Parameters in Pediatric Population
Yasemin Isik Balci, Sebahat Yilmaz Agladioglu, Kadir Agladioglu, Emine Kilic Toprak, Ozgen Kilic Erkek, Bayram Ozhan, Aziz Polat, Melek Bor Kucukatay
Effects of Subclinically Hypothyroidism on Hemorheological Parameters in Pediatric Population
Yasemin Isik Balci, Sebahat Yilmaz Agladioglu, Kadir Agladioglu, Emine Kilic Toprak, Ozgen Kilic Erkek, Bayram Ozhan, Aziz Polat, Melek Bor Kucukatay
P3-1219
Unilateral Graves Disease in an adolescent: Case report
beray selver eklioglu, mehmet emre atabek, nesibe akyurek, gungor tastekin
Unilateral Graves Disease in an adolescent: Case report
beray selver eklioglu, mehmet emre atabek, nesibe akyurek, gungor tastekin
P3-1220
Transient Hyperthyroidism Associated with a Thyroid Nodule
Alejandro Vargas Pieck, Diego Yeste Fernández, Marta Garrido Pontnou, María Clemente León, Ariadna Campos Martorell, Antonio Carrascosa Lezcano
Transient Hyperthyroidism Associated with a Thyroid Nodule
Alejandro Vargas Pieck, Diego Yeste Fernández, Marta Garrido Pontnou, María Clemente León, Ariadna Campos Martorell, Antonio Carrascosa Lezcano
P3-1221
Hyalinizing Trabecular Tumor of thyroid gland in 17-year-old boy- case report
Beata Sawicka, Janusz Dzieciol, Artur Bossowski
Hyalinizing Trabecular Tumor of thyroid gland in 17-year-old boy- case report
Beata Sawicka, Janusz Dzieciol, Artur Bossowski
P3-1222
SEVEN CASES WITH WILLIAMS BEUREN SYNDROME: ENDOCRINE EVALUATION AND LONG TERM FOLLOW-UP
Ayla Güven
SEVEN CASES WITH WILLIAMS BEUREN SYNDROME: ENDOCRINE EVALUATION AND LONG TERM FOLLOW-UP
Ayla Güven
P3-1223
Clinical course in a girl with hTPO mutation R161I in exon 5: 18 years of follow up
Iva Stoeva, Petra Ambrugger, Boris Stoilov, Ganka Dineva, Heike Biebermann, Annette Grueters
Clinical course in a girl with hTPO mutation R161I in exon 5: 18 years of follow up
Iva Stoeva, Petra Ambrugger, Boris Stoilov, Ganka Dineva, Heike Biebermann, Annette Grueters
P3-1224
Transient polyarthritis with Carbimazole treatment
Madhavi Madhusudhana, Mary Barraclough, Elaine Baguley, Sanjay Gupta
Transient polyarthritis with Carbimazole treatment
Madhavi Madhusudhana, Mary Barraclough, Elaine Baguley, Sanjay Gupta
P3-1225
Thyroid functional autonomy in adolescents with nodular goiter.
Olga Rogova, Goar Okminyan, Lubov Samsonova, Elena Kiseleva, Oleg Latyshev, Elvira Kasatkina
Thyroid functional autonomy in adolescents with nodular goiter.
Olga Rogova, Goar Okminyan, Lubov Samsonova, Elena Kiseleva, Oleg Latyshev, Elvira Kasatkina
P3-1226
A rare adverse effect of radioactive iodine therapy in a child with Graves Disease
Elizabeth Walsh, Marcie Drury Brown, David Crudo, Cathrine Constantaocs
A rare adverse effect of radioactive iodine therapy in a child with Graves Disease
Elizabeth Walsh, Marcie Drury Brown, David Crudo, Cathrine Constantaocs
P3-1227
A 7 month-old male infant with spontaneous transient Graves’ thyrotoxicosis
Shuichi Yatsuga, Takako Sasaki, Kikumi Ushijima, Junko Nishioka, Yasutoshi Koga
A 7 month-old male infant with spontaneous transient Graves’ thyrotoxicosis
Shuichi Yatsuga, Takako Sasaki, Kikumi Ushijima, Junko Nishioka, Yasutoshi Koga
P3-1228
Sex and age differences in the incidence of thyroid disease in children with obesity
Olena Budreiko, Olena Shushlyapina, Ganna Kosovtsova, Natalia Shlyachova, Larisa Nikitina
Sex and age differences in the incidence of thyroid disease in children with obesity
Olena Budreiko, Olena Shushlyapina, Ganna Kosovtsova, Natalia Shlyachova, Larisa Nikitina
P3-1229
Euthyroid sick syndrome in children presenting with diabetic ketoacidosis
Riza Taner Baran, Huseyin Demirbilek, Munevver Dundar, Mulkiye Aydin, Remezan Demir, Mustafa Karatas, Funda Tas, Kahraman Oncel, Mehmet Nuri Ozbek
Euthyroid sick syndrome in children presenting with diabetic ketoacidosis
Riza Taner Baran, Huseyin Demirbilek, Munevver Dundar, Mulkiye Aydin, Remezan Demir, Mustafa Karatas, Funda Tas, Kahraman Oncel, Mehmet Nuri Ozbek
P3-1230
THE ROLE OF THYROID FINE-NEEDLE ASPIRATION CYTOLOGY IN THE TREATMENT AND FOLLOW-UP OF THYROID NODULES IN THE PEDIATRİC POPULATION
mikayir genens, cansu yilmaz, yasemin ozluk, oguz bulent erol, zehra yavas abali, sukran poyrazoglu, firdevs bas, ruveyde bundak, pinar firat, dilek yılmaz bayhan, feyza darendeliler
THE ROLE OF THYROID FINE-NEEDLE ASPIRATION CYTOLOGY IN THE TREATMENT AND FOLLOW-UP OF THYROID NODULES IN THE PEDIATRİC POPULATION
mikayir genens, cansu yilmaz, yasemin ozluk, oguz bulent erol, zehra yavas abali, sukran poyrazoglu, firdevs bas, ruveyde bundak, pinar firat, dilek yılmaz bayhan, feyza darendeliler
P3-1231
ANGIONEUROTIC EDEMA WITH ANTITHYROID DRUGS IN THYROID STORM: WHAT IS THE BEST THERAPEUTIC OPTION
Pelin Bilir, Mehmet Isakoca, Aydan Ikinciogullari, Figen Dogu, Sule Haskaloglu, Demet Corapcioglu, Rifat Emral, Suat Fitoz, Adalet Elcin Yildiz, Metin Kir, Gulnur Göllü Bahadir, Bilge Türedi, Hüseyin Dindar
ANGIONEUROTIC EDEMA WITH ANTITHYROID DRUGS IN THYROID STORM: WHAT IS THE BEST THERAPEUTIC OPTION
Pelin Bilir, Mehmet Isakoca, Aydan Ikinciogullari, Figen Dogu, Sule Haskaloglu, Demet Corapcioglu, Rifat Emral, Suat Fitoz, Adalet Elcin Yildiz, Metin Kir, Gulnur Göllü Bahadir, Bilge Türedi, Hüseyin Dindar
P3-1232
Malabsorption of levothyroxine in a child affected by short bowel syndrome
Laura Paone, Romana Marini, Antonella Diamanti, Marco Cappa
Malabsorption of levothyroxine in a child affected by short bowel syndrome
Laura Paone, Romana Marini, Antonella Diamanti, Marco Cappa
P1-133
Improved determination of total serum estrogenic bioactivity: characterization of estrogenic activity modulators.
Paris Françoise, Grimaldi Marina, Sultan Charles, Balaguer Patrick
Improved determination of total serum estrogenic bioactivity: characterization of estrogenic activity modulators.
Paris Françoise, Grimaldi Marina, Sultan Charles, Balaguer Patrick
P1-134
Co-existing variants of FOXE1 and BMP15 genes in young females with primary ovarian insufficiency (POI): Evidence of digenic inheritance.
NIKOLAOS SETTAS, LINA MICHALA, EFTHIMIOS DELIGEOROGLOU, DIONISIOS CHRYSIS, ANDREAS PAMPANOS, ELENI THEOCHARI, OLYMPIA VALLA, CHRISTALENA SOFOCLEOUS, KITSIOU SOFIA, HELEN FRYSSIRA, EMMANUEL KANAVAKIS, CATHERINE DACOU-VOUTETAKIS, GEORGE P CHROUSOS, ANTONIS VOUTETAKIS
Co-existing variants of FOXE1 and BMP15 genes in young females with primary ovarian insufficiency (POI): Evidence of digenic inheritance.
NIKOLAOS SETTAS, LINA MICHALA, EFTHIMIOS DELIGEOROGLOU, DIONISIOS CHRYSIS, ANDREAS PAMPANOS, ELENI THEOCHARI, OLYMPIA VALLA, CHRISTALENA SOFOCLEOUS, KITSIOU SOFIA, HELEN FRYSSIRA, EMMANUEL KANAVAKIS, CATHERINE DACOU-VOUTETAKIS, GEORGE P CHROUSOS, ANTONIS VOUTETAKIS
P1-135
Sex hormones and gonadal size in pubertal girls born small or appropriate for gestational age
Indre Petraitiene, Rasa Verkauskiene, Kristina Jariene, Astra Vitkauskiene
Sex hormones and gonadal size in pubertal girls born small or appropriate for gestational age
Indre Petraitiene, Rasa Verkauskiene, Kristina Jariene, Astra Vitkauskiene
P1-56
Immunohistochemical detection of estrogen α and androgen receptors in genital tissues in girls with congenital adrenal hyperplasia
Irina Kopylova, Elizaveta Orlova, Veronika Sysoeva, Tatyana Glybina, Mariia Kareva
Immunohistochemical detection of estrogen α and androgen receptors in genital tissues in girls with congenital adrenal hyperplasia
Irina Kopylova, Elizaveta Orlova, Veronika Sysoeva, Tatyana Glybina, Mariia Kareva
P1-57
Attitudes of parents of Klinefelter boys and Flemish pediatricians towards neonatal screening and fertility preservation techniques in Klinefelter syndrome.
Inge Gies, Herman Tournaye, Jean De Schepper
Attitudes of parents of Klinefelter boys and Flemish pediatricians towards neonatal screening and fertility preservation techniques in Klinefelter syndrome.
Inge Gies, Herman Tournaye, Jean De Schepper
P2-433
Oral Contraception versus Low-Dose Pioglitazone-Spironolactone-Metformin (PioSpiMet)
for Adolescent Girls with Hyperinsulinemic Androgen Excess: On-Treatment Divergences
Lourdes Ibañez, Marta Díaz, Giorgia Sebastiani, Abel López-Bermejo, Francis de Zegher
Oral Contraception versus Low-Dose Pioglitazone-Spironolactone-Metformin (PioSpiMet)
for Adolescent Girls with Hyperinsulinemic Androgen Excess: On-Treatment Divergences
Lourdes Ibañez, Marta Díaz, Giorgia Sebastiani, Abel López-Bermejo, Francis de Zegher
P2-434
Confirmation of exogenous serum estrogenic activity in a girl with premature thelarche
Paris Françoise, Grimaldi Marina, Sultan Charles, Balaguer Patrick
Confirmation of exogenous serum estrogenic activity in a girl with premature thelarche
Paris Françoise, Grimaldi Marina, Sultan Charles, Balaguer Patrick
P2-435
Clinical criteria remain paramount for the diagnosis of polycystic ovary syndrome in the adolescent age group
Liat de Vries, Adi Weinberg, Moshe Phillip
Clinical criteria remain paramount for the diagnosis of polycystic ovary syndrome in the adolescent age group
Liat de Vries, Adi Weinberg, Moshe Phillip
P2-436
Gonadal and sexual dysfunction in childhood cancer survivors
Ju Young Yoon, Hyeon Jin Park, Jin Soo Chung, Sang Hyun Hwang, Dong Ock Lee, Hye Young Shim, Byung Kiu Park
Gonadal and sexual dysfunction in childhood cancer survivors
Ju Young Yoon, Hyeon Jin Park, Jin Soo Chung, Sang Hyun Hwang, Dong Ock Lee, Hye Young Shim, Byung Kiu Park
P2-437
Implementation of a high sensitive LC-MS/MS method for measurement of estradiol, estrone and estriol
Alexandra Kulle, Thomas Reinehr, Gunter Simic-Schleicher, Jule Roscheswsky, Maik Welzel, Paul-Martin Holterhus
Implementation of a high sensitive LC-MS/MS method for measurement of estradiol, estrone and estriol
Alexandra Kulle, Thomas Reinehr, Gunter Simic-Schleicher, Jule Roscheswsky, Maik Welzel, Paul-Martin Holterhus
P2-438
Gonadal function in the Prader-Willi syndrome from infancy to adulthood
Sakina Kherra, Mariam Kourime, Heba El-Sedfy, Wendy Paterson, M Guftar Shaikh, Malcolm Donaldson
Gonadal function in the Prader-Willi syndrome from infancy to adulthood
Sakina Kherra, Mariam Kourime, Heba El-Sedfy, Wendy Paterson, M Guftar Shaikh, Malcolm Donaldson
P2-439
Markers of fertility and quality of life in adolescents with chronic endocrine diseases at the time of transition from paediatric to adult care
Janna Mittnacht, Daniela Choukair, Daniela Klose, Ioana Inta, Markus Bettendorf
Markers of fertility and quality of life in adolescents with chronic endocrine diseases at the time of transition from paediatric to adult care
Janna Mittnacht, Daniela Choukair, Daniela Klose, Ioana Inta, Markus Bettendorf
P2-440
A NOVEL ANDROGEN RECEPTOR GENE MUTATION IN TWO PATIENTS WITH A 46,XY DISORDER OF SEX DEVELOPMENT
María Sanz Fernández, María Dolores Rodríguez Arnao, Amparo Rodríguez Sánchez, Esther González Ruiz de León, Mónica Fernández Cancio, Laura Audí Parera
A NOVEL ANDROGEN RECEPTOR GENE MUTATION IN TWO PATIENTS WITH A 46,XY DISORDER OF SEX DEVELOPMENT
María Sanz Fernández, María Dolores Rodríguez Arnao, Amparo Rodríguez Sánchez, Esther González Ruiz de León, Mónica Fernández Cancio, Laura Audí Parera
P2-441
The effect and pharmacokinetics of percutaneous administration of dihydrotestosterone gel in Chinese Children with microphallus
zhang jun, chen qiuli, guo song, du minlian, li yanhong, ma huamei, chen hongshan
The effect and pharmacokinetics of percutaneous administration of dihydrotestosterone gel in Chinese Children with microphallus
zhang jun, chen qiuli, guo song, du minlian, li yanhong, ma huamei, chen hongshan
P2-442
DIFERENTIAL REGULATION OF SERUM SEX HORMONE BINDING GLOBULING IN POLYCYSTIC OVARIAN SYNDROME GIRLS IN RELATION TO WEIGHT
Marta Murillo-Vallés, Marina Carbonell-Prat, Maria Luisa Granada, Isabel Salinas, Maria Martinez-Barahona, Joan Bel-Comós
DIFERENTIAL REGULATION OF SERUM SEX HORMONE BINDING GLOBULING IN POLYCYSTIC OVARIAN SYNDROME GIRLS IN RELATION TO WEIGHT
Marta Murillo-Vallés, Marina Carbonell-Prat, Maria Luisa Granada, Isabel Salinas, Maria Martinez-Barahona, Joan Bel-Comós
P2-443
Usefulness of 3D ultrasonography for assessment of the morphology of the ovary in adolescents with hyperandrogenism
Iwona Ben-Skowronek, Elzbieta Budzynska, Magdalena Wozniak, Pawel Wieczorek
Usefulness of 3D ultrasonography for assessment of the morphology of the ovary in adolescents with hyperandrogenism
Iwona Ben-Skowronek, Elzbieta Budzynska, Magdalena Wozniak, Pawel Wieczorek
P2-444
An unusual cause of primary amenorrhoea suggested by the urine steroid profile
Noemi Auxiliadora Fuentes-Bolanos, Norman Taylor, Christina Wei
An unusual cause of primary amenorrhoea suggested by the urine steroid profile
Noemi Auxiliadora Fuentes-Bolanos, Norman Taylor, Christina Wei
P3-1000
Final height of children with SGA TREATED WITH BIOSYNTHETIC GROWTH HORMONE : About a serie of 30 children
soumeya nora fedala, ali el mahdi haddam, leyla ahmed ali, djamila meskine, farida chentli
Final height of children with SGA TREATED WITH BIOSYNTHETIC GROWTH HORMONE : About a serie of 30 children
soumeya nora fedala, ali el mahdi haddam, leyla ahmed ali, djamila meskine, farida chentli
P3-1001
Anti-Müllerian Hormone Is a Useful Marker of Gonadotoxicity in Girls Treated for Cancer: A Prospective Study
Yoko Miyoshi, Kie Yasuda, Takako Miyamura, Emiko Miyashita, Yoshiko Hashii, Keiichi Ozono
Anti-Müllerian Hormone Is a Useful Marker of Gonadotoxicity in Girls Treated for Cancer: A Prospective Study
Yoko Miyoshi, Kie Yasuda, Takako Miyamura, Emiko Miyashita, Yoshiko Hashii, Keiichi Ozono
P3-1002
Leydig-cell tumor, a rare cause of LH-independent sexual precocity in boys.
maxime gerard, cecile thomas-teinturier, claire bouvattier, anne mantel, guenolee de lambert, sylvie beaudoin, charlotte mussini, bougneres pierre
Leydig-cell tumor, a rare cause of LH-independent sexual precocity in boys.
maxime gerard, cecile thomas-teinturier, claire bouvattier, anne mantel, guenolee de lambert, sylvie beaudoin, charlotte mussini, bougneres pierre
P3-1003
Antimullerian Hormone and Inhibin B markers of the ovarian reserve after ovariectomy
Grazia Morandi, Claudia Anita Piona, Sarah Dal Ben, Diego Ramaroli, Paolo Cavarzere, Franco Antoniazzi, Rossella Gaudino
Antimullerian Hormone and Inhibin B markers of the ovarian reserve after ovariectomy
Grazia Morandi, Claudia Anita Piona, Sarah Dal Ben, Diego Ramaroli, Paolo Cavarzere, Franco Antoniazzi, Rossella Gaudino
P3-1004
Girl with Pendred's syndrome, breast and ovary cysts (clinical case)
Olga Gumeniuk, Yuriy Chernenkov
Girl with Pendred's syndrome, breast and ovary cysts (clinical case)
Olga Gumeniuk, Yuriy Chernenkov
P3-1005
Incidence and etiology of hyperandrogenism in children and adolescent
Haddam Ali El Mahdi, Si Youcef Hafsa, Si Youcef Radhia, Meskine Djamila
Incidence and etiology of hyperandrogenism in children and adolescent
Haddam Ali El Mahdi, Si Youcef Hafsa, Si Youcef Radhia, Meskine Djamila
P3-984
Management of prepubertal gynecomastia in two patients with Peutz-Jeghers Sydrome: use of aromatase inhibitors
Laura Guazzarotti, Silvia Mauri, Federica Occhipinti, Mariangela Petruzzi, Micol Sonnino, Andrea Angela Tenconi, Laura Pogliani, Gian Vincenzo Zuccotti
Management of prepubertal gynecomastia in two patients with Peutz-Jeghers Sydrome: use of aromatase inhibitors
Laura Guazzarotti, Silvia Mauri, Federica Occhipinti, Mariangela Petruzzi, Micol Sonnino, Andrea Angela Tenconi, Laura Pogliani, Gian Vincenzo Zuccotti
P3-985
Age at Menarche (AAM) in chronic respiratory disease: Cystic Fibrosis (FC) and Asthma. Comparison with a large cohort of healthy girls living in Verona.
Rossella Gaudino, Sonia Volpi, Sarah Dal Ben, Claudia Piona, Paolo Cavarzere, Attilio Boner, Franco Antoniazzi
Age at Menarche (AAM) in chronic respiratory disease: Cystic Fibrosis (FC) and Asthma. Comparison with a large cohort of healthy girls living in Verona.
Rossella Gaudino, Sonia Volpi, Sarah Dal Ben, Claudia Piona, Paolo Cavarzere, Attilio Boner, Franco Antoniazzi
P3-986
Optimal strategy for ovarian function assessment in girls with central precocious puberty before and during GnRH analogue treatment
Analía Freire, Mirta Gryngarten, Andrea Arcari, Maria Ballerini, Nazareth Loreti, Verónica Ambao, Ignacio Bergadá, Stella Campo, Maria Ropelato
Optimal strategy for ovarian function assessment in girls with central precocious puberty before and during GnRH analogue treatment
Analía Freire, Mirta Gryngarten, Andrea Arcari, Maria Ballerini, Nazareth Loreti, Verónica Ambao, Ignacio Bergadá, Stella Campo, Maria Ropelato
P3-987
From prepuberty to adulthood: semen quality and its predictors in a prospective cohort study of Russian young men
Oleg Sergeyev, Lidia Mínguez-Alarcón, Russ Hauser, Paige L. Williams, Jane S. Burns, Susan A. Korrick, Yury Dikov, Liudmila Smigulina, Boris Revich, Mary M. Lee
From prepuberty to adulthood: semen quality and its predictors in a prospective cohort study of Russian young men
Oleg Sergeyev, Lidia Mínguez-Alarcón, Russ Hauser, Paige L. Williams, Jane S. Burns, Susan A. Korrick, Yury Dikov, Liudmila Smigulina, Boris Revich, Mary M. Lee
P3-988
Further expansion of the CHARGE geno-phenotype: a girl with a novel deletion of CHD7 and with the combination of hypogonadotropic hypogonadism and agenesis of internal genitalia.
Nele Reynaert, Francis de Zegher, Koenraad Devriendt, Inge Francois, Dominique Beckers, Kristina Casteels
Further expansion of the CHARGE geno-phenotype: a girl with a novel deletion of CHD7 and with the combination of hypogonadotropic hypogonadism and agenesis of internal genitalia.
Nele Reynaert, Francis de Zegher, Koenraad Devriendt, Inge Francois, Dominique Beckers, Kristina Casteels
P3-989
Metabolism and gonadal axis of early menarche girls and girls treated with GnRHa
Chen Qiuli, Zhang Jun, Li Yanhong, Ma Huamei, Chen Hongshan, Guo Song, Du Minlian
Metabolism and gonadal axis of early menarche girls and girls treated with GnRHa
Chen Qiuli, Zhang Jun, Li Yanhong, Ma Huamei, Chen Hongshan, Guo Song, Du Minlian
P3-990
The Consequences of Polycystic Ovary Syndrome in Adolescent Girls
Giorgiana Flavia Brad, Tamara Marcovici, Oana Belei, Calin Popoiu, Laura Olariu, Vlad David, Otilia Marginean
The Consequences of Polycystic Ovary Syndrome in Adolescent Girls
Giorgiana Flavia Brad, Tamara Marcovici, Oana Belei, Calin Popoiu, Laura Olariu, Vlad David, Otilia Marginean
P3-991
PELVIC MRI AS ALTERNATIVE TO PELVIC US FOR THE DIAGNOSIS OF PCOS IN OVERWEIGHT AND OBESE ADOLESCENT GIRLS.
Simon Kayemba-Kay's, Anne Heron, Sidi Mohamed Benosman
PELVIC MRI AS ALTERNATIVE TO PELVIC US FOR THE DIAGNOSIS OF PCOS IN OVERWEIGHT AND OBESE ADOLESCENT GIRLS.
Simon Kayemba-Kay's, Anne Heron, Sidi Mohamed Benosman
P3-992
Syndromic X-linked ichthyosis
L.Rabehi, S Azzoug, F.Chentli
Endocrine and metabolic diseases department Bab El Oued Hospital Algiers Algeria
rabehi leyla, azzoug said, chentli farida
Syndromic X-linked ichthyosis
L.Rabehi, S Azzoug, F.Chentli
Endocrine and metabolic diseases department Bab El Oued Hospital Algiers Algeria
rabehi leyla, azzoug said, chentli farida
P3-993
The effect of aromatase inhibitor in a pubertal patient with aromatase excess syndrome
Daziou Shihara, Hidetoshi Sato, Yohei Ogawa, Mami Miyado, Maki Fukami
The effect of aromatase inhibitor in a pubertal patient with aromatase excess syndrome
Daziou Shihara, Hidetoshi Sato, Yohei Ogawa, Mami Miyado, Maki Fukami
P3-994
Homozygous CYP17A1 mutation identified in a Chinese family with 46, XX and 46, XY 17α-hydroxylase deficiency
Huamei MA, Minlian DU, Jun ZHANG, Yanhong LI, Qiuli CHEN, Hongshan CHEN
Homozygous CYP17A1 mutation identified in a Chinese family with 46, XX and 46, XY 17α-hydroxylase deficiency
Huamei MA, Minlian DU, Jun ZHANG, Yanhong LI, Qiuli CHEN, Hongshan CHEN
P3-995
Puberty and gonadal function in adolescent girls after renal transplantation.
Blandine Hecquet, Marina Charbit, Michel Polak, Maud Bidet
Puberty and gonadal function in adolescent girls after renal transplantation.
Blandine Hecquet, Marina Charbit, Michel Polak, Maud Bidet
P3-996
Endocrine disruptor and premature puberty, is there any association?.
ISOLINA RIAÑO-GALAN, ADRIAN ESTRADA MENENDEZ, ANA PEREZ LOPEZ, MAR COTO FUENTE, MARGOT MORAN, CRISTINA RODRIGUEZ-DEHLI
Endocrine disruptor and premature puberty, is there any association?.
ISOLINA RIAÑO-GALAN, ADRIAN ESTRADA MENENDEZ, ANA PEREZ LOPEZ, MAR COTO FUENTE, MARGOT MORAN, CRISTINA RODRIGUEZ-DEHLI
P3-997
The effect of long term medical care on weight and body mass index (BMI) in adolescents with polycystic ovary syndrome (PCOS): a positive outcome after 3.5 years of follow up
Mariarosaria Lang-Muritano, Renate Huerlimann, Eugen J. Schoenle
The effect of long term medical care on weight and body mass index (BMI) in adolescents with polycystic ovary syndrome (PCOS): a positive outcome after 3.5 years of follow up
Mariarosaria Lang-Muritano, Renate Huerlimann, Eugen J. Schoenle
P3-998
The Changes of Body Fat and Metabolic Parameters during GnRHa treatment in Central Precocious Puberty or Early and Fast Puberty Girls
Chen Qiuli, Ma Huamei, Li Lijuan, Zhang jun, Li Yanhong, Chen Hongshan, Du Minlian, Guo Song
The Changes of Body Fat and Metabolic Parameters during GnRHa treatment in Central Precocious Puberty or Early and Fast Puberty Girls
Chen Qiuli, Ma Huamei, Li Lijuan, Zhang jun, Li Yanhong, Chen Hongshan, Du Minlian, Guo Song
P3-999
SERTOLI CELL TUMOR İN A CASE OF ANDROGEN INSENSITIVITY SYNDROME
Şenay Savaş Erdeve, Zehra Aycan, Melikşah Keskin, Semra Çetinkaya, Ayşe Karaman, Sema Apaydın, Emin Çakmakçı
SERTOLI CELL TUMOR İN A CASE OF ANDROGEN INSENSITIVITY SYNDROME
Şenay Savaş Erdeve, Zehra Aycan, Melikşah Keskin, Semra Çetinkaya, Ayşe Karaman, Sema Apaydın, Emin Çakmakçı
LBP-1261
POLR3H VARIANT IS ASSOCIATED WITH PRIMARY OVARIAN FAILURE IN TWO FAMILIES
Monica Franca, Mariana Funari, Sorahia Domenice, Mirian Nishi, Elaine Costa, Leticia Gontijo, Ana Claudia Latronico, Alexander Jorge, Antonio Lerario, Berenice Mendonca
POLR3H VARIANT IS ASSOCIATED WITH PRIMARY OVARIAN FAILURE IN TWO FAMILIES
Monica Franca, Mariana Funari, Sorahia Domenice, Mirian Nishi, Elaine Costa, Leticia Gontijo, Ana Claudia Latronico, Alexander Jorge, Antonio Lerario, Berenice Mendonca
P1-137
Normalization of puberty and adult height in girls with Turner syndrome, randomized trials versus age and dose at GH-start
Berit Kriström, Carina Ankarberg-Lindgren, Marie-Louise Barrenäs, Karlolof Nilsson, Kerstin Albertsson-Wikland
Normalization of puberty and adult height in girls with Turner syndrome, randomized trials versus age and dose at GH-start
Berit Kriström, Carina Ankarberg-Lindgren, Marie-Louise Barrenäs, Karlolof Nilsson, Kerstin Albertsson-Wikland
P1-138
Weight gain in Turner Syndrome: Association to puberty induction?
Thomas Reinehr, Anders Lindberg, Christina Toschke, Jose Cara, Dionisios Chrysis, Cecila Camacho-Hübner
Weight gain in Turner Syndrome: Association to puberty induction?
Thomas Reinehr, Anders Lindberg, Christina Toschke, Jose Cara, Dionisios Chrysis, Cecila Camacho-Hübner
P1-139
A study of arterial stiffness in Turner syndrome patients using cardio-ankle vascular index
Hae Woon Jung, Hwa Young Kim, Gyung Min Lee, So Youn Kim, Kyung A Jeong, Keun Hee Choi, Jieun Lee, Young Ah Lee, Choong Ho Shin, Sei Won Yang
A study of arterial stiffness in Turner syndrome patients using cardio-ankle vascular index
Hae Woon Jung, Hwa Young Kim, Gyung Min Lee, So Youn Kim, Kyung A Jeong, Keun Hee Choi, Jieun Lee, Young Ah Lee, Choong Ho Shin, Sei Won Yang
P1-140
Impaired motor function in Turner syndrome: what is the relationship to performal intelligence scores?
Betül Taskin, Chris Verhaak, Marlou Essink, Marlies Kempers, Anja Vinck, Ria Nijhuis-van der Sanden, Janiëlle van Alfen-van der Velden
Impaired motor function in Turner syndrome: what is the relationship to performal intelligence scores?
Betül Taskin, Chris Verhaak, Marlou Essink, Marlies Kempers, Anja Vinck, Ria Nijhuis-van der Sanden, Janiëlle van Alfen-van der Velden
P1-141
Adult height after growth hormone treatment and its association with X chromosome dosage in Turner Syndrome: a cross-sectional database analysis of the French national rare disease network.
Elodie Fiot, Delphine Zenaty, Priscilla Boizeau, Jérémie Haignere, Sophie Dos Santos, Juliane Léger, French Turner Syndrome Study Group .
Adult height after growth hormone treatment and its association with X chromosome dosage in Turner Syndrome: a cross-sectional database analysis of the French national rare disease network.
Elodie Fiot, Delphine Zenaty, Priscilla Boizeau, Jérémie Haignere, Sophie Dos Santos, Juliane Léger, French Turner Syndrome Study Group .
P1-142
Fracture incidence is not associated with the 6-year development of trabecular BMD in paediatric Turner syndrome patients
Ondrej Soucek, Zdenek Sumnik, Marta Snajderova, Stanislava Kolouskova, Jan Lebl
Fracture incidence is not associated with the 6-year development of trabecular BMD in paediatric Turner syndrome patients
Ondrej Soucek, Zdenek Sumnik, Marta Snajderova, Stanislava Kolouskova, Jan Lebl
P1-143
Is Aortic Stiffness Increased in Young Turner Syndrome Patients?
Danya Fox, Kristopher Kang, Laura Stewart, Janis Dionne, James Potts, George Sandor
Is Aortic Stiffness Increased in Young Turner Syndrome Patients?
Danya Fox, Kristopher Kang, Laura Stewart, Janis Dionne, James Potts, George Sandor
P2-547
The impact of growth hormone (GH) therapy combined with estrogens on blood pressure (BP), cardiac left ventricular (LV) dimensions and lipid metabolism in pubertal girls with Turner’s syndrome (TS).
Elena Nagaeva, Tatiana Shiryaeva, Natalia Volevodz, Olga Chikulaeva, Maria Pankratova, Anna Gavrilova, Valentina Peterkova
The impact of growth hormone (GH) therapy combined with estrogens on blood pressure (BP), cardiac left ventricular (LV) dimensions and lipid metabolism in pubertal girls with Turner’s syndrome (TS).
Elena Nagaeva, Tatiana Shiryaeva, Natalia Volevodz, Olga Chikulaeva, Maria Pankratova, Anna Gavrilova, Valentina Peterkova
P2-548
Sensitivity of measured parental height and target range in the diagnosis of Turner syndrome
Yasmine Ouarezki, Filiz Cizmecioglu, Chourouk Mansour, Jeremy Jones, Emma Jane Gault, Avril Mason, Malcolm Donaldson
Sensitivity of measured parental height and target range in the diagnosis of Turner syndrome
Yasmine Ouarezki, Filiz Cizmecioglu, Chourouk Mansour, Jeremy Jones, Emma Jane Gault, Avril Mason, Malcolm Donaldson
P2-549
Balance control in children and adolescent girls with Turner syndrome.
Laetitia Peultier, Gerome Gauchard, Bruno Leheup, Béatrice Lebon-Labich, Phlippe Perrin
Balance control in children and adolescent girls with Turner syndrome.
Laetitia Peultier, Gerome Gauchard, Bruno Leheup, Béatrice Lebon-Labich, Phlippe Perrin
P2-550
SHORT STATURE WITH NEURODEVELOPMENTAL DELAY IN FAMILIAL VARIANT TURNER SYNDROME
Madhurima Chetan, Vijith Puthi
SHORT STATURE WITH NEURODEVELOPMENTAL DELAY IN FAMILIAL VARIANT TURNER SYNDROME
Madhurima Chetan, Vijith Puthi
P3-1233
Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group
Feyza Darendeliler, Abdullah Bereket, Firdevs Bas, Ruveyde Bundak, Erkan Sari, Banu K. Aydin, Sukran Darcan, Bumin Dundar, Muammer Buyukinan, Cengiz Kara, Mümtaz M. Mazicioglu, Erdal Adal, Aysehan Akinci, Mehmet E. Atabek, Fatma Demirel, Nurullah Celik, Behzat Ozkan, Enver Simsek, Peyami Cinaz, Turner Syndrome Study Group
Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group
Feyza Darendeliler, Abdullah Bereket, Firdevs Bas, Ruveyde Bundak, Erkan Sari, Banu K. Aydin, Sukran Darcan, Bumin Dundar, Muammer Buyukinan, Cengiz Kara, Mümtaz M. Mazicioglu, Erdal Adal, Aysehan Akinci, Mehmet E. Atabek, Fatma Demirel, Nurullah Celik, Behzat Ozkan, Enver Simsek, Peyami Cinaz, Turner Syndrome Study Group
P3-1234
Cardiovascular Assessment In Turner Syndrome: Current Practice In The United Kingdom
A Mason, A Smyth, S F Ahmed, S C Wong
Cardiovascular Assessment In Turner Syndrome: Current Practice In The United Kingdom
A Mason, A Smyth, S F Ahmed, S C Wong
P3-1235
Turner syndrome in Iceland 1968-2012. Congenital anomalies and clinical outcomes.
Arndis A. Sigmarsdottir, Johann H. Johannsson, Helga A. Sigurjonsdottir, Arni V. Thorsson
Turner syndrome in Iceland 1968-2012. Congenital anomalies and clinical outcomes.
Arndis A. Sigmarsdottir, Johann H. Johannsson, Helga A. Sigurjonsdottir, Arni V. Thorsson
P3-1236
A comparison of Efficacies between rhGH and rhGH combined with stanozolol therapies in Growth of the girls with Turner Syndrome
Dan Li, Hongshan Chen, Minlian Du, Yanhong Li, Qiuli Chen, Huamei Ma, Jun Zhang
A comparison of Efficacies between rhGH and rhGH combined with stanozolol therapies in Growth of the girls with Turner Syndrome
Dan Li, Hongshan Chen, Minlian Du, Yanhong Li, Qiuli Chen, Huamei Ma, Jun Zhang
P3-1237
Clinical Features and Genetic Considerations of Turner Syndrome: A Review of our cases
Sara Berrade, María Chueca, Sada Zarikian, Arantxa Mosquera, Noelia Ulibarrena, Alberto Sola, Cristina García, Mirentxu Oyarzabal
Clinical Features and Genetic Considerations of Turner Syndrome: A Review of our cases
Sara Berrade, María Chueca, Sada Zarikian, Arantxa Mosquera, Noelia Ulibarrena, Alberto Sola, Cristina García, Mirentxu Oyarzabal
P3-1238
Growth characteristics of patient with Turner syndrome different age and karyotypes by the Ukrainian national register.
Nataliya Zelinska, Irina Shevchenko, Evgenia Globa, Nataliya Pogadaeva
Growth characteristics of patient with Turner syndrome different age and karyotypes by the Ukrainian national register.
Nataliya Zelinska, Irina Shevchenko, Evgenia Globa, Nataliya Pogadaeva
P3-1239
Nationwide study of Turner syndrome in Ukraine.
Nataliya Zelinska, Irina Shevchenko, Evgenia Globa, Nataliya Pogadaeva
Nationwide study of Turner syndrome in Ukraine.
Nataliya Zelinska, Irina Shevchenko, Evgenia Globa, Nataliya Pogadaeva
P3-1240
Patients with Turner’s syndrome should have ophthalmological examination before commencing recombinant growth hormone treatment
Hussain Alsaffar, Eleanor Thomason, Joanne Blair, Mohammed Didi
Patients with Turner’s syndrome should have ophthalmological examination before commencing recombinant growth hormone treatment
Hussain Alsaffar, Eleanor Thomason, Joanne Blair, Mohammed Didi
P3-1241
Renal problems in early adult patients with Turner syndrome
Woo Yeong Chung, Seung Hwan Oh, Dong Uk Yu
Renal problems in early adult patients with Turner syndrome
Woo Yeong Chung, Seung Hwan Oh, Dong Uk Yu
P3-1242
To predict ovarian function is a single determination of AMH useful
in patients with Turner syndrome?
Claudia Anita Piona, Paolo Cavarzere, Rossella Gaudino, Sarah Dal Ben, Diego Ramaroli, Matteo Gelati, Gian Cesare Guidi, Gian Luca Salvagno, Franco Antoniazzi
To predict ovarian function is a single determination of AMH useful
in patients with Turner syndrome?
Claudia Anita Piona, Paolo Cavarzere, Rossella Gaudino, Sarah Dal Ben, Diego Ramaroli, Matteo Gelati, Gian Cesare Guidi, Gian Luca Salvagno, Franco Antoniazzi
P3-1243
Anthropometric findings from birth to adulthood in Turkish Girls with Turner Syndrome and association with Karyotpye distribution
Erkan Sari, Abdullah Bereket, Ediz Yesilkaya, Firdevs Bas, Ruveyde Bundak, Banu K. Aydin, Sukran Darcan, Bumin Dundar, Muammer Buyukinan, Cengiz Kara, Erdal Adal, Aysehan Akinci, Mehmet E. Atabek, Fatma Demirel, Nurullah Celik, Behzat Ozkan, Bayram Ozhan, Zerrin Orbak, Oya Ercan, Turner Syndrome Study Group
Anthropometric findings from birth to adulthood in Turkish Girls with Turner Syndrome and association with Karyotpye distribution
Erkan Sari, Abdullah Bereket, Ediz Yesilkaya, Firdevs Bas, Ruveyde Bundak, Banu K. Aydin, Sukran Darcan, Bumin Dundar, Muammer Buyukinan, Cengiz Kara, Erdal Adal, Aysehan Akinci, Mehmet E. Atabek, Fatma Demirel, Nurullah Celik, Behzat Ozkan, Bayram Ozhan, Zerrin Orbak, Oya Ercan, Turner Syndrome Study Group
P3-1244
GROWS HORMONE THERAPY IN TURNER SYNDROME
Corina Galesanu, Andra Iulia Loghin, Didona Ungureanu, Mihail Romeo Galesanu
GROWS HORMONE THERAPY IN TURNER SYNDROME
Corina Galesanu, Andra Iulia Loghin, Didona Ungureanu, Mihail Romeo Galesanu
P3-1245
A Rare Variant of Turner Syndrome: First Clinical Report from Kuwait
kholoud Mohamed, Dalia Al-Abdulrazzaq
A Rare Variant of Turner Syndrome: First Clinical Report from Kuwait
kholoud Mohamed, Dalia Al-Abdulrazzaq
P3-1246
Turner Syndrome with Breast Development : Case report
Sung Won Park, Sung Yoon Cho, Jinsup Kim, Rimm Huh, Su Jin Kim, Dong-kyu Jin
Turner Syndrome with Breast Development : Case report
Sung Won Park, Sung Yoon Cho, Jinsup Kim, Rimm Huh, Su Jin Kim, Dong-kyu Jin
P1-146
Salt sensitivity of blood pressure at age 7-8 years in preterm born children.
Charlotte A. Ruys, Harrie N. Lafeber, Joost Rotteveel, Martijn J.J. Finken
Salt sensitivity of blood pressure at age 7-8 years in preterm born children.
Charlotte A. Ruys, Harrie N. Lafeber, Joost Rotteveel, Martijn J.J. Finken
P1-147
A new LC-MS/MS assay for the analysis of sulfated steroids in human serum: quantification of cholesterol sulfate, pregnenolone sulfate, 17-hydroxypregnenolone sulfate and androgen sulfates
Alberto Sánchez-Guijo, Vinzenz Oji, Michaela F. Hartmann, Heiko Traupe, Stefan A. Wudy
A new LC-MS/MS assay for the analysis of sulfated steroids in human serum: quantification of cholesterol sulfate, pregnenolone sulfate, 17-hydroxypregnenolone sulfate and androgen sulfates
Alberto Sánchez-Guijo, Vinzenz Oji, Michaela F. Hartmann, Heiko Traupe, Stefan A. Wudy
P1-165
Higher urinary iodine levels iodine correlates with lower systolic blood pressure in Chilean schoolchildren
Francisca Grob, Alejandro Martínez-Aguayo, María Clara Ateaga, Carolina Loureiro, Diego Carrillo, Caroline Hill, Carmen Campino, Carolina Mendoza, Clarita Ferrada, Rodrigo Bancalari, Constanza Pinochet, Cristian Carvajal, Marlene Aglony, Carolina Valdivia, Andrea Vecchiola, Carmen Carrasco, René Baudrand, Cristobal Fuentes, Hernán García, Carlos Fardella
Higher urinary iodine levels iodine correlates with lower systolic blood pressure in Chilean schoolchildren
Francisca Grob, Alejandro Martínez-Aguayo, María Clara Ateaga, Carolina Loureiro, Diego Carrillo, Caroline Hill, Carmen Campino, Carolina Mendoza, Clarita Ferrada, Rodrigo Bancalari, Constanza Pinochet, Cristian Carvajal, Marlene Aglony, Carolina Valdivia, Andrea Vecchiola, Carmen Carrasco, René Baudrand, Cristobal Fuentes, Hernán García, Carlos Fardella
P2-177
Analysis the relationship between clinical characteristics and genotype of six cases of Bartter syndrome and Gitelman syndrome in children
zhang jun, chen qiuli, guo song, yang ping, ma huamei, li yanhong, du minlian
Analysis the relationship between clinical characteristics and genotype of six cases of Bartter syndrome and Gitelman syndrome in children
zhang jun, chen qiuli, guo song, yang ping, ma huamei, li yanhong, du minlian
P2-178
Genotypic heterogeneity and clinical phenotype in two patients with triple A syndrome (AAAS).
Antonella Meloni, Maria Rosaria Casini, Roberta Mazzitti, Riccardo Congia, Maria Cristina Rosatelli, Marco Bonomi
Genotypic heterogeneity and clinical phenotype in two patients with triple A syndrome (AAAS).
