(Q34400405)

1 August 2017

title

Spinocerebellar ataxia type 10: Frequency of epilepsy in a large sample of Brazilian patients (English)

1 reference

spinocerebellar ataxia type 10

1 August 2017

main subject

1 reference

6

Lineu C Werneck

1 reference

1 August 2017

1

Hélio A G Teive

1 reference

1 August 2017

2

Renato P Munhoz

1 reference

1 August 2017

Salmo Raskin

3

1 reference

1 August 2017

Walter O Arruda

series ordinal

4

1 reference

1 August 2017

Luciano de Paola

series ordinal

5

1 reference

1 August 2017

Tetsuo Ashizawa

series ordinal

7

1 reference

1 August 2017

language of work or name

English

0 references

publication date

1 December 2010

1 reference

1 August 2017

1 reference

1 August 2017

volume

25

1 reference

1 August 2017

issue

16

1 reference

1 August 2017

page(s)

2875-2878

1 reference

The descriptive epidemiology of epilepsy-a review

1 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3000879

Ancestral origin of the ATTCT repeat expansion in spinocerebellar ataxia type 10 (SCA10)

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3000879

The global burden and stigma of epilepsy

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3000879

Interruptions in the expanded ATTCT repeat of spinocerebellar ataxia type 10: repeat purity as a disease modifier?

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3000879

Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3000879

Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3000879

Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3000879

Clinical phenotype of Brazilian families with spinocerebellar ataxia 10.

6 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FMDS.23324

Spinocerebellar ataxia type 10 is rare in populations other than Mexicans

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FMDS.23324

Ethnic origin and extrapyramidal signs in an Argentinean spinocerebellar ataxia type 10 family

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3000879

Reduced penetrance in a Brazilian family with spinocerebellar ataxia type 10

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3000879

Clinical features and ATTCT repeat expansion in spinocerebellar ataxia type 10.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3000879

Clinical and genetic analysis of four Mexican families with spinocerebellar ataxia type 10.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3000879

Mapping of the gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsy

27 October 2018

1 reference

12 December 2020

Demonstration Project on Epilepsy in Brazil: situation assessment

1 reference

12 December 2020

The history of spinocerebellar ataxia type 10 in Brazil: travels of a gene

1 reference

12 December 2020

The ATTCT repeats of spinocerebellar ataxia type 10 display strong nucleosome assembly which is enhanced by repeat interruptions

1 reference

12 December 2020

Identifiers

DOI

10.1002/MDS.23324

1 reference

1 August 2017

1 reference

1 August 2017

1 reference