Stratification of disease progression in a broad spectrum of degenerative cerebellar ataxias with a clustering method using MRI-based atrophy rates of brain structures-Reference-Cited by-同舟云学术

Stratification of disease progression in a broad spectrum of degenerative cerebellar ataxias with a clustering method using MRI-based atrophy rates of brain structures

Published:2017-06-29 Issue:1 Volume:4 Page:
ISSN:2053-8871
Container-title:Cerebellum & Ataxias
language:en
Short-container-title:cerebellum ataxias

Author:

Sasaki Rie,Maki Futaba,Hara Daisuke,Tanaka Shigeaki,Hasegawa Yasuhiro

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology

Link

http://link.springer.com/content/pdf/10.1186/s40673-017-0068-4.pdf

Reference35 articles.

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2. Kawaguchi Y, Okamoto T, Taniwaki M, Aizawa M, Inoue M, Katayama S, et al. CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1. Nat Genet. 1994;8:221–8.

3. Paulson HL. The spinocerebellar ataxias. J Neuroophthalmol. 2009;29:227–37.

4. Riess O, Schols L, Bottger H, Nolte D, Vieira-Saecker AM, Schimming C, et al. SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel gene. Hum Mol Genet. 1997;6:1289–93.

5. Schols L, Bauer P, Schmidt T, Schulte T, Riess O. Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis. Lancet Neurol. 2004;3:291–304.

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