Antonella Meloni, Maria Rosaria Casini, Roberta Mazzitti, Riccardo Congia, Maria Cristina Rosatelli, Marco Bonomi
P2-216
A CASE WITH ACRODYSOSTOSIS AND HORMONE RESISTANCE
Selma Tunç, Korcan Demir, Filiz Hazan, Özgür Kırbıyık, Eren Soyaltın, Özlem Nalbantoğlu, Melek Yıldız, Hüseyin Anıl Korkmaz, Behzat Özkan
A CASE WITH ACRODYSOSTOSIS AND HORMONE RESISTANCE
Selma Tunç, Korcan Demir, Filiz Hazan, Özgür Kırbıyık, Eren Soyaltın, Özlem Nalbantoğlu, Melek Yıldız, Hüseyin Anıl Korkmaz, Behzat Özkan
P2-242
THE ASSOCIATION OF ATTENTION DEFICIT HYPERACTIVITY DISORDER (ADHD) AND AUTISM SPECTRUM DISORDERS (ASD) WITH THE MEAN PLATELET VOLUME (MPV) AND VITAMIN D
Keziban Aslı Bala, Murat Doğan, Tuba Mutluer, Sultan Kaba, Oktay Aslan, Nihat Demir, Lokman Üstyol
THE ASSOCIATION OF ATTENTION DEFICIT HYPERACTIVITY DISORDER (ADHD) AND AUTISM SPECTRUM DISORDERS (ASD) WITH THE MEAN PLATELET VOLUME (MPV) AND VITAMIN D
Keziban Aslı Bala, Murat Doğan, Tuba Mutluer, Sultan Kaba, Oktay Aslan, Nihat Demir, Lokman Üstyol
P2-340
Prevalence of scoliosis in a large cohort of pediatric and adolescent Prader-Willi Syndrome: a Scottish-Italian study
Sara Ciccone, Danilo Fintini, Andreas Kyriakou, Sarah Bocchini, Marco Crostelli, Heather Read, Malcolm Donaldson, Marco Cappa, Guftar Shaikh, Antonino Crinò
Prevalence of scoliosis in a large cohort of pediatric and adolescent Prader-Willi Syndrome: a Scottish-Italian study
Sara Ciccone, Danilo Fintini, Andreas Kyriakou, Sarah Bocchini, Marco Crostelli, Heather Read, Malcolm Donaldson, Marco Cappa, Guftar Shaikh, Antonino Crinò
P2-353
A new mutation of PCSK1 revealed by neonatal malabsorptive diarrhea, panhypopituitarism and major obesity.
Natacha BOUHOURS-NOUET, Aurélie DONZEAU, Anne DECREQUY, Marion GOIDEAU, Alban ZIEGLER, Estelle COLIN, Dominique BONNEAU, Régis COUTANT
A new mutation of PCSK1 revealed by neonatal malabsorptive diarrhea, panhypopituitarism and major obesity.
Natacha BOUHOURS-NOUET, Aurélie DONZEAU, Anne DECREQUY, Marion GOIDEAU, Alban ZIEGLER, Estelle COLIN, Dominique BONNEAU, Régis COUTANT
P2-366
Homozygous mutation in FBN1 gen in patient with Prader Willi syndrome: variant Marfan syndrome?
Yvonne van den Boom - Rijk, Marlies Kempers, Ria Nijhuis-van der Sanden, Janielle van Alfen-van der Velden
Homozygous mutation in FBN1 gen in patient with Prader Willi syndrome: variant Marfan syndrome?
Yvonne van den Boom - Rijk, Marlies Kempers, Ria Nijhuis-van der Sanden, Janielle van Alfen-van der Velden
P2-445
The late effects after the hematopoietic stem cells transplantation (HSCT) for patients with non-neoplastic disease
Akito Sutani, Yuichi Miyakawa, Atsumi Tsuji, Yuki Aoki, Kei Takasawa, Masatoshi Takagi, Kohsuke Imai, Kenichi Kashimada, Tomohiro Morio
The late effects after the hematopoietic stem cells transplantation (HSCT) for patients with non-neoplastic disease
Akito Sutani, Yuichi Miyakawa, Atsumi Tsuji, Yuki Aoki, Kei Takasawa, Masatoshi Takagi, Kohsuke Imai, Kenichi Kashimada, Tomohiro Morio
P2-457
Low Plasma Ghrelin Levels in Children with Severe Protein Energy Malnutrition
Harikrishnan V, Rakesh Kumar, Naresh Sachdeva, Devi Dayal
Low Plasma Ghrelin Levels in Children with Severe Protein Energy Malnutrition
Harikrishnan V, Rakesh Kumar, Naresh Sachdeva, Devi Dayal
P2-507
Fanconi Anemia Endocrine Abnormalities - case report
Liliana Abreu, Sofia Martins, Olinda Marques
Fanconi Anemia Endocrine Abnormalities - case report
Liliana Abreu, Sofia Martins, Olinda Marques
P2-536
Ultra-deep next-generation sequencing: a reliable method for the molecular diagnosis of McCune Albright syndrome.
Delphine Mallet-Moták, Florence Roucher-Boulez, Marc Nicolino, Yves Morel
Ultra-deep next-generation sequencing: a reliable method for the molecular diagnosis of McCune Albright syndrome.
Delphine Mallet-Moták, Florence Roucher-Boulez, Marc Nicolino, Yves Morel
P2-537
Increased ambulatory blood pressure in adolescents with gender dysphoria treated with gonadotropin- releasing hormone analogues
Daniel Klink, Arend Bokenkamp, Eline Atsma, Joost Rotteveel
Increased ambulatory blood pressure in adolescents with gender dysphoria treated with gonadotropin- releasing hormone analogues
Daniel Klink, Arend Bokenkamp, Eline Atsma, Joost Rotteveel
P2-538
Plasma humanin levels during normal childhood and puberty. Study of possible correlations with sex, age, and insulin levels.
Valeria De Dona, Marta Ciaccio, Junxiang Wan, Gabriela Guercio, Elisa Vaiani, Gabriela Krochik, Mercedes Maceiras, Juan Manuel Lazzati, Marco Rivarola, Pinchas Cohen, Alicia Belgorosky
Plasma humanin levels during normal childhood and puberty. Study of possible correlations with sex, age, and insulin levels.
Valeria De Dona, Marta Ciaccio, Junxiang Wan, Gabriela Guercio, Elisa Vaiani, Gabriela Krochik, Mercedes Maceiras, Juan Manuel Lazzati, Marco Rivarola, Pinchas Cohen, Alicia Belgorosky
P3-1006
Early and sever manifestation of McCune-Albright syndrome with GNAS mutation in the liver tissue
Fahad Aljuraibah, Wael Alohali, Mohammed Albalawi, Angham Almutair
Early and sever manifestation of McCune-Albright syndrome with GNAS mutation in the liver tissue
Fahad Aljuraibah, Wael Alohali, Mohammed Albalawi, Angham Almutair
P3-1040
Psychomotor development in children born small for gestational age (SGA) during early infancy.
BEATRIZ PUGA, MARÍA J. OLIVAN, ZENAIDA GALVE, SEGUNDO RITE, ANTONIO DE ARRIBA, MARTA FERRER, JOSÉ IGNACIO LABARTA, ÁNGEL FERRÁNDEZ
Psychomotor development in children born small for gestational age (SGA) during early infancy.
BEATRIZ PUGA, MARÍA J. OLIVAN, ZENAIDA GALVE, SEGUNDO RITE, ANTONIO DE ARRIBA, MARTA FERRER, JOSÉ IGNACIO LABARTA, ÁNGEL FERRÁNDEZ
P3-1156
Eating disorders in Greek adolescents: frequency and characteristics
Ioannis Kyrgios, Vagia Papageorgiou, Eleni Kotanidou, Paraskevi Kokka, Angeliki Kleisarchaki, Konstantina Mouzaki, Iro Tsara, Efthimia Efstratiou, Anna-Bettina Haidich, Assimina Galli-Tsinopoulou
Eating disorders in Greek adolescents: frequency and characteristics
Ioannis Kyrgios, Vagia Papageorgiou, Eleni Kotanidou, Paraskevi Kokka, Angeliki Kleisarchaki, Konstantina Mouzaki, Iro Tsara, Efthimia Efstratiou, Anna-Bettina Haidich, Assimina Galli-Tsinopoulou
P3-1157
Assessment of endocrine function in Egyptian adolescent B-thalassemia major patients
Soha Abd El Dayem, Mona Abd El Kader
Assessment of endocrine function in Egyptian adolescent B-thalassemia major patients
Soha Abd El Dayem, Mona Abd El Kader
P3-1247
The association between selected endocrinopathies and central arterial pressure in children and adolescents
Klaudyna Noiszewska, Anna Krentowska, Anna Skoneczny, Agnieszka Mazur, Hanna Borysewicz-Sanczyk, Artur Bossowski
The association between selected endocrinopathies and central arterial pressure in children and adolescents
Klaudyna Noiszewska, Anna Krentowska, Anna Skoneczny, Agnieszka Mazur, Hanna Borysewicz-Sanczyk, Artur Bossowski
P3-1248
The Development of a Publication Presentation Workshop: Enhancing the Publication of African Paediatric Endocrinological Research.
François de Villiers
The Development of a Publication Presentation Workshop: Enhancing the Publication of African Paediatric Endocrinological Research.
François de Villiers
P3-596
Transient pseudohypoaldosteronism as a complication of infected obstructive uropathy in infancy, a case series.
Alexandra Rodrigues Da Costa, Simon Glew, Geetha Fonseka, Dunia Ismail
Transient pseudohypoaldosteronism as a complication of infected obstructive uropathy in infancy, a case series.
Alexandra Rodrigues Da Costa, Simon Glew, Geetha Fonseka, Dunia Ismail
P3-717
Seip-Berardinelli syndrome in a patient referred by low weight gain
Cristiane Kopacek, Luciana Amorim Beltrão, Victória Bernardes Guimarães, Julia Santana Trombetta, Karen Lizeth Puma Lliguin, Rosana Cardoso Manique Rosa, Vinicius Freitas de Mattos, Carla Graziadio, Paulo Ricardo Gazzola Zen, Rafael Fabiano Machado Rosa
Seip-Berardinelli syndrome in a patient referred by low weight gain
Cristiane Kopacek, Luciana Amorim Beltrão, Victória Bernardes Guimarães, Julia Santana Trombetta, Karen Lizeth Puma Lliguin, Rosana Cardoso Manique Rosa, Vinicius Freitas de Mattos, Carla Graziadio, Paulo Ricardo Gazzola Zen, Rafael Fabiano Machado Rosa
P3-903
GENOTYPE AND PHENOTYPE CHARACTERIZATION IN TWO PATIENTS WITH MEHMO SYNDROME
Juraj Staník, Martina Škopková, Daniela Staníková, Jozef Ukropec, Daniel Daniš, Timea Kurdiová, Barbara Ukropcová, Ľubica Tichá, Iwar Klimeš, Daniela Gašperíková
GENOTYPE AND PHENOTYPE CHARACTERIZATION IN TWO PATIENTS WITH MEHMO SYNDROME
Juraj Staník, Martina Škopková, Daniela Staníková, Jozef Ukropec, Daniel Daniš, Timea Kurdiová, Barbara Ukropcová, Ľubica Tichá, Iwar Klimeš, Daniela Gašperíková
LBP-1265
Profiling of a novel NSIAD-causing mutation of vasopressin receptor 2 and its differential effect on receptor trafficking compared to previously identified mutations
Anatoly Tiulpakov, Carl W. White, Rekhati Abhayawardana, Natalia Zubkova, Ruth M. Seeber, Heng B. See, Kevin D.G. Pfleger
Profiling of a novel NSIAD-causing mutation of vasopressin receptor 2 and its differential effect on receptor trafficking compared to previously identified mutations
Anatoly Tiulpakov, Carl W. White, Rekhati Abhayawardana, Natalia Zubkova, Ruth M. Seeber, Heng B. See, Kevin D.G. Pfleger
LBP-1257
Prepubertal and pubertal predictors of semen quality in a prospective cohort study of Russian young men: focus on endocrine disrupting chemicals
Oleg Sergeyev, Lidia Mínguez-Alarcón, Russ Hauser, Paige L. Williams, Jane S. Burns, Susan A. Korrick, Yury Dikov, Liudmila Smigulina, Boris Revich, Mary M. Lee
Prepubertal and pubertal predictors of semen quality in a prospective cohort study of Russian young men: focus on endocrine disrupting chemicals
Oleg Sergeyev, Lidia Mínguez-Alarcón, Russ Hauser, Paige L. Williams, Jane S. Burns, Susan A. Korrick, Yury Dikov, Liudmila Smigulina, Boris Revich, Mary M. Lee
P1-148
The analysis of occurrence the zinc transporter antibodies ZnT8 in children with Graves’ disease and Hashimoto’s thyroiditis.
Artur Bossowski, Hanna Borysewicz-Sanczyk, Anna Bossowska, Mieczyslaw Szalecki, Anna Kucharska, Beata Pyrzak, Mieczyslaw Walczak, Elzbieta Petriczko, Katarzyna Ziora, Maria Del Pilar Larosa, Shu Chen, Michael Powell, Jadwiga Furmaniak, Bernard Rees Smith
The analysis of occurrence the zinc transporter antibodies ZnT8 in children with Graves’ disease and Hashimoto’s thyroiditis.
Artur Bossowski, Hanna Borysewicz-Sanczyk, Anna Bossowska, Mieczyslaw Szalecki, Anna Kucharska, Beata Pyrzak, Mieczyslaw Walczak, Elzbieta Petriczko, Katarzyna Ziora, Maria Del Pilar Larosa, Shu Chen, Michael Powell, Jadwiga Furmaniak, Bernard Rees Smith
P1-149
Recombinant Parathyroid Hormone (1-34) replacement treatment of Hypoparathyroidism in the alfacalcidol-resistant patient with severe Autoimmune Polyendocrinopathy Syndrome type 1
Leila Sozaeva, Elizaveta Orlova, Maria Kareva
Recombinant Parathyroid Hormone (1-34) replacement treatment of Hypoparathyroidism in the alfacalcidol-resistant patient with severe Autoimmune Polyendocrinopathy Syndrome type 1
Leila Sozaeva, Elizaveta Orlova, Maria Kareva
P1-150
Severe immunodysregulation phenotypes including infancy-onset type 1 diabetes mellitus in two siblings with a homozygous mutation in the LPS-responsive beige-like anchor (LRBA) gene
Felix Schreiner, Michaela Plamper, Gesche Düker, Stefan Schoenberger, Janine Altmueller, Alina Hilger, Heiko Reutter, Joachim Woelfle
Severe immunodysregulation phenotypes including infancy-onset type 1 diabetes mellitus in two siblings with a homozygous mutation in the LPS-responsive beige-like anchor (LRBA) gene
Felix Schreiner, Michaela Plamper, Gesche Düker, Stefan Schoenberger, Janine Altmueller, Alina Hilger, Heiko Reutter, Joachim Woelfle
P1-151
A case of autoimmune polyglandular syndrome type I presenting as progressive generalized lipodystrophy in a 15-month-old child.
Ekaterina Sorkina, Elena Frolova, Dina Rusinova, Svetlana Polyakova, Evgeny Vasilyev, Vasily Petrov, Anatoly Tiulpakov
A case of autoimmune polyglandular syndrome type I presenting as progressive generalized lipodystrophy in a 15-month-old child.
Ekaterina Sorkina, Elena Frolova, Dina Rusinova, Svetlana Polyakova, Evgeny Vasilyev, Vasily Petrov, Anatoly Tiulpakov
P1-45
IMMUNE/INFLAMMATORY PROFILE IN CHILDREN WITH TYPE 1 DIABETES MELLITUS AND CELIAC DISEASE AND/OR AUTOIMMUNE THYROIDITIS
Valentina Fattorusso, Mario Galgani, Enza Mozzillo, Marianna Santopaolo, Rosa Nugnes, Giuseppe Matarese, Adriana Franzese
IMMUNE/INFLAMMATORY PROFILE IN CHILDREN WITH TYPE 1 DIABETES MELLITUS AND CELIAC DISEASE AND/OR AUTOIMMUNE THYROIDITIS
Valentina Fattorusso, Mario Galgani, Enza Mozzillo, Marianna Santopaolo, Rosa Nugnes, Giuseppe Matarese, Adriana Franzese
P2-202
Autoimmune polyglandular syndrome type 1 in Russia: clinical experience in 112 patients.
Elizaveta Orlova, Leila Sozaeva, Maria Kareva, Bergithe E. Oftedal, Lars Breivik, Per M. Knappskog, Ekaterina Zakharova, Eystein S. Husebye, Valentina Peterkova
Autoimmune polyglandular syndrome type 1 in Russia: clinical experience in 112 patients.
Elizaveta Orlova, Leila Sozaeva, Maria Kareva, Bergithe E. Oftedal, Lars Breivik, Per M. Knappskog, Ekaterina Zakharova, Eystein S. Husebye, Valentina Peterkova
P2-203
Autoimmune encephalitis - a newly recognised clinical manifestation of autoimmune polyendocrine syndrome type 1?
Juliana Ferenczova, Veronika Vargova, David Krysl, Erika Banoova, Eva Sadova
Autoimmune encephalitis - a newly recognised clinical manifestation of autoimmune polyendocrine syndrome type 1?
Juliana Ferenczova, Veronika Vargova, David Krysl, Erika Banoova, Eva Sadova
P2-484
Challenged diagnosis on hypoglycemia: Hirata Disease X Factitious Hypoglycemia
Tiago Jeronimo dos Santos, Caroline Passone, Simone Ito, Roberta Savoldelli, Hilton Kuperman, Hamilton Cabral de Menezes Filho, Leandra Steinmetz, Vae Dichtchekenian, Thais Della Manna, Durval Damiani
Challenged diagnosis on hypoglycemia: Hirata Disease X Factitious Hypoglycemia
Tiago Jeronimo dos Santos, Caroline Passone, Simone Ito, Roberta Savoldelli, Hilton Kuperman, Hamilton Cabral de Menezes Filho, Leandra Steinmetz, Vae Dichtchekenian, Thais Della Manna, Durval Damiani
P2-551
Diagnostic significance of serum concentrations of osteoprotegerin and proinflammatory cytokine IL-1β in children with autoimmune thyroid disease.
Hanna Mikos, Marcin Mikos, Marek Niedziela
Diagnostic significance of serum concentrations of osteoprotegerin and proinflammatory cytokine IL-1β in children with autoimmune thyroid disease.
Hanna Mikos, Marcin Mikos, Marek Niedziela
P3-628
Assessment of ovarian function and reserve based on hormonal parameters, ovarian volume, and follicle count in euthyroid girls with Hashimoto thyroiditis
Cigdem Kasikara, Ozgur Pirgon, Hakan Demirtas, Bumin Dundar
Assessment of ovarian function and reserve based on hormonal parameters, ovarian volume, and follicle count in euthyroid girls with Hashimoto thyroiditis
Cigdem Kasikara, Ozgur Pirgon, Hakan Demirtas, Bumin Dundar
P3-629
Early-onset type 1 diabetes and multiorgan autoimmunity in a girl with partial monosomy 2q and trisomy 10p
Carla Bizzarri, Maria Cristina Matteoli, Ippolita Patrizia Patera, Marco Cappa
Early-onset type 1 diabetes and multiorgan autoimmunity in a girl with partial monosomy 2q and trisomy 10p
Carla Bizzarri, Maria Cristina Matteoli, Ippolita Patrizia Patera, Marco Cappa
P3-630
CTLA4 A49G and C60T genetic polymorphism in Croatian children and young adults with autoimmune thyroid disease
Natasa Rojnic Putarek, Vesna Kusec, Zorana Grubic, Jadranka Knezevic-Cuca, Jasenka Ille, Biserka Stajnkler, Bruna Jaksic, Miroslav Dumic
CTLA4 A49G and C60T genetic polymorphism in Croatian children and young adults with autoimmune thyroid disease
Natasa Rojnic Putarek, Vesna Kusec, Zorana Grubic, Jadranka Knezevic-Cuca, Jasenka Ille, Biserka Stajnkler, Bruna Jaksic, Miroslav Dumic
P3-631
Oocyte cryopreservation in a patient with premature ovarian failure due to autoimmune polyendocrine syndrome type 2.
Claudia Balsamo, Eleonora Porcu, Federico Baronio, Luisa Forchielli, Antonia Bazzocchi, Laura Mazzanti, Alessandra Cassio
Oocyte cryopreservation in a patient with premature ovarian failure due to autoimmune polyendocrine syndrome type 2.
Claudia Balsamo, Eleonora Porcu, Federico Baronio, Luisa Forchielli, Antonia Bazzocchi, Laura Mazzanti, Alessandra Cassio
P3-632
Thyroid function and autoimmunity in children with newly diagnosed type 1 diabetes mellitus.
Elzbieta Niechcial, Bogda Skowronska, Anna Gertig-Kolasa, Izabela Krzysko, Witold Stankiewicz, Michal Michalak, Piotr Fichna
Thyroid function and autoimmunity in children with newly diagnosed type 1 diabetes mellitus.
Elzbieta Niechcial, Bogda Skowronska, Anna Gertig-Kolasa, Izabela Krzysko, Witold Stankiewicz, Michal Michalak, Piotr Fichna
P3-633
HYPERCALCAEMIA AS AN INDICATION OF ADRENAL INSUFFICIENCY IN A PATIENT WITH AUTOIMMUNE POLYENDOCRINOPATHY-CANDIDIASIS-ECTODERMAL DYSTROPHY (APECED)
EIRINI DIKAIAKOU, ELPIDA-ATHINA VLACHOPAPADOPOULOU, ELLI ANAGNOSTOU, IOANNIS PANAGIOTOPOULOS, ASPASIA PHOTINOU, STEPHANOS MICHALACOS
HYPERCALCAEMIA AS AN INDICATION OF ADRENAL INSUFFICIENCY IN A PATIENT WITH AUTOIMMUNE POLYENDOCRINOPATHY-CANDIDIASIS-ECTODERMAL DYSTROPHY (APECED)
EIRINI DIKAIAKOU, ELPIDA-ATHINA VLACHOPAPADOPOULOU, ELLI ANAGNOSTOU, IOANNIS PANAGIOTOPOULOS, ASPASIA PHOTINOU, STEPHANOS MICHALACOS
P3-634
Stevens Johnson Syndrome in a case with type 1 diabetes mellitus: Relation or coincidince?
Onur AKIN, Esra DOGER, Emine DEMET AKBAS, Arzu BAKIRTAS, Orhun CAMURDAN, Aysun BIDECI, Peyami CINAZ
Stevens Johnson Syndrome in a case with type 1 diabetes mellitus: Relation or coincidince?
Onur AKIN, Esra DOGER, Emine DEMET AKBAS, Arzu BAKIRTAS, Orhun CAMURDAN, Aysun BIDECI, Peyami CINAZ
P3-635
Radiologic appearance is important for diagnosis of autoimmune hypophysitis
Erkan Sari, Ediz Yesilkaya, Onur Akin, Orhan Gursel, Sebahattin Sari
Radiologic appearance is important for diagnosis of autoimmune hypophysitis
Erkan Sari, Ediz Yesilkaya, Onur Akin, Orhan Gursel, Sebahattin Sari
P3-636
Functional status of the thyroid gland in children with diabetes mellitus type 1.
Oleg Latyshev, Lubov Samsonova, Goar Okminyan, Elena Kiseleva, Yuryi Lobanov, Dmitriy Latyshev
Functional status of the thyroid gland in children with diabetes mellitus type 1.
Oleg Latyshev, Lubov Samsonova, Goar Okminyan, Elena Kiseleva, Yuryi Lobanov, Dmitriy Latyshev
P3-637
About a case of Basedow-Graves' disease in a infant
M.A.Bassaid , K.Bouriche , D.Senouci , W,Mazari , F.Hadj Kaddour , F.Ghellai , A.Bendjelloul , A.S.Bendeddouche "Pédiatrics"
A.Medjahdi, N.Berber "Nuclear Medicine"
Faculty of Medicine and Hospital of Tlemcen, Algeria
M.A Bassaid, K. Bouriche, D. Senouci, W. Mazari, F. Hadj Kaddour, F. Ghellai, A. Bendjelloul, A. Medjahdi, N. Berber, A.S. Bendeddouche
About a case of Basedow-Graves' disease in a infant
M.A.Bassaid , K.Bouriche , D.Senouci , W,Mazari , F.Hadj Kaddour , F.Ghellai , A.Bendjelloul , A.S.Bendeddouche "Pédiatrics"
A.Medjahdi, N.Berber "Nuclear Medicine"
Faculty of Medicine and Hospital of Tlemcen, Algeria
M.A Bassaid, K. Bouriche, D. Senouci, W. Mazari, F. Hadj Kaddour, F. Ghellai, A. Bendjelloul, A. Medjahdi, N. Berber, A.S. Bendeddouche
P3-638
THE AUTOIMMUNE POLYENDOCRINOPATHIES in children and Adolescents
soumeya nora fedala, ali el mahdi haddam, leyla ahmed ali, djamila meskine, farida chentli
THE AUTOIMMUNE POLYENDOCRINOPATHIES in children and Adolescents
soumeya nora fedala, ali el mahdi haddam, leyla ahmed ali, djamila meskine, farida chentli
P1-155
Prospective Cognitive Assessment in Children with Craniopharyngioma Identifies Dysfunction at Diagnosis, After Conservative Surgery and Before Adjuvant Radiation.
Penelope Rodriguez-Cabrera, Adam Kuczynski, Maria Michaelidou, Laura Losa, Helen Spoudeas
Prospective Cognitive Assessment in Children with Craniopharyngioma Identifies Dysfunction at Diagnosis, After Conservative Surgery and Before Adjuvant Radiation.
Penelope Rodriguez-Cabrera, Adam Kuczynski, Maria Michaelidou, Laura Losa, Helen Spoudeas
P1-156
CUSHING SYNDROME DUE TO ADRENOCORTICAL CARCINOMA IN A 3 MONTH OLD INFANT WITH A LARGE INTERSTITIAL DELETION OF CHROMOSOME 5Q INCLUDING THE APC GENE
Halit Ilker Akkurt, Esther Schulz, Konrad Reinshagen, Inga Vater, Almuth Caliebe, Jessika Johannsen
CUSHING SYNDROME DUE TO ADRENOCORTICAL CARCINOMA IN A 3 MONTH OLD INFANT WITH A LARGE INTERSTITIAL DELETION OF CHROMOSOME 5Q INCLUDING THE APC GENE
Halit Ilker Akkurt, Esther Schulz, Konrad Reinshagen, Inga Vater, Almuth Caliebe, Jessika Johannsen
P1-157
How do Adolescent Minors Banking Sperm Before Cancer Therapy Subsequently Use the Fertility Service? A Post Banking Re-evaluation.
James Pigot, Maria Michaelidou, Elizabeth Williamson, Alison Webb, Hoong-Wei Gan, Helen Spoudeas
How do Adolescent Minors Banking Sperm Before Cancer Therapy Subsequently Use the Fertility Service? A Post Banking Re-evaluation.
James Pigot, Maria Michaelidou, Elizabeth Williamson, Alison Webb, Hoong-Wei Gan, Helen Spoudeas
P2-380
Insulin-resistance and abnormal glucose tolerance after paediatric hematopoietic stem cell transplantation in blood-cancer survivors.
Sara Ciccone, Carla Bizzarri, Rita Maria Pinto, Letizia Pomponia Brescia, Franco Locatelli, Marco Cappa
Insulin-resistance and abnormal glucose tolerance after paediatric hematopoietic stem cell transplantation in blood-cancer survivors.
Sara Ciccone, Carla Bizzarri, Rita Maria Pinto, Letizia Pomponia Brescia, Franco Locatelli, Marco Cappa
P2-432
A perioperative movement of Anti-Mullerian Hormone (AMH) and E2 in a patient with SCTAT
Aya Shimada, Masaki Takagi, Kentaro Miyai, Ryuji Fukuzawa, Yukihiro Hasegawa
A perioperative movement of Anti-Mullerian Hormone (AMH) and E2 in a patient with SCTAT
Aya Shimada, Masaki Takagi, Kentaro Miyai, Ryuji Fukuzawa, Yukihiro Hasegawa
P3-811
Cushing's syndrome (CS) due to ectopic ACTH secretion by a germline tumor in the cross-tail area in a 7 month old female infant.
Artur Bossowski, Marta Kuzmicz, Anna Kitszel, Dariusz Polnik, Martin Savage, Maryna Krawczuk-Rybak
Cushing's syndrome (CS) due to ectopic ACTH secretion by a germline tumor in the cross-tail area in a 7 month old female infant.
Artur Bossowski, Marta Kuzmicz, Anna Kitszel, Dariusz Polnik, Martin Savage, Maryna Krawczuk-Rybak
P3-812
Uterine Bleeding: a rare side effect of mitotane treatment for recurrent adrenal carcinoma
Hilton Kuperman, Israel Bendit, Maria Fernanda Carvalho de Camargo, Decio Blucher
Uterine Bleeding: a rare side effect of mitotane treatment for recurrent adrenal carcinoma
Hilton Kuperman, Israel Bendit, Maria Fernanda Carvalho de Camargo, Decio Blucher
P3-813
Metabolic syndrome in childhood acute lymphoblastic leukemia survivors
Maurizio Delvecchio, Vincenza Luce, Mariantonietta Monteduro, Paola Giordano, Paola Muggeo, Nicola Santoro, Luciano Cavallo, Maria Felicia Faienza
Metabolic syndrome in childhood acute lymphoblastic leukemia survivors
Maurizio Delvecchio, Vincenza Luce, Mariantonietta Monteduro, Paola Giordano, Paola Muggeo, Nicola Santoro, Luciano Cavallo, Maria Felicia Faienza
P3-814
Results of growth hormone treatment in childhood brain tumors survivors
Nadia Mazerkina, Sergey Gorelyshev, Olga Geludkova
Results of growth hormone treatment in childhood brain tumors survivors
Nadia Mazerkina, Sergey Gorelyshev, Olga Geludkova
P3-815
Craniopharyngioma – symptoms, treatment and follow up – an analysis of 100 cases
Elzbieta Moszczynska, Agnieszka Bogusz, Anna Bendysz – Golatowska, Mieczyslaw Szalecki
Craniopharyngioma – symptoms, treatment and follow up – an analysis of 100 cases
Elzbieta Moszczynska, Agnieszka Bogusz, Anna Bendysz – Golatowska, Mieczyslaw Szalecki
P3-816
Von Hippel-Lindau disease in an adolescent with a newly described alteration in the VHL gene
Sevil Ari Yuca, Emine Ayca Cimbek, Yasar Sen, Fuat Bugrul, Dogan Kose, Yavuz Koksal
Von Hippel-Lindau disease in an adolescent with a newly described alteration in the VHL gene
Sevil Ari Yuca, Emine Ayca Cimbek, Yasar Sen, Fuat Bugrul, Dogan Kose, Yavuz Koksal
P3-817
TWO SYNCHRONOUS CENTRAL NERVOUS SYSTEM TUMORS IN A CHILD WITH NEUROFIBROMATOSIS TYPE 1.
Rodica Elena Cornean, Monica Scutariu, Gheorghe Ungureanu, Dorin Farcau, Stefan Florian
TWO SYNCHRONOUS CENTRAL NERVOUS SYSTEM TUMORS IN A CHILD WITH NEUROFIBROMATOSIS TYPE 1.
Rodica Elena Cornean, Monica Scutariu, Gheorghe Ungureanu, Dorin Farcau, Stefan Florian
P3-818
Endocrine evaluation in children and adolescents submitted to allogenic bone marrow tranplantation
Hilton Kuperman, Thais Della Manna, Vaê Dichtchkenian, Hamilton Cabral de Menezes Filho, Leandra Steinmetz, Louise Cominato, Juliana Folloni Fernandes, Angela Mandelli, Luiz Fernando Mantovani, Maria Aparecida Zanichelli, Maria Dulce Colassanti, Lilian Maria Cristófani, Vicente Odone Filho, Durval Damiani
Endocrine evaluation in children and adolescents submitted to allogenic bone marrow tranplantation
Hilton Kuperman, Thais Della Manna, Vaê Dichtchkenian, Hamilton Cabral de Menezes Filho, Leandra Steinmetz, Louise Cominato, Juliana Folloni Fernandes, Angela Mandelli, Luiz Fernando Mantovani, Maria Aparecida Zanichelli, Maria Dulce Colassanti, Lilian Maria Cristófani, Vicente Odone Filho, Durval Damiani
P3-819
EARLY ENDOCRINE COMPLICATIONS IN SURVIVORS OF CHILDHOOD MALIGNANT TUMORS
Cristina Sánchez-González, Mónica Andrades-Toledo, Álvaro Cárdeno-Morales, Alicia Torralbo-Carmona, Emilio García-García
EARLY ENDOCRINE COMPLICATIONS IN SURVIVORS OF CHILDHOOD MALIGNANT TUMORS
Cristina Sánchez-González, Mónica Andrades-Toledo, Álvaro Cárdeno-Morales, Alicia Torralbo-Carmona, Emilio García-García
P3-820
AIP POLYMORPHISM IN FAMILIAR ISOLATED PITUITARY ADENOMAS. CASE REPORT
María Lorena Viale, Claudia L. Hernandez, María Gabriela Rampi, María Pia Serra, Verónica Figueroa, Patricia Fainstein Day, Oscar H. Brunetto
AIP POLYMORPHISM IN FAMILIAR ISOLATED PITUITARY ADENOMAS. CASE REPORT
María Lorena Viale, Claudia L. Hernandez, María Gabriela Rampi, María Pia Serra, Verónica Figueroa, Patricia Fainstein Day, Oscar H. Brunetto
P3-821
PRIMARY HYPOGONADISM AFTER HEMATOPOIETIC STEM CELL TRANSPLANT IN PEDIATRIC PATIENTS WITH CANCER
maria del carmen de mingo alemany, raquel segovia orti, francisca moreno macián, sara león cariñena, maría del mar andrés moreno, josé maría fernández navarro
PRIMARY HYPOGONADISM AFTER HEMATOPOIETIC STEM CELL TRANSPLANT IN PEDIATRIC PATIENTS WITH CANCER
maria del carmen de mingo alemany, raquel segovia orti, francisca moreno macián, sara león cariñena, maría del mar andrés moreno, josé maría fernández navarro
P3-823
LHRH ANALOGUES (LHRHa) SUCCESSFULLY SUPPRESS MENSTRUATION DURING CHEMOTHERAPY IN TEENAGERS AND YOUNG ADULTS (TYA)
Martha Perisoglou, Sujata Edate, Assunta Albanese
LHRH ANALOGUES (LHRHa) SUCCESSFULLY SUPPRESS MENSTRUATION DURING CHEMOTHERAPY IN TEENAGERS AND YOUNG ADULTS (TYA)
Martha Perisoglou, Sujata Edate, Assunta Albanese
P3-824
Suprasellar brain tumours related endocrinopathies
Amir Babiker, Amani Edrees, Iman Al Gadi, Sharefah Al Issa, Safdar Malik, Sharief Al Watedi, Ayman Al Aeyadhy, Saeed Hassan, Hessah Al Otaibi, Nasir Al Jurayyan
Suprasellar brain tumours related endocrinopathies
Amir Babiker, Amani Edrees, Iman Al Gadi, Sharefah Al Issa, Safdar Malik, Sharief Al Watedi, Ayman Al Aeyadhy, Saeed Hassan, Hessah Al Otaibi, Nasir Al Jurayyan
P3-825
GROWTH HORMONE AND PROLACTIN SECRETING ADENOMA IN AN ADOLESCENT BOY
Fatma Dursun, Heves Kirmizibekmez, Adnan Dagcinar
GROWTH HORMONE AND PROLACTIN SECRETING ADENOMA IN AN ADOLESCENT BOY
Fatma Dursun, Heves Kirmizibekmez, Adnan Dagcinar
P3-826
The evaluation of bone mass density (BMD) in patients after therapy of solid tumors
Joanna Polubok, Olimpia Jasielska, Aleksandra Gonera, Marta Kozicka, Katarzyna Dubienska, Bernarda Kazanowska, Ewa Barg
The evaluation of bone mass density (BMD) in patients after therapy of solid tumors
Joanna Polubok, Olimpia Jasielska, Aleksandra Gonera, Marta Kozicka, Katarzyna Dubienska, Bernarda Kazanowska, Ewa Barg
LBP-1256
Higher Expression of the Oncogene YAP1, a Wnt/ß-Catenin Target, is associated with Poor Outcome in Pediatric Patients with Adrenocortical Tumors
Rafael H. Abduch, Ana Carolina Bueno, Leticia F. Leal, Marcelo M. Cavalcanti, Silvia R. Brandalise, Maria J. Masterallo, José A. Yunes, Carlos E. Martinelli Jr, Carlos A. Scrideli, Luiz G. Tone, Silvio Tucci, Ayrton C. Moreira, Leandra Z. Ramalho, Margaret Castro, Sonir R. Antonini
Higher Expression of the Oncogene YAP1, a Wnt/ß-Catenin Target, is associated with Poor Outcome in Pediatric Patients with Adrenocortical Tumors
Rafael H. Abduch, Ana Carolina Bueno, Leticia F. Leal, Marcelo M. Cavalcanti, Silvia R. Brandalise, Maria J. Masterallo, José A. Yunes, Carlos E. Martinelli Jr, Carlos A. Scrideli, Luiz G. Tone, Silvio Tucci, Ayrton C. Moreira, Leandra Z. Ramalho, Margaret Castro, Sonir R. Antonini
P1-158
The Expression of Related Neuroendocrine Factors with Puberty Onset in Rat at Different Developmental Stages
Mo Kyung Jung, Ki Eun Kim, Ah Reum Kwon, Hyun Wook Hyun Wook, Duk Hee Kim, Ho-Seong Kim
The Expression of Related Neuroendocrine Factors with Puberty Onset in Rat at Different Developmental Stages
Mo Kyung Jung, Ki Eun Kim, Ah Reum Kwon, Hyun Wook Hyun Wook, Duk Hee Kim, Ho-Seong Kim
P1-159
FOXL2 gene and combined pituitary hormone deficiency: a possible link
Sarah Castets, Alexandru Saveanu, Christine Raybaud, Delphine Mallet, Florence Roucher, Yves Morel, Thierry Brue, Rachel Reynaud, Marc Nicolino
FOXL2 gene and combined pituitary hormone deficiency: a possible link
Sarah Castets, Alexandru Saveanu, Christine Raybaud, Delphine Mallet, Florence Roucher, Yves Morel, Thierry Brue, Rachel Reynaud, Marc Nicolino
P1-160
Septo-optic dysplasia (SOD) associated with Koolen-de Vries syndrome (KDVS): a case report
Ani Aroyo, Iva Stoeva, Gergana Stancheva, Reni Koleva, Radka Kaneva
Septo-optic dysplasia (SOD) associated with Koolen-de Vries syndrome (KDVS): a case report
Ani Aroyo, Iva Stoeva, Gergana Stancheva, Reni Koleva, Radka Kaneva
P1-161
Screening of IGSF1 in patients with Central Hypothyroidism and GH deficiency, participating in the Dutch HYPOPIT study
Melitza Elizabeth, Robin Peeters, Theo Visser, Anita Hokken-Koelega, Laura de Graaff
Screening of IGSF1 in patients with Central Hypothyroidism and GH deficiency, participating in the Dutch HYPOPIT study
Melitza Elizabeth, Robin Peeters, Theo Visser, Anita Hokken-Koelega, Laura de Graaff
P1-98
Growth Hormone Excess in McCune-Albright Syndrome
Daniele Tessaris, Alison M. Boyce, Patrizia Matarazzo, Roberto Lala, Michael T. Collins
Growth Hormone Excess in McCune-Albright Syndrome
Daniele Tessaris, Alison M. Boyce, Patrizia Matarazzo, Roberto Lala, Michael T. Collins
P1-99
Growth hormone hypersecretion in children with NF1 and optic pathway gliomas
Stefania Pedicelli, Paola Cambiaso, Marina Macchiaiolo, Stefania Galassi, Angela Mastronuzzi, Francesca Del Bufalo, Graziamaria Ubertini, Marco Cappa
Growth hormone hypersecretion in children with NF1 and optic pathway gliomas
Stefania Pedicelli, Paola Cambiaso, Marina Macchiaiolo, Stefania Galassi, Angela Mastronuzzi, Francesca Del Bufalo, Graziamaria Ubertini, Marco Cappa
P2-389
Childhood Craniopharyngioma with Hypothalamic Obesity – No Long-term Weight Reduction due to Rehabilitation Programs
Anthe S. Sterkenburg, Anika Hoffmann, Ursel Gebhardt, Hermann L. Müller
Childhood Craniopharyngioma with Hypothalamic Obesity – No Long-term Weight Reduction due to Rehabilitation Programs
Anthe S. Sterkenburg, Anika Hoffmann, Ursel Gebhardt, Hermann L. Müller
P2-508
The IGSF-1 Deficiency Syndrome: An Unusual Case
Javier Aisenberg, Steven Ghanny, Amy Chartoff, Aliza Zidell, Helio Pedro, Sjoerd Joustra, Monique Losekoot, Jan Wit
The IGSF-1 Deficiency Syndrome: An Unusual Case
Javier Aisenberg, Steven Ghanny, Amy Chartoff, Aliza Zidell, Helio Pedro, Sjoerd Joustra, Monique Losekoot, Jan Wit
P2-509
Survival, Hypothalamic Obesity, and Neuropsychological/Psychosocial Status after
Childhood-onset Craniopharyngioma: Newly reported Long-term Outcomes
Anthe S. Sterkenburg, Anika Hoffmann, Ursel Gebhardt, Monika Warmuth-Metz, Anna M.M. Daubenbüchel, Hermann L. Müller
Survival, Hypothalamic Obesity, and Neuropsychological/Psychosocial Status after
Childhood-onset Craniopharyngioma: Newly reported Long-term Outcomes
Anthe S. Sterkenburg, Anika Hoffmann, Ursel Gebhardt, Monika Warmuth-Metz, Anna M.M. Daubenbüchel, Hermann L. Müller
P2-510
CHRONIC INAPPROPRIATE ANTIDIURESIS IN CHILDHOOD: EXPERIENCE WITH TOLVAPTAN
Rossella Gaudino, Claudia Piona, Grazia Morandi, Paolo Cavarzere, Milena Brugnara
CHRONIC INAPPROPRIATE ANTIDIURESIS IN CHILDHOOD: EXPERIENCE WITH TOLVAPTAN
Rossella Gaudino, Claudia Piona, Grazia Morandi, Paolo Cavarzere, Milena Brugnara
P2-511
Pituitary hormone secretion profiles in IGSF1 deficiency syndrome
Sjoerd Joustra, Ferdinand Roelfsema, Eric Endert, Bart Ballieux, Paul van Trotsenburg, Erik Fliers, Noortje Corssmit, Daniel Bernard, Wilma Oostdijk, Jan Maarten Wit, Alberto Pereira, Nienke Biermasz
Pituitary hormone secretion profiles in IGSF1 deficiency syndrome
Sjoerd Joustra, Ferdinand Roelfsema, Eric Endert, Bart Ballieux, Paul van Trotsenburg, Erik Fliers, Noortje Corssmit, Daniel Bernard, Wilma Oostdijk, Jan Maarten Wit, Alberto Pereira, Nienke Biermasz
P2-512
Pituitary function after mild to severe traumatic brain injury in children 2-18 years old: a prospective study.
Karine Braun, Claire Briet, Patrick Toussaint, Helene Bony Trifunovic, Bernard Boudailliez
Pituitary function after mild to severe traumatic brain injury in children 2-18 years old: a prospective study.
