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Loss-of-function mutations in SOX10 cause Kallmann syndrome with deafness.
Veronique Pingault
,
Virginie Bodereau
,
Viviane Baral
,
Severine Marcos
,
Yuli Watanabe
,
et al.
Journal articles
inserm-00836181v1
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Classification of Patients With GH Disorders May Vary According to the IGF-I Assay
Maria Mavromati
,
Emmanuelle Kuhn
,
Hélène Agostini
,
Sylvie Brailly-Tabard
,
Catherine Massart
,
et al.
Journal articles
hal-01579404v1
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Consensus statement by the French Society of Endocrinology (SFE) and French Society of Pediatric Endocrinology & Diabetology (SFEDP) on diagnosis of Cushing's syndrome
Antoine Tabarin
,
Guillaume Assie
,
Pascal Barat
,
Fideline Bonnet
,
Jean Francois Bonneville
,
et al.
Journal articles
hal-03604251v1
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European Consensus Statement on congenital hypogonadotropic hypogonadism—pathogenesis, diagnosis and treatment
Ulrich Boehm
,
Pierre-Marc Bouloux
,
Mehul Dattani
,
Nicolas de Roux
,
Catherine Dodé
,
et al.
Journal articles
inserm-03204444v1
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Human fetal testis: source of estrogen and target of estrogen action.
Kahina Boukari
,
Maria-Luisa Ciampi
,
Anne Guiochon-Mantel
,
Jacques Young
,
Marc Lombès
,
et al.
Journal articles
inserm-00135609v1
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SEMA3A, a Gene Involved in Axonal Pathfinding, Is Mutated in Patients with Kallmann Syndrome
Naresh Kumar Hanchate
,
Paolo Giacobini
,
Pierre Lhuillier
,
Jyoti Parkash
,
Cécile Espy
,
et al.
Journal articles
inserm-03204465v1
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Epicardial and Pericardial Adiposity Without Myocardial Steatosis in Cushing Syndrome
Peter Wolf
,
Benjamin Marty
,
Khaoula Bouazizi
,
Nadjia Kachenoura
,
Céline Piedvache
,
et al.
Journal articles
hal-04021022v1
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Familial glucocorticoid receptor haploinsufficiency by non-sense mediated mRNA decay, adrenal hyperplasia and apparent mineralocorticoid excess.
Jérôme Bouligand
,
Brigitte Delemer
,
Annie-Claude Hecart
,
Géri Meduri
,
Say Viengchareun
,
et al.
Journal articles
inserm-00524824v1
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