(Q45300182)

11 December 2017

Molecular diagnosis of Huntington disease in Brazilian patients (English)

1 reference

11 December 2017

0 references

4

1 reference

11 December 2017

T C Lima E Silva

1

1 reference

PubMed ID

10770860

11 December 2017

H G Serra

series ordinal

2

1 reference

PubMed ID

10770860

11 December 2017

C S Bertuzzo

series ordinal

3

1 reference

11 December 2017

1 March 2000

1 reference

Arquivos de Neuro-Psiquiatria

11 December 2017

1 reference

11 December 2017

58

1 reference

11 December 2017

1

1 reference

11 December 2017

11-17

1 reference

Huntington's disease. Pathogenesis and management

11 December 2017

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

A polymorphic DNA marker genetically linked to Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

Dynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

Expansion of the (CAG)n repeat causing Huntington's disease in 352 patients of German origin

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

Analysis of the trinucleotide repeat expansion in Italian families affected with Huntington disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

A study of the Huntington's disease associated trinucleotide repeat in the Scottish population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

Widespread expression of Huntington's disease gene (IT15) protein product

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

When more is less: pathogenesis of glutamine repeat neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

The CAG/polyglutamine tract diseases: gene products and molecular pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

Ectopically expressed CAG repeats cause intranuclear inclusions and a progressive late onset neurological phenotype in the mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

Site of (CCG) polymorphism in the HD gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

Instability of CAG repeats in Huntington's disease: relation to parental transmission and age of onset

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

De novo expansion of a (CAG)n repeat in sporadic Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

Mutation analysis in patients with possible but apparently sporadic Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

Diagnosis of "sporadic" Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

Trinucleotide repeat length instability and age of onset in Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

Ethical issues policy statement on Huntington's disease molecular genetics predictive test. International Huntington Association. World Federation of Neurology

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

Guidelines for the molecular genetics predictive test in Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

The expanding world of ataxins

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

Laboratory Guidelines for Huntington Disease Genetic Testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2000000100002

10.1590/S0004-282X2000000100002

21 January 2018

Identifiers

DOI

1 reference

11 December 2017

1 reference

PubMed ID

10770860