Savine Vicart

Electromyography guides toward subgroups of mutations in muscle channelopathies

Emmanuel Fournier, Marianne Arzel, Damien Sternberg et al. · Annals of Neurology · 2004 · 305 citations

Spectrum of<i>HSPG2</i>(Perlecan) mutations in patients with Schwartz-Jampel syndrome

Morgane Stum, Claire-Sophie Davoine, Savine Vicart et al. · Human Mutation · 2006 · 104 citations

Hspg2 Gene, Mendelian Disorder, Schwartz-jampel Syndrome +11

New mutations of <i>SCN4A</i> cause a potassium-sensitive normokalemic periodic paralysis

Savine Vicart, Damien Sternberg, Emmanuel Fournier et al. · Neurology · 2004 · 78 citations

Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patients

J. Molenaar, Jamie I. Verhoeven, Richard J. Rodenburg et al. · Brain · 2019 · 40 citations · Full text

Homozygosity for dominant mutations increases severity of muscle channelopathies

Marianne Arzel-Hézode, Damien Sternberg, Nacira Tabti et al. · Muscle & Nerve · 2009 · 34 citations

Muscle Function, Genetics, Muscle Channelopathies +22