J Reboul

Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31–32 in three European families

B. Fontaine, J. Vale-Santos, K Jurkat-Rott et al. · Nature Genetics · 1994 · 234 citations

Health Sciences, Cytogenetics, European Families +8

Familial factors influence disability in MS multiplex families

David Brassat, C. Azais-Vuillemin, Jacqueline Yaouanq et al. · Neurology · 1999 · 82 citations

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

Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP)

Emmanuelle Plassart, Alexis Elbaz, JoseVale Santos et al. · Human Genetics · 1994 · 45 citations

Electrolyte Disorder, Genetics, Physiology +5

Cytokines in genetic susceptibility to multiple sclerosis: a candidate gene approach

J Reboul, Caroline Mertens, Florence Levillayer et al. · Journal of Neuroimmunology · 2000 · 40 citations

Cytokine, Disease Susceptibility, Allergy +11