Nathalie Petit

Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndrome

Behzad Moghadaszadeh, Nathalie Petit, Céline Jaillard et al. · Nature Genetics · 2001 · 364 citations

Rare Diseases, Developmental Biology, Mendelian Disorder +9

Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p (RSMD1)

Eugenio Mercuri, Beril Talim, Behzad Moghadaszadeh et al. · Neuromuscular Disorders · 2002 · 213 citations

Rare Diseases, Mendelian Disorder, Genetic Disorder +5

Colon luminal content and epithelial cell morphology are markedly modified in rats fed with a high-protein diet

Mireille Andriamihaja, Anne‐Marie Davila, Mamy Eklou-Lawson et al. · American Journal of Physiology-Gastrointestinal and Liver Physiology · 2010 · 143 citations · Full text

Nutrition, Gastroenterology, Pathology +21

Tissue-specific conditional<i>CCM2</i>knockout mice establish the essential role of endothelial CCM2 in angiogenesis: implications for human cerebral cavernous malformations

Gwénola Boulday, Anne Blécon, Nathalie Petit et al. · Disease Models & Mechanisms · 2009 · 108 citations · Full text

<i>technical knockout</i>, a Drosophila Model of Mitochondrial Deafness

Janne M. Toivonen, Kevin M.C. O’Dell, Nathalie Petit et al. · Genetics · 2001 · 99 citations · Full text