(Q43910526)

28 November 2017

title

Autosomal dominant cerebellar ataxias in ethnic Bengalees in West Bengal - an Eastern Indian state (English)

1 reference

28 November 2017

1 reference

A Chakravarty

1

1 reference

28 November 2017

S C Mukherjee

series ordinal

2

1 reference

28 November 2017

language of work or name

English

0 references

publication date

1 March 2002

1 reference

Acta Neurologica Scandinavica

28 November 2017

published in

1 reference

28 November 2017

volume

105

1 reference

28 November 2017

issue

3

1 reference

28 November 2017

page(s)

202-208

1 reference

A new form of heredo-familial spinocerebellar degeneration with slow eye movements (nine families)

28 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.1O054.X

A clinicogenetic analysis of six Indian spinocerebellar ataxia (SCA2) pedigrees. The significance of slow saccades in diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.1O054.X

Eight families with Joseph's disease in India

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.1O054.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.1O054.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/10.1034%2FJ.1600-0404.2002.1O054.X

Spinocerebellar ataxia type 2 in seven Korean families: CAG trinucleotide expansion and clinical characteristics

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.1O054.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/10.1034%2FJ.1600-0404.2002.1O054.X

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/10.1034%2FJ.1600-0404.2002.1O054.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.1O054.X

Cognitive deficits in spinocerebellar ataxia 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.1O054.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/10.1034%2FJ.1600-0404.2002.1O054.X

Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.1O054.X

Spinocerebellar ataxia type 1 in Russia

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.1O054.X

A common disease haplotype segregating in spinocerebellar ataxia 2 (SCA2) pedigrees of diverse ethnic origin

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.1O054.X

7 January 2021

Machado-Joseph-Azorean disease in India

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.1O054.X

7 January 2021

Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2 and SCA6 loci in nine ethnic populations of eastern India

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.1O054.X

7 January 2021

Autosomal dominant cerebellar ataxias in the Kinki area of Japan

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.1O054.X

7 January 2021

Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.1O054.X

7 January 2021

Prevalence of triplet repeat expansion in ataxia patients from Hokkaido, the northernmost island of Japan

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.1O054.X

7 January 2021

10.1034/J.1600-0404.2002.1O054.X

Identifiers

DOI

1 reference

28 November 2017

1 reference