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  • Mutations in FUS cause FALS and SALS in French and French Canadian populations
    [作者:Belzil, VV; Valdmanis, PN; Dion, PA; Daoud, H; Kabashi, E; Noreau, A; Gauthier, J; Hince, P; Desjarlais, A; Bouchard, JP; Lacomblez, L; Salachas, F; Pradat, PF; Camu, W; Meininger, V; Dupre, N; Rouleau, GA,期刊:Neurology, 页码:1176-1179 , 文章类型: Article,,卷期:2009年73-15]
  • Background: The identification of mutations in the TARDBP and more recently the identification of mutations in the FUS gene as the cause of amyotrophic lateral sclerosis (ALS) is providing the field with new insight abou...
  • Relationships between biomarkers in aging and dementia
    [作者:Jagust, WJ; Landau, SM; Shaw, LM; Trojanowski, JQ; Koeppe, RA; Reiman, EM; Foster, NL; Petersen, RC; Weiner, MW; Price, JC; Mathis, CA,期刊:Neurology, 页码:1193-1199 , 文章类型: Article,,卷期:2009年73-15]
  • Background: PET imaging using [F-18]fluorodeoxyglucose (FDG) and [C-11]Pittsburgh compound B (PIB) have been proposed as biomarkers of Alzheimer disease (AD), as have CSF measures of the 42 amino acid beta-amyloid protei...
  • Deletions involving both KCNQ2 and CHRNA4 present with benign familial neonatal seizures
    [作者:Kurahashi, H; Wang, JW; Ishii, A; Kojima, T; Wakai, S; Kizawa, T; Fujimoto, Y; Kikkawa, K; Yoshimura, K; Inoue, T; Yasumoto, S; Ogawa, A; Kaneko, S; Hirose, S,期刊:Neurology, 页码:1214-1217 , 文章类型: Article,,卷期:2009年73-15]
  • Objective: Mutations of the genes encoding subunits of potassium voltage-gated channel, KCNQ2 and KCNQ3, have been identified in patients with benign familial neonatal seizures (BFNS). This study set out to determine the...