P. Pigny

Patients with Familial Partial Lipodystrophy of the Dunnigan Type Due to a<i>LMNA</i>R482W Mutation Show Muscular and Cardiac Abnormalities

Marie‐Christine Vantyghem, P. Pigny, C. A. Maurage et al. · The Journal of Clinical Endocrinology & Metabolism · 2004 · 121 citations · Full text

Life Sciences, Endocrinology, Genetics +16

Primary hyperparathyroidism as first manifestation in multiple endocrine neoplasia type 2A: an international multicenter study

Louise Vølund Larsen, Delphine Mirebeau‐Prunier, Tsuneo Imai et al. · Endocrine Connections · 2020 · 34 citations · Full text

Medicine, Endocrinology, Pathology +17

Efficient mutation detection in <b><i>MEN1</i></b> gene using a combination of single‐strand conformation polymorphism (MDGA™) and heteroduplex analysis

Michel Crépin, Fabienne Escande, P. Pigny et al. · Electrophoresis · 2003 · 22 citations

Life Sciences, Genetics, Molecular Genetics +17

Identification by array-Comparative Genomic Hybridization (array-CGH) of a large deletion of luteinizing hormone receptor gene combined with a missense mutation in a patient diagnosed with a 46,XY disorder of sex development and application to prenatal diagnosis

Nicolas Richard, Céline Leprince, Nicolas Gruchy et al. · Endocrine Journal · 2011 · 17 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Evaluation of denaturing high performance liquid chromatography for the mutational analysis of the MEN1 gene

Michel Crépin, P. Pigny, Fabienne Escande et al. · Journal of Molecular Endocrinology · 2006 · 16 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17