Bernard Prudhon

Dynamin 2 mutations cause sporadic centronuclear myopathy with neonatal onset

Marc Bitoun, Jorge A. Bevilacqua, Bernard Prudhon et al. · Annals of Neurology · 2007 · 149 citations · Full text

Medicine, Neurology, Pediatrics +8

Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy

Johann Böhm, Valérie Biancalana, Elizabeth T. DeChene et al. · Human Mutation · 2012 · 137 citations · Full text

Medicine, Genetics, Neurology +17

A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice

Anne‐Cécile Durieux, Alban Vignaud, Bernard Prudhon et al. · Human Molecular Genetics · 2010 · 125 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosis

Marc Bitoun, Anne‐Cécile Durieux, Bernard Prudhon et al. · Human Mutation · 2009 · 81 citations · Full text

Life Sciences, Cell Biology, Neurology +17

A Centronuclear Myopathy – Dynamin 2 Mutation Impairs Autophagy in Mice

Anne‐Cécile Durieux, Stéphane Vassilopoulos, Jeanne Lainé et al. · Traffic · 2012 · 64 citations · Full text

Life Sciences, Genetics, Molecular Biology +17