Pierre Bouloux

Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism

Nelly Pitteloud, Richard Quinton, Simon H. S. Pearce et al. · Journal of Clinical Investigation · 2007 · 378 citations · Full text

Life Sciences, Endocrinology, Genetics +17

Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome

Jean‐Pierre Hardelin, Jacqueline Levilliers, Stéphane Blanchard et al. · Human Molecular Genetics · 1993 · 205 citations

Life Sciences, Genetics, Molecular Genetics +9

Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes

Nelly Pitteloud, Astrid U. Meysing, Richard Quinton et al. · Molecular and Cellular Endocrinology · 2006 · 198 citations

Life Sciences, Genetics, Molecular Genetics +12

Landscape of Familial Isolated and Young-Onset Pituitary Adenomas: Prospective Diagnosis in<i>AIP</i>Mutation Carriers

Laura C. Hernández‐Ramírez, Plamena Gabrovska, Judit Dénes et al. · The Journal of Clinical Endocrinology & Metabolism · 2015 · 170 citations · Full text

Medicine, Endocrinology, Genetics +17

Methodological Considerations in the Determination of Plasma Catecholamines by High-Performance Liquid Chromatography with Electrochemical Detection

Pierre Bouloux, David I. Perrett, G. M. Besser · Annals of Clinical Biochemistry International Journal of Laboratory Medicine · 1985 · 156 citations · Full text

Pharmacy, Chemistry, Pharmacology +9