Clinical features, disease progression, and nuclear imaging in ATXN2-related parkinsonism in a longitudinal cohort-Reference-Cited by-同舟云学术

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Clinical features, disease progression, and nuclear imaging in ATXN2-related parkinsonism in a longitudinal cohort

Published:2024-02-10 Issue:7 Volume:45 Page:3191-3200
ISSN:1590-1874
Container-title:Neurological Sciences
language:en
Short-container-title:Neurol Sci

Author:

Xu Yi-Dan,Zhou Xin-Yue,Wei Si-Di,Liu Feng-Tao,Zhao Jue,Tang Yi-Lin,Shen Bo,Ding Zheng-Tong,Wu Jian-Jun,Sun Yi-Min,Wang Jian^ORCID

Funder

Science and Technology Commission of Shanghai Municipality

National Health Commission of the People's Republic of China

National Natural Science Foundation of China

National Health Commission of China

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s10072-024-07383-1.pdf

Reference30 articles.

1. Furtado S, Payami H, Lockhart PJ et al (2004) Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2). Mov Disord 19(6):622–629

2. Gwinn-Hardy K, Chen JY, Liu HC et al (2000) Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese. Neurology 55(6):800–805

3. Shan DE, Soong BW, Sun CM, Lee SJ, Liao KK, Liu RS (2001) Spinocerebellar ataxia type 2 presenting as familial levodopa-responsive parkinsonism. Ann Neurol 50(6):812–815

4. Lu CS, Wu Chou YH, Kuo PC, Chang HC, Weng YH (2004) The parkinsonian phenotype of spinocerebellar ataxia type 2. Arch Neurol 61(1):35–38

5. Charles P, Camuzat A, Benammar N et al (2007) Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism? Neurology 69(21):1970–1975

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