Karine Braun, Claire Briet, Patrick Toussaint, Helene Bony Trifunovic, Bernard Boudailliez
P2-513
A novel mutation within the AVP gene in an 18-year-old male patient with Kallmann syndrome and combined pituitary hormone deficiency
Won Bok Choi, Soo Young Kim, Lira Yoon, Young Mi Kim, Min-Jung Cho, Chang-Seok Ki, Sung Yoon Cho, Dong-Kyu Jin, Min Jung Kwak
A novel mutation within the AVP gene in an 18-year-old male patient with Kallmann syndrome and combined pituitary hormone deficiency
Won Bok Choi, Soo Young Kim, Lira Yoon, Young Mi Kim, Min-Jung Cho, Chang-Seok Ki, Sung Yoon Cho, Dong-Kyu Jin, Min Jung Kwak
P2-514
Hydrocephalus and Hypothalamic Involvement in Pediatric Patients with Craniopharyngioma or Cysts of Rathke’s Pouch: Impact on Long-term Prognosis
Anna M.M. Daubenbüchel, Anika Hoffmann, Ursel Gebhardt, Monika Warmuth-Metz, Anthe S. Sterkenburg, Hermann L. Müller
Hydrocephalus and Hypothalamic Involvement in Pediatric Patients with Craniopharyngioma or Cysts of Rathke’s Pouch: Impact on Long-term Prognosis
Anna M.M. Daubenbüchel, Anika Hoffmann, Ursel Gebhardt, Monika Warmuth-Metz, Anthe S. Sterkenburg, Hermann L. Müller
P2-515
Contrasting central diabetes insipidus due to preproAVP mutations: earlier onset of symptoms in recessive than in dominant forms
Karine Bourdet, Sophie Valette, Johnny Deladoëy, Guy Van Vliet
Contrasting central diabetes insipidus due to preproAVP mutations: earlier onset of symptoms in recessive than in dominant forms
Karine Bourdet, Sophie Valette, Johnny Deladoëy, Guy Van Vliet
P2-516
ENDOCRINE DISORDERS IN CHILDREN WITH OPTIC CHIASM GLIOMA
Alicia Torralbo-Carmona, Mar Domínguez-Begines, Laura Barchino-Muñoz, Emilio García-García
ENDOCRINE DISORDERS IN CHILDREN WITH OPTIC CHIASM GLIOMA
Alicia Torralbo-Carmona, Mar Domínguez-Begines, Laura Barchino-Muñoz, Emilio García-García
P2-517
Be aware of congenital panhypopituitarism in children with a family history of polydactyly
Idske Kremer Hovinga, Jacques Giltay, Hetty van der Kamp
Be aware of congenital panhypopituitarism in children with a family history of polydactyly
Idske Kremer Hovinga, Jacques Giltay, Hetty van der Kamp
P2-518
A Novel Single Nucleotide Variation Contributing to the Expression of Isolated Hypogonadotropic Hypogonadism
Ahmed Khattab, Cuiqi Zhou, Maria New, Shlomo Melmed
A Novel Single Nucleotide Variation Contributing to the Expression of Isolated Hypogonadotropic Hypogonadism
Ahmed Khattab, Cuiqi Zhou, Maria New, Shlomo Melmed
P2-519
Eating behavior, weight problems and eating disorders in 101 long-term survivors of childhood-onset craniopharyngioma
Anika Hoffmann, Anthe S. Sterkenburg, Ursel Gebhardt, Hermann L. Müller
Eating behavior, weight problems and eating disorders in 101 long-term survivors of childhood-onset craniopharyngioma
Anika Hoffmann, Anthe S. Sterkenburg, Ursel Gebhardt, Hermann L. Müller
P2-520
Two novel LHX3 mutations in patients with combined pituitary hormone deficiency and sensorineural hearing loss
Bassam Bin-Abbas, Khushnooda Ramzan, Rabab Allam, Mohammed Al-Owain, Faiqa Imtiaz
Two novel LHX3 mutations in patients with combined pituitary hormone deficiency and sensorineural hearing loss
Bassam Bin-Abbas, Khushnooda Ramzan, Rabab Allam, Mohammed Al-Owain, Faiqa Imtiaz
P2-521
A novel entity characterized by Growth Hormone Deficiency and Central Precocious Puberty in two siblings and their father, in the absence of Central Nervous System defect.
Antonis Voutetakis, Dimitris Chiotis, Maria Dracopoulou-Vabouli, Alexandra-Maria Magiakou, Georgia Chrousos, George Chrousos, Catherine Dacou-Voutetakis
A novel entity characterized by Growth Hormone Deficiency and Central Precocious Puberty in two siblings and their father, in the absence of Central Nervous System defect.
Antonis Voutetakis, Dimitris Chiotis, Maria Dracopoulou-Vabouli, Alexandra-Maria Magiakou, Georgia Chrousos, George Chrousos, Catherine Dacou-Voutetakis
P2-522
Effect of specimen repeated freeze-thaw cycles on urinary gonadotropin determined by immunochemiluminometric assays
Yaping Ma, Zhuangjian Xu, Yu Hu, Wenying Zhu, Qing Wang
Effect of specimen repeated freeze-thaw cycles on urinary gonadotropin determined by immunochemiluminometric assays
Yaping Ma, Zhuangjian Xu, Yu Hu, Wenying Zhu, Qing Wang
P2-539
GnRH Infusion in Females with Hypogonadotrophic Hypogonadism
Analía Freire, Andrea Arcari, Romina Grinspon, María Gabriela Ballerini, Nora Sanguineti, Ignacio Bergadá, María Eugenia Escobar, María Gabriela Ropelato, Mirta Gryngarten
GnRH Infusion in Females with Hypogonadotrophic Hypogonadism
Analía Freire, Andrea Arcari, Romina Grinspon, María Gabriela Ballerini, Nora Sanguineti, Ignacio Bergadá, María Eugenia Escobar, María Gabriela Ropelato, Mirta Gryngarten
P3-1099
Isolated Growth Hormone Deficiency (IGHD) Associated with 7q11.23 Duplication Syndrome -a Case Report
Ani Aroyo, Iva Stoeva, Gergana Stancheva, Daniela Avdshieva, Radka Kaneva
Isolated Growth Hormone Deficiency (IGHD) Associated with 7q11.23 Duplication Syndrome -a Case Report
Ani Aroyo, Iva Stoeva, Gergana Stancheva, Daniela Avdshieva, Radka Kaneva
P3-1100
Cushing disease in a patient with Beckwith Wiedemann: an unusual association.
Frederic Brioude, Carole Nicolas, Irene Netchine, Isabelle Marey, Yves Le Bouc, Philippe Touraine
Cushing disease in a patient with Beckwith Wiedemann: an unusual association.
Frederic Brioude, Carole Nicolas, Irene Netchine, Isabelle Marey, Yves Le Bouc, Philippe Touraine
P3-1101
Baseline characteristics, growth hormone response, and long term evolution in 67 patients with pituitary stalk interruption according to the initial presentation
Céline Bar, Charline Zadro, Gwenaelle Diene, Isabelle Oliver, Catherine Pienkowski, Béatrice Jouret, Cartault Audrey, Annick Sevely, Maithé Tauber, Thomas Edouard
Baseline characteristics, growth hormone response, and long term evolution in 67 patients with pituitary stalk interruption according to the initial presentation
Céline Bar, Charline Zadro, Gwenaelle Diene, Isabelle Oliver, Catherine Pienkowski, Béatrice Jouret, Cartault Audrey, Annick Sevely, Maithé Tauber, Thomas Edouard
P3-1102
Clinical characteristics of children with congenital combined growth hormone deficiency without associated syndrome in Belgium
Renate Zeevaert, Franciska Verlinde, Muriel Thomas, Francis De Zegher, Martine Cools, Claudine Heinrichs, Véronique Beauloye, Annick France, Marie-Christine Lebrethon, Guy Massa
Clinical characteristics of children with congenital combined growth hormone deficiency without associated syndrome in Belgium
Renate Zeevaert, Franciska Verlinde, Muriel Thomas, Francis De Zegher, Martine Cools, Claudine Heinrichs, Véronique Beauloye, Annick France, Marie-Christine Lebrethon, Guy Massa
P3-1103
Pitfalls in reporting of paediatric pituitary scans
Dalia Hammouche, Aufrey Ebita-Gama, Vijith Puthi
Pitfalls in reporting of paediatric pituitary scans
Dalia Hammouche, Aufrey Ebita-Gama, Vijith Puthi
P3-1104
Long term follow-up of a child treated with CyberKnife radiosurgery for ACTH-secreting pituitary adenoma after bilateral adrenalectomy
Tommaso Aversa, Malgorzata Wasniewska, Maria Francesca Messina, Mariarosa Calafiore, Filippo De Luca
Long term follow-up of a child treated with CyberKnife radiosurgery for ACTH-secreting pituitary adenoma after bilateral adrenalectomy
Tommaso Aversa, Malgorzata Wasniewska, Maria Francesca Messina, Mariarosa Calafiore, Filippo De Luca
P3-1105
Off-label use of vaptans in children with severe symptomatic hyponatremia due to SIADH
Gerdi Tuli, Daniele Tessaris, Serena Di Taranto, Alberto Giorgis, Silvia Einaudi, Patrizia Matarazzo
Off-label use of vaptans in children with severe symptomatic hyponatremia due to SIADH
Gerdi Tuli, Daniele Tessaris, Serena Di Taranto, Alberto Giorgis, Silvia Einaudi, Patrizia Matarazzo
P3-1106
Acquired long QT syndrome in a 14-year-old boy with panhypopituitarism
Yoo-Mi Kim, Jung-Ho Seo, Chong Kun Cheon, Young-Tak Yim, Su Young Kim
Acquired long QT syndrome in a 14-year-old boy with panhypopituitarism
Yoo-Mi Kim, Jung-Ho Seo, Chong Kun Cheon, Young-Tak Yim, Su Young Kim
P3-1107
Between three to four years after severe traumatism brain injury 22% at least of children and adolescents do have persistent pituitary dysfunction
Yamina DASSA, Claire PERSONNIER, Hélène CROSNIER, Mathilde CHEVIGNARD, Marie BOURGEOIS, Magali VIAUD, Michel POLAK
Between three to four years after severe traumatism brain injury 22% at least of children and adolescents do have persistent pituitary dysfunction
Yamina DASSA, Claire PERSONNIER, Hélène CROSNIER, Mathilde CHEVIGNARD, Marie BOURGEOIS, Magali VIAUD, Michel POLAK
P3-1108
Causes and consequences of thickened pituitary stalk found by MRI in children and adolescents with central diabetes insipidus
Julián Martínez-Villanueva, Beatriz Corredor-Andrés, María Teresa Muñoz-Calvo, Miguel Ángel López-Pino, Claudio Laganá, Mariana Campderá, Jesús Pozo-Román, Jesús Argente
Causes and consequences of thickened pituitary stalk found by MRI in children and adolescents with central diabetes insipidus
Julián Martínez-Villanueva, Beatriz Corredor-Andrés, María Teresa Muñoz-Calvo, Miguel Ángel López-Pino, Claudio Laganá, Mariana Campderá, Jesús Pozo-Román, Jesús Argente
P3-1109
Acute phase proteins and endocrine dysfunction after traumatic brain injury in childhood
Olga Verigaki, Ioannis Papassotiriou, Neofytos Prodromou, George Sfakianos3, George Chrousos, Christina Kanaka-Gantenbein
Acute phase proteins and endocrine dysfunction after traumatic brain injury in childhood
Olga Verigaki, Ioannis Papassotiriou, Neofytos Prodromou, George Sfakianos3, George Chrousos, Christina Kanaka-Gantenbein
P3-1110
Two Cases of Combined Pituitary Hormone Deficiency Proven to Have Mutations of GLI2
Yuka Nagashima, Masaki Takagi, Yukihiro Hasegawa, Takeshi Sato, Tomohiro Ishii, Tomonobu Hasegawa
Two Cases of Combined Pituitary Hormone Deficiency Proven to Have Mutations of GLI2
Yuka Nagashima, Masaki Takagi, Yukihiro Hasegawa, Takeshi Sato, Tomohiro Ishii, Tomonobu Hasegawa
P3-1111
AVP-NPII gene mutations and clinical characteristics of the patients with autosomal dominant familial central diabetes insipidus
Doga Turkkahraman, Emel Saglar, Tugce Karaduman, Hatice Mergen
AVP-NPII gene mutations and clinical characteristics of the patients with autosomal dominant familial central diabetes insipidus
Doga Turkkahraman, Emel Saglar, Tugce Karaduman, Hatice Mergen
P3-1112
A boy with Combined Pituitary Hormone Deficiency and Agenesis of Right Internal Carotid Artery: a rare association or a simple coincidence?
TC Vieira, Carolina Ramos, Eduardo Vellutini
A boy with Combined Pituitary Hormone Deficiency and Agenesis of Right Internal Carotid Artery: a rare association or a simple coincidence?
TC Vieira, Carolina Ramos, Eduardo Vellutini
P3-1113
A rare case of Congenital Hyperinsulinism associated with Hypopituitarism due to Pituitary Stalk Interruption Syndrome
Hussain Alsaffar, Supriya Phanse, Mohammed Didi, Senthil Senniappan
A rare case of Congenital Hyperinsulinism associated with Hypopituitarism due to Pituitary Stalk Interruption Syndrome
Hussain Alsaffar, Supriya Phanse, Mohammed Didi, Senthil Senniappan
P3-1114
Management of Risperidone induced Hyperprolactinemia in an Adolescent with Severe Autism
Dinesh Giri, Tayyaba Sanam, A Oppenheim, Senthil Senniappan, Urmi Das
Management of Risperidone induced Hyperprolactinemia in an Adolescent with Severe Autism
Dinesh Giri, Tayyaba Sanam, A Oppenheim, Senthil Senniappan, Urmi Das
P3-1115
Pituitary hyperplasia due to primary hypothyroidism in a case with Neurofibromatosis Type 1
Esra DOGER, Orhun CAMURDAN, Emine DEMET AKBAS, Onur AKIN, Ozge YUCE, Nurullah CELIK, Aysun BIDECI, Peyami CINAZ
Pituitary hyperplasia due to primary hypothyroidism in a case with Neurofibromatosis Type 1
Esra DOGER, Orhun CAMURDAN, Emine DEMET AKBAS, Onur AKIN, Ozge YUCE, Nurullah CELIK, Aysun BIDECI, Peyami CINAZ
P3-1116
HORMONE DISORDER AND VITAMIN DEFICIENCY IN ATTENTION DEFICIT HYPERACTIVITY DISORDER (ADHD) AND AUTISM SPECTRUM DISORDERS (ASD)
Murat Doğan, Keziban Aslı Bala, Tuba Mutluer, Sultan Kaba, Oktay Aslan, Şekibe Zehra Doğan
HORMONE DISORDER AND VITAMIN DEFICIENCY IN ATTENTION DEFICIT HYPERACTIVITY DISORDER (ADHD) AND AUTISM SPECTRUM DISORDERS (ASD)
Murat Doğan, Keziban Aslı Bala, Tuba Mutluer, Sultan Kaba, Oktay Aslan, Şekibe Zehra Doğan
P3-1117
Two novel mutations in GLI2 gene in two unrelated Argentinean prepuberal patients, one with isolated growth hormone deficiency, and another with multiple pituitary hormone deficiency, both with developmental defects in posterior pituitary gland.
Roxana Marino, Matias Juanes, Pablo Ramirez, Natalia Perez Garrido, Marta Ciaccio, Isabel Di Palma, Mercedes Maceiras, Juan Manuel Lazzati, Marco Aurelio Rivarola, Alicia Belgorosky
Two novel mutations in GLI2 gene in two unrelated Argentinean prepuberal patients, one with isolated growth hormone deficiency, and another with multiple pituitary hormone deficiency, both with developmental defects in posterior pituitary gland.
Roxana Marino, Matias Juanes, Pablo Ramirez, Natalia Perez Garrido, Marta Ciaccio, Isabel Di Palma, Mercedes Maceiras, Juan Manuel Lazzati, Marco Aurelio Rivarola, Alicia Belgorosky
P3-1118
Pituitary Stalk Interruption Syndrome Presenting with Normogonadotropic Amenorrhea and Hypoprolactinemia
Gonul Catli, Cemil Kocyigit, Sule Penbe Can, Bumin Nuri Dundar
Pituitary Stalk Interruption Syndrome Presenting with Normogonadotropic Amenorrhea and Hypoprolactinemia
Gonul Catli, Cemil Kocyigit, Sule Penbe Can, Bumin Nuri Dundar
P3-1119
PEDIATRIC CENTRAL NERVOUS SYSTEM GERM CELL TUMORS: ENDOCRINE OUTCOME
Alicia Torralbo-Carmona, Laura Barchino-Muñoz, Mar Domínguez-Begines, Emilio García-García
PEDIATRIC CENTRAL NERVOUS SYSTEM GERM CELL TUMORS: ENDOCRINE OUTCOME
Alicia Torralbo-Carmona, Laura Barchino-Muñoz, Mar Domínguez-Begines, Emilio García-García
P3-1120
Description of patients diagnosed with central diabetes insipidus, 14 year experience at the National Children´s Hospital, Costa Rica.
Fred Cavallo-Aita, Jiulliana Montenegro-Villalobos
Description of patients diagnosed with central diabetes insipidus, 14 year experience at the National Children´s Hospital, Costa Rica.
Fred Cavallo-Aita, Jiulliana Montenegro-Villalobos
P3-1121
Pegvisomant in child acromegaly.
Vaczlavik Anna, Teinturier Cécile, Gaillard Stephan, Bougnères Pierre-François, Chanson Philippe
Pegvisomant in child acromegaly.
Vaczlavik Anna, Teinturier Cécile, Gaillard Stephan, Bougnères Pierre-François, Chanson Philippe
P3-1122
Case Series; Central Diabetes Insipidus Presenting to a District General Hospital
Gemma Keelty, Kamal Weerasinghe, John Gregory
Case Series; Central Diabetes Insipidus Presenting to a District General Hospital
Gemma Keelty, Kamal Weerasinghe, John Gregory
P3-1123
A 5-year-old patient with Cushing’s disease
Kikumi Ushijima, Takako Sasaki, Syuichi Yatsuga, Koga Yasutoshi
A 5-year-old patient with Cushing’s disease
Kikumi Ushijima, Takako Sasaki, Syuichi Yatsuga, Koga Yasutoshi
P3-1125
COMBINED PITUITARY HORMONE DEFICIENCY
Karolina Kot, Elzbieta Moszczynska, Mieczyslaw Szalecki
COMBINED PITUITARY HORMONE DEFICIENCY
Karolina Kot, Elzbieta Moszczynska, Mieczyslaw Szalecki
P3-1126
Outstanding growth response to growth hormone replacement therapy in 3 different cases of growth hormone deficiency (GHD)
Ljiljana Saranac, Zlatko Djuric, Ivana Markovic, Hristina Stamenkovic, Dragoljub Lazarevic, Vesna Cvetkovic
Outstanding growth response to growth hormone replacement therapy in 3 different cases of growth hormone deficiency (GHD)
Ljiljana Saranac, Zlatko Djuric, Ivana Markovic, Hristina Stamenkovic, Dragoljub Lazarevic, Vesna Cvetkovic
P3-1127
Pituitary Stalk Interruption Syndrome : a case of an infant
Havva Nur Peltek Kendirci, Zafer Kaya
Pituitary Stalk Interruption Syndrome : a case of an infant
Havva Nur Peltek Kendirci, Zafer Kaya
P3-1128
Congenital adiptical diabetes insipidus: a clinical case
Olga Zagrebaeva, Anzhalika Solntsava, Olga Kniazkina, Olga Barash, Natalia Kizevich
Congenital adiptical diabetes insipidus: a clinical case
Olga Zagrebaeva, Anzhalika Solntsava, Olga Kniazkina, Olga Barash, Natalia Kizevich
P3-1129
Thickened Pituitary stalk with central diabetes insipidus: what diagnosis?
amel Merazka, S Achir, O Baz, D Foudil, S Mimouni
Thickened Pituitary stalk with central diabetes insipidus: what diagnosis?
amel Merazka, S Achir, O Baz, D Foudil, S Mimouni
P1-49
Can hypothalamic obesity be treated with stimulants? -Follow up
Friederike Denzer, Belinda Lennerz, Heike Vollbach, Christian Denzer, Martin Wabitsch
Can hypothalamic obesity be treated with stimulants? -Follow up
Friederike Denzer, Belinda Lennerz, Heike Vollbach, Christian Denzer, Martin Wabitsch
P1-50
A feasibility study of intra-gastric balloons (supported by a lifestyle programme) for the treatment of severe adolescent obesity - the (BOB) Study.
Pooja Sachdev, Lindesy Reece, Rob Copeland, Mike Thomson, Anuja Natarajan, Jerry Wales, Neil Wright
A feasibility study of intra-gastric balloons (supported by a lifestyle programme) for the treatment of severe adolescent obesity - the (BOB) Study.
Pooja Sachdev, Lindesy Reece, Rob Copeland, Mike Thomson, Anuja Natarajan, Jerry Wales, Neil Wright
P1-51
Distribution of obesity indices among European preschool children and associated risk factors: the ToyBox-study
Sonya Galcheva, Mina Lateva, Violeta Iotova, Ilse De Bourdeaudhuij, Greet Cardon, Odysseas Androutsos, Zbigniew Kulaga, Piotr Socha, Luis Moreno, Berthold Koletzko, Yannis Manios, ToyBox-study Group
Distribution of obesity indices among European preschool children and associated risk factors: the ToyBox-study
Sonya Galcheva, Mina Lateva, Violeta Iotova, Ilse De Bourdeaudhuij, Greet Cardon, Odysseas Androutsos, Zbigniew Kulaga, Piotr Socha, Luis Moreno, Berthold Koletzko, Yannis Manios, ToyBox-study Group
P1-52
A Randomized Trial of the Effects of Perinatal Education of Overweight Pregnant Women to Prevent Childhood Overweight: the ETOIG study.
Sophie PARAT, Emmanuel COSSON, Amandine BAPTISTE, Marie-Therese TAUBER, Paul VALENSI, Anne-Marie BERTRAND, Myriam DABBAS, Caroline ELIE, Françoise LORENZINI, Veronique NEGRE
A Randomized Trial of the Effects of Perinatal Education of Overweight Pregnant Women to Prevent Childhood Overweight: the ETOIG study.
Sophie PARAT, Emmanuel COSSON, Amandine BAPTISTE, Marie-Therese TAUBER, Paul VALENSI, Anne-Marie BERTRAND, Myriam DABBAS, Caroline ELIE, Françoise LORENZINI, Veronique NEGRE
P1-53
Perypheral neuroblastic tumors and ROHHADNET syndrome (Rapid-onset Obesity with Hypothalamic dysfunction, Hypoventilation, Autonomic Dysregulation and NEural Tumor)
Flavia Napoli, Ramona Tallone, Annalisa Calcagno, Stefania Sorrentino, Anna Allegri, Natascia Di Iorgi, Mohamad Maghnie
Perypheral neuroblastic tumors and ROHHADNET syndrome (Rapid-onset Obesity with Hypothalamic dysfunction, Hypoventilation, Autonomic Dysregulation and NEural Tumor)
Flavia Napoli, Ramona Tallone, Annalisa Calcagno, Stefania Sorrentino, Anna Allegri, Natascia Di Iorgi, Mohamad Maghnie
P1-54
“bestPWS EU”: A Phase 3 study in adolescent and adult patients with PWS in Europe
Maithe Tauber, Terri Kim, Nerissa Kreher, Dennis Kim, Berthold Hauffa
“bestPWS EU”: A Phase 3 study in adolescent and adult patients with PWS in Europe
Maithe Tauber, Terri Kim, Nerissa Kreher, Dennis Kim, Berthold Hauffa
P1-55
Intrauterine growth restriction is associated with greater severity in childhood obesity-associated metabolic impairment and poorer adult height prediction
Rocío González-Leal, Julián Martínez-Villanueva, Jesús Argente, Gabriel Á. Martos-Moreno
Intrauterine growth restriction is associated with greater severity in childhood obesity-associated metabolic impairment and poorer adult height prediction
Rocío González-Leal, Julián Martínez-Villanueva, Jesús Argente, Gabriel Á. Martos-Moreno
P1-67
miR-146a-mediated suppression of the inflammatory response in human adipocytes
Julian Roos, Eveliina Enlund, Daniel Tews, Jan-Bernd Funcke, Verena Zoller, Klaus-Michael Debatin, Martin Wabitsch, Pamela Fischer-Posovszky
miR-146a-mediated suppression of the inflammatory response in human adipocytes
Julian Roos, Eveliina Enlund, Daniel Tews, Jan-Bernd Funcke, Verena Zoller, Klaus-Michael Debatin, Martin Wabitsch, Pamela Fischer-Posovszky
P1-68
Leptin resistance alteration after modulation of dopamine system funcional activity in rat's diet-induced obesity
Liudmila Viazava, Angzhalika Solntsva, Alexander Sukalo, Alena Dashkevich, Julia Stukach
Leptin resistance alteration after modulation of dopamine system funcional activity in rat's diet-induced obesity
Liudmila Viazava, Angzhalika Solntsva, Alexander Sukalo, Alena Dashkevich, Julia Stukach
P1-70
Outcome of Adolescents Undergoing Bariatric Surgery – One Year Follow-up
Michal Ben-Ami, Maayan Bacher, Irena Vusiker, Reut Pink, Daniel Stein, Benjamin Vagner, Gal Raz-Dubnov, Danny Yardeni, Orit PInhas-Hamiel
Outcome of Adolescents Undergoing Bariatric Surgery – One Year Follow-up
Michal Ben-Ami, Maayan Bacher, Irena Vusiker, Reut Pink, Daniel Stein, Benjamin Vagner, Gal Raz-Dubnov, Danny Yardeni, Orit PInhas-Hamiel
P1-71
Identifying critical periods for maintaining weight loss in obese children
Amanda Peacock, Talat Mushtaq, Erin Alexander, Helen Truby, Darren Greenwood, Vince Russo, Steven Yau, George Werther, Matthew Sabin
Identifying critical periods for maintaining weight loss in obese children
Amanda Peacock, Talat Mushtaq, Erin Alexander, Helen Truby, Darren Greenwood, Vince Russo, Steven Yau, George Werther, Matthew Sabin
P1-72
Use of topiramate in severe hyperphagia associated to neuropsychiatric features in a boy with congenital proopiomelanocortin deficiency (POMC)
Romana Marini, Sara Ciccone, Paolo Alfieri, Stefania Pedicelli, Marco Cappa
Use of topiramate in severe hyperphagia associated to neuropsychiatric features in a boy with congenital proopiomelanocortin deficiency (POMC)
Romana Marini, Sara Ciccone, Paolo Alfieri, Stefania Pedicelli, Marco Cappa
P1-73
CIRCULATING miR146a AND 486-5p ARE ALTERED IN OBESE CHILDREN WITH AND WITHOUT NON-ALCOHOLIC FATTY LIVER DISEASE (NAFLD) AND CORRELATE WITH ABDOMINAL FAT AND BMI.
Luisa Montanini, Viviana D. Patianna, Chiara Sartori, Barbara Predieri, Patrizia Bruzzi, Pietro Lazzeroni, Silvia Merli, Paolo Bergamaschi, Sergio Bernasconi, Lorenzo Iughetti, Maria Elisabeth Street
CIRCULATING miR146a AND 486-5p ARE ALTERED IN OBESE CHILDREN WITH AND WITHOUT NON-ALCOHOLIC FATTY LIVER DISEASE (NAFLD) AND CORRELATE WITH ABDOMINAL FAT AND BMI.
Luisa Montanini, Viviana D. Patianna, Chiara Sartori, Barbara Predieri, Patrizia Bruzzi, Pietro Lazzeroni, Silvia Merli, Paolo Bergamaschi, Sergio Bernasconi, Lorenzo Iughetti, Maria Elisabeth Street
P1-74
Erythropoietin activates heat production and lipolysis on brown adipose tissue and consequently reduces obesity in dietary-induced obese mice
Kazuki Kodo, Hisakazu Nakajima, Satoru Sugimoto, Ikuyo Itoh, Shota Fukuhara, Shigehara keiichi, Taichiro Nishikawa, Jun Mori, Kitaro Kosaka, Hajime Hosoi
Erythropoietin activates heat production and lipolysis on brown adipose tissue and consequently reduces obesity in dietary-induced obese mice
Kazuki Kodo, Hisakazu Nakajima, Satoru Sugimoto, Ikuyo Itoh, Shota Fukuhara, Shigehara keiichi, Taichiro Nishikawa, Jun Mori, Kitaro Kosaka, Hajime Hosoi
P1-75
Ghrelin and brain-derived neurotrophic factor in children with Prader-Willi syndrome.
Elena Bogova, Natalya Volevodz, Valentina Peterkova
Ghrelin and brain-derived neurotrophic factor in children with Prader-Willi syndrome.
Elena Bogova, Natalya Volevodz, Valentina Peterkova
P1-76
Endothelial Progenitor Cells in Obese Non-diabetic Children and Adolescents: Relations to Some Metabolic Parameters, Echocardiographic Parameters and Tissue Doppler Imaging
Alaa Ahmed, Omneya Youssef, Botheina Thabet
Endothelial Progenitor Cells in Obese Non-diabetic Children and Adolescents: Relations to Some Metabolic Parameters, Echocardiographic Parameters and Tissue Doppler Imaging
Alaa Ahmed, Omneya Youssef, Botheina Thabet
P1-77
Evaluation of adiponectin concentrations in obese children and its correlation with lipid and carbohydrate parameters
Malgorzata Ruminska, Anna Majcher, Beata Pyrzak
Evaluation of adiponectin concentrations in obese children and its correlation with lipid and carbohydrate parameters
Malgorzata Ruminska, Anna Majcher, Beata Pyrzak
P2-328
miR-122 and non-alcoholic fatty liver disease in prepubertal obese children
Elena Inzaghi, Stephanie Brandt, Julian Roos, Stefano Cianfarani, Valerio Nobili, Mauro Colajacomo, Tadej Battelino, Kotnik Primoz, Martin Wabitsch, Pamela Fischer-Posovszky
miR-122 and non-alcoholic fatty liver disease in prepubertal obese children
Elena Inzaghi, Stephanie Brandt, Julian Roos, Stefano Cianfarani, Valerio Nobili, Mauro Colajacomo, Tadej Battelino, Kotnik Primoz, Martin Wabitsch, Pamela Fischer-Posovszky
P2-329
Meteorin-like (METRNL) expression in human adipose tissue is associated with adipocyte hypertrophy and inflammation and is down-regulated during human adipogenesis
Dennis Löffler, Denise Rockstroh, Julian Schwartze, Kathrin Landgraf, Antje Körner
Meteorin-like (METRNL) expression in human adipose tissue is associated with adipocyte hypertrophy and inflammation and is down-regulated during human adipogenesis
Dennis Löffler, Denise Rockstroh, Julian Schwartze, Kathrin Landgraf, Antje Körner
P2-330
Abdominal fat distribution measured by Magnetic Resonance Imaging in 197 children aged 10 to 15 years – correlation to anthropometry and Dual X-ray Absorptiometry
Jeanette Tinggaard, Casper P Hagen, Annette Mouritsen, Mikkel G Mieritz, Christine Wohlfahrt-Veje, Eva Fallentin, Rasmus Larsen, Anders N Christensen, Rikke B Jensen, Anders Juul, Katharina Main
Abdominal fat distribution measured by Magnetic Resonance Imaging in 197 children aged 10 to 15 years – correlation to anthropometry and Dual X-ray Absorptiometry
Jeanette Tinggaard, Casper P Hagen, Annette Mouritsen, Mikkel G Mieritz, Christine Wohlfahrt-Veje, Eva Fallentin, Rasmus Larsen, Anders N Christensen, Rikke B Jensen, Anders Juul, Katharina Main
P2-331
Autonomic nervous system function assessed by heart rate variability in children and adolescents with long term follow up of craniopharyngioma
Hae Woon Jung, Hwa Young Kim, Gyung Min Lee, So Youn Kim, Kyung A Jeong, Keun Hee Choi, Jieun Lee, Young Ah Lee, Choong Ho Shin, Sei Won Yang
Autonomic nervous system function assessed by heart rate variability in children and adolescents with long term follow up of craniopharyngioma
Hae Woon Jung, Hwa Young Kim, Gyung Min Lee, So Youn Kim, Kyung A Jeong, Keun Hee Choi, Jieun Lee, Young Ah Lee, Choong Ho Shin, Sei Won Yang
P2-332
SIRT1 and SIRT2 gene expression in peripheral blood mononuclear cells of obese children and adolescents and their relationship with metabolic parameters and insulin resistance
Mitra Nourbakhsh, Maryam Razzaghy-Azar, Zahra Arab, Parvin Pasalar, Abolfazl Golestani, Bagher Larijani
SIRT1 and SIRT2 gene expression in peripheral blood mononuclear cells of obese children and adolescents and their relationship with metabolic parameters and insulin resistance
Mitra Nourbakhsh, Maryam Razzaghy-Azar, Zahra Arab, Parvin Pasalar, Abolfazl Golestani, Bagher Larijani
P2-333
Leptin replacement improves central ventilation in a patient with congenital leptin deficiency: first report in childhood.
Laura Lucaccioni, Philip L. Davies, Neil A. Gibson, Sadaf Farooqi, M. Guftar Shaikh
Leptin replacement improves central ventilation in a patient with congenital leptin deficiency: first report in childhood.
Laura Lucaccioni, Philip L. Davies, Neil A. Gibson, Sadaf Farooqi, M. Guftar Shaikh
P2-334
Childhood obesity negatively influences adult Leydig cell function
Isabel V. Wagner, Nora Klöting, Wieland Kiess, Olle Söder, Konstantin Svechnikov
Childhood obesity negatively influences adult Leydig cell function
Isabel V. Wagner, Nora Klöting, Wieland Kiess, Olle Söder, Konstantin Svechnikov
P2-335
Network Coordinated Primary Care Intervention in obese children and adolescents: almost a decade of experience.
Sophie Guilmin-Crépon, Amine Arsan, Priscilla Boizeau, Corinne Alberti, Laurent Fidalgo, Bertrand Chevallier, Patricia Lubelski, Jacques Cheymol, Alain Zaluski, Patrick Tounian, Jean-Claude Carel, on behalf of REPOP Ile-de-France
Network Coordinated Primary Care Intervention in obese children and adolescents: almost a decade of experience.
Sophie Guilmin-Crépon, Amine Arsan, Priscilla Boizeau, Corinne Alberti, Laurent Fidalgo, Bertrand Chevallier, Patricia Lubelski, Jacques Cheymol, Alain Zaluski, Patrick Tounian, Jean-Claude Carel, on behalf of REPOP Ile-de-France
P2-336
Diagnosing the metabolic syndrome in survivors of childhood haematopoietic stem cell transplantation and total body irradiation (HSCT/TBI)
Christina Wei, Linda Hunt, Ruth Elson, Rachel Cox, Karin Bradley, Julian Shield, Michael Stevens, Elizabeth Crowne
Diagnosing the metabolic syndrome in survivors of childhood haematopoietic stem cell transplantation and total body irradiation (HSCT/TBI)
Christina Wei, Linda Hunt, Ruth Elson, Rachel Cox, Karin Bradley, Julian Shield, Michael Stevens, Elizabeth Crowne
P2-337
Laparoscopic sleeve gastrectomy in adolescents: metabolic consequences.
Marina Ybarra, Ruth Franco, Louise Cominato, Manoel Carlos Velhote, Durval Damiani
Laparoscopic sleeve gastrectomy in adolescents: metabolic consequences.
Marina Ybarra, Ruth Franco, Louise Cominato, Manoel Carlos Velhote, Durval Damiani
P2-338
A novel melanocortin 4 receptor (MC4R) gene mutation associated with early onset severe obesity.
Christos Shammas, Vassos Neocleous, Marie Phelan, Nicos Skordis, Leonidas Phylactou, Christos Mantzoros, Meropi Toumba
A novel melanocortin 4 receptor (MC4R) gene mutation associated with early onset severe obesity.
Christos Shammas, Vassos Neocleous, Marie Phelan, Nicos Skordis, Leonidas Phylactou, Christos Mantzoros, Meropi Toumba
P2-339
Hypothalamic obesity, Hyperphagia and Hyperinsulinaemia: time for a paradigm shift in assumptions?
Hoong-Wei Gan, Clare Leeson, Helen Aitkenhead, Helen Spoudeas, Mehul Dattani
Hypothalamic obesity, Hyperphagia and Hyperinsulinaemia: time for a paradigm shift in assumptions?
Hoong-Wei Gan, Clare Leeson, Helen Aitkenhead, Helen Spoudeas, Mehul Dattani
P2-341
Palmitic acid could modify cognitive and behavioral functions through sex specific activation of hippocampal astrocytes
Laura M Frago, Alejandra Freire-Regatillo, Pilar Argente-Arizón, Jesús Argente, Julie A Chowen
Palmitic acid could modify cognitive and behavioral functions through sex specific activation of hippocampal astrocytes
Laura M Frago, Alejandra Freire-Regatillo, Pilar Argente-Arizón, Jesús Argente, Julie A Chowen
P2-342
Changes in insulin sensitivity in adolescents who underwent bariatric surgery: effects of laparoscopic sleeve gastrectomy and laparoscopic gastric banding.
Gianpaolo De Filippo, Guillaume Pourcher, Naziha Khen-Dunlop, Christèle Kyheng, Ibrahim Dagher, Pierre Bougnères
Changes in insulin sensitivity in adolescents who underwent bariatric surgery: effects of laparoscopic sleeve gastrectomy and laparoscopic gastric banding.
Gianpaolo De Filippo, Guillaume Pourcher, Naziha Khen-Dunlop, Christèle Kyheng, Ibrahim Dagher, Pierre Bougnères
P2-343
Chronodisruption in Obese Children
Christoph Saner, Primus Mullis, Giacomo D Simonetti, Marco Janner
Chronodisruption in Obese Children
Christoph Saner, Primus Mullis, Giacomo D Simonetti, Marco Janner
P2-344
Configuring a Better Estimation of Obese Children’s Kidney Size
Fahimeh Soheilipour, Nahid Rahimzade, Fatemeh Jesmi, Mohadeseh Pishgahroudsari, Sarah Kaviani, Mahnaz Sadeghian, Fariba Almassinokiani
Configuring a Better Estimation of Obese Children’s Kidney Size
Fahimeh Soheilipour, Nahid Rahimzade, Fatemeh Jesmi, Mohadeseh Pishgahroudsari, Sarah Kaviani, Mahnaz Sadeghian, Fariba Almassinokiani
P2-345
Early onset of adiposity rebound is associated with higher leptin concentrations in 12-year old children
Satomi Koyama, Toshimi Sairenchi, Osamu Arisaka
Early onset of adiposity rebound is associated with higher leptin concentrations in 12-year old children
Satomi Koyama, Toshimi Sairenchi, Osamu Arisaka
P2-346
Metformin treatment for obese children and adolescents with insulin resistance
Zdravka Todorova, Elissaveta Stefanova, Krasimira Kazakova, Desislava Yordanova
Metformin treatment for obese children and adolescents with insulin resistance
Zdravka Todorova, Elissaveta Stefanova, Krasimira Kazakova, Desislava Yordanova
P2-347
A double-blind, placebo-controlled comparison of cinnamon extract to metformin effects upon insulin resistance, apolipoprotein B/ apolipoprotein A1 ratio, and body mass index of obese adolescent girls with polycystic ovarian syndrome
Shadab Salehpour, Somayeh Setavand, Samaneh Onsori
A double-blind, placebo-controlled comparison of cinnamon extract to metformin effects upon insulin resistance, apolipoprotein B/ apolipoprotein A1 ratio, and body mass index of obese adolescent girls with polycystic ovarian syndrome
Shadab Salehpour, Somayeh Setavand, Samaneh Onsori
P2-348
Pantoprazole treatment of Exogenous Obesity and Hyperinsulinism in Childhood
Murat Doğan, Sultan Kaba, Keziban Bulan, Şukran Akgeyik, Şekibe Zehra Doğan
Pantoprazole treatment of Exogenous Obesity and Hyperinsulinism in Childhood
Murat Doğan, Sultan Kaba, Keziban Bulan, Şukran Akgeyik, Şekibe Zehra Doğan
P2-349
Subepicardial Adipose Tissue and Carotid Intima Media Thickness in Obese Children and Their Relationship Between Metabolic and Clinical Parameters
Mehmet Boyraz, Fatma Uzun, Sancar Eminoğlu
Subepicardial Adipose Tissue and Carotid Intima Media Thickness in Obese Children and Their Relationship Between Metabolic and Clinical Parameters
Mehmet Boyraz, Fatma Uzun, Sancar Eminoğlu
P2-350
The switch in eating behavior in infants with Prader-Willi syndrome is associated with an increase in the acylated to unacylated ghrelin ratio: Results of a longitudinal study
Renske Kuppens, Aart Jan van der Lely, Patric Delhanty, Martin Huisman, Anita Hokken-Koelega
The switch in eating behavior in infants with Prader-Willi syndrome is associated with an increase in the acylated to unacylated ghrelin ratio: Results of a longitudinal study
Renske Kuppens, Aart Jan van der Lely, Patric Delhanty, Martin Huisman, Anita Hokken-Koelega
P2-351
Domino liver transplantation for the pre-emptive therapy of compound heterozygous familial hypercholesterolemia : A case of 2-year-old girl
Hiroyuki Tanaka, Daisuke Sugawara, Yasuko Tanaka, Tomoko Yoshida, Kanako Nakao, Noboru Uchida, Akiko Yamamoto, Akinari Fukuda, Mureo Kasahara, Reiko Horikawa
Domino liver transplantation for the pre-emptive therapy of compound heterozygous familial hypercholesterolemia : A case of 2-year-old girl
Hiroyuki Tanaka, Daisuke Sugawara, Yasuko Tanaka, Tomoko Yoshida, Kanako Nakao, Noboru Uchida, Akiko Yamamoto, Akinari Fukuda, Mureo Kasahara, Reiko Horikawa
P2-352
Metformin Prescriptions as a Proxy for Pediatric Type 2 Diabetes (T2D) Burden
Ann Marie McNeill, Tongtong Wang, Yong Chen, Ravi Shankar
Metformin Prescriptions as a Proxy for Pediatric Type 2 Diabetes (T2D) Burden
Ann Marie McNeill, Tongtong Wang, Yong Chen, Ravi Shankar
P2-354
Overweight and obesity in childhood cancer survivors
Christian Denzer, Louise Breuninger, Daniel Steinbach, Holger Cario, Klaus-Michael Debatin, Martin Wabitsch
Overweight and obesity in childhood cancer survivors
Christian Denzer, Louise Breuninger, Daniel Steinbach, Holger Cario, Klaus-Michael Debatin, Martin Wabitsch
P2-355
BERARDINELLI SEIP CONGENITAL LIPODYSTROPHY. A LIGTH OF HOPE.
Maria Ruiz del Campo, Isabel Saenz Moreno, Jose Julian Revorio Gonzalez, David Araujo-Vilar
BERARDINELLI SEIP CONGENITAL LIPODYSTROPHY. A LIGTH OF HOPE.
Maria Ruiz del Campo, Isabel Saenz Moreno, Jose Julian Revorio Gonzalez, David Araujo-Vilar
P2-356
Physical and metabolic evolution of obese children and adolescents after the attainment of intense weight reduction
Gabriel Á. Martos-Moreno, Julián Martínez-Villanueva, Rocío González-Leal, Jesús Argente
Physical and metabolic evolution of obese children and adolescents after the attainment of intense weight reduction
Gabriel Á. Martos-Moreno, Julián Martínez-Villanueva, Rocío González-Leal, Jesús Argente
P2-357
TG/HDL ratio as best predictor for IGT screening in overweight children
Maria Chiara Pellegrin, Lucia Radillo, Andrea Grillo, Gianluca Tornese, Elena Faleschini, Alessandro Ventura
TG/HDL ratio as best predictor for IGT screening in overweight children
Maria Chiara Pellegrin, Lucia Radillo, Andrea Grillo, Gianluca Tornese, Elena Faleschini, Alessandro Ventura
P2-358
Elevated Serum Irisin Level is not Related to Metabolic and Anthropometric Parameters in Obese Children
Ayhan Abaci, Gonul Catli, Hale Unver Tuhan, Ahmet Anik, Tuncay Küme, Özlem Gürsoy Calan, Ece Böber
Elevated Serum Irisin Level is not Related to Metabolic and Anthropometric Parameters in Obese Children
Ayhan Abaci, Gonul Catli, Hale Unver Tuhan, Ahmet Anik, Tuncay Küme, Özlem Gürsoy Calan, Ece Böber
P2-359
FTO rs9939609 polymorphism is associated with the presence of obstructive sleep apnoea in obese youth.
Kung-Ting Kao, Erin Alexander, Brooke E. Harcourt, Richard Saffery, Melissa Wake, Zoe McCallum, George Werther, Matthew Sabin
FTO rs9939609 polymorphism is associated with the presence of obstructive sleep apnoea in obese youth.
Kung-Ting Kao, Erin Alexander, Brooke E. Harcourt, Richard Saffery, Melissa Wake, Zoe McCallum, George Werther, Matthew Sabin
P2-360
Increasing waist/height ratio and BMI Z-score are associated with increased comorbidities in obese youth, although neither accurately identifies those with abnormal glucose metabolism.
Kung-Ting Kao, Erin Alexander, Brooke E. Harcourt, Zoe McCallum, Melissa Wake, George Werther, Matthew Sabin
Increasing waist/height ratio and BMI Z-score are associated with increased comorbidities in obese youth, although neither accurately identifies those with abnormal glucose metabolism.
