Spinocerebellar ataxia type 17 repeat in patients with Huntington's disease-like and ataxia

被引：11
|
作者：
Cellini, E [1 ]
Forleo, P [1 ]
Nacmias, B [1 ]
Tedde, A [1 ]
Bagnoli, S [1 ]
Piacentini, S [1 ]
Sorbi, S [1 ]
机构：
[1] Univ Florence, Dept Neurol & Psychiat Sci, I-50121 Florence, Italy
来源：
ANNALS OF NEUROLOGY | 2004年 / 56卷 / 01期
关键词：
D O I：
10.1002/ana.20146
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：163 / 163
页数：1
相关论文
共 50 条
  • [21] Dysarthria in patients with Friedreich's ataxia and spinocerebellar ataxia
    Brendel, B.
    Schoelderle, T.
    Lindig, T.
    Synofzik, M.
    Schoels, L.
    Ackermann, H.
    Ziegler, W.
    MOVEMENT DISORDERS, 2011, 26 : S2 - S2
  • [22] Molecular Mechanisms of Spinocerebellar Ataxia Type 17
    Davidenko, Alina
    Bogomazova, Alexandra
    Illarioshkin, Sergey
    Lagarkova, Maria
    MOLECULAR NEUROBIOLOGY, 2024, : 5720 - 5729
  • [23] Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: A population genetics model for CAG repeat expansions
    Frontali, M
    Sabbadini, G
    Novelletto, A
    Jodice, C
    Naso, F
    Spadaro, M
    Giunti, P
    Jacopini, AG
    Veneziano, L
    Mantuano, E
    Malaspina, P
    Ulizzi, L
    Brice, A
    Durr, A
    Terrenato, L
    ANNALS OF HUMAN GENETICS, 1996, 60 : 423 - 435
  • [24] Evaluation of ataxia in patients with Huntington's Disease
    Franklin, Gustavo
    Teive, Helio Afonso
    Germiniani, Francisco Branco
    Milano, Sibele
    Pavanelli, Giovanna
    Lima, Nayra
    Raskin, Salmo
    Ribas, Gustavo
    NEUROLOGY, 2018, 90
  • [25] Genetic analysis of Spinocerebellar ataxia type 17 in Parkinson's disease in mainland China
    Xu, Qian
    Jia, Dandan
    Wang, Junling
    Guo, Jifeng
    Jiang, Hong
    Lei, Lifang
    Shen, Lu
    Pan, Qian
    Xia, Kun
    Yan, Xinxiang
    Tang, Beisha
    PARKINSONISM & RELATED DISORDERS, 2010, 16 (10) : 700 - 702
  • [26] The molecular diagnosis of spinocerebellar ataxia type 1 in patients with ataxia
    Koefoed, P
    Nielsen, JE
    Hasholt, L
    Jensen, PKA
    Fenger, K
    Sorensen, SA
    EUROPEAN JOURNAL OF NEUROLOGY, 1997, 4 (06) : 586 - 592
  • [27] Trehalose Attenuates the Gait Ataxia and Gliosis of Spinocerebellar Ataxia Type 17 Mice
    Zhi-Zhong Chen
    Chien-Ming Wang
    Guan-Chiun Lee
    Ho-Chiang Hsu
    Tzu-Ling Wu
    Chia-Wei Lin
    Chih-Kang Ma
    Guey-Jen Lee-Chen
    Hei-Jen Huang
    Hsiu Mei Hsieh-Li
    Neurochemical Research, 2015, 40 : 800 - 810
  • [28] Trehalose Attenuates the Gait Ataxia and Gliosis of Spinocerebellar Ataxia Type 17 Mice
    Chen, Zhi-Zhong
    Wang, Chien-Ming
    Lee, Guan-Chiun
    Hsu, Ho-Chiang
    Wu, Tzu-Ling
    Lin, Chia-Wei
    Ma, Chih-Kang
    Lee-Chen, Guey-Jen
    Huang, Hei-Jen
    Hsieh-Li, Hsiu Mei
    NEUROCHEMICAL RESEARCH, 2015, 40 (04) : 800 - 810
  • [29] Spinocerebellar ataxia type 10: A disease caused by a large ATTCT repeat expansion
    Matsuura, T
    Ashizawa, T
    TRIPLE REPEAT DISEASES OF THE NERVOUS SYSTEMS, 2002, 516 : 79 - 97
  • [30] Single cell analysis of trinucleotide repeat expansion mutations in Huntington disease, spinocerebellar ataxia type 1, and myotonic dystrophy
    Chong, SS
    Liu, L
    Hughes, MR
    IN VITRO FERTILIZATION AND ASSISTED REPRODUCTION, 1997, : 751 - 757
12345