Mohamed Abdullah
Fri 19 14:25 - 14:35
WG8.2
Working Group for Global Paediatric Endocrinology and Diabetes (GPED)
Inequities of treatment options in developing countries: Inequities in treatment options type 1 diabetes in Sudan
John Achermann
London, United Kingdom
Thu 18 08:00 - 08:30
WG3.1
ESPE Disorders of Sex Development Working Group (DSD)
Genetic variation in human SF-1 (NR5A1): clinical consequences for individuals, families and populations
London, United Kingdom
Fri 19 14:15
S5.1
Symposium 5 - Novel Insights into Hypoadrenalism
Aetiology of Congenital Hypoadrenalism
London, United Kingdom
Professor Faisal Ahmed
Glasgow, United Kingdom
Thu 18
Education and Training Update
Update of the 28th ESPE Summer School
Glasgow, United Kingdom
Kyriaki Alatzoglou
Sat 20 12:10
FC11.2
Free Communication 11 - Pituitary
Novel SOX2 mutation: identification of new molecular mechanisms of SOX2 action and interactions.
Janielle Alfen
Nijmegen, the Netherlands
Thu 18 09:45 - 10:15
WG6.4
ESPE Turner Syndrome Working Group (TS)
Motor performance in TS
Nijmegen, the Netherlands
Emmanuel Ameyaw
Ghana
Fri 19 15:15 - 15:25
WG8.6
Working Group for Global Paediatric Endocrinology and Diabetes (GPED)
Neonatal screening for congenital hypothyroidism: Don’t take it for granted! (Ghana)
Ghana
Professor Wiebke Arlt
London, UK
Fri 19 15:15
S5.3
Symposium 5 - Novel Insights into Hypoadrenalism
CAH: Health Status in Adults (CaHASE)
London, UK
Galit Asher
Ramat-Gan, Israel
Fri 19 14:35
WG7.2
ESPE Working Group for Paediatric Endocrine Nurse Specialists and Allied Health Professionals
Evolving Growth Hormone Therapy (GHT) Patient Training in a Digital World
Ramat-Gan, Israel
Patrick Aubourg
Paris, France
Fri 19 11:45
PL4
Plenary Session 4
Gene therapy in cerebral form of X-linked adrenoleukodystrophy
Paris, France
Peter Bang
Linköping, Sweden
Thu 18 08:15 - 08:40
WG2.2
ESPE Working Group on Diabetes Technology and Therapeutics
Non-Insulin Glucoregulatory therapy for type 1 diabetes
Linköping, Sweden
Thu 18
Education and Training Update
ESPE Research Fellowship programme
Linköping, Sweden
Murat Bastepe
Boston MA, USA
Thu 18 08:30 – 09:00
WG1.2
ESPE Bone and Growth Plate Working Group (BGP)
The effect of stimulatory G proteins on differentiation within the growth plate
Boston MA, USA
Thu 18 14:00
S1.1
Symposium 1 - Disorders of Gsalpha Signaling
Pseudohypoparathyroidism
Boston MA, USA
Professor Tadej Battelino
Ljubljana, Slovenia
Thu 18 09:40 - 10:15
WG2.5
ESPE Working Group on Diabetes Technology and Therapeutics
Debate: Sensor/pump therapy from onset of diabetes?
Ljubljana, Slovenia
Jacques Beltrand
Paris, France)
Sat 20 09:35
FC9.6
Free Communication 9 - Beta Calls
Sulfonylurea therapy corrects hypotonia, attention deficits, improves complex neuropsychological functions and motricity in patients with neonatal diabetes secondary to mutation in potassium channel subunits, through a central nervous system effect.
Paris, France)
Melissa Benoit
Toronto, Canada
Fri 19 14.15
WG7.1
ESPE Working Group for Paediatric Endocrine Nurse Specialists and Allied Health Professionals
Quality of life and anxiety in adolescents with differentiated thyroid cancer
Toronto, Canada
Iwona Ben-Skowronek
Sat 20 12:40
FC13.5
Free Communication 13 - Thyroid
THE ULTRASTRUCTURAL CHANGES IN THYROID CELLS IN THE COURSE OF DAMAGE IN HASHIMOTO’S THYROIDITIS
Professor Daniel Bernard
Montreal, Canada
Thu 18 14:30
S4.2
Symposium 4 - Recent Advances in Our Understanding of Hypothyroidism
Novel role(s) for immunoglobulin superfamily, member 1 (IGSF1) in the hypothalamic-pituitary-thyroid axis
Montreal, Canada
Gerhard Binder
Tübingen, Germany
Sat 20 12:20
FC12.3
Free Communication 12 - Obesity
Increased resting energy expenditure in girls with Turner syndrome
Tübingen, Germany
Nicholas Bishop
Fri 19 08:55
FC2.2
Free Communication 2- Bone & Mineral
Hypophosphatasia: Gross motor function and height improvement in infants and young children treated with asfotase alfa for up to 3 years
Ulrich Boehm
Fri 19 15:15
S6.3
Symposium 6 - New Concepts in the Gonadotropic Axis
Genetic Dissection of Puberty in Mice
Roberto Bogarin
Fri 19 15:05 - 15:15
WG8.5
Working Group for Global Paediatric Endocrinology and Diabetes (GPED)
Neonatal screening for congenital hypothyroidism: Don’t take it for granted! (Costa Rica)
Jean-Pierre Bourguignon
Liège, Belgium
Thu 18 08:50 - 09:15
WG5.3
ESPE Working Group on Paediatric and Adolescent Gynaecology (PAG)
Delay or advancement of female puberty after early life exposure to Bisphenol A and neuroendocrine mechanism
Liège, Belgium
Maria Luisa Brandi
Florence, Italy
Thu 18 14:30
S2.2
Symposium 2 - Endocrine Cancer Syndromes: An Update
MEN1 in Children and Adolescents
Florence, Italy
Laura Breij
Sat 20 12:30
FC10.4
Free Communication 10 - Programming & Early
Influence of newborn and maternal factors on neonatal body composition
Jillian Bryce
Glasgow, UK
Thu 18 10:25 - 10:35
WG3.6
ESPE Disorders of Sex Development Working Group (DSD)
I-DSD and I-CAH registry update
Glasgow, UK
Kanetee Busiah
Paris, France
Sat 20 09:25
FC9.5
Free Communication 9 - Beta Calls
TRANSIENT NEONATAL DIABETES IN ADULTHOOD: METABOLIC AND NEURODEVELOPMENTAL OUTCOMES
Paris, France
Núria Camats
Sat 20 09:05
FC6.3
Free Communication 6 - Gonads & DSD
LRH-1 rescues SF-1 deficiency for steroidogenesis in vitro but cannot explain the broad phenotype of SF-1 deficiency in men
Fergus Cameron
Victoria, Australia
Thu 18 16:00 - 17:00
MTE4.1
Meet the Expert Parallel Sessions
Management and prevention of complications in adolescents with Diabetes
Victoria, Australia
Angel Campos-Barros
Fri 19 08:45
FC4.1
Free Communication 4- Growth
HETEROZYGOUS IGF1R MUTATIONS REPRESENT A FREQUENT FINDING IN PATIENTS WITH PRE- AND/OR POSTNATAL PROPORTIONAL UNDERGROWTH AND LOW, NORMAL OR SUPRANORMAL IGF1
James Cantley
Oxford, UK
Thu 18 10:00 - 10:30
WG4.4
ESPE Obesity Working Group (OWG)
Identification of fatty acid binding protein 4 as an adipokine that regulates insulin secretion during obesity
Oxford, UK
Jean-Claude Carel
Paris, France
Sat 20 12:40
FC14.5
Free Communication 14 - Puberty
Fertility of women treated during childhood for precocious puberty with triptorelin: PREFER retrospective study
Paris, France
Gabriela Carren
London, UK
Sat 20 08:55
FC-LB-2
Free Communications - Late Breaking
Sonic Hedgehog is required for cell specification of Rathke’s pouch progenitors during normal development and is over-expressed in adamantinomatous craniopharyngioma
London, UK
Gemma Carreras-Badosa
Girona, Spain
Sat 20 12:10
FC10.2
Free Communication 10 - Programming & Early
STK11 EXPRESSION IN ADIPOSE TISSUE FOLLOWING FETAL GROWTH RESTRICTION: RELATION TO CATCH-UP GROWTH AND VISCERAL FAT MASS.
Girona, Spain
Manuela Cerbone
London, UK
Sat 20 12:40
FC11.5
Free Communication 11 - Pituitary
ENDOCRINE FEATURES OF A LARGE COHORT OF CHILDREN WITH SEPTO-OPTIC DYSPLASIA AND CONGENITAL MULTIPLE PITUITARY HORMONAL DEFICIENCIES
London, UK
Jean-Pierre Chanoine
Vancouver, Canada
Fri 19 14:15 - 14:25
WG8.1
Working Group for Global Paediatric Endocrinology and Diabetes (GPED)
Word from GPED’s President
Vancouver, Canada
Professor Evangelia Charmandari
Athens, Greece
Thu 18
Education and Training Update
ESPE Science School: the past and the future
Athens, Greece
Sat 20 16:00
S8.3
Symposium 8 - Novel Therapies in Paediatric Endocrinology
Congenital Adrenal Hyperplasia
Athens, Greece
Professor Krishna Chatterjee
Cambridge, UK
Thu 18 15:00
S4.3
Symposium 4 - Recent Advances in Our Understanding of Hypothyroidism
Novel Insights into Thyroid Hormone Resistence
Cambridge, UK
Julie Chowen
Sat 20 12:00
FC12.1
Free Communication 12 - Obesity
High-fat diet rapidly triggers circadian de-synchronization of clock genes, neuropeptides and inflammation mediators in the hypothalamus of C57BL mice
Professor Stefano Cianfarani
Rome, Italy
Thu 18
Education and Training Update
Seminars in Developmental Endocrinology: Diving in Paediatric Endocrinology sea
Rome, Italy
Florencia Clément
Fri 19 09:25
FC5.5
Free Communication 5- Neuroendocrinology
Characterization of IGF-I receptor expression and localization in paediatric gliomas upon diagnosis according to WHO 2007 grading
Professor Michael Collins
Bethesda MD, USA
Thu 18 09:30 – 10.00
WG1.3
ESPE Bone and Growth Plate Working Group (BGP)
Denosumab as an emerging therapy in pediatric metabolic bone diseases
Bethesda MD, USA
Thu 18 14:30
S1.2
Symposium 1 - Disorders of Gsalpha Signaling
McCune Albright Syndrome
Bethesda MD, USA
Gerard Conway
Thu 18 08:45 - 09:15
WG6.2
ESPE Turner Syndrome Working Group (TS)
Gastrointestinal disease in TS
Fri 19 14:30
S7.2
Symposium 7 - Controversies in the Surgical Management of DSD
Pros and Cons of Early or Late Feminising Genitoplasty
Professor Sabine Costagliola
Brussels, Belgium
Sat 20 09:15
NP2.2
New Perspectives 2
Formation of a Thyroid Gland from Embryonic Stem Cells
Brussels, Belgium
Nicola Crabtree
Birmingham, UK
Fri 19 09:15
FC2.4
Free Communication 2- Bone & Mineral
Fractures in children with chronic inflammatory and/or disabling conditions: the SNAP study
Birmingham, UK
Jovanna Dahlgren
Sweden
Sat 20 09:15
FC7.4
Free Communication 7 - Growth Promoting Therapies
A decade of clinical experience in a Swedish university centre using prediction models to optimize growth hormone (GH) treatment in prepubertal children
Sweden
Feyza Darendeliler
Istanbul, Turkey
Thu 18
Education and Training Update
Harmonization of Paediatric Endocrinology training in EU
Istanbul, Turkey
Sat 20 12:10
FC14.2
Free Communication 14 - Puberty
Infancy growth rate predicts timing of puberty both in girls and boys
Istanbul, Turkey
Ms Kate Davies
London, UK
Fri 19 14:55
WG7.3
ESPE Working Group for Paediatric Endocrine Nurse Specialists and Allied Health Professionals
Endocrine Nursing, social media and research: results of an international study
London, UK
Carine de Beaufort
Luxembourg, Luxembourg
Thu 18 10:15 - 10:50
WG2.7
ESPE Working Group on Diabetes Technology and Therapeutics
Debate: Do we need long acting insulin analogs?
Luxembourg, Luxembourg
Asma Deeb
Thu 18
Education and Training Update
Paediatric Endocrinology in the Middle East & North Africa; future plans and collaboration
Violeta Delgado-Carballar
Sat 20 12:30
FC11.4
Free Communication 11 - Pituitary
Management of hyperhydration in a child with Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH) using a selective vasopresin receptor agonist.
Huseyin Demirbilek
Ankara, Turkey
Sat 20 09:15
FC9.4
Free Communication 9 - Beta Calls
Clinical characteristics and molecular genetics analysis of 20 patients with neonatal diabetes mellitus from a single centre of the South-Eastern region of Turkey
Ankara, Turkey
Phillip Dennis
Baltimore, USA
Thu 18 14:00
S2.1
Symposium 2 - Endocrine Cancer Syndromes: An Update
PTEN: A Gene Involved in Overgrowth and Cancer
Baltimore, USA
Natascia Di Iorgi
Sat 20 12:20
FC11.3
Free Communication 11 - Pituitary
Early-Onset Central Diabetes Insipidus is associated with De novo Arginine Vasopressin-Neurophysin II or Wolfram Syndrome 1 gene mutations
Malcolm Donaldson
Glasgow, United Kingdom
Thu 18
Education and Training Update
The Winter School journey – past, present and future
Glasgow, United Kingdom
Stenvert Drop
Thu 18
Education and Training Update
Drop on behalf of e-learning team - the espe-elearning.org portal: Learning and teaching paediatric endocrinology on demand
Fri 19 07:30
NTA2.1
New Technological Aids in Clinical Paediatric Endocrinology 2
Two girls with precocious puberty; application of the www.espe-elearning.org portal for interactive classroom teaching on your personal mobile device.
Jacques Drouin
Montreal, Canada
Sat 20 16:00
S9.3
Symposium 9 - Novel Insights into Pituitary Development and Function
Pax7 dictates alternate pituitary cell fates during development
Montreal, Canada
Klas Ekström
Fri 19 09:05
FC3.3
Free Communication 3 - Diabetes
Improved hepatic insulin sensitivity in children randomized to CSII treatment from onset of type 1 diabetes
Charlotte Elder
Fri 19 09:15
FC1.4
Free Communication 1 - Adrenal
A novel non-invasive Short Synacthen Test
Alaa El-Ghoneimi
Paris, France
Fri 19 15:00
S7.3
Symposium 7 - Controversies in the Surgical Management of DSD
Masculinising Genitoplasty
Paris, France
Sian Ellard
Thu 18 14:30
S3.2
Symposium 3 - Novel Insights into Monogenic Diabetes
New Genes, New Mechanisms, New Phenotypes
Professor Sadaf Farooqi
Cambridge, UK
Thu 18 09:30 - 10:00
WG4.3
ESPE Obesity Working Group (OWG)
Making a diagnosis in Severe Complex Obesity
Cambridge, UK
Sat 20 17:00
PL6
Plenary 6
Genetics of Obesity
Cambridge, UK
Colin Farquharson
Thu 18 08:00 - 08:30
WG1.1
ESPE Bone and Growth Plate Working Group (BGP)
Unravelling GH actions on the growth plate and its promotion of linear growth
Pamela Fischer-Posovszky
Sat 20 12:50
FC12.6
Free Communication 12 - Obesity
Resveratrol inhibits inflammation-induced production of cytokines in human adipocytes
William Foulkes
Montreal, Canada
Thu 18 15:00
S2.3
Symposium 2 - Endocrine Cancer Syndromes: An Update
DICER1 syndrome: a erview of the syndrome with a focus on endocrine aspects
Montreal, Canada
Jan-Bernd Funcke
Sat 20 09:05
FC8.3
Free Communication 8 - Fat Metabolism
Identification of death ligand TRAIL (TNF-related apoptosis-inducing ligand) as a potent mitogen in human preadipocytes
Rachel Gafni
Bethesda, USA
Fri 19 07:30 - 08:30
MTE5.1
Meet the Expert Parallel Sessions
Management of childhood fractures
Bethesda, USA
Hoong-Wei Gan
London, UK
Fri 19 09:35
FC5.6
Free Communication 5- Neuroendocrinology
The diencephalic syndrome (DS) of emaciation in infantile hypothalamochiasmatic low-grade gliomas (HCLGGs): a retrospective case-control study of diagnostic parameters and long-term outcomes over 30 years of follow-up
London, UK
Tommaso Giorgis
Sat 20 08:45
FC8.1
Free Communication 8 - Fat Metabolism
Activation of the ER stress response in cultured human umbilical vein endothelial cells (HUVECs) by plasma obtained from prepubertal obese children.
Debora Gomes
Sat 20 12:00
FC11.1
Free Communication 11 - Pituitary
ABNORMAL SONIC HEDGEHOG SIGNALING IN ADAMANTINOMATOUS CRANIOPHARYNGIOMAS AND ITS ASSOCIATION WITH CTNNB1/BETA-CATENIN MUTATIONS
Catherine Gordon
Boston, USA
Thu 18 10:10 - 10:35
WG5.5
ESPE Working Group on Paediatric and Adolescent Gynaecology (PAG)
Contraception in adolescence: current options
Boston, USA
Anna Grandone
Naples, Italy
Sat 20 09:25
FC-LB-5
Free Communications - Late Breaking
CB2 polymorphism could modulate the relationship between childhood obesity and age at menarche
Naples, Italy
Louise Gregory
London, UK
Sat 20 12:20
FC14.3
Free Communication 14 - Puberty
Novel genetic variants in a cohort of paediatric and adolescent patients with Hypogonadotrophic Hypogonadism and Kallmann syndrome
London, UK
Aliesha Griffin
Fri 19 09:05
FC1.3
Free Communication 1 - Adrenal
Genetic engineering using TALENs to study the redox regulation of steroidogenesis in vivo
Virginie Grybek
Sat 20 12:20
FC10.3
Free Communication 10 - Programming & Early
Genetic and epigenetic defects at the GNAS locus lead to opposite patterns of fetal and postnatal growth
Anja Gucht
Sat 20 12:50
FC13.6
Free Communication 13 - Thyroid
ABNORMAL THYROID HORMONE METABOLISM IN PATIENTS WITH THRA MUTATIONS DUE TO IMPAIRED EXPRESSION OF THE TYPE 3 DEIODINASE
Maria Güemes
Madrid, Spain
Sat 20 12:50
FC11.6
Free Communication 11 - Pituitary
Clinical and neuroradiological characteristics in children and adolescents with Septo-Optic Dysplasia, Multiple Pituitary Hormone Deficiencies and Optic Nerve Hypoplasia: Experience from a single tertiary centre.
Madrid, Spain
Casper Hagen
Copenhagen, Denmark
Sat 20 09:25
FC6.5
Free Communication 6 - Gonads & DSD
Serum levels of AMH reflect ovarian morphology by MRI in 109 healthy peripubertal girls
Copenhagen, Denmark
Rasha Hamza
Cairo, Egypt
Fri 19 09:05
FC2.3
Free Communication 2- Bone & Mineral
Calcium Homeostasis in Adolescents with Beta-Thalassemia Major: Effect of Intramuscular Injection of a Megadose of Cholecalciferol
Cairo, Egypt
Bing Han
Manchester, UK
Sat 20 08:45
FC9.1
Free Communication 9 - Beta Calls
Inappropriately High Rates of Cell Proliferation in Diffuse Congenital Hyperinsulinism are Linked to Nuclear Expression of CDK6
Manchester, UK
Ragnar Hanas
Uddevalla, Sweden
Thu 18 10:15 - 10:50
WG2.8
ESPE Working Group on Diabetes Technology and Therapeutics
Debate: Do we need long acting insulin analogs?
Uddevalla, Sweden
Dr Sabine Hannema
Amsterdam, The Netherlands
Sat 20 12:00
FC14.1
Free Communication 14 - Puberty
Brain structure and function in gender dysphoric adolescents
Amsterdam, The Netherlands
Matthias Herrath
LA, USA
Thu 18 12:00
PL2
Plenary Session 1 & 2
Learning from histopathology to design novel immune-therapies for type 1 and 2 diabetes
LA, USA
Olaf Hiort
Lübeck, Germany
Thu 18 10:45 - 10:55
WG3.8
ESPE Disorders of Sex Development Working Group (DSD)
DSDnet: A COST Action on the systematic elucidation of differences of sex development
Lübeck, Germany
Wolfgang Högler
Linz, Austria
Sat 20 09:35
FC-LB-6
Free Communications - Late Breaking
Global Consensus Recommendations on Prevention and Management of Nutritional Rickets
Linz, Austria
Anita Hokken-Kolega
Rotterdam, The Netherlands
Thu 18 16:30
NTA1.2
New Technological Aids in Clinical Paediatric Endocrinology 1
Growth monitor platform: New application to predict growth and synchronize data between devices
Rotterdam, The Netherlands
PD Nadine Hornig, PhD
Kiel, Germany
Sat 20 08:55
FC6.2
Free Communication 6 - Gonads & DSD
Next generation sequencing of the androgen receptor (AR) gene in patients with androgen insensitivity syndrome (AIS) and controls
Kiel, Germany
Stephen Hsu
Florida, USA
Sat 20 09:35
FC7.6
Free Communication 7 - Growth Promoting Therapies
Topicon™ ThermoMatrix™-Mediated Passive Transdermal Delivery of Human Growth Hormone (hGH) Across EpidermFT™ Full-Thickness Human Skin Equivalent (HSE): Towards an Extended-Wear hGH Patch
Florida, USA
John Hughes
Thu 18
Education and Training Update
Reflections on an African (PETCA) safari
Claire Hughes
Fri 19 08:55
FC1.2
Free Communication 1 - Adrenal
Clinical phenotype of patients with MCM4 mutation suggests pubertal delay in males in addition to adrenal failure, absent adrenarche and short stature in boys and girls
Professor Khalid Hussain
Doha, Qatar
Sat 20 15:00
S8.1
Symposium 8 - Novel Therapies in Paediatric Endocrinology
Hyperinsulinaemia
Doha, Qatar
A. Iglesias
Sat 20 12:00
FC13.1
Free Communication 13 - Thyroid
Massive sequencing of thyroidal genes reveals unexpected polygenic defects in dyshormonogenic hypothyroidism.
Jarmo Jääskeläinen
Kuopio, Finland
Thu 18 16:00 - 17:00
MTE3.1
Meet the Expert Parallel Sessions
Evaluation of Precocious Pubarche
Kuopio, Finland
Rikke Jensen
Copenhagen, Denmark
Sat 20 08:45
FC7.1
Free Communication 7 - Growth Promoting Therapies
Genetic markers of insulin resistance are associated with growth hormone response in short SGA children – the North European SGA Study (NESGAS)
Copenhagen, Denmark
Anders Juul
Copenhagen, Denmark
Thu 18 08:00 - 08:25
WG5.1
ESPE Working Group on Paediatric and Adolescent Gynaecology (PAG)
New markers of Ovarian Function
Copenhagen, Denmark
Clemens Kamrath
Giessen, Germany
Thu 18 08:30 - 08:50
WG3.2
ESPE Disorders of Sex Development Working Group (DSD)
The potential role of the alternative ‘backdoor’ pathway for androgen synthesis and virilisation in CAH
Giessen, Germany
Christina Kanaka-Gantenbein
Sat 20 12:40
FC12.5
Free Communication 12 - Obesity
Low Circulating Levels of DKK-1 Protein in Obese Children Indicate Suppression of Canonical Wnt Signaling
Birgit Köhler
Berlin, Germany
Thu 18 10:35 - 10:45
WG3.7
ESPE Disorders of Sex Development Working Group (DSD)
DSDlife
Berlin, Germany
Antje Körner
Leipzig, Germany
Sat 20 12:30
FC12.4
Free Communication 12 - Obesity
Pediatric reference values for insulin from oGTT and prevalence of hyperinsulinemia in obese children
Leipzig, Germany
Tanja Kuiri-Hänninen
Fri 19 09:15
FC5.4
Free Communication 5- Neuroendocrinology
Reference values for urinary gonadotropins in preterm and full-term infants in “minipuberty”
Svetlana Lajic
Stockholm, Sweden
Thu 18 08:50 - 09:15
WG3.3
ESPE Disorders of Sex Development Working Group (DSD)
Long term outcome of prenatal CAH- therapy
Stockholm, Sweden
Agaristi Lamprokostopoulou
Sat 20 12:10
FC12.2
Free Communication 12 - Obesity
Obesity in childhood and adolescence is associated with shorter leucocyte telomere length
Juliane Léger
Paris, France
Thu 18
Education and Training Update
ESPE Maghreb School: training in French
Paris, France
Chiara Leonibus
Fri 19 08:55
FC4.2
Free Communication 4- Growth
The effect of GRB10-deficiency in Zebrafish: a translational animal model to study human growth
Sat 20 08:55
FC7.2
Free Communication 7 - Growth Promoting Therapies
The rs1024531 GRB10 promoter polymorphism is associated with response to growth hormone (GH) therapy in patients with GH deficiency (GHD): validation by in vitro functional analysis
Agnès Linglart, MD, PhD
Paris, France
Thu 18 10:00 – 10:30
WG1.4
ESPE Bone and Growth Plate Working Group (BGP)
New therapies in Metabolic bone disease: PTH
Paris, France
Thu 18 15:00
S1.3
Symposium 1 - Disorders of Gsalpha Signaling
Acrodysostosis
Paris, France
Robin Lovell-Badge
London, UK
Fri 19 10:15
PL3
Plenary Session 3
Sex, Stem Cells and Decision of Cell Fate
London, UK
Katherine Madson
Fri 19 08:45
FC2.1
Free Communication 2- Bone & Mineral
Asfotase Alfa: Sustained Improved Growth and Function with Extended Treatment in Children with Hypophosphatasia
Katharina Main
Copenhagen, Denmark
Thu 18 16:00 - 17:00
MTE1.1
Meet the Expert Parallel Sessions
Management of a Child with Cryptorchidism
Copenhagen, Denmark
David Martin
Tuebingen, Germany
Thu 18 16:00
NTA1.1
New Technological Aids in Clinical Paediatric Endocrinology 1
The BoneXpert methods for fully automated assessment of skeletal maturity ('bone age') and adult height prediction
Tuebingen, Germany
Laetitia Martinerie
Paris, France
Sat 20 12:50
FC10.6
Free Communication 10 - Programming & Early
The PremAldo Study: Impaired Aldosterone Signaling Worsens Renal Sodium Loss in Preterm Infants
Paris, France
J.P Martinez-Barbera
London, UK
Sat 20 15:30
S9.2
Symposium 9 - Novel Insights into Pituitary Development and Function
Sox2+ve cells in the adult murine pituitary are stem cells with tumour-inducing potential
London, UK
M. Mavinkurve
Sat 20 09:35
FC8.6
Free Communication 8 - Fat Metabolism
A Novel Missense Variant in the Insulin Receptor Gene in 3 unrelated Irish families with severe Insulin Resistance Syndrome - Evidence for an Irish Founder Effect.
Nancy Mekhail
Fri 19 08:55
FC5.2
Free Communication 5- Neuroendocrinology
Mutations in the maternally imprinted gene MKRN3 are a frequent cause of familial central precocious puberty
Muriel Meso
Sat 20 12:00
FC10.1
Free Communication 10 - Programming & Early
A role for Delta-like homologue 1 (DLK1) in a secretory placental population and implications for foetal growth
Pierre-André Michaud
Lausanne, Switzerland
Thu 18 09:45 - 10:10
WG5.4
ESPE Working Group on Paediatric and Adolescent Gynaecology (PAG)
Contraception in Adolescence from a Public Health Perspective
Lausanne, Switzerland
Mikkel Mieritz
Sat 20 12:30
FC14.4
Free Communication 14 - Puberty
Development of pubertal gynaecomastia - A longitudinal cohort study
Professor Rod Mitchell
Edinburgh, UK
Sat 20 09:35
FC6.6
Free Communication 6 - Gonads & DSD
Effects of exposure to the endocrine disruptor di(n-butyl) phthalate on testicular dysgenesis and fetal germ cell development in the rat and human fetal testis.
Edinburgh, UK
Wojciech Mlynarski
Lodz, Poland
Thu 18 15:00
S3.3
Symposium 3 - Novel Insights into Monogenic Diabetes
Epidemiology of Monogenic Diabetes
Lodz, Poland
Patrice Mollard
Montpellier, France
Sat 20 15:00
S9.1
Symposium 9 - Novel Insights into Pituitary Development and Function
Paracrine Regulation in the Pituitary
Montpellier, France
Dénes Molnar
Pecs, Hungary
Sat 20 15:00
S10.1
Symposium 10 - Childhood Obesity: Challenges in Management
The Metabolically Healthy Obese Child
Pecs, Hungary
Rebecca Moon
Southampton, UK
Sat 20 12:40
FC10.5
Free Communication 10 - Programming & Early
Contrasting associations of maternal smoking and alcohol intake in late pregnancy and offspring body composition in childhood
Southampton, UK
Nicolas Nicolaides
Athens, Greece
Fri 19 08:45
FC1.1
Free Communication 1 - Adrenal
Molecular Mechanisms of Nongenomic Glucocorticoid Actions: The Role of Human Glucocorticoid Receptor S-Palmitoylation.
Athens, Greece
Dr Ola Nilsson
Stockholm, Sweden
Fri 19 09:15
FC4.4
Free Communication 4- Growth
Short stature, accelerated bone maturation, and early growth cessation due to heterozygous aggrecan mutations
Stockholm, Sweden
Revital Nimri
Petah Tikva, Israel
Thu 18 09:40 - 10:15
WG2.6
ESPE Working Group on Diabetes Technology and Therapeutics
Debate: Sensor/pump therapy from onset of diabetes?
Petah Tikva, Israel
Munier Nour
Sat 20 09:25
FC7.5
Free Communication 7 - Growth Promoting Therapies
Impact of Growth Hormone on Adult Bone Quality in Turner Syndrome – A High Resolution Peripheral Quantitative Computed Tomography Study
Stephen O’Riordan
Cork, Ireland
Fri 19 07:30 - 08:30
MTE7.1
Meet the Expert Parallel Sessions
Clinical Management of Cystic Fibrosis Related Diabetes (CFRD) in Childhood
Cork, Ireland
Ken Ong
Cambridge, United Kingdom
Sat 20 09:05
FC-LB-3
Free Communications - Late Breaking
Parent-of-origin specific allelic associations among 106 genomic loci for age at menarche
Cambridge, United Kingdom
Professor Donal O'Shea
Dublin, Ireland
Sat 20 10:15
PL5
Plenary Session 5
Obesity: Novel Treatments and the Imperative for Prevention
Dublin, Ireland
Yasmine Ouarezki
Sat 20 12:30
FC13.4
Free Communication 13 - Thyroid
The prevalence of congenital malformations in infants with TSH elevation on newborn screening – the importance of distinguishing between true and transient congenital hypothyroidism
Katharine Owen
Thu 18 14:00
S3.1
Symposium 3 - Novel Insights into Monogenic Diabetes
Differential Diagnosis of Monogenic Diabetes
Jacques Pantel
Sat 20 09:25
FC8.5
Free Communication 8 - Fat Metabolism
Putative gain-of-function in rats carrying the Ghsr Q343X mutation
Munro Peacock
Indianapolis, USA
Fri 19 09:35
FC2.6
Free Communication 2- Bone & Mineral
Efficacy and Safety Following Four Monthly Subcutaneous (SC) Doses of a Human Anti-FGF23 (Fibroblast Growth Factor 23) Antibody (KRN23) in Adults with X-Linked Hypophosphatemia (XLH)
Indianapolis, USA
Lenka Petruzelkova
Fri 19 08:55
FC3.2
Free Communication 3 - Diabetes
HbA1c level as a predictive marker of progression to clinical diabetes
Moshe Phillip
Israel
Thu 18 08:00 - 08:15
WG2.1
ESPE Working Group on Diabetes Technology and Therapeutics
Technological horizon for diabetes treatment
Israel
Thu 18 11:30
PL1
Plenary Session 1 & 2
Closed-Loop System: Dream or Reality?
Israel
Joao Pippi-Salle
Toronot, Canada
Fri 19 14:15
S7.1
Symposium 7 - Controversies in the Surgical Management of DSD
Evolution of Feminising Genitoplasty
Toronot, Canada
Nelly Pitteloud
Lausanne, Switzerland
Thu 18 08:25 - 08:50
WG5.2
ESPE Working Group on Paediatric and Adolescent Gynaecology (PAG)
Lessons drawn from gynecological disorders in relation with hypothalamic-pituitary malfunction
Lausanne, Switzerland
Michel Polak
Paris, France
Thu 18 10:35 - 11:00
WG5.6
ESPE Working Group on Paediatric and Adolescent Gynaecology (PAG)
Lessons drawn from rare gynecological disorders in relation with ovarian malfunction
Paris, France
Anna Prats-Puig
Girona, Spain
Sat 20 09:15
FC8.4
Free Communication 8 - Fat Metabolism
CREB-REGULATED TRANSCRIPTION COACTIVATOR 3 (CRTC3): A NEW ADIPOKINE RELATED TO CHILDHOOD OBESITY
Girona, Spain
Vincent Prevot
Lille, France
Fri 19 08:45
NP1.1
New Perspectives 1
Non Coding RNA's: Introduction to Non-Coding RNAs and the Role of MicroRNAs in GnRH Neurons
Lille, France
Aman Pulungan
Fri 19 14:35 - 14:45
WG8.3
Working Group for Global Paediatric Endocrinology and Diabetes (GPED)
Inequities of treatment options in developing countries: Osteogenesis imperfecta in Indonesia
Sofia Rahman
Sat 20 08:55
FC9.2
Free Communication 9 - Beta Calls
Characterising the immunohistochemical expression of dipeptidyl peptidase-4 in pancreatic tissue from patients with diffuse and focal congential hyperinsulinism.
William Rainey
Michigan, USA
Fri 19 14:45
S5.2
Symposium 5 - Novel Insights into Hypoadrenalism
Adrenarche: Coming of age in the era of genomics and metabolomics
Michigan, USA
Taneli Raivio
Helsinki, Finland
Fri 19 08:45
FC5.1
Free Communication 5- Neuroendocrinology
Derivation of GnRH neuron-like cells from human embryonic stem cell-derived neural crest progenitors
Helsinki, Finland
Romano Regazzi
Lausanne, Switzerland
Fri 19 09:15
NP1.2
New Perspectives 1
The Role of MicroRNAs in Diabetes
Lausanne, Switzerland
Thomas Reinehr
Datteln, Germany
Thu 18 08:30 - 09:00
WG4.2
ESPE Obesity Working Group (OWG)
Type 2 diabetes in children and adolescents
Datteln, Germany
Sat 20 16:00
S10.3
Symposium 10 - Childhood Obesity: Challenges in Management
Natural Course of Impaired Glucose Tolerance in Obese Children
Datteln, Germany
Cheryl Rockman-Greenberg
Manitoba, Canada
Sat 20 15:30
S8.2
Symposium 8 - Novel Therapies in Paediatric Endocrinology
Treatment of Hypophosphatasia
Manitoba, Canada
Ron Rosenfeld
Oregon, USA
Sat 20 08:45
FC-LB-1
Free Communications - Late Breaking
Top Line Results of Once-Weekly, CTP-Modified Human Growth Hormone (MOD-4023): Phase 2 Dose Finding Study in Children with Growth Hormone Deficiency (GHD)
Oregon, USA
Dominique Roulot
Paris, France
Thu 18 08:00 - 08.45
WG6.1
ESPE Turner Syndrome Working Group (TS)
Liver involvement in Turner syndrome
Paris, France
Nicolas de Roux
Paris, France
Fri 19 14:45
S6.2
Symposium 6 - New Concepts in the Gonadotropic Axis
New Syndromes Resulting in Secretory Pathway and Gonadotropic Axis Regulation Defects
Paris, France
Joanne Rovel
Toronto, Canada
Sat 20 09:15
FC-LB-4
Free Communications - Late Breaking
Does Severity of Hypothyroidism at Birth Contribute to Abnormal Cortical Development among Children with Congenital Hypothyroidism (CH)?
Toronto, Canada
Lars Sävendahl
Stockholm, Sweden
Thu 18
Education and Training Update
Welcome and meeting new ESPE members and trainees
Stockholm, Sweden
Fri 19 07:30 - 08:30
MTE8.1
Meet the Expert Parallel Sessions
Evaluation and the Management of Tall Stature
Stockholm, Sweden
Andrea Scaramuzza
Asola, Italy
Fri 19 09:35
FC3.6
Free Communication 3 - Diabetes
ALPHA-LIPOIC ACID AND ANTI-OXIDANT DIET HELPS TO IMPROVE ENDOTHELIAL DYSFUNCTION IN CHILDREN AND ADOLESCENTS WITH TYPE 1 DIABETES.
Asola, Italy
Raphael Scharfmann
Paris, France
Sat 20 08:45
NP2.1
New Perspectives 2
Pancreatic Beta Cell Development: from rodent to human
Paris, France
Nikolaos Settas
Bethesda, USA
Sat 20 08:45
FC6.1
Free Communication 6 - Gonads & DSD
Search for genetic defects in the transcription factor genes FOXL2, FOXE1, BMP15, NOBOX and GDF9 in children, adolescents and young adults with premature ovarian insufficiency (POI).
Bethesda, USA
Deimante Simaite
Sat 20 09:05
FC9.3
Free Communication 9 - Beta Calls
In search for new monogenic diabetes genes: PCBD1
David Skuse
London, UK
Thu 18 10:15 – 11:00
WG6.3
ESPE Turner Syndrome Working Group (TS)
Autism and the X-chromosome
London, UK
Evelien Smeets
Fri 19 09:35
FC1.6
Free Communication 1 - Adrenal
Molecular Characterization of Testicular Adrenal Rest Tumours (TART) in Congenital Adrenal Hyperplasia (CAH); Lesions with both Adrenocortical and Leydig Cell Features
Adam Stevens
Manchester, United Kingdom
Fri 19 09:05
FC4.3
Free Communication 4- Growth
Oscillations in gene expression profiles across childhood highlight the relation of growth and specific metabolic functions in both sexes
Manchester, United Kingdom
Sat 20 09:05
FC7.3
Free Communication 7 - Growth Promoting Therapies
Gene expression networks associated with changes in serum markers of metabolism and growth in growth hormone (GH)-treated children with GH deficiency (GHD)
Manchester, United Kingdom
Maria Elizabeth Street
Parma, Italy
Fri 19 08:45
FC3.1
Free Communication 3 - Diabetes
HIGH MOBILITY GROUP BOX-1(HMGB-1) SERUM CONCENTRATIONS INCREASE AT ONSET OF DIABETES IN CYSTIC FIBROSIS (CF) PATIENTS
Parma, Italy
Manuel Tena-Sempere
Córdoba, Spain
Fri 19 14:15
S6.1
Symposium 6 - New Concepts in the Gonadotropic Axis
Role of The Hypothalamic MicroRNA in Puberty Regulations
Córdoba, Spain
Ali Topaloglu
Fri 19 09:05
FC5.3
Free Communication 5- Neuroendocrinology
Loss of Function Mutations in PNPLA6 Cause Hypogonadotropic Hypogonadism due to Impaired LH Release from Pituitary Gonadotropes
Ericka Trarbach
Sat 20 12:20
FC13.3
Free Communication 13 - Thyroid
Overexpression of supressor tumoral PTEN, but not DREAM, was detected in multinodular goiter in humans.
Paul Trotsenburg
Amsterdam, The Netherlands
Thu 18 14:00
S4.1
Symposium 4 - Recent Advances in Our Understanding of Hypothyroidism
Management of Central Hypothyroidism
Amsterdam, The Netherlands
Nadia Tubiana-Rufi
Paris, France
Thu 18 08:40 - 09:15
WG2.3
ESPE Working Group on Diabetes Technology and Therapeutics
Debate: Should all newly diagnosed patients with diabetes need to be hospitalized?
Paris, France
Elisa Vaiani
Sat 20 09:15
FC6.4
Free Communication 6 - Gonads & DSD
FAMILIAL 46,XY COMPLETE FEMALE EXTERNAL SEX DEVELOPMENT AND PRIMARY AMENORRHEA ALONG WITH HIDDEN GONADAL TUMORS, SECONDARY TO A NOVEL p.MET64VAL SRY GENE MUTATION
Tero Varimo
Helsinki, Finland
Sat 20 12:50
FC14.6
Free Communication 14 - Puberty
QUALITY OF LIFE IN PATIENTS WITH CONGENITAL HYPOGONADOTROPIC HYPOGONADISM (CHH)
Helsinki, Finland
Rasa Verkauskiene
Kaunas, Lithuania
Thu 18
Education and Training Update
ESPE Clinical Fellowship programme: starting opportunity for young Paediatric Endocrinologists
Kaunas, Lithuania
Thu 18
Education and Training Update
ESPE Caucasus and Central Asia School: starting in 2014
Kaunas, Lithuania
Guy Vliet
Montréal, Canada
Fri 19 07:30 - 08:30
MTE6.1
Meet the Expert Parallel Sessions
Assessment of Thyroid Nodules
Montréal, Canada
Bibian Voorn
Fri 19 09:25
FC1.5
Free Communication 1 - Adrenal
Antenatal glucocorticoid treatment and polymorphisms in glucocorticoid and mineralocorticoid receptor genes are associated with long-term
Liat Vries
Petah Tikva, Israel
Thu 18 08:40 - 09:15
WG2.4
ESPE Working Group on Diabetes Technology and Therapeutics
Debate: Should all newly diagnosed patients with diabetes need to be hospitalized?
Petah Tikva, Israel
Nina Vuorela
Fri 19 09:35
FC4.6
Free Communication 4- Growth
LONGITUDINAL GROWTH OF FINNISH CHILDREN WITH GESTATIONAL DIABETES IN MOTHERS
Ram Weiss
Jerusalem, Israel
Thu 18 08:00 - 08:30
WG4.1
ESPE Obesity Working Group (OWG)
Metabolic syndrome in youth: current insights and novel serum biomarkers
Jerusalem, Israel
Sat 20 15:30
S10.2
Symposium 10 - Childhood Obesity: Challenges in Management
Childhood and Adolescent Obesity - Can Treatment Response be Predicted?
Jerusalem, Israel
Michelle Welsh
Glasgow, UK
Thu 18 09:45 - 10:05
WG3.4
ESPE Disorders of Sex Development Working Group (DSD)
Detailed phenotyping of DSD: external virilisation
Glasgow, UK
Alena Welters
Fri 19 09:25
FC3.5
Free Communication 3 - Diabetes
Pancreatic N-Methyl-D-Aspartate receptors as novel drug targets for the treatment of diabetes mellitus
Theda Wessel
Sat 20 12:10
FC13.2
Free Communication 13 - Thyroid
Thyroid agenesis and severe thyroid hypoplasia caused by a new inactivating TSH receptor mutation Ala579Val
Susanna Wiegand
Berlin, Germany
Fri 19 09:15
FC3.4
Free Communication 3 - Diabetes
Genetics of pediatric type 2 diabetes: ABCC8 mutation in obesity-associated insulin secretion defects
Berlin, Germany
Lutz Wünsch
Lubeck, Germany
Thu 18 10:05 - 10:25
WG3.5
ESPE Disorders of Sex Development Working Group (DSD)
Imaging of the urogenital tract
Lubeck, Germany
Xiao-qin Xu
Sat 20 08:55
FC8.2
Free Communication 8 - Fat Metabolism
MicroRNA-152 promotes hepatic steatosis by suppressing the Wnt signaling pathway
Iroro Yahere
Fri 19 15:25 - 15:35
WG8.7
Working Group for Global Paediatric Endocrinology and Diabetes (GPED)
Neonatal screening for congenital hypothyroidism: Don’t take it for granted! (Nigeria)
Margaret Zacharin
Fri 19 14:45 - 14:55
WG8.4
Working Group for Global Paediatric Endocrinology and Diabetes (GPED)
Inequities of treatment options in developing countries: Congenital Adrenal Hyperplasia
Delphine Zenaty
Paris, France
Fri 19 09:25
FC4.5
Free Communication 4- Growth
Fetal and postnatal growth in Turner Syndrome and their associations with the dosage effects of the X-linked gene: a cross-sectional data base analysis of the French national rare disease network
Paris, France
Xiaoping Zhang
Fri 19 09:25
FC2.5
Free Communication 2- Bone & Mineral
Pharmacokinetics (PK) and Pharmacodynamics (PD) of a Human Monoclonal Anti-FGF23 (Fibroblast Growth Factor 23) Antibody (KRN23) Following Four Month Intra-Dose Escalation in Adults with X-linked Hypophosphatemia (XLH)
LB-D3-1001
HISTOLOGICAL EVALUATION OF PATIENTS WITH PARTIAL GONADAL DYSGENESIS AND NR5A1 MUTATIONS: REVIEW IN LEYDIG AND GERM CELL PATTERN.
