Natural History of Spinocerebellar Ataxia Type 31: a 4-Year Prospective Study-Reference-Cited by-同舟云学术

Natural History of Spinocerebellar Ataxia Type 31: a 4-Year Prospective Study

Published:2016-11-09 Issue:2 Volume:16 Page:518-524
ISSN:1473-4222
Container-title:The Cerebellum
language:en
Short-container-title:Cerebellum

Author:

Nakamura Katsuya,Yoshida Kunihiro,Matsushima Akira,Shimizu Yusaku,Sato Shunichi,Yahikozawa Hiroyuki,Ohara Shinji,Yazawa Masanobu,Ushiyama Masao,Sato Mitsuto,Morita Hiroshi,Inoue Atsushi,Ikeda Shu-ichi

Funder

The Ministry of Health, Labor, and Welfare, Japan

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,Neurology

Link

http://link.springer.com/content/pdf/10.1007/s12311-016-0833-6.pdf

Reference32 articles.

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2. Onodera Y, Aoki M, Mizuno H, Warita H, Shiga Y, Itoyama Y. Clinical features of chromosome 16q22.1 linked autosomal dominant cerebellar ataxia in Japanese. Neurology. 2006;67:1300–2.

3. Nozaki H, Ikeuchi T, Kawakami A, Kimura A, Koide R, Tsuchiya M, et al. Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese population. Mov Disord. 2007;22:857–62.

4. Basri R, Yabe I, Soma H, Sasaki H. Spectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan: a study of 113 Japanese families. J Hum Genet. 2007;52:848–55.

5. Hayashi M, Adachi Y, Mori M, Nakano T, Nakashima K. Clinical and genetic epidemiological study of 16q22.1-linked autosomal dominant cerebellar ataxia in western Japan. Acta Neurol Scand. 2007;116:123–7.

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