The aetiology of sporadic adult-onset ataxia (Q44858419)

6 December 2017

title

The aetiology of sporadic adult-onset ataxia (English)

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6 December 2017

Abele M

1

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6 December 2017

Bürk K

2

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6 December 2017

Schöls L

3

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6 December 2017

Schwartz S

4

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6 December 2017

Besenthal I

5

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6 December 2017

Dichgans J

6

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6 December 2017

Zühlke C

7

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6 December 2017

Riess O

8

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6 December 2017

Klockgether T

9

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6 December 2017

language of work or name

English

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publication date

1 May 2002

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6 December 2017

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6 December 2017

volume

125

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6 December 2017

issue

Pt 5

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6 December 2017

page(s)

961-968

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Recessive ataxia with ocular apraxia: review of 22 Portuguese patients

6 December 2017

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An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)

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The distribution of oligodendroglial inclusions in multiple system atrophy and its relevance to clinical symptomatology

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SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel gene

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Trinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patients

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Different types of repeat expansion in the TATA-binding protein gene are associated with a new form of inherited ataxia

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Autosomal recessive spastic ataxia of Charlevoix–Saguenay

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Identifiers

DOI

10.1093/BRAIN/AWF107

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6 December 2017

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