Clinical characteristics of combined cases of spinocerebellar ataxia types 6 and 31.

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Clinical characteristics of combined cases of spinocerebellar ataxia types 6 and 31.

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2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

@zh-my

2015年学术文章

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2015年學術文章

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2015年學術文章

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2015年學術文章

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Clinical characteristics of combined cases of spinocerebellar ataxia types 6 and 31.

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Clinical characteristics of combined cases of spinocerebellar ataxia types 6 and 31.

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Clinical characteristics of combined cases of spinocerebellar ataxia types 6 and 31.

@en

Clinical characteristics of combined cases of spinocerebellar ataxia types 6 and 31.

@nl

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Clinical characteristics of combined cases of spinocerebellar ataxia types 6 and 31.

@en

Clinical characteristics of combined cases of spinocerebellar ataxia types 6 and 31.

@nl

P1476

Clinical characteristics of combined cases of spinocerebellar ataxia types 6 and 31.

@en

P2093

Akio Hara

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Hidehiro Mizusawa

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Hiroyuki Ohmori

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Kinya Ishikawa

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P2860

Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1

Abundant expression and cytoplasmic aggregations of [alpha]1A voltage-dependent calcium channel protein associated with neurodegeneration in spinocerebellar ataxia type 6

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

The carboxy-terminal fragment of alpha(1A) calcium channel preferentially aggregates in the cytoplasm of human spinocerebellar ataxia type 6 Purkinje cells.

The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.

Autosomal dominant cerebellar ataxia type III: a review of the phenotypic and genotypic characteristics.

A 3-year cohort study of the natural history of spinocerebellar ataxia type 6 in Japan.

Scale for the assessment and rating of ataxia: development of a new clinical scale.

The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study.

P304

80-84

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P31

scholarly article

P356

10.3109/01677063.2015.1054992

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P433

2-3

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P478

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P50

Yukio Ando

P577

2015-05-25T00:00:00Z

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P698

26004545

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