Neuropathology in a patient with ataxia and the SCA8 genotype

被引：0
|
作者：
Factor, SA [1 ]
Qian, J [1 ]
Lava, NS [1 ]
机构：
[1] Albany Med Ctr, Albany, NY USA
来源：
MOVEMENT DISORDERS | 2003年 / 18卷 / 09期
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：1095 / 1095
页数：1
相关论文
共 50 条
  • [21] SCA8 mRNA expression suggests an antisense regulation of KLHL1 and correlates to SCA8 pathology
    Chen, Wei-Lun
    Lin, Jun-Wei
    Huang, Hei-Jen
    Wang, Su-Min
    Su, Ming-Tsan
    Lee-Chen, Guey-Jen
    Chen, Chiung-Mei
    Hsieh-Li, Hsiu Mei
    BRAIN RESEARCH, 2008, 1233 : 176 - 184
  • [22] Analysis of SCA8, SCA12, SCA17 and SCA19 in Thai patients with unknown spinocerebellar ataxia: A multicenter study
    Choubtum, Lulin
    Pulkes, Teeratorn
    Boonkongchuen, Pairoj
    Dejthevaporn, Charungthai
    Pongpakdee, Sunsanee
    Wetchaphanphesat, Suppachok
    Jindahra, Panitha
    Jitkritsadakul, Onanong
    Bhidayasiri, Roongroj
    Hanchaiphiboolkul, Suchat
    MOVEMENT DISORDERS, 2014, 29 : S59 - S59
  • [23] The Phenotypical Presentation of SCA8 in Taiwan
    Liaw, Y. C.
    Chiang, H. L.
    MOVEMENT DISORDERS, 2020, 35 : S534 - S534
  • [24] Atypical Parkinsonism and SCA8 - Reply
    Baba, Yasuhiko
    Uitti, Ryan J.
    Wszolek, Zbigniew K.
    Farrer, Matthew J.
    PARKINSONISM & RELATED DISORDERS, 2006, 12 (06) : 396 - 396
  • [25] Understanding the dynamics of Spinocerebellar Ataxia 8 (SCA8) locus through a comparative genetic approach in humans and apes
    Andrés, AM
    Soldevila, M
    Saitou, N
    Volpini, V
    Calafell, F
    Bertranpetit, J
    NEUROSCIENCE LETTERS, 2003, 336 (03) : 143 - 146
  • [26] Analysis of SCA8, SCA10, SCA12, SCA17 and SCA19 in patients with unknown spinocerebellar ataxia: a Thai multicentre study
    Lulin Choubtum
    Pirada Witoonpanich
    Suchat Hanchaiphiboolkul
    Roongroj Bhidayasiri
    Onanong Jitkritsadakul
    Sunsanee Pongpakdee
    Suppachok Wetchaphanphesat
    Pairoj Boonkongchuen
    Teeratorn Pulkes
    BMC Neurology, 15
  • [27] Analysis of SCA8, SCA10, SCA12, SCA17 and SCA19 in patients with unknown spinocerebellar ataxia: a Thai multicentre study
    Choubtum, Lulin
    Witoonpanich, Pirada
    Hanchaiphiboolkul, Suchat
    Bhidayasiri, Roongroj
    Jitkritsadakul, Onanong
    Pongpakdee, Sunsanee
    Wetchaphanphesat, Suppachok
    Boonkongchuen, Pairoj
    Pulkes, Teeratorn
    BMC NEUROLOGY, 2015, 15
  • [28] Novel neuronal cytoplasmic inclusions in a patient carrying SCA8 expansion mutation
    Yokoyama, Teruo
    Ishiyama, Miyako
    Hasegawa, Kazuko
    Uchihara, Toshiki
    Yagishita, Saburo
    NEUROPATHOLOGY, 2014, 34 (01) : 27 - 31
  • [29] SCA8 expansion in the Spanish population including one homozygous patient.
    Mila, M
    Tazon, B
    Muñoz, E
    Jimenez, D
    Badenas, C
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 652 - 652
  • [30] SCA8 CTG expansion: evidence for a common haplotype and highly mutable region on both ataxia and non-ataxia chromosomes.
    Moseley, M
    Jacobsen, J
    Liquori, C
    Durand, A
    Davis, L
    Ikeda, Y
    Bird, T
    Spiegel, R
    Ashizawa, T
    Pandolfo, M
    Potter, N
    Schaefer, F
    Milunsky, A
    Kennedy, J
    Seltzer, W
    Atwood, L
    Vincent, J
    Day, J
    Ranum, L
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 363 - 363
12345