Kung-Ting Kao, Erin Alexander, Brooke E. Harcourt, Zoe McCallum, Melissa Wake, George Werther, Matthew Sabin
P2-362
Nonalcoholic fatty liver disease and intestinal inflammation in obese children
Zehra Yavas Abali, Seha Saygili, Tulin Ozden, Serdar Cantez, Firdevs Bas, Vildan Ertekin, Ruveyde Bundak, Ozlem Durmaz, Feyza Darendeliler
Nonalcoholic fatty liver disease and intestinal inflammation in obese children
Zehra Yavas Abali, Seha Saygili, Tulin Ozden, Serdar Cantez, Firdevs Bas, Vildan Ertekin, Ruveyde Bundak, Ozlem Durmaz, Feyza Darendeliler
P2-363
Sleep and weight status at 4 years in the Inma Asturias cohort
ISOLINA RIAÑO-GALAN, CRISTINA RODRIGUEZ-DEHLI, ANA FERNANDEZ-SOMOANO, ADONINA TARDON
Sleep and weight status at 4 years in the Inma Asturias cohort
ISOLINA RIAÑO-GALAN, CRISTINA RODRIGUEZ-DEHLI, ANA FERNANDEZ-SOMOANO, ADONINA TARDON
P2-364
Evaluation of acylated ghrelin and obestatin levels and ghrelin/obestatin ratio in obesity
Maryam Razzaghy-Azar, Mitra Nourbakhsh, Abdolreza Pourmoteabed, Mona Nourbakhsh, Davoud Illbeigi, Zahra Arab
Evaluation of acylated ghrelin and obestatin levels and ghrelin/obestatin ratio in obesity
Maryam Razzaghy-Azar, Mitra Nourbakhsh, Abdolreza Pourmoteabed, Mona Nourbakhsh, Davoud Illbeigi, Zahra Arab
P2-365
A novel MC4R mutation associated with infancy-onset obesity
Damla Goksen, Huseyin Onay, Samim Ozen, Ferda Ozkinay, Sukran Darcan
A novel MC4R mutation associated with infancy-onset obesity
Damla Goksen, Huseyin Onay, Samim Ozen, Ferda Ozkinay, Sukran Darcan
P2-367
Residual excess weight difference between BMI 35-40 and BMI over 40 after laparoscopic sleeve gastrectomy in severely obese adolescents. Midterm outcomes.
Jeannette Linares, Rodrigo Villagran, Michael Gallardo, Isabela García, Sofia Araya, Carlos Flores, Mario Cariaga, Paulina Fuentes, Marisol Yañez
Residual excess weight difference between BMI 35-40 and BMI over 40 after laparoscopic sleeve gastrectomy in severely obese adolescents. Midterm outcomes.
Jeannette Linares, Rodrigo Villagran, Michael Gallardo, Isabela García, Sofia Araya, Carlos Flores, Mario Cariaga, Paulina Fuentes, Marisol Yañez
P2-368
Effect of visfatin on gene expression of insulin signaling molecules in SW872 Adipocytes
Li Ruizhen
Effect of visfatin on gene expression of insulin signaling molecules in SW872 Adipocytes
Li Ruizhen
P2-370
Information technology (IT) supported treatment of obese children and their families: a pilot study*
Dagmar Lallemand, Tobias Kowatsch, Irena Pletikosa, Björn Brogle, Anneco Dintheer, Dunja Wiegand, Dominique Durrer, Wolfgang Maass, Dirk Büchter
Information technology (IT) supported treatment of obese children and their families: a pilot study*
Dagmar Lallemand, Tobias Kowatsch, Irena Pletikosa, Björn Brogle, Anneco Dintheer, Dunja Wiegand, Dominique Durrer, Wolfgang Maass, Dirk Büchter
P2-371
Prevalence and phenotype characterization of MC4R mutations in a large paediatric cohort
Heike Vollbach, Stephanie Brandt, Georgina Lahr, Martin Wabitsch
Prevalence and phenotype characterization of MC4R mutations in a large paediatric cohort
Heike Vollbach, Stephanie Brandt, Georgina Lahr, Martin Wabitsch
P2-372
The effect of ABCA1 gene C69T single nucleotide polymorphism on dyslipidemia and insulin resistance in obese children
Ilker Tolga Ozgen, Ufuk Erenberk, Ozlem Gok, Ulkan Kilic, Bilge Bayraktar-Tanyeri, Emel Torun, Mehmet Sirin Aksu, Yasar Cesur
The effect of ABCA1 gene C69T single nucleotide polymorphism on dyslipidemia and insulin resistance in obese children
Ilker Tolga Ozgen, Ufuk Erenberk, Ozlem Gok, Ulkan Kilic, Bilge Bayraktar-Tanyeri, Emel Torun, Mehmet Sirin Aksu, Yasar Cesur
P2-374
Lifestyle habits and arterial hypertension in children and adolescents
Maria Daratsianou, Anastasios Ioannidis, Sofia Zyga, Paraskevas Koutsovitis, Athanasios Sachlas, Maria Xrona, Maria Batsikoura, Maria Efthymia Katsa, Maria Magana, Eleftherios Andronikakis, Andrea Paola Rojas Gil
Lifestyle habits and arterial hypertension in children and adolescents
Maria Daratsianou, Anastasios Ioannidis, Sofia Zyga, Paraskevas Koutsovitis, Athanasios Sachlas, Maria Xrona, Maria Batsikoura, Maria Efthymia Katsa, Maria Magana, Eleftherios Andronikakis, Andrea Paola Rojas Gil
P2-375
The Relation of Serum Nesfatin-1 Level with Anthropometric and Metabolic Parameters in Korean Children and Young Adolescents
Shin-Hee Kim, Moonbae Ahn, In-Ah Jung, Yeon Jin Jeon, Won Kyoung Cho, Kyoung Soon Cho, So Hyun Park, Min Ho Jung, Byoung-Kyu Suh
The Relation of Serum Nesfatin-1 Level with Anthropometric and Metabolic Parameters in Korean Children and Young Adolescents
Shin-Hee Kim, Moonbae Ahn, In-Ah Jung, Yeon Jin Jeon, Won Kyoung Cho, Kyoung Soon Cho, So Hyun Park, Min Ho Jung, Byoung-Kyu Suh
P2-376
Metabolic syndrome components of normal weight central obese adolescents in Korea stratified by waist to height ratio: Results from K-NHANES 2008-2010
Won Kyoung cho, Hyun young Lee, Moonbae Ahn, In Ah Jung, Shin Hee Kim, Kyoung Soon Cho, So Hyun Park, Min Ho Jung, Byung-Kyu Suh
Metabolic syndrome components of normal weight central obese adolescents in Korea stratified by waist to height ratio: Results from K-NHANES 2008-2010
Won Kyoung cho, Hyun young Lee, Moonbae Ahn, In Ah Jung, Shin Hee Kim, Kyoung Soon Cho, So Hyun Park, Min Ho Jung, Byung-Kyu Suh
P2-377
The Effect of Exenatide on Weight and Appetite in Overweight Adolescents and Young Adults with Prader-Willi Syndrome
Parisa Salehi, Isabel Hsu, Colleen G. Azen, Steven D. Mittelman, Mitchell E. Geffner, Debra Jeandron
The Effect of Exenatide on Weight and Appetite in Overweight Adolescents and Young Adults with Prader-Willi Syndrome
Parisa Salehi, Isabel Hsu, Colleen G. Azen, Steven D. Mittelman, Mitchell E. Geffner, Debra Jeandron
P2-378
Early-onset obesity and adrenal insufficiency associated with a homozygous POMC mutation.
Antonella Meloni, Maria Rosaria Casini, Emanuele Miraglia Del Giudice, Loredana Boccone
Early-onset obesity and adrenal insufficiency associated with a homozygous POMC mutation.
Antonella Meloni, Maria Rosaria Casini, Emanuele Miraglia Del Giudice, Loredana Boccone
P2-379
Clinical and Laboratory Differences between Metabolically Healthy and Unhealthy Obese Children
Selin Elmaogullari, Fatma Demirel, Nihal Hatipo
Clinical and Laboratory Differences between Metabolically Healthy and Unhealthy Obese Children
Selin Elmaogullari, Fatma Demirel, Nihal Hatipo
P2-381
Metformin in combination with lifestyle changes effectively reduces body mass index and waist circumference in overweight/obese children and adolescents
Natalija Smetanina, Adrone Seibokaite, Raimondas Valickas, Gintaras Kuprionis, Jolanta Janina Grigoniene, Ruta Rokaite, Astra Vitkauskiene, Kerstin Albertsson-Wikland, Rasa Verkauskiene
Metformin in combination with lifestyle changes effectively reduces body mass index and waist circumference in overweight/obese children and adolescents
Natalija Smetanina, Adrone Seibokaite, Raimondas Valickas, Gintaras Kuprionis, Jolanta Janina Grigoniene, Ruta Rokaite, Astra Vitkauskiene, Kerstin Albertsson-Wikland, Rasa Verkauskiene
P2-382
Insulin-like factor 5 –a novel orexigenic hormone in humans is dysregulated in obesity
Isabel V. Wagner, Gesine Flehmig, Kathrin Scheuermann, Dennis Löffler, Antje Körner, Wieland Kiess, Michael Stumvoll, Arne Dietrich, Matthias Blueher, Nora Klöting, Olle Söder, Konstantin Svechnikov
Insulin-like factor 5 –a novel orexigenic hormone in humans is dysregulated in obesity
Isabel V. Wagner, Gesine Flehmig, Kathrin Scheuermann, Dennis Löffler, Antje Körner, Wieland Kiess, Michael Stumvoll, Arne Dietrich, Matthias Blueher, Nora Klöting, Olle Söder, Konstantin Svechnikov
P2-383
TRYPTOPHAN SUPPLEMENTATION AS CONJUNCTIVE THERAPY TO LIFE STYLE CHANGES IN OBESE ADOLESCENTS
Adriana Jaramillo, Caterina Calderón, Marina Llobet, Laura Sole, Larisa Suarez-Ortega, Carles Lerin, Marta Ramon-Krauel
TRYPTOPHAN SUPPLEMENTATION AS CONJUNCTIVE THERAPY TO LIFE STYLE CHANGES IN OBESE ADOLESCENTS
Adriana Jaramillo, Caterina Calderón, Marina Llobet, Laura Sole, Larisa Suarez-Ortega, Carles Lerin, Marta Ramon-Krauel
P2-384
Obesity in ROHHADNET syndrome: does cortisol play a role?
Vera van Tellingen, Paul van Trotsenburg
Obesity in ROHHADNET syndrome: does cortisol play a role?
Vera van Tellingen, Paul van Trotsenburg
P2-385
TNFα downregulates CIDEC via MEK/ERK-dependent PPARγ phosphorylation and nuclear exportation in human adipocytes
Xinrui Tan, Yanfeng Xiao, Zhenzhen Cao
TNFα downregulates CIDEC via MEK/ERK-dependent PPARγ phosphorylation and nuclear exportation in human adipocytes
Xinrui Tan, Yanfeng Xiao, Zhenzhen Cao
P2-386
The Sequence of Prenatal Growth Restraint and Postnatal Catch-Up Growth Leads to a Thicker Intima Media and More Pre-Peritoneal and Hepatic Fat by Age 3-6 years
Giorgia Sebastiani, Marta Díaz, Judit Bassols, Abel Lopez-Bermejo, Francis De Zegher, Lourdes Ibañez
The Sequence of Prenatal Growth Restraint and Postnatal Catch-Up Growth Leads to a Thicker Intima Media and More Pre-Peritoneal and Hepatic Fat by Age 3-6 years
Giorgia Sebastiani, Marta Díaz, Judit Bassols, Abel Lopez-Bermejo, Francis De Zegher, Lourdes Ibañez
P2-387
Biovascular markers in children with Kabuki syndrome
Dina Schott, Berbel Kooger, Jörgen Bierau, Willem-Jan Gerver, Luc Zimmermann, Constance Stumpel
Biovascular markers in children with Kabuki syndrome
Dina Schott, Berbel Kooger, Jörgen Bierau, Willem-Jan Gerver, Luc Zimmermann, Constance Stumpel
P2-388
Phthalate exposure and metabolic parameters in Korean girls
Shin Hye Kim, Heesoo Pyo, Mi-Jung Park
Phthalate exposure and metabolic parameters in Korean girls
Shin Hye Kim, Heesoo Pyo, Mi-Jung Park
P3-828
Long-term effects of a ketogenic versus a hypocaloric diet in children and adolescents with obesity.
Ioanna Partsalaki, Alexia Karvela, Bessie E. Spiliotis
Long-term effects of a ketogenic versus a hypocaloric diet in children and adolescents with obesity.
Ioanna Partsalaki, Alexia Karvela, Bessie E. Spiliotis
P3-829
METABOLICALLY UNHEALTHY OBESE CHILDREN UNDER THE RISK OF EXERCISE INDUCED CHRONOTROPIC INCOMPETENCE
Tetyana Chaychenko, Olena Rybka
METABOLICALLY UNHEALTHY OBESE CHILDREN UNDER THE RISK OF EXERCISE INDUCED CHRONOTROPIC INCOMPETENCE
Tetyana Chaychenko, Olena Rybka
P3-830
DETERMINANTS OF SERUM INTERLEUKIN-1 RECEPTOR ANTAGONIST CONCENTRATIONS IN 12-YEAR-OLD CHILDREN BORN SMALL OR APPROPRIATE FOR GESTATIONAL AGE
Satu Seppä, Raimo Voutilainen, Sirpa Tenhola
DETERMINANTS OF SERUM INTERLEUKIN-1 RECEPTOR ANTAGONIST CONCENTRATIONS IN 12-YEAR-OLD CHILDREN BORN SMALL OR APPROPRIATE FOR GESTATIONAL AGE
Satu Seppä, Raimo Voutilainen, Sirpa Tenhola
P3-831
Evaluation of Renal Functions in Obese Children and Adolescents with Cystatin-C and Creatinin Based GFR: Is Increasing GFR Reflected Hyperfiltration and Possible Renal Damage in Future?
Dilsah Onerli Salman, Zeynep Siklar, Nisa Eda Cullas Ilarslan, Pinar Kocaay, Birsin Ozcakar, Merih Berberoglu
Evaluation of Renal Functions in Obese Children and Adolescents with Cystatin-C and Creatinin Based GFR: Is Increasing GFR Reflected Hyperfiltration and Possible Renal Damage in Future?
Dilsah Onerli Salman, Zeynep Siklar, Nisa Eda Cullas Ilarslan, Pinar Kocaay, Birsin Ozcakar, Merih Berberoglu
P3-832
THE FRENCH EXPERIENCE IN BARIATRIC SURGERY “Laparoscopic adjustable gastric banding (LAGB)” IN ADOLESCENCE.
Myriam DABBAS, Naziha KHEN-DUNLOP, Jean Paul DE FILIPPO, Pierre BOUGNERES, Olivier GOULET, Yann REVILLON
THE FRENCH EXPERIENCE IN BARIATRIC SURGERY “Laparoscopic adjustable gastric banding (LAGB)” IN ADOLESCENCE.
Myriam DABBAS, Naziha KHEN-DUNLOP, Jean Paul DE FILIPPO, Pierre BOUGNERES, Olivier GOULET, Yann REVILLON
P3-833
Correlation of serum fibroblast growth factor 21 levels with metabolic parameters in Korean children and adolescents
Joonwoo Baek, Hyo-Kyoung Nam, Young-Jun Rhie, Kee-Hyoung Lee
Correlation of serum fibroblast growth factor 21 levels with metabolic parameters in Korean children and adolescents
Joonwoo Baek, Hyo-Kyoung Nam, Young-Jun Rhie, Kee-Hyoung Lee
P3-834
Liver steatosis in obese children courses with enhanced insulin resistance and dyslipidemia, which are influenced by gender, puberty, race and body fat distribution.
Gabriel Á. Martos-Moreno, Julián Martínez-Villanueva, Rocío González-Leal, Sara Sirvent, Arturo Mínguez, Guillermo Martínez, Federico G. Hawkins, Jesús Argente
Liver steatosis in obese children courses with enhanced insulin resistance and dyslipidemia, which are influenced by gender, puberty, race and body fat distribution.
Gabriel Á. Martos-Moreno, Julián Martínez-Villanueva, Rocío González-Leal, Sara Sirvent, Arturo Mínguez, Guillermo Martínez, Federico G. Hawkins, Jesús Argente
P3-835
HOW EARLY ARE VASCULAR CHANGES IN OBESE CHILDREN AMONG NORTH INDIAN POPULATION?
Krishna Kishore Umapathi, Sangeeta Yadav, Sanjay Tyagi, T K Mishra
HOW EARLY ARE VASCULAR CHANGES IN OBESE CHILDREN AMONG NORTH INDIAN POPULATION?
Krishna Kishore Umapathi, Sangeeta Yadav, Sanjay Tyagi, T K Mishra
P3-836
Prader-Willi Syndrome – a general picture of 51 cases
Simone Ito, Tiago Jeronimo dos Santos, Caroline Passone, Ruth Franco, Durval Damiani
Prader-Willi Syndrome – a general picture of 51 cases
Simone Ito, Tiago Jeronimo dos Santos, Caroline Passone, Ruth Franco, Durval Damiani
P3-837
Comparison of two family-intervention (parents only versus parent and child) in the treatment of childhood obesity.
Joseph Meyerovitch, Michal Yackobovitch-Gavan, Dafna Wolf, , Moshe Phillip, Shlomit Shalitin
Comparison of two family-intervention (parents only versus parent and child) in the treatment of childhood obesity.
Joseph Meyerovitch, Michal Yackobovitch-Gavan, Dafna Wolf, , Moshe Phillip, Shlomit Shalitin
P3-838
Bioavailable Vitamin D in Obese Children: The Role of Insulin Resistance.
anna grandone, emanuele Miraglia del Giudice, Grazia Cirillo, Anna Di Sessa, Giuseppina Umano, Pierluigi Marzuillo, Carlo Capristo, Laura Perrone
Bioavailable Vitamin D in Obese Children: The Role of Insulin Resistance.
anna grandone, emanuele Miraglia del Giudice, Grazia Cirillo, Anna Di Sessa, Giuseppina Umano, Pierluigi Marzuillo, Carlo Capristo, Laura Perrone
P3-839
AGE AT MENARCHE IN RELATION TO BODY MASS INDEX. DATA FROM THE HELLENIC ACTION PLAN FOR THE ASSESSMENT, PREVENTION AND TREATMENT FOR CHILDHOOD OBESITY
ELPIS VLACHOPAPADOPOULOU, FOTINI-ELENI KARACHALIOU, THEODORA PSALTOPOULOU, DIMITRA KOUTSOUKI, YANNIS MANIOS, GRIGORIS BOGDANIS, VILEELMINI KARAGIANNI, STEFANOS MICHALACOS
AGE AT MENARCHE IN RELATION TO BODY MASS INDEX. DATA FROM THE HELLENIC ACTION PLAN FOR THE ASSESSMENT, PREVENTION AND TREATMENT FOR CHILDHOOD OBESITY
ELPIS VLACHOPAPADOPOULOU, FOTINI-ELENI KARACHALIOU, THEODORA PSALTOPOULOU, DIMITRA KOUTSOUKI, YANNIS MANIOS, GRIGORIS BOGDANIS, VILEELMINI KARAGIANNI, STEFANOS MICHALACOS
P3-840
Are age and initial BMI-SDS in obese children and adolescents associated with the BMI-SDS courses during and after the attendance of an inpatient weight-loss program (LOGIC-trial)?
Stephanie Brandt, Martin Wabitsch, Melanie Heitkamp, Barbara Geilhof, Helmut Langhof, Martin Halle, Monika Siegrist
Are age and initial BMI-SDS in obese children and adolescents associated with the BMI-SDS courses during and after the attendance of an inpatient weight-loss program (LOGIC-trial)?
Stephanie Brandt, Martin Wabitsch, Melanie Heitkamp, Barbara Geilhof, Helmut Langhof, Martin Halle, Monika Siegrist
P3-841
Turn off and turn in: the influence of television viewing and sleep on lipid profiles in children.
Despoina Manousaki, Sanyath Radji, Tracie Barnett, Marie-Eve Mathieu, Katherine Gray-Donald, Mélanie Henderson
Turn off and turn in: the influence of television viewing and sleep on lipid profiles in children.
Despoina Manousaki, Sanyath Radji, Tracie Barnett, Marie-Eve Mathieu, Katherine Gray-Donald, Mélanie Henderson
P3-842
Hepatic steatosis influences significantly the cardiovascular risk in children with metabolic syndrome
Irene Rutigliano, Gianpaolo De Filippo, Roberta Vinci, Christèle Kyheng, Agostino Petraccaro, Michele Conoscitore, Massimo Pettoello-Mantovani, Angelo Campanozzi
Hepatic steatosis influences significantly the cardiovascular risk in children with metabolic syndrome
Irene Rutigliano, Gianpaolo De Filippo, Roberta Vinci, Christèle Kyheng, Agostino Petraccaro, Michele Conoscitore, Massimo Pettoello-Mantovani, Angelo Campanozzi
P3-843
Increased GLP-1 response to oral glucose in prepubertal obese children
M. Loredana Marcovecchio, Nella Polidori, Cosimo Giannini, Tommaso De Giorgis, Francesco Chiarelli, Angelika Mohn
Increased GLP-1 response to oral glucose in prepubertal obese children
M. Loredana Marcovecchio, Nella Polidori, Cosimo Giannini, Tommaso De Giorgis, Francesco Chiarelli, Angelika Mohn
P3-844
The risk of metabolic syndrome among dyslipidemic children and adolescents.
Barbara Predieri, Giulia Colombini, Silvia Mazzoni, Patrizia Bruzzi, Laura Lucaccioni, Lorenzo Iughetti
The risk of metabolic syndrome among dyslipidemic children and adolescents.
Barbara Predieri, Giulia Colombini, Silvia Mazzoni, Patrizia Bruzzi, Laura Lucaccioni, Lorenzo Iughetti
P3-845
RNAi as tool to study molecular mechanisms of metabolic adverse reactions in Caenorhabditis elegans
Manuela Hörnle, Isabelle Hellwig, Steve Hodgkinson, Wolfgang Kaschka
RNAi as tool to study molecular mechanisms of metabolic adverse reactions in Caenorhabditis elegans
Manuela Hörnle, Isabelle Hellwig, Steve Hodgkinson, Wolfgang Kaschka
P3-846
Hypertriglicerydemia in a boy with Bardet-Biedl syndrome – case report
Malgorzata Wojcik, Katarzyna Rogulska, Dawid Piotrowski, Agata Zygmunt-Gorska, Dominika Janus, Jerzy B. Starzyk
Hypertriglicerydemia in a boy with Bardet-Biedl syndrome – case report
Malgorzata Wojcik, Katarzyna Rogulska, Dawid Piotrowski, Agata Zygmunt-Gorska, Dominika Janus, Jerzy B. Starzyk
P3-847
Uric acid and Triglycerides/HDL ratio as a predisposing factor for metabolic syndrome in children
Maria Efthymia Katsa, Anastasios Ioannidis, Sofia Zyga, Maria Tsironi, Paraskevas Koutsovitis, Athanasios Sachlas, Petros Kolovos, Maria Magana, Maria Daratsianou, Andrea Paola Rojas Gil
Uric acid and Triglycerides/HDL ratio as a predisposing factor for metabolic syndrome in children
Maria Efthymia Katsa, Anastasios Ioannidis, Sofia Zyga, Maria Tsironi, Paraskevas Koutsovitis, Athanasios Sachlas, Petros Kolovos, Maria Magana, Maria Daratsianou, Andrea Paola Rojas Gil
P3-848
Increased prevalence of 25-hydroxyvitamin D insufficiency and deficiency among overweight and obese children and adolescents in GREECE
Christos Giannios, Ioanna Farakla, Georgios Papadopoulos, Eleni Koniari, Chrysanthi Papathanasiou, Penio Kassari, Evangelia Charmandari
Increased prevalence of 25-hydroxyvitamin D insufficiency and deficiency among overweight and obese children and adolescents in GREECE
Christos Giannios, Ioanna Farakla, Georgios Papadopoulos, Eleni Koniari, Chrysanthi Papathanasiou, Penio Kassari, Evangelia Charmandari
P3-849
The triglyceride-to-high density lipoprotein cholesterol ratio in overweight Korean children
YU SUN KANG, Eun-Gyong Yoo
The triglyceride-to-high density lipoprotein cholesterol ratio in overweight Korean children
YU SUN KANG, Eun-Gyong Yoo
P3-850
Waist Height Ratio As a Marker of Obesity and Insulin Resistance in Adolescents
V. Sri Nagesh, RAKESH KUMAR SAHAY, NEELAVENI KUDUGUNTI, VISHNUVARDHAN RAO, SYED MUSTAFA HASHMI, ADITYA VIKRAM, SANIA JIWANI, SANA HYDER
Waist Height Ratio As a Marker of Obesity and Insulin Resistance in Adolescents
V. Sri Nagesh, RAKESH KUMAR SAHAY, NEELAVENI KUDUGUNTI, VISHNUVARDHAN RAO, SYED MUSTAFA HASHMI, ADITYA VIKRAM, SANIA JIWANI, SANA HYDER
P3-851
Genotype and Clinical Characteristics in Korean patients with Prader-Willi Syndrome: a single center study
Yoo-Mi Kim, Chong Kun Cheon, Su Young Kim
Genotype and Clinical Characteristics in Korean patients with Prader-Willi Syndrome: a single center study
Yoo-Mi Kim, Chong Kun Cheon, Su Young Kim
P3-852
Comparison of the insulin resistance index HOMA-IR between obese and normal children
Ghislain ROCHELEAU, Aude DEWITTE, Amelie BONNEFOND, Jacques WEILL
Comparison of the insulin resistance index HOMA-IR between obese and normal children
Ghislain ROCHELEAU, Aude DEWITTE, Amelie BONNEFOND, Jacques WEILL
P3-853
Nonalcoholic steatohepatitis leading to cirrhosis of the liver as a complication of hypothalamic disorders in a course of craniopharyngioma- case report
Urszula Watrobinska, Anna Bendysz- Golatowska, Elzbieta Moszczynska, Mieczyslaw Szalecki
Nonalcoholic steatohepatitis leading to cirrhosis of the liver as a complication of hypothalamic disorders in a course of craniopharyngioma- case report
Urszula Watrobinska, Anna Bendysz- Golatowska, Elzbieta Moszczynska, Mieczyslaw Szalecki
P3-854
Association of sleep habits and risk factors for metabolic disorders in children
Maria Magana, Sofia Zyga, Anastasios Ioannidis, Athanasios Sachlas, Maria Efthymia Katsa, Anna Maria Pistikou, Dafni Eleni Kougioumtzi Dimoliani, Maria Daratsianou, Petros Kolovos, Andrea Paola Rojas Gil
Association of sleep habits and risk factors for metabolic disorders in children
Maria Magana, Sofia Zyga, Anastasios Ioannidis, Athanasios Sachlas, Maria Efthymia Katsa, Anna Maria Pistikou, Dafni Eleni Kougioumtzi Dimoliani, Maria Daratsianou, Petros Kolovos, Andrea Paola Rojas Gil
P3-855
Plasminogen activator inhibitor-1(PAI-1) as a marker of insulin resistance in obese adolescents
Ozlem Engiz, Bulent Alioglu, Denizhan Bagrul, Jale Karakaya, Yıldız Bilge Dallar
Plasminogen activator inhibitor-1(PAI-1) as a marker of insulin resistance in obese adolescents
Ozlem Engiz, Bulent Alioglu, Denizhan Bagrul, Jale Karakaya, Yıldız Bilge Dallar
P3-856
Relationship between Visceral Obesity and Plasma Fibrinogen in Obese Children
Mona Hafez, Sahar El Masry, Noha Musa, Marwa Fathy, Mona Hassan, Nayera Hassan, Mahmoud Tareef, Mohamed El Husseiny
Relationship between Visceral Obesity and Plasma Fibrinogen in Obese Children
Mona Hafez, Sahar El Masry, Noha Musa, Marwa Fathy, Mona Hassan, Nayera Hassan, Mahmoud Tareef, Mohamed El Husseiny
P3-857
INFLUENCE OF GNRH ANALOGUE THERAPY ON BODY MASS INDEX IN GIRLS WITH PRECOCIOUS PUBERTY
Heshmat MOAYERI
INFLUENCE OF GNRH ANALOGUE THERAPY ON BODY MASS INDEX IN GIRLS WITH PRECOCIOUS PUBERTY
Heshmat MOAYERI
P3-858
Prevalence of asthma symptoms and association with obesity, sedentary lifestyle and sociodemographic factors: Data from the Hellenic National Plan for the Assessment, Prevention and Treatment of Childhood Obesity
Feneli Karachaliou, Elpis Vlachopapadopoulou, Theodora Psaltopoulou, Dimitra Koutsouki, Ioannis Manios, Grigoris Bogdanis, Theodoros Sergentanis, Ioannis Panagiotopoulos, Anastasia Papadopoulou, Agelos Chatzakis, Stefanos Michalakos
Prevalence of asthma symptoms and association with obesity, sedentary lifestyle and sociodemographic factors: Data from the Hellenic National Plan for the Assessment, Prevention and Treatment of Childhood Obesity
Feneli Karachaliou, Elpis Vlachopapadopoulou, Theodora Psaltopoulou, Dimitra Koutsouki, Ioannis Manios, Grigoris Bogdanis, Theodoros Sergentanis, Ioannis Panagiotopoulos, Anastasia Papadopoulou, Agelos Chatzakis, Stefanos Michalakos
P3-859
Long-term effects of neonatal over-nutrition on metabolic equilibrium are age and sex dependant
Pilar Argente-Arizón, Purificación Ros, Francisca Díaz, Esther Fuente-Martín, Vicente Barrios, Julie A. Chowen, Jesús Argente
Long-term effects of neonatal over-nutrition on metabolic equilibrium are age and sex dependant
Pilar Argente-Arizón, Purificación Ros, Francisca Díaz, Esther Fuente-Martín, Vicente Barrios, Julie A. Chowen, Jesús Argente
P3-860
Metabolic syndrome in Greek adolescents and the effect of six-month educational/behavioral school interventions
Flora Bacopoulou, Vassiliki Efthymiou, Maria Papaefthymiou, Georgios Landis, George Palaiologos, Maria Kaklea, Ioannis Papassotiriou, George Chrousos
Metabolic syndrome in Greek adolescents and the effect of six-month educational/behavioral school interventions
Flora Bacopoulou, Vassiliki Efthymiou, Maria Papaefthymiou, Georgios Landis, George Palaiologos, Maria Kaklea, Ioannis Papassotiriou, George Chrousos
P3-861
Decreased insulin sensitivity and secretion in obese youth with high OGTT derived one hour blood glucose
M. Loredana M. Loredana, Elsa Marisi, Ilaria Di Giovanni, Chiara De Leonibus, Francesco Chiarelli, Angelika Mohn
Decreased insulin sensitivity and secretion in obese youth with high OGTT derived one hour blood glucose
M. Loredana M. Loredana, Elsa Marisi, Ilaria Di Giovanni, Chiara De Leonibus, Francesco Chiarelli, Angelika Mohn
P3-862
Diagnosis and treatment of familial hypercholesterolemia in children – a preliminary report.
Agnieszka Brandt, Joanna Bautembach-Minkowska, Matylda Hennig, Bartosz Wasąg, Janusz Limon, Małgorzata Myśliwiec
Diagnosis and treatment of familial hypercholesterolemia in children – a preliminary report.
Agnieszka Brandt, Joanna Bautembach-Minkowska, Matylda Hennig, Bartosz Wasąg, Janusz Limon, Małgorzata Myśliwiec
P3-863
Metabolic syndrome risk factors in obese children and adolescents
Shahnoza Azimova, Gulnora Rakhimova
Metabolic syndrome risk factors in obese children and adolescents
Shahnoza Azimova, Gulnora Rakhimova
P3-864
A Systemic Approach for the Management of the Program entitled “Development of a National System for the Prevention and Management of Overweight and Obesity in Childhood and Adolescence in Greece”
Penio Kassari, Panagiotis Papaioannou, Evangelia Charmandari
A Systemic Approach for the Management of the Program entitled “Development of a National System for the Prevention and Management of Overweight and Obesity in Childhood and Adolescence in Greece”
Penio Kassari, Panagiotis Papaioannou, Evangelia Charmandari
P3-865
Waist circumference to body height (WHtR) is a suitable measure of cardiovascular risk in overweight and obese children.
Vira Yakovenko, Ulrike Teufel, Laura Henn, Markus Bettendorf, Georg F. Hoffmann, Juergen Grulich-Henn
Waist circumference to body height (WHtR) is a suitable measure of cardiovascular risk in overweight and obese children.
Vira Yakovenko, Ulrike Teufel, Laura Henn, Markus Bettendorf, Georg F. Hoffmann, Juergen Grulich-Henn
P3-866
The Effectiveness of a Comprehensive and Personalized Plan of Action in the Prevention and Management of Overweight and Obesity in Childhood and Adolescence
George Papadopoulos, Ioanna Farakla, Sophia Bakopoulou, Christos Giannios, Eleni Koui, Alexandra Georgiou, Stamatis Romas, Eleni Terzioglou, Eleni Koniari, Chryssanthi Papathanasiou, Penio Kassari, Nicolas Nicolaides, Elena Critselis, Yannis Manios, Evangelia Charmandari
The Effectiveness of a Comprehensive and Personalized Plan of Action in the Prevention and Management of Overweight and Obesity in Childhood and Adolescence
George Papadopoulos, Ioanna Farakla, Sophia Bakopoulou, Christos Giannios, Eleni Koui, Alexandra Georgiou, Stamatis Romas, Eleni Terzioglou, Eleni Koniari, Chryssanthi Papathanasiou, Penio Kassari, Nicolas Nicolaides, Elena Critselis, Yannis Manios, Evangelia Charmandari
P3-867
Insulin resistance in adolescents with screen addiction and attention-deficit/hyperactivity disorder
Ozge Koprulu, Sukran Darcan, Burcu Ozbaran, Emsal Ata, Yasemin Altinok, Samim Ozen, Damla Goksen
Insulin resistance in adolescents with screen addiction and attention-deficit/hyperactivity disorder
Ozge Koprulu, Sukran Darcan, Burcu Ozbaran, Emsal Ata, Yasemin Altinok, Samim Ozen, Damla Goksen
P3-869
Severe hypothalamic obesity in a girl with craniopharyngioma – case report.
Monika Obara-Moszynska, Marek Harat, Marek Niedziela
Severe hypothalamic obesity in a girl with craniopharyngioma – case report.
Monika Obara-Moszynska, Marek Harat, Marek Niedziela
P3-870
The changes of neuroendocrine status in children with different forms of obesity
Olga Zagrebaeva, Anzhalika Solntsava, Hanna Mikhno, Helena Dashkevich
The changes of neuroendocrine status in children with different forms of obesity
Olga Zagrebaeva, Anzhalika Solntsava, Hanna Mikhno, Helena Dashkevich
P3-871
Body composition and metabolic risk factors in preschool children.
Mina Lateva, Ralitsa Popova, Sonya Galcheva, Miglena Georgieva, Violeta Iotova
Body composition and metabolic risk factors in preschool children.
Mina Lateva, Ralitsa Popova, Sonya Galcheva, Miglena Georgieva, Violeta Iotova
P3-872
Evaluation of alternatives to OGTT to assess glucose intolerance and diabetes in an obese paediatric population
Eglantine Elowe-Gruau, Thérèse Bouthors, Gael Vadnaï, Mihaela Buzduga, Daniel Laufer, Manuela Decarli, Sylvie Borloz, Sophie Stoppa-Vaucher, Franziska Phan-Hug, Michael Hauschild, Nelly Pitteloud
Evaluation of alternatives to OGTT to assess glucose intolerance and diabetes in an obese paediatric population
Eglantine Elowe-Gruau, Thérèse Bouthors, Gael Vadnaï, Mihaela Buzduga, Daniel Laufer, Manuela Decarli, Sylvie Borloz, Sophie Stoppa-Vaucher, Franziska Phan-Hug, Michael Hauschild, Nelly Pitteloud
P3-873
Sex differences in the response to high fat diet intake during adolescence
Alejandra Freire-Regatillo, Pilar Argente-ARizón, Francisca Diaz, Vicente Barrios, Angeles Arevalo, Jesús Argente, Luis Miguel García-Segura, Iñigo Azcoitia, Julie A. Chowen
Sex differences in the response to high fat diet intake during adolescence
Alejandra Freire-Regatillo, Pilar Argente-ARizón, Francisca Diaz, Vicente Barrios, Angeles Arevalo, Jesús Argente, Luis Miguel García-Segura, Iñigo Azcoitia, Julie A. Chowen
P3-874
RELATION BETWEEN THYROID FUNCTION TESTS AND CARDIOMETABOLIC RISK FACTORS IN CHILDHOOD OBESITY
Dogus Vuralli, Esra Tapci, Yildiz Bilge Dallar
RELATION BETWEEN THYROID FUNCTION TESTS AND CARDIOMETABOLIC RISK FACTORS IN CHILDHOOD OBESITY
Dogus Vuralli, Esra Tapci, Yildiz Bilge Dallar
P3-875
İnsulin infusion treatment option in severe hypertriglyceridemia induced pancreatitis
Ala Üstyol, Mehmet Emre Atabek, Hasan Ali Yüksekkaya, Meltem Dorum
İnsulin infusion treatment option in severe hypertriglyceridemia induced pancreatitis
Ala Üstyol, Mehmet Emre Atabek, Hasan Ali Yüksekkaya, Meltem Dorum
P3-876
Obesity has a significant impact on hyperandrogenemia only after puberty in Korean girls
Min Jae Kang, Young Suk Shim, Yeon Joung Oh, Il Tae Hwang, Seung Yang
Obesity has a significant impact on hyperandrogenemia only after puberty in Korean girls
Min Jae Kang, Young Suk Shim, Yeon Joung Oh, Il Tae Hwang, Seung Yang
P3-877
Higher Hb1Ac in Obese Prader-Willi Syndrome patients versus Obese controls
Caroline Passone, Tiago Jeronimo dos Santos, Simone Sakura Ito, Marina Ybarra, Louise Cominato, Ruth Franco, Durval Damiani
Higher Hb1Ac in Obese Prader-Willi Syndrome patients versus Obese controls
Caroline Passone, Tiago Jeronimo dos Santos, Simone Sakura Ito, Marina Ybarra, Louise Cominato, Ruth Franco, Durval Damiani
P3-878
Obese children and adolescents: Reasons for non-compliance with follow-up scheduling
Chrysoula Drosatou, Elpis-Athina Vlachopapadopoulou, Feneli Karachaliou, Eirini Dikaiakou, Elli Anagnostou, Ioanna Patinioti, Vassilios Petrou, Stefanos Michalakos
Obese children and adolescents: Reasons for non-compliance with follow-up scheduling
Chrysoula Drosatou, Elpis-Athina Vlachopapadopoulou, Feneli Karachaliou, Eirini Dikaiakou, Elli Anagnostou, Ioanna Patinioti, Vassilios Petrou, Stefanos Michalakos
P3-879
Cardiometabolic risk factors in overweight/obese children and adolescents and family history of cardiovascular disease
Zacharoula Karabouta, Dimitrios Papandreou, Areti Makedou, Israel Rousso, Fani Athanassiadou-Piperopoulou
Cardiometabolic risk factors in overweight/obese children and adolescents and family history of cardiovascular disease
Zacharoula Karabouta, Dimitrios Papandreou, Areti Makedou, Israel Rousso, Fani Athanassiadou-Piperopoulou
P3-880
Healthcare professionals’ perception of overweight in preschool-aged children.
Gianni Bocca, Eva Corpeleijn, Jasper Broens, Ronald Stolk, Pieter Sauer
Healthcare professionals’ perception of overweight in preschool-aged children.
Gianni Bocca, Eva Corpeleijn, Jasper Broens, Ronald Stolk, Pieter Sauer
P3-881
EVALUATION OF THE RELATIONSHIP BETWEEN SERUM ADROPIN LEVELS AND BLOOD PRESSURE IN OBESE CHILDREN
Ayça Altıncık, Oya Sayın
EVALUATION OF THE RELATIONSHIP BETWEEN SERUM ADROPIN LEVELS AND BLOOD PRESSURE IN OBESE CHILDREN
Ayça Altıncık, Oya Sayın
P3-882
Adipocyte fatty acid binding protein (aFABP) is related to weight status and metabolic risk markers in childhood obesity
Jakob Kaepplinger, David Petroff, Sabine Herget, Sandra Reichardt, Andrea Grimm, Jürgen Kratzsch, Susann Blüher
Adipocyte fatty acid binding protein (aFABP) is related to weight status and metabolic risk markers in childhood obesity
Jakob Kaepplinger, David Petroff, Sabine Herget, Sandra Reichardt, Andrea Grimm, Jürgen Kratzsch, Susann Blüher
P3-883
Investigating predisposing factors for childhood obesity
Maria Magana, Kleopatra Routsi, Sofia Zyga, George Panoutsopoulos, Anastasios Ioannidis, Maria Tsironi,, Anna-Maria Pistikou, Dafni-Eleni Kougioumtzi-Dimoliani, Petros Kolovos, Andrea Paola Rojas Gil
Investigating predisposing factors for childhood obesity
Maria Magana, Kleopatra Routsi, Sofia Zyga, George Panoutsopoulos, Anastasios Ioannidis, Maria Tsironi,, Anna-Maria Pistikou, Dafni-Eleni Kougioumtzi-Dimoliani, Petros Kolovos, Andrea Paola Rojas Gil
P3-884
Vitamin D status in Iranian obese and non-obese children
Fatemeh Sayarifard, Yasaman Motlaghzadeh, Azadeh Sayarifard, Bahar Allahverdi
Vitamin D status in Iranian obese and non-obese children
Fatemeh Sayarifard, Yasaman Motlaghzadeh, Azadeh Sayarifard, Bahar Allahverdi
P3-885
IS VITAMIN D IMPORTANT PLAYER IN HEPATOSTEATOSIS IN CHILDHOOD OBESITY ?
Elif Ozsu, Feyza Nur Topcu, Derya Acar Tepe
IS VITAMIN D IMPORTANT PLAYER IN HEPATOSTEATOSIS IN CHILDHOOD OBESITY ?
Elif Ozsu, Feyza Nur Topcu, Derya Acar Tepe
P3-886
Obesity in school children of Zahedan-Iran; double burden of weight disorders
Fahimeh Soheilipour, Zeinab Pourzahabi, Maryam Lotfi, Maziar Moradi-Lakeh, Atefeh Ghanbari Jolfaie
Obesity in school children of Zahedan-Iran; double burden of weight disorders
Fahimeh Soheilipour, Zeinab Pourzahabi, Maryam Lotfi, Maziar Moradi-Lakeh, Atefeh Ghanbari Jolfaie
P3-887
Sports regulated and lipid profile in children and adolescents with overweight
Rosaura Leis Trabazo, Rocío Vázquez Cobela, Concepción Aguilera García, Gloria Bueno Lozano, Josune Olza Meneses, Mercedes Gil Campos, Juan José Bedoya Carpente, Lidia Castro Feijoo, Luis Moreno Aznar, Angel Gil Hernández
Sports regulated and lipid profile in children and adolescents with overweight
Rosaura Leis Trabazo, Rocío Vázquez Cobela, Concepción Aguilera García, Gloria Bueno Lozano, Josune Olza Meneses, Mercedes Gil Campos, Juan José Bedoya Carpente, Lidia Castro Feijoo, Luis Moreno Aznar, Angel Gil Hernández
P3-888
Weight and the factors influencing it in a cohort of school aged children
Raluca Pop, Oana Capraru, Ionela Pascanu
Weight and the factors influencing it in a cohort of school aged children
Raluca Pop, Oana Capraru, Ionela Pascanu
P3-890
Does vitamin D influence energy metabolism in children and adolescents?
Anna Wedrychowicz, Krystyna Sztefko, Jerzy Starzyk
Does vitamin D influence energy metabolism in children and adolescents?
