(Q33425580)

26 July 2017

Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study (English)

1 reference

26 July 2017

1 reference

Jeanette Koht

2

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author name string

Anne Kjersti Erichsen

1

1 reference

26 July 2017

Asbjørg Stray-Pedersen

3

1 reference

26 July 2017

Michael Abdelnoor

4

1 reference

26 July 2017

Chantal M E Tallaksen

5

1 reference

26 July 2017

language of work or name

English

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publication date

31 March 2009

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26 July 2017

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26 July 2017

132

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26 July 2017

Pt 6

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26 July 2017

1577-1588

1 reference

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

26 July 2017

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Dominant ataxias and Friedreich ataxia: an update

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Survival probability in ataxia telangiectasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Frequency analysis and clinical characterization of different types of spinocerebellar ataxia in Serbian patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Clinical features and molecular genetics of autosomal recessive cerebellar ataxias

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Autosomal dominant cerebellar ataxias in Spain: molecular and clinical correlations, prevalence estimation and survival analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Characterization of ATM mutations in 41 Nordic families with ataxia telangiectasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Population genetics of wild-type CAG repeats in the Machado-Joseph disease gene in Portugal

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Friedreich's ataxia: an epidemiological study in Valencia, Spain, based on consanguinity analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

The prevalence of "pure" autosomal dominant hereditary spastic paraparesis in the island of Ireland.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Population based study of late onset cerebellar ataxia in south east Wales.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Hereditary ataxias and paraplegias in Cantabria, Spain. An epidemiological and clinical study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Hereditary ataxias and spastic paraplegias: methodological aspects of a prevalence study in Portugal.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Spinocerebellar ataxias: an update

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Prevalence and pattern of spinocerebellar degenerations in northeastern Libya

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Alpha fetoprotein is increasing with age in ataxia-telangiectasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

The impact of an early truncating founder ATM mutation on immunoglobulins, specific antibodies and lymphocyte populations in ataxia-telangiectasia patients and their parents

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Recent advances in hereditary spastic paraplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Recent advances in hereditary spinocerebellar ataxias

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP056

21 January 2018

Identifiers

DOI

10.1093/BRAIN/AWP056

1 reference

26 July 2017

1 reference