B. Eymard

Mutations in dynamin 2 cause dominant centronuclear myopathy

Marc Bitoun, Svetlana Maugenre, Pierre‐Yves Jeannet et al. · Nature Genetics · 2005 · 452 citations · Full text

Mitochondrial Myopathy, Mendelian Disorder, Genetic Disorder +5

Electromyography guides toward subgroups of mutations in muscle channelopathies

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

Phenotypic Study in 40 Patients With Dysferlin Gene Mutations

Karine Nguyen, Guillaume Bassez, Martin Krahn et al. · Archives of Neurology · 2007 · 262 citations

Distinct muscle imaging patterns in myofibrillar myopathies

Dirk Fischer, Rudolf A. Kley, Katharina Strach et al. · Neurology · 2008 · 252 citations · Full text

High Incidence of Sudden Death with Conduction System and Myocardial Disease Due to Lamins A and C Gene Mutation

Henri-Marc Bécane, Gisèle Bonne, Shaïda Varnous et al. · Pacing and Clinical Electrophysiology · 2000 · 250 citations