Effectiveness of Deep Brain Stimulation (DBS) in Mice with Spinocerebellar Ataxia (SCA1)

被引：0
|
作者：
Vedam-Mai, V.
McFarland, K.
Nathu, R.
Kurtovic, S.
Zhang, Q.
Ashizawa, T.
Okun, M.
机构：
来源：
MOVEMENT DISORDERS | 2017年 / 32卷
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：
799
引用
收藏
页数：1
相关论文
共 50 条
  • [41] Comparison of peripheral nervous system damage in patients with type 1 (SCA1) and type 2 (SCA2) spinocerebellar ataxia
    Niewiadomska, M.
    Rakowicz, M.
    Wochnik-Dyjas, D.
    Glazowski, C. Z.
    Zaremba, J.
    EUROPEAN JOURNAL OF NEUROLOGY, 2004, 11 : 158 - 158
  • [42] Cerebellar atrophy patterns in Paraneoplastic Cerebellar Degeneration (PCD) and Spinocerebellar Ataxia type-1 (SCA1)
    de Pemille, C. Vialatte
    Psimaras, D.
    Adanyegu, I.
    Graus, F.
    Durr, A.
    Honnorat, J.
    Delattre, J. -Y.
    Alentorn, A.
    EUROPEAN JOURNAL OF NEUROLOGY, 2018, 25 : 457 - 458
  • [43] Analysis of spinocereballar ataxia type 1 (SCA1) knock-in mice.
    Watase, K
    Lorenzetti, D
    Xu, B
    Armstrong, D
    Orr, HT
    Zoghbi, HY
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A114 - A114
  • [44] Frequency of SCA1, DRPLA, MJD, SCA2 and SCA6 mutations in a large group of Portuguese families with spinocerebellar ataxia
    Silveira, I
    Coutinho, P
    Maciel, P
    Hayes, S
    Dias, A
    Guimaraes, J
    Loureiro, LL
    Barros, J
    Chorao, R
    Ribeiro, P
    Bettencourt, M
    Serrano, P
    Silva, C
    Rouleau, GA
    Sequeiros, J
    EUROPEAN JOURNAL OF HUMAN GENETICS, 1998, 6 : 160 - 160
  • [45] LINKAGE STUDIES ON GLYOXALASE-I (GLO), PEPSINOGEN (PG), SPINOCEREBELLAR ATAXIA (SCA1), AND HLA
    WHITTINGTON, JE
    KEATS, BJB
    JACKSON, JF
    CURRIER, RD
    TERASAKI, PI
    CYTOGENETICS AND CELL GENETICS, 1980, 28 (03): : 145 - 150
  • [46] Expanded CAG repeats in spinocerebellar ataxia (SCA1) segregate with distinct haplotypes in South African families
    R. S. Ramesar
    Soraya Bardien
    Peter Beighton
    Alan Bryer
    Human Genetics, 1997, 100 : 131 - 137
  • [47] Expanded CAG repeats in spinocerebellar ataxia (SCA1) segregate with distinct haplotypes in South African families
    Ramesar, RS
    Bardien, S
    Beighton, P
    Bryer, A
    HUMAN GENETICS, 1997, 100 (01) : 131 - 137
  • [48] Early electrophysiological anomalies of Purkinje cells in a transgenic mouse model of spinocerebellar ataxia type 1 (SCA1)
    Hourez, R
    Millard, I
    Servais, L
    Vig, P
    Orr, HT
    Gall, D
    Pandolfo, M
    Schiffmann, SN
    NEUROLOGY, 2006, 66 (05) : A333 - A333
  • [49] SPINOCEREBELLAR-ATAXIA-1 (SCA1) IN THE JAPANESE IN HOKKAIDO MAY DERIVE FROM A SINGLE COMMON ANCESTRY
    WAKISAKA, A
    SASAKI, H
    TAKADA, A
    FUKAZAWA, T
    SUZUKI, Y
    HAMADA, T
    IWABUCHI, K
    TASHIRO, K
    YOSHIKI, T
    JOURNAL OF MEDICAL GENETICS, 1995, 32 (08) : 590 - 592
  • [50] LINKAGE DISEQUILIBRIUM BETWEEN SPINOCEREBELLAR ATAXIA (SCA1) AND D6S89 LOCI
    TERRENATO, L
    JODICE, C
    MALASPINA, P
    NOVELLETTO, A
    PERSICHETTI, F
    SCHINAIA, G
    FRONTALI, M
    LULLI, P
    CAPPELLACCI, S
    GIUNTI, P
    SPADARO, M
    ANTONELLI, A
    PANDOLFO, M
    CYTOGENETICS AND CELL GENETICS, 1993, 62 (2-3): : 80 - 80
12345