B Bady

Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins.

Isabelle Richard, L. Brenguier, Pervin Dinçer et al. · PubMed · 1997 · 119 citations

Medicine, Genetics, Molecular Genetics +11

Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families.

Alexis Elbaz, J. Vale-Santos, Karin Jurkat‐Rott et al. · PubMed · 1995 · 113 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Congenital Lambert-Eaton myasthenic syndrome.

B Bady, G Chauplannaz, Howard Carrier · Journal of Neurology Neurosurgery & Psychiatry · 1987 · 65 citations · Full text

Medicine, Neurology, Pediatrics +13

Clinical validation of antidromic stimulation of the ring finger in early electrodiagnosis of mild carpal tunnel syndrome

Christophe Vial, G Chauplannaz, B Bady · Electroencephalography and Clinical Neurophysiology · 1990 · 61 citations

Medicine, Neurology, Electrodiagnostic Medicine +6

Mutations in the Muscle SodiumChannel Gene (SCN4A) in 13 FrenchFamilies with Hyperkalemic PeriodicParalysis and ParamyotoniaCongenita: Phenotype to GenotypeCorrelations and Demonstration of thePredominance of Two Mutations

Emmanuelle Plassart, J Reboul, Claire-Sophie Rime et al. · European Journal of Human Genetics · 1994 · 56 citations

Life Sciences, Genetics, Molecular Genetics +17