Anna Wedrychowicz, Krystyna Sztefko, Jerzy Starzyk
P3-891
Bone age assessment and glucose metabolism in overweight and obese children
Corina Paul, Mirela Mogoi, Iulian Velea
Bone age assessment and glucose metabolism in overweight and obese children
Corina Paul, Mirela Mogoi, Iulian Velea
P3-892
The triglyceride-to-HDL cholesterol ratio is associated with insulin resistance in obese boys but not in obese girls
Guy Massa, Liene Bervoets, Jonas Massa, Renate Zeevaert
The triglyceride-to-HDL cholesterol ratio is associated with insulin resistance in obese boys but not in obese girls
Guy Massa, Liene Bervoets, Jonas Massa, Renate Zeevaert
P3-893
Experience with sleeve gastrectomy in adolescent obese subjects and in Prader-Willi Syndrome
Danilo Fintini, Sarah Bocchini, Romina Caccamo, Graziano Grugni, Marco Cappa, Francesco De Peppo, Antonino Crinò
Experience with sleeve gastrectomy in adolescent obese subjects and in Prader-Willi Syndrome
Danilo Fintini, Sarah Bocchini, Romina Caccamo, Graziano Grugni, Marco Cappa, Francesco De Peppo, Antonino Crinò
P3-894
Metabolic syndrome and inflammatory markers in obese children
at Chiang Mai University Hospital
Watchareewan Sontichai, Prapai Dejkhamron, Kevalee Unachak, Prachya Kongtaweelert
Metabolic syndrome and inflammatory markers in obese children
at Chiang Mai University Hospital
Watchareewan Sontichai, Prapai Dejkhamron, Kevalee Unachak, Prachya Kongtaweelert
P3-895
Evaluating liver enzymes and cholesterol levels in newly diagnosed obese children attending the University of Port Harcourt Teaching Hospital
IRORO YARHERE, TAMUNOPRIYE JAJA
Evaluating liver enzymes and cholesterol levels in newly diagnosed obese children attending the University of Port Harcourt Teaching Hospital
IRORO YARHERE, TAMUNOPRIYE JAJA
P3-896
Prevalence of excess weight in adolescents at primary health care units in South Brazil.
Deisi Maria Vargas, Ana Carolina Santin de Medeiros, Elis Klieman, Isabel Eberhardt, Vera Janete Piesanti, Simone Pasa, Claudia Regina Lima Duarte da Silva, Luciane Azevedo Coutinho, Vilma Margarete Simão
Prevalence of excess weight in adolescents at primary health care units in South Brazil.
Deisi Maria Vargas, Ana Carolina Santin de Medeiros, Elis Klieman, Isabel Eberhardt, Vera Janete Piesanti, Simone Pasa, Claudia Regina Lima Duarte da Silva, Luciane Azevedo Coutinho, Vilma Margarete Simão
P3-897
Effect of overweight and obesity on spinal deformities for children 5-7 years
marzieh aghaei, javad shapoori
Effect of overweight and obesity on spinal deformities for children 5-7 years
marzieh aghaei, javad shapoori
P3-898
A Case of rapid Onset Obesity, hypoventilation, hypothalamic dysregulation and neuroendocrine tumours-ROHHADNET syndrome
Navoda Atapattu, Lalitha Dissanayaka, S Arulmoli
A Case of rapid Onset Obesity, hypoventilation, hypothalamic dysregulation and neuroendocrine tumours-ROHHADNET syndrome
Navoda Atapattu, Lalitha Dissanayaka, S Arulmoli
P3-899
The influence of physical activity and physical fitness in the metabolic profile and microcirculation of eutrophic, overweight and obese children 5 to 12 years of age
Jociene Terra da Penha, Fernanda Mussi Gazolla, Cecilia Noronha de Miranda Carvalho, Isabel Rey Madeira, Flavio Rodrigues Jr., Elisabeth de Amorim Machado, Fernando Lencastre Sicuro, Paulo de Tarso Veras Farinatti, Paulo Ferrez Collett-Solberg
The influence of physical activity and physical fitness in the metabolic profile and microcirculation of eutrophic, overweight and obese children 5 to 12 years of age
Jociene Terra da Penha, Fernanda Mussi Gazolla, Cecilia Noronha de Miranda Carvalho, Isabel Rey Madeira, Flavio Rodrigues Jr., Elisabeth de Amorim Machado, Fernando Lencastre Sicuro, Paulo de Tarso Veras Farinatti, Paulo Ferrez Collett-Solberg
P3-900
PREDICTING EARLY CARDIOVASCULAR RISK IN OBESE CHILDREN BASED ON ANTHROPOMETRY
Claudia Cipollone, Alessandra Piccorossi, Annarita Antenucci, Carla Greco, Stefania Lasorella, Giovanni Farello
PREDICTING EARLY CARDIOVASCULAR RISK IN OBESE CHILDREN BASED ON ANTHROPOMETRY
Claudia Cipollone, Alessandra Piccorossi, Annarita Antenucci, Carla Greco, Stefania Lasorella, Giovanni Farello
P3-901
Metabolic syndrome rates among adolescents of the Greek school community.
Eleni Kotanidou, Angeliki Kleisarchaki, Konstantina Mouzaki, Paraskevi Kokka, Ioannis Kyrgios, Iro Tsara, Efthimia Efstratiou, Anna-Bettina Haidich, Vagia Papageorgiou, Maria Eboriadou-Petikopoulou, Assimina Galli-Tsinopoulou
Metabolic syndrome rates among adolescents of the Greek school community.
Eleni Kotanidou, Angeliki Kleisarchaki, Konstantina Mouzaki, Paraskevi Kokka, Ioannis Kyrgios, Iro Tsara, Efthimia Efstratiou, Anna-Bettina Haidich, Vagia Papageorgiou, Maria Eboriadou-Petikopoulou, Assimina Galli-Tsinopoulou
P3-902
Identification and Management of Obesity by General Paediatricians in the UK.
Madhu Easwariah, Jake Mann, Rajiv Goonetilleke
Identification and Management of Obesity by General Paediatricians in the UK.
Madhu Easwariah, Jake Mann, Rajiv Goonetilleke
P3-905
Potential connection of dyslipidemia with BMI and associated disorders in obese children and adolescents
Lusine Navasardyan, Renata Markosyan
Potential connection of dyslipidemia with BMI and associated disorders in obese children and adolescents
Lusine Navasardyan, Renata Markosyan
P3-906
Deficiency of 25- (OH) D-vitamin in adolescents with obesity.
Mariia Matveeva, Julia Samoylova
Deficiency of 25- (OH) D-vitamin in adolescents with obesity.
Mariia Matveeva, Julia Samoylova
P3-907
THE CORRELATION STUDY ON CHILDHOOD OBESITY, INSULIN RESISTANCE
AND ANDROGENS
Feng Xiong, Yu-Qing Zhang, Xiao-Yan Ding, Dong-Gang Wang, Min Zhu
THE CORRELATION STUDY ON CHILDHOOD OBESITY, INSULIN RESISTANCE
AND ANDROGENS
Feng Xiong, Yu-Qing Zhang, Xiao-Yan Ding, Dong-Gang Wang, Min Zhu
P3-908
The prevalence of obesity in children and adolescents in the Udmurt Republic
Tatiana Kovalenko, Maria Larionova
The prevalence of obesity in children and adolescents in the Udmurt Republic
Tatiana Kovalenko, Maria Larionova
P3-909
Survey Serum 25-Hdroxyvitamin D concentration in obese children and clinical significance in chinese population
Yu YANG, Lei XU
Survey Serum 25-Hdroxyvitamin D concentration in obese children and clinical significance in chinese population
Yu YANG, Lei XU
P3-910
CLINICO-BIOCHEMICAL CORRELATION AMONG CHILDREN WITH OBESITY AND METABOLIC SYNDROME
Sangita Yadav, Krishna Kishore Umapathi, T K Mishra
CLINICO-BIOCHEMICAL CORRELATION AMONG CHILDREN WITH OBESITY AND METABOLIC SYNDROME
Sangita Yadav, Krishna Kishore Umapathi, T K Mishra
P3-912
IN DIFFERENT METHOD OF THE EVALUATION
OF STATE OF FEELING
( cognitive functions/ socioemotional adaptation)
OF OBESE CHILDREN;
Goodenough Harris ‘The Draw-A-Person’ Test
Ayça Törel Ergür, Gaye Aşık Kırdağ, Seda Uçar
IN DIFFERENT METHOD OF THE EVALUATION
OF STATE OF FEELING
( cognitive functions/ socioemotional adaptation)
OF OBESE CHILDREN;
Goodenough Harris ‘The Draw-A-Person’ Test
Ayça Törel Ergür, Gaye Aşık Kırdağ, Seda Uçar
P3-913
Phenotypic study of obesity in children and adolescents
Soumeya nora Fedala, Ali el mahdi Haddam, leyla ahmed ali, djamila meskine, farida chentli
Phenotypic study of obesity in children and adolescents
Soumeya nora Fedala, Ali el mahdi Haddam, leyla ahmed ali, djamila meskine, farida chentli
P3-914
Association of serum levels of 25(OH)cholecalciferol and childhood obesity
Maria Laura Iezzi, Gaia Varriale, Anastasios Megalooikonomou, Simona Di Loreto, Luca Zagaroli, Nunzia Torge
Association of serum levels of 25(OH)cholecalciferol and childhood obesity
Maria Laura Iezzi, Gaia Varriale, Anastasios Megalooikonomou, Simona Di Loreto, Luca Zagaroli, Nunzia Torge
P3-915
Comparison of lipid profile in active and non active obese children IN Qom -Iran
javad shapoori, marzieh aghaei
Comparison of lipid profile in active and non active obese children IN Qom -Iran
javad shapoori, marzieh aghaei
LBP-1260
Decreased AMY1 gene copy number is associated with increased obesity risk in a population of Caucasian school-children
M. Loredana Marcovecchio, Rosalba Florio, Fabio Verginelli, Laura De Lellis, Delfina Verzilli, Francesco Chiarelli, Alessandro Cama, Angelika Mohn
Decreased AMY1 gene copy number is associated with increased obesity risk in a population of Caucasian school-children
M. Loredana Marcovecchio, Rosalba Florio, Fabio Verginelli, Laura De Lellis, Delfina Verzilli, Francesco Chiarelli, Alessandro Cama, Angelika Mohn
P1-58
Long-Term Endocrine Outcome In Men With Partial Androgen Insensitivity Syndrome
Angela K Lucas-Herald, S Faisal Ahmed, Silvano Bertelloni, Anders Juul, Jillian Bryce, Jipu Jiang, Martina Rodie, Marie L Johansen, Olaf Hiort, Paul-Martin Holterhus, Martine Cools, An Desloovere, Naomi Weintrob, Sabine E Hannema, Tulay Guran, Feyzad Darendeliler, Anna Nordenstrom, Ieuan Hughes
Long-Term Endocrine Outcome In Men With Partial Androgen Insensitivity Syndrome
Angela K Lucas-Herald, S Faisal Ahmed, Silvano Bertelloni, Anders Juul, Jillian Bryce, Jipu Jiang, Martina Rodie, Marie L Johansen, Olaf Hiort, Paul-Martin Holterhus, Martine Cools, An Desloovere, Naomi Weintrob, Sabine E Hannema, Tulay Guran, Feyzad Darendeliler, Anna Nordenstrom, Ieuan Hughes
P1-59
Novel Genetic Associations In Children With Disorders Of Sex Development (DSD) And Neurodevelopment Disorders – Insights From The Deciphering Developmental Disorders (DDD) Study
Gabriella Gazdagh, DDD Study, Edward S. Tobias, S. Faisal Ahmed, Ruth McGowan
Novel Genetic Associations In Children With Disorders Of Sex Development (DSD) And Neurodevelopment Disorders – Insights From The Deciphering Developmental Disorders (DDD) Study
Gabriella Gazdagh, DDD Study, Edward S. Tobias, S. Faisal Ahmed, Ruth McGowan
P1-60
Insight into the Human Ovarian Sex Development Networks
Leila Bouazzi, Mariangela Franco, Wassim Eid, Monika Meyer-Böni, Patrick Sproll, Alexander Maret, Anna Lauber-Biason
Insight into the Human Ovarian Sex Development Networks
Leila Bouazzi, Mariangela Franco, Wassim Eid, Monika Meyer-Böni, Patrick Sproll, Alexander Maret, Anna Lauber-Biason
P1-61
Current Models Of Practice & Professional Development Of Clinicians In DSD Centres – Results From An International Survey Of Specialist Care For DSD.
Andreas Kyriakou, Arianne B Dessens, Jillian Bryce, Ira Haraldsen, Violeta Iotova, Anders Juul, Maciej Krawczynski, Agneta Nordenskjöld, Marta Rozas, Caroline Sanders, Olaf Hiort, S Faisal Ahmed
Current Models Of Practice & Professional Development Of Clinicians In DSD Centres – Results From An International Survey Of Specialist Care For DSD.
Andreas Kyriakou, Arianne B Dessens, Jillian Bryce, Ira Haraldsen, Violeta Iotova, Anders Juul, Maciej Krawczynski, Agneta Nordenskjöld, Marta Rozas, Caroline Sanders, Olaf Hiort, S Faisal Ahmed
P1-62
Prediction of germ cell cancer occurrence in postpubertal individuals with androgen insensitivity based on pathological findings and cancer predisposition SNPs
Martine Cools, Katja P Wolffenbuttel, Jana Kaprova, Berenice B Mendonca, Sten LS Drop, Remko Hersmus, Hans Stoop, Ad JM Gillis, Elaine MF Costa, Soraiah Domenice, Lutsz Wunsch, Charmian Quigley, Wiebke Arlt, Guy T'Sjoen, Leendert HJ Looijenga
Prediction of germ cell cancer occurrence in postpubertal individuals with androgen insensitivity based on pathological findings and cancer predisposition SNPs
Martine Cools, Katja P Wolffenbuttel, Jana Kaprova, Berenice B Mendonca, Sten LS Drop, Remko Hersmus, Hans Stoop, Ad JM Gillis, Elaine MF Costa, Soraiah Domenice, Lutsz Wunsch, Charmian Quigley, Wiebke Arlt, Guy T'Sjoen, Leendert HJ Looijenga
P1-63
Gender identity prediction in adulthood by HTP test (House-Tree-Family) in 46, XY DSD patients
Rafael Loch Batista, Marlene Inacio, Ari Oliveira Jr, Vinicius N Brito, Elaine M F Costa, Sorahia Domenice, Berenice B Mendonça
Gender identity prediction in adulthood by HTP test (House-Tree-Family) in 46, XY DSD patients
Rafael Loch Batista, Marlene Inacio, Ari Oliveira Jr, Vinicius N Brito, Elaine M F Costa, Sorahia Domenice, Berenice B Mendonça
P1-64
MAMLD1 mutations seem not sufficient to explain a 46,XY DSD phenotype. What else?
Núria Camats, Mónica Fernández-Cancio, Laura Audí, Primus E Mullis, Francisca Moreno, Isabel González Casado, Juan Pedro López-Siguero, Raquel Corripio, José Antonio Bermúdez de la Vega, José Antonio Blanco, Christa E Flück
MAMLD1 mutations seem not sufficient to explain a 46,XY DSD phenotype. What else?
Núria Camats, Mónica Fernández-Cancio, Laura Audí, Primus E Mullis, Francisca Moreno, Isabel González Casado, Juan Pedro López-Siguero, Raquel Corripio, José Antonio Bermúdez de la Vega, José Antonio Blanco, Christa E Flück
P1-65
Subcutaneous continuous administration of recombinant human luteinizing and follicle-stimulating hormones is an effective treatment for micropenis during the mini-puberty
Athanasia Stoupa, Dinane Samara-Boustani, Isabelle Flechtner, Graziella Pinto, Isabelle Jourdon, Kathleen Laborde, Didier Chevenne, Anne-Elodie Millischer-Bellaiche, Michel Polak, Jacques Beltrand
Subcutaneous continuous administration of recombinant human luteinizing and follicle-stimulating hormones is an effective treatment for micropenis during the mini-puberty
Athanasia Stoupa, Dinane Samara-Boustani, Isabelle Flechtner, Graziella Pinto, Isabelle Jourdon, Kathleen Laborde, Didier Chevenne, Anne-Elodie Millischer-Bellaiche, Michel Polak, Jacques Beltrand
P1-66
46,XX ovotesticular DSD in the absence of SRY gene associated to SOX3 duplication
Romina P. Grinspon, Julián Nevado, María de los Angeles Mori Alvarez, Rodolfo A. Rey, Graciela del Rey, Ana Chiesa
46,XX ovotesticular DSD in the absence of SRY gene associated to SOX3 duplication
Romina P. Grinspon, Julián Nevado, María de los Angeles Mori Alvarez, Rodolfo A. Rey, Graciela del Rey, Ana Chiesa
P2-303
Multiple malformations extending the phenotypic spectrum of Antley-Bixler syndrome in a patient with P450 oxidoreductase deficiency due to two novel mutations of the POR gene
Aleksandra Janchevska, Jan Idkowiak, Elisabeta Caredda, Jane Hurst, Mehul T. Dattani, Wiebke Arlt, Helen A. Spoudeas
Multiple malformations extending the phenotypic spectrum of Antley-Bixler syndrome in a patient with P450 oxidoreductase deficiency due to two novel mutations of the POR gene
Aleksandra Janchevska, Jan Idkowiak, Elisabeta Caredda, Jane Hurst, Mehul T. Dattani, Wiebke Arlt, Helen A. Spoudeas
P2-304
A novel homozygous missense mutation in RSPO1 associated with a familial case of 46,XX testicular and ovotesticular DSD
Yassine Naasse, Farida Jennane, Sibai Hicham, Ken McElreavey, Anu Bashamboo
A novel homozygous missense mutation in RSPO1 associated with a familial case of 46,XX testicular and ovotesticular DSD
Yassine Naasse, Farida Jennane, Sibai Hicham, Ken McElreavey, Anu Bashamboo
P2-305
“www.steroidogenicfactor-1.info”: An online database of variants in steroidogenic factor-1 (SF-1, NR5A1) and resource for families and professional healthcare providers
Jenifer Suntharalingham, Federica Buonocore, Andrew Duncan, John Achermann
“www.steroidogenicfactor-1.info”: An online database of variants in steroidogenic factor-1 (SF-1, NR5A1) and resource for families and professional healthcare providers
Jenifer Suntharalingham, Federica Buonocore, Andrew Duncan, John Achermann
P2-306
Two testes and 2 X chromosomes – Why?
AL JASER, FAHED, WHERRETT, DIANE. Division of Endocrinology, Department of Pediatrics,
Hospital for Sick Children, University of Toronto, ON.
Fahed Aljaser, Diane Wherrett
Two testes and 2 X chromosomes – Why?
AL JASER, FAHED, WHERRETT, DIANE. Division of Endocrinology, Department of Pediatrics,
Hospital for Sick Children, University of Toronto, ON.
Fahed Aljaser, Diane Wherrett
P2-307
Diagnostic Approach To A Newborn With Suspected DSD - Results From An International Survey Of Specialist Care For DSD.
Andreas Kyriakou, Arianne B Dessens, Jillian Bryce, Ira Haraldsen, Violeta Iotova, Anders Juul, Maciej Krawczynski, Agneta Nordenskjöld, Marta Rozas, Caroline Sanders, Olaf Hiort, S Faisal Ahmed
Diagnostic Approach To A Newborn With Suspected DSD - Results From An International Survey Of Specialist Care For DSD.
Andreas Kyriakou, Arianne B Dessens, Jillian Bryce, Ira Haraldsen, Violeta Iotova, Anders Juul, Maciej Krawczynski, Agneta Nordenskjöld, Marta Rozas, Caroline Sanders, Olaf Hiort, S Faisal Ahmed
P2-308
MAP3K1 mutation in a patient with complete XY gonadal dysgenesis
Birgit Köhler, Nicole Gehrmann, Annette Grüters-Kieslich, Joelle Bignon-Topalovic, Kenneth McElreavey, Anu Bashamboo
MAP3K1 mutation in a patient with complete XY gonadal dysgenesis
Birgit Köhler, Nicole Gehrmann, Annette Grüters-Kieslich, Joelle Bignon-Topalovic, Kenneth McElreavey, Anu Bashamboo
P2-309
Alterations in Germ Cell Memory and Mini-Puberty Induce Infertility in Cryptorchidism
Faruk Hadziselimovic, Maria-Jose Docampo-Garcia, Nils Hadziselimovic, Gunthild Kray, Philipp Demougin
Alterations in Germ Cell Memory and Mini-Puberty Induce Infertility in Cryptorchidism
Faruk Hadziselimovic, Maria-Jose Docampo-Garcia, Nils Hadziselimovic, Gunthild Kray, Philipp Demougin
P2-310
Management of gonads in adults with androgen insensitivity: an international survey
Ellen Maris, LHJ Looijenga, Martine Cools
Management of gonads in adults with androgen insensitivity: an international survey
Ellen Maris, LHJ Looijenga, Martine Cools
P2-311
The localization of cells with XX and XY in gonadal tissues associated with ovotesticular disorder of sexual development with a 46,XX/46,XY karyotype
Noriko Nishina, Ryuji Fukuzawa, Tomohiro Ishii, Tomonobu Hasegawa, Yukihiro Hasegawa
The localization of cells with XX and XY in gonadal tissues associated with ovotesticular disorder of sexual development with a 46,XX/46,XY karyotype
Noriko Nishina, Ryuji Fukuzawa, Tomohiro Ishii, Tomonobu Hasegawa, Yukihiro Hasegawa
P2-312
Birth Weight in Different Aetiologies of Disorder of Sex Development
Sukran Poyrazoglu, Feyza Darendeliler, Syed Faisal Ahmed, Jillian Bryce, Jipu Jiang, Martina Rodie, Olaf Hiort, Sabine E. Hannema, Silvano Bertelloni, Lidka Lisa, Tulay Guran, Ieuan Hughes, Martine Cools, Pierre Chatelain, Hedi L. Claahsen-van der Grinten, Anna Nordenstrom, Paul-Martin Holterhus, Birgit Köhler, Marek Niedziela, Nils Krone
Birth Weight in Different Aetiologies of Disorder of Sex Development
Sukran Poyrazoglu, Feyza Darendeliler, Syed Faisal Ahmed, Jillian Bryce, Jipu Jiang, Martina Rodie, Olaf Hiort, Sabine E. Hannema, Silvano Bertelloni, Lidka Lisa, Tulay Guran, Ieuan Hughes, Martine Cools, Pierre Chatelain, Hedi L. Claahsen-van der Grinten, Anna Nordenstrom, Paul-Martin Holterhus, Birgit Köhler, Marek Niedziela, Nils Krone
P2-313
A novel human CYP19A1 deletion-insertion mutation reveals that the C-terminus of the aromatase protein is crucial for its activity
Asmahane Ladjouze, Kay-Sarah Sauter, Yasmine Ouarezki, Leila Kedji, Abdenour Laraba, Amit V. Pandey, Christa E. Flück
A novel human CYP19A1 deletion-insertion mutation reveals that the C-terminus of the aromatase protein is crucial for its activity
Asmahane Ladjouze, Kay-Sarah Sauter, Yasmine Ouarezki, Leila Kedji, Abdenour Laraba, Amit V. Pandey, Christa E. Flück
P2-314
Pubertal virilization in two unrelated XY teenagers with female phenotype due to NR5A1/SF-1 gene mutation
Pascal PHILIBERT, Patrick FENICHEL, Didier DEWAILLY, Françoise AUDRAN, Nadege FAUCONNET-SERVANT, Françoise PARIS, Charles SULTAN
Pubertal virilization in two unrelated XY teenagers with female phenotype due to NR5A1/SF-1 gene mutation
Pascal PHILIBERT, Patrick FENICHEL, Didier DEWAILLY, Françoise AUDRAN, Nadege FAUCONNET-SERVANT, Françoise PARIS, Charles SULTAN
P2-315
Chimerism in a teenager with ovotesticular disorder of sexual development (DSD)
Mihaela Buzduga, Blaise Meyrat, Sofia Anna Typaldou, Vanina Estremadoyro, Leonor Alamo Maestre, Andrew Dwyer, Nelly Pitteloud, Franziska Phan-Hug
Chimerism in a teenager with ovotesticular disorder of sexual development (DSD)
Mihaela Buzduga, Blaise Meyrat, Sofia Anna Typaldou, Vanina Estremadoyro, Leonor Alamo Maestre, Andrew Dwyer, Nelly Pitteloud, Franziska Phan-Hug
P2-316
Partial androgen insensitivity: syndrome or symptoms?
Sultan Charles, Philibert Pascal, Kalfa Nicolas, Maïmoun Laurent, Audran Françoise, Servant Nadège, Gaspari Laura, Paris Françoise
Partial androgen insensitivity: syndrome or symptoms?
Sultan Charles, Philibert Pascal, Kalfa Nicolas, Maïmoun Laurent, Audran Françoise, Servant Nadège, Gaspari Laura, Paris Françoise
P2-317
Next-generation Sequencing as a Rapid Molecular Diagnosis in Patients with 46,XY Disorder of Sex Development (DSD)
Samim Ozen, Huseyin Onay, Tahir Atik, Asli Ece Solmaz, Damla Goksen, Ferda Ozkinay, Sukran Darcan
Next-generation Sequencing as a Rapid Molecular Diagnosis in Patients with 46,XY Disorder of Sex Development (DSD)
Samim Ozen, Huseyin Onay, Tahir Atik, Asli Ece Solmaz, Damla Goksen, Ferda Ozkinay, Sukran Darcan
P2-318
When, If Ever, Should the Müllerian Remnants Be Removed from Subjects with Mixed Gonadal Dysgenesis Raised as Males?
Anat Segev-Becker, Sarah Meisler, Ori Eyal, Asaf Oren, Anita Schachter Davidov, Naomi Weintrob
When, If Ever, Should the Müllerian Remnants Be Removed from Subjects with Mixed Gonadal Dysgenesis Raised as Males?
Anat Segev-Becker, Sarah Meisler, Ori Eyal, Asaf Oren, Anita Schachter Davidov, Naomi Weintrob
P2-319
Gonadotropin surge during the early postnatal activation period in 46,XX testicular/ovotesticular disorder of sex development (DSD) patients
Mariana Costanzo, Gabriela Guercio, Roxana Marino, Pablo Ramirez, Natalia Perez Garrido, Elisa Vaiani, Esperanza Berensztein, Juan Manuel Lazzati, Mercedes Maceiras, Marco A Rivarola, Alicia Belgorosky
Gonadotropin surge during the early postnatal activation period in 46,XX testicular/ovotesticular disorder of sex development (DSD) patients
Mariana Costanzo, Gabriela Guercio, Roxana Marino, Pablo Ramirez, Natalia Perez Garrido, Elisa Vaiani, Esperanza Berensztein, Juan Manuel Lazzati, Mercedes Maceiras, Marco A Rivarola, Alicia Belgorosky
P2-320
The Evaluation of AR and SRD5A2 Gene Mutations in 87 Patients with 46, XY DSD Children in Turkey
Nese Akcan, Guven Toksoy, Oya Uyguner, Nurcin Saka, Umut Altunoglu, Zehra Yavas Abali, Mikayir Genens, Sukran Poyrazoglu, Firdevs Bas, Ruveyde Bundak, Hulya Kayserili, Feyza Darendeliler
The Evaluation of AR and SRD5A2 Gene Mutations in 87 Patients with 46, XY DSD Children in Turkey
Nese Akcan, Guven Toksoy, Oya Uyguner, Nurcin Saka, Umut Altunoglu, Zehra Yavas Abali, Mikayir Genens, Sukran Poyrazoglu, Firdevs Bas, Ruveyde Bundak, Hulya Kayserili, Feyza Darendeliler
P2-321
Familial mutation of NR5A1/SF-1 gene associated with DSD and spleen agenesis: a new syndrome?
Pascal PHILIBERT, Francis POULAT, Françoise AUDRAN, Maryse CARTIGNY, Françoise PARIS, Charles SULTAN, Sylvie MANOUVRIER-HANU
Familial mutation of NR5A1/SF-1 gene associated with DSD and spleen agenesis: a new syndrome?
Pascal PHILIBERT, Francis POULAT, Françoise AUDRAN, Maryse CARTIGNY, Françoise PARIS, Charles SULTAN, Sylvie MANOUVRIER-HANU
P2-322
Clinical spectrum of 45,X/46,XY mosaicism and variants in children.
Hae Woon Jung, Hwa Young Kim, Gyung Min Lee, So Youn Kim, Kyung A Jeong, Keun Hee Choi, Jieun Lee, Young Ah Lee, Choong Ho Shin, Sei Won Yang
Clinical spectrum of 45,X/46,XY mosaicism and variants in children.
Hae Woon Jung, Hwa Young Kim, Gyung Min Lee, So Youn Kim, Kyung A Jeong, Keun Hee Choi, Jieun Lee, Young Ah Lee, Choong Ho Shin, Sei Won Yang
P2-323
Chromosomal variations in children and adolescents with gender dysphoria: is routine karyotyping indicated?
Claire Goedhart, Caroline Brain, Russell M Viner, Sabah Alvi, Talat Mushtaq, Jenny Walker, Polly Carmichael, Gary Butler
Chromosomal variations in children and adolescents with gender dysphoria: is routine karyotyping indicated?
Claire Goedhart, Caroline Brain, Russell M Viner, Sabah Alvi, Talat Mushtaq, Jenny Walker, Polly Carmichael, Gary Butler
P2-324
DSD 46,XY and serum steroid profile ambiguity due to combined 17-beta hydroxysteroid dehydrogenase/21-hydroxylase deficiencies
Elena Kuznetsova, Vitaliy Ioutsi, Anna Kolodkina, Natalia Kalinchenko, Anatoly Tiulpakov
DSD 46,XY and serum steroid profile ambiguity due to combined 17-beta hydroxysteroid dehydrogenase/21-hydroxylase deficiencies
Elena Kuznetsova, Vitaliy Ioutsi, Anna Kolodkina, Natalia Kalinchenko, Anatoly Tiulpakov
P2-325
FREQUENCY OF CRYPTORCHIDISM AND AGE AT OPERATION IN HELSINKI AREA BETWEEN 2004 AND 2014
Ella Kohva, Päivi Miettinen, Seppo Taskinen, Taneli Raivio
FREQUENCY OF CRYPTORCHIDISM AND AGE AT OPERATION IN HELSINKI AREA BETWEEN 2004 AND 2014
Ella Kohva, Päivi Miettinen, Seppo Taskinen, Taneli Raivio
P2-326
Prevalence of partial androgen insensitivity syndrome (PAIS) in 3 cohorts of 46,XY children presenting with isolated hypospadias, isolated micropenis or isolated persistent pubertal gynecomastia (PPG)
Paris Françoise, Philibert Pascal, Gaspari Laura, Audran Françoise, Kalfa Nicolas, Sultan Charles
Prevalence of partial androgen insensitivity syndrome (PAIS) in 3 cohorts of 46,XY children presenting with isolated hypospadias, isolated micropenis or isolated persistent pubertal gynecomastia (PPG)
Paris Françoise, Philibert Pascal, Gaspari Laura, Audran Françoise, Kalfa Nicolas, Sultan Charles
P2-327
A novel mutation of anti-Mullerian hormone receptor gene in a male with Persistent Mullerian Duct Syndrome
Ghadir Elias-Assad, Marwan Elias, Asher Pressman, Yardena Tenenbaum-Rakover
A novel mutation of anti-Mullerian hormone receptor gene in a male with Persistent Mullerian Duct Syndrome
Ghadir Elias-Assad, Marwan Elias, Asher Pressman, Yardena Tenenbaum-Rakover
P3-780
Clinical findings, endocrine profile and genetic features of 5alpha-reductase-2 deficiency
Gianni Russo, Fulvia Baldinotti, Paolo Ghirri, Silvia Meroni, Ilaria Colombo, Francesca Moscuzza, Giampiero I. Baroncelli, Maria R. Sessa, Eleonora Dati, Silvano Bertelloni
Clinical findings, endocrine profile and genetic features of 5alpha-reductase-2 deficiency
Gianni Russo, Fulvia Baldinotti, Paolo Ghirri, Silvia Meroni, Ilaria Colombo, Francesca Moscuzza, Giampiero I. Baroncelli, Maria R. Sessa, Eleonora Dati, Silvano Bertelloni
P3-781
Aromatase deficiency due to novel CYP19A1 mutation in an Egyptian patient with ambiguous genitalia
Inas Mazen, Ken Mclreavey, Mohamed Abdel hamid
Aromatase deficiency due to novel CYP19A1 mutation in an Egyptian patient with ambiguous genitalia
Inas Mazen, Ken Mclreavey, Mohamed Abdel hamid
P3-782
The time of first presentation at the department of paediatric endocrinology of patients with 46,XY DSD.
Zofia Kolesinska, Marek Niedziela
The time of first presentation at the department of paediatric endocrinology of patients with 46,XY DSD.
Zofia Kolesinska, Marek Niedziela
P3-783
Impact of neonatal exposure to different doses of bisphenol A on the hypothalamic-pituitary-testicle axis in male rat
Lin Qi Chen, Wen Wen Zhou, Fan Yang, Hai Ying Wu, Mei Fang Jin
Impact of neonatal exposure to different doses of bisphenol A on the hypothalamic-pituitary-testicle axis in male rat
Lin Qi Chen, Wen Wen Zhou, Fan Yang, Hai Ying Wu, Mei Fang Jin
P3-784
A cross-sectional growth reference and chart of stretched penile length for Japanese boys aged 0–7 years: Ethnic differences and secular changes
Tomohiro Ishii, Nobutake Matsuo, Mikako Inokuchi, Tomonobu Hasegawa
A cross-sectional growth reference and chart of stretched penile length for Japanese boys aged 0–7 years: Ethnic differences and secular changes
Tomohiro Ishii, Nobutake Matsuo, Mikako Inokuchi, Tomonobu Hasegawa
P3-785
Recurrent orchitis in a patient with true hermaphroditism
Letícia Guimarães de Souza, Bárbara Berrutti, José Antônio Diniz Faria Junior, Marina Ybarra, Leandra Steinmetz, Louise Cominato, Hamilton de Cabral Menezes Filho, Hilton Kuperman, Thais Della Manna, Durval Damiani
Recurrent orchitis in a patient with true hermaphroditism
Letícia Guimarães de Souza, Bárbara Berrutti, José Antônio Diniz Faria Junior, Marina Ybarra, Leandra Steinmetz, Louise Cominato, Hamilton de Cabral Menezes Filho, Hilton Kuperman, Thais Della Manna, Durval Damiani
P3-786
Isolated persistent pubertal gynecomastia in three adolescent males as the only phenotypic expression of PAIS with androgen receptor gene mutations
Pascal PHILIBERT, Felicien M'BOU, Françoise AUDRAN, Laura GASPARI, Françoise PARIS, Charles SULTAN
Isolated persistent pubertal gynecomastia in three adolescent males as the only phenotypic expression of PAIS with androgen receptor gene mutations
Pascal PHILIBERT, Felicien M'BOU, Françoise AUDRAN, Laura GASPARI, Françoise PARIS, Charles SULTAN
P3-788
Persistent Müllerian duct syndrome associated with anorchia caused by a compound heterozygous mutation in the AMHR-II gene
Jaime Cruz Rojo, Lucía Garzón Lorenzo, Jone Agirregoitia Fernández, Cristina Martínez del Pozo, Jean-Yves Picard, Jaime Sánchez del Pozo
Persistent Müllerian duct syndrome associated with anorchia caused by a compound heterozygous mutation in the AMHR-II gene
Jaime Cruz Rojo, Lucía Garzón Lorenzo, Jone Agirregoitia Fernández, Cristina Martínez del Pozo, Jean-Yves Picard, Jaime Sánchez del Pozo
P3-789
A Novel Mutation in Steroidogenic Factor (SF1) Gene in a Patient with 46, XY DSD without Adrenal Insufficiency
Ahmet Anik, Gonul Catli, Ayhan Abaci, Hale Unver Tuhan, Huseyin Onay, Ayca Aykut, Ece Bober
A Novel Mutation in Steroidogenic Factor (SF1) Gene in a Patient with 46, XY DSD without Adrenal Insufficiency
Ahmet Anik, Gonul Catli, Ayhan Abaci, Hale Unver Tuhan, Huseyin Onay, Ayca Aykut, Ece Bober
P3-790
Evaluation of two new anti-Müllerian hormone (AMH) assays for the investigation of disorders of sexual development in neonates
Clement KM Ho, Johnson WS Setoh
Evaluation of two new anti-Müllerian hormone (AMH) assays for the investigation of disorders of sexual development in neonates
Clement KM Ho, Johnson WS Setoh
P3-791
"Female", "Male", or "Between" in a 46,XY-Patient with a 17ß-HSD3-Mutation
Rolf Peter Willig, Petra Algenstaedt, Klaus Mohnike, Olaf Hiort
"Female", "Male", or "Between" in a 46,XY-Patient with a 17ß-HSD3-Mutation
Rolf Peter Willig, Petra Algenstaedt, Klaus Mohnike, Olaf Hiort
P3-792
Physical assessment and growth curve of 46, XY Disorders of Sex Development children who aged 0-16 years old
Di WU, Chunxiu GONG, Hui CHEN
Physical assessment and growth curve of 46, XY Disorders of Sex Development children who aged 0-16 years old
Di WU, Chunxiu GONG, Hui CHEN
P3-793
A Novel Mutation of the AR Gene Causes Androgen Insensitivity Syndrome :
A Case Report
Zhang longjiang, Xian xionghui, Tian shufeng, Liu xia, Su zhe
A Novel Mutation of the AR Gene Causes Androgen Insensitivity Syndrome :
A Case Report
Zhang longjiang, Xian xionghui, Tian shufeng, Liu xia, Su zhe
P3-794
A Novel Androgen Receptor Gene Mutation in a 46, XY Patient: Complete Androgen Insensitivity Syndrome
Hale Tuhan, Ahmet Anik, Ayca Aykut, Huseyin Onay, Ece Bober, Ayhan Abaci
A Novel Androgen Receptor Gene Mutation in a 46, XY Patient: Complete Androgen Insensitivity Syndrome
Hale Tuhan, Ahmet Anik, Ayca Aykut, Huseyin Onay, Ece Bober, Ayhan Abaci
P3-795
Polymorphisms and mutations of the genes INSL3 and HOXD13 in the pathogenesis of isolated cryptorchidism in Greece.
Sofia Vappa, Christalena Sofocleous, Konstantinos Nikas, Georgios Mastorakos, Emmanouel Kanavakis, Christina Kanaka-Gantenbein
Polymorphisms and mutations of the genes INSL3 and HOXD13 in the pathogenesis of isolated cryptorchidism in Greece.
Sofia Vappa, Christalena Sofocleous, Konstantinos Nikas, Georgios Mastorakos, Emmanouel Kanavakis, Christina Kanaka-Gantenbein
P3-796
Tumors of gonads in patients with disorders of sex development – 46,XY gonadal disgenesis
Oleg Latyshev, Lubov Samsonova, Alexey Okulov, Elena Kiseleva, Guar Okmynuan
Tumors of gonads in patients with disorders of sex development – 46,XY gonadal disgenesis
Oleg Latyshev, Lubov Samsonova, Alexey Okulov, Elena Kiseleva, Guar Okmynuan
P3-797
Screening for Y Microdeletions in Patients With Hypergonadotropic Hypogonadism Due to Disorder of Sexual Development
Murat Karaoglan, Mehmet Keskin, Ozlem Keskin
Screening for Y Microdeletions in Patients With Hypergonadotropic Hypogonadism Due to Disorder of Sexual Development
Murat Karaoglan, Mehmet Keskin, Ozlem Keskin
P3-798
'I AM A BOY SINCE 8-YEARS-OLD’:FEMALE DURING CHILDHOOD, VIRILIZATION AT PUBERTY
Suna Kılınç, Ayla Guven, Didem Helvacıoğlu
'I AM A BOY SINCE 8-YEARS-OLD’:FEMALE DURING CHILDHOOD, VIRILIZATION AT PUBERTY
Suna Kılınç, Ayla Guven, Didem Helvacıoğlu
P3-799
A novel mutation in human androgen receptor gene causing partial androgen insensitivity syndrome in a patient presenting with gynecomastia at puberty
Cemil Kocyigit, Gonul Catli, Serdar Saritas, Huseyin Onay, Bumin Nuri Dundar
A novel mutation in human androgen receptor gene causing partial androgen insensitivity syndrome in a patient presenting with gynecomastia at puberty
Cemil Kocyigit, Gonul Catli, Serdar Saritas, Huseyin Onay, Bumin Nuri Dundar
P3-800
A novel mutation of the AMH in an Egyptian male with persistent Mullerian duct syndrome
Inas Mazen, Mona El Gammal, Mohamed Abdel Hamid
A novel mutation of the AMH in an Egyptian male with persistent Mullerian duct syndrome
Inas Mazen, Mona El Gammal, Mohamed Abdel Hamid
P3-801
PSEUDO-PRECOCIOUS PUBERTY IN ANDROGEN INSENSITIVITY SYNDROME SECONDARY TO A PREPUBERTAL ESTROGEN PRODUCING SERTOLI CELL TUMOR
Diana Monica WARMAN, Esperanza BERENSZTEIN, Roxana MARINO, Pablo RAMIREZ, Mariana COSTANZO, Mercedes MACEIRAS, Marco A. RIVAROLA, Alicia BELGOROSKY
PSEUDO-PRECOCIOUS PUBERTY IN ANDROGEN INSENSITIVITY SYNDROME SECONDARY TO A PREPUBERTAL ESTROGEN PRODUCING SERTOLI CELL TUMOR
Diana Monica WARMAN, Esperanza BERENSZTEIN, Roxana MARINO, Pablo RAMIREZ, Mariana COSTANZO, Mercedes MACEIRAS, Marco A. RIVAROLA, Alicia BELGOROSKY
P3-802
Gender reassignment in Muslim communities
Amir Babiker, Amer Al Ali, Turki Al Batti, Nasir Al Jurayyan, Stenvert L Drop
Gender reassignment in Muslim communities
Amir Babiker, Amer Al Ali, Turki Al Batti, Nasir Al Jurayyan, Stenvert L Drop
P3-803
A CASE OF KLINEFELTER SYNDROME WITH AN ATYPICAL PRESENTATION
Ulku Gul, Veysel Nijat Bas, Deniz Okdemir, Leyla Akin, Nihal Hatipoglu, Mustafa Kendirci, Selim Kurtoglu
A CASE OF KLINEFELTER SYNDROME WITH AN ATYPICAL PRESENTATION
Ulku Gul, Veysel Nijat Bas, Deniz Okdemir, Leyla Akin, Nihal Hatipoglu, Mustafa Kendirci, Selim Kurtoglu
P3-804
A Practical and Integrative Approach to Differantial Diagnosis Between 46XY Disorder of Sexual Development
Murat Karaoglan, Mehmet Keskin, Ayhan Ozkur, Ozlem Keskin
A Practical and Integrative Approach to Differantial Diagnosis Between 46XY Disorder of Sexual Development
Murat Karaoglan, Mehmet Keskin, Ayhan Ozkur, Ozlem Keskin
P3-805
Patient with primary amenorrhea and glomerular nephropathy
Sara Santini, Franziska Phan-Hug, Cheng Xu, Faiza Lamine, Nicolas Moser, Anna Surbone, Patrice Mathevet, Benoit Lhermitte, Chahin Achtari, Nelly Pitteloud
Patient with primary amenorrhea and glomerular nephropathy
Sara Santini, Franziska Phan-Hug, Cheng Xu, Faiza Lamine, Nicolas Moser, Anna Surbone, Patrice Mathevet, Benoit Lhermitte, Chahin Achtari, Nelly Pitteloud
P3-806
The advent of Disorders of sexual differentiation team at a major teaching Nigeria: impact on patient management and outcome.
Olumide Jarrett, Taiwo Lawal, Oluyomi Esan, Adenike Sofoluwe, Oladapo Olayemi
The advent of Disorders of sexual differentiation team at a major teaching Nigeria: impact on patient management and outcome.
