(Q42503095)

1 November 2017

title

An approach to the patient with late-onset cerebellar ataxia (English)

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1 November 2017

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Brent L Fogel

1

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1 November 2017

Susan Perlman

series ordinal

2

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1 November 2017

publication date

1 November 2006

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Nature Clinical Practice Neurology

1 November 2017

published in

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1 November 2017

volume

2

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1 November 2017

issue

11

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1 November 2017

page(s)

629-35; quiz 1 p following 635

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Clinical feature profile of spinocerebellar ataxia type 1-8 predicts genetically defined subtypes.

1 November 2017

cites work

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https://api.crossref.org/works/10.1038%2FNCPNEURO0319

Late-onset pure cerebellar ataxia: differentiating those with and without identifiable mutations

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

21 January 2018

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Recent advances in hereditary spinocerebellar ataxias

21 January 2018

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

21 January 2018

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Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes

21 January 2018

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Symptomatic and disease-modifying therapy for the progressive ataxias

21 January 2018

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The wide spectrum of spinocerebellar ataxias (SCAs)

21 January 2018

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An overview of the patient with ataxia

21 January 2018

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The complex clinical and genetic classification of inherited ataxias. II. Autosomal recessive ataxias

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Late-onset Friedreich ataxia: phenotypic analysis, magnetic resonance imaging findings, and review of the literature

21 January 2018

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Late-onset Tay-Sachs disease: phenotypic characterization and genotypic correlations in 21 affected patients.

21 January 2018

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Initial diagnoses given to persons with the fragile X associated tremor/ataxia syndrome (FXTAS).

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Multiple system atrophy

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Phenotypic variability in human prion diseases.

21 January 2018

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The aetiology of sporadic adult-onset ataxia

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RNAi suppresses polyglutamine-induced neurodegeneration in a model of spinocerebellar ataxia.

21 January 2018

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A clinical and genetic study in a large cohort of patients with spinocerebellar ataxia type 6

21 January 2018

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inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NCPNEURO0319

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1 November 2017

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