Juliana Gabriel Ribeiro de Andrade, Ralf Werner, Helena Campos Fabbri, Gil Guerra-Junior, Andrea Trevas Maciel-Guerra, Maricilda Palandi de Mello, Konstanze Holl-Ulrich, Olaf Hiort
P1-D1-184
Very low birth weight <1,500g is associated with reduced sex-typical behaviour in childhood
Ulla Sankilampi, Melissa Hines, Annamarja Lamminmäki
P1-D3-100
QUALITY OF LIFE IN A LARGE COHORT OF ADULT BRAZILIAN PATIENTS WITH 46,XX AND 46,XY DISORDERS OF SEX DEVELOPMENT FROM A SINGLE TERTIARY CENTRE
Rita Amaral, Marlene Inacio, Vinicius Brito, Tania Bachega, Ari Oliveira Jr, Sorahia Domenice, Francisco Denes, Maria Helena Sircilli, Ivo Arnhold, Guiomar Madureira, Larissa Gomes, Elaine Costa, Berenice Mendonca
P1-D3-101
Subjective need for psychological support in parents of children with dsd - Results from the German Clinical Evaluation Study
Elena Bennecke, Knut Werner-Rosen, Heiko Krude, Ute Thyen, Anke Lux, Eva Kleinemeier, Martina Jürgensen, Birgit Köhler, Group DSD Network Working
P1-D3-102
FOUR CASES OF ISOLATED PARTIAL GONADAL DYSGENESIS DUE TO NR0B1 (DAX1) LOCUS DUPLICATION INHERITED IN A LARGE FAMILY
Kathy Wagner Mahler, Caroline Devos, Jean Yves Kurzenne, Frederique Gastaud, Marie Hoflack, Delphine Mallet, Houda Karmous Benailly, Fabienne Giuliano, Gilbert Simonin, Damien Sanlaville, Yves Morel
P1-D3-92
Mutations involving FIBULIN2 are a novel cause of 46,XY DSD
Anu Bashamboo, Chiara Palka, Angelika Mohn, Valentina Chiavaroli, Francesco Chiarelli, Raja Brauner, Ken McElreavey
P1-D3-93
Ex vivo culture of human fetal gonads: Manipulation of meiosis regulation affects testis development
Anne Jørgensen, John E Nielsen, Signe Perlman, Lene Lundvall, Anders Juul, Ewa Rajpert-De Meyts
P1-D3-94
Prenatal exposure to phthalates and phenols in relation to anogenital distance (AGD) at birth in male infants
Benjamin G. Fisher, Ajay Thankamony, Ken K. Ong, David B. Dunger, Ieuan A. Hughes, Carlo L. Acerini
P1-D3-95
Ovarian development and hormonal feedback mechanism in a 46 XX Patient with CYP19A1 Deficiency under low dose Estrogen Replacement
Marie-Anne Burckhardt, Verena Obmann, Marco Janner, Primus E. Mullis
P1-D3-96
Isolated hypospadias (IH) and exposure to endocrine disrupting chemicals (EDC) during pregnancy: a multi-institutional controlled study in a high prevalence area
Nicolas Kalfa, Pascal Philibert, Sylvie Broussous, Taieb Chouikh, Mohamed Masmoudi, Francoise Audran, Françoise Paris, Nadège Servant, Charles Sultan, Mattea Orsini, Amel Zahhaf, Jean Pierre Daures, Hélène Lehors, Jean Michel Guys, Rachel Reynaud, Pierre Alessandrini, Florence Bastiani, Jean Yves Kurzenne, Kathy Wagner, Gérard Morisson Lacombe
P1-D3-97
46 XX ovotesticular disorder of sex development: potential role of 13q31.1
Céline M Girardin, Mirjam Dirlewanger, Frédérique Bena, Serge Nef, Anne-Laure Rougemont, Jacques Birraux, Valérie M Schwitzgebel
P1-D3-98
A novel NR5A1 mutation with preserved fertility.
Hiroko Yagi, Masaki Takagi, Yukihiro Hasegawa, Maki Igarashi, Masafumi Kon, Maki Fukami
P1-D3-99
Development of a next generation sequencing panel for Disorders of Sex Development (DSDs)
Graham A Fews, Lowri Hughes, Kirsten McKay Bounford, Trevor Cole, NIls Krone, Fiona Madonald
P2-D1-564
46,XY neonates and infants with ambiguous genitalia: who to investigate?
Dorien Baetens, Wilhelm Mladenov, Barbara Delle Chiaie, An Desloovere, Violeta Iotova, Bjorn Menten, Eric Van Laecke, Piet Hoebeke, Elfride De Baere, Martine Cools
P2-D1-565
Novel NR5A1 gene mutations associated with 46,XY Disorders of Sex Development
Helena Fabbri, Juliana Gabriel Ribeiro de Andrade, Andrea Trevas Maciel-Guerra, Gil Guerra-Junior, Maricilda Palandi de Mello
P2-D1-566
The Research about SF1 gene abnormality in 45 children with micropenis
Pin Li, Yan Gong, Ying Zhuzhi
P2-D1-567
A new mutation of MAMLD1 (CXorf6) associated with NR5A1 (SF1) variant in a patient with 46,XY DSD
Asmahane Ladjouze, Pascal Philibert, yasmine Ouarezki, Adel Djermane, Leila Kedji, Abdeljalil Maoudj, Karima Berkouk, Charles Sultan, Abdenour Laraba
P2-D1-568
46XY,DSD Due To 5α-Reductase Type 2 Deficiency In 19 Chinese Patients
Yan-Hong Li, Min-Lian Du, Hua-Mei Ma, Hong-Shan Chen, Qiu-Li Chen
P2-D1-569
Experience of feminizing operations in cases of incomplete sexual development of girls
Alena Shybeka, Hanna Milkhno, Herman Druzhynin, Vitali Dubrov, Anzhalika Solntsava, Izaokas Skobejus
P2-D1-570
FOUR CASES OF ISOLATED PARTIAL GONADAL DYSGENESIS DUE TO NR0B1 (DAX1) LOCUS DUPLICATION INHERITED IN A LARGE FAMILY
WAGNER MAHLER Kathy, DEVOS Caroline, KURZENNE Jean Yves, GASTAUD Frédérique, HOFLACK Marie, MALLET Delphine, KARMOUS BENAILLY Houda, GIULIANO Fabienne, SIMONIN Gilbert, SANLAVILLE Damien, MOREL Yves
P2-D1-571
Identification of a missense MAP3K1 mutation in a patient with hypospadias
Maki Igarashi, Reiko Horikawa, Kazuhiko Nakabayashi, Kenichirou Hata, Tsutomu Ogata, Maki Fukami
P2-D1-572
Anogenital Distance, Penis Growth, and Masculine Behavior: Evidence for Independent Neurobehavioral Effects of Foetal versus Postnatal Androgen Exposure in Boys
Vickie Pasterski, Carlo Acerini, David Dunger, Ken Ong, Ieuan Hughes, Ajay Thankamony, Melissa Hines
P2-D1-573
Mutation analysis of KDM3A (lysine-specific demethylase 3A) in patients with hypospadias
Masafumi Kon, Maki Igarashi, Yoko Izumi, Yuko Kato-Fukui, Kentaro Mizuno, Yutaro Hayashi, Kenjiro Kohri, Yoshiyuki Kojima, Katsuya Nonomura, Tsutomu Ogata, Maki Fukami
P2-D2-574
Analysis of steroid 5-alpha reductase 2 (SRD5A2) gene in patients with 46,XY disorder of sex development (DSD)
Giselle Neres de Souza, Aline Zamboni Machado, Ivo Jorge Prado Arnhold, Berenice Mendonca, Maria Helena Palma Sircili, Mirian Yumie Nishi, Rosana Barbosa Silva, Elaine Maria Frade Costa, Sorahia Domenice
P2-D2-575
AMH Levels in Pediatric Girls with Chronic Disease
Chelsey Grimbly, Connie Prosser
P2-D2-576
The Utility Of AMH For Predicting Testosterone Response To HCG Stimulation In Children With Suspected DSD
Andreas Kyriakou, Jane D McNeilly, Guftar M Shaikh, Avril Mason, David Shapiro, Syed Faisal Ahmed
P2-D2-577
A NOVEL CYP19A1 GENE MUTATION IDENTIFIED IN THREE TURKISH FAMILIES
Sema Akcurin, Erdem Durmaz, Woo-Young Kim, Doga Turkkahraman, Joe-Gook Shin, Su-Jun Lee
P2-D2-578
46,XX ovotesticular DSD: is it lawful to wait for gonadal surgery ?
Claire Bouvattier, Ariane Cuny, Sylvie Beaudoin, Frédéric Bargy
P2-D2-579
45,X/46,Xidic(Y) mosaicism: study of nine patients
Laura Mazzanti, Federico Baronio, Rita Ortolano, Emanuela Scarano, Federica Tamburrino, Angela Colangiulo, Ilaria Bettocchi, Alessandra Cassio, Antonio Balsamo
P2-D2-580
The V89L polymorphism in the SRD5A2 gene in cases with undescended testis
Elif Yesilada, Aysehan Akinci, Gonca Gulbay, Sengul Yuksel, Serap Savaci
P2-D2-581
Rare Disease Registries - Perception Of Parents & Young People
Arundathi Jayasena, Miriam Muscarella, Faisal Ahmed
P2-D2-582
Down syndrome and disorders of sex development – only coincidence or more?
Joyce Pupo, Tiago Jeronimo dos Santos, Leandra Steinmetz, Louise Cominato, Thais Della Manna, Hamilton Menezes Filho, Hilton Kuperman, Vaê Dichtchekenian, Nuvarte Setian, Durval Damiani
P2-D2-583
NOVEL MUTATION IN A NEWBORN WITH A RARE CAUSE OF 46,XY SEX REVERSAL: 17β- HYDROXYSTEROID DEHYDROGENASE TYPE 3 DEFICIENCY
Korcan Demir, Melek Yildiz, Özlem Nalbantoglu Elmas, Hüseyin Anil Korkmaz, Behzat Özkan
P3-D1-952
Discordant genotypic sex and concordant phenotypes in two Spanish siblings with 17α-hydroxylase/17,20-lyase deficiency carrying the most prevalent mutated alleles in Brazilian patients
Laura Audí, Mónica Fernández-Cancio, Marta Melón-Pardo, Emilio García-García
P3-D1-953
The development of gonadoblastoma in a 3-year-old girl with 46X,del(Y)p11.3, gonadal dysgenesis and associated congenital anomalies.
Zofia Kolesinska, Aleksandra Rojek, Helena Kedzia, Michal Blaszczynski, Anna Latos-Bielenska, Karina Kapczuk, Marek Niedziela
P3-D1-954
46,XX DSD: bilateral ovotestis with SOX9
Alessandra di Lascio, Silvia Laura Carla Meroni, Moira Gianninoto, Orsetta Zuffardi, Gianni Russo
P3-D1-956
Gonadoblastoma and papillary tubal hyperplasia in ovotesticular syndrome
Enver Simsek, Cigdem Binay, Baran Tokar, Sare Kabukcuoglu, Melek Ustun
P3-D1-957
5α-Steroid Reductase 2 Deficiency in a Large Family
eda mengen ucakturk, yılmaz kor, fatih gurbuz, ali kemal topaloglu, bilgin yuksel
P3-D1-958
17βHSD-3 Enzyme Deficiency in Newborn due to A Novel Mutation in HSD17B3 Gene
ELIF SAGSAK, ZEHRA AYCAN, SENAY SAVAS ERDEVE, MELIKSAH KESKIN, SEMRA CETINKAYA, KADRI KARAER
P3-D1-959
Partial androgen insensitivity syndrome in a boy with inactivating androgen receptor mutation and somatic mosaicism
Johanna Tommiska, Päivi Keskinen, Taneli Raivio
P3-D1-960
CLINICAL CHARACTERISTICS OF 30 PATIENTS WITH 45,X/46,XY MOSAICISM
Sukran Poyrazoglu, Nurcin Saka, Firdevs Bas, Ruveyde Bundak, Feyza Darendeliler
P3-D1-961
Three Siblings extremely Androgen Insensitivity Syndrome due to an AR mutation with Differing Phenotypes
bilgin yuksel, eda mengen ucakturk, fatih gurbuz, ali kemal topaloglu
P3-D1-995
Severe undervirilisation in a 46,XY case due to a novel mutation in HSD17B3 gene
Ayfer Alikasifoglu, Dogus Vuralli, Olaf Hiort, E.Nazli Gonc, Z.Alev Ozon, Nurgun Kandemir
P3-D2-964
An ovulating testis
Jaya Sujatha Gopal Kothandapani, Pooja Sachdev, Neil Wright
P3-D2-965
Mosaicism ratios of 45,X to 46,X idicY explained a phenotype in a case with mixed gonadal dysgenesis.
Megumi Hatano, Ryuji Fukuzawa, Yukihiro Hasegawa
P3-D2-966
A Rare Case of Swyer Syndrome with Spontaneous Breast Development and Menstruation
Bumin Nuri Dundar, P. Sule Can, Caner Alparslan, Sinem Akbay, Gonul Catli, Sefa Kelekci
P3-D2-967
Phenotypic and genotypic variability of patients with 5-α reductase type 2 deficiency
Kun Hu, Nils Krone, Jeremy Kirk
P3-D2-968
The Novel Mutation in the Steroidogenic Acute Regulatory Protein (StAR) in 46, XY Case with Adrenal Insufficiency and Complete Sex Reversal
Fatih Gurbuz, L. Damla Kotan, Eda Mengen, Ali Kemal Topaloglu, Bilgin Yuksel
P3-D2-969
A challenging diagnosis in three 46, XY females from two related families.
Raffaella Di Mase, Nicola Improda, Manuela Cerbone, Lucia De Martino, Donatella Capalbo, Lilia Baldazzi, Mariacarolina Salerno
P3-D2-971
A case of 46,Y,dup(X)(p21.2p22.2) DSD caused by overexpressed DAX1
Sasaki Takako, Izumi Youko, Fukami Maki, Yatsuga Shuichi, Koga Yasutoshi
P3-D2-972
Disorders of sexual differentiation observed in endocrinology
Ali el mahdi Haddam, Soumeya Fedala, Djamila Meskine, Farida Chentli, Leyla ahmed ali, Naziha Fedala
P3-D2-973
INCIDENS OF SEX DIFFERENTIONE DISORDER - 46XY Sultanova Sh.T. , R.A Yakubova The Centre of Scientific and Clinical Study of Endocrinology in Republic of Uzbekistan. Contact e-mail: sultanova_69@mail.ru.
Shakhrizada Sultanova, Rano Yakupova
P3-D3-970
A familial case of complete androgen insensitivity syndrome
Evelina Maines, Claudia Piona, Grazia Morandi, Fulvia Baldinotti, Franco Antoniazzi, Rossella Gaudino
LB-D3-1002
Pseudoexon activation in nicotinamide nucleotide transhydrogenase (NNT) in two siblings with Familial Glucocorticoid Deficiency
Li Chan, Tatiana Novoselova, Shoshana Rath, Karen Carpenter, H Atkinson, Jan Dickinson, Nick Pachter, G Price, Cathy Choong, Lou Metherell
LB-D3-1009
Family studies of CYP21A2 gene identify different haplotypes for nonclassical 21-hydroxylase deficiency in Brazilian population.
Débora de Paula Michelatto, Larissa Magalhães Grimaldi, Marcel Costa Alpiste, Maria Tereza Matias Baptista, Gil Guerra-Júnior, Sofia Helena Valente de Lemos-Marini, Maricilda Palandi de Mello
LB-D3-1013
Copy number determination of CYP21A2 gene supplements the molecular biological analysis of Hungarian patients with 21-hydroxylase deficiency
Koncz Klara, Luczay Andrea, Doleschall Márton, Károly Rácz, Patócs Attila
P1-D2-1
Allelic frequencies of CYP21A2 variants and genotype-phenotype correlations in a cohort of 660 CAH patients from Germany and Austria
Stefan Riedl, Friedrich-Wilhelm Röhl, Susann Empting, Walter Bonfig, Helmuth-Günther Dörr, Reinhard Holl, Klaus Mohnike
P1-D2-11
Identification of a novel large CYP17A1 deletion by multiplex ligation-dependent probe amplification analysis in patients with classic 17-hydroxylase deficiency
Tulay Guran, Doga Turkkahraman, Hannah Ivison, Aliesha Griffin, Raymon Vijzelaar, Nils Krone
P1-D2-2
Functional Characterization of a Novel Heterozygous Point Mutation in the Human Glucocorticoid Receptor Gene Causing Primary Generalized Glucocorticoid Resistance.
Nicolas C. Nicolaides, Dimitris Vlachakis, Amalia Sertedaki, Sophia Kossida, George P. Chrousos, Evangelia Charmandari
P1-D2-3
Transient Generalized Glucocorticoid Hypersensitivity: Clinical Manifestations, Endocrinologic Evaluation and Transcriptomic Profile: The Potential Role of NF-κB.
Nicolas C. Nicolaides, Agaristi Lamprokostopoulou, Alexandros Polyzos, Tomoshige Kino, Eleni Katsantoni, Panagiota Triantafyllou, Athanasios Christophoridis, George Katzos, Maria Drakopoulou, Amalia Sertedaki, George P. Chrousos, Evangelia Charmandari
P1-D2-4
Mineralo and glucocorticoid deficiency in early infancy are caused by a founder novel mutation in the Nicotinamide Nucleotide Transhydrogenase gene
Abdulsalam Abu-Libdeh, Ariella Weinberg-Shukron, Sharon Zeligson, Fouad Zhadeh, Liran Carmel, Paul Renbaum, Ephrat Levy-Lahad, David Zangen
P1-D2-5
Carbohydrate metabolism in children and adolescents with classical congenital adrenal hyperplasia due to 21-hydoxylase deficiency (CAH).
Helmuth G. Dörr, Carolin Pichl, Michaela Marx, Nadine Herzog, Daniela Klaffenbach, Thomas Völkl
P1-D2-6
Diagnosis of 21-Hydroxylase Deficiency by urinary Gas Chromatography-Mass Spectrometry Analysis: Reference Values for Neonates and Infants in a large Cohort of 95 untreated Patients with special Emphasis on Glucocorticoid Metabolism
Clemens Kamrath, Michaela Hartmann, Claudia Boettcher, Stefan Wudy
P1-D2-7
A novel founder mutation of CYP21A2 in patients with CAH due to 21-hydroxylase deficiency
Aysenur Ökten, Gülay Karagüzel, Bayram Toraman, Ersan Kalay, Tugba Dincer
P1-D2-9
Mast cells in human adrenal gland during fetal development
Alexandre Naccache, Céline Duparc, Estelle Louiset, Hervé Lefebvre, Mireille Castanet
P1-D3-12
Adrenal Rest Tumors in patients with Primary Adrenal Insufficiency
Zehra Yavas Abali, Nurcin Saka, Oguz Bulent Erol, Banu Kucukemre Aydin, Tulay Guran, Firdevs Bas, Sukran Poyrazoglu, Ruveyde Bundak, Feyza Darendeliler
P1-D3-13
Assessment of Blood Pressure and Left Ventricular Parameters in Children with Classical Congenital Adrenal Hyperplasia due to 21 hydroxylase deficiency
Shereen Abdelghaffar, Reem Ibrahim, Osama Abdelaziz, Mona Hafez, Mona Mamdouh, Abeer Alashmawy, Fatma Elmougy, Sahar Abdelaty, Amany Ibrahim, Hend Mehawed, Isis Ghaly
P1-D3-14
Clinical, biological and genetic characteristics of 48 pediatric patients with micronodular adrenal hyperplasia (MAH).
Anya Rothenbuhler, Evgenia Gourgari, Maya Lodish, Constantine Stratakis
P1-D3-16
A novel mutation in exon 5 of TP53 gene in a familial adrenocortical carcinoma
Enver Simsek, Cigdem Binay, Baran Tokar, Emine Dündar, Meliha Demiral
P1-D3-17
Aldosterone/Renin Ratio as a Key Player in the Diagnosis of Primary Hypoaldosteronism in Newborns and Infants
Beate Ruecker, Mariarosaria Lang-Muritano, Katharina Spanaus, Maik Welzel, Dagmar Lallemand, Franziska Phan-Hug, Daniel Konrad, Claudia Katschnig, Paul-Martin Holterhus, Eugen Schoenle
P1-D3-18
Zenhale Inhaled Corticosteroid therapy: useful second line therapy for Asthma in children but be wary of adrenal suppression
Rebecca Perry, Wendy Schwarz, Karen Stosky, Jonathan Dawrant, Daniele Pacaud, Mary Noseworthy, Mark Anselmo
P1-D3-19
Development of Scotland Wide Process for Management of Acute Adrenal Insufficiency
Barbara .S. Wardhaugh, Jacquie Reid
P1-D3-20
Salivary cortisol as a diagnostic tool of Hypercortisolism in Primary Pigmented Nodular Adrenocortical Disease (PPNAD).
AYRTON MOREIRA, PAULA ELIAS, MARCELO BITTAR, CARLOS EDUARDO MARTINELLI JR, SONIR ANTONINI, MARGARET CASTRO
P1-D3-21
HOW TO INTERPRET CORTISOL RESPONSES TO ACTH IN PATIENTS WITH NON-CLASSIC CONGENITAL ADRENAL HYPERPLASIA
M BELEN ROLDAN MARTIN, YOKO OYAKAWA BARCELLI, RAQUEL BARRIO CASTELLANOS, MARIA MARTIN FRIAS, DANIEL ALONSO MARTIN, MILAGROS ALONSO BLANCO
P1-D3-22
Clinical Utility Of Urinary Steroid Metabolite Ratios In Children Undergoing Investigations For Suspected Disorders Of Steroid Synthesis
Angela Lucas-Herald, Martina Rodie, Laura Lucaccioni, Karen Rankin, Guftar Shaikh, Jane McNeilly, David Shapiro, Faisal Ahmed
P2-D1-257
Growth Pattern in Infants with Congenital Adrenal Hyperplasia During the First Year of Life
Heba Elsedfy, Rasha Hamza
P2-D1-258
Adrenocorticotropic hormone and cortisol levels are associated with cardiovascular risk in pediatric obesity: A cross-sectional study in China
jianfeng liang, JUNFEN FU, jinling wang, youjun jiang, guanping dong
P2-D1-259
Inadequate cortisol response to tetracosactide (Synacthen®) test in NCCAH patients, an exception to the rule?
Athanasia Stoupa, Laura González Briceño, Graziella Pinto, Dinane Samara-Boustani, Isabelle Flechtner, Caroline Thalassinos, Maud Bidet, Albane Simon, Yves Morel, Christine Béllanné-Chantelot, Philippe Touraine, Michel Polak
P2-D1-260
Genotype-Phenotype Non-Concordance: How Prevalent Is It? How To Explain It
Ahmed Khattab, Mabel Yau, Maria New
P2-D1-261
PARADOXICAL INCREASE IN URINAY CORTISOL EXCRETION IN CHILDREN WITH PRIMARY PIGMENTED NODULAR ADRENAL DISEASE
Ana Beatriz Fraga, João Anselmo, Catarina Franco, Sara Vaz, Fernanda Gomes
P2-D1-262
Mutation spectrum of CYP11B1 gene in Turkish patients with 11β-hydroxylase deficiency
Nurgun Kandemir, Didem Yucel Yilmaz, E. Nazli Gonc, Z. Alev Ozon, Ayfer Alikasifoglu, Ali Dursun, R. Koksal Ozgul
P2-D1-263
Genotype and Phenotype Characteristics of Patients with Nonclassical Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency
Nese Akcan Tombalak, Oya Uyguner, Guven Toksoy, Esin Karakilic, Banu Aydin, Firdevs Bas, Nurcin Saka, Sukran Poyrazoglu, Ruveyde Bundak, Hulya Kayserili, Feyza Darendeliler
P2-D1-264
LCMSMS profiling of plasma steroids in different types of congenital adrenal hyperplasia
Alexandra E. Kulle, Thomas Reinehr, Halit Ilker Akkurt, Christian Commentz, Sabine Heger, Gunter Simic-Schleicher, Maik Welzel, Nadine C. Hornig, Paul-Martin Holterhus
P2-D1-265
Two brothers with late onset apparent mineralocorticoid excess
Grazia Morandi, Evelina Maines, Francesca Malesani, Paolo Cavarzere, Rossella Gaudino, Franco Antoniazzi
P2-D1-266
Is Basal 17 - hydroxyprogesterone a Sensitive Marker for Diagnosis of Non-Classical Congenital Adrenal Hyperplasia?
Rachel Bello, Yael Lebenthal, Moshe Phillip, Liat de Vries
P2-D1-267
An adolescent with hypertension caused by primary hyperaldosteronism due to KCNJ5 mutation
Annelieke van der Linde, Jaap Deinum, Yvette Konijnenberg, Mandy Keijzer – Veen, Hedi Claahsen - van der Grinten
P2-D1-268
Analysis of Prospective Annual Adrenocorticotropin Stimulation Testing among Survivors of Intracranial Tumor
Marjorie Golekoh, Manasa Mantravadi, Lindsey Hornung, Jane Khoury, Maryam Fouladi, Susan Rose, Sarah Lawson
P2-D1-269
Congenital adrenal hyperplasia caused by 11ß-hydroxylase-deficiency as a rare differential diagnosis of precocious pseudo-puberty and hypertension
Vira Yakovenko, Anke Simon, Egbert Schulze, Jürgen Grulich-Henn, Markus Bettendorf
P2-D2-270
Osteoporosis in triple A syndrome – an overlooked symptom of unexplained etiology
Miroslav Dumic, Natasa Rojnic Putarek, Vesna Kusec, Nina Barisic, Katrin Koehler, Angela Huebner
P2-D2-271
The results of CYP21A2 mutation analysis in adolescent with polycystic ovary syndrome
Elif Yagli Çolakoglu, Derya Bulus, Nesibe Andiran, Ugur Ufuk Isin
P2-D2-272
Timing of precocious pubarche in girls: Does a contemporary subgroup exist?
FERIDE TAHMISCIOGLU, OYA ERCAN, BAHAR OZCABI, OLCAY EVLIYAOGLU
P2-D2-273
Nonclassic lipoid adrenal hyperplasia with R272C STAR mutation: a case report
Tatsuya Miyoshi, Masaki Takagi, Yukihiro Hasegawa
P2-D2-274
Severe 21-hydroxylase deficiency Congenital Adrenal Hyperplasia and Congenital Hypothyroidism due to Thyroglobulin mutations in a single family: 2 distinct genetic disorders with phenotypic variability within a single family
Caroline Ponmani, Abigail Atterbury, Senthil Seniappan, Nadia Schoenmakers, Adeline K Nicholas, Krishna Chatterjee, Mehul Dattani
P2-D2-275
Non-Virilizing Congenital Adrenal Hyperplasia in a Female Patient - Report of a Novel HSD3B2 Mutation
Ursina Probst-Scheidegger, Christa Flück, Dagmar l'Allemand, Nùria Camats
P2-D2-276
Waist-to-height ratio, waist-to-hip ratio, waist circumference, and BMI in children and adolescents with classical congenital adrenal hyperplasia due to 21-hydoxylase deficiency (CAH).
Helmuth G. Dörr, Michaela Marx, Nadine Herzog, Katja Gassmann, Carolin Pichl, Thomas Völkl
P2-D2-277
Psychological and Behavioral Outcome of Female patients with Congenital Adrenal Hyperplasia
abeer el ashmawy, amany abdou, mohamed nasr, sameh tawfik, shereen abdelghaffar, amany ibrahim
P2-D2-278
Do neonates need a short synacthen test to investigate the adrenal axis?
Usha Niranjan, Victoria Franklin, Imran Bashir, Sarah Martin, Alan Gibson, Neil Wright, Paul Dimitri
P2-D2-279
GENOTYPE –PHENOTYPE DISCORDANT PATIENTS WITH HOMOZYGOUS INTRON 2 MUTATION (IVS2) OF CYP21 GENE
Emine Camtosun, Zeynep Siklar, Hatice Ilgin Ruhi, Nukhet Yurur Kutlay, Pinar Kocaay, Ajlan Tukun, Merih Berberoglu
P2-D2-280
A 26-day-old Japanese girl with aldosterone synthase deficiency caused by a novel mutation in the CYP11B2 gene
Satomi Koyama, Tatsuo Tsuboi, Naoto Shimura, Akie Nakamura, Toshihiro Tajima, Osamu Arisaka
P2-D2-281
NONCLASSIC CYP21A2 DEFICIENCY: DIAGNOSIS AND CLINICAL EVOLUTION
Cristina Luzuriaga, María Laura Bertholt, Cristina Naranjo, Begoña Ezquieta
P2-D2-282
Steroid 11β-hydroxylase deficiency due to CYP11B1 mutations in females with hyperandrogenemia
Christos Shammas, Stefania Byrou, Alexia AP Phedonos, Stella Nicolaou, Meropi Toumba, Nicos Skordis, Vassos Neocleous, Leonidas A Phylactou
P2-D2-636
Neonatal hpercalcaemia associated with congenital adrenal hyperplasia
Cigdem Binay, Enver Simsek, Neslihan Tekin, Meliha Demiral
P3-D1-621
The effect of working in a children´s hospital on urinary catecholamine excretion rates in male and female physicians
Claudia Boettcher, Mirko Peitzsch, Graeme Eisenhofer, Stefan A. Wudy
P3-D1-622
Body Composition Analysis in Girls with Premature Adrenarche
Ayse Nurcan CEBECI, Aysegul TAS
P3-D1-623
PseudoHypoAldosteronism Type 1 (PHA1): role of urinary steroid profiling (USP) in specific and early diagnosis – lessons in differential diagnosis of PHA1 vs PHA2 (renal tract anomaly)
V ABBOT, L GHATAORE, DJ PIETERSE, S CHAPMAN, RR KAPOOR, NF TAYLOR, CR BUCHANAN
P3-D1-624
Genotype-phenotype correlations in Bulgarian patients with I2G splice mutation of 21CYPA2 picked up by neonatal screening (NS)
Iva Stoeva, Ganka Dineva, Andrey Kirov, Antoaneta Kostova, Tihomir Todorov, Ani Aroyo, Albena Todorova, Vanio Mitev
P3-D1-625
A Pediatric Case of Cushing’s Disease Presenting with Diabetic Ketoacidosis
Gonul Catli, Ozgur Tanrisever, P. Sule Can, Bumin Nuri Dundar
P3-D1-626
CYP21A2 mutation spectrum in Bulgarian CAH patients
Albena Todorova, Andrey Kirov, Iva Stoeva, Tihomir Todorov, Ganka Dineva, Antoaneta Kostova, Ani Aroyo, Vanio Mitev
P3-D1-627
A Rare Cause of Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency: A Case Report
Peyami Cinaz, Hamdi Cihan Emeksiz, Nurullah Çelik, Esra Döğer, Özge Yüce, Orhun Çamurdan, Aysun Bideci
P3-D1-628
Familial glucocorticoid deficiency (FGD): masked diagnosis by hydrocortisone life-saving treatment
Federico Baronio, Angelica Marsigli, Ilaria Bettocchi, Davide Tassinari, Laura Mazzanti, Louise Metherell, Antonio Balsamo
P3-D1-629
Clinical and genetic diagnosis of Allgrove syndrome
Zdravka Todorova, Elissaveta Stefanova, Ivan Litvinenko, Krasimira Kazakova, Penka Yaneva, Desislava Yordanova, Mihaela Dimitrova
P3-D1-630
Clinical case of Cushing syndrome in secreting NET
Gianluca Musolino, Marzia Piran, Stefano Chiaravalli, Luigi Nespoli, Alessandro Salvatoni
P3-D1-631
Homozygous c.923dupT combined with heterozygous c.334G>A CYP21A2 mutation – a case report from the Bulgarian CAH screening programme
Antoaneta Kostova, Iva Stoeva, Andrey Kirov, Ganka Dineva, Tihomir Todorov, Albena Todorova, Elissaveta Stefanova, Krassimira Kazakova, Ani Aroyo, Vanio Mitev
P3-D1-632
Secondary Pseudohypoaldosteronism Type 1 – the role of a Urinary Steroid Profile in diagnosis.
ML Grace, DM Murray, C Joyce, NF Taylor, L Ghataore, SM O'Connell
P3-D1-633
Steroid 11βHydroxylase deficiency in Egyptian children
Noha Musa, Isis Ghali, Sara Farag, Maha Amin, Mona Hafez
P3-D1-900
Effect of Pubertal status, Age and Gender on Cortisol Response to Insulin Induced Hypoglycaemia in Children and Adolescents.
Dinesh Giri, Ian Robert Mulvey, Arundoss Gangadharan, K Saravanai-Prabu, Jo Blair, Poonam Dharmaraj, Urmi Das, Senthil Senniappan, Mohammed Didi
P3-D1-901
Music benefits on postoperative distress and pain in Pediatric Day Care Surgery
Valeria Calcaterra, Daniela Larizza, Ghassan Nakib, Selene Ostuni, Irene Bonomelli, Simonetta Mencherini, Elisa Zambaiti, Savina Mannarino, Riccardo Albertini, Carmine Tinelli, Gloria Pelizzo
P3-D1-902
A Case of Congenital Isolated Adrenocorticotropin Deficiency due to TBX19 Gene Mutation
Natalya Kazachenko, Anatoly Tiulpakov, Yulia Skorodok, Dmitry Ivanov, Zukhra Mullakhmetova
P3-D2-634
PRENATAL DEXAMETHASONE USE FOR THE PREVENTION OF VIRILIZATION IN PREGNANCY AT RISK FOR CLASSICAL CONGENITAL ADRENAL HYPERPLASIA
María Sanz Fernández, Esther González Ruíz de León, Elena Dulín Iñiguez, Begoña Ezquieta Zubicaray, Dolores Rodríguez Arnao, Amparo Rodríguez Sánchez
P3-D2-635
Congenital Adrenal Hyperplasia- Survey of the management in children across U.K
Usha Niranjan, Anuja Natarajan
P3-D2-637
Clinical and genetic analysis of congenital adrenal hypoplasia due to DAX-1 gene mutations
Duan Li, Jipeng Zheng, Yonglan Huang, Chun Fan, Jing Cheng
P3-D2-638
ADDISON DISEASE AND ATROPHIC GASTRITIS: HIGH PERSISTENT ACTH LEVELS ALTHOUGH AN ADEQUATE TREATMENT
Eugenia Prinzi, Francesca Serraino, Maria Cristina Maggio, Giovanni Corsello
P3-D2-639
Four Cases of Ovarian Adrenal Rest Tumors in Chinese Girls with Congenital Adrenal Hyperplasia due to 21-hydroxylase deficiency.
Su Zhe, Zhang Jun, Ma Huamei, Chen Qiuli, Du Minlian, Li Yanhong, Chen Hongshan
P3-D2-640
Therapeutic troubles of Cushing's disease in adolescence: report of a case
Manuela Deiana, Marco Losa, Adolfo Trettene, Alessandra Scolari, Alessandro Salvatoni
P3-D2-641
Congenital Hypoaldosteronism of Unknown Etiology in Five Half-Siblings
Jan Foote, Jennifer Cook
P3-D2-642
X-linked adrenoleukodystrophy in 8 patients.
Zhe Meng, Liyang Liang, Lina Zhang, LeLe Hou, Zulin Liu
P3-D2-643
The ganglioneuromas: About eight cases
Ali el mahdi Haddam, Soumeya Fedala, Djamila Meskine, Farida Chentli, Amina laloui, leila ahmed ali
P3-D2-644
Cushing Syndrome without origin
Sara Queirolo, Piero Balice
P3-D2-645
Untreated congenital hyperplasia with central precocious puberty
Mihaela Dimitrova, Elisaveta Stefanova, Krasimira Kazakova, Desislava Yordanova, Zdravka Todorova
P3-D2-963
HYPOSPADIAS IN A MALE PATIENT WITH 21-HYDROXYLASE DEFICIENCY AND ATYPICAL CLINICAL COURSE: PRESENTATİON OF TWO BROTHERS
Ayla Güven, Suna Hancili, Wiebke Arlt
LB-D3-1003
Increasing incidence of infants born small and large for gestational age over 20 years
Valentina Chiavaroli, Valeria Castorani, Paola Guidone, Ilaria Di Giovanni, Marco Liberati, Francesco Chiarelli, Angelika Mohn
LB-D3-1004
Methyl donor deficiency impairs pre-osteoblast differentiation through PGC-1α hypomethylation and increased ERRα
Eva Feigerlova, Essi Ewu, Georges Weryha, Brigitte Leininger, Jean-Louis Guéant
LB-D3-1014
CpG methylation changes within the INS, HLA-G and PTPN-22 promoters in childhood type 1 diabetes.
Ioannis Kyrgios, Konstantina Mouzaki, Theodoros Spandonidis, Aikaterini Fragou, Georgios Tzimagiorgis, Maria Eboriadou-Petikopoulou, Assimina Galli-Tsinopoulou
P1-D1-173
A girl with Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B, a unique example of multiple imprinting defects
Boudewijn Bakker, Laura Sonneveld, Claire Woltering, Sarina Kant
P1-D2-155
Clinical Characteristics and Imprinting Analysis of Chinese Silver Russell Syndrome
Di WU, Chunxiu GONG, Yang ZHAO
P2-D3-508
Various presentations of X-linked adrenoleukodystrophy: case reports.
Alina Daniela Fădur, Aurora Constantinescu, Cristina Rusu, Adina Manolachie, Ioana Bodescu, Dumitru D. Brănișteanu, Cristina Preda, Voichița Mogoș, Carmen Vulpoi
P3-D1-886
3-ketothiolase deficiency induced by ACAT1 gene mutation
Li Li, Zhu Min, Mao Huiying, Xiong Feng
LB-D3-1005
A Two-Year Multi-Centre, Open Label, Randomized Two Arm Study of Genotropin Treatment In Very Young Children Born Small For Gestational Age: Early Growth And Neurodevelopment (EGN)
Jean De Schepper, Johan Vanderfaeillie, Primus-E Mullis, Raoul Rooman, Lisa Matthews, Maria Dilleen, Richard Browning, Roy Gomez, Hartmut Wollmann
P1-D1-204
The influence of GH treatment on the Oral Disposition Index (ODI) in Turner Syndrome girls and in GH deficient children : eight years of follow-up
Federico Baronio, Fiorenzo Lupi, Benedetta Siroli, Silvia Longhi, Federica Tamburrino, Emanuela Scarano, Laura Mazzanti, Giorgio Radetti
P1-D2-148
Beneficial effects of long-term growth hormone treatment on adaptive functioning in infants with Prader-Willi syndrome.
Sin Lo, Dederieke Festen, Roderick Tummers-de Lind van Wijngaarden, Philippe Collin, Anita Hokken-Koelega
P1-D2-149
EARLY DEVELOPMENT, GROWTH AND PUBERTY BEFORE AND DURING TREATMENT OF CONGENITAL IGHD
Keren Samuel, Rivka Kauli, Zvi Laron
P1-D2-151
Sequential measurements of IGF-I serum concentrations in patients with severe primary IGF-I deficiency (SPIGFD) and growth failure treated with recombinant IGF-I (Increlex®)
Markus Bettendorf, Klaus Kapelari, Carolin Kneppo, Hermann L Müller, Dirk Schnabel, Joachim Wölfle
P1-D2-153
Intima media thickness in children treated with growth hormone
Caroline Knop, Barbara Wolters, Nina Lass, Rainer Wunsch, Thomas Reinehr
P1-D2-154
Clinical and laboratory parameters predicting a requirement for reevaluation of growth hormone status during growth hormone treatment
Dogus Vuralli, Nazli Gonc, Alev Ozon, Ayfer Alikasifoglu, Nurgun Kandemir
P1-D2-26
Influence of growth hormone therapy on the occurrence of second neoplasms in survivors of childhood cancer.
Cecile Thomas-Teinturier, Isabelle Oliver-Petit, Chiraz El Fayech, Helene Pacquement, Odile Oberlin, Martine Munzer, Ibrahima Diallo, Florent De Vathaire
P1-D3-160
Final Height and Safety Outcomes in Growth Hormone (GH)-Treated Children with Short Stature Homeobox-Containing Gene (SHOX) Deficiency: Experience from a Large, Multinational, Prospective Observational Study
Christopher Child, Charmian Quigley, Alan Zimmermann, Judith Ross, Cheri Deal, Stenvert Drop, Werner Blum
P1-D3-161
Safety and Effectiveness of Increlex® therapy in children enrolled in the Increlex Growth Forum Database (IGFD) in Europe: 4 years interim results
Michel Polak, Joachim Woelfle, Peter Bang, Aude Sicsic, Bruno Fiorentino
P1-D3-163
Six months Follow-up Pharmacokinetics and Pharmacodynamics Profile of Once-Weekly, CTP-Modified Human Growth Hormone (MOD-4023;): Phase 2 Dose Finding Study in Children with GHD Deficiency
Gili Hart, Zvi Zadik, Klaudziya Kradziu, Nataliya Zelinska, Oleg Malievsky, Violeta Iotova, Julia Skorodok, Ronit Koren, Leanne Amitzi, Eyal Fima
P1-D3-164
CHARACTERIZATION OF MOD-4023 GLYCOSYLATION, A CTP MODIFIED LONG ACTING GROWTH HORMONE IN ADVANCED CLINICAL STAGES
Oren Herskovitz, Laura Moschovich, Rachel Guy, Yana Felikman, Eyal Fima
P1-D3-165
Validating genetic markers of response to recombinant human growth hormone (r-hGH) in children with growth hormone deficiency (GHD) or Turner Syndrome (TS): Results from the PREDICT Validation study
Pierre Chatelain, Adam Stevens, Chiara De Leonibus, Peter Clayton, Jerome Wojcik
P1-D3-166
Short-term changes in bone formation markers following growth hormone (GH) treatment in short prepubertal children with a broad range of GH secretion
Björn Andersson, Diana Swolin-Eide, Per Magnusson, Kerstin Albertsson-Wikland
P1-D3-168
Effect of One-Year Growth Hormone Therapy on Left Ventricular Dimensions and Functions in Children with Growth Hormone Deficiency
Randa Khalaf
P1-D3-170
The ZOMATRIP study: Four year combination therapy of GH and GnRHa in girls with a short predicted adult height during early puberty.Interim results at the end of the treatment phase
Raoul Rooman, Annick France, Claudine Heinrichs, Sylvie Tenoutasse, Cecile Brachet, Martine Cools, Kathleen De Waele, Guy Masa, Marie-Christine Lebrethon, Jean-Pierre Bourguignon, Inge Gies, Jesse Van Besien, Christine De Rycke, Jean De Schepper
P1-D3-172
3-years height outcome during rh-growth hormone therapy in subjects with achondroplasia and hypochondroplasia
Francesco Massart, Francesco Vierucci, Mario Miccoli, Angelo Baggiani
P2-D1-418
Response to growth hormone treatment in patients with Silver Russell syndrome
C.C.J. Smeets, J.S. Renes, M. van der Steen, A.C.S. Hokken-Koelega
P2-D1-419
Pubertal development during growth hormone (GH) treatment with or without additional gonadotropin releasing hormone analogue (GnRHa) treatment in short children born small for gestational age (SGA)
M. van der Steen, A.J. Lem, A.C.S. Hokken-Koelega
P2-D1-420
Subcutaneous Injections of a Reversible Albumin-binding Growth Hormone Derivative (NNC0195-0092) in Adult Subjects with Growth Hormone Deficiency is well tolerated
Michael Højby Rasmussen, Jurgita Janukonyté, Marianne Klose, Djordje Marina, Mette Tanvig, Lene Nielsen, Charlotte Höybye, Marianne Andersen, Ulla Feldt-Rasmussen, Jens Christiansen
P2-D1-421
The Effects of Delaying Puberty with Gonadotropin-Releasing Hormone Agonists (GnRHa) in Patients with Idiopathic Growth Hormone Deficiency (IGHD)
David B Dunger, Anders Lindberg, Helmut G Dörr, Cecilia Camacho-Hübner, Mitchell E Geffner
P2-D2-422
Perceptions and expectations of patients and their families for the effects of Growth Hormone treatment.
Chrysoula Drosatou, Elpis-Athina Vlachopapadopoulou, Feneli Karachaliou, Vassileios Petrou, Eirini Kaloumenou, Stefanos Michalakos
P2-D2-423
Normal onset of clinical puberty for age in growth hormone-treated children with Noonan syndrome or Turner syndrome: data from the NordiNet® IOS and ANSWER® Program
Judith Ross, Henrik Christesen, Peter Lee, John Germak, Birgitte Tønnes Pedersen, Primoz Kotnik
P2-D2-424
What dose of hGH is adequate as a substitution therapy in growth hormone deficient children?