Olumide Jarrett, Taiwo Lawal, Oluyomi Esan, Adenike Sofoluwe, Oladapo Olayemi
P3-807
An interesting case of a phenotypic female with a 46 XY karyotype, uterus and menstruation
Mabel Yau, Ahmed Khattab, Maria New
An interesting case of a phenotypic female with a 46 XY karyotype, uterus and menstruation
Mabel Yau, Ahmed Khattab, Maria New
P3-808
Characteristic of children with mixed gonadal dysgenesis
Natallia Akulevich, Yulia Makarava, Irina Khmara, Anzhalika Solntseva
Characteristic of children with mixed gonadal dysgenesis
Natallia Akulevich, Yulia Makarava, Irina Khmara, Anzhalika Solntseva
P3-809
A 19-year-old adolescent with short stature and scrotal tumor
Katrin Heldt, Dagmar L`Allemand, Peter Waibel
A 19-year-old adolescent with short stature and scrotal tumor
Katrin Heldt, Dagmar L`Allemand, Peter Waibel
P3-810
An atypical case of Mayer-Rokitansky-Kuster-Hauser syndrome with hyperandrogenemia
Ala Üstyol, Mehmet Emre Atabek
An atypical case of Mayer-Rokitansky-Kuster-Hauser syndrome with hyperandrogenemia
Ala Üstyol, Mehmet Emre Atabek
LBP-1263
LATE SURGICAL CORRECTION OF HYPOSPADIAS INCREASES THE RISK OF COMPLICATION: A 501 CONSECUTIVE PATIENTS SERIES.
SARAH GARNIER, CLEMENT JEANDEL, BARBARA CEREDA, SYLVIE BROUSSOUS, OLIVIER MAILLET, CHRISTOPHE LOPEZ, FRANCOISE PARIS, LAURA GASPARI, PASCAL PHILIBERT, CLAIRE JEANDEL, AMANDINE COFFY, JEAN PIERRE DAURES, CHARLES SULTAN, NICOLAS KALFA
LATE SURGICAL CORRECTION OF HYPOSPADIAS INCREASES THE RISK OF COMPLICATION: A 501 CONSECUTIVE PATIENTS SERIES.
SARAH GARNIER, CLEMENT JEANDEL, BARBARA CEREDA, SYLVIE BROUSSOUS, OLIVIER MAILLET, CHRISTOPHE LOPEZ, FRANCOISE PARIS, LAURA GASPARI, PASCAL PHILIBERT, CLAIRE JEANDEL, AMANDINE COFFY, JEAN PIERRE DAURES, CHARLES SULTAN, NICOLAS KALFA
LBP-1264
FAMILY HISTORY OF GENITAL MALFORMATION IS UNDER-ESTIMATED IN CHILDREN WITH ISOLATED HYPOSPADIAS: A CLINICAL REPORT OF 105 FAMILIES.
NICOLAS KALFA, PASCAL PHILIBERT, SYLVIE BROUSSOUS, LAURA GASPARI, AMANDINE COFFY, NADÈGE FAUCONNET-SERVANT, FRANÇOISE AUDRAN, HÉLÈNE LEHORS, JEAN MICHEL GUYS, RACHEL REYNAUD, THIERRY MERROT, KATHY WAGNER, JEAN BRÉAUD, JEAN YVES KURZENNE, FLORENCE BASTIANI, JEAN STÉPHANE VALLA, ERIC DOBREMEZ, JEAN-PIERRE DAURES, FRANÇOISE PARIS, CHARLES SULTAN
FAMILY HISTORY OF GENITAL MALFORMATION IS UNDER-ESTIMATED IN CHILDREN WITH ISOLATED HYPOSPADIAS: A CLINICAL REPORT OF 105 FAMILIES.
NICOLAS KALFA, PASCAL PHILIBERT, SYLVIE BROUSSOUS, LAURA GASPARI, AMANDINE COFFY, NADÈGE FAUCONNET-SERVANT, FRANÇOISE AUDRAN, HÉLÈNE LEHORS, JEAN MICHEL GUYS, RACHEL REYNAUD, THIERRY MERROT, KATHY WAGNER, JEAN BRÉAUD, JEAN YVES KURZENNE, FLORENCE BASTIANI, JEAN STÉPHANE VALLA, ERIC DOBREMEZ, JEAN-PIERRE DAURES, FRANÇOISE PARIS, CHARLES SULTAN
LBP-1262
The Existence Of An Androgen Responsive Transcriptome In The Peripheral Blood Of Boys Extends The Utility Of The HCG Stimulation Test
Martina Rodie, Pawel Herzyk, Manikhandan Mudaliar, Sandra Chudleigh, Edward Tobias, Faisal Ahmed
The Existence Of An Androgen Responsive Transcriptome In The Peripheral Blood Of Boys Extends The Utility Of The HCG Stimulation Test
Martina Rodie, Pawel Herzyk, Manikhandan Mudaliar, Sandra Chudleigh, Edward Tobias, Faisal Ahmed
P1-78
Influence of Genetic Variation on the Response to Recombinant Human Growth Hormone (GH) Treatment in Children with GH Deficiency: An Analysis of 13 Single Nucleotide Polymorphisms and the GH Receptor Exon 3 Deletion
Anna-Maria Jung, Paul Francois Hoffmann, Dominik Monz, Christina Lissewski, Denny Schanze, Martin Zenker, Tilman Robert Rohrer
Influence of Genetic Variation on the Response to Recombinant Human Growth Hormone (GH) Treatment in Children with GH Deficiency: An Analysis of 13 Single Nucleotide Polymorphisms and the GH Receptor Exon 3 Deletion
Anna-Maria Jung, Paul Francois Hoffmann, Dominik Monz, Christina Lissewski, Denny Schanze, Martin Zenker, Tilman Robert Rohrer
P1-79
Decrease of jumping power in adolescents with severe GHD (sGHD) after stop of GH-therapy
Roland Schweizer, Julian Ziegler, Gerhard Binder
Decrease of jumping power in adolescents with severe GHD (sGHD) after stop of GH-therapy
Roland Schweizer, Julian Ziegler, Gerhard Binder
P1-80
GOOD CLINICAL RESPONSE TO GROWTH HORMONE THERAPY IN A BOY WITH A COMBINATION OF FAMILIAR SHORT STATURE CAUSED BY NOVEL p.Val478Serfs*14 MUTATION IN ACAN GENE AND ISOLATED GROWTH HORMONE DEFICIENCY
Stepanka Pruhova, Lenka Dusatkova, Petra Dusatkova, Dana Zemkova, Jan Lebl
GOOD CLINICAL RESPONSE TO GROWTH HORMONE THERAPY IN A BOY WITH A COMBINATION OF FAMILIAR SHORT STATURE CAUSED BY NOVEL p.Val478Serfs*14 MUTATION IN ACAN GENE AND ISOLATED GROWTH HORMONE DEFICIENCY
Stepanka Pruhova, Lenka Dusatkova, Petra Dusatkova, Dana Zemkova, Jan Lebl
P1-81
The growth response to growth hormone treatment is greater in patients with SHOX enhancer deletions compared to SHOX defects.
Stephany Donze, Caroline Meijer, Sarina Kant, Gladys Zandwijken, Annemieke van der Hout, Resie van Spaendonk, Ans van den Ouweland, Jan Maarten Wit, Monique Losekoot, Wilma Oostdijk
The growth response to growth hormone treatment is greater in patients with SHOX enhancer deletions compared to SHOX defects.
Stephany Donze, Caroline Meijer, Sarina Kant, Gladys Zandwijken, Annemieke van der Hout, Resie van Spaendonk, Ans van den Ouweland, Jan Maarten Wit, Monique Losekoot, Wilma Oostdijk
P1-82
Assessment of Primary Cancers in Growth Hormone (GH)–Treated Paediatric Patients Compared with General Population Registries: An Epidemiological Analysis of a Large, Multinational, Prospective Observational Study
Christopher Child, Alan Zimmermann, Nan Jia, Leslie Robison, Jürgen Brämswig, Werner Blum
Assessment of Primary Cancers in Growth Hormone (GH)–Treated Paediatric Patients Compared with General Population Registries: An Epidemiological Analysis of a Large, Multinational, Prospective Observational Study
Christopher Child, Alan Zimmermann, Nan Jia, Leslie Robison, Jürgen Brämswig, Werner Blum
P1-83
Genetic markers contribute to the Prediction of response to GH in severe but not mild GH deficiency
Adam Stevens, Philip Murray, Jerome Wojcik, John Raelson, Ekaterina Koledova, Pierre Chatelain, Peter Clayton
Genetic markers contribute to the Prediction of response to GH in severe but not mild GH deficiency
Adam Stevens, Philip Murray, Jerome Wojcik, John Raelson, Ekaterina Koledova, Pierre Chatelain, Peter Clayton
P1-84
Disease and Treatment Burden In Children And Adolescents with Growth Hormone Deficiency (GHD)
Meryl Brod, Lise Højbjerre, Suzanne Alolga, Alise Nacson, Lars Nordholm, Michael Højby Rassmussen
Disease and Treatment Burden In Children And Adolescents with Growth Hormone Deficiency (GHD)
Meryl Brod, Lise Højbjerre, Suzanne Alolga, Alise Nacson, Lars Nordholm, Michael Højby Rassmussen
P1-85
EFFECTS OF GROWTH HORMONE TREATMENT ON IMMUNITY
Ramón Cañete, María Dolores Caballero, Rocío Aguado, Manuel Santamaría
EFFECTS OF GROWTH HORMONE TREATMENT ON IMMUNITY
Ramón Cañete, María Dolores Caballero, Rocío Aguado, Manuel Santamaría
P1-86
The growth hormone treatment results in the increase of irisin concentration in plasma
Beata Wikiera, Katarzyna Pukajlo, Lukasz Laczmanski, Natalia Sloka, Aleksander Basiak, Anna Noczynska, Marek Bolanowski, Jacek Daroszewski
The growth hormone treatment results in the increase of irisin concentration in plasma
Beata Wikiera, Katarzyna Pukajlo, Lukasz Laczmanski, Natalia Sloka, Aleksander Basiak, Anna Noczynska, Marek Bolanowski, Jacek Daroszewski
P1-87
A novel OTX2 gene mutation in a child with growth hormone deficiency
Antonella Lonero, Maurizio Delvecchio, Paola Primignani, Roberto Caputo, Fabrizia De Palma, Vincenza Luce, Maria Felicia Faienza, Luciano Cavallo
A novel OTX2 gene mutation in a child with growth hormone deficiency
Antonella Lonero, Maurizio Delvecchio, Paola Primignani, Roberto Caputo, Fabrizia De Palma, Vincenza Luce, Maria Felicia Faienza, Luciano Cavallo
P1-88
The dose dependent effect of growth hormone therapy in patients with IGF-1 receptor haploinsufficiency due to heterozygous deletion
Haruo Mizuno, Kohei Aoyama, Tatsushi Tanaka, Shinji Saitoh
The dose dependent effect of growth hormone therapy in patients with IGF-1 receptor haploinsufficiency due to heterozygous deletion
Haruo Mizuno, Kohei Aoyama, Tatsushi Tanaka, Shinji Saitoh
P2-406
Metabolic Health in short children born SGA treated with GH and GnRHa: Results of a randomized, dose-response trial.
M. van der Steen, A.J. Lem, D.C.M. van der Kaay, W.M. Bakker-van Waarde, F.J.P.C.M. van der Hulst, F.S. Neijens, C. Noordam, R.J. Odink, W. Oostdijk, E.J. Schroor, E.J. Sulkers, C. Westerlaken, A.C.S. Hokken-Koelega
Metabolic Health in short children born SGA treated with GH and GnRHa: Results of a randomized, dose-response trial.
M. van der Steen, A.J. Lem, D.C.M. van der Kaay, W.M. Bakker-van Waarde, F.J.P.C.M. van der Hulst, F.S. Neijens, C. Noordam, R.J. Odink, W. Oostdijk, E.J. Schroor, E.J. Sulkers, C. Westerlaken, A.C.S. Hokken-Koelega
P2-407
A Phase 2, six-month, randomized, active-controlled, safety and efficacy study of TransCon hGH compared to daily hGH in children with Growth Hormone Deficiency (GHD)
Pierre Chatelain, Oleg Malievsky, Klaudziya Radziuk, Ganna Senatorova, Michael Beckert
A Phase 2, six-month, randomized, active-controlled, safety and efficacy study of TransCon hGH compared to daily hGH in children with Growth Hormone Deficiency (GHD)
Pierre Chatelain, Oleg Malievsky, Klaudziya Radziuk, Ganna Senatorova, Michael Beckert
P2-408
Does skeletal disproportion in children with idiopathic short stature influence response to Growth Hormone (GH) therapy?
Wayne S Cutfield, Anders Lindberg, Paul Hofman, Jose Derraik, Mitchell E Geffner, Cecilia Camacho-Hubner
Does skeletal disproportion in children with idiopathic short stature influence response to Growth Hormone (GH) therapy?
Wayne S Cutfield, Anders Lindberg, Paul Hofman, Jose Derraik, Mitchell E Geffner, Cecilia Camacho-Hubner
P2-409
THE INFLUENCE OF GROWTH HORMONE THERAPY ON CHEMERIN CONCENTRATION, BODY MASS AND SELECTED PARAMETERS OF CARBOHYDRATE METABOLISM IN PREPUBERTAL NON-OBESE CHILDREN WITH GROWTH HORMONE DEFICIENCY
Agnieszka Rudzka-Kocjan, Mieczyslaw Szalecki
THE INFLUENCE OF GROWTH HORMONE THERAPY ON CHEMERIN CONCENTRATION, BODY MASS AND SELECTED PARAMETERS OF CARBOHYDRATE METABOLISM IN PREPUBERTAL NON-OBESE CHILDREN WITH GROWTH HORMONE DEFICIENCY
Agnieszka Rudzka-Kocjan, Mieczyslaw Szalecki
P2-410
Response to growth hormone treatment in the very young with growth hormone deficiency
Semra Cetinkaya, Sukran Poyrazoglu, Zehra Aycan, Zeynep Siklar, Merih Berberoglu, Zeynep Atay, Abdullah Bereket, Oya Ercan, Eda Mengen, Fatma Demirel, Sukran Darcan, Feyza Darendeliler
Response to growth hormone treatment in the very young with growth hormone deficiency
Semra Cetinkaya, Sukran Poyrazoglu, Zehra Aycan, Zeynep Siklar, Merih Berberoglu, Zeynep Atay, Abdullah Bereket, Oya Ercan, Eda Mengen, Fatma Demirel, Sukran Darcan, Feyza Darendeliler
P2-411
ESTIMATION OF ADIPSIN, OMENTIN AND VASPIN CONCENTRATION IN PREPUBERTAL CHILDREN WITH GROWTH HORMONE DEFICIENCY BEFORE AND AFTER 6 MONTHS OF GROWTH HORMONE TREATMENT
Agnieszka Rudzka-Kocjan, Mieczyslaw Szalecki
ESTIMATION OF ADIPSIN, OMENTIN AND VASPIN CONCENTRATION IN PREPUBERTAL CHILDREN WITH GROWTH HORMONE DEFICIENCY BEFORE AND AFTER 6 MONTHS OF GROWTH HORMONE TREATMENT
Agnieszka Rudzka-Kocjan, Mieczyslaw Szalecki
P2-412
Final Height and Safety Outcomes in Growth Hormone (GH)-Treated Children Born Small for Gestational Age (SGA): Experience from the Prospective GeNeSIS Observational Study
Chris Child, Charmian Quigley, Alan Zimmermann, Cheri Deal, Judith Ross, Eckhard Schönau, Werner Blum
Final Height and Safety Outcomes in Growth Hormone (GH)-Treated Children Born Small for Gestational Age (SGA): Experience from the Prospective GeNeSIS Observational Study
Chris Child, Charmian Quigley, Alan Zimmermann, Cheri Deal, Judith Ross, Eckhard Schönau, Werner Blum
P2-413
Results up to January 2015 from PATRO Children, a multi-centre, non-interventional study of the long-term safety and efficacy of Omnitrope® in children requiring growth hormone treatment
Roland Pfaffle, Shankar Kanumakala, Charlotte Höybye, Berit Kriström, Ellen Schuck, Markus Zabransky, Tadej Battelino, Michel Colle
Results up to January 2015 from PATRO Children, a multi-centre, non-interventional study of the long-term safety and efficacy of Omnitrope® in children requiring growth hormone treatment
Roland Pfaffle, Shankar Kanumakala, Charlotte Höybye, Berit Kriström, Ellen Schuck, Markus Zabransky, Tadej Battelino, Michel Colle
P2-414
Growth Hormone (GH) treatment prevents hypoxia-induced decrease of GH and IGF-1 plasma concentrations in neonatal mice
Susan Jung, Mandy Richter-Kraus, Florian Brackmann, Helmut G. Dörr, Regina Trollmann
Growth Hormone (GH) treatment prevents hypoxia-induced decrease of GH and IGF-1 plasma concentrations in neonatal mice
Susan Jung, Mandy Richter-Kraus, Florian Brackmann, Helmut G. Dörr, Regina Trollmann
P2-415
The Pharmacokinetics and Pharmacodynamics of TV-1106, a Once Weekly Growth Hormone Supplement: Results from a Phase 2 Study of TV-1106 in Adults with Growth Hormone Deficiency
Orit Cohen-Barak, Jens Sendahl Christiansen, Martin Bidlingmaier, Kurt Brown, Anat Sakov, Gaya Anscheutz, Kathleen Butler
The Pharmacokinetics and Pharmacodynamics of TV-1106, a Once Weekly Growth Hormone Supplement: Results from a Phase 2 Study of TV-1106 in Adults with Growth Hormone Deficiency
Orit Cohen-Barak, Jens Sendahl Christiansen, Martin Bidlingmaier, Kurt Brown, Anat Sakov, Gaya Anscheutz, Kathleen Butler
P2-416
EFFECTS OF GROWTH HORMONE TREATMENT ON THE HEART IN CHILDREN WITH GH DEFICIENCY
Elena Gómez-Guzmán, Mará Dolores Cañete, Miguel Valle-Jiménez, Javier Caballero-Villarraso, Ramón Cañete
EFFECTS OF GROWTH HORMONE TREATMENT ON THE HEART IN CHILDREN WITH GH DEFICIENCY
Elena Gómez-Guzmán, Mará Dolores Cañete, Miguel Valle-Jiménez, Javier Caballero-Villarraso, Ramón Cañete
P2-417
GH THERAPY IN SKELETAL DYSPLASIAS: FINAL HEIGHT (FH) DATA.
Emanuela Scarano, Matteo Procopio, Federica Tamburrino, Annamaria Perri, Ilaria Bettocchi, Benedetta Vestrucci, Alessandra Rollo, Antonio Balsamo, Laura Mazzanti
GH THERAPY IN SKELETAL DYSPLASIAS: FINAL HEIGHT (FH) DATA.
Emanuela Scarano, Matteo Procopio, Federica Tamburrino, Annamaria Perri, Ilaria Bettocchi, Benedetta Vestrucci, Alessandra Rollo, Antonio Balsamo, Laura Mazzanti
P2-418
Random forest classification predicts response to growth hormone (GH) in GH deficient children using baseline clinical parameters and genetic markers
Adam Stevens, Philip Murray, Jerome Wojcik, John Raelson, Ekaterina Koledova, Pierre Chatelain, Peter Clayton
Random forest classification predicts response to growth hormone (GH) in GH deficient children using baseline clinical parameters and genetic markers
Adam Stevens, Philip Murray, Jerome Wojcik, John Raelson, Ekaterina Koledova, Pierre Chatelain, Peter Clayton
P2-419
Safety evaluation of long-term recombinant growth hormone treatment in childhood: interim analysis of the NordiNet® International Outcome Study
Lars Sävendahl, Effie Pournara, Tilman R. Rohrer, Birgitte Tønnes Pedersen, Marja-Terttu Saha, Oliver Blankenstein
Safety evaluation of long-term recombinant growth hormone treatment in childhood: interim analysis of the NordiNet® International Outcome Study
Lars Sävendahl, Effie Pournara, Tilman R. Rohrer, Birgitte Tønnes Pedersen, Marja-Terttu Saha, Oliver Blankenstein
P2-420
Hypoglycaemic adverse events reported in children enrolled in the European Increlex® Growth Forum Database (EU-IGFD) in Europe (5-year interim data)
Joachim Woelfle, Michel Polak, Peter Bang, Aude Houchard, Caroline Sert
Hypoglycaemic adverse events reported in children enrolled in the European Increlex® Growth Forum Database (EU-IGFD) in Europe (5-year interim data)
Joachim Woelfle, Michel Polak, Peter Bang, Aude Houchard, Caroline Sert
P2-421
Application of neural networks for final height prediction based on pre-treatment data in children with growth hormone (GH) deficiency treated with GH
Joanna Smyczynska, Urszula Smyczynska, Renata Stawerska, Andrzej Lewinski, Ryszard Tadeusiewicz, Maciej Hilczer
Application of neural networks for final height prediction based on pre-treatment data in children with growth hormone (GH) deficiency treated with GH
Joanna Smyczynska, Urszula Smyczynska, Renata Stawerska, Andrzej Lewinski, Ryszard Tadeusiewicz, Maciej Hilczer
P2-422
Physical performance and right ventricular function in children with growth hormone (GH) deficiency (GHD) before and after 12 months-GH replacement therapy
Flavia Barbieri, Donatella Capalbo, Rosa Lucci, Alessandra Vitelli, Andrea Esposito, Elisa Di Pietro, Antonio Rapacciuolo, Carlo Vigorito, Mariacarolina Salerno
Physical performance and right ventricular function in children with growth hormone (GH) deficiency (GHD) before and after 12 months-GH replacement therapy
Flavia Barbieri, Donatella Capalbo, Rosa Lucci, Alessandra Vitelli, Andrea Esposito, Elisa Di Pietro, Antonio Rapacciuolo, Carlo Vigorito, Mariacarolina Salerno
P2-423
The accuracy of bioelectrical impedance analysis (BIA) to detect the body composition changes in adolescents with severe GHD during transition
Julian Ziegler, Roland Schweizer, Gerhard Binder
The accuracy of bioelectrical impedance analysis (BIA) to detect the body composition changes in adolescents with severe GHD during transition
Julian Ziegler, Roland Schweizer, Gerhard Binder
P2-424
Timing of GH peak in provocation tests is important in predicting the effectiveness of treatment with rhGH in prepubertal children with GHD
Irene Georeli, Panagiota Triantafyllou, Aris Slavakis, Athanasios Christoforidis
Timing of GH peak in provocation tests is important in predicting the effectiveness of treatment with rhGH in prepubertal children with GHD
Irene Georeli, Panagiota Triantafyllou, Aris Slavakis, Athanasios Christoforidis
P2-425
Comparison of baseline parameters and response to GH treatment in 125 children with short stature with eight different diagnosis.
Irene Ioimo, Alessandro Mussa, Silvia Vannelli, Francesca Feyles, Silvia Einaudi, Patrizia Matarazzo
Comparison of baseline parameters and response to GH treatment in 125 children with short stature with eight different diagnosis.
Irene Ioimo, Alessandro Mussa, Silvia Vannelli, Francesca Feyles, Silvia Einaudi, Patrizia Matarazzo
P2-426
The ALS dose matters? Response to human growth hormone treatment in patients with acid-labile subunit deficiency
Susanne Bechtold, Julia Roeb, Claudia Weissenbacher, Carmen Sydlik, Heinrich Schmidt
The ALS dose matters? Response to human growth hormone treatment in patients with acid-labile subunit deficiency
Susanne Bechtold, Julia Roeb, Claudia Weissenbacher, Carmen Sydlik, Heinrich Schmidt
P2-427
rhGH replacement therapy ameliorates body composition substantially but has no effect in the quality of life in adolescents with GH deficiency– A cross-sectional study
Charikleia Stefanaki, George Paltoglou, Flora Bacopoulou, Dario Boschiero, George P. Chrousos
rhGH replacement therapy ameliorates body composition substantially but has no effect in the quality of life in adolescents with GH deficiency– A cross-sectional study
Charikleia Stefanaki, George Paltoglou, Flora Bacopoulou, Dario Boschiero, George P. Chrousos
P2-428
Evaluation of the effect of growth hormone treatment on insulin resistance and cardiovascular tissue
Seha Kamil Saygili, Mehmet Kocaaga, Gamze Kaya, Mine Sukur, Pelin Ozer, Firdevs Bas, Ruveyde Bundak, Feyza Darendeliler
Evaluation of the effect of growth hormone treatment on insulin resistance and cardiovascular tissue
Seha Kamil Saygili, Mehmet Kocaaga, Gamze Kaya, Mine Sukur, Pelin Ozer, Firdevs Bas, Ruveyde Bundak, Feyza Darendeliler
P2-429
EFFECTIVENESS OF RECOMBINANT IGF-I TREATMENT IN A PATIENT WITH ISOLATED GH IA DEFICIT PRODUCER OF ANTI-GH ANTIBODIES.
INES PORCAR, JOSEP ORIOLA, JÜRGEN KRATZSCH, JOAQUIN ESCRIBANO, ALBERT FELIU
EFFECTIVENESS OF RECOMBINANT IGF-I TREATMENT IN A PATIENT WITH ISOLATED GH IA DEFICIT PRODUCER OF ANTI-GH ANTIBODIES.
INES PORCAR, JOSEP ORIOLA, JÜRGEN KRATZSCH, JOAQUIN ESCRIBANO, ALBERT FELIU
P2-430
Analysis of CD133+CD45+ hematopoietic progenitor/stem cells and CD133+/CD45- very small embryonic-like stem cells in children with growth hormone deficiency subjected to growth hormone (GH) therapy
A. Bossowski, P. Singh, K. Grubczak, U. Radzikowska, B. Sawicka, P. Miklasz, M. Dabrowska, A. Bossowska, M. Moniuszko
Analysis of CD133+CD45+ hematopoietic progenitor/stem cells and CD133+/CD45- very small embryonic-like stem cells in children with growth hormone deficiency subjected to growth hormone (GH) therapy
A. Bossowski, P. Singh, K. Grubczak, U. Radzikowska, B. Sawicka, P. Miklasz, M. Dabrowska, A. Bossowska, M. Moniuszko
P2-431
Effectiveness of rhIGF-I treatment in a girl with Leprechaunism
Clemens Kamrath, Claudia Boettcher, Stefan Wudy
Effectiveness of rhIGF-I treatment in a girl with Leprechaunism
Clemens Kamrath, Claudia Boettcher, Stefan Wudy
P3-930
IGF-1 deficiency: an important differential diagnosis in severe growth failure and its excellent response to rhIGF-1 replacement therapy
Dinesh Giri, Helen Storr, Martin O. Savage, Renuka Ramakrishnan
IGF-1 deficiency: an important differential diagnosis in severe growth failure and its excellent response to rhIGF-1 replacement therapy
Dinesh Giri, Helen Storr, Martin O. Savage, Renuka Ramakrishnan
P3-931
Five-year response to growth hormone in children with Noonan syndrome and growth hormone deficiency: our experience and review of the literature.
Cristina Meazza, Niki Zavras, Alba Pilotta, Chiara Gertosio, Sara Pagani, Carmine Tinelli, Mauro Bozzola
Five-year response to growth hormone in children with Noonan syndrome and growth hormone deficiency: our experience and review of the literature.
Cristina Meazza, Niki Zavras, Alba Pilotta, Chiara Gertosio, Sara Pagani, Carmine Tinelli, Mauro Bozzola
P3-932
Modification of cardiovascular risk factors in children treated with growth hormone.
Maria Escolà Llop, Raquel Monné Gelonch, Montse Olona Cabases, Àngels Vilanova Navarro, Diana Sofia de Melo Canhoto, Encarnación Torruz Yuste
Modification of cardiovascular risk factors in children treated with growth hormone.
Maria Escolà Llop, Raquel Monné Gelonch, Montse Olona Cabases, Àngels Vilanova Navarro, Diana Sofia de Melo Canhoto, Encarnación Torruz Yuste
P3-933
Adult height in children born small for gestational age and treated with GH: data from the French KIGS database
Michel POLAK, Paul CZERNICHOW
Adult height in children born small for gestational age and treated with GH: data from the French KIGS database
Michel POLAK, Paul CZERNICHOW
P3-934
Psychosocial functioning and self-perception of children and adolescents treated with Growth Hormone
Chrysoula Drosatou, Elpis-Athina Vlachopapadopoulou, Feneli Karachaliou, Apostolos Prodromidis, Stefanos Michalakos, Konstantinos Tsoumakas
Psychosocial functioning and self-perception of children and adolescents treated with Growth Hormone
Chrysoula Drosatou, Elpis-Athina Vlachopapadopoulou, Feneli Karachaliou, Apostolos Prodromidis, Stefanos Michalakos, Konstantinos Tsoumakas
P3-935
Do IGF-I Generation Test Results Predict First Year Growth Response to GH Treatment in Idiopathic Short Stature?
Mohammad Ajmal Masoom, Oya Ercan, Feride Tahmiscioglu Bucak, Bahar Taskin Ozcabi, Olcay Evliyaoglu
Do IGF-I Generation Test Results Predict First Year Growth Response to GH Treatment in Idiopathic Short Stature?
Mohammad Ajmal Masoom, Oya Ercan, Feride Tahmiscioglu Bucak, Bahar Taskin Ozcabi, Olcay Evliyaoglu
P3-936
Adherence to growth hormone treatment: impact of actual height, treatment duration, and puberty
Juliane Rothermel, Karl Scheite, Nadine Nazari, Berthold Hauffa, Thomas Reinehr
Adherence to growth hormone treatment: impact of actual height, treatment duration, and puberty
Juliane Rothermel, Karl Scheite, Nadine Nazari, Berthold Hauffa, Thomas Reinehr
P3-937
The Blood Oxidant System and Insulin Resistance in Girls with Turner Syndrome after 1 Year of Growth Hormone Therapy
Maria Pankratova, Maria Faassen, Tatyana Shiryaeva, Elena Nagaeva, Valentina Peterkova, Adil Baizhumanov, Alexander Yusipovich, Alexander Cherkashin, Georgy Maksimov
The Blood Oxidant System and Insulin Resistance in Girls with Turner Syndrome after 1 Year of Growth Hormone Therapy
Maria Pankratova, Maria Faassen, Tatyana Shiryaeva, Elena Nagaeva, Valentina Peterkova, Adil Baizhumanov, Alexander Yusipovich, Alexander Cherkashin, Georgy Maksimov
P3-938
An Open-label Phase 2 Dose-Finding Study Comparing 3 Different Doses of Weekly TV-1106 and Daily Recombinant Human Growth Hormone (Genotropin®) in Treatment-Naive, Pre-Pubertal, Growth Hormone-Deficient Children
Ron G Rosenfeld, Jan M Wit, Oleg Malievsky, Elena Bolshova, Kurt Brown, Anat Sakov, Gaya Anscheutz, Merav Bassan, Kathleen Butler
An Open-label Phase 2 Dose-Finding Study Comparing 3 Different Doses of Weekly TV-1106 and Daily Recombinant Human Growth Hormone (Genotropin®) in Treatment-Naive, Pre-Pubertal, Growth Hormone-Deficient Children
Ron G Rosenfeld, Jan M Wit, Oleg Malievsky, Elena Bolshova, Kurt Brown, Anat Sakov, Gaya Anscheutz, Merav Bassan, Kathleen Butler
P3-939
Increasing Lean Body Mass (LBM), Phase Angle (PA), and Total Body Water (TBW) but decreasing Body Fat (BF) among short-statured children born Small-for-Gestational Age on Growth Hormone Treatment
Thomas MK Völkl, Isabel Stumpf, Helmuth-G Dörr
Increasing Lean Body Mass (LBM), Phase Angle (PA), and Total Body Water (TBW) but decreasing Body Fat (BF) among short-statured children born Small-for-Gestational Age on Growth Hormone Treatment
Thomas MK Völkl, Isabel Stumpf, Helmuth-G Dörr
P3-940
Growth hormone (GH) dosing patterns in children with isolated GH deficiency (IGHD) and multiple pituitary hormone deficiency (MPHD) enrolled in the NordiNet® International Outcome Study (IOS)
Marta Šnajderová, Effie Pournara, Birgitte Tønnes Pedersen, Oliver Blankenstein
Growth hormone (GH) dosing patterns in children with isolated GH deficiency (IGHD) and multiple pituitary hormone deficiency (MPHD) enrolled in the NordiNet® International Outcome Study (IOS)
Marta Šnajderová, Effie Pournara, Birgitte Tønnes Pedersen, Oliver Blankenstein
P3-941
Decrease of small dense LDL and lipoprotein-associated phospholipase A2 due to human growth hormone treatment in short children with growth hormone deficiency and small for gestational age status
Andreas Krebs, Thomas Kratzin, Jürgen Doerfer, Karl Winkler, Michael Wurm, Natascha van der Werf-Grohmann, Alexandra Krause, Karl Otfried Schwab
Decrease of small dense LDL and lipoprotein-associated phospholipase A2 due to human growth hormone treatment in short children with growth hormone deficiency and small for gestational age status
Andreas Krebs, Thomas Kratzin, Jürgen Doerfer, Karl Winkler, Michael Wurm, Natascha van der Werf-Grohmann, Alexandra Krause, Karl Otfried Schwab
P3-942
Long-term insulin sensitivity and beta-cell function in short children born SGA treated with GH and GnRHa: Results of a randomized, dose-response trial
Manouk van der Steen, Annemieke J. Lem, Danielle C.M. van der Kaay, Anita C.S. Hokken-Koelega
Long-term insulin sensitivity and beta-cell function in short children born SGA treated with GH and GnRHa: Results of a randomized, dose-response trial
Manouk van der Steen, Annemieke J. Lem, Danielle C.M. van der Kaay, Anita C.S. Hokken-Koelega
P3-943
Influence of the application of the POI score on the results of GH therapy in Prader-Willi.
Alessandro Salvatoni, Sarah Bocchini, Antonino Crinò, Stefania Di Candia, Graziano Grugni, Lorenzo Iughetti, Luigi Nespoli, Luana Nosetti, Giovanni Padoan, Alba Pilotta, Marzia Piran, Valeria Spica Russotto
Influence of the application of the POI score on the results of GH therapy in Prader-Willi.
Alessandro Salvatoni, Sarah Bocchini, Antonino Crinò, Stefania Di Candia, Graziano Grugni, Lorenzo Iughetti, Luigi Nespoli, Luana Nosetti, Giovanni Padoan, Alba Pilotta, Marzia Piran, Valeria Spica Russotto
P3-944
The impact of growth hormone therapy in Noonan Syndrome children with identified mutations in RAS/MAPK pathway
Alexsandra Malaquias, Michelle Moraes, Mariana Funari, Alexandre Pereira, Debora Bertola, Alexander Jorge
The impact of growth hormone therapy in Noonan Syndrome children with identified mutations in RAS/MAPK pathway
Alexsandra Malaquias, Michelle Moraes, Mariana Funari, Alexandre Pereira, Debora Bertola, Alexander Jorge
P3-945
As great intra as interindividual variability in uptake of subcutaneous GH injections in longitudinally followed GH treated children
Elena Lundberg, Berit Kriström, Björn Andersson, Sten Rosberg, Kerstin Albertsson-Wikland
As great intra as interindividual variability in uptake of subcutaneous GH injections in longitudinally followed GH treated children
Elena Lundberg, Berit Kriström, Björn Andersson, Sten Rosberg, Kerstin Albertsson-Wikland
P3-946
The correlation between the increase in insulin-like growth factor I and the growth improvement induced by growth hormone treatment in short children born small for gestational age
Atsushi Hattori, Junya Eto, Atsuko Kawano, Kenichi Miyako
The correlation between the increase in insulin-like growth factor I and the growth improvement induced by growth hormone treatment in short children born small for gestational age
Atsushi Hattori, Junya Eto, Atsuko Kawano, Kenichi Miyako
P3-947
Medical and biochemical effects of intervention program in patients with poor adherence to rhGH treatment.
María Martínez, Marta Murillo, Estefania Guerrini, Maria Luisa Granada, Joan Bel
Medical and biochemical effects of intervention program in patients with poor adherence to rhGH treatment.
María Martínez, Marta Murillo, Estefania Guerrini, Maria Luisa Granada, Joan Bel
P3-948
Favourable growth hormone treatment response in a young boy with achondroplasia
Marina Krstevska - Konstantinova, Nevenka Slaveska
Favourable growth hormone treatment response in a young boy with achondroplasia
Marina Krstevska - Konstantinova, Nevenka Slaveska
P3-949
Plexiform neurofibroma and demielinisant lesions in a patient with GH deficiency treated with rGH
Luminita-Nicoleta Cima, Alice Albu, Simona Fica, Carmen Gabriela Barbu
Plexiform neurofibroma and demielinisant lesions in a patient with GH deficiency treated with rGH
Luminita-Nicoleta Cima, Alice Albu, Simona Fica, Carmen Gabriela Barbu
P3-950
Growth, development and puberty of patients with congenital multiple pituitary hormone deficiencies (MPHD)
Hadar Haim-Pinhas, Rivka Kauli, Zvi Laron
Growth, development and puberty of patients with congenital multiple pituitary hormone deficiencies (MPHD)
Hadar Haim-Pinhas, Rivka Kauli, Zvi Laron
P3-951
PREDICTORS OF RESPONSE TO rhGH TREATMENT IN 125 CHILDREN WITH SHORT STATURE OF VARIOUS ETIOLOGIES
Irene Ioimo, Alessandro Mussa, Silvia Vannelli, Francesca Verna, Alberto Borraccino, Patrizia Matarazzo
PREDICTORS OF RESPONSE TO rhGH TREATMENT IN 125 CHILDREN WITH SHORT STATURE OF VARIOUS ETIOLOGIES
Irene Ioimo, Alessandro Mussa, Silvia Vannelli, Francesca Verna, Alberto Borraccino, Patrizia Matarazzo
P3-952
Linear regression model of final height prediction based on pre-treatment data in children with growth hormone (GH) deficiency treated with GH
Maciej Hilczer, Joanna Smyczynska, Urszula Smyczynska, Renata Stawerska, Andrzej Lewinski
Linear regression model of final height prediction based on pre-treatment data in children with growth hormone (GH) deficiency treated with GH
Maciej Hilczer, Joanna Smyczynska, Urszula Smyczynska, Renata Stawerska, Andrzej Lewinski
P3-953
Vitamin D levels and not vitamin A are correlated with height velocity in children with growth hormone (GH) deficiency who are under GH treatment
Maria Xatzipsalti, Ioulia Polychroni, Andriani Vazeou, Vasiliki Maravelia, Eirini Papadimitriou, Lela Stamogiannou
Vitamin D levels and not vitamin A are correlated with height velocity in children with growth hormone (GH) deficiency who are under GH treatment
Maria Xatzipsalti, Ioulia Polychroni, Andriani Vazeou, Vasiliki Maravelia, Eirini Papadimitriou, Lela Stamogiannou
P3-954
Long-term effects of GH replacement therapy on hematopoiesis in GH deficient children
Andrea Esposito, Lucia De Martino, Flavia Barbieri, Martina Rezzuto, Nicola Improda, Manuela Cerbone, Donatella Capalbo, Mariacarolina Salerno
Long-term effects of GH replacement therapy on hematopoiesis in GH deficient children
Andrea Esposito, Lucia De Martino, Flavia Barbieri, Martina Rezzuto, Nicola Improda, Manuela Cerbone, Donatella Capalbo, Mariacarolina Salerno
P3-955
Thyroid function in children treated with rhGH for growth hormone deficiency
Panagiota Triantafyllou, Irene Georeli, Meropi Dimitriadou, Olga Maliahova, Anreas Daflos, Athanasios Christoforidis
Thyroid function in children treated with rhGH for growth hormone deficiency
Panagiota Triantafyllou, Irene Georeli, Meropi Dimitriadou, Olga Maliahova, Anreas Daflos, Athanasios Christoforidis
P3-956
A 5-year follow-up of adults, with childhood-onset GH deficiency, treated with GENOTONORM® in France
Philippe Touraine, Françoise Borson-Chazot, Brigitte Delemer, Thierry Brue
A 5-year follow-up of adults, with childhood-onset GH deficiency, treated with GENOTONORM® in France
Philippe Touraine, Françoise Borson-Chazot, Brigitte Delemer, Thierry Brue
P3-957
Somatotropic pituitary insufficiency in Kearns-Sayre syndrome – the clinical picture, genetic diagnosis and efficacy of rhGH therapy
Aleksandra Rojek, Marek Niedziela
Somatotropic pituitary insufficiency in Kearns-Sayre syndrome – the clinical picture, genetic diagnosis and efficacy of rhGH therapy
Aleksandra Rojek, Marek Niedziela
P3-958
The correlation between the increase in insulin-like growth factor-I 24 hours after the first injection of growth hormone and the improved growth.
Kenichi Miyako, Yuichi Mushimoto, Atsuko Kawano
The correlation between the increase in insulin-like growth factor-I 24 hours after the first injection of growth hormone and the improved growth.
Kenichi Miyako, Yuichi Mushimoto, Atsuko Kawano
P3-959
Late diagnosis of a type II/III mucolipidoses treated with GH replacement therapy
Iulia Crumpei, Alina Belceanu, Ioana Armasu, Elena Braha, Cristina Rusu, Adina Manolachie, Zmau George, Cristina Preda, Carmen Vulpoi
Late diagnosis of a type II/III mucolipidoses treated with GH replacement therapy
Iulia Crumpei, Alina Belceanu, Ioana Armasu, Elena Braha, Cristina Rusu, Adina Manolachie, Zmau George, Cristina Preda, Carmen Vulpoi
P3-960
DOES APPLYING REGULAR QUESTIONNAIRE TO PATIENTS ON GROWTH HORMONE INCREASE THE COMPLIANCE ?
mikayir genens, sukran poyrazoglu, mine sukur, firdevs bas, ruveyde bundak, feyza darendeliler
DOES APPLYING REGULAR QUESTIONNAIRE TO PATIENTS ON GROWTH HORMONE INCREASE THE COMPLIANCE ?
mikayir genens, sukran poyrazoglu, mine sukur, firdevs bas, ruveyde bundak, feyza darendeliler
P3-961
Characterization of Children Born Small for Gestational Age (SGA) Within the Australian Indications for Growth Hormone (GH) Therapy: An OZGROW Analysis
Ian Hughes, Mark Harris, Andrew Cotterill
Characterization of Children Born Small for Gestational Age (SGA) Within the Australian Indications for Growth Hormone (GH) Therapy: An OZGROW Analysis
Ian Hughes, Mark Harris, Andrew Cotterill
P3-962
Effectiveness of rhGH treatment in a boy with nephrogenic diabetes insipidus
Clemens Kamrath, Stefan Wudy
Effectiveness of rhGH treatment in a boy with nephrogenic diabetes insipidus
Clemens Kamrath, Stefan Wudy
P3-963
The Easypod™ Connect Observational Study (ECOS): comparison of results from interim analyses
Peter Davies, Marc Nicolino, Svante Norgren, George Stoyanov, Ekaterina Koledova, John VanderMeulen
The Easypod™ Connect Observational Study (ECOS): comparison of results from interim analyses
Peter Davies, Marc Nicolino, Svante Norgren, George Stoyanov, Ekaterina Koledova, John VanderMeulen
P3-964
EVALUATION OF THE FACILITY OF USE OF A NEW GROWTH HORMONE ADMINISTRATION DEVICE. STUDY DAGH2014.
María José Rivero-Martín, Ana Ontañón-Nasarre, María José Alcázar-Villar, America Carrasco-Torrents, Ana Andrés-Rosado, David Montes-Bentura
EVALUATION OF THE FACILITY OF USE OF A NEW GROWTH HORMONE ADMINISTRATION DEVICE. STUDY DAGH2014.
