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Page 1
Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and demonstration of the predominance of two mutations.
Plassart E, Reboul J, Rime CS, Recan D, Millasseau P, Eymard B, Pelletier J, Thomas C, Chapon F, Desnuelle C, et al. Plassart E, et al. Among authors: reboul j. Eur J Hum Genet. 1994;2(2):110-24. doi: 10.1159/000472351. Eur J Hum Genet. 1994. PMID: 8044656
A systematic study of oligodendrocyte growth factors as candidates for genetic susceptibility to MS. French Multiple Sclerosis Genetics Group.
Mertens C, Brassat D, Reboul J, Eichenbaum-Voline S, Vuillemin-Azais C, Cournu I, Babron MC, Semana G, Edan G, Clanet M, Clerget-Darpoux F, Baron-Van Evercooren A, Lyon-Caen O, Liblau R, Fontaine B. Mertens C, et al. Among authors: reboul j. Neurology. 1998 Sep;51(3):748-53. doi: 10.1212/wnl.51.3.748. Neurology. 1998. PMID: 9748021
Apolipoprotein E polymorphism in multiple sclerosis.
Gervais A, Gaillard O, Plassart E, Reboul J, Fontaine B, Schuller E. Gervais A, et al. Among authors: reboul j. Ann Clin Biochem. 1998 Jan;35 ( Pt 1):135-6. doi: 10.1177/000456329803500119. Ann Clin Biochem. 1998. PMID: 9463752 No abstract available.
Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP).
Plassart E, Elbaz A, Santos JV, Reboul J, Lapie P, Chauveau D, Jurkat-Rott K, Guimaraes J, Saudubray JM, Weissenbach J, et al. Plassart E, et al. Among authors: reboul j. Hum Genet. 1994 Nov;94(5):551-6. doi: 10.1007/BF00211025. Hum Genet. 1994. PMID: 7959693
Periodic paralysis and voltage-gated ion channels.
Fontaine B, Lapie P, Plassart E, Tabti N, Nicole S, Reboul J, Rime-Davoine CS. Fontaine B, et al. Among authors: reboul j. Kidney Int. 1996 Jan;49(1):9-18. doi: 10.1038/ki.1996.2. Kidney Int. 1996. PMID: 8770943 Free article. Review. No abstract available.
270 results