Valérie Allamand

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

Steven L. Roberds, France Leturcq, Valérie Allamand et al. · Cell · 1994 · 456 citations

Rare Diseases, Missense Mutations, Developmental Biology +9

β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12

Leland E. Lim, Franck Duclos, Odile Broux et al. · Nature Genetics · 1995 · 447 citations

Mechanobiology, Skeletal Muscle, Pathology +3

Disruption of the β-Sarcoglycan Gene Reveals Pathogenetic Complexity of Limb-Girdle Muscular Dystrophy Type 2E

Madeleine Durbeej, Ronald D. Cohn, Ronald F. Hrstka et al. · Molecular Cell · 2000 · 208 citations · Full text

Skeletal Muscle, Medicine, Pathology +4

Mutations in COL6A3 Cause Severe and Mild Phenotypes of Ullrich Congenital Muscular Dystrophy

Ercan Demir, Patrizia Sabatelli, Valérie Allamand et al. · The American Journal of Human Genetics · 2002 · 167 citations · Full text

Rare Diseases, Mendelian Disorder, Genetic Disorder +9

Premature stop codons involved in muscular dystrophies show a broad spectrum of readthrough efficiencies in response to gentamicin treatment

Laure Bidou, Isabelle Hatin, Norma Pérez et al. · Gene Therapy · 2004 · 150 citations

Medicine, Degenerative Disease, Broad Spectrum +6