María José Rivero-Martín, Ana Ontañón-Nasarre, María José Alcázar-Villar, America Carrasco-Torrents, Ana Andrés-Rosado, David Montes-Bentura
P3-965
Effect of human growth hormone on growth rate of short stature children with low birth weight
Fatemeh Saffari, Hoda Hassani, Neda Esmailzadehha, Amir Javadi
Effect of human growth hormone on growth rate of short stature children with low birth weight
Fatemeh Saffari, Hoda Hassani, Neda Esmailzadehha, Amir Javadi
P3-966
GH treatment and first year response: a retrospective study
Catarina Moniz, Carlos Vasconcelos, Clotilde Limbert, Catarina Saraiva
GH treatment and first year response: a retrospective study
Catarina Moniz, Carlos Vasconcelos, Clotilde Limbert, Catarina Saraiva
P3-967
Usefulness of reevaluation of Growth Hormone secretion during puberty
Paolo Cavarzere, Diego Ramaroli, Silvana Lauriola, Grazia Morandi, Rossella Gaudino, Franco Antoniazzi
Usefulness of reevaluation of Growth Hormone secretion during puberty
Paolo Cavarzere, Diego Ramaroli, Silvana Lauriola, Grazia Morandi, Rossella Gaudino, Franco Antoniazzi
P3-968
Bone age maturation in Prader-Willi Syndrome on GH treatment is accelerated in pre-pubertal age without affecting final height
Urs Eiholzer, Carla Obwegeser, Fabienne Witassek, Udo Meinhardt
Bone age maturation in Prader-Willi Syndrome on GH treatment is accelerated in pre-pubertal age without affecting final height
Urs Eiholzer, Carla Obwegeser, Fabienne Witassek, Udo Meinhardt
P3-969
Evaluating First Year Response and Final Height to Growth Hormone Treatment in Growth Hormone Deficiency based on Peak GH levels on Testing
Saygin Abali, Serpil Bas, Azad Akbarzade, Zeynep Atay, Belma Haliloglu, Tulay Guran, Serap Turan, Abdullah Bereket
Evaluating First Year Response and Final Height to Growth Hormone Treatment in Growth Hormone Deficiency based on Peak GH levels on Testing
Saygin Abali, Serpil Bas, Azad Akbarzade, Zeynep Atay, Belma Haliloglu, Tulay Guran, Serap Turan, Abdullah Bereket
P3-970
Growth hormone therapy in children: predictive factors and short-term and long-term response criteria in an Italian cohort
Cristina Partenope, Giulia Pruccoli, Chiara Maria Damia, Maria Piera Ferrarello, Gisella Garbetta, Sara Osimani, Giovanna Weber, Gabriella Pozzobon
Growth hormone therapy in children: predictive factors and short-term and long-term response criteria in an Italian cohort
Cristina Partenope, Giulia Pruccoli, Chiara Maria Damia, Maria Piera Ferrarello, Gisella Garbetta, Sara Osimani, Giovanna Weber, Gabriella Pozzobon
P3-971
PATIENTS WITH CHILDHOOD ONSET GROWTH HORMONE DEFICIENCY TREATED WITH rhGH – REEVALUATION IN THE TRANSITION PERIOD BETWEEN CHILDHOOD AND ADULTHOOD – PRELIMINARY STUDY
Camelia Procopiuc, Andra Caragheorgheopol, Iuliana Gherlan, Andreea Brehar, Adriana Padure, Andra Dumitrascu, Mariana Costache, Ioana Ardeleanu, Crisina Dumitrescu
PATIENTS WITH CHILDHOOD ONSET GROWTH HORMONE DEFICIENCY TREATED WITH rhGH – REEVALUATION IN THE TRANSITION PERIOD BETWEEN CHILDHOOD AND ADULTHOOD – PRELIMINARY STUDY
Camelia Procopiuc, Andra Caragheorgheopol, Iuliana Gherlan, Andreea Brehar, Adriana Padure, Andra Dumitrascu, Mariana Costache, Ioana Ardeleanu, Crisina Dumitrescu
P3-972
Time trends in baseline characteristics (2006–2014) in short children with growth hormone deficiency (GHD), born small for gestational age (SGA) and with Ullrich-Turner syndrome (TS) enrolled in NordiNet® International Outcomes Study (IOS) in Germany and Czech Republic.
Helmuth Gunther Dörr, Jürgen Bramswig, Stefanie Meckes-Ferber, Effie Pournara, Birgitte Tønnes Pedersen, Marta Šnajderová
Time trends in baseline characteristics (2006–2014) in short children with growth hormone deficiency (GHD), born small for gestational age (SGA) and with Ullrich-Turner syndrome (TS) enrolled in NordiNet® International Outcomes Study (IOS) in Germany and Czech Republic.
Helmuth Gunther Dörr, Jürgen Bramswig, Stefanie Meckes-Ferber, Effie Pournara, Birgitte Tønnes Pedersen, Marta Šnajderová
P3-973
A patient with an 13q deletion syndrome, important growth delay and somatotropine insufficiency undergoing growth hormone therapy– case report.
Kinga Wolaniecka-Deahan, Mieczysław Szalecki, Krystyna Chrzanowska
A patient with an 13q deletion syndrome, important growth delay and somatotropine insufficiency undergoing growth hormone therapy– case report.
Kinga Wolaniecka-Deahan, Mieczysław Szalecki, Krystyna Chrzanowska
P3-974
Linear Growth in a Child with Ellis Van Creveld Syndrome: Positive Effect of growth hormone therapy .
Ashraf Soliman, Fawzia Alyafei
Linear Growth in a Child with Ellis Van Creveld Syndrome: Positive Effect of growth hormone therapy .
Ashraf Soliman, Fawzia Alyafei
P3-975
Factors Effecting Response to Growth Hormone Treatment in Children with Turner Syndrome
Serpil Bas, Saygin Abali, Zeynep Atay, Belma Haliloglu, Ziya Gurbanov, Tulay Guran, Abdullah Bereket, Serap Turan
Factors Effecting Response to Growth Hormone Treatment in Children with Turner Syndrome
Serpil Bas, Saygin Abali, Zeynep Atay, Belma Haliloglu, Ziya Gurbanov, Tulay Guran, Abdullah Bereket, Serap Turan
P3-976
Thyroid function in children with Prader-Willi syndrome, the first 12 months of Growth Hormone Therapy.
Yassmin M. Musthaffa, Ian P. Hughes, Mark Harris, Gary Leong
Thyroid function in children with Prader-Willi syndrome, the first 12 months of Growth Hormone Therapy.
Yassmin M. Musthaffa, Ian P. Hughes, Mark Harris, Gary Leong
P3-977
Congenital hypopituitarism and severe developmental delay associated with homozygous POUF1 mutation.
Maria Melikian, Anatoly Tiulpakov, Anna Gavrilova
Congenital hypopituitarism and severe developmental delay associated with homozygous POUF1 mutation.
Maria Melikian, Anatoly Tiulpakov, Anna Gavrilova
P3-978
GH therapy in Lery Weill Syndrome: report of three cases
Elisa Guidoni, Michela Franceschini, Cristina Mucaria, Renato Scarinci, Giovanna Municchi
GH therapy in Lery Weill Syndrome: report of three cases
Elisa Guidoni, Michela Franceschini, Cristina Mucaria, Renato Scarinci, Giovanna Municchi
P3-979
The assessment of quality of life and new technologies for therapeutic monitoring in a cohort of pediatric patients treated with growth hormone
Giulia Pruccoli, Cristina Partenope, Maria Piera Ferrarello, Chiara Maria Damia, Sara Osimani, Gisella Garbetta, Giovanna Weber, Gabriella Pozzobon
The assessment of quality of life and new technologies for therapeutic monitoring in a cohort of pediatric patients treated with growth hormone
Giulia Pruccoli, Cristina Partenope, Maria Piera Ferrarello, Chiara Maria Damia, Sara Osimani, Gisella Garbetta, Giovanna Weber, Gabriella Pozzobon
P3-980
Final height in patients with isolated growth hormone deficiency and multiple pituitary hormone deficiencies, treated with growth hormone
Elena Bashnina, Olga Berseneva, Sergey Fogt
Final height in patients with isolated growth hormone deficiency and multiple pituitary hormone deficiencies, treated with growth hormone
Elena Bashnina, Olga Berseneva, Sergey Fogt
P3-981
CURRENT PRACTICE IN DIAGNOSIS AND TREATMENT OF GROWTH HORMONE DEFICIENCY IN CHILDHOOD: A SURVEY FROM TURKEY
Sukran Poyrazoglu, Teoman Akcay, Mehmet Emre Atabek, Aysun Bideci, Iffet Bircan, Ece Bober, Sule Can, Sukran Darcan, Betul Ersoy, Ayla Guven, Cengiz Kara, Mehmet Keskin, Selim Kurtoglu, Mehmet Nuri Ozbek, Tolga Ozgen, Zeynep Siklar, Enver Simsek, Serap Turan, Bilgin Yuksel, Feyza Darendeliler
CURRENT PRACTICE IN DIAGNOSIS AND TREATMENT OF GROWTH HORMONE DEFICIENCY IN CHILDHOOD: A SURVEY FROM TURKEY
Sukran Poyrazoglu, Teoman Akcay, Mehmet Emre Atabek, Aysun Bideci, Iffet Bircan, Ece Bober, Sule Can, Sukran Darcan, Betul Ersoy, Ayla Guven, Cengiz Kara, Mehmet Keskin, Selim Kurtoglu, Mehmet Nuri Ozbek, Tolga Ozgen, Zeynep Siklar, Enver Simsek, Serap Turan, Bilgin Yuksel, Feyza Darendeliler
P3-982
Experience of the use of genetically engineered growth hormone "Rastan" by children in clinical practice.
Kulagina E.P., Savelyeva E.V., Chistousova G.V.
SBME “Orenburg children”s clinical hospital”, Orenburg
SBME “Perm regional children”s clinical hospital”, Perm
Elena Kulagina, Elena Savelyeva, Galina Chistousova
Experience of the use of genetically engineered growth hormone "Rastan" by children in clinical practice.
Kulagina E.P., Savelyeva E.V., Chistousova G.V.
SBME “Orenburg children”s clinical hospital”, Orenburg
SBME “Perm regional children”s clinical hospital”, Perm
Elena Kulagina, Elena Savelyeva, Galina Chistousova
P3-983
Growth Hormone Therapy in Kuwait: First Report on Characteristics and Response in Treated Children
Dalia Al-Abdulrazzaq, Iman Al-Basari
Growth Hormone Therapy in Kuwait: First Report on Characteristics and Response in Treated Children
Dalia Al-Abdulrazzaq, Iman Al-Basari
LBP-1270
Long-term Safety and Effectiveness of daily and weekly growth hormone treatment in pediatric patients
Jae Hyun Kim, Il Tae Hwang, Sochung Chung, Young-Jun Rhie, Hyun-Wook Chae, Choong Ho Shin
Long-term Safety and Effectiveness of daily and weekly growth hormone treatment in pediatric patients
Jae Hyun Kim, Il Tae Hwang, Sochung Chung, Young-Jun Rhie, Hyun-Wook Chae, Choong Ho Shin
LBP-1267
Safety and Efficacy of Long-Acting Growth Hormone (VRS-317) in Children with GHD: Effects of Dose Change in the Second Treatment Year
George Bright, Wayne V. Moore, Huong Jil Nguyen, Gad B. Kletter, Bradley S. Miller, Patricia Y. Fechner, David Ng, Eric Humphriss, Jeffrey L. Cleland
Safety and Efficacy of Long-Acting Growth Hormone (VRS-317) in Children with GHD: Effects of Dose Change in the Second Treatment Year
George Bright, Wayne V. Moore, Huong Jil Nguyen, Gad B. Kletter, Bradley S. Miller, Patricia Y. Fechner, David Ng, Eric Humphriss, Jeffrey L. Cleland
P1-89
Royal Jelly supplementation induces the growth plate development and increases plasma growth hormone and estradiol levels in prepubertal rats
Murat Sever, Ozgur Pirgon, Metin Ciris, Bunyamin Aydin
Royal Jelly supplementation induces the growth plate development and increases plasma growth hormone and estradiol levels in prepubertal rats
Murat Sever, Ozgur Pirgon, Metin Ciris, Bunyamin Aydin
P1-90
Silver-Russell syndrome without body asymmetry in three patients with duplications of maternally derived chromosome 11p15 involving CDKN1C
Shinichi Nakashima, Fumiko Kato, Tomoki Kosho, Keisuke Nagasaki, Toru Kikuchi, Masayo Kagami, Maki Fukami, Tsutomu Ogata
Silver-Russell syndrome without body asymmetry in three patients with duplications of maternally derived chromosome 11p15 involving CDKN1C
Shinichi Nakashima, Fumiko Kato, Tomoki Kosho, Keisuke Nagasaki, Toru Kikuchi, Masayo Kagami, Maki Fukami, Tsutomu Ogata
P1-91
Mutation in RTTN, a regulator of ciliary function, causes a complex syndrome characterized by severe congenital microcephaly, lissencephaly and profound growth failure in two siblings
Anna Grandone, Vincenzo Nigro, Annalaura Torella, Adalgisa Festa, Caterina Luongo, Pierluigi Marzuillo, Ruggero Coppola, Emanuele Miraglia del Giudice, Laura Perrone
Mutation in RTTN, a regulator of ciliary function, causes a complex syndrome characterized by severe congenital microcephaly, lissencephaly and profound growth failure in two siblings
Anna Grandone, Vincenzo Nigro, Annalaura Torella, Adalgisa Festa, Caterina Luongo, Pierluigi Marzuillo, Ruggero Coppola, Emanuele Miraglia del Giudice, Laura Perrone
P1-92
Chronic Effects of Bisphenol A administration on Growth Hormone Activity
Mohammed AL-Masroori, Mohammed Hebais, Amnah AL-Araimi, Fahad Zadjali
Chronic Effects of Bisphenol A administration on Growth Hormone Activity
Mohammed AL-Masroori, Mohammed Hebais, Amnah AL-Araimi, Fahad Zadjali
P1-93
Severe IGF-I deficiency and multi-organ autoimmune disease associated with novel germline STAT3 mutations.
Paula Scaglia, Ana Keselman, Mariana Gutiérrez, Sabina Domené, Miguel Blanco, Nora Sanguinetti, Liliana Bezrodnik, Daniela Di Giovanni, María Soledad Caldirola, Lucia Martucci, Liliana Karabatas, Ashish Kumar, Nana-Hawa Jones, Vivian Hwa, Santiago Revale, Martín Vázquez, Héctor Jasper, Horacio Domené
Severe IGF-I deficiency and multi-organ autoimmune disease associated with novel germline STAT3 mutations.
Paula Scaglia, Ana Keselman, Mariana Gutiérrez, Sabina Domené, Miguel Blanco, Nora Sanguinetti, Liliana Bezrodnik, Daniela Di Giovanni, María Soledad Caldirola, Lucia Martucci, Liliana Karabatas, Ashish Kumar, Nana-Hawa Jones, Vivian Hwa, Santiago Revale, Martín Vázquez, Héctor Jasper, Horacio Domené
P1-95
Various imprinting disorders underlying Silver-Russell Syndrome-compatible phenotype
Masayo Kagami, Keiko Matsubara, Shinichiro Sano, Akie Nakamura, Seiji Mizuno, Naoki Hamajima, Atsuhiro Yanagisawa, Miyuki Hashimoto, Akira Yukote, Maki Fukami, Tsutomu Ogata
Various imprinting disorders underlying Silver-Russell Syndrome-compatible phenotype
Masayo Kagami, Keiko Matsubara, Shinichiro Sano, Akie Nakamura, Seiji Mizuno, Naoki Hamajima, Atsuhiro Yanagisawa, Miyuki Hashimoto, Akira Yukote, Maki Fukami, Tsutomu Ogata
P1-96
Ligase IV deficiency syndrome as a cause of microcephalic primordial dwarfism in dizygotic twins
Céline Girardin, Emmanuelle Ranza, Philippe Klee, Mirjam Dirlewanger, Marianne Caflisch, Armand Bottani, Valérie Schwitzgebel
Ligase IV deficiency syndrome as a cause of microcephalic primordial dwarfism in dizygotic twins
Céline Girardin, Emmanuelle Ranza, Philippe Klee, Mirjam Dirlewanger, Marianne Caflisch, Armand Bottani, Valérie Schwitzgebel
P1-97
HIGH FREQUENCY OF HYPOMORPHIC ALLELIC HAPLOTYPES OF THE GH1 PROXIMAL PROMOTER IN PATIENTS WITH PROPORTIONAL UNDERGROWTH AND ISOLATED GH DEFICIENCY
Angel Campos-Barros, Ana Gómez-Núñez, Olga Zurita-Múñoz, Elena Gallego-Gómez, Jaime Cruz-Rojo, Lucía Garzón, Cristina Luzuriaga-Tomás, Isolina Riaño-Galán, Carolina Bezanilla-López, José María Donate-Legaz, Mercedes Marbán-Calzón, Sara Rupérez, Florinda Hermoso, Emma Lara-Orejas, Mª Victoria Borrás-Pérez, Jose Manuel Rius-Peris, Beatriz García-Cuartero, Isabel González-Casado
HIGH FREQUENCY OF HYPOMORPHIC ALLELIC HAPLOTYPES OF THE GH1 PROXIMAL PROMOTER IN PATIENTS WITH PROPORTIONAL UNDERGROWTH AND ISOLATED GH DEFICIENCY
Angel Campos-Barros, Ana Gómez-Núñez, Olga Zurita-Múñoz, Elena Gallego-Gómez, Jaime Cruz-Rojo, Lucía Garzón, Cristina Luzuriaga-Tomás, Isolina Riaño-Galán, Carolina Bezanilla-López, José María Donate-Legaz, Mercedes Marbán-Calzón, Sara Rupérez, Florinda Hermoso, Emma Lara-Orejas, Mª Victoria Borrás-Pérez, Jose Manuel Rius-Peris, Beatriz García-Cuartero, Isabel González-Casado
P2-446
Body mass index negatively correlates with growth hormone response to GH provocation testing.
Ioannis- Anargyros Vasilakis, Ruth Gausche, Christoph Beger, Juergen Kratzsch, Wieland Kiess, Antje Koerner, Roland Pfaeffle
Body mass index negatively correlates with growth hormone response to GH provocation testing.
Ioannis- Anargyros Vasilakis, Ruth Gausche, Christoph Beger, Juergen Kratzsch, Wieland Kiess, Antje Koerner, Roland Pfaeffle
P2-447
SHOX mutation spectrum in an unbiased cohort of 585 patients referred for Leri-Weill dyschondrosteosis or idiopathic short stature.
Alberta Belinchón, Sara Benito-Sanz, Carolina de la Torre, Ana C. Barreda-Bonís, Isabel González-Casado, Karen E. Heath
SHOX mutation spectrum in an unbiased cohort of 585 patients referred for Leri-Weill dyschondrosteosis or idiopathic short stature.
Alberta Belinchón, Sara Benito-Sanz, Carolina de la Torre, Ana C. Barreda-Bonís, Isabel González-Casado, Karen E. Heath
P2-448
Determination of the pathogenicity of SHOX P2 promoter variants, identified in patients with Léri-Weill dyschondrosteosis or idiopathic short stature
Alberta Belinchón, Sara Benito-Sanz, Karen E. Heath
Determination of the pathogenicity of SHOX P2 promoter variants, identified in patients with Léri-Weill dyschondrosteosis or idiopathic short stature
Alberta Belinchón, Sara Benito-Sanz, Karen E. Heath
P2-449
Risk for non-alcoholic fatty liver disease in young adults born preterm
Laura M. Breij, Gerthe F. Kerkhof, Anita C.S. Hokken-Koelega
Risk for non-alcoholic fatty liver disease in young adults born preterm
Laura M. Breij, Gerthe F. Kerkhof, Anita C.S. Hokken-Koelega
P2-450
Pharmacokinetics and Efficacy of a long-acting human growth hormone with Fc fusion protein
SUJIN KIM, DONG-KYU JIN, SUNGYOON CHO, RIMM HUH, JINSUP KIM, ARAM YANG, HYUNHEE KWAK
Pharmacokinetics and Efficacy of a long-acting human growth hormone with Fc fusion protein
SUJIN KIM, DONG-KYU JIN, SUNGYOON CHO, RIMM HUH, JINSUP KIM, ARAM YANG, HYUNHEE KWAK
P2-451
SHOX deficiency: clinical, radiological signs and value of screening scores
Giulia Genoni, Sandra Esposito, Valentina Agarla, Alice Monzani, Matteo Castagno, Silvia Raviolo, Antonella Petri, Flavia Prodam, Simonetta Bellone, Gianni Bona
SHOX deficiency: clinical, radiological signs and value of screening scores
Giulia Genoni, Sandra Esposito, Valentina Agarla, Alice Monzani, Matteo Castagno, Silvia Raviolo, Antonella Petri, Flavia Prodam, Simonetta Bellone, Gianni Bona
P2-452
Skeletal Dysplasia with Short Stature and a Larsen-like Phenotype due to a Homozygous Mutation in B3GAT3
Elisabeth Steichen-Gersdorf, Franco Laccone
Skeletal Dysplasia with Short Stature and a Larsen-like Phenotype due to a Homozygous Mutation in B3GAT3
Elisabeth Steichen-Gersdorf, Franco Laccone
P2-453
Cross-sectional and longitudinal follow-up of changes in glucose metabolism in prepubertal growth-hormone (GH)-treated SGA-patients: results of an unicentric study.
Carmen Sydlik, Susanne Bechtold, Claudia Weissenbacher, Julia Roeb, Matthias Buckl, Stefanie Putzker, Heinrich Schmidt
Cross-sectional and longitudinal follow-up of changes in glucose metabolism in prepubertal growth-hormone (GH)-treated SGA-patients: results of an unicentric study.
Carmen Sydlik, Susanne Bechtold, Claudia Weissenbacher, Julia Roeb, Matthias Buckl, Stefanie Putzker, Heinrich Schmidt
P2-454
Growth Pattern in children affected of Lowe Syndrome. Descriptive multicenter international study: Preliminary data
Larisa Suarez-Ortega, Anna Casteràs Román, Marisa Loranca, Jaime Sánchez del Pozo, Rare Commons Group
Growth Pattern in children affected of Lowe Syndrome. Descriptive multicenter international study: Preliminary data
Larisa Suarez-Ortega, Anna Casteràs Román, Marisa Loranca, Jaime Sánchez del Pozo, Rare Commons Group
P2-455
Effect of aromatase inhibitor treatment during adolescence on the final adult height in males with idiopathic short stature
Li Yan-hong, Du Min-lian, Ma Hua-mei, Chen Hong-shan, Chen Qiu-li, Zhang Jun
Effect of aromatase inhibitor treatment during adolescence on the final adult height in males with idiopathic short stature
Li Yan-hong, Du Min-lian, Ma Hua-mei, Chen Hong-shan, Chen Qiu-li, Zhang Jun
P2-456
The Effect of Inhaled Glucocorticoid Therapy on Growth Patterns in Pre-Pubertal Children with Asthma Compared to Controls
Chiara De Leonibus, Zane Roze, Marina Attanasi, Maria Loredana Marcovecchio, Sabrina Di Pillo, Francesco Chiarelli, Angelika Mohn
The Effect of Inhaled Glucocorticoid Therapy on Growth Patterns in Pre-Pubertal Children with Asthma Compared to Controls
Chiara De Leonibus, Zane Roze, Marina Attanasi, Maria Loredana Marcovecchio, Sabrina Di Pillo, Francesco Chiarelli, Angelika Mohn
P2-459
Heterozygous NPR2 mutations cause disproportionate short stature, similar to Léri-Weill dyschondrosteosis
Alfonso Hisado-Oliva, Ana Isabel Garre-Vázquez, Fabiola Santaolalla-Caballero, Alberta Belinchón, Ana Coral Barreda-Bonis, Gabriela A Vasques, Joaquin Ramirez, Cristina Luzuriaga, Isabel González-Casado, Sara Benito-Sanz, Alexander A Jorge, Angel Campos-Barros, Karen E Heath
Heterozygous NPR2 mutations cause disproportionate short stature, similar to Léri-Weill dyschondrosteosis
Alfonso Hisado-Oliva, Ana Isabel Garre-Vázquez, Fabiola Santaolalla-Caballero, Alberta Belinchón, Ana Coral Barreda-Bonis, Gabriela A Vasques, Joaquin Ramirez, Cristina Luzuriaga, Isabel González-Casado, Sara Benito-Sanz, Alexander A Jorge, Angel Campos-Barros, Karen E Heath
P2-460
INDIVIDUALS WITH COW'S MILK ALLERGY ARE AT RISK FOR NOT REACHING THEIR GROWTH POTENTIAL
Tali Sinai, Roni Amitzur-Levy, Liat Nachshon, Tamar Yihye, Michael R. Goldberg, Efrat Monsonego-Ornan, Yitzhak Katz
INDIVIDUALS WITH COW'S MILK ALLERGY ARE AT RISK FOR NOT REACHING THEIR GROWTH POTENTIAL
Tali Sinai, Roni Amitzur-Levy, Liat Nachshon, Tamar Yihye, Michael R. Goldberg, Efrat Monsonego-Ornan, Yitzhak Katz
P2-461
French growth reference charts should be updated
Athanasia Stoupa, Alexandra Goischke, Camille Garcin, Caroline Elie, Magali Viaud, Anne Thery, Geneviève Richard, Michel Polak
French growth reference charts should be updated
Athanasia Stoupa, Alexandra Goischke, Camille Garcin, Caroline Elie, Magali Viaud, Anne Thery, Geneviève Richard, Michel Polak
P2-462
Advanced bone age and accelerated dental development associated with elevated retinoic acid levels and haploinsufficiency of CYP26A1 and CYP26C1
Ola Nilsson, Nina Isoherranen, Ines Guttmann-Bauman, YouHee Jee, Michael Guo, Julian Lui, Andrew Dauber
Advanced bone age and accelerated dental development associated with elevated retinoic acid levels and haploinsufficiency of CYP26A1 and CYP26C1
Ola Nilsson, Nina Isoherranen, Ines Guttmann-Bauman, YouHee Jee, Michael Guo, Julian Lui, Andrew Dauber
P2-463
Recurrent IGFALS gene mutations p.E35Gfs*17 and p.[L409F;A475V]: hot spot or founder effect?
Paula Scaglia, Andrea Sala, Ignacio Bergadá, Debora Braslavsky, Ana Keselman, Angela Espínola-Castro, Sabina Domené, Héctor Jasper, Daniel Corach, Horacio Domené
Recurrent IGFALS gene mutations p.E35Gfs*17 and p.[L409F;A475V]: hot spot or founder effect?
Paula Scaglia, Andrea Sala, Ignacio Bergadá, Debora Braslavsky, Ana Keselman, Angela Espínola-Castro, Sabina Domené, Héctor Jasper, Daniel Corach, Horacio Domené
P2-464
INFANT WITH PHENOTYPE SUGGESTIVE OF SILVER-RUSSELL SYNDROME AND STUDY OF NORMAL METHYLATION: CONSIDER 12Q14.3Q15 MICRODELETION SYNDROME.
NATALIA VARGAS, BLANCA LIDIA GALO, ARIADNA CAMPOS, TERESA VENDRELL, ANTONIO PLAJA, DIEGO YESTE
INFANT WITH PHENOTYPE SUGGESTIVE OF SILVER-RUSSELL SYNDROME AND STUDY OF NORMAL METHYLATION: CONSIDER 12Q14.3Q15 MICRODELETION SYNDROME.
NATALIA VARGAS, BLANCA LIDIA GALO, ARIADNA CAMPOS, TERESA VENDRELL, ANTONIO PLAJA, DIEGO YESTE
P2-465
Making adult height prediction complete: Forecasting the age of the growth spurt and the height & velocity trajectories until adulthood
David Martin, Sofus Mortensen, Oscar Jenni, Hans Henrik Thodberg
Making adult height prediction complete: Forecasting the age of the growth spurt and the height & velocity trajectories until adulthood
David Martin, Sofus Mortensen, Oscar Jenni, Hans Henrik Thodberg
P2-466
Whole exome identifies de novo HRAS mutation underlying primary IGF-1 deficiency (PIGFD)
Greta Grosse, Alina Hilger, Markus Draaken, Michael Ludwig, Heiko Reutter, Franziska Lorenzen, Joachim Woelfle
Whole exome identifies de novo HRAS mutation underlying primary IGF-1 deficiency (PIGFD)
Greta Grosse, Alina Hilger, Markus Draaken, Michael Ludwig, Heiko Reutter, Franziska Lorenzen, Joachim Woelfle
P2-467
Clinical and Biochemical Characteristics of a Female Patient with a Novel Homozygous STAT5B Mutation but Lack of Pulmonary Disease
Gonul Catli, Vivian Hwa, Monique Loseqoot, Berk Ozyilmaz, Neslihan Edeer, Bumin Nuri Dundar, Jan Marteen Wit
Clinical and Biochemical Characteristics of a Female Patient with a Novel Homozygous STAT5B Mutation but Lack of Pulmonary Disease
Gonul Catli, Vivian Hwa, Monique Loseqoot, Berk Ozyilmaz, Neslihan Edeer, Bumin Nuri Dundar, Jan Marteen Wit
P2-468
Novel heterozygous ACAN mutations in short stature: expanding the clinical spectrum
Lucia Sentchordi, Jimena Barraza, Carlos Iván Rivera, M. Victoria Marcos, M. Consuelo Sanchez, Elena Vallespín, Angela del Pozo, Karen E. Heath
Novel heterozygous ACAN mutations in short stature: expanding the clinical spectrum
Lucia Sentchordi, Jimena Barraza, Carlos Iván Rivera, M. Victoria Marcos, M. Consuelo Sanchez, Elena Vallespín, Angela del Pozo, Karen E. Heath
P2-469
Major improvement in parental perception of their children’s height-specific quality of life after one year of GH treatment - our experience with the QoLiSSY questionnaire.
Laura Gabriela González-Briceño, Magali Viaud, Isabelle Flechtner, Yamina Dassa, Dinane Samara-Boustani, Caroline Thalassinos, Christian Pauwels, Jacques Beltrand, Kanetee Busiah, Graziella Pinto, Michel Polak
Major improvement in parental perception of their children’s height-specific quality of life after one year of GH treatment - our experience with the QoLiSSY questionnaire.
Laura Gabriela González-Briceño, Magali Viaud, Isabelle Flechtner, Yamina Dassa, Dinane Samara-Boustani, Caroline Thalassinos, Christian Pauwels, Jacques Beltrand, Kanetee Busiah, Graziella Pinto, Michel Polak
P2-472
Characterisation of partial SHOX deletions/duplications reveals intron 3 to be a hotspot region
Sara Benito-Sanz, Alberta Belinchón, Karen E Heath
Characterisation of partial SHOX deletions/duplications reveals intron 3 to be a hotspot region
Sara Benito-Sanz, Alberta Belinchón, Karen E Heath
P2-473
The pubertal gain in height is inversely related to BMI in childhood
Anton Holmgren, Aimon Niklasson, Andreas F.M. Nierop, Lars Gelander, A. Stefan Aronson, Agneta Sjöberg, Lauren Lissner, Kerstin Albertsson-Wikland
The pubertal gain in height is inversely related to BMI in childhood
Anton Holmgren, Aimon Niklasson, Andreas F.M. Nierop, Lars Gelander, A. Stefan Aronson, Agneta Sjöberg, Lauren Lissner, Kerstin Albertsson-Wikland
P2-474
Growth curves for height, weight, body mass index and head circumference in children with achondroplasia
Andrea Merker, Lars Hagenäs, Thomas Hertel, Lo Neumeyer
Growth curves for height, weight, body mass index and head circumference in children with achondroplasia
Andrea Merker, Lars Hagenäs, Thomas Hertel, Lo Neumeyer
P2-475
Growth hormone deficiency and pituitary dysgenesis in a girl with microdeletion 2q31.1
Elke Hammer, Andreas Busche, Gabriele Gillessen-Kaesbach
Growth hormone deficiency and pituitary dysgenesis in a girl with microdeletion 2q31.1
Elke Hammer, Andreas Busche, Gabriele Gillessen-Kaesbach
P2-476
One Year Screening Program for Stature Deviations - Strategy and Outcome
Galina Yordanova, Violeta Iotova, Mina Lateva, Sonya Galcheva, Rositsa Stoycheva, Vilchelm Mladenov, Vesselin Boyadjiev, Yulia Bazdarska, Antonia Ivanova
One Year Screening Program for Stature Deviations - Strategy and Outcome
Galina Yordanova, Violeta Iotova, Mina Lateva, Sonya Galcheva, Rositsa Stoycheva, Vilchelm Mladenov, Vesselin Boyadjiev, Yulia Bazdarska, Antonia Ivanova
P2-478
Comparison of the Turkish Growth Standards with the WHO standards
Zehra Yavas Abali, Ruveyde Bundak, Andrezj Furman, Gulbin Gokcay, Hulya Gunoz, Firdevs Bas, Feyza Darendeliler, Olcay Neyzi
Comparison of the Turkish Growth Standards with the WHO standards
Zehra Yavas Abali, Ruveyde Bundak, Andrezj Furman, Gulbin Gokcay, Hulya Gunoz, Firdevs Bas, Feyza Darendeliler, Olcay Neyzi
P2-479
Moya Moya syndrome in a patient with growth hormone deficiency and hypergonadotropic hypogonadism: to treat or not to treat with growth hormone therapy?
Laura Gabriela González Briceño, Athanasia Stoupa, Graziella Pinto, Philippe Touraine, Michel Polak
Moya Moya syndrome in a patient with growth hormone deficiency and hypergonadotropic hypogonadism: to treat or not to treat with growth hormone therapy?
Laura Gabriela González Briceño, Athanasia Stoupa, Graziella Pinto, Philippe Touraine, Michel Polak
P2-480
In vitro functional characterization of IGFALS gene variants found in ALS deficient or idiopathic short stature (ISS) children
Lucia Martucci, Paula Scaglia, Liliana Karabatas, Rodolfo Rey, Horacio Domené, Sabina Domené, Héctor Jasper
In vitro functional characterization of IGFALS gene variants found in ALS deficient or idiopathic short stature (ISS) children
Lucia Martucci, Paula Scaglia, Liliana Karabatas, Rodolfo Rey, Horacio Domené, Sabina Domené, Héctor Jasper
P2-481
KLINEFELTER SYNDROME WITH SHORT STATURE AND MICROCEPHALY: AN UNUSUAL COMBINATION
BLANCA LIDIA GALO, NATALIA VARGAS, MARIA CLEMENTE, TERESA VENDRELL, ALBERTO PLAJA, DIEGO YESTE
KLINEFELTER SYNDROME WITH SHORT STATURE AND MICROCEPHALY: AN UNUSUAL COMBINATION
BLANCA LIDIA GALO, NATALIA VARGAS, MARIA CLEMENTE, TERESA VENDRELL, ALBERTO PLAJA, DIEGO YESTE
P2-482
Childhood Growth of Boys with Congenital Hypogonadotropic Hypogonadism
Tero Varimo, Matti Hero, Eeva-Maria Laitinen, Päivi Miettinen, Johanna Tommiska, Anders Juul, Taneli Raivio
Childhood Growth of Boys with Congenital Hypogonadotropic Hypogonadism
Tero Varimo, Matti Hero, Eeva-Maria Laitinen, Päivi Miettinen, Johanna Tommiska, Anders Juul, Taneli Raivio
P3-1007
Depth And Timing Of Hypoglycaemia Achieved During Insulin Tolerance Test In Children
S C Wong, M Boroujerdi, J McNeilly, W Morris, C Carson, A Mason, G Shaikh, S F Ahmed
Depth And Timing Of Hypoglycaemia Achieved During Insulin Tolerance Test In Children
S C Wong, M Boroujerdi, J McNeilly, W Morris, C Carson, A Mason, G Shaikh, S F Ahmed
P3-1008
Presenting characteristics, auxological, and etiologic evaluation of 364 patients with growth hormone deficiency
Mehmet Nuri Ozbek, Birsen Baysal, Sibel Tanriverdi, Ahmet Deniz, Kahraman Oncel, Murat Ocal, Riza Taner Baran, Huseyin Demirbilek
Presenting characteristics, auxological, and etiologic evaluation of 364 patients with growth hormone deficiency
Mehmet Nuri Ozbek, Birsen Baysal, Sibel Tanriverdi, Ahmet Deniz, Kahraman Oncel, Murat Ocal, Riza Taner Baran, Huseyin Demirbilek
P3-1009
Nutritional Supplementation, Sleep Patterns and Growth in Short and Lean Prepubertal Children
Ayelet Machtei, Yael Lebenthal, Liora Lazar, Raanan Shamir, Moshe Phillip, Michal Yackobovitch-Gavan
Nutritional Supplementation, Sleep Patterns and Growth in Short and Lean Prepubertal Children
Ayelet Machtei, Yael Lebenthal, Liora Lazar, Raanan Shamir, Moshe Phillip, Michal Yackobovitch-Gavan
P3-1010
Disease-specific growth charts of Marfan syndrome in Korea
SUJIN KIM, SUNGYOON CHO, YOUNGBAE SOHN, SUNGWON PARK, DONG-KYU JIN, RIMM HUH, JINSUP KIM, ARAM YANG
Disease-specific growth charts of Marfan syndrome in Korea
SUJIN KIM, SUNGYOON CHO, YOUNGBAE SOHN, SUNGWON PARK, DONG-KYU JIN, RIMM HUH, JINSUP KIM, ARAM YANG
P3-1011
Targeted birth length and parental height measurement in babies with birthweight ≤ 9th centile; improved uptake during second study during one calendar year in a single newborn unit.
Colette Montgomery Sardar, Sharon Donnelly, Jamila Siddique, Emma Jane Gault, Sheena Kinmond, Malcolm Donaldson
Targeted birth length and parental height measurement in babies with birthweight ≤ 9th centile; improved uptake during second study during one calendar year in a single newborn unit.
Colette Montgomery Sardar, Sharon Donnelly, Jamila Siddique, Emma Jane Gault, Sheena Kinmond, Malcolm Donaldson
P3-1012
Case report of Wolf-Hirschhorn Syndrome by Chromosomal Microarray Analysis: Importance of the Molecular Investigation for the Etiological Diagnosis of Short Stature.
Renata Pinto, Irene Pinto, Lysa Minasi, Damiana Cunha, Cristiano Ribeiro, Cláudio Silva, Aparecido Cruz
Case report of Wolf-Hirschhorn Syndrome by Chromosomal Microarray Analysis: Importance of the Molecular Investigation for the Etiological Diagnosis of Short Stature.
Renata Pinto, Irene Pinto, Lysa Minasi, Damiana Cunha, Cristiano Ribeiro, Cláudio Silva, Aparecido Cruz
P3-1013
Achondroplasia reference as background matrix for following children with extreme short stature
Andrea Merker, Lars Hagenäs, Thomas Hertel, Lo Neumeyer
Achondroplasia reference as background matrix for following children with extreme short stature
Andrea Merker, Lars Hagenäs, Thomas Hertel, Lo Neumeyer
P3-1014
Altered gene-expression in human growth plate cartilage tissue exposed to dexamethasone.
Therése Cedervall, Farasat Zaman, Lars Sävendahl
Altered gene-expression in human growth plate cartilage tissue exposed to dexamethasone.
Therése Cedervall, Farasat Zaman, Lars Sävendahl
P3-1015
Reversible Growth Hormone Excess (GHE) in Two Girls with Neurofibromatosis Type 1 (NF-1) and Optic Pathway Glioma (OPG)
Ilaria Sani, Patrizia Bruzzi, Assunta Albanese
Reversible Growth Hormone Excess (GHE) in Two Girls with Neurofibromatosis Type 1 (NF-1) and Optic Pathway Glioma (OPG)
Ilaria Sani, Patrizia Bruzzi, Assunta Albanese
P3-1016
Autosomal recessive omodysplasia: a rare cause of disproportionate short stature
Cristiane Kopacek, Luciana Amorim Beltrão, Victória Bernardes Guimarães, Julia Santana Trombetta, Karen Lizeth Puma Lliguin, Vinicius de Souza, Géssica Haubert, André Campos da Cunha, Paulo Ricardo Gazzola Zen, Rafael Fabiano Machado Rosa
Autosomal recessive omodysplasia: a rare cause of disproportionate short stature
Cristiane Kopacek, Luciana Amorim Beltrão, Victória Bernardes Guimarães, Julia Santana Trombetta, Karen Lizeth Puma Lliguin, Vinicius de Souza, Géssica Haubert, André Campos da Cunha, Paulo Ricardo Gazzola Zen, Rafael Fabiano Machado Rosa
P3-1017
The growth characteristics of patients with Noonan syndrome, and first two years results of GH treatment: A Nationwide multicenter study
Zeynep SIKLAR, Merih BERBEROGLU, Mikayir GENENS, sükran POYRAZOGLU, Firdevs BAS, Feyza DARENDELıLER, Rüveyde BUNDAK, Zehra AYCAN, Senay SavaS ERDEVE, Semra CETINKAYA, Saygin ABALI, Zeynep ATAY, Serap TURAN, Cengiz KARA, Gülay Can YILMAZ, Nesibe AKYUREK, Ayhan ABACI, Erkan SARI, Semih BOLU, Huseyin ANIL KORKMAZ, Enver SIMSEK, Gönül CATLI, Atilla CAYIR, Olcay EVLIYAGLU, Sukriye Pinar ISGUVEN
The growth characteristics of patients with Noonan syndrome, and first two years results of GH treatment: A Nationwide multicenter study
Zeynep SIKLAR, Merih BERBEROGLU, Mikayir GENENS, sükran POYRAZOGLU, Firdevs BAS, Feyza DARENDELıLER, Rüveyde BUNDAK, Zehra AYCAN, Senay SavaS ERDEVE, Semra CETINKAYA, Saygin ABALI, Zeynep ATAY, Serap TURAN, Cengiz KARA, Gülay Can YILMAZ, Nesibe AKYUREK, Ayhan ABACI, Erkan SARI, Semih BOLU, Huseyin ANIL KORKMAZ, Enver SIMSEK, Gönül CATLI, Atilla CAYIR, Olcay EVLIYAGLU, Sukriye Pinar ISGUVEN
P3-1018
Vitamin D in short children on Growth Hormone Therapy: effects of vitamin D status and vitamin D supplementation on glucose homeostasis
CRISTINA DUMITRESCU, ANDRA CARAGHEORGHEOPOL, IULIANA GHERLAN, ANDREEA BREHAR, ADRIANA PADURE, MARIA OLARU, CAMELIA PROCOPIUC
Vitamin D in short children on Growth Hormone Therapy: effects of vitamin D status and vitamin D supplementation on glucose homeostasis
CRISTINA DUMITRESCU, ANDRA CARAGHEORGHEOPOL, IULIANA GHERLAN, ANDREEA BREHAR, ADRIANA PADURE, MARIA OLARU, CAMELIA PROCOPIUC
P3-1019
LARON SYNDROME CAUSED BY A LARGE DELETION IN GROWTH HORMONE RECEPTOR GENE
Gul Yesiltepe Mutlu, Heves Kirmizibekmez, Ahmet Arman, Sukru Hatun
LARON SYNDROME CAUSED BY A LARGE DELETION IN GROWTH HORMONE RECEPTOR GENE
Gul Yesiltepe Mutlu, Heves Kirmizibekmez, Ahmet Arman, Sukru Hatun
P3-1020
Growth hormone deficiency and glucose 1 transporter deficiency syndrome
GIUSEPPA PATTI, GIANLUCA TORNESE, PAOLA COSTA, ELENA FALESCHINI, ALESSANDRO VENTURA
Growth hormone deficiency and glucose 1 transporter deficiency syndrome
GIUSEPPA PATTI, GIANLUCA TORNESE, PAOLA COSTA, ELENA FALESCHINI, ALESSANDRO VENTURA
P3-1021
Response to rhGH treatment in patients with transient or permanent growth hormone deficiency
BEATRIZ VILLAFUERTE, RAQUEL BARRIO, MARIA MARTIN-FRIAS, MILAGROS ALONSO, YOKO OYAKAWA, BELEN ROLDAN
Response to rhGH treatment in patients with transient or permanent growth hormone deficiency
BEATRIZ VILLAFUERTE, RAQUEL BARRIO, MARIA MARTIN-FRIAS, MILAGROS ALONSO, YOKO OYAKAWA, BELEN ROLDAN
P3-1022
Postnatal growth and biochemical markers of late preterm infants: prospective birth cohort
Tomoko Yoshida, Reiko Horikawa
Postnatal growth and biochemical markers of late preterm infants: prospective birth cohort
Tomoko Yoshida, Reiko Horikawa
P3-1023
ALTERATIONS OF SHOX AND ITS ENHANCERS AS A CAUSE OF SHORT STATURE: EVOLUTION OF OUR CASES
MARIA LAURA BERTHOLT ZUBER, CRISTINA LUZURIAGA TOMAS, KAREN HEATH, CONCEPCIÓN FREIJO MARTIN, CRISTINA NARANJO GONZALEZ
ALTERATIONS OF SHOX AND ITS ENHANCERS AS A CAUSE OF SHORT STATURE: EVOLUTION OF OUR CASES
MARIA LAURA BERTHOLT ZUBER, CRISTINA LUZURIAGA TOMAS, KAREN HEATH, CONCEPCIÓN FREIJO MARTIN, CRISTINA NARANJO GONZALEZ
P3-1024
Vitamin D Status in Pre-pubertal children with Isolated Idiopathic Growth Hormone Deficiency: Effect of Growth Hormone Therapy
Rasha Hamza, Amira Hamed, Rehab Abdelmohsen
Vitamin D Status in Pre-pubertal children with Isolated Idiopathic Growth Hormone Deficiency: Effect of Growth Hormone Therapy
Rasha Hamza, Amira Hamed, Rehab Abdelmohsen
P3-1025
New point mutation in short stature homeobox (SHOX) gene leads to phenotype of Lery-Weill dyschondrosteosis.
