11 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 33058338 | A Novel Duplication in ATXN2 as Modifier for Spinocerebellar Ataxia 3 (SCA3) and C9ORF72-ALS. | 2021 Feb | 2 |
2 | 32340607 | Late-onset oro-facial dyskinesia in Spinocerebellar Ataxia type 2: a case report. | 2020 Apr 27 | 3 |
3 | 30120431 | Repeat length variations in polyglutamine disease-associated genes affect body mass index. | 2019 Mar | 1 |
4 | 29427106 | The Neuropathology of Spinocerebellar Ataxia Type 3/Machado-Joseph Disease. | 2018 | 1 |
5 | 29756284 | Factors associated with ATXN2 CAG/CAA repeat intergenerational instability in Spinocerebellar ataxia type 2. | 2018 Oct | 3 |
6 | 26095883 | Motor neurone disease/amyotrophic lateral sclerosis associated with intermediate-length CAG repeat expansions in Ataxin-2 does not have 1C2-positive polyglutamine inclusions. | 2016 Jun | 2 |
7 | 22037902 | Epigenetics DNA methylation in the core ataxin-2 gene promoter: novel physiological and pathological implications. | 2012 Apr | 4 |
8 | 21399888 | A comprehensive review of spinocerebellar ataxia type 2 in Cuba. | 2011 Jun | 2 |
9 | 11396263 | [Autosomal dominant cerebellar ataxias in the Netherlands: a national inventory]. | 2001 May 19 | 1 |
10 | 10210910 | Clinical and molecular analysis of 11 Sicilian SCA2 families: influence of gender on age at onset. | 1999 May | 2 |
11 | 9630233 | The hereditary ataxias. | 1998 Jun | 1 |