Presence of spinocerebellar ataxia type 2 gene mutation in a patient with apparently sporadic Parkinson's disease: Clinical implications-Reference-Cited by-同舟云学术

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Presence of spinocerebellar ataxia type 2 gene mutation in a patient with apparently sporadic Parkinson's disease: Clinical implications

Published:2004-11 Issue:11 Volume:19 Page:1357-1360
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Shan Din-E,Liu Ren-Shyan,Sun Chen-Ming,Lee Shwn-Jen,Liao Kwong-Kum,Soong Bing-Wen

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference19 articles.

1. Genes and parkinsonism;Hardy;Lancet Neurol,2003

2. Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese;Gwinn-Hardy;Neurology,2000

3. Spinocerebellar ataxia type 2 presenting as familial levodopa-responsive parkinsonism;Shan;Ann Neurol,2001

4. Dopa-responsive parkinsonism phenotype of spinocerebellar ataxia type 2;Lu;Mov Disord,2002

5. The parkinsonian phenotype of spinocerebellar ataxia type 2;Lu;Arch Neurol,2004

Cited by 29 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetic Movement Disorders Commonly Seen in Asians;Movement Disorders Clinical Practice;2023-05-08

2. Detection of ATXN2 Expansions in an Exome Dataset: An Underdiagnosed Cause of Parkinsonism;Movement Disorders Clinical Practice;2023-03-07

3. Spinocerebellar Ataxia Type 2: A Family Re-port;Advances in Clinical Medicine;2023

4. Unraveling movement disorders in spinocerebellar ataxia;Annals of Movement Disorders;2022-05

5. Spinocerebellar ataxia type 2 from an evolutionary perspective: Systematic review and meta‐analysis;Clinical Genetics;2021-05-27

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