Eva Koffeman, Gera Hoorweg-Nijman, Hanneke van Santen, Nienke Volker-Touw
New point mutation in short stature homeobox (SHOX) gene leads to phenotype of Lery-Weill dyschondrosteosis.
Eva Koffeman, Gera Hoorweg-Nijman, Hanneke van Santen, Nienke Volker-Touw
P3-1026
Fasting and post-meal levels of appetite regulating hormones, before and following growth hormone treatment, in children with idiopathic short stature
Michal Yackobovitch-Gavan, Galia Gat-Yablonski, Biana Shtaif, Moshe Phillip, Liora Lazar
Fasting and post-meal levels of appetite regulating hormones, before and following growth hormone treatment, in children with idiopathic short stature
Michal Yackobovitch-Gavan, Galia Gat-Yablonski, Biana Shtaif, Moshe Phillip, Liora Lazar
P3-1027
Impact of using WHO vs national growth charts on the clinical performance of a decision rule for growth monitoring
Pauline Scherdel, Soraya Matczak, Raja Brauner, Jean-François Salaun, Chalumeau Martin, Barbara Heude
Impact of using WHO vs national growth charts on the clinical performance of a decision rule for growth monitoring
Pauline Scherdel, Soraya Matczak, Raja Brauner, Jean-François Salaun, Chalumeau Martin, Barbara Heude
P3-1028
Comparison of the performance of algorithms proposed to standardize growth monitoring
Pauline Scherdel, Soraya Matczak, Raja Brauner, Jean-François Salaün, Barbara Heude, Martin Chalumeau
Comparison of the performance of algorithms proposed to standardize growth monitoring
Pauline Scherdel, Soraya Matczak, Raja Brauner, Jean-François Salaün, Barbara Heude, Martin Chalumeau
P3-1029
Evaluation of 207 Danish Girls with Constitutional Tall Stature (CTS): Diagnostic Characteristics and Effects of Oral Administration of 17-β Estradiol.
Emmie Nicolina Upners, Anders Juul
Evaluation of 207 Danish Girls with Constitutional Tall Stature (CTS): Diagnostic Characteristics and Effects of Oral Administration of 17-β Estradiol.
Emmie Nicolina Upners, Anders Juul
P3-1030
Sitting height/height ratio: an indicator for genetic study of the SHOX gene in children with disharmonic short stature. An in-house analysis.
Diego Yeste, Mildred Domínguez, Ariadna Campos, Maria Clemente, Paula Fernández, Alberto Plaja, Antonio Carrascosa
Sitting height/height ratio: an indicator for genetic study of the SHOX gene in children with disharmonic short stature. An in-house analysis.
Diego Yeste, Mildred Domínguez, Ariadna Campos, Maria Clemente, Paula Fernández, Alberto Plaja, Antonio Carrascosa
P3-1031
Final height in survivors of childhood acute leukemia
In Ah Jung, Yeon Jin Jeon, Shin Hee Kim, Won Kyoung Cho, So Hyun Park, Kyoung Soon Cho, Min Ho Jung, Byung Kyu Suh, Hyo Jin Kim
Final height in survivors of childhood acute leukemia
In Ah Jung, Yeon Jin Jeon, Shin Hee Kim, Won Kyoung Cho, So Hyun Park, Kyoung Soon Cho, Min Ho Jung, Byung Kyu Suh, Hyo Jin Kim
P3-1032
IMPACT OF RECOMBINANT HUMAN GROWTH HORMONE ON HEIGHT IN CHILDREN WITH CHRONIC KIDNEY DISEASE
Polina MIteva, Dimitar Roussinov, Elissaveta Stefanova, Russka Shumnalieva
IMPACT OF RECOMBINANT HUMAN GROWTH HORMONE ON HEIGHT IN CHILDREN WITH CHRONIC KIDNEY DISEASE
Polina MIteva, Dimitar Roussinov, Elissaveta Stefanova, Russka Shumnalieva
P3-1033
Birth length and metabolic syndrome in obese children.
Elena Inzaghi, Barbara Baldini Ferroli, Danilo Fintini, Armando Grossi, Rossana Fiori, Gianluigi Spadoni, Giuseppe Scirè, Stefano Cianfarani
Birth length and metabolic syndrome in obese children.
Elena Inzaghi, Barbara Baldini Ferroli, Danilo Fintini, Armando Grossi, Rossana Fiori, Gianluigi Spadoni, Giuseppe Scirè, Stefano Cianfarani
P3-1034
Birth characteristics influence the male to female diagnostic prevalence of idiopathic growth hormone deficiency
Cecilia Camacho-Hubner, Anders Lindberg, Ivo JP Arnhold, Michael B Ranke
Birth characteristics influence the male to female diagnostic prevalence of idiopathic growth hormone deficiency
Cecilia Camacho-Hubner, Anders Lindberg, Ivo JP Arnhold, Michael B Ranke
P3-1035
Two cases with decelerated linear growth, normal growth hormone (GH) – insulin-like
growth factor –I(IGF-I) axis with an exceptional response to GH therapy
Fawzia Alyafei, Ashraf Soliman
Two cases with decelerated linear growth, normal growth hormone (GH) – insulin-like
growth factor –I(IGF-I) axis with an exceptional response to GH therapy
Fawzia Alyafei, Ashraf Soliman
P3-1036
IMPACT OF GROWHT HORMONE (GH) TREATMENT IN CHILDREN FINAL HEIGHT AND WEIGHT STATUS
Daniela Guelho, Maria Miguel Almiro, Rosa Dantas, Isabel Paiva, Margarida Bastos, Joana Serra-Caetano, Rita Cardoso, Isabel Dinis, Alice Mirante
IMPACT OF GROWHT HORMONE (GH) TREATMENT IN CHILDREN FINAL HEIGHT AND WEIGHT STATUS
Daniela Guelho, Maria Miguel Almiro, Rosa Dantas, Isabel Paiva, Margarida Bastos, Joana Serra-Caetano, Rita Cardoso, Isabel Dinis, Alice Mirante
P3-1037
Expanding the role of nurses in improving patient care and clinical outcomes in growth disorders
Angela Casey, Lori Casnellie
Expanding the role of nurses in improving patient care and clinical outcomes in growth disorders
Angela Casey, Lori Casnellie
P3-1038
Short stature in a rare 15q duplication – is hGH treatment beneficial?
Adina Manolachie, Cristina Rusu, Elena Braha, Iulia Crumpei, Alina Belceanu, Mirela Puiu, Mihaela Anton, Letitia Leustean, Carmen Vulpoi
Short stature in a rare 15q duplication – is hGH treatment beneficial?
Adina Manolachie, Cristina Rusu, Elena Braha, Iulia Crumpei, Alina Belceanu, Mirela Puiu, Mihaela Anton, Letitia Leustean, Carmen Vulpoi
P3-1039
Sotos syndrome. Why is better an early diagnosis?
María Magdalena Hawkins Solís, Maria Royo Gómez, Ana Dolores Alcalde de Alvaré, Julia Yebra Yebra, Araceli García Pose, Alfonso Cañete Díaz
Sotos syndrome. Why is better an early diagnosis?
María Magdalena Hawkins Solís, Maria Royo Gómez, Ana Dolores Alcalde de Alvaré, Julia Yebra Yebra, Araceli García Pose, Alfonso Cañete Díaz
P3-1041
PATIENT WITH CLASSIC PHENOTYPE OF HYPOCHONDROPLASIA AND DELETION OF THE GENE SHOX
Mildred Domínguez, Sonia Amoretti, Esther Ropero, Ariadna Campos, María Clemente, Diego Yeste, Paula Fernández
PATIENT WITH CLASSIC PHENOTYPE OF HYPOCHONDROPLASIA AND DELETION OF THE GENE SHOX
Mildred Domínguez, Sonia Amoretti, Esther Ropero, Ariadna Campos, María Clemente, Diego Yeste, Paula Fernández
P3-1042
Growth Hormone Treatment in Survivors of Pediatric Brain Tumors
Sukran Darcan, Nurhan Ozcan, Damla Goksen, Mehmet Kantar, Tuncer Turhan, Nazan Cetingul, Samim Ozen
Growth Hormone Treatment in Survivors of Pediatric Brain Tumors
Sukran Darcan, Nurhan Ozcan, Damla Goksen, Mehmet Kantar, Tuncer Turhan, Nazan Cetingul, Samim Ozen
P3-1043
Growth Hormone Deficiency in a patient with 4p16 Deletion: an infrequent association with Wolf-Hirschhorn syndrome
Ioulia Polychroni, Maria Xatzipsalti, Helen Fryssira, Lela Stamogiannou
Growth Hormone Deficiency in a patient with 4p16 Deletion: an infrequent association with Wolf-Hirschhorn syndrome
Ioulia Polychroni, Maria Xatzipsalti, Helen Fryssira, Lela Stamogiannou
P3-1044
Value of alkaline phosphatase assay in short stature exploration
Alexandre NACCACHE, Claire GAYET, Marie Claire WIELICZKO, Mireille CASTANET
Value of alkaline phosphatase assay in short stature exploration
Alexandre NACCACHE, Claire GAYET, Marie Claire WIELICZKO, Mireille CASTANET
P3-1045
SGA incidence in one of the regions of the Russian Federation
Irina Petrova, Marina Shtina, Tatiana Kovalenko
SGA incidence in one of the regions of the Russian Federation
Irina Petrova, Marina Shtina, Tatiana Kovalenko
P3-1046
Final Height (FH) in patients with and without pituitary abnormalities detected by MRI and/or CT treated with growth hormone.
Maria Cláudia Schmitt-Lobe, Paula Webster, Roberta Webster
Final Height (FH) in patients with and without pituitary abnormalities detected by MRI and/or CT treated with growth hormone.
Maria Cláudia Schmitt-Lobe, Paula Webster, Roberta Webster
P3-1047
CONGENITAL HEART DISEASE AND ITS EFFECTS ON GROWTH IN CHILDREN
Ileana Puiu, Veronica Elena Maria, Alexandra Oltea Puiu
CONGENITAL HEART DISEASE AND ITS EFFECTS ON GROWTH IN CHILDREN
Ileana Puiu, Veronica Elena Maria, Alexandra Oltea Puiu
P3-1048
A Rare Cause of Short Stature : The Floating Harbor Syndrome.
A Case Report.
SIMON KAYEMBA-KAY'S, ODILE MAILLET, ANNE HERON
A Rare Cause of Short Stature : The Floating Harbor Syndrome.
A Case Report.
SIMON KAYEMBA-KAY'S, ODILE MAILLET, ANNE HERON
P3-1049
CORRELATIONS BETWEEN IGF1 LEVELS AND ANTHROPOMETRICAL PARAMETERS IN CHILDREN UNDER GROWTH HORMONE THERAPY
Simona Hutu, Raluca Pop, Ionela Pascanu
CORRELATIONS BETWEEN IGF1 LEVELS AND ANTHROPOMETRICAL PARAMETERS IN CHILDREN UNDER GROWTH HORMONE THERAPY
Simona Hutu, Raluca Pop, Ionela Pascanu
P3-1050
Body Mass Index and Total Cholesterol Are Negative Predictors of Peak Stimulated Growth Hormone in Han Children with Short Stature
Su Wu, Wei Gu, Ziyang Zhu, Shining Ni, Xing Shi, Qianqi Liu
Body Mass Index and Total Cholesterol Are Negative Predictors of Peak Stimulated Growth Hormone in Han Children with Short Stature
Su Wu, Wei Gu, Ziyang Zhu, Shining Ni, Xing Shi, Qianqi Liu
P3-1051
A 4 month-old boy with Beckwith Wiedemann Syndrome (BWS)
Aleksandra Janchevska, Velibor Tasic, Zoran Gucev, Nadine Bachmann, Carsten Bergmann
A 4 month-old boy with Beckwith Wiedemann Syndrome (BWS)
Aleksandra Janchevska, Velibor Tasic, Zoran Gucev, Nadine Bachmann, Carsten Bergmann
P3-1052
MEGHA : Observational study on prescription of the growth hormone Saizen® in adults in France
Christine Cortet, Michel Pugeat, Laurence Fresneau, Jean-Louis Sadoul, Jacques Young, Jean-Claude Souberbielle, Philippe Chanson
MEGHA : Observational study on prescription of the growth hormone Saizen® in adults in France
Christine Cortet, Michel Pugeat, Laurence Fresneau, Jean-Louis Sadoul, Jacques Young, Jean-Claude Souberbielle, Philippe Chanson
P3-1053
Comparative study of low-dose growth hormone treatment in children with idiopathic short stature and growth hormone deficiency
Hwalrim Jeong, Eunbyul Kwon, Haesang Lee, Jinsoon Hwang, Jungsub Lim, Youngseok Shim
Comparative study of low-dose growth hormone treatment in children with idiopathic short stature and growth hormone deficiency
Hwalrim Jeong, Eunbyul Kwon, Haesang Lee, Jinsoon Hwang, Jungsub Lim, Youngseok Shim
P3-1054
To investigate the changes of hormone levels and body composition in pubertal children with growth retardation: A clinical controlled study
Su Wu, Qian-qi Liu, Wei Gu, Zi-yang Zhu, Xing Shi, Shi-ning Ni
To investigate the changes of hormone levels and body composition in pubertal children with growth retardation: A clinical controlled study
Su Wu, Qian-qi Liu, Wei Gu, Zi-yang Zhu, Xing Shi, Shi-ning Ni
P3-1055
the effect of BMI in reducing risk of refractory seizure due to probable lipoid tissue factors
setila dalili, vahid aminzadeh, shahin koohmanaee, yalda ashoorian, afagh hassanzadeh rad
the effect of BMI in reducing risk of refractory seizure due to probable lipoid tissue factors
setila dalili, vahid aminzadeh, shahin koohmanaee, yalda ashoorian, afagh hassanzadeh rad
P3-1057
The frequency study and the Etiological profile of short stature in 2-15 years old children admitted in endocrinology clinic of 17 Shahrivar Hospital, Rasht, between 2008-2013
shahin koohmanaee, setila dalili, romisa majdi
The frequency study and the Etiological profile of short stature in 2-15 years old children admitted in endocrinology clinic of 17 Shahrivar Hospital, Rasht, between 2008-2013
shahin koohmanaee, setila dalili, romisa majdi
LBP-1268
GENETIC CAUSES OF DISPROPORTIONAL SHORT STATURE IDENTIFIED BY WHOLE EXOME SEQUENCING
Mariana F. A. Funari, Gabriela A. Vasques, Antonio M. Lerario, Bruna L. Freire, Mirian Y. Nishi, Monica M. França, Sueli M. O. Shinjo, Suely K. N. Marie, Ivo J. P. Arnhold, Alexander A. L. Jorge
GENETIC CAUSES OF DISPROPORTIONAL SHORT STATURE IDENTIFIED BY WHOLE EXOME SEQUENCING
Mariana F. A. Funari, Gabriela A. Vasques, Antonio M. Lerario, Bruna L. Freire, Mirian Y. Nishi, Monica M. França, Sueli M. O. Shinjo, Suely K. N. Marie, Ivo J. P. Arnhold, Alexander A. L. Jorge
P2-390
PROGRAMMING OF RAT BEHAVIORS AND THE STRESS RESPONSE BY DURATION OF THE INFANCY STAGE
Yonatan Crispel, Oren Katz, Ze'ev Hochberg
PROGRAMMING OF RAT BEHAVIORS AND THE STRESS RESPONSE BY DURATION OF THE INFANCY STAGE
Yonatan Crispel, Oren Katz, Ze'ev Hochberg
P2-391
POMC DNA hypermethylation variant is highly associated with obesity in adults
Peter Kühnen, Daniela Handke, Jochen Spranger, Antje Fischer-Rosinsky, Anke Hinney, Johannes Hebebrand, Annette Grüters, Heiko Krude
POMC DNA hypermethylation variant is highly associated with obesity in adults
Peter Kühnen, Daniela Handke, Jochen Spranger, Antje Fischer-Rosinsky, Anke Hinney, Johannes Hebebrand, Annette Grüters, Heiko Krude
P2-458
Sleep apneas in Silver Russell syndrome : A constant finding
Eloïse Giabicani, Michèle Boulé, Eva Galliani, Irène Netchine
Sleep apneas in Silver Russell syndrome : A constant finding
Eloïse Giabicani, Michèle Boulé, Eva Galliani, Irène Netchine
P2-470
HYPOMETHYLATION WITHIN THE IMPRINTED DLK1 - DIO3 DOMAIN : A POTENTIAL REGULATORY MECHANISM OF PRE AND POSTNATAL GROWTH
Anna Prats-Puig, Gemma Carreras-Badosa, Judit Bassols, Patricia Cavelier, Agnés Magret, Cristina Sabench, Francis de Zegher, Lourdes Ibáñez, Robert Feil, Abel López-Bermejo
HYPOMETHYLATION WITHIN THE IMPRINTED DLK1 - DIO3 DOMAIN : A POTENTIAL REGULATORY MECHANISM OF PRE AND POSTNATAL GROWTH
Anna Prats-Puig, Gemma Carreras-Badosa, Judit Bassols, Patricia Cavelier, Agnés Magret, Cristina Sabench, Francis de Zegher, Lourdes Ibáñez, Robert Feil, Abel López-Bermejo
P2-471
Growth and Metabolic Phenotypes in patients with SRS: A Multi-Centre Cross-sectional Observational Study
Kayleigh Aston, Gemma Grosvenor, Catherine Peters, Verghese Mathew, Joanne Blair, Simon Chapman, Charles Buchanan, Eamonn Maher, Renuka Dias
Growth and Metabolic Phenotypes in patients with SRS: A Multi-Centre Cross-sectional Observational Study
Kayleigh Aston, Gemma Grosvenor, Catherine Peters, Verghese Mathew, Joanne Blair, Simon Chapman, Charles Buchanan, Eamonn Maher, Renuka Dias
P2-483
HYPERMETHYLATION AT THE IMPRINTED C19MC microRNA CLUSTER: A NEW LINK BETWEEN MATERNAL METABOLISM AND INFANT’S GROWTH.
Anna Prats-Puig, Gemma Carreras-Badosa, Judit Bassols, Michael Girardot, Empar Carrion, Radu Gehmis, Francis de Zegher, Lourdes Ibáñez, Robert Feil, Abel López-Bermejo
HYPERMETHYLATION AT THE IMPRINTED C19MC microRNA CLUSTER: A NEW LINK BETWEEN MATERNAL METABOLISM AND INFANT’S GROWTH.
Anna Prats-Puig, Gemma Carreras-Badosa, Judit Bassols, Michael Girardot, Empar Carrion, Radu Gehmis, Francis de Zegher, Lourdes Ibáñez, Robert Feil, Abel López-Bermejo
P3-1249
Telomere length in young adults born preterm and the risk for cardiovascular disease;
Support for accelerated biological ageing in subjects born preterm
Carolina Smeets, Veryan Codd, Nilesh Samani, Anita Hokken-Koelega
Telomere length in young adults born preterm and the risk for cardiovascular disease;
Support for accelerated biological ageing in subjects born preterm
Carolina Smeets, Veryan Codd, Nilesh Samani, Anita Hokken-Koelega
P3-1250
A survival analysis approach to assess the association between maternal prepregnancy overweight and childhood overweight – Results of the Ulm Birth Cohort Study (UBCS)
Stephanie Brandt, Hermann Brenner, Jon Genuneit, Dietrich Rothenbacher, Martin Wabitsch
A survival analysis approach to assess the association between maternal prepregnancy overweight and childhood overweight – Results of the Ulm Birth Cohort Study (UBCS)
Stephanie Brandt, Hermann Brenner, Jon Genuneit, Dietrich Rothenbacher, Martin Wabitsch
P3-1251
Sexually dimorphic methylation of SF-1 gene in rat placenta after gestational exposure to BPA
Julie Fudvoye, Pierre Dehan, Mehdi Liénard, Geert Trooskens, Arlette Gérard, Jean-Pierre Bourguignon, Anne-Simone Parent
Sexually dimorphic methylation of SF-1 gene in rat placenta after gestational exposure to BPA
Julie Fudvoye, Pierre Dehan, Mehdi Liénard, Geert Trooskens, Arlette Gérard, Jean-Pierre Bourguignon, Anne-Simone Parent
P3-1252
Pregnancy-induced rise in circulating Delta-like homologue-1 (DLK1) is derived from the conceptus and promotes ‘accelerated starvation’.
Mary Cleaton, Anne Ferguson-Smith, Marika Charalambous
Pregnancy-induced rise in circulating Delta-like homologue-1 (DLK1) is derived from the conceptus and promotes ‘accelerated starvation’.
Mary Cleaton, Anne Ferguson-Smith, Marika Charalambous
P3-1253
Newborns with Longest Telomeres are Big at Birth and have Most Lean Mass – not Most Fat – in Late Infancy.
Marta Díaz Silva, Abel López-Bermejo, Lourdes Ibáñez Toda, Francis de Zeguer
Newborns with Longest Telomeres are Big at Birth and have Most Lean Mass – not Most Fat – in Late Infancy.
Marta Díaz Silva, Abel López-Bermejo, Lourdes Ibáñez Toda, Francis de Zeguer
P3-1254
Untargeted Plasma Metabolomics in Prepubertal ICSI and naturally conceived Children Unravels Gender - dimorphic Metabolic Trajectories after ICSI
Alexandra Gkourogianni, Aristeidis G. Telonis, Ioanna Kosteria, Alexandra Margeli, Emilia Mantzou, Maria Konsta, Dimitrios Loutradis, George Mastorakos, Ioannis Papassotiriou, Christina Kanaka-Gantenbein, Maria I. Klapa, George P. Chrousos
Untargeted Plasma Metabolomics in Prepubertal ICSI and naturally conceived Children Unravels Gender - dimorphic Metabolic Trajectories after ICSI
Alexandra Gkourogianni, Aristeidis G. Telonis, Ioanna Kosteria, Alexandra Margeli, Emilia Mantzou, Maria Konsta, Dimitrios Loutradis, George Mastorakos, Ioannis Papassotiriou, Christina Kanaka-Gantenbein, Maria I. Klapa, George P. Chrousos
P3-1255
Analysis of gene methylation difference and evaluation the effect of growth hormone in Silver Russell syndrome
Di WU, Chunxiu GONG, Yang ZHAO, Chang SU, Bingyan CAO
Analysis of gene methylation difference and evaluation the effect of growth hormone in Silver Russell syndrome
Di WU, Chunxiu GONG, Yang ZHAO, Chang SU, Bingyan CAO
P2-392
UNALTERED RATIO OF CIRCULATING LEVELS OF GROWTH HORMONE (GH) ISOFORMS AFTER ADMINISTRATION OF DIFFERENT GH PROVOCATIVE TESTS IN A POPULATION OF SHORT STATURE CHILDREN
Antonello Rigamonti, Cristina Meazza, Martin Bidlingmaier, Valentina Muratore, Luparia Martina, Silvia Bini, Sara Pagani, Silvano Cella, Mauro Bozzola
UNALTERED RATIO OF CIRCULATING LEVELS OF GROWTH HORMONE (GH) ISOFORMS AFTER ADMINISTRATION OF DIFFERENT GH PROVOCATIVE TESTS IN A POPULATION OF SHORT STATURE CHILDREN
Antonello Rigamonti, Cristina Meazza, Martin Bidlingmaier, Valentina Muratore, Luparia Martina, Silvia Bini, Sara Pagani, Silvano Cella, Mauro Bozzola
P2-393
STUDY OF IGF1 RECEPTOR (IGF1R) GENE IN SMALL FOR GESTATIONAL AGE (SGA) PATIENTS WITH SHORT STATURE TREATED WITH RhGH.
Marta Ferrer, Antonio de Arriba, Jose Miguel Martinez de Zabarte, Eva Barrio, Jose Ignacio Labarta
STUDY OF IGF1 RECEPTOR (IGF1R) GENE IN SMALL FOR GESTATIONAL AGE (SGA) PATIENTS WITH SHORT STATURE TREATED WITH RhGH.
Marta Ferrer, Antonio de Arriba, Jose Miguel Martinez de Zabarte, Eva Barrio, Jose Ignacio Labarta
P2-394
Gene expression profiles in growth hormone deficient (GHD) children relate peak GH levels to circadian clock, chromatin remodelling and WNT signalling pathways
Philip Murray, Adam Stevens, Chiara DeLeonibus, Ekaterina Koledova, Pierre Chatelain, Peter Clayton
Gene expression profiles in growth hormone deficient (GHD) children relate peak GH levels to circadian clock, chromatin remodelling and WNT signalling pathways
Philip Murray, Adam Stevens, Chiara DeLeonibus, Ekaterina Koledova, Pierre Chatelain, Peter Clayton
P2-395
Growth and growth hormone in Kabuki syndrome
Dina Schott, Willem-Jan Gerver, Luc Zimmermann, Constance Stumpel
Growth and growth hormone in Kabuki syndrome
Dina Schott, Willem-Jan Gerver, Luc Zimmermann, Constance Stumpel
P2-396
IGF-II and lipid profile in pediatric obesity: a marker of cardio-metabolic risk?
elena inzaghi, Barbara Baldini Ferroli, Daniela Germani, Antonella Puglianiello, Armando Grossi, Danilo Fintini, Rossana Fiori, Stefano Cianfarani
IGF-II and lipid profile in pediatric obesity: a marker of cardio-metabolic risk?
elena inzaghi, Barbara Baldini Ferroli, Daniela Germani, Antonella Puglianiello, Armando Grossi, Danilo Fintini, Rossana Fiori, Stefano Cianfarani
P2-397
Silver Russell Syndrome (SRS): a cause of partial IGF-I resistance?
Marie-Noëlle DUFOURG, Laurence PERIN, Muriel HOUANG, Marie-Laure DAUBARD, Frédéric BRIOUDE, Yves LE BOUC, Irène NETCHINE
Silver Russell Syndrome (SRS): a cause of partial IGF-I resistance?
Marie-Noëlle DUFOURG, Laurence PERIN, Muriel HOUANG, Marie-Laure DAUBARD, Frédéric BRIOUDE, Yves LE BOUC, Irène NETCHINE
P2-398
The in vitro functional analysis of gene promoter region single nucleotide polymorphisms (SNPs) associated with growth hormone (GH) response in children with GH deficiency
Chiara De Leonibus, Philip Murray, Dan Hanson, Adam Stevens, Peter Clayton
The in vitro functional analysis of gene promoter region single nucleotide polymorphisms (SNPs) associated with growth hormone (GH) response in children with GH deficiency
Chiara De Leonibus, Philip Murray, Dan Hanson, Adam Stevens, Peter Clayton
P2-399
IS RETESTING IN GROWTH HORMONE DEFICIENT CHILDREN REALLY USEFUL?
Sara Pagani, Cristina Meazza, Chiara Gertosio, Chaira Donati, Francesca Scavuzzo, Alba Pilotta, Fabio Buzi, Daniela Larizza, Mauro Bozzola
IS RETESTING IN GROWTH HORMONE DEFICIENT CHILDREN REALLY USEFUL?
Sara Pagani, Cristina Meazza, Chiara Gertosio, Chaira Donati, Francesca Scavuzzo, Alba Pilotta, Fabio Buzi, Daniela Larizza, Mauro Bozzola
P2-400
Regulation of IGF1R mRNA expression by GnRH agonist may be involved in the decrease of height velocity during Central Precocious Puberty therapy.
MARIANA SARTI DE PAULA, RAFAELA RICCO, RODRIGO CUSTODIO, SORAYA MILANI, PATRICIA ATIQUE, AYRTON MOREIRA, SONIR ANTONINI, RAPHAEL LIBERATOREJr, CARLOS MARTINELLIJr
Regulation of IGF1R mRNA expression by GnRH agonist may be involved in the decrease of height velocity during Central Precocious Puberty therapy.
MARIANA SARTI DE PAULA, RAFAELA RICCO, RODRIGO CUSTODIO, SORAYA MILANI, PATRICIA ATIQUE, AYRTON MOREIRA, SONIR ANTONINI, RAPHAEL LIBERATOREJr, CARLOS MARTINELLIJr
P2-401
GRB10 knockdown in Zebrafish is associated with decreased weight-to-length ratio without alterations in AKT and ERK activity: a model to study human growth regulation
Chiara De Leonibus, Jack Broadbent, Philip Murray, Joseph Whitehead, Adam Hurlstone, Holly Shiels, Peter Clayton, Adam Stevens
GRB10 knockdown in Zebrafish is associated with decreased weight-to-length ratio without alterations in AKT and ERK activity: a model to study human growth regulation
Chiara De Leonibus, Jack Broadbent, Philip Murray, Joseph Whitehead, Adam Hurlstone, Holly Shiels, Peter Clayton, Adam Stevens
P2-402
The involvement of the Epidermal Growth Factor Receptor (EGFR) in the successful Growth Hormone (GH) signaling and the role of p21 in the negative regulation of the GH/GHR and EGF/EGFR pathways, in Growth Hormone Transduction Defect (GHTD).
Eirini Kostopoulou, Andrea Paola Rojas Gil, Alexia Karvela, Bessie Eugenia Spiliotis
The involvement of the Epidermal Growth Factor Receptor (EGFR) in the successful Growth Hormone (GH) signaling and the role of p21 in the negative regulation of the GH/GHR and EGF/EGFR pathways, in Growth Hormone Transduction Defect (GHTD).
Eirini Kostopoulou, Andrea Paola Rojas Gil, Alexia Karvela, Bessie Eugenia Spiliotis
P2-403
Homozygous carriers of a novel IGFALS mutation are 1.5 SD shorter than heterozygous relatives and tend to have lower bone mineral density
Emregül Isık, Jaap van Doorn, Hüseyin Demirbilek, Monique Losekoot, Jan-Maarten Wit
Homozygous carriers of a novel IGFALS mutation are 1.5 SD shorter than heterozygous relatives and tend to have lower bone mineral density
Emregül Isık, Jaap van Doorn, Hüseyin Demirbilek, Monique Losekoot, Jan-Maarten Wit
P2-404
The role of beta-TrCP (β-TrCP), an E3 ubiquitin ligase, in the signaling of the Growth Hormone (GH) and Epidermal Growth Factor (EGF) pathways in Growth Hormone Transduction Defect (GHTD).
Eirini Kostopoulou, Andrea Paola Rojas Gil, Alexia Karvela, Bessie Eugenia Spiliotis
The role of beta-TrCP (β-TrCP), an E3 ubiquitin ligase, in the signaling of the Growth Hormone (GH) and Epidermal Growth Factor (EGF) pathways in Growth Hormone Transduction Defect (GHTD).
Eirini Kostopoulou, Andrea Paola Rojas Gil, Alexia Karvela, Bessie Eugenia Spiliotis
P2-405
SGA Short Stature Bearing with a Novel Nonsense Mutation (p.W1249X) in the IGF1R Gene
Masanobu Fujimoto, Yuki Kawashima, Takashi Hamajima, Naoki Miyahara, Rei Nishimura, Keiichi Hanaki, Susumu Kanzaki
SGA Short Stature Bearing with a Novel Nonsense Mutation (p.W1249X) in the IGF1R Gene
Masanobu Fujimoto, Yuki Kawashima, Takashi Hamajima, Naoki Miyahara, Rei Nishimura, Keiichi Hanaki, Susumu Kanzaki
P3-916
Vitamin D deficiency can modulate GH/IGF-1 axis in growth hormone deficient children.
Ewelina Witkowska-Sedek, Anna Kucharska, Anna Majcher, Beata Pyrzak
Vitamin D deficiency can modulate GH/IGF-1 axis in growth hormone deficient children.
Ewelina Witkowska-Sedek, Anna Kucharska, Anna Majcher, Beata Pyrzak
P3-917
Serum IGF-I concentration and growth during infancy correlate to polyunsaturated fatty acid pattern
Jovanna Dahlgren, Emma Kjellberg, Birgitta Strandvik, Josefine Roswall
Serum IGF-I concentration and growth during infancy correlate to polyunsaturated fatty acid pattern
Jovanna Dahlgren, Emma Kjellberg, Birgitta Strandvik, Josefine Roswall
P3-918
Are short children with low GH secretion metabolically different from children of normal height?
Anders Tidblad, Klas Ekström, Martin Ritzén, Claude Marcus
Are short children with low GH secretion metabolically different from children of normal height?
Anders Tidblad, Klas Ekström, Martin Ritzén, Claude Marcus
P3-919
Familial short stature associated to terminal microdeletion of 15q26.3: variable phenotype not involving the IGF-I receptor gene.
Laura Lucaccioni, Simona F. Madeo, Ilaria Stanghellini, Patrizia Bruzzi, Barbara Predieri, Lorenzo Iughetti, Antonio Percesepe
Familial short stature associated to terminal microdeletion of 15q26.3: variable phenotype not involving the IGF-I receptor gene.
Laura Lucaccioni, Simona F. Madeo, Ilaria Stanghellini, Patrizia Bruzzi, Barbara Predieri, Lorenzo Iughetti, Antonio Percesepe
P3-920
Is the insulin secretion in pancreatic beta cells related with IGF-1/IGFBP-1 axis in Korean children?
Min Sun Kim, Dae-Yeol Lee
Is the insulin secretion in pancreatic beta cells related with IGF-1/IGFBP-1 axis in Korean children?
Min Sun Kim, Dae-Yeol Lee
P3-921
SEVERE ISOLATED GROWTH HORMONE DEFICENCY AND MYOPATHY IN TWO BROTHERS WITH RNPC3 MUTATION
Zoran Gucev, Momir Polenakovic, Velibor Tasic, Yves LeBouc, Jurgen Klammt, Roland Pfaeffle, Aleksandra Filipovska
SEVERE ISOLATED GROWTH HORMONE DEFICENCY AND MYOPATHY IN TWO BROTHERS WITH RNPC3 MUTATION
Zoran Gucev, Momir Polenakovic, Velibor Tasic, Yves LeBouc, Jurgen Klammt, Roland Pfaeffle, Aleksandra Filipovska
P3-922
Gigantism Secondary to Growth Hormone Secreting Pituitary Macrodenoma
Andrew Sng, Kah Yin Loke
Gigantism Secondary to Growth Hormone Secreting Pituitary Macrodenoma
Andrew Sng, Kah Yin Loke
P3-923
IGF-I and relation to growth in infancy and early childhood in very-low-birth-weight infants and term appropriate for gestational age infants
Miranda de Jong, Anneke Cranendonk, Mirjam M. van Weissenbruch
IGF-I and relation to growth in infancy and early childhood in very-low-birth-weight infants and term appropriate for gestational age infants
Miranda de Jong, Anneke Cranendonk, Mirjam M. van Weissenbruch
P3-924
SEVERE ISOLATED GROWTH HORMONE DEFICENCY AND MYOPATHY IN TWO BROTHERS WITH RNPC3 MUTATION
Zoran Gucev, Momir Polenakovic, Velibor Tasic, Yves LeBouc, Serge Amselem, Jurgen Klammt, Roland Pfaeffle, Aleksandra Filipovska
SEVERE ISOLATED GROWTH HORMONE DEFICENCY AND MYOPATHY IN TWO BROTHERS WITH RNPC3 MUTATION
Zoran Gucev, Momir Polenakovic, Velibor Tasic, Yves LeBouc, Serge Amselem, Jurgen Klammt, Roland Pfaeffle, Aleksandra Filipovska
P3-925
Influence of The -202 A/C IGFBP-3 Promoter Polymorphism on Individual Variation in Body Height in Korean Girls
Seung Yang, Young Suk Shim, Min Jae Kang, Yeon Joung Oh, Il Tae Hwang
Influence of The -202 A/C IGFBP-3 Promoter Polymorphism on Individual Variation in Body Height in Korean Girls
Seung Yang, Young Suk Shim, Min Jae Kang, Yeon Joung Oh, Il Tae Hwang
P3-926
Usefulness of priming with gonadal steroids prior to growth hormone (GH) stimulation with clonidine in the evaluation of the GH status of short children
Gulnara Rakhimova, Kamil Gilyazetdinov
Usefulness of priming with gonadal steroids prior to growth hormone (GH) stimulation with clonidine in the evaluation of the GH status of short children
Gulnara Rakhimova, Kamil Gilyazetdinov
P3-927
Comparison of two IGF-I assays in patients treated with GH
María Martínez, Marta Murillo, M.Luisa Granada, Marta Aldea, Estefanía Guerrini, Joan Bel
Comparison of two IGF-I assays in patients treated with GH
María Martínez, Marta Murillo, M.Luisa Granada, Marta Aldea, Estefanía Guerrini, Joan Bel
P3-928
Acute effects of a training session on IGF-I and IGFBP-3 concentrations in Brazilian Jiu-Jitsu fighters
Hugo Tourinho Filho, Enrico Puggina, Camila Moraes, L Oliveira, Carlos Martinelli Jr
Acute effects of a training session on IGF-I and IGFBP-3 concentrations in Brazilian Jiu-Jitsu fighters
Hugo Tourinho Filho, Enrico Puggina, Camila Moraes, L Oliveira, Carlos Martinelli Jr
P3-929
Biochemical profiles differentials by SGA children catch up
Ignacio Diez-Lopez, Ainhoa Sarasua-Miranda, Marta del Hoyo-Moracho, Raquel Gomez de Segura, Dorleta Pérez-Campos, Maria Teresa Mararulla-Arenaza, Victor Manuel Rodriguez-Rivera
Biochemical profiles differentials by SGA children catch up
Ignacio Diez-Lopez, Ainhoa Sarasua-Miranda, Marta del Hoyo-Moracho, Raquel Gomez de Segura, Dorleta Pérez-Campos, Maria Teresa Mararulla-Arenaza, Victor Manuel Rodriguez-Rivera
Workshop
0
Oral
15
Expert
4
Plenary
6
Catering and Social
6
Nurse
0
Other
28
Symposium
10
No Session Type
8
Fri 02 09:25
FC2.2
Identification of mutations in TBX1 and AIRE in isolated hypoparathyroidism patients
Philadelphia, USA
Fri 02 09:15
FC3.1
RNA-based MAFA over-expression is sufficient to drive human pancreatic duct-derived cells toward a -cell-like phenotype
Brussels, Belgium
Fri 02 09:55
FC3.5
C-peptide levels and glycemic control in children, adolescents and young adults with type 1 diabetes (TID)
Athens, Greece
Fri 02 10:05
FC3.6
First report of nationwide incidence and prevalence of type 1 diabetes among children in Turkey
Ankara, Turkey
Fri 02 09:45
FC4.4
Modulation of GH-1 splicing as potential strategy to rescue growth hormone deficiency type II
Bern, Switzerland
Fri 02 09:55
FC4.5
Fri 02 10:05
FC4.6
Positive association between height and cancer in the Swedish population
Stockholm, Sweden
Fri 02 09:25
FC5.2
MEN1 syndrome because of combined germline and somatic mosaicism, with important consequences for relatives
Nijmegen, The Netherlands
Sat 03 09:15
FC6.1
Correlation of AR expression and AR transcriptional activity in cultured human genital fibroblasts
Kiel, Germany
Sat 03 09:35
FC6.3
Establishing the role of the steroid backdoor pathway for androgen biosynthesis in the human ovary
Bern, Switzerland
Sat 03 09:35
FC7.3
IGF-I levels, complex formation and igf-bioactivity in growth hormone treated children with Prader-Willi syndrome
Rotterdam, The Netherlands
Sat 03 09:35
FC8.3
Sat 03 10:05
FC8.6
Metabolic effects of ADP355, protein-based adiponectin receptor agonist, on mice with high-fat diet induced fatty liver disease
Inchon, Republic of Korea
Sat 03 09:15
FC9.1
Sat 03 12:30
FC10.1
Effect of sonic hedgehog signalling on regulation the expression of 11β-HSD2 in the placenta
Hangzhou, China
Sat 03 12:50
FC10.3
Sat 03 13:00
FC10.4
Sat 03 13:10
FC10.5
Lack of association between transient hypothyroxinaemia of prematurity and neurodevelopmental and behavioral outcomes in young adulthood
Amsterdam, The Netherlands
Sat 03 12:50
FC11.3
Next generation sequencing: towards a new clinical frontier in the diagnosis and management of pituitary tumours
New South Wales, Australia
Sat 03 13:00
FC11.4
Idiopathic multiple pituitary hormone deficiency (IMPHD): radiological and perinatal factors
Birmingham, UK
Sat 03 13:20
FC11.6
Sat 03 12:30
FC12.1
Evaluation of cardiovascular risk in childhood: data from a survey of dyslipidaemic children
Modena, Italy
Sat 03 12:50
FC12.3
Sat 03 13:20
FC13.6
TRIAC treatment of allan-herndon-dudley syndrome (AHDS) due to defects in thyroid hormone transporter MCT8
Madrid, Spain
Sat 03 12:30
FC14.1
KLB, encoding the co-receptor for FGF21, is mutated in congenital hypogonadotropic hypogonadism
Lausanne, Switzerland
Sat 03 13:00
FC14.4
Genetic variation of AMH signaling affects AMH and inhibin B levels in healthy peripubertal girls
Copenhagen, Denmark
Sat 03 13:10
FC14.5
Sat 03 13:20
FC14.6
An evaluation of glandular breast tissue development and volume by MRI in 121 healthy peripubertal girls
Copenhagen, Denmark
Sat 03 13:00
FC-LB-4
Long-term cognitive effects of antenatal dexamethasone treatment in Swedish adolescents with and without CAH
Stockholm, Sweden
Sat 03 13:10
FC-LB-5
Paternally inherited IGF2 mutation results in intrauterine and postnatal growth retardation
Tübingen, Germany
Fri 02
MTE6.1
Sat 03
MTE6.2
Fri 02 10:45
PL3
Fri 02 12:15
PL4
Sat 03 17:45
PL6
The complex relationship between the GH/IGF axis and aging and longevity – the interface with diet and mitochondrial peptides
Los Angeles, USA
Thu 01 08:30
WG3.2
DSD in Indonesia: the course of psychological development in late identified patients
Rotterdam, The Netherlands
Thu 01 08:40
WG4.2
Thu 01 09:40
WG4.3
Thu 01 09:00
WG5.3
Restoration of fertility in cancer adolescents after chemotherapy
Brussels, Belgium
Thu 01 08:05
WG6.1
Incidental prenatal diagnosis of Turner Syndrome, perspectives of parents and professionals
Leiderdorp, The Netherlands
Thu 01 10:00
WG6.4
Management of middle ear and hearing problems in Turner's syndrome - how can we do better?
Glasgow, United Kingdom
Thu 01 10:30
WG6.5
Report on the progress and difficulties on transdermal Estradiol supplementation in Europe
Rotterdam, The Netherlands
Fri 02
NP1.1
Fri 02
NP1.2
Fri 02 14:45
SS1.3
Fri 02 15:20
SS1.6
Pro-Con debate - Arguments in favour of screening survivors at risk with palpation of the neck
Vienna, Austria
Fri 02 15:35
SS1.6
Pro - Con Debate: Arguments in favour of screening survivors at risk with thyroid ultrasound
Gainesville, USA
Fri 02 14:30
S5.1
Fri 02 15:30
S6.3
Fri 02 15:30
S7.3
Modeling GnRH deficiency with the use of human pluripotent cells
Helsinki, Finland
Sat 03 15:30
S8.1
Disentangling disease and drug signatures in the human gut microbiome
Copenhagen, Denmark
Sat 03 15:30
S10.1
Molecular mechanisms of growth plate adaptation during undernutrition
Philadelphia, USA
Sat 03 16:00
S10.2
Molecular response of the growth plate to inflammatory cytokines
Stockholm, Sweden
Sat 03 16:30
S10.3
0 result(s) found.