Antonis Voutetakis, Maria-Alexandra Magiakou, Catherine Dacou-Voutetakis, George Chrousos, Christina Kanaka-Gantenbein
P2-D2-425
Electronic devices and single-dose dispensing systems GH are the most efficient and less loss of drug
Ignacio Diez-Lopez, Ainhoa Sarasua-Miranda, Miriam Miriam Elizalde, Isabel Lorente-Blazquez, Cristina Minguez, Carlos Martínez-Martínez
P2-D2-426
The level and conformation of blood plasma carotenoids in growth hormone deficient children after 1 year of GH therapy
Maria Faassen, Maria Pankratova, Tatyana Shiryaeva, Elena Nagaeva, Valentina Peterkova, Svetlana Kovalenko, Adil Baizhumanov, Evgenia Parshina, Alexander Yusipovich, Georgy Maksimov
P2-D2-427
Effects and Safety of Recombinant Human Growth Hormone in Growth Hormone Deficient Children with Rathke Cyst
Liyang Liang, Lina Zhang, Zhe Meng, Hui Ou, Zhanwen He, Lele Hou, Dongfang Li, Pinggan Li, Xiangyang Luo
P2-D2-428
The interconnectivity between growth hormone replacement therapy and subclinical hypothyroidism on growth response in children with pituitary dwarfism
Ioana Bodescu, Jeanina Idriceanu, Ioana Vasiliu, Adina Manolachie, Irina Oana Chifu, Iulia Crumpei, Cristina Cristea, Cristina Preda, Voichita Mogos, Carmen Vulpoi
P2-D2-429
What should be the diagnosis and management of short children with IGF-I deficiency, responding to growth hormone (GH) administration despite normal GH secretion?
Joanna Smyczynska, Renata Stawerska, Andrzej Lewinski, Maciej Hilczer
P2-D2-430
A REAPPRAISAL OF THE CUT-OFF LIMITS OF THE PEAK GH RESPONSE TO STIMULATION TESTS FOR THE DIAGNOSIS OF GH DEFICIENCY IN CHILDREN AND ADOLESCENTS
Chiara Guzzetti, Anastasia Ibba, Sabrina Pilia, Nadia Beltrami, Natascia Di Iorgi, Alessandra Rollo, Giorgio Radetti, Stefano Zucchini, Mohamed Maghnie, Marco Cappa, Sandro Loche
P2-D2-431
Vitamin D concentrations in children with growth hormone deficiency during first year of GH treatment
Beata Pyrzak, Ewelina Witkowska-Sedek, Anna Kucharska, Magdalena Sagala, Anna Majcher
P2-D2-432
GROWTH HORMONE TREATMENT IN CHILDREN WITH SGA DURING A 5 YEAR PERIOD, ASSESSMENT OF AUXOLOGICAL DEVELOPMENT AND INSULIN RESISTANCE
JP López-Siguero, MJ Martínez-Aedo, JA Bermúdez, N Cabrinety, J Bosch, JL Lechuga, R Torralba
P2-D2-433
Comparison of measured lean body mass (LBM by DXA) and estimated LBM by BIA in children with growth hormone deficiency (GHD)
Roland Schweizer, Julian Ziegler, Laura Frank, Gerhard Binder
P2-D2-434
Metabolic assessment in children with growth hormone deficiency before, during and after human GH replacement therapy.
Barbara Predieri, Silvia Mazzoni, Valentina Paraluppi, Viviana Patianna, Laura Lucaccioni, Simona Madeo, Patrizia Bruzzi, Lorenzo Iughetti
P2-D3-435
First-year growth response to growth hormone in relation to final height outcome in prepubertal children with idiopathic growth hormone deficiency.
Saartje Straetemans, Muriel Thomas, Sylvie Tenoutasse, Jean De Schepper, Raoul Rooman
P2-D3-436
Reevaluation of growth hormone secretion during puberty in children diagnosed as GH-deficient during childhood
Diego Ramaroli, Evelina Maines, Claudia Anita Piona, Grazia Morandi, Rossella Gaudino, Franco Antoniazzi
P2-D3-437
Long-term effects of GH replacement therapy on thyroid function in GH deficiency children.
Andrea Esposito, Iolanda Di Donato, Martina Rezzuto, Sara Alfano, Cristina Moracas, Donatella Capalbo, Mariacarolina Salerno
P2-D3-438
Does priming with sex steroids before growth hormone stimulation test increase the diagnosis of normal GH secretion in short children?
Ashraf Soliman, Vincenzo De sanctis, Elkhansa Elgaali, Hannah Ahmed, Aml Sabt, Randa Nassar
P2-D3-439
Growth hormone (GH) dosing patterns in short children born small for gestational age (SGA)
Isabelle Oliver Petit, Oliver Blankenstein, Dragan Zdravkovic, Birgitte Tønnes Pedersen, Effie Pournara
P2-D3-440
Two-year data from a long-term, phase IV study of Omnitrope®, a recombinant human growth hormone (rhGH), in short children born small for gestational age (SGA)
Hans-Peter Schwarz, Dorota Birkholz-Walerzak, Mieczyslaw Szalecki, Mieczyslaw Walczak, Corina Galesanu, David Metreveli, Jasmin Khan-Boluki, Ellen Schuck
P2-D3-441
Effects of gender and gestational age on growth hormone (GH) treatment in very young children born small for gestational age (SGA)
Margaret Boguszewski, Anders Lindberg, Hartmut A Wollmann
P2-D3-442
Two-year results from PATRO Children, a multi-centre, non-interventional study of the long-term efficacy and safety 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-D3-443
The effect of two different GH dosages on final height and bone geometry
Fiorenzo Lupi, Mauro Bozzola, Fabio Buzi, Silvia Longhi, Amelia Mascolo, Alba Pilotta, Rossella Porto, Giulia Ruffinazzi, Valentina Zattoni, Giorgio Radetti
P2-D3-444
Baseline body composition of children with short stature diagnosed for growth hormone deficiency (GHD)
Pawel Matusik, Aleksandra Barylak, Patrycja Cholewka, Marta Klesiewicz, Karolina Klos, Martyna Stasiulewicz, Maria Cetera, Ewa Malecka-Tendera
P2-D3-445
GROWTH HORMONE TREATMENT TO FINAL HEIGHT IN CHILDREN WITH IDIOPATHIC SHORT STATURE: EVIDENCE FOR AN EARLY THERAPY INITIATION EFFECT
Kiriaki Hatziagapiou, Paraskevi Zosi, Dionisis Karakaidos, Eleftheria Kaiafa, Thomais Vlahou, Likourgos Kanaris, Georgios Kafalidis
P2-D3-446
Evaluation of the safety and usability of FlexPro® 30 mg/3 mL, for the delivery of Norditropin® in patients requiring growth hormone (GH) therapy
Gitte Schøning Fuchs, Yanhong Wen, Rasmus Klinck, Marianne Qvist, Anne-Marie Kappelgaard
P2-D3-447
Efficacy , adherence and cost study according to pathology and treatment devices in children treated with GHRH
Ignacio Diez-Lopez, Ainhoa Sarasua-Miranda, Miriam Miriam Elizalde, Isabel Lorente-Blazquez, Cristina Minguez, Carlos Martínez-Martínez
P3-D1-817
Increased required dose of growth hormone in children with inborn panhypopituitarism
Michael Wurm, Natascha van der Werf-Grohmann, Alexandra Krause, Cordula Roemer-Pergher, Karl Otfried Schwab
P3-D1-818
Assessment of compliance with Growth Hormone (GH) therapy.
Chrysoula Drosatou, Feneli Karachaliou, Elpis-Ahina Vlachopapadopoulou, Vassileios Petrou, Eirini Kaloumenou, Stefanos Michalakos
P3-D1-819
Body composition in GH deficient children: effects of GH therapy and comparison between DXA and anthropometric data.
Donatella Capalbo, Andrea Esposito, Manuela Cerbone, Martina Rezzuto, Rosita Di Pinto, Ciro Mainolfi, Mariacarolina Salerno
P3-D1-820
Socioeconomic factors influence rhGH treatment adherence and its response in children
Joan Bel, María Martínez, Marta Murillo, Silvina de Pedro, Maria Luisa Granada
P3-D1-821
Study of Growth Hormone Receptor（GHR）exon 3 polymorphism in children with Prader-Willi Syndrome
Feihong Luo, Wei Lu, Zhou Pei, Zhangqian Zheng
P3-D2-823
Correlation between Initial Treatment Effect of Recombinant Human Growth Hormone and Exon 3 Polymorphism of Growth Hormone Receptor in Chinese Growth Hormone Deficiency Children
Zhangqian Zheng, Linfeng Cao, Zhou Pei, Feihong Luo, Dijing Zhi, Zhuhui Zhao, Rong Ye, Ruoqian Cheng, Xiaojing Li
P3-D2-824
Growth hormone deficiency in a case with Neurofibromatosis-Noonan Syndrome (NFNS)
Dogus Vuralli, E.Nazli Gonc, Dominique Vidaud, Z.Alev Ozon, Ayfer Alikasifoglu, Nurgun Kandemir
P3-D2-825
Monitoring of Growth Hormone Treatment by the Electronic Auto-Injection Device easypod™ allows to improve the outcome and maximize adherence in patients with generally high adherence rates.
Klaus Hartmann
P3-D2-826
Usability and safety of FlexPro® PenMate® in patients, caregivers and healthcare professionals (HCPs)
Yanhong Wen, Conny Nøhr Korsholm, Rasmus Klinck, Anne-Marie Kappelgaard
P3-D2-827
Impairment of glucose metabolism in Growth Hormone (GH) deficient children under GH replacement
MARIA XATZIPSALTI, VASILIKI-IOANNA MITRAVELA, IOULIA POLICHRONI, DIMITRIOS DELIS, ANDRIANI VAZEOU, LELA STAMOGIANNOU
P3-D2-828
Growth response after 1 year of growth hormone (GH) treatment in children born small for gestational (SGA) without GH deficiency: our experience
Gisella Garbetta, Gabriella Pozzobon, Sara Osimani, Chiara Damia, Maria Piera Ferrarello, Andrea Voto, Giulia Pruccoli, Cristina Partenope, Giovanna Weber, Giuseppe Chiumello
P3-D2-829
CROSS- SECTIONAL AND PROSPECTIVE STUDY OF THE EFFECTS OF GH THERAPY ON METABOLIC PANEL IN CHILDREN WITH GH DEFICIENCY
Vincenzo Ramistella, Malgorzata Wasniewska, Mariella Valenzise, Tommaso Aversa, Stefania Arasi, Maria Rosa Velletri, Filippo De Luca
P3-D2-830
Prader Willi Syndrome and growth hormone therapy: valuable effects and adverse events
Magdalena Wilk, Katarzyna Wzorek, Ewa Tobór, Barbara Dejniak, Anna Wedrychowicz, Katarzyna Dolezal-Oltarzewska, Agata Zygmunt-Gorska, Jerzy Starzyk
P3-D2-831
Recovery of central fever after GH therapy in a patient with GH deficiency secondary to posttraumatic brain injury
Hale Unver Tuhan, Ahmet Anik, Gonul Catli, Ayhan Abaci, Ece Bober
P3-D2-832
The impact of growth hormone replacement therapy in children born small-for-gestational-age – growth response and safety profile
Irina Oana Chifu, Ioana Bodescu, Ioana Vasiliu, Jeanina Idriceanu, Alina Fadur, Ana Hreniuc, Maria Christina Ungureanu, Letitia Leustean, Voichita Mogos, Carmen Vulpoi
P3-D2-833
GROWTH HORMONE TREATMENT IN 50 CHILD WITH SHORT STATURE: LEBANESE EXPERIENCE.
ELIE ABI NADER, IMAD MELKI, CARLO AKATCHERIAN, BERNARD GERBAKA, ELIANE KHALLOUF-CALLAS
P3-D2-834
Effectiveness of growth hormone (GH) therapy in children with short stature and decreased GH peak in stimulating tests is independent from GH secretion after falling asleep
Maciej Hilczer, Joanna Smyczynska, Renata Stawerska, Andrzej Lewinski
P3-D3-836
WHAT IS THE PROFIL OF GIGANTISM :7 observations
SAMIA ACHIR, MOURAD SEMROUNI
P3-D3-837
GH treatment in Dent’s disease: a case report
Simona Falcone, Elisa Guidoni, Giovanna Municchi, Maddalena Cioni
P3-D3-838
ANALYSIS OF THE EFFECTIVENESS OF TREATMENT WITH GROWTH HORMONE IN A TERTIARY HOSPITAL IN THE LAST 30 YEARS
Jaime Cruz Rojo, Lucía Garzón Lorenzo, Mª Elena Gallego Gómez, Jaime Sánchez del Pozo
P3-D3-839
A Rare Syndrome Benefits From Growth Hormone Therapy: Hypotonia-Cystinuria Syndrome
ONUR AKIN, BULENT HACIHAMDİOĞLU, EDİZ YEŞİLKAYA
P3-D3-840
Changes in body mass index in GHD and SGA children in the first year of treatment
Juan-Pablo Llano, Teresa Ortiz Picon, Mauricio Llano
P3-D3-841
Study of the effect of growth hormone treatment on growth in patients with methylmalonic acidemia.
Francois Eyskens
P3-D3-842
Pubertal development of isolated GH deficient patients
Soumeya Fedala, Mahdi el mahdi Haddam, Farida Chentli
P3-D3-843
TWO YEARS OF GROWTH HORMONE THERAPY IN CHILDREN WITH GROWTH DEFICIENCY
Mimouna Bessahraoui, Sakina Niar, Malika Naceur, Karim Bouziane-Nedjadi
LB-D3-1006
Morphologic change of growth plate after 6 months of recombinant growth hormone therapy in normal short children : Three-dimensional MRI Analysis
Ji-Young Seo
P1-D2-34
High prevalence of low bone mass in adolescents with non-transfusion dependent Hb E/ß-thalassemia
Pairunyar Nakavachara, Jaturat Petchkul, Gritta Jeerawongpanich, Vip Viprakasit
P1-D2-35
Assessment of Quality of Life Data After Four Monthly Subcutaneous (SC) Doses of a Human Monoclonal Anti-FGF23 (Fibroblast Growth Factor 23) Antibody (KRN23) in Adults with X-linked Hypophosphatemia (XLH)
Mary Ruppe, Xiaoping Zhang, Erik Imel, Thomas Weber, Mark Klausner, Takahiro Ito, Maria Vergeire, Jeffrey Humphrey, Francis Glorieux, Anthony Portale, Karl Insogna, Munro Peacock, Thomas Carpenter
P1-D2-36
Sun protection habits and calcium intake in children with malignancy
Yael Levy-Shraga, Orit Pinhas-Hamiel, Michal Ben Ami, Yonatan Yeshayahu, Vered Temam, Rinat Cohen, Dalit Modan-Moses
P1-D2-37
Vitamin D levels and effects of vitamin D replacement in children with Periodic Fever, Aphthous stomatitis, Pharyngitis, and cervical Adenitis (PFAPA) syndrome
Perla Scalini, Stefano Stagi Stagi, Chiara Iurato, Camilla Menchini, Cristina Manoni, Giulia Anzillotti, Maurizio de Martino, Salvatore Seminara
P1-D2-38
Increased rates of infantile hypercalcaemia following guidelines for antenatal vitamin D3 supplementation
Lisa A Amato, Kristen A Neville, Shihab Hameed, Wei Shern Quek, Charles F Verge, Helen J Woodhead, Chris P White, Andrea Rita Horvath, Jan L Walker
P1-D2-39
Continuous Subcutaneous Recombinant PTH1-34 Pump Therapy in Congenital Hypoparathyroidism associated with malabsorption.
Vrinda Saraff, Wolfgang Högler
P1-D2-40
Effects and Limitations of Cinacalcet Therapy in Neonatal Severe Hyperparathyroidism (NSHPT)
Ulla Doehnert, Wolfgang Goepel, Wolfgang Hoeppner, Olaf Hiort
P1-D2-41
Young adults with Klinefelter Syndrome and Congenital Anorchia treated with testosterone have normal bone and muscle mass but increased central adiposity
SC Wong, D Scott, S Tandon, P Ebeling, M Zacharin
P1-D2-42
Decreased Bone Density In Boys With Klinefelter Syndrome: Results Of A Placebo-Controlled Clinical Trial Using Low-Dose Androgen Treatment For Two Years
Judith Ross, Hans Henrik Thodberg, Martha Bardsley, Ania Gosek
P1-D2-43
STUDY OF MINERAL AND BONE METABOLISM IN PEDIATRIC PATIENTS WITH INFLAMMATORY BOWEL DISEASE
María Aguilar-Quintero, Javier Caballero-Villarraso, Maria Dolores Cañete, Alicia Romero-Urrutia, Ramon Cañete
P1-D2-44
Vitamin D Deficiency: a national threat to adolescent health in Saudi Arabia
Mohammed Al Dubayee, Fadia Albuhairan, Ibrahim Alalwan, Suleiman Al Shahri, Hani Tamim, Mohieldin Magzoub, Walid Al Tamim, Nasreldin Ahmed
P1-D2-45
Longitudinal Changes Of Bone Mineral Content In Children With Cystic Fibrosis
Adela Chirita-Emandi, Sheila Khanna, Andreas Kyriakou, Jane McNeilly, Anne Devenny, Faisal Ahmed
P1-D3-46
Loss of function CYP24A1 mutations in patients with hypercalcemia and low PTH level: an autosomal dominant or recessive trait?
Arnaud Molin, Roseline Baudouin, Nadia Coudray, Marie-Lucille Figueres, Glennville Jones, Marie-Laure Kottler
P1-D3-47
Relation between CNP signaling pathway and the effect of combined treatment with GnRHa and rhGH on the linear growth in mid/late pubertal girls at great bone ages with CPP or EFP
Hua-mei MA, Zhe SU, Yin-ya LI
P1-D3-48
Paternal Isodisomy and sporadic pseudohypoparathyroidism I-b
Cindy Colson, Anne Claire Brehin, Geneviève Abeguile, Matthieu Decamp, Nicolas Richard, Marie-Laure Kottler
P1-D3-49
Vertebral Fracture Assessment In a Paediatric Population Using Dual-Energy X-ray Absorptiometry.
Andreas Kyriakou, Sheila Shepherd, Guftar M Shaikh, Syed Faisal Ahmed, Avril Mason
P1-D3-50
Genetic study of Osteogenesis Imperfecta. Two novel mutations in COL1A1 and COL1A2.
Lidia Castro-Feijóo, Lourdes Loidi, Nuria Quiroga, Paloma Cabanas, Claudia Heredia, Rosaura Leis, Francisco Barros, Manuel Pombo, Jesús Barreiro
P1-D3-51
Bone geometry, volumetric density, microarchitecture and estimated bone strength assessed by HR-pQCT in adult patients with Hypophosphatemic Rickets
Vikram v. Shanbhogue, Stinus Hansen, Lars Folkestad, Kim Brixen, Signe Sparre Beck-Nielsen
P1-D3-52
Opposing effects of childhood obesity on radial and tibial bone microstructure
Paul Dimitri, Richard Jacques, Margaret Paggiosi, David King, Jennifer Walsh, Nick Bishop, Richard Eastell
P1-D3-53
Bone Mineral Density evaluation in children with Gaucher Disease.
Maria Silvia Larroude, Guillermo Drelichman, Hamilton Cassinelli, Lucia Richard, Alba Ruiz, Paola Reicher, Fernanda Cuello, Victoria Lanza, Ramiro Fernandez, Alejandra Maro, Marcela Corrales, Adriana Arizo, Nicolas Fernandez Escobar, Cristina Rapetti, Hugo Donato, Juan Jose Chain, Sandra Zirone, Alejandra Cedola, Julieta Bietti, Maia Sweri
P1-D3-54
CORRELATION OF SCLEROSTIN LEVELS WITH BONE METABOLISM MARKERS AND BONE MINERAL DENSITY IN CHILDREN AND ADOLESCENTS WITH TYPE 1 DIABETES MELLITUS (T1DM)
Charalampos Tsentidis, Dimitrios Gourgiotis, Lydia Kossiva, Antonios Marmarinos, Asteroula Papathanasiou, Artemis Doulgeraki, Kyriaki Karavanaki
P1-D3-55
INCREASED OSTEOCLAST ACTIVITY IN CHILDREN AND ADOLESCENTS WITH TYPE 1 DIABETES MELLITUS (T1DM) INDICATED BY HIGHER LEVELS OF OSTEOPROTEGERIN AND S-RANKL MAY PREDISPOSE TO LOWER BONE MASS.
Charalampos Tsentidis, Dimitrios Gourgiotis, Lydia Kossiva, Artemis Doulgeraki, Antonios Marmarinos, Triantafillia Sdogou, Kyriaki Karavanaki
P1-D3-56
Effect of a Vibration Based Rehabilitation Concept on Bone and Muscle Development in Children with Osteogenesis Imperfecta
Oliver Semler, Heike Hoyer-Kuhn, Christina Stark, Nora Struebing, Oranna Goebel, Eckhard Schoenau
P1-D3-57
25OHD status and pro or anti-inflammatory cytokines in obese children and normal weight controls
Aoife Carroll, Chike Onwuneme, Malachi McKenna, Philip Mayne, Eleanor Molloy
P2-D1-283
Hypophosphatemic rickets in Norwegian children: genotypes, phenotypes and complications.
Silje Rafaelsen, Helge Ræder, Stefan Johansson, Robert Bjerknes
P2-D1-284
Increased fracture rate in children and adolescents with Marfan Syndrome
Giuliana Trifirò, Susan Marelli, Stefano Mora, Alessandro Pini
P2-D1-285
Mutations in IFITM5 leading to prenatal and postnatal signs of dominant Osteogenesis imperfecta
Heike Hoyer-Kuhn, Christian Netzer, Jutta Becker, Eckhard Schoenau, Oliver Semler
P2-D1-286
Musculoskeletal Health in Children with Crohn’s Disease at Diagnosis: Dynamic Muscle Function, Tibia Cortical and Trabecular Bone Density and Vertebral Fracture Prevalence
Leanne M Ward, Frank Rauch, Jinhui Ma, Maya Scharke, Heather Cosgrove, Mary Ann Matzinger, Nazih Shenouda, Eric I Benchimol, David R Mack
P2-D1-287
Case Report: A novel mutation in the calcium sensing receptor in a Welsh family with hypercalcaemia
Astha Soni, Carley Frerichs, Renuka Ramakrishnan, Poonam Dharmaraj
P2-D1-288
A new missense mutation in FGF23 gene in a male with hyperostosis-hyperphosphatemia syndrome (HHS)
Farzaneh Abbasi, Soudeh Ghafouri-Fard, Azadeh Ebrahim-Habibi
P2-D1-289
Pseudohypoparathyroidism type 1A due to novel GNAS mutation
Yael Levy-Shraga, Noah Gruber, Kineret Mazor-Aronovitch, Dalit Modan-Moses, Orit Pinhas-Hamiel
P2-D1-290
Sleep-Related Breathing Disorders in Pycnodysostosis
Serap Turan, Zeynep Atay, Yasemin Gokdemir, Nilay Bas, Belma Haliloglu, Saygin Abali, Serpil Bas, Refika Ersu, Abdullah Bereket
P2-D1-291
Cystinosis as a cause of hypophosphatemic rickets: A single-center experience
Murat DOGAN, Keziban BULAN, Sultan KABA
P2-D1-292
Pseudohypoparathyroidism type Ib: two cases with different clinical presentation.
Claudia Balsamo, Federico Baronio, Angelica Marsigli, Valentina Bonifacci, Giovanna Mantovani, Angelo Molinaro, Harald Jüppner, Paola Visconti, Laura Mazzanti, Antonio Balsamo
P2-D1-293
A very rare case of rickets: Fanconi-Bickel syndrome
Adel Djermane, Asmahane Ladjouze, Yasmine Ouarezki, Sandrine Vuillaumier-Barrot, Benfetima Ali Khodja, Leila Kedji, Abdeljalil Maoudj, Karima Berkouk, Menoubia Bensmina, Tahar Anane, Abdennour Laraba
P2-D1-294
Determinants of Vitamin D Levels in Children and Adolescents with Down Syndrome
Stefano Stagi, Elisabetta Lapi, Perla Scalini, Paolo Del Greco, Franco Ricci, Achille Marino, Maurizio de Martino, Salvatore Seminara
P2-D2-295
Determinants of Vitamin D Levels in Children, Adolescents, and Young Adults with Juvenile Idiopathic Arthritis
Stefano Stagi, Laura Capirchio, Achille Marino, Federico Bertini, Salvatore Seminara, Maurizio de Martino, Fernanda Falcini
P2-D2-296
Determinants of Vitamin D Levels in Italian Children and Adolescents of Mugello, an Area of Tuscany: a Longitudinal Evaluation
Perla Scalini, Stefano Stagi, Chiara Iurato, Cristina Manoni, Paola Pelosi, Laura Capirchio, Maurizio de Martino, Salvatore Seminara
P2-D2-297
Severe heterotopic ossifications in a 10 year old boy with PHP1a
Adalbert Raimann, Diana Alexandra Ertl, Stefan Riedl, Werner Schlegel, Gabriele Haeusler
P2-D2-298
Zoledronic Acid for management of osteopenia of prematurity and associated ventilator dependency
Mary White, Anastasia Pellicano, Margaret Zacharin, Peter Simm
P2-D2-299
Mutation in the TBCE Gene associated with Kenny-Caffey type 1 syndrome:A rare cause of hypocalcemia
Bensalah Meriem, Bouzidi Fatma Zohra, Véronique Beauloye, Hoyos Maria Garcia, Kemali Zahra
P2-D2-300
Vitamin D levels in children, adolescents, and young adults with juvenile onset systemic lupus erythematosus: A cross-sectional study
Stefano Stagi, Laura Capirchio, Federico Bertini, Camilla Menchini, Perla Scalini, Salvatore Seminara, Maurizio de Martino, Fernanda Falcini
P2-D2-301
Disproportionate short stature with advanced bone age due to PTHLH mutation
Annemieke Boot, Irene Stolte-Dijkstra, Irma Veenstra-Knol
P2-D2-302
PLASMA 25-OH VITAMIN D AND PTH CONCENTRATIONS IN CORD BLOOD. RELATIONSHIP WITH ETHNIC GROUPS, NUTRICIONAL HABITS AND DEGREE OF MATERNAL SUN EXPOSURE
Sandra Ortigosa Gómez, Oscar Garcia Algar, Antonio Mur Sierra, Roser Ferrer Costa, Antonio Carrascosa Lezcano, Diego Yeste Fernández
P2-D2-303
Cleidocranial dysplasia misdiagnosed as rickets in three generations
Roberto Franceschi, Evelina Maines, Michela Fedrizzi, Maria Rosaria Piemontese, Maria Bellizzi, Vittoria Cauvin, Annunziata Di Palma
P2-D2-304
Age and gender specific reference values of bone mineral density in Korean adolescents and young adults
Shin Hye Kim, Mi Jung Park, Duk Hee Kim
P2-D2-305
Status of vitamin D in pregnancy to childhood in northern Spain: seasonality, sun exposure and intake
Ana Cristina Rodríguez-Dehli, Isolina Riaño-Galán, Inés Olaya Velázquez, Ana Fernández-Somoano, Ane Miren Castilla, Mercedes Espada, Eva M Navarrete-Muñoz, Adonina Tardon
P2-D2-306
Effects of recombinant human growth hormone on bone mass and body composition in paediatric inflammatory bowel disease (IBD)
M.A. Altowati, S. Shepherd, P. McGrogan, R.K. Russell, S.F. Ahmed, SC Wong
P2-D2-676
A case of autosomal dominant hypocalcemia caused by an activating mutation of calcium sensing receptor gene (L773R): effects of phosphate binder and dietary phosphate restriction
Sumie Yamashita, Takakazu Yoshioka, Hiroshi Mizumoto, Mitsutaka Shiota, Atsuko Hata, Ken Watabane, Daisuke Hata, Masahiko Kawai
P2-D3-307
Suppression Of Bone Turnover & Its Determinants In Children Receiving Bisphosphonate Therapy
Andreas Kyriakou, Jane D McNeilly, Martin McMillan, Guftar M Shaikh, Avril Mason, Syed Faisal Ahmed
P2-D3-308
A Case of Vitamin D Dependent Rickets Type 1 With A Novel Mutation in CYP27B1 (25-OH Vitamin D-1-α-hydroxylase) Gene
BAHAR OZCABI, OLCAY EVLIYAOGLU, OYA ERCAN, FERIDE TAHMISCIOGLU, SEVINC JAFEROVA, CIGDEM ORUC, AMRA ADROVIC
P2-D3-309
Risedronate Use in Duchenne Muscular Dystrophy (DMD): A Pilot Randomised Control Trial
Niamh Mc Sweeney, Malachi Mc Kenna, Susan van der Kamp, Mark Kilbane, Ciara Mc Donnell, Nuala Murphy, David Webb, Bryan Lynch
P2-D3-310
Outcomes of vitamin D analogues and phosphate supplements in patients with hereditary hypophosphatemic rickets (HHR), comparison with non-treated patients.
Emese Boros, Anya Rothenbuhler, Claudine Heinrichs, Cécile Brachet, Laure Esterle, Peter Kamenicky, Pol Harvengt, Sylvie Brailly-Tabard, Hazar Haidar, Céline Gaucher, Caroline Silve, Charles Gossiome, Philippe Wicart, Martin Biosse Duplan, Frederic Courson, Catherine Chaussain, Agnès Linglart
P2-D3-311
Hyperostosis-hyperphosphataemia syndrome – shortening a diagnostic odyssey
Jaya Sujatha Gopal Kothandapani, Amaka Offiah, Sally Hobson, Paul Arundel
P2-D3-312
SEVERE OSTEOGENESIS IMPERFECTA and EPIDERMOLYSIS BULLOSA SIMPLEX CAUSED BY FKBP10 MUTATION: New Case
Ayla Güven, Mukaddes Kavala, A. Nurten Akarsu
P2-D3-313
Osteogenesis imperfecta type I caused by a novel mutation in the start codon of the COL1A1 gene in a Korean family and the course of pamidronate treatment for 1 year
Sung Yoon Cho, Dong-Kyu Jin, Jae-Hong Yu, Heon-Seok Han
P2-D3-314
Early calcinosis cutis, short stature and brachydactyly: a case evolution
Isolina Riaño-Galan, Cristina Rodriguez-Dehli, Belen Huidobro-Fernandez, M Victoria Alvarez, Silvia Avila Flores, Joaquin Fernández Toral
P2-D3-315
DOES VITAMIN D AFFECT MEAN PLATELET VOLUME VALUES OR NOT
Keziban BULAN, Murat DOGAN, Sultan KABA, Oktay ASLAN
P2-D3-316
Bone Size and Bone Mineral Content in Adolescents and Young Adults with Eating Disorders
Avril Mason, Sheila Shepherd, Charlotte Oakley, Michelle Thrower, Andreas Kyriakou, Guftar Shaikh, Syed Faisal Ahmed
P2-D3-317
Infantile Hypercalcemia – Still A Diagnostic And Therapeutic Enigma
Veselin Boyadzhiev, Dimitrichka Bliznakova, Violeta Iotova, Karl Schlingmann
P3-D1-660
Normal serum calcium levels and vitamin-D dependent rickets type 2 (VDDR-II): A novel vitamin D receptor mutation
Damla Goksen, Samim Ozen, Sachiko Kitanaka, Tsuyoshi Isojima, Ozgur Cogulu, Sukran Darcan
P3-D1-661
No gene alterations in eleven genes associated with isolated hypoparathyroidism (IHPT)
Zoran Gucev, Vesna Sabolic, Velibor Tasic, Toshikatsu Mitsui, Toshikatsu Hasegawa
P3-D1-662
HYPERCALCEMIA DUE TO SUBCUTANEOUS FAT NECROSIS IN A NEWBORN SUCCESSFULLY TREATED WITH PAMIDRONATE INFUSION THERAPY
Ali Atas, Suleyman Geter, M. Emin Guldur
P3-D1-663
HYPOVITAMINOSIS D: FACTORS AFFECTING IN SPANISH CHILDREN AND ADOLESCENTS
Rosaura Leis, Rocio Vazquez, Luisa Maria Seoane, Silvia Barja-Fernandez, Isabel Martinez-Silva, Concepcion M Aguilera, Josune Olza, Mercedes Gil-Campos, Lidia Castro-Feijoo, Carmen Cadarso-Suarez, Angel Gil, Rafael Tojo
P3-D1-664
HYPERCALCAEMIA DUE TO JANSEN’S METAPHYSEAL CHONDRODYSPLASIA: A CASE REPORT
Amanda Scott, Valli Velayutham, Andrew Cotterill, Michael Gabbett, Mark Harris
P3-D1-665
Survey of vitamin D status in breastfeeding infants under the age of 6 months attending the growth monitoring clinic at Rubaga hospital.
Nalunkuma Cissy, Laigong Paul, Mworozi Edison, Larry Fox
P3-D1-666
Hypercalciuria in Patients with Coexisting Osteogenesis Imperfecta and Renal Tubular Acidosis
Luisa Aguiar, Gregory Braden, Holley Allen
P3-D1-667
METABOLIC AND BONE DISORDERS IN VERTICALLY HIV-INFECTED CHILDREN
MARITZA VIVANCO, CONSTANZA RIVEROS, PAULINA BALBOA, MARIANA HEVIA, ELOISA VIZUETA, ANA MARIA CHAVEZ, JULIA VILLARROEL, ANA MARIA ALVAREZ, CLAUDIA TORREJON
P3-D1-668
Lumbar spine areal bone mineral density and 25-Hydroxyvitamin D serum concentrations at two-year follow-up in patients with osteogenesis imperfecta
Claudia Piona, Giovanni Moser, Diego Ramaroli, Malesani Francesca, Grazia Morandi, Rossella Gaudino, Franco Antoniazzi
P3-D1-669
Achondroplasia and neurological disorders
Fatima Saraoui, Soumeya fedala, ali el mahdi haddam, farida chentli, djamila meskine, leila ahmed ali
P3-D1-670
Primary hypomagnesaemia with secondary hypocalcaemia (HSH) : An uncommon diagnosis for a 2 month old Afro-Caribbean formula fed infant presenting with seizures.
Chibuzor Ihe, Jennifer Kalitsi, Ritika Kapoor, Charles Buchanan
P3-D1-671
A Challenging Diagnosis of Pseudohypoparathyroidism type 1a and practical management: a case report
ML Grace, S O'Riordan, SM O'Connell, C Bogue, C Joyce, J Allgrove
P3-D1-672
Obese adolescent with limp and depression
Vera Zdravkovic, Vladan Zivaljevic, Vadislav Bojic, Maja Jesic, Natasa Dragutinovic, Silvija Sajic
P3-D2-154
Autosomal-dominant hypocalcaemia, new clinical features
Isabel Leiva Gea, Noemi Auxiliadora Fuentes-Bolaños, Araceli Muñoz-Garach, Luis Castaño González, Maria Jose Martinez-Aedo Ollero, Juan Pedro Lopez-Siguero
P3-D2-673
Normal bone mineral acquisition in Korean adolescents; Korea National Health and Nutrition Examination Surveys
Hye Won Park, Byung Ok Kwak, Kyo Sun Kim, Sochung Chung
P3-D2-674
Klippel -Trenaunay -Weber Syndrome : the first case report in an African child.
Olumide Jarrett, Kehinde Fasina
P3-D2-675
FGFR3 GENE: A VERY RARE MUTATION
Magdalena Hawkins, Ana Alcalde, Julia Yebra, Victor Quintero, María Jose Trujillo-Tiebas, Alfonso Cañete
P3-D2-677
Risk factors affecting the development of nephrocalcinosis, the most common complication of hypophosphatemic rickets
Meliksah Keskin, Senay SavaS Erdeve, Elif Sagsak, Zehra Aycan, Semra Cetinkaya
P3-D2-678
When is epilepsy not epilepsy
Richard Lloyd-Nash, Tabitha Randell
P3-D2-679
Evaluation of Patients with Stunting in Armenia
Renata Markosyan, Natalya Volevodz, Anush Perikhanyan
P3-D2-680
Fluctuation in cerebral calcification in a patient with pseudohypoparathyroidism type II
Elena Sukarova-Angelovska, Mirjana Kocova, Olivera Lekovska
P3-D2-681
VARIABILITY IN CLINICAL AND GENETIC SPECTRUM IN HYPOPHOSPHATASIA: NATURAL HISTORY IN TWO PATIENTS
Gabriel Á. Martos-Moreno, Sergio Lerma, Elena García-Esparza, Jesús Argente
P3-D2-682
Cautionary Tales in the Management of Transient Neonatal Hypoparathyroidism
Ian Robert Mulvey, Carley Frerichs, Poonam Dharmaraj, Renuka Ramakrishnan
P3-D2-683
TWO DİFFERENT DİAGNOSİS OF PSEUDOHİPOALDOSTERONİSM
Derya Bulus, Nesibe Andiran, Elif Yagli colakoglu, Nilgün Altuntas
P3-D2-684
Clinical phenotype and molecular studies in patients with hypophosphatemic rickets
Monika Obara-Moszynska, Aleksandra Rojek, Zofia Kolesinska, Malgorzata Slomko-Jozwiak, Marek Niedziela
P3-D3-686
Bone Health in a cohort of Irish Spinal Muscular Atrophy (SMA) Patients
Niamh Mc Sweeney, Malachi Mc Kenna, David Webb, Susan van der Kamp, Mark Kilbane, Myra O' Keane, Bryan Lynch
P3-D3-687
Endocrinological assessment of children with bronchiectasis
Ilker Tolga Ozgen, Erkan Cakir, Hakan Gedik, Selim Gökce, Mustafa Atilla Nursoy, Yasar Cesur
P3-D3-688
Infantile hypophosphatasia
Nevenka Slaveska, Marina Krstevska-Konstantinova, Zoran Trajkovski
P3-D3-689
Vitamin D levels in short prepubertal children born small for gestational age (SGA)
Maria Korpal- Szczyrska
P3-D3-690
Prospective evaluation of bone mineralization, PTH regulation and metabolic profile in adult patients with hereditary hypophosphatemic rickets.
Emese Boros, Anya Rothenbuhler, Hazar Haidar, Dominique Prie, Pol Harvengt, Lavinia Vija, Sylvie Brailly-Tabard, Philippe Chanson, Agnès Linglart, Peter Kamenicky
P3-D3-691
Bone mineral density and vitamine D status in girls and adolescents with Turner Syndrome:
ouidad BAZ, Mourad SEMROUNI, Samia SAKHER, Lakhdar GRIENE, Nadir HAMMOMRAOUI, H DJOUDI
P3-D3-692
Vitamin D deficiency in children
Andreea Dobrescu, Adela Chirita-Emandi, Maria Papa, Maria Puiu
P3-D3-693
THE USE OF PAMIDRONATE IN PEDIATRIC PATIENTS WITH DISEASE OF OTHER THAN OSTEOGENESIS IMPERFECTA: THE EXPERIENCE OF OUR CENTER
Ayla Güven, Didem Helvacıoğlu, Suna Hancili, Metin Yıldız
P3-D3-694
McCune-Albright Syndrome associated to hypophosphatemic rickets
Tiago Jeronimo dos Santos, Caroline Passone, Hamilton Menezes Filho, Hilton Kuperman, Thaís Della Manna, Leandra Steinmetz, Louise Cominato, Vaê Dichtchekenian, Joyce Pupo, Nuvarte Setian, Durval Damiani
P3-D3-695
Clinical Effects Of Vitamin D In Asthma
MAHMUT DOGRU, HEVES KIRMIZIBEKMEZ, GUL YESILTEPE MUTLU, ALEV AKTAS
P3-D3-696
A Korean boy with pseudohypoparathyrodism type Ia presenting with congenital megacolon and spinal stenosis : Identification of a novel GNAS gene mutation
JE Lee, SH Lee, SY Cho, CS Ki, DK Jin
P3-D3-697
A CASE WITH ODONTOHYPOPHOSPHATASIA AND FAMILY INVESTIGATION
ESRA DENIZ PAPATYA CAKIR, MEHMET TURE, HALIL SAGLAM, SEYIT AHMET UCAKTURK, SAHIN ERDOL, ERDAL EREN, TAHSIN YAKUT, OMER TARIM
LB-D3-1007
Hepatic NAD metabolism is dysregulated by an excessive supply of lipids
Wieland Kiess, Melanie Penke, Jonas T. Treebak, Susanne Schuster, Theresa Gorski, Antje Garten
LB-D3-1011
The circulating miRNAs expression in simple obese children
Liyang Liang, Zhe Meng, Zulin Liu, Lele Hou, Lina Zhang, Wenqin Lao
P1-D1-103
TRAIL (TNF-related apoptosis-inducing ligand) induces a pro-inflammatory secretion profile in human adipocytes
Verena Zoller, Muad Abd El Hay, Jan-Bernd Funcke, Klaus-Michael Debatin, Martin Wabitsch, Pamela Fischer-Posovszky
P1-D1-104
Coexistence of elevated chitinase 3-like protein 1 (YKL-40) and von Willebrand levels in prepubertal obese children.
Ioannis Kyrgios, Charilaos Stylianou, Eleni Kotanidou, Assimina Galli-Tsinopoulou
P1-D1-105
Being overweight during the peripubertal period modifies the leptin induced changes in hypothalamic neuropeptides involved in metabolism but not those involved in pubertal onset
David Castro-González, Esther Fuente-Martín, Miguel A. Sánchez-Garrido, Pilar Argente-Arizón, Manuel Tena-Sempere, Julie A. Chowen, Jesús Argente
P1-D1-106
Natural antibiotics: New biomarkers of childhood obesity
Anna Prats-Puig, Montserrat Gispert-Saüch, Gemma Carreras-Badosa, Ferran Díaz-Roldán, Francis de Zegher, Lourdes Ibánez, Judit Bassols, Abel López-Bermejo
P1-D1-107
Evidence of early alterations in adipose tissue biology and function in obese children
Katrhin Landgraf, Denise Rockstroh, Isabel Wagner, Roy Tauscher, Julian Schwartze, Ulf Bühligen, Holger Till, Magdalena Wojan, Jürgen Kratzsch, Wieland Kiess, Matthias Blüher, Antje Körner
P1-D1-108
The impact of antibiotic exposure during infancy on weight and height
Antti Saari, Lauri Virta, Ulla Sankilampi, Harri Saxen, Leo Dunkel
P1-D1-109
Identification of brown adipocyte progenitor marker genes in progenitor cells from human deep neck and subcutaneous adipose tissue by gene array analysis
Daniel Tews, Verena Schwar, Theresia Weber, Marc Scheithauer, Tobias Fromme, Martin Klingenspor, Thomas F Barth, Peter Möller, Pamela Fischer-Posovszky, Martin Wabitsch
P1-D1-11
A multiplatform non-targeted metabolomics approach to investigate insulin resistance associated to obesity in childhood.
Annalaura Mastrangelo, Gabriel Martos-Moreno, Antonia García, Francisco Rupérez, Julie Chowen, Luis Pérez-Jurado, Coral Barbas, Jesús Argente
P1-D1-110
Free fatty acids activate hypothalamic astrocytes in a sexually dimorphic manner
Pilar Argente-Arizón, Esther Fuente-Martín, Francisca Díaz, Alejandra Freire-Regatillo, Jesús Argente, Julie A. Chowen
P1-D1-112
MIR-146a AND -155 ARE INVOLVED IN FOXO-1 REGULATION AND NON ALCOHOLIC FATTY LIVER DISEASE (NAFLD) IN CHILDHOOD OBESITY
Luisa Montanini, Pietro Lazzeroni, Chiara Sartori, Valerio Nobili, Pellegrino Crafa, Sergio Bernasconi, Maria E. Street
P1-D2-113
Prenatal maternal weight and weight status and lipid profile of the offspring
Isolina Riaño-Galan, Cristina Rodriguez-Dehli, Ines Olaya Velázquez, Ana Fernández-Somoano, Damaskini Valvi, Marisa Rebagliato, Jesus Ibarluzea, Adonina Tardon
P1-D2-114
Pro-inflammatory (M1) and anti-inflammatory (M2) profiles in adipose tissue of lean and obese children and adolescents.
Alexia Karvela, Aikaterini Avgeri, Eleni D. Vlotinou, George Georgiou, Dionysios J. Papachristou, Bessie E. Spiliotis
P1-D2-115
Important Links between Fat Derived Proteins and Bone Remodeling Factors in Lean and Obese Girls
Christina Kanaka-Gantenbein, Evangelos Terpos, George Chrousos, Ioannis Papassotiriou
P1-D2-116
Characterizing the Metabolically Obese Normal Weight phenotype in youth
Melanie Henderson, Marie-Eve Mathieu, Andrea Benedetti, Tracie Barnett
P1-D2-117
Ratio of TriGlycerides to High-density lipoprotein Cholesterol compared with Homeostasis Model Assessment Insulin Resistance indexes in screening the Metabolic Syndrome in Chinese obese children
JIANFENG LIANG, JUNFEN FU, jinling wang, youjun jiang, guanping dong
P1-D2-118
Plasminogen activator inhibitor-1(PAI-1) levels, PAI-1 gene polymorphism, and family history of cardiovascular disease in relation to metabolic parameters in a sample of obese children.
Zacharoula Karabouta, Areti Makedou, Anagnostis Argiriou, Dimitrios Papandreou, Eleni Xanthopoulou, Vasiliki Bisbinas, Fani Athanassiadou-Piperopoulou, Israel Rousso
P1-D2-119
How production of vascular endothelial growth factor (VEGF) influences formation of vascular disorders in children with obesity
Olena Budreiko, Nataly Shlyachova, Larisa Nikitina, Svitlana Chumak, Anna Kosovtsova
P1-D2-120
RANKL and osteoprotegerin serum levels in obese children and adolescents
Maria Felicia Faienza, Maria Rosaria Vulpi, Laura Piacente, Annamaria Ventura, Antonella Lonero, Vincenza Luce, Fabrizia De Palma, Angelo Acquafredda, Clara Zecchino, Antonio Minenna, Maurizio Delvecchio, Maria Grano, Luciano Cavallo, Giacomina Brunetti
P1-D2-121
Sex-, age- and height-specific Reference Curves for the Six- Minute Walk Test in Healthy Children and Adolescents.
