(Q50434198)

13 March 2018

title

Comparisons of acoustic function in SCA31 and other forms of ataxias. (English)

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13 March 2018

author name string

Yoshio Ikeda

1

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13 March 2018

Makiko Nagai

2

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13 March 2018

Tomoko Kurata

3

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13 March 2018

Toru Yamashita

4

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13 March 2018

Yasuyuki Ohta

5

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13 March 2018

Shoko Nagotani

6

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13 March 2018

Kentaro Deguchi

7

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13 March 2018

Yasushi Takehisa

8

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13 March 2018

Yoshihiko Shiro

9

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13 March 2018

Tohru Matsuura

10

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13 March 2018

Koji Abe

11

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13 March 2018

publication date

1 May 2011

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13 March 2018

published in

Neurological Research

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13 March 2018

volume

33

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13 March 2018

issue

4

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13 March 2018

page(s)

427-432

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13 March 2018

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis

cites work

1 reference

https://api.crossref.org/works/10.1179%2F1743132810Y.0000000011

Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)n

21 January 2018

1 reference

https://api.crossref.org/works/10.1179%2F1743132810Y.0000000011

A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III.

21 January 2018

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https://api.crossref.org/works/10.1179%2F1743132810Y.0000000011

Second consensus statement on the diagnosis of multiple system atrophy

21 January 2018

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https://api.crossref.org/works/10.1179%2F1743132810Y.0000000011

Sporadic adult onset ataxia of unknown etiology : a clinical, electrophysiological and imaging study

21 January 2018

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https://api.crossref.org/works/10.1179%2F1743132810Y.0000000011

Spinocerebellar ataxia type 8: molecular genetic comparisons and haplotype analysis of 37 families with ataxia

21 January 2018

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https://api.crossref.org/works/10.1179%2F1743132810Y.0000000011

Hearing impairment and health-related quality of life: the Blue Mountains Hearing Study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1179%2F1743132810Y.0000000011

Severity and progression rate of cerebellar ataxia in 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA) in the endemic Nagano Area of Japan.

21 January 2018

1 reference

https://api.crossref.org/works/10.1179%2F1743132810Y.0000000011

16q-linked autosomal dominant cerebellar ataxia: a clinical and genetic study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1179%2F1743132810Y.0000000011

Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese population.

21 January 2018

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https://api.crossref.org/works/10.1179%2F1743132810Y.0000000011

Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1179%2F1743132810Y.0000000011

The (-16C > T) substitution in the PLEKHG4 gene is not present among European ADCA patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1179%2F1743132810Y.0000000011

16q-linked autosomal dominant cerebellar ataxia in a Korean family.

21 January 2018

1 reference

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10.1179/1743132810Y.0000000011

21 January 2018

Identifiers

DOI

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13 March 2018

PubMed ID

21535943

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13 March 2018