Maryse Cartigny

Phenotypical, Biological, and Molecular Heterogeneity of 5α-Reductase Deficiency: An Extensive International Experience of 55 Patients

Laurent Maı̈moun, Pascal Philibert, B. Cammas et al. · The Journal of Clinical Endocrinology & Metabolism · 2010 · 210 citations

Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study

Pamela Bowman, Åsta Sulen, Fabrizio Barbetti et al. · The Lancet Diabetes & Endocrinology · 2018 · 169 citations · Full text

Clinical Outcome, Hormonal Status, Gonadotrope Axis, and Testicular Function in 219 Adult Men Born With Classic 21-Hydroxylase Deficiency. A French National Survey

Claire Bouvattier, Laure Esterle, Peggy Renoult-Pierre et al. · The Journal of Clinical Endocrinology & Metabolism · 2015 · 112 citations · Full text

Familial reciprocal translocation t(7;16) associated with maternal uniparental disomy 7 in a Silver‐Russell patient

Jean‐Michel Dupont, Laurence Cuisset, Maryse Cartigny et al. · American Journal of Medical Genetics · 2002 · 112 citations

Deferring surgical treatment of ambiguous genitalia into adolescence in girls with 21-hydroxylase deficiency: a feasibility study

Pierre Bougnères, Claire Bouvattier, Maryse Cartigny et al. · International Journal of Pediatric Endocrinology · 2017 · 46 citations · Full text