Vrinda Saraff, Johanna Schneider, Valeria Colleselli, Monika Ruepp, Sabrina Neururer, Markus Rauchenzauner, Ralf Geiger, Wolfgang Högler
P1-D2-122
Predictive value of excess body weight in childhood and adolescence compared to body mass index and waist to height ratio
David Petroff, Katrin Kromeyer-Hauschild, Susanna Wiegand, Dagmar L’Allemand-Jander, Gerhard Binder, Karl Otfried Schwab, Rainer Stachow, Wieland Kiess, Elke Hammer, Sirid Sturm, Reinhard Holl, Susann Blüher
P1-D2-123
Cardiovascular risk markers in metabolically healthy and metabolically unhealthy obese adolescents
Tetyana Chaychenko
P1-D2-124
A dual role of Fetuin A on cardiovascular risk in obese children and adolescents.
Susanna Wiegand, Mareike Buermann, Andrea Ernert, Silvia Briese, Ann-Madeleine Bau, Heiko Krude
P1-D3-125
Impairment of adipose tissue in Prader-Willi syndrome rescued by growth hormone treatment
Thomas CADOUDAL, Gwenaelle DIENE, Coralie SENGENES, Catherine MOLINAS, Flavie DESNEULIN, Sanaa EDDIRY, Francoise CONTE AURIOL, Daniele DAVIAUD, Anne BOULOUMIE, Jean Pierre SALLES, Philippe VALET, Maithe TAUBER
P1-D3-126
Dysautonomia and acyl ghrelin in Prader-Willi syndrome (PWS)
Ohn Nyunt, Sinead Archbold, Jennifer Donelly, Penelope Jeffery, Andrew Cotterill, Peter Davies, Mark Harris
P1-D3-127
Infancy lipidomic analyses and associations with early nutrition and growth
Philippa Prentice, Albert Koulman, Lee Matthews, Carlo Acerini, Ken Ong, David Dunger
P1-D3-128
Acylated and unacylated ghrelin levels in children and young adults with Prader-Willi syndrome.
Renske Kuppens, Gwenaelle Diène, Nienke Bakker, Catherine Molinas, S Faye, Marc Nicolino, Delphine Bernoux, Patric Delhanty, Aart Jan van der Lelij, Soraya Allas, Michiel Julien, Thomas Delale, Maïthé Tauber, Anita Hokken-Koelega
P1-D3-129
The Effect of Honey on Plasma Glucose and Insulin Concentrations in Obese Prepubertal Girls.
Ioanna Farakla, Georgios E. Papadopoulos, Eleni Koui, Jessica Arditi, Paraskevi Moutsatsou, Maria Drakopoulou, Ioannis Papassotiriou, George P. Chrousos, Evangelia Charmandari
P1-D3--130
Features of neuroendocrine status in children with different forms of obesity
Anzhalika Solntsava, Olga Zagrebaeva, Hanna Mikhno, Helena Dashkevich, Alexandr Sukalo, Katsiaryna Konchyts
P1-D3-131
UNDER-DIAGNOSED BECKWITH-WIEDEMANN SYNDROME AMONG EARLY-ONSET OBESE CHILDREN
Gabriel Á. Martos-Moreno, Clara Serra-Juhé, Luis A. Pérez-Jurado, Jesús Argente
P1-D3-132
IMPACT OF MATERNAL AND FETAL INFLAMMATORY MARKERS ON NEONATAL AND INFANT ADIPOSITY
Jean M Donnelly, Jennifer M Walsh, Mary Horan, Eleanor J Molloy, Fionnuala Mc Auliffe
P1-D3-133
CAN WE PREDICT THE RISK OF OBESITY?
Antonio de Arriba, Javier Pascual, Mario de Francisco, Marta Ferrer, Ignacio Martínez, José Ignacio Labarta, Ángel Ferrández
P1-D3-134
Can hypothalamic obesity be treated with stimulants?
Friederike Denzer, Belinda Lennerz, Christian Denzer, Martin Wabitsch
P2-D1-362
Age at onset of weight gain in Prader-Willi syndrome is often between 1 and 2 years, preceding the hyperphagic phase; implications for management
Malcolm Donaldson, Noran Abu-Of Hammed, M. Guftar Shaikh
P2-D1-363
Novel uncoupling protein-1 (UCP1) expression in white adipocytes of subcutaneous abdominal adipose tissue in children and adolescents: a protective mechanism for metabolic equilibrium?
Alexia Karvela, Aikaterini Avgeri, Eleni D. Vlotinou, George Georgiou, Dionysios J. Papachristou, Bessie E. Spiliotis
P2-D1-364
The Association between Self-reported Sleep Quality, Ghrelin hormone and Obese Children and Adolescents.
abeer el-ashmawy, iman eyada, nahed mohamed, mona attya, shereen Abdel-Ghaffar, marwa farouk
P2-D1-365
Large-Born Infants Switch from an Adipose to a Lean and Insulin-Sensitive State with Low Concentrations of Circulating Myostatin and Follistatin
Giorgia Sebastiani, Miriam Perez Cruz, Marta Díaz Silva, María Dolores Gomez Roig, Abel Lopez Bermejo, Lourdes Ibañez Toda, Francis De Zegher
P2-D1-366
URIC ACID AND RISK FOR ATHEROSCLEROTIC DISEASE EARLY IN LIFE
Judit Bassols, Jose-Maria Martínez-Calcerrada, Anna Prats-Puig, Gemma Carreras-Badosa, Ferran Díaz-Roldán, Inés Osiniri, Elena Riera-Pérez, Francis de Zegher, Lourdes Ibáñez, Abel López-Bermejo
P2-D1-367
Prevalence of idiopathic intracranial hypertension and related factors in obese children and adolescents.
Derya Tepe, Fatma Demirel, Esra Dag Seker, Meltem Tayfun, Ihsan Esen, Ozlem Kara, Ebru Petek Arhan
P2-D1-368
MAINTAIN: An intervention study of weight regain after weight loss in adolescents and children reveals an only minor role of leptin in weight regain
Susanna Wiegand, Anne-Madeleine Bau, Andrea Ernert, Heiko Krude
P2-D1-369
The expression of Insulin-Like Growth Factor type 1 receptor (IGF1R) is increased in obese children.
Rafaela Ricco, Rodrigo Custódio, Patricia Atique, Raphael Liberatore, Rubens Ricco, Carlos Martinelli
P2-D1-370
Childhood obesity, renal injury and future disease risk.
Mina Lateva, Dimitrichka Bliznakova, Sonya Galcheva, Maria Neshkinska, Vilhelm Mladenov, Veselin Boyadzhiev, Irina Halvadzhiyan, Galina Yordanova, Violeta Iotova
P2-D1-371
Replacement of the neonatal leptin surge during maternal deprivation normalizes some endocrine parameters but exacerbates others
Virginia Mela, Alvaro Lopez-Rodriguez, Sara Peñasco, Vicente Barrios, Jesús Argente, María-Paz Viveros, Julie A. Chowen
P2-D1-372
Longitudinal development of adiponectin in early childhood and the influence of breastfeeding and essential fatty acid status
Josefine Roswall, Emma Kjellberg, Birgitta Strandvik, Jovanna Dahlgren
P2-D1-373
Expression levels of the Growth-arrest-specific transcript 5 (Gas5) in overweight and obese children and adolescents
Terpsihori Fragouli, Amalia Sertedaki, Ioanna Farakla, Nicolas C. Nicolaides, Maria Dracopoulou, Ioannis Papassotiriou, George P. Chrousos, Evangelia Charmandari
P2-D2-374
The role of bone and fat tissue in glucose metabolism in two different metabolic conditions: obesity and diabetes mellitus type 1 – pilot study
Anna Wedrychowicz, Krystyna Sztefko, Jerzy Starzyk
P2-D2-375
FAMILY AND GENETIC FACTORS INFLUENCE THE METABOLIC CHANGES IN CHILDREN
Anzhalika Solntsava, Liudmila Viazava, Alexander Sukalo, Elena Aksionava, Nina Danilenko
P2-D2-376
Non-Alcoholic Fatty Liver Disease (NAFLD) in children/adolescent affected by Prader WIlli Syndrome
danilo fintini, elena inzaghi, sarah bocchini, graziano grugni, mauro colajacomo, claudia brufani, marco cappa, valerio nobili, stefano cianfarani, antonino crinò
P2-D2-377
Short-term results of single-port sleeve gastrectomy in adolescents with severe obesity.
Gianpaolo De Filippo, Guillaume Pourcher, Catherine Piquard, Stefano Ferretti, Ibrahim Dagher, Pierre Bougnères
P2-D2-378
CIRCULATING CONCENTRATIONS OF FIBROBLAST GROWTH FACTOR-21 (FGF21) ARE UNDETECTABLE IN HUMAN INFANTS AT TERM BIRTH AND SURGE WITHIN HOURS AFTER BIRTH
David Sánchez-Infantes, José Miguel Gallego-Escudero, Rubén Cereijo, Marta Díaz, Gemma Aragonés, Abel López-Bermejo, Francis de Zegher, Francesc Villarroya, Lourdes Ibáñez
P2-D2-379
Severe childhood-onset obesity and testicular function after puberty
Saila Laakso, Heli Viljakainen, Marita Lipsanen-Nyman, Ursula Turpeinen, Tero Saukkonen, Outi Mäkitie
P2-D2-380
A new case of Proopiomelanocortin Deficiency
Noemi Auxiliadora Fuentes-Bolaños, Francisco Jose Tinahones Madueño, Luis Castaño González, Isabel Leiva Gea, Maria Jose Martínez-Aedo Ollero, Juan Pedro Lopez-Siguero
P2-D2-381
Neuroendocrine and psychological status in obese children
Anzhalika Solntsava, Olga Zagrebaeva, Tatsiana Yemelyantsava, Hanna Mikhno, Helena Dashkevich, Yuliya Tkachova
P2-D2-382
Is 24-hour blood pressure monitoring necessary in obese children and adolescents ?
Malgorzata Wojcik, Jadwiga Malek, Dominika Janus, Anna Kalicka-Kasperczyk, Katarzyna Tyrawa, Jerzy B. Starzyk
P2-D2-383
Fetuin A Serum Levels in Children with Nonalcoholic Fatty Liver Disease (NAFLD)
Valentina Pampanini, Elena Inzaghi, Valerio Nobili, Daniela Germani, Antonella Puglianiello, Stefano Cianfarani
P2-D2-384
Ambulatory Arterial Stiffness Index in Obese Children
Christoph Saner, Primus Mullis, Giacomo Simonetti, Marco Janner
P2-D2-385
Evaluation of the risk of dyslipidemia in adolescents with obesity
Jurgita Gailite, Urzula Nora Urbane, Ieva Strele, Renars Erts, Una Lauga-Tunina, Inara Kirillova, Dace Gardovska, Iveta Dzivite-Krisane
P2-D3-386
Miglitol upregulates uncoupling protein 1 (UCP1) by enhancing β3-adrenergic signaling in mature brown adipocytes of rat.
Satoru Sugimoto, Hisakazu Nakajima, Taichiro Nishikawa Nishikawa, Kazuki Kodo, Ikuyo Itoh, Kitaro Kosaka, Hajime Hosoi
P2-D3-387
Enhanced liver fibrosis test in obese children with ultrasound-proven steatosis
Krystyna Sztefko, Patrycja Szybowska, Malgorzata Wojcik, Jerzy B. Starzyk
P2-D3-388
METFORMIN TREATMENT IN OBESE CHILDREN ENHACES WEIGHT LOSS RELATED IMPROVEMENT IN IMPAIRED GLUCOSE TOLERANCE
Andrea Bartucci, Gabriel Á. Martos-Moreno, Vicente Barrios, Jesús Argente
P2-D3-389
TYPE AND TIME OF FEEDING IN THE FIRST YEAR OF LIFE ARE NOT ASSOCIATED TO CIRCULATING MULTIMERIC ADIPONECTIN LEVELS IN OBESE CHILDREN
Simonetta Bellone, Flavia Prodam, Letizia Trovato, Marta Roccio, Agostina Marolda, Cristina Fiorito, Enza Giglione, Gianni Bona
P2-D3-390
POMC DEFICIENCY MIMICKING NEUROMETABOLIC DISEASE
Samim Ozen, Nurhan Ozcan, Sema Kalkan Ucar, Damla Goksen, Sukran Darcan
P2-D3-391
The relationship between weight-related anthropometric parameters and menarche in Norwegian girls
Heiko Bratke, Bente Ellingsen Brannsether, Jörg Aßmus, Robert Bjerknes, Pétur B. Júlíusson
P2-D3-392
HbA1c AND METABOLIC PARAMETERS IN A PEDIATRIC OVERWEIGHT/OBESE POPULATION.
Maria Chiara Pellegrin, Andrea Grillo, Elena Faleschini, Gianluca Tornese, Alessandro Ventura
P2-D3-393
Comparison of FMDXA and FMBIA in obese adolescents
Julian Ziegler, Roland Schweizer, Gerhard Binder
P2-D3-394
From the need of preventing infantile obesity as soon as possible: a new SCORE at birth
Nuria Sanz, M.Jesus Asencio, Angeles Buj, Corpus Marzo, Juan Manuel Rodriguez, Consol Sanchez, Lourdes Ibañez, Maria Victoria Marcos
P2-D3-395
Body composition in 10-15 year old children exposed to pesticides prenatally
Jeanette Tinggaard, Christine Wohlfahrt-Veje, Ida M Schmidt, Malene Boas, Steffen Husby, Katharina M Main, Niels E Skakkebæk, Tina K Jensen, Helle R Andersen
P2-D3-396
D2 DOPAMINE RECEPTOR AGONISTS INFLUENCE IN THE ANIMAL MODEL OF DIETARY OBESITY
Liudmila Viazava, Anzhalika Solntsava, Alexander Sukalo, Elena Dashkevich, Yuliya Stukach
P2-D3-397
Combined evaluation of glucose levels at fasting state and one-hour after glucose load can safely predict prediabetes in obese youth
Eleni P Kotanidou, Ioannis Kyrgios, Assimina Galli-Tsinopoulou
P2-D3-398
Association between calcium deficiency and obesity in children
Hanna Mikhno, Anzhalika Solntsava, Olga Zagrebaeva, Katsiaryna Konchyts
P2-D3-399
Is small for gestational age status associated with an increase risk of atherogenesis?
Ramona Stroescu, Ioana Micle, Monica Marazan, Otilia Marginean, Teofana Bizerea, Gabriela Doros
P2-D3-400
Association between lipid profile, body mass index and insulin resistance markers in obese prepubertal children.
Ramon Cañete, Miguel Valle, Rosario Martos, Maria Dolores Cañete, Rosario Valle-Martos
P2-D3-401
Mannose binding lectin and carotid intima-media thickness in Chinese obese children.
Wei WU, Liqing Cheng, Junfen Fu
P2-D3-402
Usefulness of hypertriglyceridemic waist phenotype in obese Indian children
Janani Ravi, Hemchand Krishna Prasad, Lakshmi Venugopalan, Gowrishankar Chokanathan, Nedunchelian Krishnamoorthy, Kannan Narayanaswamy
P2-D3-403
Concomitant changes in Full Body DXA Values and BMI SDS during Multidisciplinary Treatment of Childhood Obesity
Tenna RH Nielsen, Cilius E Fonvig, Thomas A Gerds, Ulrik Lausten-Thomsen, Jens-Christian Holm
P2-D3-404
Cystic fibrosis - dyslipidemia in Brazilian Children
Ana Catarina Araujo, Ana Cristina Bezerra, Luciana Monte, Cristina Moreira, Andrea Abdalla
P2-D3-405
Do children with Down Syndrome show lipid profile disorders?
Dominika Zimny, Marta Szatkowska, Julian Maciaszek, Mikolaj Machaj, Ewa Barg
P2-D3-406
Relationship between obesity and platelet indices in children
Elif Özsu, Bahadir Yazicioglu
P2-D3-407
Examining beta-cell reserve in extremely obese children
Maria Neshkinska, Sonya Galcheva, Mina Lateva, Violeta Iotova
P2-D3-408
SHBG INTEGRATES THE CARDIOVASCULAR RISK AND METABOLIC DYSFUNCTION OF GESTATIONAL OBESITY
Judit Bassols, Pilar Soriano-Rodríguez, Anna Prats-Puig, Gemma Carreras-Badosa, Miguel-Angel Miranda-Arce, Elena Álvarez-Castaño, Francis de Zegher, Lourdes Ibáñez, Abel López-Bermejo
P3-D1-1771
Level of non-high-density-lipoprotein cholesterol and its related factors in Chinese Han students
Fang Yanlan, Liang Li, Fu Junfen
P3-D1-760
Association of ghrelin gene polymorphisms with obesity in Japanese children
Ikuyo Itoh, Hisakazu Nakajima, Kazuki Kodo, Satoru Sugimoto, Kitaro Kosaka, Hajime Hosoi
P3-D1-761
25-Hydroxy vitamin D Deficiency and It's relationship to Obesity and other Risk Factors in a group of Iranian children and adolescents
Heshmat Moayeri, Maral Ghasemzadeh
P3-D1-762
A rare case of sea-blue histiocytosis associated with Niemann-Pick disease type B in a 8-year and 9-month old boy with hypertension.
Hua-mei MA, Zhe SU, Yan-hong LI
P3-D1-763
Association of lifestyle with metabolic syndrome in children
Maria Efthymia Katsa, Sofia Zyga, Maria Tsironi, Anastasios Ioannidis, Athanasios Sachlas, Petros Kolobos, Maria Magana, Anna Maria Pistikou, Dafni Eleni Kougioumtzi Dimoliani, Andrea Paola Rojas GIl
P3-D1-764
PREVALENCE OF METABOLIC SYNDROME AND INSULIN RESISTANCE AMONG AGED 3 TO 9 CHILDREN
Nihal Hatipoglu, Selim Kurtoglu, Mumtaz Mazicioglu, Deniz Okdermir, Ulku Gul
P3-D1-765
The Relation of Serum Leptin and Soluble Leptin Receptor Levels with Metabolic and Clinical Parameters in Obese and Healthy Children
Gönül ÇATLI, Ahmet ANIK, Hale ÜNVER TUHAN, Tuncay KUME, Ece BÖBER, Ayhan ABACI
P3-D1-766
Positive association of pro-oxidative stress markers with adipose mass in pre- and early-pubertal boys
George Paltoglou, Maria Schoina, George Valsamakis, Alexandra Avloniti, Athanasios Chatzinikolaou, Antonis Kambas, Dimitris Draganidis, Ioannis Papassotiriou, Alexandra Margeli, Nicolaos Salakos, Maria Papagianni, Christina Kanaka-Gantenbein, George P. Chrousos, Ioannis G. Fatouros, George Mastorakos
P3-D1-767
Prevalence metabolic syndrome and its components among children with obesity
Oleg Latyshev, Elena Kiseleva, Goar Okminyan, Lubov Samsonova, Irina Kolomina
P3-D1-768
Serum Omentin-1 and Vaspin Levels in Obese Children and Their Correlation With Lipid Metabolism
Hong-Shan Chen, Ling-Ling Xu, Shun-Ye Zhu, Si-Nian Pan, Min-lian Du, Zhe Su
P3-D1-769
THE IMPORTANCE OF WEIGHT FOR HEIGHT FOR PREDICTION OF METABOLIC SYNDROME IN OBESE CHILDREN AND ADOLESCENTS : IMPACT OF GENDER AND PUBERTAL STATUS
Bayram Özhan, Betül Ersoy, Seniha Kiremitçi
P3-D1-770
Understanding How Race Influences Plasma Peptide YY in the Aging Population
Kamille Camacho-Monclova, Dillip Jeste, Pei-an Betty Shih
P3-D1-772
Do children with Down Syndrome show lipid profile disorders?
Dominika Zimny, Marta Szatkowska, Julian Maciaszek, Mikolaj Machaj, Ewa Barg
P3-D1-924
Leptin Levels in Boys with Pubertal Gynecomastia
Atilla Buyukgebiz, Bumin Dundar, Nihal Dundar, Ece Bober
P3-D2-773
Trends in obesity prevalence and body-mass index among pre-pubertal Bulgarian children, 1990-2007
Violeta Iotova, Sonya Galcheva, Yoto Yotov, Kera Grozdeva, Velin Stratev
P3-D2-774
The prevalence of 25-hydroxyvitamin D insufficiency and deficiency among overweight and obese children and adolescents in Greece.
Christos Giannios, Ioanna Farakla, Georgios Papadopoulos, Ioanna Bakopoulou, Nicolas C. Nicolaides, Chryssanthi Papathanasiou, Maria Drakopoulou, George P. Chrousos, Evangelia Charmandari
P3-D2-775
Metabolic and lifestyle correlates of health-related quality of life among Taiwanese obese adolescents
Meng-Che Tsai, Yen-Yin Chou
P3-D2-776
Prevalence of Dyslipidemia and Associated Factors Among Obese Turkish Children
Selin Elmaogullari, Derya Tepe, Ahmet Ucakturk, Fatma Demirel
P3-D2-777
THE INTERACTION OF EXOPHTALMOS WITH OBESITY IN TURKISH CHILDREN AND ADOLESCENTS
Betul Cicek, Ahmet Ozturk, Mumtaz Mazicioglu, Selim Kurtoglu, Tuncay Kara, Nihal Hatipoglu
P3-D2-778
Reproducibility of the glucose tolerance test in overweight children
shokery awadalla
P3-D2-779
Younger age and BMI>3SD are risk factors for mortality in children with Hypothalamic Obesity
Belma Haliloglu, Serap Turan, Zeynep Atay, Tulay Guran, Saygın Abalı, Serpil Bas, Abdullah Bereket
P3-D2-780
Age-related characteristics of nutritional status in children with alimentary obesity
Nataliya Volkova, Anzhalika Solntsava, Olga Zagrebaeva
P3-D2-781
Relationship between adiposity degree and physical activity and inactivity among children and adolescents
Rosaura Leis, Rocio Vázquez-Cobela, Juan José Bedoya, Luisa María Seoane, Silvia Barja-Fernández, Concepción Aguilera, Josune Olza, Gloria Bueno, Mercedes Gil-Campos, Lidia Castro-Feijoo, Luis Moreno, Angel Gil, Rafael Tojo
P3-D2-782
Antenatal and early childhood determinants of the development of obesity in children
Yauhenia Dzmitrovich, Anzhalika Solntsava, Olga Zagrebaeva, Hanna Mikhno, Yuliya Tkachova, Katsiaryna Konchyts
P3-D2-783
The association hypothyroidism – obesity in a group of children and adolescents
Corina Paul, Mirela Mogoi, Iulian Velea
P3-D2-784
A new lipodystrophy syndrome?
Julia von Schnurbein, Pamela Fischer-Posovszky, Abhimanyu Garg, Martin Wabitsch
P3-D2-785
Prevalence of excessive body mass and obesity among children and adolescents residing in Tashkent, Uzbekistan
Shakhnoza Azimova, Gulnara Rakhimova
P3-D3-659
Evaluation of the Relation Between Thyroid Dysfunction and Oxidant/ Antioxidant Status in Obese Children
Ali Asci, Derya Bulus, Nesibe Andiran, Belma Kocer-Gumusel
P3-D3-759
Diabetes mellitus type 2 in Pediatrics : an emerging reality in our country. First cases described at Spain
Ignacio Diez-Lopez, Ainhoa Sarasua-Miranda, Isabel Lorente-Blazquez
P3-D3-786
Hypothalamic Obesity in Children and Adolescents: a multi-disciplinary approach and novel therapeutic tools.
Daniele Tessaris, Antonella Tuscano, Ivana Rabbone, Antonella Lezo, Giorgia Fenocchio, Fabio Broglio, Alessandra Spinardi, Roberto Lala, Patrizia Matarazzo
P3-D3-787
OBESE TEENAGERS AND RISK OF INJURIES DURING SCHOOL PHISICAL ACTIVITY
Francesco Lemma, Beatrice Messini
P3-D3-788
ERYTHROCYTE SEDIMENTATION RATE AND CRP LEVELS IN CHILDHOOD OBESITY
Dilek Ozcelik Ersu, Lale Seren, Rahime Gul Yesiltepe Mutlu, Heves Kirmizibekmez
P3-D3-789
Bone age advancement in prepubertal children with overweight and obesity
Hae Sang Lee, Jung Sub Lim, Jin Soon Hwang, Eun Young Kim
P3-D3-790
Obesity correlates in adolescence
Ioannis Papandreou, Eleni Kotsalidou, Aikaterini Tselenti, Zoi Gerle
P3-D3-791
Correlation between Fasting blood glucose and glucose tolerance test in overweight children
Shokery Awadalla
P3-D3-792
Frequency of vegetable and fruit consumption in overweight children and their parents
sandra beatriz Escobar Escobar, shokery Awadalla
P3-D3-793
Prevalence of abnormalities of glucose metabolism in obese Greek children and adolescents
Feneli Karachaliou, Irene Kaloumenou, Elpis-Athina Vlachopapadopoulou, Paraskeui Katsixti, Aspasia Fotinou, Stefanos Michalacos
P3-D3-794
PRADER WILLI SYNDROME (PWS): REPORTS OF TWO PATIENTS WITH CONGENITAL ABNORMALITIES OF KIDNEY AND URINARY TRACT.
Federica Tamburrino, Emanuela Scarano, Francesca Mencarelli, Annamaria Perri, Angela Colangiulo, Benedetta Siroli, Anna Lisa Martini, Laura Mazzanti
P3-D3-795
RESPONSE TO TREATMENT IN A GROUP OF PATIENTS WITH CHILDHOOD OBESITY.
Concepción Freijo Martín, María Laura Bertholt Zuber, Inmaculada Palenzuela Revuelta, Ana Rebollo Rebollo
P3-D3-796
PREVALENCE OF OVERWEIGHT AND OBESITY IN CHILDREN AND ADOLESCENTS AT PUBLIC AND PRIVATE SCHOOLS FROM UBERABA BRAZIL
Adriana Paula Silva, Taciana Carla Maia Feibelmann, Daniela Cristina Silva, Heloisa Marcelina Cunha Palhares, Lúcia Marina Scatena, Maria de Fátima Borges
P3-D3-797
Gene Mutation and Clinical Characteristics Analysis in Progressive Familial Intrahepatic Cholestasis
Ruizhu Lin, Li Liu, Huiying Sheng
P3-D3-798
Characteristics of a Population of Obese Children and Adolescents: Suggesting a new paradigm.
Quentin Van Meter, Bethany Welstead, Joey Low
P3-D3-938
Hyperandrogenism doesn’t increase the insulin resistance in overweight and obese adolescent girls with polycystic ovary syndrome
Natalija Smetanina, Audrone Seibokaite, Raimondas Valickas, Rasa Verkauskiene
LB-D3-1008
LONG-TERM IMPACT OF CHILDHOOD-ONSET TYPE 1 DIABETES: SOCIAL INSERTION, QUALITY OF LIFE, SEXUALITY
Hélène Mellerio, Sophie Guilmin-Crépon, Paul Jacquin, Corinne Alberti, Claire Levy-Marchal
P1-D1-58
A Leu402Pro mutation of the non-HLA gene IL18RAP in aggressive neonatal type 1 diabetes mellitus
Mirjam Dirlewanger, Jean-Louis Blouin, Jeremy Bevillard, Federico Santoni, Valérie Schwitzgebel
P1-D1-59
A randomized, crossover pilot study comparing glycemic control and satisfaction with an indwelling catheter (I-PORT Advance) for insulin administration in children and adolescents with type 1 diabetes on basal-bolus treatment
Giulio Maltoni, Anna Lisa Martini, Alessandra Rollo, Annamaria Perri, Stefano Zucchini
P1-D1-60
Activity of neutral alfa-glucosidase in the urine of children and adolescents with type 1 diabetes mellitus and diabetic nephropathy
Akidahon Sadykova, Gulnara Rakhimova
P1-D1-61
EVALUATION OF S-100B, ANTIOXIDANT AND OXIDATIVE CAPACITY BEFORE AND AFTER THE TREATMENT IN CHILDREN WITH DIABETIC KETOACIDOSIS
Cemil Kaya, Ali Atas, Nurten Aksoy
P1-D1-62
Effect of adjunctive therapy with cholecalciferol on residual β-cell function in recent-onset Type 1 Diabetes Mellitus – a prospective pilot study
Ana Laura Fitas, Ana Filipa Almeida, Catarina Limbert, Lurdes Lopes
P1-D1-63
Th17 cells in children with new onset type 1 diabetes
Robert Piekarski, Iwona Ben-Skowronek, Agnieszka Bojarska-Junak, Jacek Tabarkiewicz, Leszek Szewczyk
P1-D1-64
BIOMARKERS OF SUBCLINICAL INFLAMMATION IN AN INFANT-JUVENIL POPULATION WITH TYPE 1 DIABETES
Maria Bazan, Sofia Casella, Santiago Lopez, Teresita Carrizo, Maria Velarde, Elba Díaz, Adela Abregu
P1-D1-65
Glycaemic control and acute complications in European children, adolescents and young adults with Type 1 Diabetes (T1D) in the TEENs study
Moshe Phillip, Lori Laffel, Catherine Domenger, Marie-Paule Dain, Valerie Pilorget, Christophe Candelas, Thomas Danne, Carmen Mazza, Barbara Anderson, Ragnar Hanas, Sheridan Waldron, Roy Beck, Chantal Mathieu
P1-D1-66
Metabolic consequences of antipsychotic medication in youths with type 1 diabetes: analysis from the prospective nationwide German and Austrian diabetes survey DPV
Angela Galler, Esther Molz, Michael Meusers, Bela Bartus, Andrea Näke, Holger Haberland, Edith Schober, Reinhard W. Holl
P1-D1-67
Protective Effects of Combined Intervention with Adenovirus Vector Mediated IL-10 and IGF-1 Genes on Endogenous Islet β Cells in Nonobese Diabetes Mice with Onset of Type 1 Diabetes Mellitus
Tang Li, Lijuan Zhang, Yanyan Chen, Cheng Li, Xiaojie Lin
P1-D1-68
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
P1-D2-29
Standard Population Screening for Diabetes mellitus has low sensitivity in identifying diabetes in adult survivors of childhood bone marrow transplantation with total body irradiation (BMT/TBI)
Christina Wei, Rebecca Unsworth, Nikki Davis, Ruth Elson, Karin Bradley, Michael Stevens, Elizabeth Crowne
P1-D2-69
Activation of insulin/IGF-I signaling could increase hypothalamic lipid anabolism in non-diabetic IRS2-deficient mice
Vicente Barrios, Eva Baquedano, Sandra Canelles, Águeda González-Rodríguez, Emma Burgos-Ramos, Julie A. Chowen, Laura M. Frago, Ángela M. Valverde, Jesús Argente
P1-D2-70
Evaluation of Subclinical Atherosclerosis by Non-Invasive Radiological Methods and Its Relation with Endoglin and Nitric Oxide Levels
Hamdi Cihan Emeksiz, Aysun Bideci, Nurullah Çelik, Özge Yüce, Esra Döğer, Çağrı Damar, Öznur Boyunağa, Orhun Çamurdan, Peyami Cinaz
P1-D2-71
Identification of Novel Candidate Gene Variants for MODY by Whole Exome Sequencing in Korean MODY Families
Un Mi Cho, Yae Ji Shim, Byung Ho Choi, Cheol Woo Ko
P1-D2-72
Protective potential of metformin on membrane linked functions in diabetic aging female rats.
Pardeep Kumar, R Kale, N Baquer
P1-D2-73
A novel mutation of WFS1 gene in a Japanese infant of diabetes mellitus, deafness and congenital cataract.
Shuntaro Morikawa, Akie Nakamura, Katsura Ishizu, Satoru Kumaki, Toshihiro Tajima
P1-D2-74
Transient hyperglycaemia preceded by neonatal hyperinsulinaemic hypoglycaemia in an infant with a novel HNF1A mutation
Barbora Obermannova, Klara Rozenkova, Petra Dusatkova, Stepanka Pruhova, Zdenek Sumnik, Jan Lebl
P1-D2-75
LPL gene mutation and polymorphism of APOC2 and APOC5 genes in a patient with diabetes mellitus type 1
Julita Nocon-Bohusz, Beata Wikiera, Aleksander Basiak, Anna Noczynska
P1-D2-76
DETERMINANTS OF SERUM OSTEOCALCIN CONCENTRATIONS IN 12-YEAR-OLD CHILDREN BORN SMALL OR APPROPRIATE FOR GESTATIONAL AGE
Sirpa Tenhola, Satu Seppä, Raimo Voutilainen
P1-D2-77
MOLECULAR GENETIC ANALYSIS OF MATURITY ONSET DIABETES OF THE YOUNG (MODY) GENES IN CHILDREN BY USING TARGETED NEXT-GENERATION SEQUENCING
Ahmet ANIK, Gönül ÇATLI, Hale ÜNVER TUHAN, Ayhan ABACI, Hüseyin Anil KORKMAZ, Behzat ÖZKAN, Erkan SARI, Ediz YESILKAYA, Ayça ALTINCIK, Sefa KIZILDAG, Ece BÖBER
P1-D2-78
Hormonal and Lipid Profile in Correlation with Anthropometric Measurements Among Offspring of Diabetic Mothers
Nancy Elbarbary, Mohammed AboElAsrar, Eman El-Hadidy, Marwa Maghrabi
P1-D2-79
Sequence Analysis of 11 Known Causative Genes in Clinically Diagnosed Children as Maturity Onset Diabetes of Youth (MODY) by Next Generation Sequencing
Sebahat Yilmaz Agladioglu, Zehra Aycan, Semra Cetinkaya, Veysel Nijat Bas, Asan Onder, Havva Nur Peltek Kendirci, Haldun Dogan, Serdar Ceylaner
P1-D2-80
Methylmalonic acidemia (MMA) with unusual presentation mimicking diabetic ketoacidosis (DKA)
Prapai Dejkhamron, Karn Wejaphikul, Kamornwan Katanyuwong, Kevalee Unachak, Duangrurdee Wattanasirichaigoon, Pranoot Tanpaiboon
P1-D3-189
An Unusual case of Hereditary Nephrogenic Diabetes Insipidus (HNDI) affecting Mother and Daughter
Dinesh Giri, Caroline Jones, Ian Ellis, Renuka Ramakrishnan
P1-D3-190
A rare cause of diabetes insipidus: Congenital proprotein convertase 1/3 deficiency
Gülay Karagüzel, Murat Cakir, Ulas Akbulut, Andreas Janecke, Aysenur Ökten
P1-D3-81
mHealth app for young people with diabetes type 1 transferring from pediatric to adult care.
Grete Teilmann, Kirsten Boisen, Eva Hommel, Birthe Olsen, Ulrik Pedersen-Bjergaard, Pernille Castensøe-Seidenfaden
P1-D3-82
Holding the Horses of Insulin Pump Infusion: Usage and Effectiveness of the Low Glucose Suspend Feature During Fasting in Ramadan Among Adolescents With Type 1 Diabetes Mellitus to Prevent Hypoglycemia
Nancy Elbarbary
P1-D3-83
DKA during diabetes therapy: Multinational comparison with 59,191 Pediatric Patients from England, Wales, the United States, Austria and Germany
Justin Warner, Julia Hermann, Thomas Kapellen, Sabine Hofer, Stephanie Dubose, Des Schatz, Roy Beck, Claudia Schweiger, David Maahs, Reinhard Holl
P1-D3-84
Children and adolescents with type 1 diabetes have higher plasma visfatin levels than healthy controls
Julia Höntzsch, Hildegard Jasser-Nitsche, Marlene Grillitsch, Elisabeth Suppan, Gudrun Weinhandl, Regina Riedl, Christine Barowitsch, Martin Borkenstein, Elke Fröhlich-Reiterer
P1-D3-85
Algorithm-based cholesterol monitoring in diabetic children related to non-diabetic peers
K. Otfried Schwab, Juergen Doerfer, Christa Scheidt-Nave, Bärbel-Maria Kurth, Andreas Hungele, Nicole Scheuing, Andreas Krebs, Axel Dost, Tilman R. Rohrer, Edith Schober, Reinhard W. Holl
P1-D3-86
Implementation of Effective Transition from Paediatric to Adult Diabetes Care with an Outpatient Transition Nurse
Eglantine Elowe-Gruau, Marie-Paule Aquarone, Virginie Schlüter, Sophie Stoppa-Vaucher, Franziska Phan-Hug, Andrew Dwyer, Nelly Pitteloud, Michael Hauschild
P1-D3-87
The natural evolution of impaired glucose homeostasis among obese adolescents in a high - risk diabetes prone population
Nehama Zuckerman-Levin, Idit Pasternak, Sami Najjar, Doron Hermoni, Naim Shehadeh
P1-D3-88
Improved Health-related Quality of Life with insulin therapy in children with Cystic Fibrosis Related Diabetes - a prospective cohort study
Sherly George, Hilary MCV Hoey, Colm Costigan, Nuala Murphy, Edna F Roche, Stephen MP O'Riordan
P1-D3-89
Nutritional status and respiratory function in patients affected by cystic fibrosis and glucose metabolism derangements after 4 years of insulin therapy with glargine.
Enza Mozzillo, Valeria Raia, Valentina Fattorusso, Carla Cerrato, Elena De Nitto, Fabiola De Gregorio, Angela Sepe, Giuliana Valerio, Adriana Franzese
P1-D3-90
The Relationship of Serum 25-Hydroxyvitamin D with Glucose Homeostasis in Obese Children and Adolescents in Zhejiang, China
You-jun Jiang, Ke Huang, Jun-fen FU, Jian-feng LIANG, Hong ZHU, Zhi-wei ZHU, Li-fei HU, Guan-pin DONG, Xue-feng CHEN
P1-D3-91
Feasibility and Acceptability of Robot Assistant in Self-Management of Type 1 Diabetes in Children
Majid Al-Taee, S Abood, Christopher Garrett, Pratik Choudhary, Ritika R Kapoor
P2-D1-319
Simultaneous changes in trends in incidence of children diabetes type 1 in distant geopraphic regions
Noemi Auxiliadora Fuentes-Bolaños, Francisco Javier Arroyo Díez, Violeta Delgado Carballar, Pilar Méndez Pérez, Manuela Núñez Estevez
P2-D1-320
Risk factors for Type 2 diabetes mellitus in secondary school students in Port Harcourt
TAMUNOPRIYE JAJA, IRORO YARHERE
P2-D1-321
Interaction of pubertal development and metabolic control in 1303 adolescents with Diabetes mellitus type 1
Michaela Hamm, Bettina Gohlke, Joachim Wölfle, Katharina Fink, Katja Konrad, Tilman Rohrer, Sabine Hofer, Reinhard Holl
P2-D1-322
Quality of Life and Glycaemic Assessment Before and After Pump School
Patricia Leahy, Norma O'Toole, Susan O'Connell, Stephen O'Riordan
P2-D1-323
Improving paediatric diabetes care with the use of an electronic diabetes information management system (Twinkle.Net) and routine uploading of glucose meters and insulin pumps (Diasend) in outpatient clinic
Sze May Ng, Linda Connellan, Lynne Finnigan
P2-D1-324
Two novel homozygous mutations in WFS1 gene in two Turkish families with mild phenotypic expression of Wolfram syndrome
Maha Sherif, Huseyin Demirbilek, Atilla Cayir, Mehmet Nuri Ozbek, Riza Taner Baran, Ayse Nurcan Cebeci, Sophia Tahir, Sofia Rahman, Mehul Dattani, Khalid Hussain
P2-D1-325
Imbalance between pro-oxidative and anti-oxidative mechanisms in children and adolescents with Type 1 Diabetes Mellitus
Maria Karampali, Ioannis Kyrgios, Stavros Kalogiannis, Efthimia Efstratiou, Assimina Galli-Tsinopoulou
P2-D1-326
Trends in incidence and prevalence of DM type 1 in children in Ukraine during 2002–2012.
Evgenia Globa, Nataliya Zelinska
P2-D1-327
Effectiveness of insulin pump therapy in children and adolescents with type 1 diabetes.
Darya Osokina, Irina Osokina
P2-D1-328
Functional condition of the kidneys (K/DOQI , 2002) by ACE gene I/D polymorphism in children and adolescents with type I diabetes mellitus
Akidahon Sadykova, Gulnara Rakhimova
P2-D2-330
A multicentre study evaluating the risk and prevalence of diabetic retinopathy in children and young people with Type 1 Diabetes Mellitus
Sze May Ng, Omolola O Ayoola, Michael McGuigan, Surendran Chandrasekaran
P2-D2-331
ACE Gene Insertion/ Deletion Polymorphism and ACE enzymatic activity in Egyptian Children withType 1 Diabetes with and without Microalbuminuria
Ghada Anwar, Hafez Bazaraa, Olfat Shaker, Noha Arafa, Mona Hafez, Noha Mousa
P2-D2-332
Game interaction between a humanoid robot and a diabetic teenager: might this improve motivation to fill in the nutritional diary?
Alberto Sanna, Ilaria Baroni, Elettra Oleari, Maria Iole Colombini, Clara Pozzi, Gianni Russo, Andrea Rigamonti, Giulio Frontino, Valeria Favalli, Roseila Battaglino, Clara Bonura, Riccardo Bonfanti, Giusy Ferro, Giuseppe Chiumello
P2-D2-333
A novel AVPR2 mutation (L161P) causing partial nephrogenic diabetes insipidus
Sumie Yamashita, Astuko Hata, Naoto Kaneko, Takeshi Usui, Daisuke Hata
P2-D2-334
New-onset Type 2 diabetes presenting with Hyperglycaemic Hyperosmolar State in a renal transplant patient on growth hormone treatment.
Francesca Harrington, Taffy Makaya, Helen Wolfenden
P2-D2-335
Insulin therapy via tubeless patch pump – really an alternative?
Claudia Boettcher, Maike Schaefer, Lucia Weiss, Stefan A. Wudy
P2-D2-336
GAD antibody positivity is associated with higher prevalence of autoimmun thyroiditis in children with type 1 Diabetes Mellitus
Saygin Abali, Enes Celik, Belma Haliloglu, Serpil Bas, Zeynep Atay, Serap Turan, Abdullah Bereket
P2-D2-337
The length of the deletion in the region 17q contributes to the individual variability of the phenotype of patients with renal cysts and diabetes syndrome (RCAD, HNF1B-MODY)
Stepanka Pruhova, Petra Dusatkova, Michal Malina, Zuzana Slamova, Kveta Blahova, Radana Kotalova, Jiri Dusek, Jan Lebl, Tomas Seeman, Ondrej Cinek
P2-D2-338
Urinary vitamin E metabolites as a biomarker of oxidative stress in type 1 diabetes
Chloe Bulwer, Peter Hindmarsh, Simon Pope, Sally Tollerfield, Ernestas Sirka, Kevin Mills
P2-D2-339
DIRECT COSTS OF DIABETES CARE IN PEDIATRIC PATIENTS WITH TYPE 1 DIABETES IN GREECE
Feneli Karachaliou, Konstantinos Athanasakis, Charalabos Tsendidis, Maria Kitra, Stefanos Michalakos, Kyriaki Karavanaki
P2-D2-723
Estimation of compensation and prevalence of chronic complications of type 1 DM in children according to the screening data
Nasiba Alimova, Gulnara Rakhimova
P2-D2-736
Metabolic compensation correlation with chronic complications of type 1 diabetes in children in Latvia
Zane Eglite, Iveta Dzivite-Krisane, Una Lauga-Tunina, Inara Kirilova
P2-D3-329
Lipid profile is related to androgen level in adolescent girls with type 1 diabetes mellitus
Agnieszka Zachurzok, Grażyna Deja, Aneta Gawlik, Agnieszka Drosdzol-Cop, Ewa Malecka-Tendera
P2-D3-340
Coated Pellets with Controlled Glucose Release in Treatment of Children with Diabetes
David Neumann, Ales Franc, Jan Muselik
P2-D3-341
A RARE CAUSE OF OBESITY AND TYPE2 DIABETES: A NOVEL ALMS1 MUTATION IN TWO SIBLINGS WITH ALSTROM SYDROME
Suna Hancili, Ayla Güven, Süheyla Apaydin, Aylin Ardagil, Diana Valverde Perez
P2-D3-342
Prolonged treatment with vitamin D supplementation and high dose is necessary to treat vitamin D deficiency/insufficiency (VDD/I) in children and adolescents with type 1 diabetes
MARIA XATZIPSALTI, MARIA DOLIANITI, KONSTANTINA PAPADOPOULOU, PENELOPE KOULOUFAKOU, VASILIKI-IOANNA MITRAVELA, MARIA DRACOPOULOU, LELA STAMOGIANNOU, ANDRIANI VAZEOU
P2-D3-343
No association between serum vitamin D and Left Ventricular Mass Index in children and adolescent with type 1 diabetes mellitus
Angeliki Klissarhaki, Kyriaki Papadopoulou-Legbelou, Ioannis Kyrgios, Maria Eboriadou-Petikopoulou, Assimina Galli-Tsinopoulou
P2-D3-344
Lifestyle and Health Related Quality of Life in adolescents with Diabetes Mellitus Type 1.
