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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.
American Journal of Human Genetics, 2013, 92 (5), pp.707-24. ⟨10.1016/j.ajhg.2013.03.024⟩
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 of Clinical Endocrinology and Metabolism, 2017, 102 (8), pp.2844-2852. ⟨10.1210/jc.2017-00202⟩
Journal articles hal-01579404v1

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.
Annales d'Endocrinologie, 2022, ⟨10.1016/j.ando.2022.02.001⟩
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.
Nature Reviews Endocrinology, 2015, 11 (9), pp.547-564. ⟨10.1038/nrendo.2015.112⟩
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.
Human Reproduction, 2007, 22 (7), pp.1885-92. ⟨10.1093/humrep/dem091⟩
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.
PLoS Genetics, 2012, 8 (8), pp.e1002896. ⟨10.1371/journal.pgen.1002896⟩
Journal articles inserm-03204465v1

Epicardial and Pericardial Adiposity Without Myocardial Steatosis in Cushing Syndrome

Peter Wolf , Benjamin Marty , Khaoula Bouazizi , Nadjia Kachenoura , Céline Piedvache , et al.
Journal of Clinical Endocrinology and Metabolism, 2021, 185 (2), pp.299-311. ⟨10.1210/clinem/dgab556⟩
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.
PLoS ONE, 2010, 5 (10), pp.e13563. ⟨10.1371/journal.pone.0013563⟩
Journal articles inserm-00524824v1