The Initial Symptom and Motor Progression in Spinocerebellar Ataxias-Reference-Cited by-同舟云学术

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The Initial Symptom and Motor Progression in Spinocerebellar Ataxias

Published:2016-11-15 Issue:3 Volume:16 Page:615-622
ISSN:1473-4222
Container-title:The Cerebellum
language:en
Short-container-title:Cerebellum

Author:

Luo Lan,Wang Jie,Lo Raymond Y,Figueroa Karla P,Pulst Stefan M,Kuo Pei-Hsin,Perlman Susan,Wilmot George,Gomez Christopher M,Schmahmann Jeremy D.,Paulson Henry,Shakkottai Vikram G,Ying Sarah H,Zesiewicz Theresa,Bushara Khalaf,Geschwind Michael,Xia Guangbin,Subramony S H,Ashizawa Tetsuo,Kuo Sheng-Han

Funder

National Institute of Neurological Disorders and Stroke

Louis V. Gerstner Jr. Scholarship

Parkinson’s Disease Foundation

Rare Disease Clinical Research Network

Government of Jiangsu Province

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

Link

http://link.springer.com/content/pdf/10.1007/s12311-016-0836-3.pdf

Reference25 articles.

1. Durr A. Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond. Lancet Neurol. 2010;9:885–94.

2. Lo RY, Figueroa KP, Pulst SM, Perlman S, Wilmot G, Gomez C, et al. Depression and clinical progression in spinocerebellar ataxia. Parkinsonism Relat Disord. 2016;22:87–92.

3. Orr HT, Chung MY, Banfi S, Kwiatkowski TJ, Servadio A, Beaudet AL, et al. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nat Genet. 1993;4:221–6.

4. Schöls L, Amoiridis G, Büttner T, Przuntek H, Epplen JT, Riess O, et al. Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes? Ann Neurol. 1997;42:924–32.

5. Stevanin G, Durr A, Brice A. Clinical and molecular advances in autosomal dominant cerebellar ataxias: from genotype to phenotype and physiopathology. Eur J Hum Genet. 2000;8:4–18.

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