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55th Annual ESPE

Paris, France
10 Sep 2016 - 12 Sep 2016

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Paris, France: 10-12 September 2016 Further information

Free Communications

Neuroendocrinology

Rabconnectin3-[alpha] is Indispensable for the Activation and Maturation of the GnRH Neuronal Network
aHopital Robert Debré, Inserm U1141, Paris, France; bInserm U1172, Lille, France; cParis Diderot University-Bio Sorbonne Cité, Paris, France
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LGR4 and EAP1 Mutations are Implicated in the Phenotype of Self-limited Delayed Puberty
aCentre for Endocrinology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK; bCentre for Translational Bioinformatics, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK; cNIHR Barts Cardiovascular Biomedical Research Unit, Queen Mary University of London, London, UK
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Inactivating Mutations in CCDC141 Causing Idiopathic Hypogonadotrophic Hypogonadism/Kallmann Syndrome
aCukurova University, Division of Pediatric Endocrinology, Adana, Turkey; bCellular and Developmental Neurobiology Section, National Institute of Neurological Disorders and Stroke, Bethesda, USA; cDepartment of Pediatric Endocrinology, GATA Medical Faculty, Istanbul, Turkey; dDepartment of Pediatric Endocrinology, Diyarbakir Children’s State Hospital, Diyarbakir, Turkey; eDepartment of Endocrinology, Firat University, Elazig, Turkey
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Idiopathic Hypogonadotrophic Hypogonadism Caused by Inactivating Mutations in SRA1
aCukurova University, Division of Pediatric Endocrinology,
Adana, Turkey; bUniversity of Manitoba, Manitoba, Canada;
cEge University, Izmir, Turkey; dUniversity of Leeds, Leeds, UK; eDepartment of Forensic Medicine, Cukurova University, Adana, Turkey; fCukurova University, Division of Endocrinology, Adana, Turkey
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Abnormal Corticospinal Tract Decussation in Kallmann Syndrome due to ANOS1 (KAL1) Mutations: An Explanation of the Mirror Movements Frequently Observed in These Patients
aPediatric Endocrinology, Necker Hospital, Paris, France;
bEndocrinology Unit, Brest Hospital, Brest, France; cUnidad de Endocrinología Pediátrica, Hospital de Clínicas, Caracas, Venezuela; dInserm U1141, Paris Diderot University, Paris, France;
eFoetopathology, Paris, France; fFoetopathology, Rouen, France; gRadiology Department, Brest, France; hBiochemistry Laboratory, Robert Debré Hospital, Paris, France
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Pubertal Onset in Boys is Influenced by BMI and Genetic Variation of Fshb and Fshr: A Study in Two Population-Based Cohorts of Different Genetic Ancestry
aDepartment of Growth and Reproduction & EDMaRC, Rigshospitalet, Copenhagen, Denmark; bInstitute of Maternal and Child Research, University of Chile, Santiago, Chile
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