Enza Mozzillo, Eugenio Zito, Elena De Nitto, Carla Cerrato, Rosa Nugnes, Valentina Fattorusso, Adriana Franzese, Giuliana Valerio
P2-D3-345
Improvement in type 1 diabetes mellitus metabolic control: from conventional to functional insulin therapy
Joana Serra-Caetano, Sara Ferreira, Helena Lourenço, Lina Aveiro, Nanci Batista, Filomena Freitas, Luísa Simão, Rita Cardoso, Isabel Dinis, Alice Mirante
P2-D3-346
TWO CASES OF “UNKNOWN” LIPOPROTEIN LIPASE (LPL) DEFICIENCY AND DIABETES MELITUS
Carla Bizzarri, Sara Ciccone, Stefania Pedicelli, Danila Benevento, Francesca Baldari, Ippolita Patrizia Patera, Maria Cristina Matteoli, Marco Cappa
P2-D3-347
PREDICTORS OF DIRECT COSTS OF PEDIATRIC DIABETES IN GREECE
Feneli Karachaliou, Konstantinos Athanasakis, Charalabos Tsendidis, Maria Kitra, Stefanos Michalacos, Kyriaki Karavanaki
P2-D3-348
Early detection and treatment of Cystic Fibrosis Related Diabetes Mellitus in a Tertiary Paediatric Centre: A Case Series
Eirin Carolan, Claire Murphy, Caoimhe Howard, Dubhfeasa Slattery, Fiona Healy, Ciara Mc Donnell, Nuala Murphy
P2-D3-349
Retinol binding protein 4 and adiponectin levels during oral glucose tolerance test in obese children newly diagnosed of type 2 diabetes
SO HYUN PARK, JAE HONG KIM, kYUNG SOON CHO, MIN SUN CHO, IN A JUNG, SIN HEE KIM, MIN HO JUNG, BYUNG KYU SUH
P2-D3-350
Wellbeing of adolescents with type 1 diabetes: influence of metabolic control and family factors.
Jesse Vanbesien, Laurence Berlanger, Susanne Böhler, Jolien Laridaen, Inge Gies, Sara Van Aken, Kathleen De Waele, Martine Cools, Ellen Maris, Johan Vanderfaeillie, Jean De Schepper
P2-D3-351
Wolcott-Rallison Syndrome: new mutations and report of two cases
Erdal Eren, Esra Deniz Papatya Cakir, Sefika Elmas Bozdemir, Solmaz Celebi, Cécile Julier, Halil Saglam, Omer Tarim
P2-D3-352
Socioeconomic deprivation is associated with increased hospital admissions in children with Type 1 Diabetes Mellitus
Louise Apperley, Sze May Ng
P2-D3-353
Household unemployment and low levels of education are associated with poor glycaemic control in children and young people with Type 1 Diabetes Mellitus
Louise Apperley, Sze May Ng
P2-D3-354
An infant with a novel Kir6.2 mutation causing neonatal diabetes and unexplained lack of response to sulphonylurea
Susan M O'Connell, Aoife McDonald, Norma O'Toole, Anne Bradfield, Maura Bradley, Andrew Hattersley, Sian Ellard, Peter Proks, Katia K Mattis, Frances Ashcroft, Stephen MP O'Riordan
P2-D3-355
Glycaemic control and microvascular complications in adolescents and young adults with type 1 diabetes: outcome following transfer of care to adult services
Suma Uday, Fiona Campbell, James Yong, Ramzi Ajjan
P2-D3-356
DIABETIC KETOACIDOSIS AT THE ONSET OF TYPE I DIABETES: A RETROSPECTIVE STUDY IN A PAEDIATRIC POPULATION.
Gerdi Tuli, Giovanna Maria Ignaccolo, Davide Tinti, Elisa Gioia, Sabrina Sicignano, Franco Cerutti, Ivana Rabbone
P2-D3-357
EARLY-ONSET AUTOINFLAMMATORY PARTIAL LIPODYSTROPHY CHARACTERIZED BY RECURRENT FEVER AND RASH: CANDLE SYNDROME
Korcan Demir, Melek Yildiz, Balahan Makay, Hüseyin Anil Korkmaz, Özlem Nalbantoglu Elmas, Behzat Özkan
P2-D3-358
Is there a change in the presentation of childhood Type-1 Diabetes Mellitus in the last 15 years?: data from a tertiary care center in Turkey
Saygin Abali, Enes Celik, Belma Haliloglu, Serpil Bas, Zeynep Atay, Serap Turan, Abdullah Bereket
P2-D3-359
The Sugarsquare study: a multicenter randomized controlled trial concerning a web-based patient portal for parents of a child with type 1 diabetes
Emiel Boogerd, Christianne Verhaak, Jan Kremer, Judith Prins, Kees Noordam
P2-D3-360
"My diabetes" application for android devices as a diabetes mangement tool
María José Ballester, Luis Alberto Santillana, Rossen Varvanov, Katarzyna Buch-Gasz, Adam Gasz, María José Sanchez, Carmen maría Lopez, Elena Martín, Enrique Palomo
P2-D3-361
Comparison of HbA1c and OGTT to diagnose diabetes in Korean children
Min Sun Kim, Dae-Yeol Lee
P3-D1-699
Efficacy and safety of CSII treatment in paediatric age. Long term experience of a tertiary care centre in Spain.
Belen Roldan, Esmeralda Colino, Maria Martin-Frias, Angeles Alvarez, Rosa Yelmo, Raquel Barrio
P3-D1-700
Diabetic ketoacidosis (DKA) in children with T1DM: an Italian multicentre survey
Stefano Zucchini, Riccardo Bonfanti, Pietro Buono, Francesca Cardella, Vittoria Cauvin, Valentino Cherubini, Giovanni Chiari, Giuseppe D'Annunzio, Anna Paola Frongia, Dario Iafusco, Giulio Maltoni, Patrizia Ippolita Patera, Andrea Scaramuzza, Sonia Toni, Stefano Tumini, Ivana Rabbone
P3-D1-701
Changing Presentation of Type 1 Diabetes to a Tertiary Paediatric Centre
Niamh Mc Grath, SM Mc Glacken-Byrne, CP Hawkes, NP Murphy
P3-D1-702
Abnormal blood glucose as a prognostic factor for adverse clinical outcome among children with acute medical conditions in Ghana.
Emmanuel Ameyaw
P3-D1-703
Urinary C-Peptid/Creatinine Ratio in Children and Adolescents Diagnosed with Maturity-Onset Diabetes of the Young (MODY)
Sebahat Yilmaz Agladioglu, Zehra Aycan
P3-D1-704
A case with neonatal diabetes and congenital hypothyroidism due to GLIS3 gene deletion
Ilker Tolga Ozgen, Mehmet Kücükkoc, Jayne Houghton, Selim Gökce, Yasar Cesur
P3-D1-705
Glycemic control of patients with type 1 Diabetes using automated bolus calculator glucometer
Jaime Cruz Rojo, Lucía Garzón Lorenzo, Jaime Sánchez del Pozo, Mª Elena Gallego Gómez
P3-D1-706
CONGENITAL HYPERINSULINISM LINKED TO INS-R MUTATION: CASE REPORT
Marcello Vitaliti, Maria Cristina Maggio, Giuliana Vitaliti, Valeria Grasso, Amalia Ciofalo, Grazia Rinaudo, Elisa Tranchina, Giuseppina Costantino, Giovanni Corsello, Fabrizio Barbetti
P3-D1-707
The Lung Endothelin System: A Potent Therapeutic Target with Bosentan for The Amelioration Of Lung Alterations In A Rat Model of Diabetes Mellitus
Atilla Cayir, Zekai Halici, Erol Akpinar, Zafer Bayraktutan, Mustafa Kara
P3-D1-708
Clinical significance of typing fulminant type 1 diabetes in children and adolescents
yi wang, chunxiu gong
P3-D1-709
Continuous Subcutaneous Insulin Infusion Therapy in Preschool Children with Type 1 Diabetes Mellitus
Rita Moinho, Dora Martins, Ângela Almeida, Estefânia Maia, Nanci Batista, Lina Aveiro, Rita Capitão, Rita Cardoso, Isabel Dinis, Alice Mirante
P3-D1-710
Health-related quality of life among Turkish children and adolescents with type 1 diabetes
Turgay Aydin, Cengiz Kara
P3-D2-712
Audit of the use of integrated care pathway in the management of Diabetic keto acidosis in children
Ravi Palakurthi, Kamal Weerasinghe
P3-D2-713
Development of diabetes mellitus after hematopoietic stem cell transplantation for childhood leukemia
In Ah Jung, Yeon Jin Jun, Won Kyoung Cho, Jae Wook Lee, Nak Gyun Chung, Min Ho Jung, Bin Cho, Byung Kyu Suh
P3-D2-714
Case of family neonatal diabetes with KCNJ11 gene mutation
Svitlana Chumak, Olena Budreiko, Evgeniy Globa
P3-D2-715
Insulin pump therapy in one case of 6q24 Transient Neonatal Diabetes for three years
Liu Wangkai, Li Xiaoyu, Su Yihua, Zhuang Siqi, Li Yijuan, Ma Huamei, Du Minlian, Chen Weiqi
P3-D2-716
Uptake of a novel tool to adjust insulin boluses, based on CGM trend arrows and insulin sensitivity (Trend Arrow Adjustment Tool); in children with type 1 diabetes, who are using insulin pump therapy and continuous glucose monitoring.
Emmeline Heffernan, Margaret Lawson
P3-D2-717
Diabetes Mellitus a late complication in glycogen storage disease Type 1b
Kiran Kumar, Pooja Sachdev, Tabitha Randell, Louise Denvir
P3-D2-718
INCIDENCE OF DIABETES MELLITUS AND ASSOCIATED COMPLICATIONS AMONG CHILDREN: RESULTS FROM AZERBAIJAN DIABETES REGISTRY 1997-2007
Gunduz Ahmadov
P3-D2-719
Arabic Translation and Validation of the Newest Vital Sign Health Literacy Tool: A Pilot Project to Test Health Literacy of Caregivers of Children with Type 1 Diabetes in Kuwait
Dalia Al-Abdulrazzaq, Muneera Al-Haddad, Majedah AbdulRasoul, Iman Al-Basari, Abdulla Al-Taiar
P3-D2-720
ANTI-CYCLIC CITRULLINATED PEPTIDE ANTIBODIES ARE NOT FREQUENT IN CHILDREN WITH TYPE 1 DIABETES
Melek Yildiz, Figen Isleten, Korcan Demir, Nilüfer Celik, Hüseyin Anil Korkmaz, Birsen Tuglu, Özlem Nalbantoglu Elmas, Behzat Özkan
P3-D2-721
GLYCEMIC VARIABILITY AND METABOLIC CONTROL IN PEDIATRIC PATIENTS WITH TYPE 1 DIABETES MELLITUS
Maria Martin-Frias, M Belen Roldan, M Milagros Alonso, Yoko Patricia Oyakawa, Daniel Alonso, Raquel Barrio
P3-D2-722
Knowledge base and attitudes of senior medical staff to insulin therapy in children with diabetes
Amith Nuti, Christopher Bidder, Geraldine Phillips, Puvaneswary Vamadevan, Carol Fraser
P3-D2-737
IGF-I levels in children with type 1 diabetes are primarily related to glycemic control and residual beta cell mass, and not affected by different modalities of insulin therapy
Carla Bizzarri, Danila Benevento, Ippolita Patrizia Patera, Romana Marini, Marzia Bongiovanni, Marco Anziano, Marco Cappa
P3-D2-738
When should we suspect maturity onset diabetes of the young in children and adolescents?
Sarar Mohamed, Iman Talaat, Ali Hellani
P3-D2-739
Cystic Fibrosis-Related Diabetes in children and adolescents in the Russian Federation. Kondratyeva E.I. Kapranov N.I. Sherman V.D Research and Clinical Department of cystic fibrosis Medical Genetics Research Center, Russian Federation
elena Kondratyeva, Nicolay Kapranov, Victoria Sherman
P3-D2-740
Continuous Glucose Monitoring System (CGMS) in the Diagnosis of Early Glycemic Abnormalities in High Risk Groups
Ashraf Soliman, Mohamed Yassin, Ahmed Elawwa, Rania Elalaily, Vincenzo De sanctis
P3-D2-741
Incidence of dyslipidemia and its association with glycemic control in adolescents and young adults with type 1 diabetes
Shin-Hee Kim, In-Ah Jung, Won Kyoung Cho, Kyoung Soon Cho, So Hyun Park, Min Ho Jung, Byoung Kyu Suh
P3-D2-742
“Learning by doing approach”: use of multimedia applications in type 1 diabetic children.
Federica Ortolani, Marcella Vendemiale, Albina Tummolo, Pierpaolo Di Bitonto, Veronica Rossano, Teresa Roselli, Elvira Piccinno
P3-D2-743
Seip Berardinelli Syndrome Case Report
Doly Pantoja, Liliana Mejia
P3-D2-744
9-year old boy with Wolfram syndrome - case report
Ewa Jakubowska, Justyna Michalak, Bożena Florys, Wojciech Młynarski, Agnieszka Zmysłowska, Agnieszka Szadkowska, Włodzimierz Łuczyński, Barbara Olszewska-Głowińska, Artur Bossowski
P3-D2-745
A case of type 2 diabetes associated with ichthyosis : Chanarin-Dorfman syndrome
Nihal Hatipoğlu, Deniz Ökdemir, Leyla Akın, Songül Gökay, Fatih Kardaş, Mustafa Kendirci, Ülkü Gül, Selim Kurtoğlu
P3-D2-746
CURRENT STATUS OF DIABETES MANAGEMENT , GLYCEMIC CONTROL AND COMPLICATIONS IN CHILDREN AND ADOLESCENTS WITH DIABETES: A REGISTRY-BASED STUDY IN EGYPT. WHERE DO WE STAND NOW? AND WHERE DO WE GO FROM HERE?
Nancy Elbarbary, Mona Elsamahy, Hala Elmorsi
P3-D2-747
Comparison the clinical efficacy of autologous hematopoietie stem cell transplantation and traditional insulin therapy in newly diagnosed primary childhood type 1 diabetes.
GU YI, GONG Chunxiu, Peng xiaoxia, Wei liya, Su Chang, Li fengting, Wang Yi
P3-D3-724
Prevalence of impaired glucose tolerance and insulin resistance in a sample of the 6- to 16-year-old overweight or obese pediatric population
Fatemeh Saffari, Mahmood Vandaei, Sonia Oveisi, Neda Esmailzadehha
P3-D3-725
Differences in pubertal development and anthropometry between normal population and type1 diabetic child at debut in Spain
Ignacio Diez-Lopez, Ainhoa Sarasua-Miranda, Sonia Sanchez-Antonio, Isabel Lorente-Blazquez
P3-D3-726
Effect Of Vitamin D Treatment On Glucose And Insulin Metabolism, And Bone Turnover In Children With Symptomatic Vitamin D Deficiency
Nagla El-fakhri, Martin McMillan, Jane McNeilly, S.F Ahmed, Helen McDevitt
P3-D3-727
Evaluation of HbA1c measurement in Trinidad and Tobago
Maynika Rastogi, Paul Ladenson, David Goldstein, Randie Little
P3-D3-728
THE RESULT OF SULPHONYLUREAS TREATMENT IN PATIENTS WITH NEONATAL DIABETES MELLITUS DUE TO KCNJ11/ABCC8 GENE MUTATIONS IN VIETNAM
Ngoc Can Thi Bich, Dung Vu Chi, Thao Bui Phuong, Khanh Nguyen Ngoc, Dat Nguyen Phu, Sian Ellard, Maria Craig, Hoan Nguyen Thi
P3-D3-729
Prevalence of secondary diabetes and related factors in China Hospitalized children
LI Yu-Chuan, CAO Bing-yan, GONG Chun-xiu, LIANG Xue-jun
P3-D3-730
Wolcott-Rallison Syndrome In Two Siblings With No Implication Of EIF2AK3 Mutation
Ayca Altincik, Bayram Ozhan, Sarah Flanagan, Sian Ellard
P3-D3-731
Prevalence of atopic diseases in diabetic children and adolescents
Hildegard Jasser-Nitsche, Eva-Maria Varga, Elke Fröhlich-Reiterer, Julia Höntzsch, Lisa Pieringer, Alexander Avian, Martin Borkenstein
P3-D3-732
The Pattern of Body Composition Change in Type 1 Diabetes by Gender
Yong Hyuk Kim, Hye Won Park, Kyo Sun Kim, Sochung Chung
P3-D3-733
Transient Neonatal Diabetes and intermediate DEND phenotype with KCNJ11 mutation
Ana Laura Fitas, Rita Belo Morais, Eulália Viveiros, Anabela Simões, Ana Raposo, João Anselmo, Catarina Limbert, Lurdes Lopes
P3-D3-734
Offspring of parents with obesity. Complex investigations. Risk of carbohydrate disturbances and diabetes.
Renata Wasik, Maria Dziura, Aleksander Basiak
P3-D3-735
Metabolic control in a pediatric population with type 1 diabetes mellitus
Joana Andrade, Clara Gomes, Assunção Luís, Gabriela Laranjo, Joana Campos
P3-D3-748
Monogenic Diabetes in a Paediatric Population: finding the needle in the haystack.
M Mavinkurve, N Johnston, A Carroll, C Mc Donnell, M M Byrne, N P Murphy
P3-D3-749
Hyperglycemia – MODY a diagnosis to remember
Ricardo Monteiro, Ana Laura Fitas, Marta Amado, Rosa Pina, Lurdes Lopes
P3-D3-750
A case of Type 1 Diabetes associated with cerebellar ataxia: Stiff-person syndrome
Selim Kurtoğlu, Deniz Ökdemir, Nihal Hatipoğlu, Leyla Akın, Ülkü Gül, Mehmet Canpolat, Mustafa Kendirci
P3-D3-751
Continuous glucose monitoring (CGMS) versus oral glucose tolerance test (OGTT) and glycated hemoglobin(HbA1C) in the evaluation of glycemic abnormalities in an obese adolescent before versus after partial gastrectomy.
Ashraf Soliman, Aml Sabt, Fawzia Alyafei, Nagwa Eldarsy
P3-D3-752
The psychological impact of diabetes on glycaemic control in affected Saudi children at different developmental age groups
Amir Babiker, Mona El Rashid, Nasir Al Jurayyan, Maralyn Druce, Aban Bahebri, Mohamed El Ahmedi, Ahmed H Errasoul, Hala Gasim, Simon Coppack
P3-D3-753
Type 1 diabetes mellitus in pediatric population: chronic complications and associated diseases
Joana Andrade, Clara Gomes, Assunção Luís, Gabriela Laranjo, Joana Campos
P3-D3-754
Ketoacidosis-associated stroke: cerebral infarction
zerrin orbak, hakan doneray, seda yesilcibik, mecit kantarci, huseyin tan, nuran kucuk, celalettin kosan
P3-D3-755
MULTIPLE DAILY INJECTIONS SINCE THE DIAGNOSIS OF TYPE 1 DIABETES MELLITUS IN CHILDREN AND ADOLESCENTS – ASSESSMENT OF 3 YEARS
Rita Cardoso, Dora Martins, Nanci Batista, Lina Aveiro, Rita Capitão, Helena Ribeiro, Filomena Freitas, Luisa Simão, Isabel Dinis, Alice Mirante
P3-D3-756
Haemolysis and acute pancreatitis during diabetic ketoacidosis treatment in a 14-year-old boy with unknown glucose-6-phosphate dehydrogenase deficiency.
Federica Ortolani, Albina Tummolo, Cataldo Torelli, Maristella Masciopinto, Stefania Fedele, Maria Paola Lanzillotto, Francesco Nicastro, Francesco Papadia, Marcella Vendemiale, Elvira Piccinno
P3-D3-757
Pneumothorax, pneumomediastinum and subcutaneous emphysema: complications of severe DKA in T2DM obese patient.
Federica Ortolani, Albina Tummolo, Cataldo Torelli, Maristella Masciopinto, Stefania Fedele, Francesco Nicastro, Francesco Papadia, Marcella Vendemiale, Elvira Piccinno
P3-D3-758
DIABETES INSIPIDUS IN PEDIATRIC PRACTICE Sultanova Sh.T. * Bobohodzhaeva Sh.A. ** The center for the Scientific and clinical study of Endocrinology, Republic of Uzbekistan , Tashkent * . Tashkent Pediatric Medical Institute, Department of Pediatric Endocrinology ** Contact e-mail: sultanova_69@mail.ru.
Shakhrizada Sultanova, Shakhlo Bobohodzhaeva
LB-D3-1010
Effect of Triptorelin 3.75 mg subcutaneously injection every 6 weeks on adult height in girls with idiopathic central precocious puberty
Yan Liang, Hong Wei, Jie Li, Ling Hou, Jianling Zhang, Wei Wu, Yanqin Ying, Xiaoping Luo
P1-D1-200
Testes in infants with Prader-Willi syndrome: hCG treatment, surgery and histology
Nienke Bakker, Katja Wolffenbuttel, Leendert Looijenga, Anita Hokken-Koelega
P1-D2-211
The incidence of childhood Gonadoblastoma over fifteen years in the Republic of Ireland
Susan M O'Connell, Sally-Ann Lynch, David Coyle, Michael McDermott, Maureen O'Sullivan, Edna Roche, Feargal Quinn, Declan Cody
P1-D2-215
Serum inhibin-B values in boys with unilateral cryptorchidism and boys with unilateral vanished testis
Dina Cortes, Jorgen Thorup
P1-D2-220
Successful treatment of male congenital hypogonadotropic hypogonadism with rFSH pretreatment followed by GnRH
Haruo Mizuno, Kohei Aoyama, Shinji Saitoh
P1-D3-15
Testicular adrenal rest tumors and Sertoli cell function in adolescents with CAH
Igor Chugunov, Maria Kareva, Elizaveta Orlova, Elvira Kuznecova, Sergey Bogolubov
P1-D3-228
Impact of bisphenol-A on the puberty of female rats
chen linqi
P1-D3-229
The role of Bisphenol A in etiopathogenesis of polycystic ovary syndrome in adolescent girls
Leyla Akin, Mustafa Kendirci, Figen Narin, Selim Kurtoglu, Recep Saraymen, Meda Kondolot, Selda Ozkan Kocak, Nihal Hatipoglu, Ferhan Elmali
P2-D1-529
Is there any influence of TSH serum levels on insulin resistance in euthyroid adolescents with polycystic ovary syndrome?
Alice Albu, Serban Radian, Suzana Florea, Simona Fica
P2-D1-530
The Vaginal Maturation Index as a marker of local sensitivity to estrogens in girls with congenital adrenal hyperplasia (CAH) during puberty
Irina Kopylova, Sofya Blokh, Elizaveta Orlova, Irina Yarovaya, Maria Kareva
P2-D1-531
Very low Estradiol levels are independent from duration of amenorrhea in girls with severe Anorexia Nervosa
Christèle Kyheng, Gianpaolo De Filippo, Anne-Laure Castell, Jennifer Flandrin, Julie Durin, Manon Delafoy, Lise Duranteau
P2-D1-532
Evaluation Of The Free Androgen Index in Adolesent Females Diagnosed With Obesity, Hirsutism and PCOS
ELIF SAGSAK, ZEHRA AYCAN, MELIKSAH KESKIN, SENAY SAVAS ERDEVE, FUNDA CENESIZ, FATMA DOGA OCAL, SEMRA CETINKAYA
P2-D1-533
Polycystic Ovarian Syndrome in Adolescents (PCOS): Metabolic profile at diagnosis, during and after treatment with Oral Contraceptive (OC)
Andrea Arcari, Mirta Gryngarten, María Gabriela Ballerini, Analía Freire, María Eugenia Rodríguez, María Gabriela Ropelato, Ignacio Bergadá, María Eugenia Escobar
P2-D1-534
Endocrine disruptors and polycytic ovary syndrome:Phthalates
Leyla Akin, Mustafa Kendirci, Figen Narin, Selim Kurtoglu, Meda Kondolot, Recep Saraymen, Selda Ozkan Kocak, Nihal Hatipoglu, Ferhan Elmali
P2-D1-535
Corrlation research of Bisphenol A and Permature Thelarche in 6months to 2years old infant girls
haiying Wu, linqi Chen, guangzhao He, weipeng Wang
P2-D3-808
PHENOTYPIC and genotypic characteristics of patients with Turner syndrome
Soumeya Fedala, Mahdi Haddam, Farida Chentli, Djamila Meskine, Lyna Akkache, Hafsa Si youcef
P3-D3-799
EFFECTS OF GnRH ANALOGUE TREATMENT ON INTERNAL GENİTALES OF GIRLS WITH CENTRAL PRECOCIOUS
Havva Nur Peltek Kendirci, Zehra Aycan, Elif Sagsak, Yasemin Tasci Yildiz
P3-D3-800
Ovarian tumors observed in endocrinology
Amina Laloui, soumeya fedala, Ali el mahdi haddam, farida chentli, djamila meskine, leyla ahmed ali, fetta amel yaker
P3-D3-801
The usefulness of the Leuprolide stimulation test as a diagnostic method of idiopathic CPP in girls.
Joan Bel, Marta Murillo, Federico Carretto, Maria Martinez, Marisa Granada, Isabel Salinas
P3-D3-802
The effects of Rhythmical Massage Therapy and Heart rate variability-biofeedback on primary dysmenorrhea. A qualitative Study
Anna Böning, Aurelia Karutz, Jan Vagedes, Bettina Berger, David Martin
P3-D3-803
Menstrual Regularity among Early Menarche girls and CPP or EFP girls treated with GnRHa
Chen Qiuli, Li Yanhong, Su Zhe, Ma Huamei, Chen Hongshan, Zhang Jun, Du Minlian
P3-D3-804
COMPLETE BLOOD COUNT PARAMETERS IN GIRLS WITH POLYCYSTIC OVARY SYNDROME
AHMET UCAKTURK, FATMA DEMIREL, MELTEM TAYFUN, DERYA TEPE, SELIN ELMAOGULLARI, OZLEM KARA
P3-D3-805
The Genotypic and Phenotypic Variability of Mixed Gonadal Dysgenesis
Chelsey Grimbly, Robert Couch, Rose Girgis
P3-D3-806
A rare cause for 46,XX ovarian dysgenesis: Perrault syndrome
Gülay Karagüzel, Aysenur Ökten
P3-D3-807
A rare cause of ovarian failure; ovarioleucodystrophy
Erkan Sari, Mutluay Arslan, Ediz Yesilkaya, Sebahattin Vurucu, Murat Kocaoglu, Bulent Unal
P3-D3-809
THREE SIBLINGS WITH GONADAL DYSGENESIS
Fatma Dursun, Heves Kirmizibekmez
LB-D3-1012
Total and acylated Ghrelin levels in children and adolescents with growth retardation
Mitra Nourbakhsh, Mona Latifi, Davod Ilbeygi, Maryam Razzaghy Azar
P1-D1-135
The association between adipocytes and growth is mediated by growth and differentiation factor (GDF) 5
Biana Shtaif, Nitzan Dror, Meytal Bar-Maisels, Moshe Phillip, Galia Gat-Yablonski
P1-D1-136
A homozygous point mutation in the GH1 promoter (-161T>C) leads to reduced GH expression in siblings with isolated GH deficiency (IGHD)
Joao Madeira, Regina Martin, Luciana Montenegro, Marcela Franca, Everlayny Costalonga, Fernanda Correa, Aline Otto, Ivo Arnhold, Helayne Freitas, Ubiratan Machado, Berenice Mendonca, Alexander Jorge, Luciani Carvalho
P1-D1-137
Growth differentiation factor 15 and fibroblast growth factor 21: novel biomarkers for mitochondrial diseases
Shuichi Yatsuga, Yasutoshi Koga
P1-D1-138
A Novel Homozygous Mutation of the IGF1 Receptor Gene (IGF1R) in Two Siblings with Severe Short Stature, Intellectual Disability, Congenital Malformations and Deafness.
Isabelle Maystadt, Shayne F Andrew, Jean De Schepper, Nathalie Wauters, Geert Mortier, Valerie Benoît, Pascal Joset, Beatrice Oneda, Ron G Rosenfeld, Anita Rauch, Vivian Hwa
P1-D1-142
Parental Gonadal Mosaicism for Braf Mutation in Cardiofaciocutaneous Syndrome
Sarah Geoghegan, Rose Morrissey, jeniffer Shorto, Simon Ramsden, Stephen O'Riordan, Andrew Green, Susan O'Connell
P1-D1-143
Mitochondrial DNA in Placenta: Associations with Fetal Growth and Superoxide Dismutase Activity
Marta Díaz, Gemma Aragonés, David Sánchez-Infantes, Judit Bassols, Francis De Zegher, Abel López-Bermejo, Lourdes Ibáñez
P1-D1-145
Genotype-phenotype relationship in patients with SHOX region rearrangements detected by MLPA in the French population
Julie AUGER, Amandine BAPTISTE, Gaëlle THIERRY, Jean-Marc COSTA, Mélanie AMOUYAL, Marie-Laure KOTTLER, Renaud TOURAINE, Marine LEBRUN, Bruno LEHEUP, Sébastien SCHMITT, Valérie CORMIER-DAIRE, Nicolas DE ROUX, Caroline ELIE, Jean-Paul BONNEFONT
P1-D1-146
Analysis of growth hormone receptor gene expression in idiopathic tall stature children.
Sara Pagani, Giorgio Radetti, Cristina Meazza, Mauro Bozzola
P1-D1-147
The role of SHOX gene in Idiopathic Short Stature: an Italian multicenter study.
Roberta Minari, Alessandra Vottero, Sara Azzolini, Daniele Barbaro, Giuseppe Bindi, Mauro Bozzola, Carlo Burrai, Giuliana M. Cardinale, Daniela Cioffi, Mariangela Cisternino, Maria Susanna Coccioli, Maurizio Delvecchio, Enrica Fabbrizi, Mara Ferrari, Federica Gallarotti, Francesco Gallo, Lucia Ghizzoni, Maria Cristina Maggio, Benedetta Mainetti, Raffaele Montinaro
P1-D2-150
Cognitive Processing Speed as a function of growth hormone treatment in short stature children: a multiple regression analysis.
John Eric Chaplin, Berit Kriström, Björn Jonsson, Torsten Tuvemo, Kerstin Albertsson-Wikland
P1-D2-152
Longitudinal growth of healthy preterm infants born below 37 gestation weeks
Niina Hyvönen, Panu Kiviranta, Antti Saari, Leo Dunkel, Ulla Sankilampi
P1-D2-156
Gender Difference in Secular Trend in Sweden
Anton Holmgren, Aimon Niklasson, Andreas F.M. Nierop, Lars Gelander, Agneta Sjöberg, Stefan Aronson, Kerstin Albertsson-Wikland
P1-D2-157
Autoantibodies against some selected appetite-regulating peptide hormones and neuropeptides are present in serum of short children with Candida albicans colonisation and Helicobacter pylori infection.
Renata Stawerska, Elżbieta Czkwianianc, Agnieszka Matusiak, Joanna Smyczyńska, Sylwia Prymus-Kasińska, Maciej Hilczer, Magdalena Chmiela, Andrzej Lewiński
P1-D2-158
Effects of Methylphenidate on Growth and Appetite in Attention-Deficit Hyperactivity Patients
Fatih Gurbuz, Berrak Bilginer Gurbuz, Gonca Celik, Veli Yildirim, Ahmet Ucakturk, Eda Mengen, Ali Kemal Topaloglu, Bilgin Yuksel
P1-D2-159
How precisely can we measure increments of bone age and Bone Health Index with an automated method in boys with Klinefelter syndrome?
Hans Henrik Thodberg, Martha Bardsley, Ania Gosek, Judith L Ross
P1-D3-162
Infliximab improves growth in paediatric Crohn`s disease only if commenced early in puberty or prior to the onset of puberty
Arundoss Gangadharan, Joanna Metcalf, Dinesh Giri, Sharon Irving, Marcus Auth, Krishnappa Venkatesh, Balaji Krishnamurthy, Joanne C Blair, Mohammed Didi
P1-D3-167
Aromatase Inhibitors in Girls: Anastrazole Combined to an LHRH Analogue is a Safe and Effective Strategy in Girls with Early or Precocious Puberty with Compromised Growth Potential.
DIMITRIOS T. PAPADIMITRIOU, ELENI DERMITZAKI, VASSILIKI PAPAEVANGELOU, ANASTASIOS PAPADIMITRIOU
P1-D3-169
Recombinant human growth hormone therapy allows to reach a normal final adult height in coeliac children with growth hormone deficiency due to hypophysistis
Lorenzo Iughetti, Laura Lucaccioni, Patrizia Bruzzi, Anna Rita Di Biase, Anna Maira De Bellis, Barbara Predieri
P1-D3-171
Safety and efficacy results of a 6 month, randomized, multi-center trial of a novel long-acting rhGH (VRS-317) in naïve to treatment, pre-pubertal children with Growth Hormone Deficiency (GHD)
George M. Bright, Wayne V. Moore, H.Q, Nguyen, Gad B. Kletter, Bradley S. Miller, Douglas G. Rogers, Eric Humphriss, Jeffrey Cleland
P2-D1-449
FIBROBLAST GROWTH FACTOR 21 IS INVERSELY ASSOCIATED WITH GROWTH RATES IN INFANCY.
Veronica Mericq, Francesco De Luca, Maria_Isabel Hernandez, Veronica Peña, Katherine Rossel, Gabriel Cavada, Alejandra Avila, German Iñiguez
P2-D1-450
Identification of NPR2 mutations in disproportionate short stature
Alfonso Hisado-Oliva, Sara Benito-Sanz, Alberta Belinchón, Elena Vallespin, Angela del Pozo, Ana C. Barreda-Bonis, Joaquin Ramirez, Cristina Luzuriaga, Isabel González-Casado, Ángel Campos-Barros, Karen E. Heath
P2-D1-451
ELEVEN YEARS OF LETROZOLE TREATMENT IN A CHILD WITH 11-β HYDROXYLASE DEFICIENCY: EFFECT ON BONE AGE AND HEIGHT PROGNOSIS
Abdullah Bereket, Zeynep Atay, Tulay Guran, Belma Haliloglu, Saygin Abali, Serpil Bas, Serap Turan
P2-D1-452
RASOPATHIES: ASSESSMENT OF GROWTH, GENETIC STUDY, GENOTYPE-PHENOTYPE CORRELATION AND THERAPEUTIC RESPONSE TO GROWTH HORMONE IN NOONAN SYNDROME
Claudia Heredia, Francisco Barros, Lidia Castro-Feijóo, Jesús Barreiro Conde, Paloma Cabanas Rodríguez, Manuel Pombo Arias
P2-D1-453
New Reference for Height in Swedish Boys and Girls
Kerstin Albertsson-Wikland, Aimon Niklasson, Lars Gelander, Anton Holmgren, Andreas F.M. Nierop
P2-D1-454
Endocrine characteristics of patients with anorexia nervosa in a large paediatric study cohort
Moritz Toenne, Nicolin Datz, Sabine Heger, Rainhard Hartmann, Thomas Danne, Gerd Kuznik, Burkhard Neuhaus, Olga Kordonouri
P2-D1-455
The Effect of Long Term Growth Hormone Therapy in Discordant Twins Where One Twin is Born Small for Gestational Age: A Case Control Study
Johannes Letshwiti, Elaine O'Mullane, Hilary Hoey, Edna Roche
P2-D1-456
How early is the rise in Leptin levels in Small for gestational Age children with catch up growth?
Ainam Gupta, Sangita Yadav, Siddharth Ramji, T.K. Mishra
P2-D1-457
Relation between CNP and the effect of combined treatment with GnRHa and GH on the linear growth in mid/late pubertal girls with central precocious puberty or early and fast puberty at great bone ages
Hua-mei MA, Zhe SU, Yin-ya LI
P2-D1-458
Two duplications within PAR1 in a family with idiopathic short stature
Barbora Obermannova, Jana Drabova, Petra Dusatkova, Jan Lebl
P2-D1-459
Comparison between Growth hormone (GH) assays. Serum GH cut-off levels by ECLIA performed in pharmacologhical estimulation tests (PhT) in children with short stature
Cecilia Aguirre, Gabriela Sobrero, Giselle Schvab, Liliana Silvano, Julia Alvarez, Mariana Ochetti, Maria Lescurat, Alejandra Paez, Liliana Muñoz, Silvia Martin, Mirta Miras
P2-D1-460
Skeletal Disproportion and Final Adult Height In Childhood-Onset Crohn’s Disease
Avril Mason, Jelena Iljuhhina, Susan Laird, David Ross, Syed Faisal Ahmed, Dan R Gaya, Konstantinos Gerasamidis
P2-D2-461
Anophthalmia, abnormal pituitary development and suboptimal response to growth hormone therapy in two children with microdeletions of 14q22q23
Petra Dusatkova, Zuzana Slamova, Zdenek Sumnik, Martina Simandlova, Elsa Zemankova, Zdenek Sedlacek, Jan Lebl
P2-D2-462
Adiponectin levels as early marker of insulin resistance in children born small for gestational age in our cohort
Sangita Yadav, Ainam Gupta, Siddharth Ramji, T.K. Mishra
P2-D2-463
Recombinant human growth hormone effects on growth and clinical status in cystic fibrosis
Robabeh Ghergherehchi, Mandana Rafeey, Afshin Habibzadeh, Masoud Zamani, Khalil Ansarin, Mahnaz Sadeghi Shabestari
P2-D2-464
Interrelationships between BMI and other overweight related anthropometric variables in childhood
Bente Brannsether, Geir Egil Eide, Mathieu Roelants, Robert Bjerknes, Pètur Benedikt Jùlìusson
P2-D2-465
Assessment of omentin-1, vaspin and visfatin levels in pediatric patients with growth hormone deficiency
Beata Sawicka, Hanna Borysewicz-Sanczyk, Aneta Zasim, Ewa Jakubowska, Artur Bossowski
P2-D2-466
Normal growth in aromatase excess syndrome by pharmacological inhibition of aromatase activity
Beate Deubzer, Gerhard Binder
P2-D2-467
The effect of the environmental factors on growth pattern of Turkish children having the same genetic origin
Sevil Ari Yuca, Yasar Cesur, Selim Kurtoglu, Mumtaz Mustafa Mazicioglu, Emine Ayca Cimbek
P2-D2-468
Successful Growth Hormone (GH) treatment for severe growth failure in paediatric patients with Anorexia Nervosa
Anne Fjellestad-Paulsen, Anne Bargiacchi, Catherine Doyen, Cecile Raverdy, Jean-Claude Carel, Marie-France Leheuzey, Juliane Leger
P2-D2-469
The analysis of limb segments length and body proportion of children and adolescents aged 6-17 years in the main urban area of Chongqing
yanhua jiao, min zhu, feng xiong
P2-D2-470
SEVERE SHORT STATURE DUE TO A HETEROZYGOUS IGF1R MUTATION WITH A GOOD RESPONSE TO rhGH THERAPY: A FAMILY STUDY
Victoria Borrás-Pérez, Monica Fernández-Cancio, Ana Gómez-Núñez, M. Catalá-Puigbó, Laura Audí, Angel Campos-Barros
P2-D2-471
When and why should we investigate the SRCAP gene in cases of short stature?
Luiza Silveira Lucas, Kym M Boycott, Sarah M Nikkel, Elizabeth Lemos Silveira Lucas
P2-D2-472
Body Proportions estimated by Photometry
Willem Jan Gerver, Ralph Brecheisen, Bas Penders, Saartje Straetemans
P2-D2-473
Growth Hormone Deficiency (GHD) in a child with de novo 2q31.1 microdeletion
Irene Kaloumenou, Feneli Karachaliou, Elpis-Athina Vlachopapadopoulou, Aspasia Fotinou, Stefanos Michalacos
P3-D1-822
Auxological evaluation of “non-identical twins”
Raluca-Monica Pop, Marian Pop, Ionela Pascanu
P3-D2-835
An unusual case of a child with Growth Hormone Deficiency and Arnold-Chiari malformation type I.
MARIA XATZIPSALTI, IOULIA POLYCHRONI, ANDRIANI VAZEOU, LELA STAMOGIANNOU
P3-D2-849
Growth Hormone Therapy in Prepubertal Children – Results after 4 years
Corina Galesanu, Andra Iulia Loghin, Ilinka Grozavu, Luminita Apostu, Didona Ungureanu, Mihail Romeo Galesanu
P3-D2-850
A follow-up Study up to adult height of the patients included in the phase III clinical trial with the Biosimilar human recombinant Growth Hormone (Omnitrope®) on the treatment of Spanish children with Growth Hormone Deficit
Victoria Borras, Juan Pedro Lopez Siguero, Gabriela Martinez, Raquel Corripio, Juan Fernanadez, Jose Labarta, Marta Ferrer, Nuria Cabrinety, Pablo Prieto, Marta Ramon, Jordi Bosch, Rafael Espino, Margarida Palla Garcia
P3-D2-851
Growth pattern of the Nigerian child compared to International references
Jerome Elusiyan, MaryAnn Ugochi Ibekwe, Y Alkali, J. Chizo Agwu
P3-D2-852
Evaluation of potential waste of growth hormone across available growth hormone pen devices and an electronic growth hormone delivery device
JC Locklear, NC Edwards, AL Phillips
P3-D2-853
Switching from the original to the biosimilar recombinant human Growth Hormone - Omnitrope®: an experience of a single paediatric centre in Spain
Ana Gomez Gila, Margarida Palla Garcia
P3-D2-854
Descriptive Analysis of Medication Adherence for Patients Treated with Growth Hormone Therapy
SL Michels, C Uribe, Y Li, DM Meletiche, FF Velez, JC Locklear
P3-D2-855
EFFECT OF CONGENITAL HEART DISEASE ON PLACENTAL AND BIRTH SIZE.
Ashraf Soliman, Emad Shatlah, Aml Sabt, Fawzia Alyafei, Mohanad Alqadi
P3-D2-857
Differences in personality of monozygotic twins can be predicted by difference in birth weight in teen monozygotic twins
Lioba Wimmer, Joachim Woelfle, Peter Bartmann, Sandra Schulte, Bettina Gohlke
P3-D2-858
THE GROWTH SPEED OF LATE PRETEM INFANTS AGED 1 YEAR
cheng qian
P3-D2-859
Response of Growth Hormone Therapy in Six Children with Achondroplasia.
Yoon Jung Kim, Byung Wook Cho, Ji Yoon Kim, Heung Sik Kim, Hee Jung Lee
P3-D2-860
Clinical Expression of Familial Williams-Beuren Syndrome in a Turkish Family
Mesut Parlak, Banu Guzel Nur, Ercan Mihci, Erdem Durmaz, Sibel Berker Karaüzüm, Sema Akcurin, Iffet Bircan
P3-D2-861
As a rare manifestation of ichthyosis that is overlooked: TETANY SECONDARY TO VITAMIN-D DEFICIENCY RİCKETS
Murat Karaoglan, Mehmet Keskin, Ferhan Bulut, ozlem keskin
P3-D3-844
WHO growth charts replacing national reference data: Their influence on screening for over- or underweight and of growth disorders.
Celine Eisenegger, Sarina Allenspach-Moser, Dagmar Lallemand
P3-D3-845
Skeletal maturity of radius, ulna and short bones in TW3 method for children in Korea
Jieun Lee, Jaesuk Kim, Jurae Cho
P3-D3-846
Design and Recruitment of a Longitudinal Cohort Study of Growth and Puberty in Russian Boys
Oleg Sergeyev, Thuy Lam, Paige L. Williams, Jane S. Burns, Susan A. Korrick, Russ Hauser, Boris Revich, Yury Dikov, Lyubov Sergeyeva, Mary M. Lee
P3-D3-847
MULTIPLE ENDOCRINOPATHIES IN A CASE WITH H SYNDROME DUE TO A NOVEL SLC29A3 MUTATION
GUL YESILTEPE MUTLU, HEVES KIRMIZIBEKMEZ, ELIF OZSU, ABRAHAM ZLOTOGORSKI, SUKRU HATUN
P3-D3-848
Severe short stature with features of achondroplasia, later diagnosed as panhypopituitarism - a case report
Cristina Matei, Maria Karam, Catherine Peters
P3-D3-856
Anthropometric evaluation of a cohort of school-aged children: the need for national growth references in Romania
Raluca-Monica Pop, Ionela Pascanu, Marian Pop
P3-D3-862
Muccopolysacharidose and hypopituitarism: A case report
Saida Kabour, Soumeya Fedala, Farida Chentli, Fetta amel Yaker, Leila Ahmed ali
P3-D3-863
Costello Syndrome – what about GH treatment?
