Louis Viollet

Identification and characterization of a spinal muscular atrophy-determining gene

Suzie Lefebvre, Lydie Bürglen, Sophie Reboullet et al. · Cell · 1995 · 3.9K citations · Full text

Genetics, Gene Characterization, Molecular Genetics +3

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

Erin L. Heinzen, Kathryn J. Swoboda, Yuki Hitomi et al. · Nature Genetics · 2012 · 417 citations · Full text

Rare Diseases, Mendelian Disorder, Genetic Disorder +8

Structure and Organization of the Human Survival Motor Neurone (SMN) Gene

Lydie Bürglen, Suzie Lefebvre, Olivier Clermont et al. · Genomics · 1996 · 251 citations

Neurodegenerative Diseases, Neuroregeneration, Developmental Biology +9

Early onset collagen VI myopathies: Genetic and clinical correlations

Laura Briñas, Pascale Richard, Susana Quijano‐Roy et al. · Annals of Neurology · 2010 · 132 citations · Full text

Resistance strength training exercise in children with spinal muscular atrophy

Aga Lewelt, Kristin J. Krosschell, Gregory J. Stoddard et al. · Muscle & Nerve · 2015 · 102 citations · Full text