F Kurtz

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 · 213 citations

Medicine, Endocrinology, Genetics +17

Androgen Insensitivity Syndrome: Somatic Mosaicism of the Androgen Receptor in Seven Families and Consequences for Sex Assignment and Genetic Counseling

Birgit Köhler, Serge Lumbroso, Juliane Léger et al. · The Journal of Clinical Endocrinology & Metabolism · 2005 · 117 citations

Life Sciences, Endocrinology, Genetics +17

The Prevalence of<i>CHD7</i>Missense Versus Truncating Mutations Is Higher in Patients With Kallmann Syndrome Than in Typical CHARGE Patients

Séverine Marcos, Julie Sarfati, Chrystel Leroy et al. · The Journal of Clinical Endocrinology & Metabolism · 2014 · 86 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Oral L-arginine supplementation in cystic fibrosis patients: a placebo-controlled study

H. Grasemann, Corinna Grasemann, F Kurtz et al. · European Respiratory Journal · 2005 · 66 citations

Medicine, Pharmacology, Pharmacotherapy +15

Undervirilization in XY newborns may hide a 5α‐reductase deficiency: report of three new <i>SRD5A2</i> gene mutations

Pascal Philibert, B. Cammas, Françoise Audran et al. · International Journal of Andrology · 2010 · 35 citations · Full text

Life Sciences, Endocrinology, Genetics +17