Adina Manolachie, Cristina Rusu, Alina Fadur, Ioana Bodescu, Elena Braha, Voichita Mogos, Carmen Vulpoi
P3-D3-864
The Establishment of a New Paediatric Endocrinology Training Programme in South Africa
François de Villiers
P3-D3-865
Side effect of treatment with rGh
Belacel merouane, Baz O, Achir samia
P3-D3-866
Growth hormone treatment adherence in children in Latvia
Zane Eglite, Iveta Dzivite-Krisane, Una Lauga-Tunina, Inara Kirilova
LB-D3-1015
A secular trend for pubertal timing in Swedish men born 1946-1991 – the BEST cohort
Maria Bygdell, Liesbeth Vandenput, Claes Ohlsson, Jenny M Kindblom
P1-D1-206
Hypogonadotropic hypogonadism (HH) in patients with congenital adrenal hypoplasia (AHC) due to NR0B1 (DAX1) mutations: phenotype/genotype relationship
Marek Niedziela, Aleksander Jamsheer, Maciej R Krawczynski, Monika Obara-Moszynska, Aleksandra Rojek
P1-D1-207
Analysis of the WDR11 gene in patients with isolated hypogonadotropic hypogonadism with and without olfactory defects
Leticia F.G. Silveira, Luciana R. Montenegro, Elaine M.F. Costa, Ana C. Latronico
P1-D1-239
Genotype and phenotype characterization of a series of Italian patients affected with Idiopatic Central Hypothyroidism (CeH)
Marco Bonomi, Paolo Duminuco, Alessandro Salvatoni, Mario Maggi, Fabio Buzi, Alba Pilotta, Giorgio Radetti, Paolo Beck-Peccoz, Irene Campi, Nadia Schoenmakers, Sjoerd Joustra, Jan Maarten Wit, Daniel Bernard, Luigi Nespoli, Mauro Bozzola, Luca Persani
P1-D2-210
Messenger Ribonucleic Acid Expression of KiSS-1 and Serum Level of Kisspeptin in Rat at Different Developmental Stages
AH REUM KWON, DUK HEE KIM, JUNG MIN AHN, KYUNGCHUL SONG, HYUN WOOK CHAE, HO-SEONG KIM, YE JIN KIM, YONG HYUK KIM
P1-D2-212
A novel MKRN3 mutation discovered in a Korean girl with central precocious puberty
Hae Sang Lee, Jung Sub Lim, Jin Soon Hwang, Eun Young Kim
P1-D2-213
The association of Moebius syndrome and Kallman syndrome is due to a specific mutation of TUBB3.
Melanie Amouyal, Patrice Bouvagnet, Galliane Rochette, Nicolas de Roux
P1-D2-214
Early Medical Treatment of Children with Gender Dysphoria: an Empirical Ethical Study on Arguments of Proponents and Opponents concerning Early Interventions
Martine de Vries, Lieke Vrouenraets, Anne Wichmann, Maartje Schermer, Miranda Fredriks, Henriette Delemarre-van de Waal
P1-D2-216
IGSF1 variants in boys with familial delayed puberty
Sjoerd Joustra, Karoliina Wehkalampi, Wilma Oostdijk, Nienke Biermasz, Sasha Howards, Daniel Bernard, Jan Maarten Wit, Leo Dunkel, Monique Losekoot
P1-D2-217
Reference charts for testicular volume in Dutch children and adolescents
Sjoerd Joustra, Evelyn van der Plas, Joery Goede, Wilma Oostdijk, Henriette Delemarre - Van de Waal, Wilfried Hack, Stef van Buuren, Jan Maarten Wit
P1-D2-218
High incidence of genetic defects in a cohort of 24 male adolescents with persistent pubertal gynecomastia
Françoise Paris, Laura Gaspari, Felicien MBou, Pascal Philibert, Anna Lauber-Biason, Charles Sultan
P1-D2-219
Mutation analysis of the KISS1, KISS1R, LIN28A, LIN28B, TAC3, and TACR3 genes in girls with central precocious puberty
Yoo-Mi Kim, Ja Hye Kim, Ja Hyang Cho, Jin-Ho Choi, Han-Wook Yoo
P1-D3-221
The uterine artery pulsatility index as an accurate index for the assessment of puberty
Alessandra di Lascio, Caterina Colantoni, Silvia Laura Carla Meroni, Moira Gianninoto, Pierluigi Paesano, Gianni Russo
P1-D3-222
The uterine artery pulsatility index in evaluation of the GnRH-analog treatment efficacy in Central Precocious Puberty
Alessandra di Lascio, Caterina Colantuoni, Silvia Laura Carla Meroni, Moira Gianninoto, Pierluigi Paesano, Gianni Russo
P1-D3-223
Title:Serum bisphenol A concentration and premature thelarche in female infants aged 4-month to 2-year old
Fang yanlan, Chen lianhui, Liang li
P1-D3-224
Test on Kisspeptin Levels in Girls with Idiopathic Central Precocious
Yu YANG, Xiang-yu XIONG, Li YANG, Li-ling XIE, Hui HUANG
P1-D3-225
Treated and untreated women with idiopathic precocious puberty: long-term general health status and metabolic outcome between 3rd and 5th decades
Joseph Meyerovitch, Yael Lebenthal, Felice Antebi, Shlomit Shalitin, Liat de Vries, Moshe Phillip, Liora Lazar
P1-D3-226
Serum leptin, ghrelin and adiponectin levels in relation to body composition in rhythmic gymnasts entering into puberty: a 3-year follow-up study.
Vallo Tillmann, Kristel Võsaberg, Anna-Liisa JürimParm, Meeli Saar, Toivo Jürimäe, Katre Maasalu, Inga Neissaar, Evelin Lätt, Jaak Jürimäe
P1-D3-227
Impact of BMI on GnRH stimulated LH provocation peak in girls with central precocious puberty
Jun-Fen Fu, Ju-Hua Jin, Heranmaye C Prasad, Xue-Lian Zhou, Guan-Ping Dong, You-Jun Jiang
P1-D3-230
Increasing incidence of premature thelarche in the Central Denmark Region? Who evolve into precocious puberty?
Mia Elbek Sømod, Esben Thyssen Vestergaard, Kurt Kristensen, Niels Holtum Birkebæk
P2-D1-536
Monitoring Gonadotropin-Releasing Hormone Analog Treatment in Girls with Central Precocious Puberty: a Comparison of Four Methods
Amnon Zung, Ella Burundukov, Mira Ulman, Tamar Glaser, Malka Chen, Zvi Zadik
P2-D1-537
The Evaluation of Possible Role of Endocrine Disrupters in Precocious Puberty
Derya Bulus, Ali Asci, Nesibe Andiran, Belma Kocer-Gumusel, Elif Yagli Çolakoglu
P2-D1-538
Acute exposure of endocrine disruptor does not induce oxidative stress in the rat’s brain
Neeraj Kumar, Varsha Sharma
P2-D1-539
Dramatic rise in the prevalence of precocious puberty in girls over the past 20 years in the South of France
Laura Gaspari, Emilie Morcrette, Claire Jeandel, Fabienne Dalla Valé, Françoise Paris, Charles Sultan
P2-D1-540
A novel mutation at a splice acceptor site of WDR11 in a patient with combined pituitary hormone deficiency.
Yoko Izumi, Erina Suzuki, Shuichi Yatsuga, Shinichiro Sano, Kazuhiko Nakabayashi, Akihiro Umezawa, Kenichiro Hata, Tsutomu Ogata, Maki Fukami, Yasunori Yoshimura
P2-D2-541
Normal minipuberty in a patient with DAX-1 mutation: a reliable marker of the function of the hypothalamic-pituitary-gonadal axis?
Julie Fudvoye, Marie Christine Lebrethon, Jean Pierre Bourguignon, Anne Simone Parent
P2-D2-542
Growth Hormone excess and pseudoprecocious puberty in a 8 year old boy with McCune-Albright Syndrome
Diana-Alexandra Ertl, Johannes Gojo, Daniela Aubrunner, Gabriele Haeusler
P2-D2-543
Time to Menarche after Completing Gonadotropin-Releasing Hormone Agonist in Girls with Central Precocious or Early Puberty
Shin-Hee Kim, In-Ah Jung, Won Kyoung Cho, Kyoung Soon Cho, So Hyun Park, Min Ho Jung, Byoung Kyu Suh
P2-D2-544
Impact of being born small or large for gestational age on pubertal onset and progression
M. Loredana Marcovecchio, Ilaria Di Giovanni, Tommaso de Giorgis, Nella Polidori, Valentina Chiavaroli, Angelika Mohn
P2-D2-545
Diagnostic spectrum of female pubertal delay
Suma Uday, Sabah Alvi
P2-D2-546
Kallmann Syndrome: diagnosis in paediatric age
Ângela Machado, Maria João Oliveira, Teresa Borges, Helena Cardoso, Paula Fonseca, Luis Ribeiro, Catarina Gonçalves, Manuel Lemos
P2-D2-547
The Triptorelin test compares favourably with the GnRH test in the diagnosis of central precocious puberty.
Asmahane Ladjouze, Adel Djermane, Yasmine Ouarezki, Leila Kedji, Karima Berkouk, Maoudj Abdeljalil, Rawda Aboura, Minoubia Bensmina, Tahar Anane, Salah Eddine Bouyoucef, Abdenour Laraba
P2-D2-548
Puberty in children with shunted congenital hydrocephalus with and without myelomeningocele
Lemm Proos, Kai Arnell, Jan Gustafsson, Margareta Dahl
P2-D2-549
“Evaluation of age at GnRH analogue treatment discontinuation, age at menarche and adult height in girls with Central Precocious Puberty (CPP) from the Spanish Registry”
Raquel Corripio, Leandro Soriano-Guillén, Ramón Cañete, Lidia Castro-Feijoó, Arancha Escribano, Rafael Espino, Javier Herrero-Espinet, José-Ignacio Labarta, Jesús Argente
P2-D2-550
Final height in a boy with McCune-Albright syndrome and precocious puberty treated with ketoconazole, cyproterone acetate and leuprolide acetate for more than 5 years
Maria Francesca Messina, Tommaso Aversa, Mariella Valenzise, Filippo De Luca
P2-D2-551
The effect of combined growth hormone and gonadotropin-releasing hormone agonist treatment for near-final height improvement in true precocious puberty and early puberty
Se Young Kim, Eun Youn Kim, Kyung Hee Yi
P2-D2-552
Pubertal development in a cohort of Romanian school-aged children
Ionela Pascanu, Oana Capraru, Ancuta Cota, Raluca Pop
P2-D3-553
Inhibin B in the diagnosis of delayed puberty
Camelia Procopiuc, Iuliana Gherlan, Cristina Dumitrescu, Andreea Brehar, Suzana Vladoiu, Livia Procopiuc, Andra Caragheorgheopol
P2-D3-554
Predominantly matrilineal inheritance of familial precocious puberty suggests an underlying imprint anomaly
Adelaide Durand, Raja Brauner, Anu Bashamboo, Ken McElreavey
P2-D3-555
TAMOXIFEN-INDUCED HIRSUTISM: AN UNUSUAL SIDE EFFECT IN A 5 YEARS OLD GIRL WITH McCUNE- ALBRIGHT SYNDROME
Heves Kirmizibekmez, Rahime Gül Yesiltepe Mutlu, Fatma Dursun, Sükriye Pinar Isgüven
P2-D3-556
LONG TERM OUTCOMES OF PRECOCIOUS PUBERTY DUE TO HYPOTHALAMIC HAMARTOMAS
Danielle Rodrigue, Cécile Thomas-Teinturier, Emmanuelle Motte-Signoret, Pierre Bougnères, Agnès Linglart
P2-D3-557
Mutational Analysis of TAC and TACR3 in idiopathic central precocious puberty
Marina Krstevska-Konstantinova, Jana Jovanovska, Nevenka Slaveska, Velibor Tasik, Luciana Ribeiro Montenegro, Daiane Beneduzzi, Leticia Gontijo Silveira, Zoran Gucev
P2-D3-558
Pituitary-ovarian axis in patients with isolated premature thelarche.
Beata Wikiera, Julita Nocon-Bohusz, Aleksander Basiak, Jolanta Bieniasz, Ewa Glab, Anna Noczynska
P2-D3-559
The buserelin stimulation test given as an intranasal spray in diagnosing gonadotropin deficiency in males with delayed puberty
Gulnara Rakhimova, Kamil Gilyazetdinov
P2-D3-560
Adult height outcome of girls with idiopathic central precocious puberty treated with GnRH analogs is irrespective of body mass index
Tommaso Aversa, Mariella Valenzise, Malgorzata Wasniewska, Maria Francesca Messina, Alessandra Santisi, Filippo De Luca
P2-D3-561
DELAYED PUBERTY – BETWEEN CHRONOPATHOLOGY AND SUBCLINICAL PATHOLOGY
Camelia Procopiuc, Cristina Dumitrescu, Iuliana Gherlan, Andreea Brehar, Mariana Costache, Livia Procopiuc, Andra Caragheorgheopol
P2-D3-562
CENTRAL PRECOCIOUS PUBERTY AS THE INITIAL MANIFESTATION OF A PILOCYTIC ASTROCYTOMA WITH LEPTOMENINGEAL DISSEMINATION SIMULATING A HYPOTHALAMIC DYSGERMINOMA
Blanca Lidia Galo, Diego Yeste Fernandez, Ariadna Campos, Maria Clemente, Antonio Carrascosa, Anna Llort
P2-D3-563
Endocrine Abnormalities in Phosphoglucomutase 1 Deficiency
Barbara Mueksch, Eva Morava, Dirk Lefeber, Hedi Claahsen-van der Grinten, Eckhard Korsch
P3-D1-925
The timing and evolution of puberty in a sample of school-aged children in a Brazilian city
Taciana Carla Maia Feibelmann, Adriana Paula da Silva, Daniela Cristina Silva, Elisabete Aparecida Mantovani Rodrigues de Resende, Lúcia Marina Scatena, Maria de Fátima Borges
P3-D1-926
THE SIGNIFICANCE OF GONADOTROPIN RELEASING HORMONE STIMULATION TEST, LEPTIN, AND PELVIC ULTRASOUND FINDINGS FOR DIFFERENTIATING IDIOPATHIC CENTRAL PRECOCIOUS PUBERTY FROM PREMATURE TELARCHE
Betül Ersoy, Pinar Yazici, Ece Onur, Mine Ozkol
P3-D1-927
Basal Luteinizing Hormone Combined with the Tanner Stage of Breast Development Can Predict the Gonadotropin Response Following Gonadotropin-releasing Hormone Stimulation Test.
Osnat Admoni, Naama Schwartz, Yardena Tenenbaum-Rakover
P3-D1-928
CHARACTERISTICS OF CHILDREN TREATED WITH LEUPROLIDE ACETATE
gulcan seymen karabulut, ayşegül yüksel, elif özsu, gül yeşiltepe mutlu, filiz mine çizmecioğlu, şükrü hatun
P3-D1-929
Long term consequences of indirect topical exposure to testosterone gel in young children.
Inge Gies, Jesse Vanbesien, Yannick De Brucker, Caroline Ernst, Ellen Anckaert, Jean De Schepper
P3-D1-930
FINAL HEIGHT IN GIRLS WITH IDIOPATHIC CENTRAL PRECOCIOUS PUBERTY TREATED WITH GNRH ANALOG: COMPARISON WITH UNTREATED CONTROLS
Zeynep Atay, Saygin Abali, Tulay Guran, Belma Haliloglu, Serpil Bas, Serap Turan, Abdullah Bereket
P3-D1-931
X-linked recessive form of Nephrogenic Diabetes Insipidus in a 7 year old boy
Aleksandra Janchevska, Velibor Tasic, Marina Krstevska-Konstantinova, Hae Il Cheong
P3-D1-932
Idiopathic Hypogonadotropic Hypogonadism due to a GNRH1 Mutation
Eda Mengen Ucakturk, Leman Damla Kotan, Fatih Gurbuz, Bilgin Yuksel, Ali Kemal Topaloglu
P3-D1-933
Effect on body mass index of gonadotropin-releasing hormone analogue treatment in central precocious puberty or early and fast puberty girls
Chen Qiuli, Su Zhe, Li Yanhong, Ma Huamei, Chen Hongshan, Zhang Jun, Du Minlian
P3-D1-934
An unusual combination of premature ovarian failure and a history of GNRH treatment for idiopathic precocious puberty
Maria Parpagnoli, Salvatore Seminara, Giulia Anzilotti
P3-D1-935
An unusual case of early and accelerated puberty
Perla Scalini, Stefano Stagi, Paola Pelosi, Franco Ricci, Giulia Anzillotti, Paolo Del Greco, Salvatore Seminara, Maurizio de Martino
P3-D3-939
Precocious Puberty due to Duplication of the Pituitary Gland
Carla Minutti, Deborah Goldstein
P3-D3-940
Inhibin B in the boys with constitutional delay of puberty: relationship with gonadotropins, testosterone and anti-müllerian factor
Oleg Latyshev, Elena Kiseleva, Goar Okminyan, Lubov Samsonova
P3-D3-941
A rare cause of peripheric precocious puberty: Adrenocortical tumor
Erkan Sari, Erman Atas, Ahmet Guven, Ediz Yesilkaya
P3-D3-942
A severe LHRH-independent precocious puberty in a 26-month-old girl with a clinical diagnosis of McCune-Albright Syndrome.
Maciej Flader, Anna Latos-Bielenska, Karina Kapczuk, Przemyslaw Mankowski, Elzbieta Malecka, Marek Niedziela
P3-D3-943
Triptorelin test in the diagnosis of precocious puberty.
Saida Kabour, Soumeya Fedala, fetta amel Yaker, Ali el mahdi Haddam, lila rabhi, farida chentli, Djamila Meskine
P3-D3-944
Central precocious puberty and autism: 3 cases report
Daniela Amaral, Lurdes Lopes
P3-D3-945
PRECIPITATED PUBERTY - CORRELATIONS WITH EMBARRASSED OVARIAN FUNCTION
EDUARD CIRCO
P3-D3-946
Title: Impact of bisphenol-A on the puberty of female rats
chen linqi, yang fan, jin meifang, wu haiying
P3-D3-947
The Etiology of Central Precocious Puberty (CPP) and Effect of Gonadotropin Releasing Hormone (GnRH) Agonist for 2 years in Korean Boys
Young Suk Shim, Hwal Rim Jeong, Hae Sang Lee, Jung Sub Lim, Jin Soon Hwang
P3-D3-948
Hypothalamic hamartoma as a cause of central precocious puberty in 4,5-year old girl-case report
Ewa Jakubowska, Beata Sawicka, Hanna Borysewicz-Sanczyk, Aneta Zasim, Artur Bossowski
P3-D3-949
The perception of body image and self-esteem in girls with precocious puberty, being treatment with GnRH analogue
Eun Young Kim, Min Sun Choi, Se Young Kim, Il Tae Hwang
P3-D3-950
LEYDIG CELL HYPERPLASIA MIMICKING TUMOR: A RARE CAUSE OF ISOSEXUAL PRECOCCIOUS PUBERTY
gülcan seymen karabulut, şükrü hatun, ayşegül yüksel, funda özer çorapçıoğlu, yonca anık, gülşen ekingen, yeşim gürbüz
P3-D3-951
Title: Impact of different doses of bisphenol-A on the puberty of female rats
chen linqi, yang fan, Jin meifang
LB-D3-1016
THE DIVERSE PHENOTYPE OF MUTATIONS IN T3 RECEPTOR ALPHA (TRα)
Anja van Gucht, Korcan Demir, Nitash Zwaveling, Hanneke Wennink, Muammer Büyükinan, Gönül Çatli, Bumin Nuri Dündar, Marcel Meima, Edward Visser, Paul van Trotsenburg, Theo Visser, Robin Peeters
P1-D1-231
The association between rs4684677 T/A polymorphism in preproghrelin gene and predisposition to autoimmune thyroid diseases in children.
Artur Bosswski, Anna Moniuszko, Natalia Wawrusiewicz-Kurylonek, Anna Bossowska, Ewa Jakubowska, Adam Kretowski
P1-D1-232
Chosen polimorphisms in FoxP3 gene in children and adolescents with autoimmune thyroid diseases
Artur Bossowski, Hanna Borysewicz-Sanczyk, Natalia Wawrusiewicz-Kurylonek, Mieczysław Szalecki, Beata Wikiera, Ewa Barg, Małgorzata Mysliwiec, Anna Kucharska, Anna Bossowska, Joanna Goscik, Katarzyna Ziora, Maria Gorska, Adam Kretowski
P1-D1-233
TSH receptor gene (TSHR) variants in pediatric patients with non autoimmune hyperthyrotropinemia
Paula Scaglia, Ana Keselman, Laura Gruñeiro Papendieck, Patricia Papendieck, Ignacio Bergadá, Horacio Domené, Ana Chiesa
P1-D1-234
Association of Toll-Like Receptor-10 polymorphisms with autoimmune thyroid disease in Korean children.
Won Kyoung Cho, Yeon Jin Jeon, In Ah Jung, Shin Hee Kim, Jung-Pil Jang, Eun-Jeong Choi, Min Ho Jung, Tai-Gyu Kim, Byung-Kyu Suh
P1-D1-235
A nonsense thyrotropin receptor gene mutation (R609X) is associated with congenital hypothyroidism and heart defects
Hakan Cangül, Veysel Nijat Bas, Yaman Sağlam, Michaela Kendall, Timothy G Barrett, Eamonn R Maher, Zehra Aycan
P1-D1-236
Genome-wide promoter methylation analysis in cytologically indeterminate thyroid nodules.
Ericka B Trarbach, Amanda Shinzato, Chin J Lin, Suemi Marui, Antonio M Lerario
P1-D1-237
Genetic analysis of the paired box domain gene (PAX8) in a cohort of Polish patients with primary congenital hypothyroidism
Malgorzata Kumorowicz-Czoch, Anna Madetko-Talowska, Adam Dudek, Dorota Tylek-Lemanska
P1-D1-238
Homozygous deletion of the TSH beta subunit gene causes congenital secondary hypothyroidism in a consanguineous family of Turkish descent
Pia Hermanns, Cherize Klotz, Robert Couch, Norma Leonard, Joachim Pohlenz
P1-D1-240
“A novel mutation in the TITF-1 gene in a child with benign hereditary chorea”
Viviana Dora Patianna, Barbara Predieri, Livia Garavelli, Carlo Fusco, Simona Filomena Madeo, Patrizia Bruzzi, Lorenzo Iughetti
P1-D1-241
Twin couples and/or triplets discordant for congenital hypothyroidism at birth: the importance of the re-screening at 2-4 weeks of life
Antonella Olivieri, Emanuela Medda, Alessandra Cassio, Giovanna Weber, Pietro Costa, Francesca Calaciura, Maria Cristina Vigone, Valentina Di Russo, Cristina Fazzini
P1-D1-242
Congenital hypothyroidism and tuberous sclerosis: an association or a coincidence?
Francesco Gallo, Pietro Conte, Rosa Maria Alfano, Gaetano Bulfamante, Fulvio Moramarco
P1-D1-243
Evaluation of serum cytokines IL-6 and osteoprotegerin measurements in the diagnosis of chronic autoimmune thyroiditis and Graves' disease in children.
Hanna Mikos, Marcin Mikos, Marek Niedziela
P1-D2-244
Treatment of Graves’ disease with methimazole in children alters the proliferation of Treg cells and T lymphocytes
Maria Klatka, Ewelina Grywalska, Magdalena Wasiak, Jacek Rolinski
P1-D2-245
Thyroid dysfunction in children after hematopoietic stem cell transplantation : short term follow-up for 12months
Yeon Jin Jeon, In Ah Jung, Shin Hee Kim, Won-Kyoung Cho, Jae-Wook Lee, Kyoung Soon Cho, So Hyun Park, Nak-Gyun Chung, Min-Ho Jung, Bin Cho, Byung-Kyu Suh
P1-D2-246
The Effect of L-thyroxine Treatment on Left Ventricular Functions in Children with Subclinical Hypothyroidism
Gonul Catli, Mustafa Kir, Ahmet Anik, Nuh Yilmaz, Ece Bober, Ayhan Abaci
P1-D2-247
Urinary Iodine Concentrations in Mothers and Their Term Newborns.
Katerina Krylova, Radovan Bilek, Milan Bayer, Petr Dejmek, David Neumann
P1-D2-248
Vitamin D in adolescents with Hashimoto's thyroiditis
Olga Gumeniuk
P1-D2-249
Capillary TSH cut-off levels for congenital hypothyroidism screening: evidence against adopting the UK threshold of 10 mIU/L.
Jeremy Jones, Guftar Shaikh, Avril Mason
P1-D2-250
INVESTIGATION THE EFFECTS OF FUNCTIONS OF REGULATORY T CELLS AND VITAMIN D IN CHILDREN WITH CHRONIC AUTOIMMUNE THYROIDITIS
Zeynep SIKLAR, Deniz KARATAS, Figen DOGU, Pinar KOCAAY, Bulent HACIHAMDIOGLU, Aydan IKINCIOGULLARI, Merih BERBEROGLU
P1-D2-251
Triiodothyronine-predominant Graves'disease (T3-P-GD): description and management in childhood.
Julie Harvengt, Priscilla Boizeau, Delphine Zenaty, Anne Paulsen, Dominique Simon, Sophie Guilmin Crepon, Corinne Alberti, Jean-Claude Carel, Juliane Léger
P1-D2-252
AUTOIMMUNE ENCEPHALOPATHY IN A BOY WITH GRAVES' DISEASE.
Anna Kucharska, Katarzyna Kadziela, Beata Pyrzak
P1-D2-253
Maternal hypothyroxinemia in early pregnancy is associated with poorer arithmetic performance in a school test in offspring at age 5 years
Anna Noten, Eva Loomans, Tanja Vrijkotte, Paul van Trotsenburg, Manon van Eijsden, Joost Rotteveel, Martijn Finken
P1-D2-254
TSH: different normalization methods, very different normal upper limits
David Strich, Gilad Karavani, David Gillis
P1-D2-255
Usefulness of second screening strategy for congenital hypothyroidism in LBW neonates
Paolo Cavarzere, Florina Ion Popa, Monica Vincenzi, Marta Camilot, Francesca Teofoli, Lorella Morosato, Evelina Maines, Rossella Gaudino, Silvana Lauriola, Franco Antoniazzi
P1-D2-256
Screening for congenital hypothyroidism in the Russian Federation (1997-2012)
Olga Bezlepkina, Olga Chikulaeva, Olga Chumakova, Lyudmila Karavaeva, Alexey Bezlepkin, Valentina Peterkova
P2-D1-558
Investigation of Autoimmune Diseases Accompanying Hashimoto Thyroiditis in Children and Adolescents and Evaluation of Cardiac Signs
Veysel Nijat Bas, Sebahat Yilmaz Agladioglu, Senem Ozgur, Selmin Karademir, Zehra Aycan
P2-D1-584
Treatment of Pediatric Graves Disease: results of a multicenter survey in Portugal
Olinda Marques, Maria João Oliveira, Ana Antunes Antunes, Filipa Espada, Joana Guimarães, Portuguese Society of Pediatric Endocrinology and Diabetology (SPEDP), Portuguese Multicentre Group
P2-D1-585
Subclinical Hypothyroidism is associated with low IGF-I levels and decreased growth velocity.
Helena Bellini, Lea Maciel, Rodrigo Custodio, Soraia Milani, Mariana Paula, Sonir Antonini, Raphael Liberatore, Carlos Martinelli
P2-D1-586
Thyroid function and autoimmunity and their relation to weight status in healthy children and adolescents
Emilio García-García, Rafael Galera-Martínez, Icíar García-Escobar, Patricia Oliva-Pérez, José L. Gómez-Llorente, Jerónimo Momblan, María A. Vázquez-López, Antonio Bonillo Perales
P2-D1-587
MUTATION OF THE TSH RECEPTOR GENE: A LONGITUDINAL STUDY IN CHILDREN WITH NON-AUTOIMMUNE SUBCLINICAL HYPOTHYROIDISM
Maria Cristina Vigone, Micol Sonnino, Fabiana Guizzardi, Marianna Di Frenna, Silvana Caiulo, Giulia Gelmini, Luca Persani, Giovanna Weber
P2-D1-589
No difference in cognitive development of young adults and adolescents affected by congenital hypothyroidism (CH) compared to their sibling controls despite high dose L-thyroxin treatment.
Paulina Aleksander, Oliver Blankenstein, Annette Grüters, Heiko Krude
P2-D1-590
Thyroid disorders in siblings of CH patients with thyroid dysgenesis
Alessandra Cassio, Valentina Di Ruscio, Federico Baronio, Ilaria Bettocchi, Antonella Cantasano, Milva Orquidea Bal, Antonio Balsamo, Giulio Maltoni, Laura Mazzanti
P2-D1-591
Trends in median age at Guthrie sampling, laboratory receipt, notification and start of treatment for infants with TSH elevation on newborn screening
Chourouk Mansour, Yasmine Ouarezki, Jeremy Jones, Sarah Smith, Malcolm Donaldson, Avril Mason
P2-D1-592
IODINE-DEFICIENCY LEVELS IN SCHOOLCHILDREN AGED BETWEEN 6 AND 12
Ana Muñoz-Serrano, Abel González-González, José María Tenías-Burillo, Piedad Falero-Gallego, Ramon Cañete
P2-D1-593
Incidence of thyroid nodules in children affected by Hashimoto’s Thyroiditis: a 12 year survey of 567 children.
Silvia Longhi, Tommaso Aversa, Milva Bal, Antonella Cantasano, Marco Cappa, Alessandra Cassio, Andrea Corrias, Valeria D'Antonio, Filippo De Luca, Raffaella Di Mase, Roberto Gastaldi, Chiara Guzzetti, Sandro Loche, Mariacarolina Salerno, Giulia Maria Tronconi, Maria Cristina Vigone, Giovanna Weber, Giorgio Radetti
P2-D1-594
THE EVOLUTION OF IODINE STATUS IN SCHOOLCHILDREN LIVING IN FORMERLY IODINE-DEFICIENT REGION OF MURES COUNTY, ROMANIA
Zsuzsanna Szántó, Zsuzsanna Réti, Jolán Ballók, Attila Csiszér, Elod Nagy, Ildikó Kun, Imre Zoltán Kun
P2-D1-595
Papillary thyroid Cancer with diffuse pulmonary metastasis: How to manage?
Serpil Bas, Saygin Abali, Yasemin Gokdemir, Belma Haliloglu, Zeynep Atay, Bulent Karadag, Abdullah Bereket, Serap Turan
P2-D1-596
Factors useful to distinguish between children with permanent congenital hypothyroidism and transient or permanent hyperthyrotropinemia
Maria Francesca Messina, Vincenzo Ramistella, Tommaso Aversa, Mariella Valenzie, Filippo De Luca
P2-D2-559
Severe urticaria in Graves disease – Is Carbimazole to blame? A diagnostic dilemma.
Caroline Ponmani, Martin Mcclatchey, Shilpa Kanzaria, Morgan Keane, Kausik Banerjee
P2-D2-597
Thyroid nodules in childhood and adolescence; clinical, radiologic and etiological evaluation
OLCAY EVLİYAOGLU, BAHAR OZCABI, AYSE TEKİN, FERIDE BUCAK, OYA ERCAN
P2-D2-598
An unusual presentation of acquired hypothyroidism: the Van Wyk-Grumbach syndrome
Pinar Isguven, Nefise Uluc, Mustafa Kosecik, Mehmet Karacan, Bahri Ermis
P2-D2-600
Low serum free T4 concentration in a girl with McCune-Albright syndrome
Aleksandr Peet, Mart Roosimaa, Anett Pajuväli, Vallo Tillmann
P2-D2-601
Long Term Anti-Thyroid Drug Therapy in a Paediatric Population with Down Syndrome: an Irish Experience
Niall Johnston, Meenal Mavinkurve, Nuala Murphy, Sinead Moloney, Colm Costigan, Declan Cody
P2-D2-602
INFlUENCE OF AMIODARONE ON THYROID FUNCTION IN CHILDREN
Irina Nikitina, Elena Vasichkina, Irina Artemeva, Anastasia Liskina, Dmitri Lebedev
P2-D2-603
Euthyroid sick syndrome in children with diabetic ketoacidosis
Yanyan Hu, Guimei Li, Qian Wang, Zengmin Wang, Fengxue Wang
P2-D2-604
LEVOTHYROXINE REQUIREMENT IN CONGENITAL HYPOTHYROIDISM: 12-YEAR LONGITUDINAL STUDY
Maria Cristina Vigone, Rosa Lapolla, Maurizio Delvecchio, Mariacarolina Salerno, Malgorzata Wasniewska, Pietro Pio Popolo, Alessandro Mussa, Giulia Maria Tronconi, Raffaella Di Mase, Ida D'Acunzo, Rosa Maria Falcone, Andrea Corrias, Filippo De Luca, Giovanna Weber, Luciano Cavallo, Maria Felicia Faienza
P2-D2-605
Treatment of Graves’ disease with methimazole in children alters the proliferation of Treg cells and T lymphocytes
Maria Klatka, Ewelina Grywalska, Magdalena Wasiak, Jacek Rolinski
P2-D2-606
Genetic Studies in Congenital Hypothyroidism; A Regional Study
Mahin Hashemipour, Silva Hopvsepian
P2-D2-607
Premature menarche associated with Hashimoto thyroiditis at 2 years 9 months: Case report
Meliksah Keskin, Semra Cetinkaya, Elif Sagsak, Zehra Aycan, Senay Savas Erdeve
P2-D2-608
Iodine nutrition and neonatal thyrotropin levels in Lucknow, India
Vijayalakshmi Bhatia, Vignesh Gopalakrishnan, Kriti Joshi, Shubha Phadke, Preeti Dabadghao, Meenal Agarwal, Cynthia Mootheden, Vinita Das, Amita Pandey
P2-D2-609
AUXOLOGICAL PATTERN, BMI AND ENDOCRINE FOLLOW UP IN CHILDREN WITH CONGENITAL HYPOTHIROIDISM: THE DATA OF THE PEDIATRIC CLINIC OF PALERMO
Maria Cristina Maggio, Mariagrazia Irene Mineo, Marilena Maltese, Giovanni Corsello
P2-D3-509
Neonatal Pituiiary-thyroid axis dysregulation with combined thyroid hormone and thyrotropin resistance in infant with Trisomy 21 and maternal Subclinical hypothyroidism
Astha Soni, Shivaram Avula, Mohammed Didi, Sze May Ng
P2-D3-510
Neonates with Acute Kidney Injury continue to be at risk of iatrogenic iodine toxicity and hypothyroidism with attendant risk to the developing brain
Carley Frerichs, Richard Holt, Henry Morgan, Caroline Jones, Mohammed Didi
P3-D1-711
Autoimmune Thyroiditis in Georgian Children and adolescents with type 1 Diabetes Mellitus
Nino Abdushelishvili, Marine Gordeladze
P3-D1-936
ASSOCIATION OF VAN WYK GRUMBACH AND DEBRE SEMELAIGNE SYNDROMES IN TWO CASES WITH SEVERE HYPOTHROIDISM
Fatma Demirel, Alkim Oden, Meltem Tayfun, Ahmet Ucakturk, Ali Gungor
P3-D1-937
Van Wyk-Grumbach syndrome: Case report from Georgia
Irakli Paghava
P3-D1-974
INCREASING INCIDENCE OF CONGENITAL HYPOTHYROIDISM IN NEONATAL SCREENING PROGRAM IN CENTRAL SERBIA – 30 YEARS OF EXPERIENCE
Tatjana Milenkovic, Branka Opancina, Katarina Mitrovic, Sladjana Todorovic, Rade Vukovic
P3-D1-975
Prevalence of additional autoimmune diseases in autoimmune’s thyroiditis children and their first- and second-degree relatives: results from a large, single-center study
Lucia De Martino, Iolanda Di Donato, Sara Alfano, Ida D'Acunzo, Rosita Di Pinto, Donatella Capalbo, Mariacarolina Salerno
P3-D1-976
Adiposity and pubertal status effects on thyroid function in overweight children and adolescents
Aristeidis Giannakopoulos, Panagiota Pervanidou, Natalia Lazopoulou, George Chrousos, Christina Kanaka-Gantenbein
P3-D1-977
Neonatal Thyrotoxicosis in Maternal Grave’s Disease: A Case Series and Review of the Literature
Niall Johnston, Meenal Mavinjurve, Nuala Murphy, Ciara McDonnell, Sinead Moloney, Declan Cody, Colm Costigan
P3-D1-978
TREATMENT OF THE RESISTANCE TO THYROID HORMONS IN GIRL
Elzbieta Budzynska, Iwona Ben-Skowronek, Elzbieta Korobowicz, Maria Klatka
P3-D1-979
Free T3/free T4 ratios in children with hypothyroidism treated with levothyroxine monotherapy
TSUTOMU TAKAHASHI, YUKI KONNO, IKUKO TAKAHASHI
P3-D1-980
Diagnostic challenges of Thyroid dysfunction in Eating Disorders
Priyha Santhanam, Louise Denvir, Pooja Sachdev, Tabitha Randell
P3-D1-981
Kocher–Debré–Semelaigne syndrome with rhabdomyolysis and increased creatinine: a case report.
Emine Ayca Cimbek, Yasar Sen, Sevil Ari Yuca, Demet Kivanc, Celal Gur, Harun Peru
P3-D1-982
Preliminary results and normative TSH values for healthy Nigerian newborn children
IRORO YARHERE, ABIOLA ODUWOLE, SALMA SUWAID, ALKALI YAHAYA, MARYANNE IBEKWE, KAYODE ADENIRAN, BOLANLE FETUGA, JEROME ELUSIYAN, HAFSAT W IDRIS, TAMUNOPRIYE JAJA, OMOTAYO ADESIYUN, O O JARRETT
P3-D1-983
Resistance to Thyroid Hormone Syndrome from childhood to adulthood – variation in symptoms and thyroid function
Aoife Garrahy, Mariana Grace, Mary Stapleton, Carla Moran, Krishna Chatterjee, Matthew Murphy, Susan O'Connell
P3-D1-984
THYROID DISORDERS AFTER ONCOLOGIC TREATMENT IN CHILDREN
Iwona Ben-Skowronek, Elzbieta Sadurska, Agnieszka Prazmo-Zaucha, Robert Piekarski, Jerzy Kowalczyk
P3-D1-985
Trends in incidence of permanent and transient congenital hypothyroidism in Shanghai China
XIN FAN, XUEFAN GU, JINGSI LUO, WENJUAN QIU, JUN YE, SHAOKE CHEN, JIANFENG XU
P3-D1-986
Klippel-Feil syndrome and thyroiditis: a case report
Elisa Guidoni, Renato Scarinci, Giovanna Municchi
P3-D2-1000
Changes of laboratory findings before and after thyroid hormone replacement in a naïve 19.24 year-old female case of ectopic thyroid
PHIL SOO OH, Joong Wan CHOI
P3-D2-899
Iodine status in the neonate and the effect on thyroid function
Jeesuk Yu, Seung Ho Lee, Young Pyo Chang
P3-D2-987
The association of thyroid dysfunction and blood pressure in Korean children
Hae Soon Kim, Hye Sook Park, Sujin Cho, Sun Jung Baik, Bo Hyun Park, Hye Ah Lee
P3-D2-988
THYROTOXICOSIS IN CHILDHOOD AND ADOLESCENTS
Ana Hreniuc, Letitia Leustean, Ioana Bodescu, Ioana Hristov, Simona Gherasim, Cristina Preda, Carmen Vulpoi, Voichita Mogos, Christina Ungureanu
P3-D2-989
Aetiology and different clinical conditions of hyperthyroidism in children and adolescents
Bouferoua Fadila, Zeroual Zoulikha, Tari Saliha, Bouterfas Nabila, Khiari Mohamed El Mokhtar, Boukelal Houria
P3-D2-990
BMI AND AUXOLOGICAL FOLLOW UP IN CHILDREN WITH HASHIMOTO THYROIDITIS: UTILITY OF A PHISICAL ACTIVITY PROGRAM
Giovanni Corsello, Marilena Maltese, Mariagrazia Irene Mineo, Maria Cristina Maggio
P3-D2-991
MISSED CASES OF CONGENITAL HYPOTHYROIDISM DETECTED BY SCREENING PROGRAM IN CENTRAL SERBIA (1983-2014)
Sladjana Todorovic, Tatjana Milenkovic, Dragan Zdravkovic, Katarina Mitrovic, Rade Vukovic
P3-D2-992
Thyroid pathology among 14-year-old adolescents
Anastasia Statova
P3-D2-993
Raised free thyroxine levels in a boy with hypertension.
Sharon Lim
P3-D2-994
THE EVALUATION OF TRANSIENT HYPOTHYROIDISM IN PATIENTS DIAGNOSED WITH CONGENITAL HYPOTHYROIDISM
Havva Nur Peltek Kendirci, Zehra Aycan, Elif Sagsak, Meliksah Keskin, Semra Çetinkaya
P3-D2-995
Optimizing treatment in congenital hypothyroidism
Joana Serra-Caetano, Joana Miguéis, Rita Cardoso, Isabel Dinis, Alice Mirante
P3-D2-996
Report of a hurthle cell neoplasm in a boy
zerrin orbak, atilla cayir, hakan doneray, akgün oral, nesrin gursan
P3-D2-997
Delayed Diagnosis of Congenital Hypothyroidism (CH) and consequences: A case series
Tamunopriye Jaja, Iroro Yarhere, Calistus Chuku
P3-D2-998
IMPORTANCE OF EARLY INDEMNIFICATION OF HASHIMOTO THYROIDITIS AT PREGNANT WOMEN IN CONDITIONS OF IODINE DEFICIENCY IN REPUBLIC OF UZBEKISTAN
Sakhlo Muratova
P3-D2-999
Improvement of hematological values with stabilization of STH
Claudio Marcelo José Malem
P3-D3-698
TSH/fT4 ratio as a marker of TSH resistance in Pseudoparathyroidism 1A and obesity
Aurélia Alimi, Danielle Rodrigue, Agnès Linglart, Gianpaolo De Filippo
LB-D3-1017
Exploring the Pathogenesis of Hypothalamic Obesity: the Interaction of Hormonal, Neuronal and Psychological Factors
Caroline Steele, Joanne Powell, Graham Kemp, Jason Halford, John Wilding, Joanne Harrold, Kumar Das, Daniel Cuthbertson, Mohsen Javadpour, Ian MacFarlane, Andrej Stancak, Christina Daousi
P1-D2-10
AN UNUSUAL PRESENTATION OF ISOLATED ACTH-DEFICIENCY SECONDARY TO TBX19 MUTATION REVEALED BY LATE ONSET HYPOGLYCEMIA SEIZURE
Cecile Valentin, Alexandru Saveanu, Jacques Beltrand, Irene Netchine
P1-D3-185
Early-Onset Central Diabetes Insipidus is associated with De novo Arginine Vasopressin-Neurophysin II or Wolfram Syndrome 1 gene mutations
Anna Elsa Maria Allegri, Natascia Di Iorgi, Silverio Perrotta, Fulvio Della Ragione, Saverio Scianguetta, Adriana Borriello, Marcella Ferraro, Claudia Santoro, Annalisa Calcagno, Flavia Napoli, Marta Giaccardi, Marco Cappa, Maria Carolina Salerno, Mohamad Maghnie
P1-D3-186
A boy with septo-optic dysplasia identified a mutation in WDR11
Hirohito Shima, Yoko Izumi, Ikumi Umeki, Akimune Kaga, Miki Kamimura, Akiko Saito-Hakoda, Junko Kanno, Maki Fukami, Ikuma Fujiwara
P1-D3-187
Quality of Life and Psychosexual function in Young Adults with Childhood-onset hypopituitarism
Kung-Ting Kao, Robyn Stargatt, Margaret Zacharin
P1-D3-191
PHENOTYPE EVALUATION OF COMBINED PITUITARY HORMONE DEFICIENCY CAUSED BY PROP1 GENE MUTATION IN COMPARISON TO PITUITARY DEFICIENCY CAUSED BY OTHER FACTORS
Agata Zygmunt-Górska, Jerzy Starzyk, Małgorzata Wójcik, Ewa Madetko-Talowska, Piotr Sucharski, Izabela Herman-Sucharska, Jacek J. Pietrzyk
P1-D3-192
Diencephalic syndrome in childhood craniopharyngioma – Results of German multicenter studies on 485 long-term survivors of childhood craniopharyngioma
Anika Hoffmann, Ursel Gebhardt, Anthe Sterkenburg, Monika Warmuth-Metz, Hermann L. Müller
P1-D3-193
A novel mutation of OTX2 associated with neonatally diagnosed combined pituitary hormone (CPHD) deficiency and bilateral microphthalmia
Aya Shimada, Masaki Takagi, Yukihiro Hasegawa
P1-D3-194
Type 3 Congenital Multiple Pituitary Hormone Deficiency
Lucia Radillo, Antonella Fabretto, Alexandru Saveanu, Sergio Demarini, Giorgio Tonini, Elena Faleschini, Gianluca Tornese, Maria Chiara Pellegrin
P1-D3-195
Childhood Craniopharyngioma – Changes of Treatment Strategies in Multinational Trials during the last 12 years
Anika Hoffmann, Monika Warmuth-Metz, Ursel Gebhardt, Torsten Pietsch, Fabian Pohl, Rolf-Dieter Kortmann, Gabriele Calaminus, Hermann L. Müller
P1-D3-196
Rathke cleft cysts and endocrine dysfunction in children
Marie Dupre, Frederic Brioude, Laurence Berard, Blandine Esteva, Muriel Houang
P1-D3-197
Congenital nasal pyriform aperture stenosis and pituitary abnormalities: case series of 20 patients and a management guideline for early identification of pituitary insufficiency
Suet Ching Chen, Helen McDevitt, W Andrew Clement, David M Wynne, Avril Mason, Malcolm Donaldson, S Faisal Ahmed, M Guftar Shaikh
P2-D1-512
Clinical Phenotype and Complications, Endocrinopathies and Neuroimaging Findings in a Case Series of SOD
I. Maris, C. Howard, C. Bogue, R. Morrissey, LC. Gregory, SM. O'Connell, MT. Dattani, SMP. O'Riordan
P2-D1-513
Polyuria and polydipsia: the deep waters of diagnosis.
