Plassart E - Search Results

1

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

Fontaine B, Vale-Santos J, Jurkat-Rott K, Reboul J, Plassart E, Rime CS, Elbaz A, Heine R, Guimarães J, Weissenbach J, et al. Fontaine B, et al. Among authors: plassart e. Nat Genet. 1994 Mar;6(3):267-72. doi: 10.1038/ng0394-267. Nat Genet. 1994. PMID: 8012389

2

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. Hum Genet. 1994 Nov;94(5):551-6. doi: 10.1007/BF00211025. Hum Genet. 1994. PMID: 7959693

3

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. Eur J Hum Genet. 1994;2(2):110-24. doi: 10.1159/000472351. Eur J Hum Genet. 1994. PMID: 8044656

4

Genes with triplet repeats: a new class of mutations causing neurological diseases.

Plassart E, Fontaine B. Plassart E, et al. Biomed Pharmacother. 1994;48(5-6):191-7. doi: 10.1016/0753-3322(94)90133-3. Biomed Pharmacother. 1994. PMID: 7999979 Review.

5

Paramyotonia congenita: genotype to phenotype correlations in two families and report of a new mutation in the sodium channel gene.

Plassart E, Eymard B, Maurs L, Hauw JJ, Lyon-Caen O, Fardeau M, Fontaine B. Plassart E, et al. J Neurol Sci. 1996 Oct;142(1-2):126-33. doi: 10.1016/0022-510x(96)00173-6. J Neurol Sci. 1996. PMID: 8902732

6

Apolipoprotein E polymorphism in multiple sclerosis.

Gervais A, Gaillard O, Plassart E, Reboul J, Fontaine B, Schuller E. Gervais A, et al. Among authors: plassart e. Ann Clin Biochem. 1998 Jan;35 ( Pt 1):135-6. doi: 10.1177/000456329803500119. Ann Clin Biochem. 1998. PMID: 9463752 No abstract available.

7

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: plassart e. 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.

8

Apolipoprotein E and multiple sclerosis: a biochemical and genetic investigation.

Gaillard O, Gervais A, Meillet D, Plassart E, Fontaine B, Lyon-Caen O, Delattre J, Schuller E. Gaillard O, et al. Among authors: plassart e. J Neurol Sci. 1998 Jun 30;158(2):180-6. doi: 10.1016/s0022-510x(98)00118-x. J Neurol Sci. 1998. PMID: 9702689

9

Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: characterization of 14 Cx32 mutations in 35 families.

Rouger H, LeGuern E, Birouk N, Gouider R, Tardieu S, Plassart E, Gugenheim M, Vallat JM, Louboutin JP, Bouche P, Agid Y, Brice A. Rouger H, et al. Among authors: plassart e. Hum Mutat. 1997;10(6):443-52. doi: 10.1002/(SICI)1098-1004(1997)10:6<443::AID-HUMU5>3.0.CO;2-E. Hum Mutat. 1997. PMID: 9401007

10

Isolation of new genes in distal Xq28: transcriptional map and identification of a human homologue of the ARD1 N-acetyl transferase of Saccharomyces cerevisiae.

Tribioli C, Mancini M, Plassart E, Bione S, Rivella S, Sala C, Torri G, Toniolo D. Tribioli C, et al. Among authors: plassart e. Hum Mol Genet. 1994 Jul;3(7):1061-7. doi: 10.1093/hmg/3.7.1061. Hum Mol Genet. 1994. PMID: 7981673

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