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15篇 您的检索式:作者名="Plassart"
    题名 作者 年代 出处 被引量
1Mutations 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 显示文摘Plassart E Reboul J Rime CS 1994Eur J Hum Genet1994,2,2:1
2Paramyotonia congenita:genotype to phenotype correlations in two families and report of a new mutation in the sodium channel gene显示文摘Plassart E Eymard B Maurs L 1996J Neurol Sci1996,142,:1
3Genetic heterogeneity in hypokalemic periodic paralysis 显示文摘Plassart E Elbaz A Santos JV 1994Hum Genet1994,94,5:1
4Isolation of new genes in distal Xq28 : transcriptional map and identification of a human homologue of the ARD1 N-aeetyl transferase of Saccharomyces eerevisiac显示文摘Tribioli C Mancini M Plassart E 1994Hum Mol Genet1994,3,7:1
5Geretic heterogeneity in hypokalemic periodic paralysis显示文摘Plassart E Elbaz A Santos J V 1994Hum Genet1994,94,:1
6Strong correlation be- tween liver and serum levels of hepatitis C viruscoreantigen and RNA in chronically infected patients显示文摘Descamps V Op de Beeck A Plassart C 2012J Chin Microbio12012,50,2:1
7Molecular and functional responses of soil microbial communities under grassland restoration显示文摘Plassart P Vinceslas M K Gangneux C 2008Agriculture Ecosystems and Environment2008,127,3:1
8Genetic heterogeneity in hypokalemie periodic paralysis (hypoPP) 显示文摘Plassart E Elbaz A Santos JV 1994Hum Genet1994,94,:1
9Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP) 显示文摘Plassart E Elbaz A Santos JV 1994Hum Genet1994,94,5:1
10Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP) 显示文摘Plassart E Elbaz A Santos JV 1994Hum Genet1994,94,5:1
11Strong correlation between liver and serum levels of hepatitis C virus core antigen and RNA in chronically infected patients显示文摘Descamps V Op de Beeck A Plassart C 2012J Clin Microbiol2012,50,2:1
12Neurosteroids: recent findings显示文摘PLASSART SCHIESS E BAULIEU E E 2001Brain Res2001,37,13:1
13Mutations 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显示文摘Plassart E Reboul J Rime CS 0,,:1
14Genetichetorogenity in hypokalemic Periodic Paolysis显示文摘 Santis JV 1994Hum Genet1994,94,:1
15Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP)显示文摘 Elbaz A Santos JV 1994Hum Genet1994,94,:1
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