Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locus (Q48744758)

15 February 2018

title

Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locus (English)

1 reference

15 February 2018

autosomal dominant cerebellar ataxia type I

main subject

0 references

1 reference

15 February 2018

Yvon Trottier

object named as

Y Trottier

0 references

Geraldine Cancel-Tassin

G Cancel

0 references

K Bürk

1 reference

15 February 2018

O Didierjean

1 reference

15 February 2018

M Skalej

1 reference

15 February 2018

M Abele

1 reference

15 February 2018

A Brice

1 reference

15 February 2018

J Dichgans

1 reference

15 February 2018

T Klockgether

1 reference

15 February 2018

publication date

1 April 1997

1 reference

15 February 2018

published in

Journal of Neurology

1 reference

15 February 2018

volume

244

1 reference

15 February 2018

issue

1 reference

15 February 2018

page(s)

256-261

1 reference

15 February 2018

Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

Oculomotor abnormalities and MRI findings in idiopathic cerebellar ataxia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

Has spinocerebellar ataxia type 2 a distinct phenotype? Genetic and clinical study of an Italian family.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

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'.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

A genetic linkage map of human chromosome 20 composed entirely of microsatellite markers

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

Idiopathic cerebellar ataxia of late onset: natural history and MRI morphology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

Dominantly inherited olivopontocerebellar atrophy from eastern Cuba. Clinical, neuropathological, and biochemical findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

Autosomal dominant cerebellar ataxia: clinical analysis of 263 patients from a homogeneous population in Holguín, Cuba

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

Magnetic resonance imaging in hereditary and idiopathic ataxia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

HIV or zidovudine myopathy?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

Clinical criteria for diagnosis of Machado-Joseph disease: report of a non-Azorena Portuguese family

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050081

Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): genetic analysis of three unrelated SCA2 families

21 January 2018

1 reference

12 December 2020

Localization of the candidate gene D-amino acid oxidase outside the refined I-cM region of spinocerebellar ataxia 2.

1 reference

12 December 2020

Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate region

1 reference

12 December 2020

Clinical and imaging correlations in inherited ataxias.

1 reference

12 December 2020

Autosomal dominant cerebellar ataxia type I linked to chromosome 12q (SCA2: spinocerebellar ataxia type 2).

1 reference

12 December 2020

Identifiers

DOI

10.1007/S004150050081

1 reference

15 February 2018

1 reference

15 February 2018