Early electrophysiological anomalies of Purkinje cells in a transgenic mouse model of spinocerebellar ataxia type 1 (SCA1)

被引:0
|
作者
Hourez, R
Millard, I
Servais, L
Vig, P
Orr, HT
Gall, D
Pandolfo, M
Schiffmann, SN
机构
关键词
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
引用
收藏
页码:A333 / A333
页数:1
相关论文
共 50 条
  • [21] Safety and tolerability study of lithium carbonate in spinocerebellar ataxia type 1 (SCA1) patients
    Lopez, G. J.
    Considine, E.
    McElroy, B.
    Haubenberger, D.
    Razzook, A.
    Zoghbi, H.
    Hallett, M.
    MOVEMENT DISORDERS, 2009, 24 : S16 - S16
  • [22] DOMINANTLY INHERITED SPINOCEREBELLAR ATAXIA (SCA1) LINKAGE STUDIES
    SHRIMPTON, AE
    VIJAYALAXMI
    EVANS, HJ
    CYTOGENETICS AND CELL GENETICS, 1989, 51 (1-4): : 1080 - 1080
  • [23] Increased Purkinje cells acid sphingomyelinase activity: an early pathogenetic event in a spinocerebellar ataxia type 1 mouse model
    Bonato, S.
    Falcone, S.
    Bresolin, N.
    Croci, L.
    Comi, G. P.
    Gonsalez, G.
    Magnoni, R.
    Turconi, A. C.
    Pandolfo, M.
    Orr, H.
    Clementi, E.
    JOURNAL OF NEUROLOGY, 2006, 253 : 51 - 51
  • [24] Aminopyridines correct presymptomatic neuronal dysfunction and improve late behavioral and cellular phenotype in a mouse model of spinocerebellar ataxia type 1 (SCA1)
    Hourez, R.
    Servais, L.
    Gall, D.
    Pandolfo, M.
    Schiffmann, S. N.
    MOVEMENT DISORDERS, 2010, 25 (07) : S191 - S192
  • [25] Aminopyridines Correct Presymptomatic Neuronal Dysfunction and Improve Late Behavioral and Cellular Phenotype in a Mouse Model of Spinocerebellar Ataxia Type 1 (SCA1)
    Hourez, Raphael
    Servais, Laurent
    Gall, David
    Pandolfo, Massimo
    Schiffmann, Serge N.
    NEUROLOGY, 2010, 74 (09) : A359 - A359
  • [26] Partial loss of Tip60 slows mid-stage neurodegeneration in a spinocerebellar ataxia type 1 (SCA1) mouse model
    Gehrking, Kristin M.
    Andresen, J. Michael
    Duvick, Lisa
    Lough, John
    Zoghbi, Huda Y.
    Orr, Harry T.
    HUMAN MOLECULAR GENETICS, 2011, 20 (11) : 2204 - 2212
  • [27] Spinocerebellar ataxia type I (SCA1): Revised diagnosis of a familial multiple sclerosis
    Kreuz, FR
    Deike, H
    AKTUELLE NEUROLOGIE, 1999, 26 (08) : 375 - 378
  • [28] The extra-cerebellar effects of spinocerebellar ataxia type 1 (SCA1): looking beyond the cerebellum
    Victor Olmos
    Neha Gogia
    Kimberly Luttik
    Fatema Haidery
    Janghoo Lim
    Cellular and Molecular Life Sciences, 2022, 79
  • [29] Altered trafficking of membrane proteins in Purkinje cells of SCA1 transgenic mice
    Skinner, PJ
    Vierra-Green, CA
    Clark, HB
    Zoghbi, HY
    Orr, HT
    AMERICAN JOURNAL OF PATHOLOGY, 2001, 159 (03): : 905 - 913
  • [30] Clinical and genetic study of a family with spinocerebellar ataxia type 1 (SCA1) and beta-thalassemia
    V. Pietrini
    M. Godani
    S. Calzetti
    A. Negrotti
    B. Castellotti
    M. C. Riggio
    C. Toffoli
    The Italian Journal of Neurological Sciences, 1998, 19 : 345 - 350