Michele Zerah

Mutations within the MGC4607 Gene Cause Cerebral Cavernous Malformations

Christian Denier, Stéphane Goutagny, Pierre Labauge et al. · The American Journal of Human Genetics · 2004 · 238 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Analysis of Transcription Factors Key for Mouse Pancreatic Development Establishes NKX2-2 and MNX1 Mutations as Causes of Neonatal Diabetes in Man

Sarah E. Flanagan, Elisa De Franco, Hana Lango Allen et al. · Cell Metabolism · 2014 · 146 citations · Full text

Medicine, Developmental Biology, Molecular Genetics +16

No evidence of mutations in the genes for type I and type II 3 beta-hydroxysteroid dehydrogenase (3 beta HSD) in nonclassical 3 beta HSD deficiency.

Michele Zerah, Éric Rhéaume, Puurnima Mani et al. · The Journal of Clinical Endocrinology & Metabolism · 1994 · 60 citations

Life Sciences, Genetics, Pediatrics +15

Prevalence of Nonclassical Steroid 21-Hydroxylase Deficiency Based on a Morning Salivary 17-hydroxyprogesterone Screening Test: A Small Sample Study*

Michele Zerah, Hajime Ueshiba, Elizabeth Wood et al. · The Journal of Clinical Endocrinology & Metabolism · 1990 · 58 citations

Life Sciences, Endocrinology, Hormone Biochemistry +12

Morning Salivary 17-Hydroxyprogesterone Is a Useful Screening Test for Nonclassical 21-Hydroxylase Deficiency^*

Michele Zerah, Songya Pang, Maria I. New · The Journal of Clinical Endocrinology & Metabolism · 1987 · 35 citations

Dentistry, Endocrinology, Clinical Biochemistry +8