(Q46474252)

22 December 2017

title

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

1 reference

22 December 2017

author name string

Infante J

1

1 reference

22 December 2017

Combarros O

2

1 reference

22 December 2017

Volpini V

3

1 reference

22 December 2017

Corral J

4

1 reference

22 December 2017

Llorca J

5

1 reference

22 December 2017

Berciano J

6

1 reference

22 December 2017

language of work or name

English

0 references

publication date

1 June 2005

1 reference

22 December 2017

Acta Neurologica Scandinavica

published in

1 reference

22 December 2017

volume

111

1 reference

22 December 2017

issue

6

1 reference

22 December 2017

page(s)

391-399

1 reference

22 December 2017

CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia.

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00400.X

Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00400.X

The natural history of degenerative ataxia: a retrospective study in 466 patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00400.X

Regional differences in genetic subgroup frequency in hereditary cerebellar ataxia, and a morphometrical study of brain MR images in SCA1, MJD and SCA6.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00400.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00400.X

Analysis of SCA1, DRPLA, MJD, SCA2, and SCA6 CAG repeats in 48 Portuguese ataxia families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00400.X

Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00400.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00400.X

Genetic testing in spinocerebellar ataxias: defining a clinical role

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00400.X

The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00400.X

Transmission distortion of the mutant alleles in spinocerebellar ataxia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00400.X

Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00400.X

Molecular and clinical study of 18 families with ADCA type II: evidence for genetic heterogeneity and de novo mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00400.X

Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00400.X

Neurologic findings in Machado-Joseph disease: relation with disease duration, subtypes, and (CAG)n

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00400.X

Clinical, neuropathologic, and genetic studies of a large spinocerebellar ataxia type 1 (SCA1) kindred

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00400.X

10.1111/J.1600-0404.2005.00400.X

21 January 2018

Identifiers

DOI

1 reference

22 December 2017

PubMed ID

15876341

1 reference

22 December 2017