Gabriella Pozzobon, Maria Piera Ferrarello, Chiara Maria Damia, Gisella Garbetta, Sara Osimani, Andrea Voto, Cristina Partenope, Giulia Pruccoli, Giuseppe Chiumello
P2-D1-514
Urinary Gonadotrophins For Assessment And Management Of Pubertal Disorders
Laura Lucaccioni, Jane McNeilly, Avril Mason, Claudio Giacomozzi, M. Guftar Shaikh, Lorenzo Iughetti, S. Faisal Ahmed
P2-D1-515
High prevalence of PROP1 gene defects among patients with multiple pituitary hormone deficiency in Lithuania
Ruta Navardauskaite, Petra Dusatkova, Barbora Obermannova, Roland W. Pfaeffle, Werner F. Blum, Dalia Adukauskiene, Natalija Smetanina, Ondrej Cinek, Rasa Verkauskiene, Jan Lebl
P2-D1-516
NEUROENDOCRINE DYSFUNCTIONS FOLLOWING TRAUMATIC BRAIN INJURY IN CHILDREN. A TWELVE-MONTH PROSPECTIVE STUDY.
PILAR ROJO, ATILANO CARCAVILLA, IRENE ORTIZ, DAVID ARJONA, RAÚL BORREGO, ÁNGEL ARAGONÉS
P2-D1-517
COULD BRAIN MRI REPLACE GH STIMULATION TESTS IN THE WORK-UP OF GH DEFICIENCY (GHD) IN THE FIRST YEARS OF LIFE?
Stefania Pedicelli, Giuseppe Scirè, Valentina Pampanini, Jessica Gubinelli, Gian Luigi Spadoni, Maria Luisa Manca Bitti, Marco Cappa, Brunetto Boscherini, Stefano Cianfarani
P2-D1-518
GOLIATH, a variant of DAVID syndrome?
CAROLINE HASSELMANN, MARK E. SAMUELS, GUY VAN VLIET
P2-D1-519
Hyperthyroidism due to thyrotropin secreting pituitary adenoma in a 7-year-old boy
Saygin Abali, Zeynep Atay, Belma Haliloglu, Tulay Guran, Abdullah Bereket, Serap Turan
P2-D1-520
Hypothalamic obesity in children with craniopharyngioma: Prevalence and risk factors of obesity and longitudinal trends of body mass index
Ja Hyang Cho, Ja Hye Kim, Yoo-Mi Kim, Jin-Ho Choi, Han-Wook Yoo
P2-D2-521
Association of pituicytoma and Cushing’s disease: a rare pediatric case.
Sara Ciccone, Paola Cambiaso, Daniela Longo, Romana Marini, Stefania Pedicelli, Annalisa Deodati, Stefania Galassi, Marco Cappa
P2-D2-522
Treatment options in a 14-year old boy with an atypic cabergolin-resistant macroprolactinoma with somatostatin receptor 2 expression and an increased proliferation rate
Angela Huebner, Felix Reschke, Gabriele Hahn, Thomas Pinzer, Matthias Meinhardt, Anke Pyper, Salvatore Cannavò, Gunter Stalla, Lorenz C Hofbauer
P2-D2-523
Long-term data including fertility in two females with hypothalamic hamartoma associated with central precocious puberty.
Antonis Voutetakis, Christina Kanaka-Gantenbein, Maria-Alexandra Magiakou, George Chrousos, Catherine Dacou-Voutetakis
P2-D2-524
Pituitary stalk interruption syndrome: A sequential manner to gain pituitary hormone deficiencies with still unknown molecular basis
Elena Jerez, Gabriela Echeverría, Teresa Muñoz-Calvo, Jesús Pozo-Román, Gabriel Martos-Moreno, Jesús Argente
P2-D2-525
Challenging treatment of gigantism in a boy with McCune-Albright syndrome
Melanie Hess, Sara Bachmann, Gabor Szinnai, Urs Zumsteg
P2-D2-526
Child with growth hormone deficiency due to remnant craniopharyngeal duct
Elpis Vlachopapadopoulou, Evgenia Maniatakou, Spyros Sgouros, Georgia Papaioannou, Irene Dikaiakou, Stefanos Michalacos
P2-D2-527
ADOLESCENTS WITH CHRONIC ENDOCRINE DISEASES: A MULTIDISCIPLINARY APPROACH. THE EXPERIENCE OF THE PAEDIATRIC CLINIC OF PALERMO
Maria Cristina Maggio, Rita Riticella, Giuseppe Salvo, Giuseppe Santangelo, Giovanni Corsello
P2-D2-528
Atypical Presention of Hypothermia Induced Diabetes Insipidus: A Case Report
Ellen Klocker, Himala Kashmiri
P3-D1-906
Pituitary dysfunctiona with associated lesions in the hypothalamo-pituitary region: Histiocytosis or dysgerminoma?
Elpis Vlachopapadopoulou, Vassilios Papadakis, Panagiotis Nomikos, Stefanos Michalacos, Sophia Polychronopoulou
P3-D1-907
A case of combined pituitary hormone deficiency in a patient affected by osteogenesis imperfecta
Evelina Maines, Grazia Morandi, Diego Ramaroli, Claudia Anita Piona, Paolo Cavarzere, Rossella Gaudino, Franco Antoniazzi
P3-D1-908
MACROPROLACTINOMA IN ADOLESCENCE: A CASE REPORT
Amanda Scott, Valli Velayutham, Robert Campbell, Ross Cuneo, Andrew Cotterill
P3-D1-909
Idiopathic central diabetes insipidus: a case of pediatric xhantogranuloma
Gabriella Pozzobon, Chiara Damia, Andrea Voto, Maria Piera Ferrarello, Gisella Garbetta, Sara Osimani, Giulia Pruccoli, Cristina Partenope, Giuseppe Chiumello
P3-D1-910
Central Diabetes Insipidus caused by congenital cytomegalovirus: a rare association?
Tiago Jeronimo dos Santos, Caroline Passone, Leandra Steinmetz, Louise Cominato, Hilton Kuperman, Thaís Della Manna, Hamilton Menezes Filho, Vaê Dichtchekenian, Joyce Pupo, Nuvarte Setian, Durval Damiani
P3-D1-911
Primary Polydipsia in a family with mutation in the AVP gene and proven central Diabetes Insipidus
Ruth Casey, Anne marie Hannon, Caroline Joyce, Domhnall O'Halloran, Susan O'Connell
P3-D3-912
Screening for SOX2 mutations in Bulgarian patients with congenital hyposomatotropism: first results
Ani Aroyo, Iva Stoeva, Daniela Dacheva, Radka Kaneva, Atanaska Mitkova, Alexander Oscar, Vassil Haikin, Vanio Mitev
P3-D3-913
Follow up for adult height of girl with the onset of puberty at 6 or 7 years old
Zhuang-jian Xu, Ya-ping Ma, Jin-ling Zhao, Jian-mei Zhang, Bing-yang Xia
P3-D3-914
The influence of specimen pH on urinary LH and FSH by immunochemiluminometric assays
Ya-ping MA, Zhuang-jian XU, Yu HU, Wen-ying ZHU, Qing WANG
P3-D3-915
Thickened Pituitary stalk with central diabetes insipidus: what diagnosis?
AMEL MERAZKA, ACHIR SAMIA, BAZ OUIDAD, FOUDIL DALILA, SEMROUNI MOURAD
P3-D3-916
Polyuria syndrome associated with visual disorders in children: Discuss at first Craniopharyngioma, the primary polydipsia is an exclusion diagnosis.
Rahem yacine, Belacel merouane, Achir samia
P3-D3-917
MULTIPLE PITUITARY HORMONE DEFICIENCY (MPHD) WITH TRANSITORY PITUITARY ENLARGEMENT DUE TO PROP-1 MUTATION (CASE PRESENTATION)
Lavinia La Grasta Sabolic, Gordana Stipancic, Marija Požgaj Šepec
P3-D3-918
MRI in children with growth hormone deficiency:
Ouidad BAZ, Mourad SEMROUNI, Samia SAKHER, Nadia CHOUIKRAT, Mourad BENALLEGUE
P3-D3-919
Dynamic Stimulation testing in Pediatric Endocrinology – experience of a pediatric endocrine unit in a developing country
Janani Sundaram, Hemchand Krishna Prasad, Gnanabalan Murugesan, Ravisekar Vasudevan, Thangavelu Sangaralingam
P3-D3-920
A case of hypopituitarism caused by traumatic brain injury in infancy
Shinji Higuchi, Noriko Nishina, Masaki Takagi, Yukihiro Hasegawa
P3-D3-921
Severe Features of Central Hypothyroidism und Hypoadrenalism effectively resolved by Treatment with Somatropin in a Boy with Panhypopituitarism
Gunter Šimic-Schleicher
P3-D3-922
A case of combined pituitary hormone deficiency (CPHD) due to anterior pituitary hypoplasia
Ekaterine Kvaratskhelia, Maia Rekhviashvili, David Metreveli, Rolf Peter Willig
P3-D3-923
Think Histiocytosis X facing insipid diabetes with thickened pituitary stalk
Lydia Lichtenberger-Geslin, Antoine Gourmel, Christian Sainte-Rose, Hélène Trifunovic-Bony, Karine Braun, Bernard Boudailliez, Catherine Devoldere
NP1.2
The role of microRNAs in diabetes
Romano Regazzi
P1-D1-139
Functional Characterization of Three Novel Mutations in the IGF1R Gene
Matias Juanes, Gabriela Guercio, Roxana Marino, Esperanza Berensztein, Marta Ciaccio, Silvia Gil, Marco A Rivarola, Alicia Belgorosky
P1-D1-140
Severe short stature and GH insensitivity due to a De Novo Heterozygous STAT5B Missense Mutation.
Jürgen Klammt, David Neumann, Shayne F Andrew, Marcela Drahosova, Heike Stobbe, Kyle Buckham, Ron G Rosenfeld, Roland Pfäffle, Vivian Hwa
P1-D1-141
Whole exome sequencing is an efficient approach to screen for associated genetic changes inof growth-relevant genes in primary IGF-1 deficiency (PIGFD)
Greta Grosse, Alina Hilger, Markus Draaken, Michael Ludwig, Heiko Reutter, Joachim Woelfle
P1-D1-144
Genetics of growth failure in small for gestational age (SGA) children
Romy Keppler, Natascha van der Werft-Grohmann, Karl Otfried Schwab, Ekkehart Lausch
P1-D3-188
Butyrate Stimulates Growth Hormone Secretion from Rat Anterior Pituitary Cells via the G-Protein-Coupled Receptors GPR41 and 43.
Maria Consolata Miletta, Vibor Petkovic, Andrée Eblé, Roland Ammann, Christa E. Flück, Primus E. Mullis
P2-D1-409
Ternary complex formation and IGFBP-3 proteolytic activity during childhood: Age-dependent changes
Judith S. Renes, Jaap van Doorn, Anita C.S. Hokken-Koelega
P2-D1-410
GHR gene variants within coding and intronic regions in children with idiopathic short stature (ISS).
María Gabriela Ballerini, Paula Scaglia, Alicia Martínez, Ana Keselman, Débora Braslavsky, Ignacio Bergadá, Héctor Guillermo Jasper, María Gabriela Ropelato, Horacio Domené
P2-D1-411
Spontaneous baseline GH secretion signalling as a regulator of bone metabolism in children
Ralph Decker, Björn Andersson, Anders Nygren, Kerstin Albertsson-Wikland
P2-D1-412
ALS deficiency due to a novel and two already described IGFALS gene mutations in an unusual non consanguineous family: Two compound heterozygous (father and son) and two heterozygous carriers (brother and mother).
Paula Scaglia, Ana Keselman, Lucía Martucci, Liliana Karabatas, María Gabriela Ballerini, Sabina Domené, Acosta Johanna, Héctor Jasper, Horacio Domené
P2-D1-413
A re-evaluation of GH secretion with combined test (GHRH+ARG/PD) in children with Prader-Willi syndrome
danilo fintini, sarah bocchini, graziano grugni, claudia brufani, armando grossi, marco cappa, antonino crinò
P2-D1-414
Final Height (FH) SDS Gain of Growth Hormone (GH) treated Children with SHOX Deficiency describing observational and clinical trial data
Imane Benabbad, Christopher Child, Jean-Claude Carel, Myriam Rosilio
P2-D1-415
IGF-I is associated with a more favourable pattern of body composition in obese children.
elena inzaghi, valentina pampanini, paola alessio, rossana fiori, Barbara baldini ferroli, stefano cianfarani
P2-D1-417
GH STIMULATED LEVELS IN PRADER-WILLI SYNDROME DURING THE TRANSITION PERIOD BETWEEN CHILDHOOD AND ADULTHOOD.
Graziano Grugni, Andrea Corrias, Stefania Di Candia, Danilo Fintini, Luigi Gargantini, Lorenzo Iughetti, Letizia Ragusa, Alessandro Salvatoni, Alessandro Sartorio, Sarah Bocchini, Maurizio Delvecchio, Giuseppe Chiumello, Antonino Crinò
P2-D1-448
A novel homozygous missense mutation in Growth Hormone Releasing Hormone Receptor Gene (GHRHR) in a large Turkish family presenting with isolated familial growth hormone deficiency and variable anterior pituitary size
Huseyin Demirbilek, Sophia Tahir, Riza Taner Baran, Maha Sherif, Mehmet Nuri Ozbek, Khalid Hussain
P2-D1-511
Relationship between Adenoid Vegetation and Neurosecretory Dysfunction (Pituitary Dysfunction)
Murat DOGAN, Keziban BULAN, Sultan KABA, Fatih GARCA
P2-D2-416
Absence of growth hormone signaling induces hypothalamic inflammation that is reversed in response to a high fat diet.
Eva Baquedano, Ana Ruiz-López, Elena Pardo-Barquín, Elahu S Gosney, James Herpy, Julie A Chowen, Jesús Argente, John J Kopchick, Laura M Frago
P3-D1-810
The role of IGF-IR gene mutation in the development of Oligodendrocytes
Fan Yang, Mei Tang, Hedong Li
P3-D1-811
A Novel GHR mutation,c.439+1G>A;in a Family with Laron syndrome
Mona Attia, Atef Abeer, Ibrahim Makarem, Malcolm Donaldson, Lou Metherell, Sameh Tawfik, Wafaa Dowedar
P3-D1-812
Maternal inheritance of an heterozygous exon 4 IGF I gene mutation (g.65941 G>A) in an IUGR child with mild post natal growth retardation
Muriel HOUANG, Fréderic BRIOUDE, Salah AZZI, Nathalie THIBAUD, Laurence PERIN, Yves LE BOUC, Irène NETCHINE
P3-D1-813
Body Mass Index, IGF1-SDS and rhGH treatment
Ioannis Anargyros Vasiliakis, Ruth Gausche, Christoph Beger, Jürgen Kratzsch, Wieland Kieß, Roland Pfäffle
P3-D1-814
A Novel GH1 Functional Mutation in a Family with Isolated Growth Hormone Deficiency
Bilgin Yuksel, Fatih Gurbuz, Atil Bisgin, Eda Mengen Ucakturk, Ali Kemal Topaloglu
P3-D1-815
Insulin Tolerance Test and GHRH plus Arginine in the Reassessment of Pituitary Function at Adult Height Achievement
Natascia Di Iorgi, Maria Carolina Salerno, Marco Cappa, Sandro Loche, Giorgio Radetti, Donatella Capaldo, Flavia Napoli, Annalisa Calcagno, Anna Elsa Maria Allegri, Ofelia Bianca Iovovich, Serena Noli, Stefano Parodi, Mohamad Maghnie
P3-D1-816
The level and conformation of blood plasma carotenoids in girls with Turner syndrome after 1 year of growth hormone therapy
Maria Pankratova, Maria Faassen, Svetlana Kovalenko, Alexander Yusipovich, Adil Baizhumanov, Tatyana Shiryaeva, Georgy Maksimov
P1-D1-174
Use of Long Acting Somatostatin Analogue (Lanreotide) in Congenital Hyperinsulinism
Pratik Shah, Clare Gilbert, Kate Morgan, Louise Hinchey, Hannah Levy, Roberta Button, Niamh Landy, Rebecca Margetts, Senthil Senniappan, Emma Bascompta Santacreu, Carles Morte Martí, Carles Celma Lezcano, Rakesh Amin, Khalid Hussain
P1-D1-175
The role of mTORC1/RagGTPase and IGF-1R/mTORC2/Akt Pathways and the Response of Diffuse Congenital Hyperinsulinism to Sirolimus
Senthil Senniappan, Nina Tatevian, Pratik Shah, Ved Bhushan Arya, Sarah Flanagan, Sian Ellard, Robert Brown, Khalid Hussain
P1-D1-182
Clinical and Histological Heterogeneity of Congenital Hyperinsulinism due to Paternally Inherited Heterozygous ABCC8/KCNJ11 Mutations
Ved Bhushan Arya, Maria Guemes, Azizun Nessa, Syeda Alam, Pratik Shah, Clare Gilbert, Senthil Senniappan, Sarah E. Flanagan, Sian Ellard, Khalid Hussain
P1-D1-183
Molecular genetic analysis of Czech patients with congenital hyperinsulinism: surprisingly high incidence of HNF1A mutations
Klara Rozenkova, Lenka Dusatkova, Petra Dusatkova, Jitka Kytnarova, Barbora Obermannova, Blanka Rypackova, Zdenek Sumnik, Jan Lebl, Ondrej Cinek, Stepanka Pruhova
P1-D2-31
Primary pancreatic insulinomas: Clinical, morphological and genetic characteristics of 12 children
Maria Melikyan, Larisa Gurevich, Sergey Makarov, Alexey Stepanov, L Friis-Hansen, Valentina Peterkova, Henrik Christesen
P2-D3-474
Plasma Glucagon and Somatostatin levels in children with Congenital Hyperinsulinism during hypoglycaemia
Pratik Shah, Gregg Mamikunian, Clare Gilbert, Kate Morgan, Louise Hinchey, Ved Arya, Huseyin Demirbilek, Khalid Hussain
P2-D3-475
Long term follow up of children with congenital hyperinsulinism on octreotide therapy
Huseyin Demirbilek, Pratik Shah, Ved Bhushan Arya, Khalid Hussain
P2-D3-476
Glucagonsecretion in response to hypoglycemia in patients with congenital hyperinsulinism
yi wang, chunxiu gong, chang su
P2-D3-477
Opioid-induced endocrinopathy in a toddler with chronic codeine intoxication
Sara Van Aken, Saskia Van Der Straaten, Kathleen De Waele, Martine Cools, Margarita Craen, Jean De Schepper
P2-D3-478
Case Report: A Rare Cause of Hypoglycemia in a Neonate
Parissa Salemi, Jessica Strohm Farber
P2-D3-479
The Majority of Late Presenting Congenital Hypoglycaemia Disorders are Really Missed Diagnosis. What can we do to Improve Diagnosis in the New-born Period?
Lisa Troung, Paul Thornton
P2-D3-480
The role of plasma C Peptide concentration in the diagnosis of Congenital Hyperinsulinism (CHI)
Julie Green, Dinesh Giri, Arundoss Gangadharan, Jo Blair, Poonam Dharmaraj, Urmi Das, Senthil Senniappan, Mohammed Didi
P2-D3-481
Presentation, clinical and genetic outcomes in a series of infants with Congenital Hyperinsulinism
Aoife Carroll, Brian Gibney, Ciara McDonnell, Sinead Moloney, Ardeshir Monavari, Nuala Murphy
P2-D3-482
Feeding issues in children with Congenital Hyperinsulinism
Clare Gilbert, Kate Morgan, Louise Hinchey, Rebecca Margetts, Alex Forsyth, Martina Ryan, Pratik Shah, Khalid Hussain
P2-D3-483
Neurodevelopmental Outcomes In Early And Late Presenting Congenital Hyperinsulinism
Zainaba Mohamed, Jacqueline Nicholson, Imran Zamir, Thomas Butler, Lindsey Rigby, Louise Bowden, Philip Murray, Caroline Steele, Raja Narender Rao Padidela, Leena Patel, Karen Cosgrove, Peter Clayton, Mark Dunne, Indraneel Banerjee
P2-D3-484
Effects of Trigonella foenum graecum and sodium orthovanadate on antioxidant enzymes, membrane bound ATPases and glucose transporter expression in muscle, kidney and brain in female diabetic rats.
Pardeep Kumar, R Kale, N Baquer
P2-D3-485
Nocturnal hypoglycaemia in diabetic children: continuous glucose monitoring (cgms) reveals more of the iceberg.
Sara Bachmann, Eva Martin, Vreni Ritschard, Melanie Hess, Katharina Jockers, Jean-Marc Vuissoz, Urs Zumsteg
P2-D3-486
Fasting Hypoglycemia associated with hyperinsulinemia in a Child with Acute Lymphoblastic Leukemia (ALL) and 6-mercaptopurine (6-MP) therapy
Jadranka Popovic
P3-D1-874
Clinical characteristics and phenotype-genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations
Huseyin Demirbilek, Ved Bhushan Arya, Mehmet Nuri Ozbek, Aysehan Akinci, Murat Dogan, Fatma Demirel, Jayne Houghton, Sultan Kaba, Fatma Guzel, Riza Taner Baran, Sema Unal, Selahattin Tekkes, Sarah E Flanagan, Sian Ellard, Khalid Husssain
P3-D1-875
Clinical remission in a patient with congenital hyperinsulinism due to paternally inherited two novel mutations in KCJN11 gene.
Ayse Nurcan CEBECI, Jayne HOUGHTON, Sian ELLARD
P3-D1-876
Biochemical studies in patients with hyperinsulinaemic hypoglycaemia.
hessah Al Otaibi, Senthil Senniappan, Syeda Alam, Khalid Hussain
P3-D1-877
CONGENITAL HYPERINSULINISM: CLINICAL AND MOLECULAR CHARACTERISTICS OF BRAZILIAN PATIENTS
Raphael Liberatore Junior, Carlos Martinelli Junior, Gil Guerra Junior, Thais Della Manna, Ivani Silva
P3-D1-878
Clinical and genetic analysis of 95 cases of congenital hyperinsulinism
Shuyue Huang, Chunxiu Gong, Chang Su, Zhan Qi, Di Wu, Bingyan Cao, Yi Gu, Wenjing Li, Min Liu, Xuejun Liang
P3-D1-879
Congenital Hyperinsulinism: A Single-Center Experience
Murat Dogan, Sultan Kaba, Keziban Bulan
P3-D1-880
Persistent hyperinsulinemic hypoglycemia of an infancy carrying ABCC8 Arg598stop mutation
Jianfang Zhu, Weifen Zhu, Chunlin Wang, Li Liang
P3-D1-881
A Case of Hyperinsulinism/hyperammonemia Syndrome.
Young Suk Shim, Hwal Rim Jeong, Hae Sang Lee, Jung Sub Lim, Jin Soon Hwang
P1-D1-176
A novel mutation of the PCSK1 gene with surprising enzymatic consequences causes proprotein convertase 1/3 deficiency and consequent endocrinopaties
Abdulsalam Abu-Libdeh, Michael Wilschanski, Montaser Abbasi, Elias Blanco, Iris Lindberg, Michael Yourshaw, Itai Berger, Martín Martin, Orly Elpeleg, David Zangen
P1-D1-177
Growth and puberty in monozygotic twins with intra-twin birth-weight difference
Sandra Schulte, Bettina Gohlke, Peter Bartmann, Charlotte Prinz, Lioba Wimmer, Joachim Woelfle
P1-D1-178
Pubertal and adrenal hormones in monozygotic twins with intra-twin birth-weight difference
Sandra Schulte, Joachim Woelfle, Peter Bartmann, Michaela Hamm, Birgit Stoffel-Wagner, Felix Schreiner, Bettina Gohlke
P1-D1-179
VARIATIONS IN PROTEIN EXPRESSION IN SMALL-FOR-GESTATIONAL-AGE NEWBORNS
Maria Dolores Ruiz-González, Maria Dolores Cañete, José Luis Gómez-Chaparro, Juan Luis López-Barea, Ramón Cañete
P1-D1-180
Long-term Cognitive Effects of Children from Dexamethasone-treated Pregnancies
Anna Shaytarova, Elena Khramova, Lyudmila Suplotova
P1-D1-181
The Prevalence And Outcome Of Sex Chromosome Abnormalities Detected Prenatally In Scotland
Angela Lucas-Herald, Ruth McGowan, Fiona Cann, Lorna Crawford, Syed Faisal Ahmed
P1-D2-8
Normal value of steroids in Amniotic Fluid by LC-MS/MS method
Ingrid Plotton, Severine Ruet, Chantal Rigaud, Marianne Till, Damien Sanlaville, Yves Morel
P2-D3-436
Metabolic profile of neonates with different duration of gestation and different size at birth
Mirjana Kocova, Snezana Palcevska-Kocevska, Marija Krstevska, Elena Sukarova-Angelovska, Elizabeta Zisovska
P2-D3-500
The contribution of Maternal Malaria Exposure and Metabolic Markers to Change in Blood Pressure (BP) in Nigerian Children over the first 3 Years of Life.
Jasmin Farikullah-Mirza, Andrew Whatmore, Omolola Ayoola, Olayemi Omotade, Imogen Butcher, Handrean Soran, Kennedy Cruickshank, Peter Clayton
P2-D3-501
Kabuki 47,XXY syndrome: a case report.
Stefania Pedicelli, Romana Marini, Sara Ciccone, Paola Cambiaso, Maria Cristina Digilio, Carla Bizzarri, Marco Cappa
P2-D3-502
Retrospective Analysis of Cortisol Measurement in Neonates
Geetika Kumar, Jane McNeilly, Helen McDevitt, Faisal Ahmed, Avril Mason, Guftar Shaikh
P2-D3-503
Survey of opinion on the antenatal and surgical management of disorders of sex development and congenital adrenal hyperplasia
Mary White, Jacqueline Hewitt
P2-D3-504
Vitamin D deficiency as the primary cause of neonatal hypocalcemia in a tertiary hospital
ARIADNA CAMPOS-MARTORELL, KARLA NARVAEZ, MARIA CLEMENTE, DIEGO YESTE, EDUARD MOGAS, LAURA GERONES, ANTONIO CARRASCOSA
P2-D3-505
Random serial cortisol levels in neonates: does it reduce Synacthen testing?
Susannah Pye, Zoe Smith, Rakesh Amin
P2-D3-507
A couple of naturally conceived twins affected by Prader Willi syndrome.
Stefania Di Candia, Marta Massimello, Bruna Cammarata, Paola Sgaramella, Giuseppe Chiumello
P3-D1-882
PROJECT epiSGA - PreMeb . Presentation , subject recruitment and initial data
Ignacio Diez-Lopez, Ainhoa Sarasua-Miranda, Marta Hoyo-Moracho, Isabel Lorente-Blazquez, Raquel Gomez de Segura Lorente, Dorleta Pérez Campos, Victor Manuel Rodriguez-Rivera, Maria Teresa Macarulla-Arenaza
P3-D1-883
IODINE STATUS IN PREGNANT, LACTATING MOTHERS AND THEIR INFANTS AND EFFECTS OF IODINE SUPPLEMENTATION
Natalya Zelinskaya, Marina Mamenko, Natalya Belykh
P3-D1-884
Gender differences in sex steroids and insulin-like growth factor-I at birth and at five years of age
Kerstin Allvin, Ann-Katrine Karlsson, Carina Ankarberg-Lindgren, Jovanna Dahlgren
P3-D1-885
Neonatal seizures neonatal due to hypocalcemia secondary to maternal vitamin D deficiency
ARIADNA CAMPOS-MARTORELL, KARLA NARVAEZ, MARIA CLEMENTE, DIEGO YESTE, EDUARD MOGAS, LAURA GERONES, ANTONIO CARRASCOSA
P3-D2-887
Permanent Neonatal Diabetes Mellitus in China
Ke Huang, Li Liang, Junfen Fu, Guanpin Dong
P3-D2-888
Neonatal Neurogenic Diabetes Insipidus – a case report
Inês Alves, Fátima Clemente, Cíntia Castro-Correia, Helena Pinto, Hercília Guimarães, Manuel Fontoura
P3-D2-889
Evolution and epidemiological assessment of the influence of sociological variables of children born SGA in the last decade in Basque Country
Ignacio Diez-Lopez, Marta Hoyo-Moracho, Ainhoa Sarasua-Miranda, Isabel Lorente-Blazquez, Victor Manuel Rodriguez-Rivera, Maria Teresa Macarulla-Arenaza, Raquel Gomez de Segura Lorente, Dorleta Pérez Campos
P3-D2-890
A novel mutation causing Pseudohypoaldosteronsim
Emmeline Heffernan, Noina Abid, Shane McKee
P3-D2-891
A novel mutation in the NR3C2 gene causing Pseudohypoaldosteronism Type 1
Amalia Sertedaki, Christina Kanaka-Gantenbein, George P. Chrousos
P3-D2-892
Subcutaneous fat necrosis causing prolonged hypercalcaemia in a neonate: An unusual case
Usha Niranjan, Vivek Desai, Nigel Brooke, Anuja Natarajan
P3-D2-893
Severe vitamin D deficiency among pregnant women and their newborns in Turkey
Mesut Parlak, Zuhal Kalay, Ahmed Kirecci, Ozgur Guney, Esad Koklu, Salih Kalay
P3-D2-894
Relationship of birth gestational age with Insulin-like Growth Factor Binding Protein-3 beyond influences of gender, small-for-gestational-age status, caesarean section, caloric intake, parenteral nutirtion and predominant breast milk feeding in the not-life threatened newborn: relevance of not-brain-related birth body weight.
Cesare Terzi, Werner F. Blum, Sergio Zani, Marco Riani, Gabriele Tridenti, Andrea Cerioli, Lidia Garavelli, Sergio Bernasconi, Raffaele Virdis, Giacomo Banchini
P3-D2-895
Relationship of birth gestational age with the ratio between Insulin-like Growth Factor-II and Insulin-like Growth factor Binding Protein-3 in blood serum beyond influences of gender, small-for-gestational-age status, caesarean section, caloric intake and predominant breast milk feeding in the not-life-threatened newborn: relevance of parenteral nutrition.
Cesare Terzi, Raffaele Virdis, Werner F. Blum, Sergio Zani, Marco Riani, Gabriele Tridenti, Andrea Cerioli, Elena Chesi, Sergio Bernasconi, Giacomo Banchini
P3-D2-896
Cord blood vitamin D concentrations in native and immigrant population in a mediterranean area of Spain
Miguel Angel Guagnelli, Diego Yeste, Roser Ferrer, Inmaculada Comás, Antonio Carrascosa
P3-D2-897
TRANSIENT NEONATAL DIABETES MELLITUS: New Case
Suna Hancili, Ayla Güven, Ilke Mungan Akin, Ayse Nurcan Cebeci, Sian Edwards
P3-D2-898
MARFAN NEONATAL SYNDROME: A CASE REPORT
Magdalena Hawkins, Ana Alcalde, Julia Yebra, Maria Royo, Beatriz Perez-Seoane, Maria de la Serna, Teresa Raga, Ana Barrios, Sixto García-Miñaur
P1-D1-198
Stability conditions in estradiol matrix patches; in vitro studies for application in pediatrics
Carina Ankarberg-Lindgren, Theo Sas
P1-D1-199
Associations of Vascular Biomarkers and The Somatotrophic Axis with Carotid Ultrasound and Echocardiography Findings in Relation To Turner Arteriopathy
Ahmet Uçar, Fahrettin Öz, Firdevs Baş, Hüseyin Oflaz, Kemal Nişli, Melike Tuğrul, Feyza Darendeliler, Nurçin Saka, Şükran Poyrazoğlu, Rüveyde Bundak
P1-D1-201
The effect of 17ß-estradiol on uterine volume in young women with Turner syndrome – a 5 year randomized controlled clinical trial
Line Cleemann, Kirsten Holm, Eva Fallentin, Nini Møller, Bent Kristensen, Sven Oluf Skouby, Per Leth-Esbensen, Eva Mosfeldt Jeppesen, Claus Gravholt
P1-D1-202
Genetic markers in the study of chromosome Y in the population of girls with Turner syndrome
Aleksandra Rojek, Monika Obara-Moszynska, Barbara Rabska-Pietrzak, Zofia Kolesinska, Marek Niedziela
P1-D1-203
Girls with Turner syndrome have normal muscle force but decreased muscle power
Ondrej Soucek, Jan Lebl, Jana Matyskova, Marta Snajderova, Stanislava Kolouskova, Stepanka Pruhova, Zdenek Hlavka, Zdenek Sumnik
P1-D1-205
Evaluation of second sexual chromosome presence on Turner Syndrome 45,X in tissues of different embryonic origins
M. G. ASSUMPÇÃO, A. H. R. BATISTA, M. N. ROCHA, C. KOCHI, F. RICHETI, C. S. CORRÊA, C. A. LONGUI
P1-D1-208
Growth hormone therapy in Turner syndrome patients: the effects on nutritional status, adipokines and aortic dilatation
Hanna Magnuszewska, Maria Gnacinska-Szymanska, Piotr Wisniewski, Piotr Potaz, Dorota Birkholz-Walerzak, Maria Korpal-Szczyrska, Krzysztof Sworczak
P1-D1-209
EVALUATION OF SITTING HEIGHT/HEIGHT STANDARD DEVIATION SCORE IN PATIENTS WITH TURNER SYNDROME
Mikayir Genens, Gamze Kaya, Ceren Melis Ulak, Sukran Poyrazoglu, Firdevs Bas, Ruveyde Bundak, Nurcin Saka, Feyza Darendeliler
P2-D3-610
Therapeutic effects of growth hormone combined with low-dose stanozolol on growth velocity and final height of girls with Turner syndrome
Hong-Shan Chen, Min-Lian Du, Yan-Hong Li, Hui Xiong, Hua-Mei Ma, Qiu-Li Chen
P2-D3-611
Epidemiology of Turner syndrome in Iceland 1968-2012
Arndis Audur Sigmarsdottir, Johann Heidar Johannsson, Helga Agusta Sigurjonsdottir, Arni V. Thorsson
P2-D3-612
Anti-Müllerian Hormone: a marker of premature ovarian insufficiency in girls with Turner syndrome
Catarina Mendes, Liliana Pinho, Teresa Borges, Maria João Oliveira, Helena Cardoso
P2-D3-613
Nationwide Study of Turner Syndrome During Childhood in Turkey:Evaluation of Associated Problems
EDIZ YESILKAYA, FEYZA DARENDELILER, ABDULLAH BEREKET, FIRDEVS BAS, SUKRAN POYRAZOGLU, BANU KUCUKEMRE AYDIN, SUKRAN DARCAN, BUMIN DUNDAR, MUAMMER BUYUKINAN, CENGIZ KARA, ERKAN SARI, ERDAL ADAL, AYSEHAN AKINCI, MEHMET EMRE ATABEK, FATMA DEMIREL, NURULLAH CELIK, BEHZAT OZKAN, BAYRAM OZHAN, PEYAMI CINAZ, PEDIATRIC ENDOCRINOLOGY TURNER STUDY GROUP
P2-D3-614
AORTIC DILATION IN A LARGE COHORT OF PAEDIATRIC AND YOUNG ADULT PATIENTS WITH TURNER SYNDROME
Nadia Geniuk, Elisa Vaiani, Ana Rizzi, Gabriela Guercio, Monica Warman, Diego Michelli, Marco Rivarola, Alicia Belgorosky
P2-D3-615
Aortic Dimensions and cardiac anomalies in a cohort of children with Turner syndrome
Nimasari Ginige, Shamya de Silva, Shehan Perera
P2-D3-616
Improvements in bone mineral density in girls of prepubertal age with Turner syndrome
Oleg Malievsky, Natalya Volevodz, Valentina Peterkova
P2-D3-617
Early occurrence of Gonadoblastoma found at Elective Gonadectomy in Turner Syndrome mosaic for Y Chromosome
J. MacMahon, R. Morrissey, M. McDermott, M. O'Sullivan, F. Quinn, A. Green, S.A. Lynch, S.M. O'Connell
P2-D3-618
Growth hormone deficiency as a cause of persistent hypoglycaemia in a child with Turner mosaic and Kabuki Syndrome.
Michal Ajzensztejn, Pratik Shah, Noina Abid, Jane Hurst, Deborah Morrogh, Shane McKee, Khalid Hussain
P2-D3-619
A Child with Clinical and Cytogenetic Features of Male Edward Syndrome and Turner Syndrome with bilateral Gonadoblastoma in Infancy.
J. MacMahon, R. Morrissey, M. McDermott, F. Quinn, A. Green, S.M. Lynch
P2-D3-620
Turner syndrome: analysis of changes in the age at diagnosis and phenotypic and genotypic description of 174 patients
Julie AUGER, Abderrahim OUSSALAH, Laetitia LAMBERT, Jacqueline VIGNERON, Philippe JONVEAUX, Bruno LEHEUP
P3-D1-962
46,XY Female with Turner Syndrome, Crohn’s Disease and low level mosaicism for monosomy X
Emir Tas, Svetlana Yatsenko, Jadranka Popovic
P3-D3-867
The effect of GH and pubertal induction therapy in Turner Syndrome.
Sukran Darcan, Samim Ozen, Ozge Koprulu, Tahir Atik, Ferda Ozkinay, Damla Goksen
P3-D3-868
Hearing loss in Turner syndrome
Ouidad BAZ, Mourad SEMROUNI, Samia SAKHER
P3-D3-869
Genotype-Phenotype Correlation in Turner Syndrome
Adel Djermane, Asmahane Ladjouze, Yasmine Ouarezki, Belaid Ait-Abdelkader, Leila Kedji, Abdeljalil Maoudj, Karima Berkouk, Lakhder Griene, Abdennour Laraba
P3-D3-870
Primary amenorrhea with normal stature: why not Turner syndrome?
Ioana Hristov, Ana Hreniuc, Simona Gherasim, Maria-Christina Ungureanu, Cristina Preda, Carmen Vulpoi, Voichita Mogos, Letitia Leustean
P3-D3-871
The causes of short stature in Turner syndrome
Ruimin Chen, Ying Zhang, Xiaohong YANG, Xiangquan Lin, Xin YUAN
P3-D3-872
Descriptive analyses of Turner syndrome
Mimouna Bessahraoui, Malika Naceur, Sakina Niar, Amel Zennaki, Farouk Arbi, Meriem Ousaleh, Karim Bouziane-Nedjadi
P3-D3-873
Phenotypic and genotypic characteristics of patients with Turner syndrome
Soumeya Fedala, Ali el mahdi Haddam, Farida Chentli, Djamila Meskine, Lyna Akkache, Hafsa Siyoucef
P1-D2-23
Analysis of zinc transporter ZnT8 autoantibodies in children and adolescents with autoimmune thyroid diseases
Artur Bossowski, Hanna Borysewicz-Sanczyk, Barbara Glowinska-Olszewska, Beata Sawicka, Anna Bossowska, Justyna Michalak, Jadwiga Furmaniak
P1-D2-25
Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy: new insights into phenotype and genotype
Mariella Valenzise, Tommaso Aversa, Alessandra Fierabracci, Paolo Porcelli, Corrado Betterle, Filippo De Luca
P1-D2-28
Immune changes are observed after radioiodine treatment for hyperthyroidism in Graves’ disease patients
Sarah Côté-Bigras, Jean Verreault, Diane Rottembourg
P1-D2-33
Immunological studies in Rapid-onset Obesity with Hypothalamic Dysfunction, Hypoventilation, Autonomic Dysregulation and NEural Tumor (ROHHADNET) syndrome
FLAVIA NAPOLI, ANNALISA CALCAGNO, NATASCIA DI IORGI, ANNA ELSA MARIA ALLEGRI, MARIANNA VANNATI, LAURA DE MIGLIO, ROBERTA BIANCHERI, ISABELLA CECCHERINI, YAEL HACOHEN, LESLIE JACOBSON, ANGELA VINCENT, MOHAMAD MAGHNIE
P2-D1-318
Serum level of osteoprotegerin and total sRANKL in adolescents with type 1 diabetes mellitus
Mieczyslaw Szalecki, Elzbieta Wierzbicka, Pawel Pludowski, Maciej Jaworski
P2-D3-487
THE CYTOTOXIC ABILITY OF NK CELLS IN CHILDREN WITH AUTOIMMUNE THYROIDITIS.
Anna Kucharska, Katarzyna Popko, Iwona Osinska, Urszula Demkow
P2-D3-488
High prevalence of diabetes mellitus among patients with APS type 1 in Russia
Elizaveta Orlova, Leila Sozaeva, Lubov Zilberman, Galina Svetlova, Maria Kareva, Olga Ivanova, Valentina Peterkova
P2-D3-489
IMMUNOGENETICS AND CLINICAL CHARACTERISTICS OF PATIENTS WITH THE MOST COMMON ORGAN-SPESIFIC AUTOIMMUNE DISEASES : EVALUATION IN RESPECT OF GENDER AND AUTOIMMUNITY
Murat Karaoglan, Mehmet Keskin, ozlem Keskin, sibel özturk
P2-D3-490
Genetic Susceptibility in Autoimmune Polyglandular Syndrome Type 3 Variant
Amir Babiker, Iman Al Gadi, Nasir Al Jurayyan, Sarar Mohamed, Hessah Al Otaibi, Khalid Hussain
P2-D3-491
Autoimunne thyroiditis in type 1 diabetes mellitus pediatric population
Clara Gomes, Joana Andrade, Assunção Luís, Gabriela Laranjo, Joana Campos
P2-D3-492
Autoimmune Polyglandular Syndrome in a patient with Tuberous Sclerosis
Sophie Stoppa-Vaucher, Eglantine Elowe-Gruau, Franziska Phan-Hug, Nelly Pitteloud, Michael Hauschild
P3-D3-646
Hypothyroidism in anorexia nervosa due to primary autoimmune pathogenesis
Rajesh Chidanandaswamy, Mars Skae
P3-D3-647
Autoimmune disease and Arnold Chiari Syndrome: any correlation?
Federica Ortolani, Albina Tummolo, Stefania Fedele, Maristella Masciopinto, Sabino Pesce, Francesco Papadia, Domenica Cornacchia, Arianna Labbate, Marcella Vendemiale, Elvira Piccinno
P3-D3-648
Genetically proven APS type 1 in two siblings
Desislava Yordanova, Elisaveta Stefanova, Krasimira Kazakova, Zdravka Todorova, Mihaela Dimitrova
P3-D3-649
Rare association of diabetes insipidus and autoimmune thyroiditis
Mirjana Kocova, Daniela Pop Gjorceva
P3-D3-650
Coexistence of unusual and distinctive initial clinical manifestations of systemic lupus (SLE) erythematosus: A child case presentation and evaluation of polyglandular autoimmune syndrome in SLE
murat karaoglan, mehmet keskin, sibel öztürk, ozlem kesin
P1-D2-24
Final height and body mass index in English and Italian adult survivors of childhood acute lymphoblastic leukemia (ALL) treated without cranial radiotherapy.
Patrizia Bruzzi, Assunta Albanese, Stephen Nussey, Barbara Predieri, Lorenzo Iughetti, Alison Leiper
P1-D2-27
Late endocrine effects despite reduced intensity chemotherapy for bone marrow transplantation in children
Jonathan Howell, Kasiani Myers, Adam Lane, Gregory Wallace, Sonata Jodele, Susan Rose
P1-D2-30
Managing children with Thickened Pituitary Stalk (TPS) and/or Idiopathic Central Diabetes Insipidus (ICDI): A Single Centre Experience on 63 children
Manuela Cerbone, Ash Ederies, Laura Losa, Carolina Moreno, Kristi Sun, Helen A Spoudeas
P1-D2-32
Papillary thyroid cancer after hematopoietic stem cell transplantation in young age
Marta Snajderova, Petra Keslova, Pavla Sykorova, Petr Sedlacek, Renata Formankova, Jan Stary
P2-D3-493
Role of Metformin in the treatment of Hypothalamic obesity
Arundoss Gangadharan, Mohammed Didi, Barry Pizer, Lisa Howell, James Hayden, Conor Mallucci, Benedetta Pettorini, Joanne C Blair
P2-D3-494
Three Year Experience of a National Interdisciplinary Initiative to Improve Outcomes for Children with Hypothalamic Pituitary Axis Tumours (HPATs) Using Multi-site Videoconferencing for Decision Making on Behalf of the UK HPAT Interest Group.
Daniel Perelberg, Paul Morillon, Ash Ederies, Kristan Aquilina, Neil Dorward, Anton Michalski, Darren Hargrave, Yen-Ching Chang, Nillofar Bozorgi, Samantha James, Marta Korbonits, William Drake, Scott Akker, Connor Mallucci, Barry Pizer, Jo Blair, Ian Kamaly, Peter Clayton, Helen Spoudeas
P2-D3-495
Early occurrence of Graves’ disease after severe hypothyroidism in boy irradiated for Hodgkin’s disease.
Grazia Cantelmi, Anna Grandone, Caterina Luongo, Maria Carmela Affinita, Flora Micillo, Carmine Ficociello, Paolo Indolfi, Fiorina Casale, Emanuele Miraglia del Giudice, Laura Perrone
P2-D3-496
Endocrine dysfunction following treatment of medulloblastoma: a single centre experience
Suma Uday, Midhu Raju, Sabah Alvi
P2-D3-497
Gonadal tumor in 46,XY and 45,X/46,XY female patients – one clinical center experience
Aneta Gawlik, Aleksandra Antosz, Grzegorz Kudela, Agnieszka Drosdzol-Cop, Agnieszka Zachurzok, Pawel Matusik, Halla Kaminska, Tomasz Koszutski, Ewa Malecka-Tendera
P2-D3-498
A RARE BRAIN TUMOR IN NOONAN SYNDROME: REPORT OF TWO CASES.
Maria Chiara Pellegrin, Gianluca Tornese, Elisabetta Cattaruzzi, Eva Blank, Matthias Kieslich, Alessandro Ventura
P2-D3-499
Growth hormone-secreting pituitary adenoma with gigantism: A challenging case
Amish Chinoy, Dunia Ismail, Jennifer Kalitsi, Nadia Gordon, Peter Bullock, Ritika Kapoor, Simon Aylwin, Charles Buchanan
P3-D1-903
Xanthogranulomatous Hypophysitis: A rare but mistaken pituitary lesion
Jaya Sujatha Gopal Kothandapani, Veejay Bagga, Stephen Wharton, Saurabh Sinha, Paul Dimitri
P3-D1-904
Long term endocrinological follow up in diencephalic syndrome
Maria Parpagnoli, Salvatore Seminara, Giulia Anzilotti
P3-D1-905
Key-role of thyrotropin deficiency in disclosing craniopharyngioma diagnosis in a short girl with Hashimoto’s thyroiditis
Tommaso Aversa, Mariella Valenzise, Giuseppina Zirilli, Mariaausilia Catena, Filippo De Luca, Malgorzata Wasniewska
P3-D3-651
Diabetes mellitus after hematopoietic stem cell transplantation
KARLA MARIA NARVAEZ BARROS, ARIADNA CAMPOS MARTORELL, MARIA CLEMENTE LEON, IZASKUN ELORZA ALVAREZ, DIEGO YESTE FERNANDEZ, ANTONIO CARRASCOSA LEZCANO
P3-D3-652
PRESERVATION OF OVARIAN FUNCTION IN YOUNG FEMALES CANCER SURVIVORS WITH RISK OF OVARIAN FAILURE
Maria Chueca, Sara Berrade, Isabel San Miguel, Mirentxu Oyarzábal, Maria Sagaseta de Ilurdoz, Teodoro Dura, Javier Molina
P3-D3-653
Late endocrine effects in children and adolescentes submitted to allogenic bona marrow tranplantation
Hilton Kuperman, Lilian Argentino Pinchiari, Caroline Kupsch Medrado, Claudilene Battistin, Thais Della Manna, Vaê Dichtchkenian, Hamilton Cabral de Menezes Filho, Leandra Steinmetz, Louise Cominato, Juliana Folloni Fernandes, Lilian Maria Cristofani, Vicente Odone Filho, Durval Damiani
P3-D3-654
Adrenocortical tumor: a case report
Elisa Guidoni, Renato Scarinci, Giovanna Municchi
P3-D3-655
A conservative approach to the management of endocrine neoplasia in Carney Complex in an adolescent male
Carley Frerichs, Mohammed Didi, Laurence Abernethy, Simon Kenny, Ian Ellis, Joanne Blair
P3-D3-656
Two Cases of Thyroid Carcinoma in Children
Bethany Mitchell, Noina Abid, Fiona Eatock, Deirdre Donnelly
P3-D3-657
Is there any correlation between height and pediatrics’ malignancy
bahram darbandi, maryam jafroodi, adel baghersalimi, shahin koohmanaee, afagh Hassanzadeh Rad, Setila dalili
P3-D3-658
Increasing Testicular Size Due to Bilateral Large Cell Calcifying Sertoli Cell Tumours (LCCSTs) in a peri-pubertal child with Carney Complex
Sarah Geoghegan, Rose Morrissey, Michael Moore, M O'Sullivan, Michelle Murphy, Alan Irvine, Stephen O'Riordan, Fergal Quinn, Susan O'Connell
Thu 18 07:00
Registration Opens
Registration
Thu 18 08:00 - 08:15
WG2.1
ESPE Working Group on Diabetes Technology and Therapeutics
Technological horizon for diabetes treatment
Israel
Thu 18 08:15 - 08:40
WG2.2
ESPE Working Group on Diabetes Technology and Therapeutics
Non-Insulin Glucoregulatory therapy for type 1 diabetes
Linköping, Sweden
Thu 18 08:40 - 09:15
WG2.3
ESPE Working Group on Diabetes Technology and Therapeutics
Debate: Should all newly diagnosed patients with diabetes need to be hospitalized?
Paris, France
Thu 18 08:40 - 09:15
WG2.4
ESPE Working Group on Diabetes Technology and Therapeutics
Debate: Should all newly diagnosed patients with diabetes need to be hospitalized?
Petah Tikva, Israel
Thu 18 09:15 - 09:40
ESPE Working Group on Diabetes Technology and Therapeutics
Coffee Break
Thu 18 09:40 - 10:15
WG2.5
ESPE Working Group on Diabetes Technology and Therapeutics
Debate: Sensor/pump therapy from onset of diabetes?
Ljubljana, Slovenia
Thu 18 09:40 - 10:15
WG2.6
ESPE Working Group on Diabetes Technology and Therapeutics
Debate: Sensor/pump therapy from onset of diabetes?
Petah Tikva, Israel
Thu 18 10:15 - 10:50
WG2.7
ESPE Working Group on Diabetes Technology and Therapeutics
Debate: Do we need long acting insulin analogs?
Luxembourg, Luxembourg
Thu 18 10:15 - 10:50
WG2.8
ESPE Working Group on Diabetes Technology and Therapeutics
Debate: Do we need long acting insulin analogs?
Uddevalla, Sweden
Thu 18 08:00 - 08:30
WG3.1
ESPE Disorders of Sex Development Working Group (DSD)
Genetic variation in human SF-1 (NR5A1): clinical consequences for individuals, families and populations
London, United Kingdom
Thu 18 08:30 - 08:50
WG3.2
ESPE Disorders of Sex Development Working Group (DSD)
The potential role of the alternative ‘backdoor’ pathway for androgen synthesis and virilisation in CAH
Giessen, Germany
Thu 18 08:50 - 09:15
WG3.3
ESPE Disorders of Sex Development Working Group (DSD)
Long term outcome of prenatal CAH- therapy
Stockholm, Sweden
Thu 18 09:15 - 09:45
ESPE Disorders of Sex Development Working Group (DSD)
Coffee Break
Thu 18 09:45 - 10:05
WG3.4
ESPE Disorders of Sex Development Working Group (DSD)
Detailed phenotyping of DSD: external virilisation
Glasgow, UK
Thu 18 10:05 - 10:25
WG3.5
ESPE Disorders of Sex Development Working Group (DSD)
Imaging of the urogenital tract
Lubeck, Germany
Thu 18 10:25 - 10:35
WG3.6
ESPE Disorders of Sex Development Working Group (DSD)
I-DSD and I-CAH registry update
Glasgow, UK
Thu 18 10:35 - 10:45
WG3.7
ESPE Disorders of Sex Development Working Group (DSD)
DSDlife
Berlin, Germany
Thu 18 10:45 - 10:55
WG3.8
ESPE Disorders of Sex Development Working Group (DSD)
DSDnet: A COST Action on the systematic elucidation of differences of sex development
Lübeck, Germany
Thu 18 10:55 - 11:00
ESPE Disorders of Sex Development Working Group (DSD)
Open Business meeting
Thu 18 08:00 - 08:30
WG4.1
ESPE Obesity Working Group (OWG)
Metabolic syndrome in youth: current insights and novel serum biomarkers
Jerusalem, Israel
Thu 18 08:30 - 09:00
WG4.2
ESPE Obesity Working Group (OWG)
Type 2 diabetes in children and adolescents
Datteln, Germany
Thu 18 09:00 - 09:30
ESPE Obesity Working Group (OWG)
Coffee Break
Thu 18 09:30 - 10:00
WG4.3
ESPE Obesity Working Group (OWG)
Making a diagnosis in Severe Complex Obesity
Cambridge, UK
Thu 18 10:00 - 10:30
WG4.4
ESPE Obesity Working Group (OWG)
Identification of fatty acid binding protein 4 as an adipokine that regulates insulin secretion during obesity
Oxford, UK
Thu 18 10:30 - 11:00
ESPE Obesity Working Group (OWG)
Research and Business Meeting
Thu 18 08:00 - 08:25
WG5.1
ESPE Working Group on Paediatric and Adolescent Gynaecology (PAG)
New markers of Ovarian Function
Copenhagen, Denmark
Thu 18 08:25 - 08:50
WG5.2
ESPE Working Group on Paediatric and Adolescent Gynaecology (PAG)
Lessons drawn from gynecological disorders in relation with hypothalamic-pituitary malfunction
Lausanne, Switzerland
Thu 18 08:50 - 09:15
WG5.3
ESPE Working Group on Paediatric and Adolescent Gynaecology (PAG)
Delay or advancement of female puberty after early life exposure to Bisphenol A and neuroendocrine mechanism
Liège, Belgium
Thu 18 09:15 - 09:45
ESPE Working Group on Paediatric and Adolescent Gynaecology (PAG)
Coffee Break
Thu 18 09:45 - 10:10
WG5.4
ESPE Working Group on Paediatric and Adolescent Gynaecology (PAG)
Contraception in Adolescence from a Public Health Perspective
Lausanne, Switzerland
Thu 18 10:10 - 10:35
WG5.5
ESPE Working Group on Paediatric and Adolescent Gynaecology (PAG)
Contraception in adolescence: current options
Boston, USA
Thu 18 10:35 - 11:00
WG5.6
ESPE Working Group on Paediatric and Adolescent Gynaecology (PAG)
Lessons drawn from rare gynecological disorders in relation with ovarian malfunction
Paris, France
Thu 18 08:00 - 08.45
WG6.1
ESPE Turner Syndrome Working Group (TS)
Liver involvement in Turner syndrome
Paris, France
Thu 18 08:45 - 09:15
WG6.2
ESPE Turner Syndrome Working Group (TS)
Gastrointestinal disease in TS
Thu 18 09:15 - 09:45
ESPE Turner Syndrome Working Group (TS)
Coffee Break
Thu 18 09:45 - 10:15
WG6.4
ESPE Turner Syndrome Working Group (TS)
Motor performance in TS
Nijmegen, the Netherlands
Thu 18 10:15 – 11:00
WG6.3
ESPE Turner Syndrome Working Group (TS)
Autism and the X-chromosome
London, UK
Thu 18
Education and Training Update
Welcome and meeting new ESPE members and trainees
Stockholm, Sweden
Thu 18
Education and Training Update
Update of the 28th ESPE Summer School
Glasgow, United Kingdom
Thu 18
Education and Training Update
The Winter School journey – past, present and future
Glasgow, United Kingdom
Thu 18
Education and Training Update
Seminars in Developmental Endocrinology: Diving in Paediatric Endocrinology sea
Rome, Italy
Thu 18
Education and Training Update
ESPE Science School: the past and the future
Athens, Greece
Thu 18
Education and Training Update
Harmonization of Paediatric Endocrinology training in EU
Istanbul, Turkey
Thu 18
Education and Training Update
Drop on behalf of e-learning team - the espe-elearning.org portal: Learning and teaching paediatric endocrinology on demand
Thu 18
Education and Training Update
ESPE Clinical Fellowship programme: starting opportunity for young Paediatric Endocrinologists
Kaunas, Lithuania
Thu 18
Education and Training Update
Paediatric Endocrinology in the Middle East & North Africa; future plans and collaboration
Thu 18
Education and Training Update
ESPE Maghreb School: training in French
Paris, France
Thu 18
Education and Training Update
Reflections on an African (PETCA) safari
Thu 18
Education and Training Update
ESPE Caucasus and Central Asia School: starting in 2014
Kaunas, Lithuania
Thu 18
Education and Training Update
ESPE Research Fellowship programme
Linköping, Sweden
Thu 18 11:15
Opening Ceremony

Welcome and Opening Speech - ESPE President 2014

Auditorium
Hilary Hoey (Ireland)
Thu 18 11:30
PL1
Plenary Session 1 & 2
Closed-Loop System: Dream or Reality?
Israel
Thu 18 12:00
PL2
Plenary Session 1 & 2
Learning from histopathology to design novel immune-therapies for type 1 and 2 diabetes
LA, USA
Thu 18 12:30
Lunch

Visit to the Posters and Exhibition

Thu 18 12:45
Industry-sponsored Satellite Symposium 1
Liffey A
Thu 18 14:00
S1.1
Symposium 1 - Disorders of Gsalpha Signaling
Pseudohypoparathyroidism
Boston MA, USA
Thu 18 14:30
S1.2
Symposium 1 - Disorders of Gsalpha Signaling
McCune Albright Syndrome
Bethesda MD, USA
Thu 18 15:00
S1.3
Symposium 1 - Disorders of Gsalpha Signaling
Acrodysostosis
Paris, France
Thu 18 14:00
S2.1
Symposium 2 - Endocrine Cancer Syndromes: An Update
PTEN: A Gene Involved in Overgrowth and Cancer
Baltimore, USA
Thu 18 14:30
S2.2
Symposium 2 - Endocrine Cancer Syndromes: An Update
MEN1 in Children and Adolescents
Florence, Italy
Thu 18 15:00
S2.3
Symposium 2 - Endocrine Cancer Syndromes: An Update
DICER1 syndrome: a erview of the syndrome with a focus on endocrine aspects
Montreal, Canada
Thu 18 14:00
S3.1
Symposium 3 - Novel Insights into Monogenic Diabetes
Differential Diagnosis of Monogenic Diabetes
Thu 18 14:30
S3.2
Symposium 3 - Novel Insights into Monogenic Diabetes
New Genes, New Mechanisms, New Phenotypes
Thu 18 15:00
S3.3
Symposium 3 - Novel Insights into Monogenic Diabetes
Epidemiology of Monogenic Diabetes
Lodz, Poland
Thu 18 14:00
S4.1
Symposium 4 - Recent Advances in Our Understanding of Hypothyroidism
Management of Central Hypothyroidism
Amsterdam, The Netherlands
Thu 18 14:30
S4.2
Symposium 4 - Recent Advances in Our Understanding of Hypothyroidism
Novel role(s) for immunoglobulin superfamily, member 1 (IGSF1) in the hypothalamic-pituitary-thyroid axis
Montreal, Canada
Thu 18 15:00
S4.3
Symposium 4 - Recent Advances in Our Understanding of Hypothyroidism
Novel Insights into Thyroid Hormone Resistence
Cambridge, UK
Thu 18 15:30
Coffee Break
Thu 18 16:00 - 17:00
MTE1.1
Meet the Expert Parallel Sessions
Management of a Child with Cryptorchidism
Copenhagen, Denmark
Thu 18 16:00 - 17:00
MTE2.1
Meet the Expert Parallel Sessions
The challenges of extreme obesity
Thu 18 16:00 - 17:00
MTE3.1
Meet the Expert Parallel Sessions
Evaluation of Precocious Pubarche
Kuopio, Finland
Thu 18 16:00 - 17:00
MTE4.1
Meet the Expert Parallel Sessions
Management and prevention of complications in adolescents with Diabetes
Victoria, Australia
Thu 18 17:15
Industry-sponsored Satellite Symposium 2
Liffey A
Thu 18 19:00
Welcome Reception
CCD
Fri 19 07:00
Registration Opens
Fri 19 07:30 - 08:30
MTE5.1
Meet the Expert Parallel Sessions
Management of childhood fractures
Bethesda, USA
Fri 19 07:30 - 08:30
MTE6.1
Meet the Expert Parallel Sessions
Assessment of Thyroid Nodules
Montréal, Canada
Fri 19 07:30 - 08:30
MTE7.1
Meet the Expert Parallel Sessions
Clinical Management of Cystic Fibrosis Related Diabetes (CFRD) in Childhood
Cork, Ireland
Fri 19 07:30 - 08:30
MTE8.1
Meet the Expert Parallel Sessions
Evaluation and the Management of Tall Stature
Stockholm, Sweden
Fri 19 08:30
Coffee Break
Fri 19 08:45
FC1.1
Free Communication 1 - Adrenal
Molecular Mechanisms of Nongenomic Glucocorticoid Actions: The Role of Human Glucocorticoid Receptor S-Palmitoylation.
Athens, Greece
Fri 19 08:55
FC1.2
Free Communication 1 - Adrenal
Clinical phenotype of patients with MCM4 mutation suggests pubertal delay in males in addition to adrenal failure, absent adrenarche and short stature in boys and girls
Fri 19 09:05
FC1.3
Free Communication 1 - Adrenal
Genetic engineering using TALENs to study the redox regulation of steroidogenesis in vivo
Fri 19 09:15
FC1.4
Free Communication 1 - Adrenal
A novel non-invasive Short Synacthen Test
Fri 19 09:25
FC1.5
Free Communication 1 - Adrenal
Antenatal glucocorticoid treatment and polymorphisms in glucocorticoid and mineralocorticoid receptor genes are associated with long-term
Fri 19 09:35
FC1.6
Free Communication 1 - Adrenal
Molecular Characterization of Testicular Adrenal Rest Tumours (TART) in Congenital Adrenal Hyperplasia (CAH); Lesions with both Adrenocortical and Leydig Cell Features
Fri 19 08:45
FC2.1
Free Communication 2- Bone & Mineral
Asfotase Alfa: Sustained Improved Growth and Function with Extended Treatment in Children with Hypophosphatasia
Fri 19 08:55
FC2.2
Free Communication 2- Bone & Mineral
Hypophosphatasia: Gross motor function and height improvement in infants and young children treated with asfotase alfa for up to 3 years
Fri 19 09:05
FC2.3
Free Communication 2- Bone & Mineral
Calcium Homeostasis in Adolescents with Beta-Thalassemia Major: Effect of Intramuscular Injection of a Megadose of Cholecalciferol
Cairo, Egypt
Fri 19 09:15
FC2.4
Free Communication 2- Bone & Mineral
Fractures in children with chronic inflammatory and/or disabling conditions: the SNAP study
Birmingham, UK
Fri 19 09:25
FC2.5
Free Communication 2- Bone & Mineral
Pharmacokinetics (PK) and Pharmacodynamics (PD) of a Human Monoclonal Anti-FGF23 (Fibroblast Growth Factor 23) Antibody (KRN23) Following Four Month Intra-Dose Escalation in Adults with X-linked Hypophosphatemia (XLH)
Fri 19 09:35
FC2.6
Free Communication 2- Bone & Mineral
Efficacy and Safety Following Four Monthly Subcutaneous (SC) Doses of a Human Anti-FGF23 (Fibroblast Growth Factor 23) Antibody (KRN23) in Adults with X-Linked Hypophosphatemia (XLH)
Indianapolis, USA
Fri 19 08:45
FC3.1
Free Communication 3 - Diabetes
HIGH MOBILITY GROUP BOX-1(HMGB-1) SERUM CONCENTRATIONS INCREASE AT ONSET OF DIABETES IN CYSTIC FIBROSIS (CF) PATIENTS
Parma, Italy
Fri 19 08:55
FC3.2
Free Communication 3 - Diabetes
HbA1c level as a predictive marker of progression to clinical diabetes
Fri 19 09:05
FC3.3
Free Communication 3 - Diabetes
Improved hepatic insulin sensitivity in children randomized to CSII treatment from onset of type 1 diabetes
Fri 19 09:15
FC3.4
Free Communication 3 - Diabetes
Genetics of pediatric type 2 diabetes: ABCC8 mutation in obesity-associated insulin secretion defects
Berlin, Germany
Fri 19 09:25
FC3.5
Free Communication 3 - Diabetes
Pancreatic N-Methyl-D-Aspartate receptors as novel drug targets for the treatment of diabetes mellitus
Fri 19 09:35
FC3.6
Free Communication 3 - Diabetes
ALPHA-LIPOIC ACID AND ANTI-OXIDANT DIET HELPS TO IMPROVE ENDOTHELIAL DYSFUNCTION IN CHILDREN AND ADOLESCENTS WITH TYPE 1 DIABETES.
Asola, Italy
Fri 19 08:45
FC4.1
Free Communication 4- Growth
HETEROZYGOUS IGF1R MUTATIONS REPRESENT A FREQUENT FINDING IN PATIENTS WITH PRE- AND/OR POSTNATAL PROPORTIONAL UNDERGROWTH AND LOW, NORMAL OR SUPRANORMAL IGF1
Fri 19 08:55
FC4.2
Free Communication 4- Growth
The effect of GRB10-deficiency in Zebrafish: a translational animal model to study human growth
Fri 19 09:05
FC4.3
Free Communication 4- Growth
Oscillations in gene expression profiles across childhood highlight the relation of growth and specific metabolic functions in both sexes
Manchester, United Kingdom
Fri 19 09:15
FC4.4
Free Communication 4- Growth
Short stature, accelerated bone maturation, and early growth cessation due to heterozygous aggrecan mutations
Stockholm, Sweden
Fri 19 09:25
FC4.5
Free Communication 4- Growth
Fetal and postnatal growth in Turner Syndrome and their associations with the dosage effects of the X-linked gene: a cross-sectional data base analysis of the French national rare disease network
Paris, France
Fri 19 09:35
FC4.6
Free Communication 4- Growth
LONGITUDINAL GROWTH OF FINNISH CHILDREN WITH GESTATIONAL DIABETES IN MOTHERS
Fri 19 08:45
FC5.1
Free Communication 5- Neuroendocrinology
Derivation of GnRH neuron-like cells from human embryonic stem cell-derived neural crest progenitors
Helsinki, Finland
Fri 19 08:55
FC5.2
Free Communication 5- Neuroendocrinology
Mutations in the maternally imprinted gene MKRN3 are a frequent cause of familial central precocious puberty
Fri 19 09:05
FC5.3
Free Communication 5- Neuroendocrinology
Loss of Function Mutations in PNPLA6 Cause Hypogonadotropic Hypogonadism due to Impaired LH Release from Pituitary Gonadotropes
Fri 19 09:15
FC5.4
Free Communication 5- Neuroendocrinology
Reference values for urinary gonadotropins in preterm and full-term infants in “minipuberty”
Fri 19 09:25
FC5.5
Free Communication 5- Neuroendocrinology
Characterization of IGF-I receptor expression and localization in paediatric gliomas upon diagnosis according to WHO 2007 grading
Fri 19 09:35
FC5.6
Free Communication 5- Neuroendocrinology
The diencephalic syndrome (DS) of emaciation in infantile hypothalamochiasmatic low-grade gliomas (HCLGGs): a retrospective case-control study of diagnostic parameters and long-term outcomes over 30 years of follow-up
London, UK
Fri 19 08:45
NP1.1
New Perspectives 1
Non Coding RNA's: Introduction to Non-Coding RNAs and the Role of MicroRNAs in GnRH Neurons
Lille, France
Fri 19 09:15
NP1.2
New Perspectives 1
The Role of MicroRNAs in Diabetes
Lausanne, Switzerland
Fri 19 09:45
Coffee Break
Fri 19 10:15
PL3
Plenary Session 3
Sex, Stem Cells and Decision of Cell Fate
London, UK
Fri 19 10:45
ESPE Award and Activities
Auditorium
Fri 19 11:45
PL4
Plenary Session 4
Gene therapy in cerebral form of X-linked adrenoleukodystrophy
Paris, France
Fri 19 12:30
Lunch

Visit to the Posters and Exhibition

Fri 19 13:00
Industry-sponsored Satellite Symposium
Liffey B
Fri 19 14:15
S5.1
Symposium 5 - Novel Insights into Hypoadrenalism
Aetiology of Congenital Hypoadrenalism
London, United Kingdom
Fri 19 14:45
S5.2
Symposium 5 - Novel Insights into Hypoadrenalism
Adrenarche: Coming of age in the era of genomics and metabolomics
Michigan, USA
Fri 19 15:15
S5.3
Symposium 5 - Novel Insights into Hypoadrenalism
CAH: Health Status in Adults (CaHASE)
London, UK
Fri 19 14:15
S6.1
Symposium 6 - New Concepts in the Gonadotropic Axis
Role of The Hypothalamic MicroRNA in Puberty Regulations
Córdoba, Spain
Fri 19 14:45
S6.2
Symposium 6 - New Concepts in the Gonadotropic Axis
New Syndromes Resulting in Secretory Pathway and Gonadotropic Axis Regulation Defects
Paris, France
Fri 19 15:15
S6.3
Symposium 6 - New Concepts in the Gonadotropic Axis
Genetic Dissection of Puberty in Mice
Fri 19 14:15
S7.1
Symposium 7 - Controversies in the Surgical Management of DSD
Evolution of Feminising Genitoplasty
Toronot, Canada
Fri 19 14:30
S7.2
Symposium 7 - Controversies in the Surgical Management of DSD
Pros and Cons of Early or Late Feminising Genitoplasty
Fri 19 15:00
S7.3
Symposium 7 - Controversies in the Surgical Management of DSD
Masculinising Genitoplasty
Paris, France
Fri 19 14.15
WG7.1
ESPE Working Group for Paediatric Endocrine Nurse Specialists and Allied Health Professionals
Quality of life and anxiety in adolescents with differentiated thyroid cancer
Toronto, Canada
Fri 19 14:35
WG7.2
ESPE Working Group for Paediatric Endocrine Nurse Specialists and Allied Health Professionals
Evolving Growth Hormone Therapy (GHT) Patient Training in a Digital World
Ramat-Gan, Israel
Fri 19 14:55
WG7.3
ESPE Working Group for Paediatric Endocrine Nurse Specialists and Allied Health Professionals
Endocrine Nursing, social media and research: results of an international study
London, UK
Fri 19 15:15
ESPE Working Group for Paediatric Endocrine Nurse Specialists and Allied Health Professionals
Open discussion
Fri 19 14:15 - 14:25
WG8.1
Working Group for Global Paediatric Endocrinology and Diabetes (GPED)
Word from GPED’s President
Vancouver, Canada
Fri 19 14:25 - 14:35
WG8.2
Working Group for Global Paediatric Endocrinology and Diabetes (GPED)
Inequities of treatment options in developing countries: Inequities in treatment options type 1 diabetes in Sudan
Fri 19 14:35 - 14:45
WG8.3
Working Group for Global Paediatric Endocrinology and Diabetes (GPED)
Inequities of treatment options in developing countries: Osteogenesis imperfecta in Indonesia
Fri 19 14:45 - 14:55
WG8.4
Working Group for Global Paediatric Endocrinology and Diabetes (GPED)
Inequities of treatment options in developing countries: Congenital Adrenal Hyperplasia
Fri 19 14:55 - 15:05
Working Group for Global Paediatric Endocrinology and Diabetes (GPED)
Q & A
Fri 19 15:05 - 15:15
WG8.5
Working Group for Global Paediatric Endocrinology and Diabetes (GPED)
Neonatal screening for congenital hypothyroidism: Don’t take it for granted! (Costa Rica)
Fri 19 15:15 - 15:25
WG8.6
Working Group for Global Paediatric Endocrinology and Diabetes (GPED)
Neonatal screening for congenital hypothyroidism: Don’t take it for granted! (Ghana)
Ghana
Fri 19 15:25 - 15:35
WG8.7
Working Group for Global Paediatric Endocrinology and Diabetes (GPED)
Neonatal screening for congenital hypothyroidism: Don’t take it for granted! (Nigeria)
Fri 19 15:35 - 15:45
Working Group for Global Paediatric Endocrinology and Diabetes (GPED)
Q & A
Fri 19 15:45
Coffee Break
Fri 19 16:15
Industry-sponsored Satellite Symposium 4
Auditorium
Fri 19 16:15
Industry-sponsored Satellite Symposium 5
Liffey B
Fri 19 16:15
Industry-sponsored Satellite Symposium 6
Liffey A
Fri 19 19:30
Free Evening
Sat 20 07:00
Registration Opens
Sat 20 07:30 - 08:30
MTE1.2
Meet the Expert Parallel Sessions
Management of a Child with Cryptorchidism
Sat 20 07:30 - 08:30
MTE2.2
Meet the Expert Parallel Sessions
The challenges of extreme obesity
Sat 20 07:30 - 08:30
MTE3.2
Meet the Expert Parallel Sessions
Evaluation of Precocious Pubarche
Sat 20 07:30 - 08:30
MTE4.2
Meet the Expert Parallel Sessions
Management and Prevention of Complications in Adolescents with Diabetes
Sat 20 07:30 - 08:30
MTE5.2
Meet the Expert Parallel Sessions
Management of Childhood Fractures
Sat 20 08:45
FC6.1
Free Communication 6 - Gonads & DSD
Search for genetic defects in the transcription factor genes FOXL2, FOXE1, BMP15, NOBOX and GDF9 in children, adolescents and young adults with premature ovarian insufficiency (POI).
Bethesda, USA
Sat 20 08:55
FC6.2
Free Communication 6 - Gonads & DSD
Next generation sequencing of the androgen receptor (AR) gene in patients with androgen insensitivity syndrome (AIS) and controls
Kiel, Germany
Sat 20 09:05
FC6.3
Free Communication 6 - Gonads & DSD
LRH-1 rescues SF-1 deficiency for steroidogenesis in vitro but cannot explain the broad phenotype of SF-1 deficiency in men
Sat 20 09:15
FC6.4
Free Communication 6 - Gonads & DSD
FAMILIAL 46,XY COMPLETE FEMALE EXTERNAL SEX DEVELOPMENT AND PRIMARY AMENORRHEA ALONG WITH HIDDEN GONADAL TUMORS, SECONDARY TO A NOVEL p.MET64VAL SRY GENE MUTATION
Sat 20 09:25
FC6.5
Free Communication 6 - Gonads & DSD
Serum levels of AMH reflect ovarian morphology by MRI in 109 healthy peripubertal girls
Copenhagen, Denmark
Sat 20 09:35
FC6.6
Free Communication 6 - Gonads & DSD
Effects of exposure to the endocrine disruptor di(n-butyl) phthalate on testicular dysgenesis and fetal germ cell development in the rat and human fetal testis.
Edinburgh, UK
Sat 20 08:45
FC7.1
Free Communication 7 - Growth Promoting Therapies
Genetic markers of insulin resistance are associated with growth hormone response in short SGA children – the North European SGA Study (NESGAS)
Copenhagen, Denmark
Sat 20 08:55
FC7.2
Free Communication 7 - Growth Promoting Therapies
The rs1024531 GRB10 promoter polymorphism is associated with response to growth hormone (GH) therapy in patients with GH deficiency (GHD): validation by in vitro functional analysis
Sat 20 09:05
FC7.3
Free Communication 7 - Growth Promoting Therapies
Gene expression networks associated with changes in serum markers of metabolism and growth in growth hormone (GH)-treated children with GH deficiency (GHD)
Manchester, United Kingdom
Sat 20 09:15
FC7.4
Free Communication 7 - Growth Promoting Therapies
A decade of clinical experience in a Swedish university centre using prediction models to optimize growth hormone (GH) treatment in prepubertal children
Sweden
Sat 20 09:25
FC7.5
Free Communication 7 - Growth Promoting Therapies
Impact of Growth Hormone on Adult Bone Quality in Turner Syndrome – A High Resolution Peripheral Quantitative Computed Tomography Study
Sat 20 09:35
FC7.6
Free Communication 7 - Growth Promoting Therapies
Topicon™ ThermoMatrix™-Mediated Passive Transdermal Delivery of Human Growth Hormone (hGH) Across EpidermFT™ Full-Thickness Human Skin Equivalent (HSE): Towards an Extended-Wear hGH Patch
Florida, USA
Sat 20 08:45
FC8.1
Free Communication 8 - Fat Metabolism
Activation of the ER stress response in cultured human umbilical vein endothelial cells (HUVECs) by plasma obtained from prepubertal obese children.
Sat 20 08:55
FC8.2
Free Communication 8 - Fat Metabolism
MicroRNA-152 promotes hepatic steatosis by suppressing the Wnt signaling pathway
Sat 20 09:05
FC8.3
Free Communication 8 - Fat Metabolism
Identification of death ligand TRAIL (TNF-related apoptosis-inducing ligand) as a potent mitogen in human preadipocytes
Sat 20 09:15
FC8.4
Free Communication 8 - Fat Metabolism
CREB-REGULATED TRANSCRIPTION COACTIVATOR 3 (CRTC3): A NEW ADIPOKINE RELATED TO CHILDHOOD OBESITY
Girona, Spain
Sat 20 09:25
FC8.5
Free Communication 8 - Fat Metabolism
Putative gain-of-function in rats carrying the Ghsr Q343X mutation
Sat 20 09:35
FC8.6
Free Communication 8 - Fat Metabolism
A Novel Missense Variant in the Insulin Receptor Gene in 3 unrelated Irish families with severe Insulin Resistance Syndrome - Evidence for an Irish Founder Effect.
Sat 20 08:45
FC9.1
Free Communication 9 - Beta Calls
Inappropriately High Rates of Cell Proliferation in Diffuse Congenital Hyperinsulinism are Linked to Nuclear Expression of CDK6
Manchester, UK
Sat 20 08:55
FC9.2
Free Communication 9 - Beta Calls
Characterising the immunohistochemical expression of dipeptidyl peptidase-4 in pancreatic tissue from patients with diffuse and focal congential hyperinsulinism.
Sat 20 09:05
FC9.3
Free Communication 9 - Beta Calls
In search for new monogenic diabetes genes: PCBD1
Sat 20 09:15
FC9.4
Free Communication 9 - Beta Calls
Clinical characteristics and molecular genetics analysis of 20 patients with neonatal diabetes mellitus from a single centre of the South-Eastern region of Turkey
Ankara, Turkey
Sat 20 09:25
FC9.5
Free Communication 9 - Beta Calls
TRANSIENT NEONATAL DIABETES IN ADULTHOOD: METABOLIC AND NEURODEVELOPMENTAL OUTCOMES
Paris, France
Sat 20 09:35
FC9.6
Free Communication 9 - Beta Calls
Sulfonylurea therapy corrects hypotonia, attention deficits, improves complex neuropsychological functions and motricity in patients with neonatal diabetes secondary to mutation in potassium channel subunits, through a central nervous system effect.
Paris, France)
Sat 20 08:45
NP2.1
New Perspectives 2
Pancreatic Beta Cell Development: from rodent to human
Paris, France
Sat 20 09:15
NP2.2
New Perspectives 2
Formation of a Thyroid Gland from Embryonic Stem Cells
Brussels, Belgium
Sat 20 08:45
FC-LB-1
Free Communications - Late Breaking
Top Line Results of Once-Weekly, CTP-Modified Human Growth Hormone (MOD-4023): Phase 2 Dose Finding Study in Children with Growth Hormone Deficiency (GHD)
Oregon, USA
Sat 20 08:55
FC-LB-2
Free Communications - Late Breaking
Sonic Hedgehog is required for cell specification of Rathke’s pouch progenitors during normal development and is over-expressed in adamantinomatous craniopharyngioma
London, UK
Sat 20 09:05
FC-LB-3
Free Communications - Late Breaking
Parent-of-origin specific allelic associations among 106 genomic loci for age at menarche
Cambridge, United Kingdom
Sat 20 09:15
FC-LB-4
Free Communications - Late Breaking
Does Severity of Hypothyroidism at Birth Contribute to Abnormal Cortical Development among Children with Congenital Hypothyroidism (CH)?
Toronto, Canada
Sat 20 09:25
FC-LB-5
Free Communications - Late Breaking
CB2 polymorphism could modulate the relationship between childhood obesity and age at menarche
Naples, Italy
Sat 20 09:35
FC-LB-6
Free Communications - Late Breaking
Global Consensus Recommendations on Prevention and Management of Nutritional Rickets
Linz, Austria
Sat 20 10:15
PL5
Plenary Session 5
Obesity: Novel Treatments and the Imperative for Prevention
Dublin, Ireland
Sat 20 10:45
ESPE Award Session and Activities 2
Auditorium
Sat 20 12:00
FC10.1
Free Communication 10 - Programming & Early
A role for Delta-like homologue 1 (DLK1) in a secretory placental population and implications for foetal growth
Sat 20 12:10
FC10.2
Free Communication 10 - Programming & Early
STK11 EXPRESSION IN ADIPOSE TISSUE FOLLOWING FETAL GROWTH RESTRICTION: RELATION TO CATCH-UP GROWTH AND VISCERAL FAT MASS.
Girona, Spain
Sat 20 12:20
FC10.3
Free Communication 10 - Programming & Early
Genetic and epigenetic defects at the GNAS locus lead to opposite patterns of fetal and postnatal growth
Sat 20 12:30
FC10.4
Free Communication 10 - Programming & Early
Influence of newborn and maternal factors on neonatal body composition
Sat 20 12:40
FC10.5
Free Communication 10 - Programming & Early
Contrasting associations of maternal smoking and alcohol intake in late pregnancy and offspring body composition in childhood
Southampton, UK
Sat 20 12:50
FC10.6
Free Communication 10 - Programming & Early
The PremAldo Study: Impaired Aldosterone Signaling Worsens Renal Sodium Loss in Preterm Infants
Paris, France
Sat 20 12:00
FC11.1
Free Communication 11 - Pituitary
ABNORMAL SONIC HEDGEHOG SIGNALING IN ADAMANTINOMATOUS CRANIOPHARYNGIOMAS AND ITS ASSOCIATION WITH CTNNB1/BETA-CATENIN MUTATIONS
Sat 20 12:10
FC11.2
Free Communication 11 - Pituitary
Novel SOX2 mutation: identification of new molecular mechanisms of SOX2 action and interactions.
Sat 20 12:20
FC11.3
Free Communication 11 - Pituitary
Early-Onset Central Diabetes Insipidus is associated with De novo Arginine Vasopressin-Neurophysin II or Wolfram Syndrome 1 gene mutations
Sat 20 12:30
FC11.4
Free Communication 11 - Pituitary
Management of hyperhydration in a child with Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH) using a selective vasopresin receptor agonist.
Sat 20 12:40
FC11.5
Free Communication 11 - Pituitary
ENDOCRINE FEATURES OF A LARGE COHORT OF CHILDREN WITH SEPTO-OPTIC DYSPLASIA AND CONGENITAL MULTIPLE PITUITARY HORMONAL DEFICIENCIES
London, UK
Sat 20 12:50
FC11.6
Free Communication 11 - Pituitary
Clinical and neuroradiological characteristics in children and adolescents with Septo-Optic Dysplasia, Multiple Pituitary Hormone Deficiencies and Optic Nerve Hypoplasia: Experience from a single tertiary centre.
Madrid, Spain
Sat 20 12:00
FC12.1
Free Communication 12 - Obesity
High-fat diet rapidly triggers circadian de-synchronization of clock genes, neuropeptides and inflammation mediators in the hypothalamus of C57BL mice
Sat 20 12:10
FC12.2
Free Communication 12 - Obesity
Obesity in childhood and adolescence is associated with shorter leucocyte telomere length
Sat 20 12:20
FC12.3
Free Communication 12 - Obesity
Increased resting energy expenditure in girls with Turner syndrome
Tübingen, Germany
Sat 20 12:30
FC12.4
Free Communication 12 - Obesity
Pediatric reference values for insulin from oGTT and prevalence of hyperinsulinemia in obese children
Leipzig, Germany
Sat 20 12:40
FC12.5
Free Communication 12 - Obesity
Low Circulating Levels of DKK-1 Protein in Obese Children Indicate Suppression of Canonical Wnt Signaling
Sat 20 12:50
FC12.6
Free Communication 12 - Obesity
Resveratrol inhibits inflammation-induced production of cytokines in human adipocytes
Sat 20 12:00
FC13.1
Free Communication 13 - Thyroid
Massive sequencing of thyroidal genes reveals unexpected polygenic defects in dyshormonogenic hypothyroidism.
Sat 20 12:10
FC13.2
Free Communication 13 - Thyroid
Thyroid agenesis and severe thyroid hypoplasia caused by a new inactivating TSH receptor mutation Ala579Val
Sat 20 12:20
FC13.3
Free Communication 13 - Thyroid
Overexpression of supressor tumoral PTEN, but not DREAM, was detected in multinodular goiter in humans.
Sat 20 12:30
FC13.4
Free Communication 13 - Thyroid
The prevalence of congenital malformations in infants with TSH elevation on newborn screening – the importance of distinguishing between true and transient congenital hypothyroidism
Sat 20 12:40
FC13.5
Free Communication 13 - Thyroid
THE ULTRASTRUCTURAL CHANGES IN THYROID CELLS IN THE COURSE OF DAMAGE IN HASHIMOTO’S THYROIDITIS
Sat 20 12:50
FC13.6
Free Communication 13 - Thyroid
ABNORMAL THYROID HORMONE METABOLISM IN PATIENTS WITH THRA MUTATIONS DUE TO IMPAIRED EXPRESSION OF THE TYPE 3 DEIODINASE
Sat 20 12:00
FC14.1
Free Communication 14 - Puberty
Brain structure and function in gender dysphoric adolescents
Amsterdam, The Netherlands
Sat 20 12:10
FC14.2
Free Communication 14 - Puberty
Infancy growth rate predicts timing of puberty both in girls and boys
Istanbul, Turkey
Sat 20 12:20
FC14.3
Free Communication 14 - Puberty
Novel genetic variants in a cohort of paediatric and adolescent patients with Hypogonadotrophic Hypogonadism and Kallmann syndrome
London, UK
Sat 20 12:30
FC14.4
Free Communication 14 - Puberty
Development of pubertal gynaecomastia - A longitudinal cohort study
Sat 20 12:40
FC14.5
Free Communication 14 - Puberty
Fertility of women treated during childhood for precocious puberty with triptorelin: PREFER retrospective study
Paris, France
Sat 20 12:50
FC14.6
Free Communication 14 - Puberty
QUALITY OF LIFE IN PATIENTS WITH CONGENITAL HYPOGONADOTROPIC HYPOGONADISM (CHH)
Helsinki, Finland
Sat 20 12:00
Yearbook of Paediatric Endocrinology
Auditorium
Chairs: Wieland Kiess (Leipzig, Germany) & Ze'ev Hochberg (Haifa, Israel)
Sat 20 13:00
Lunch

Visit to the Posters and Exhibition

Sat 20 15:00
S8.1
Symposium 8 - Novel Therapies in Paediatric Endocrinology
Hyperinsulinaemia
Doha, Qatar
Sat 20 15:30
S8.2
Symposium 8 - Novel Therapies in Paediatric Endocrinology
Treatment of Hypophosphatasia
Manitoba, Canada
Sat 20 16:00
S8.3
Symposium 8 - Novel Therapies in Paediatric Endocrinology
Congenital Adrenal Hyperplasia
Athens, Greece
Sat 20 15:00
S9.1
Symposium 9 - Novel Insights into Pituitary Development and Function
Paracrine Regulation in the Pituitary
Montpellier, France
Sat 20 15:30
S9.2
Symposium 9 - Novel Insights into Pituitary Development and Function
Sox2+ve cells in the adult murine pituitary are stem cells with tumour-inducing potential
London, UK
Sat 20 16:00
S9.3
Symposium 9 - Novel Insights into Pituitary Development and Function
Pax7 dictates alternate pituitary cell fates during development
Montreal, Canada
Sat 20 15:00
S10.1
Symposium 10 - Childhood Obesity: Challenges in Management
The Metabolically Healthy Obese Child
Pecs, Hungary
Sat 20 15:30
S10.2
Symposium 10 - Childhood Obesity: Challenges in Management
Childhood and Adolescent Obesity - Can Treatment Response be Predicted?
Jerusalem, Israel
Sat 20 16:00
S10.3
Symposium 10 - Childhood Obesity: Challenges in Management
Natural Course of Impaired Glucose Tolerance in Obese Children
Datteln, Germany
Sat 20 15:00 - 16:00
MTE6.2
Meet the Expert Parallel Sessions
Assessment of Thyroid Nodules
Sat 20 15:00 - 16:00
MTE7.2
Meet the Expert Parallel Sessions
Clinical Management of Cystic Firbrosis Related Diabetes (CRFD) in Childhood
Sat 20 15:00 - 16:00
MTE8.2
Meet the Expert Parallel Sessions
Evaluation and the Management of Tall Stature
Sat 20 16:30
Coffee Break
Sat 20 17:00
PL6
Plenary 6
Genetics of Obesity
Cambridge, UK
Sat 20 17:30
President Poster Award
Auditorium
Sat 20 17:45
Closing Ceremony
Auditorium
Sat 20 19:00
ESPE Evening

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