Parkinsonism in spinocerebellar ataxia (Q28080641)

language of work or name

1 reference

2015

1 reference

BioMed Research International

19 March 2015

4 references

22 April 2019

25 April 2019

7 August 2019

29 May 2020

5 references

22 April 2019

25 April 2019

7 August 2019

29 May 2020

2015

1 reference

page(s)

125273

1 reference

Creative Commons Attribution 3.0 Unported

copyright license

4 references

22 April 2019

25 April 2019

7 August 2019

on focus list of Wikimedia project

29 May 2020

copyright status

copyrighted

0 references

ScienceSource

0 references

cites work

Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

The wide spectrum of spinocerebellar ataxias (SCAs)

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

Amyotrophic lateral sclerosis and spinocerebellar ataxia type 2 in a family with full CAG repeat expansions of ATXN2.

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

Severe and rapidly progressing cognitive phenotype in a SCA17-family with only marginally expanded CAG/CAA repeats in the TATA-box binding protein gene: a case report

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

Spinocerebellar ataxia type 2 is associated with Parkinsonism and Lewy body pathology

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

Brain pathology of spinocerebellar ataxias

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

ATXN8 -62 G/A promoter polymorphism and risk of Taiwanese Parkinson's disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

An autopsy case of an aged patient with spinocerebellar ataxia type 2.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

SCA8 repeat expansion: large CTA/CTG repeat alleles in neurological disorders and functional implications

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

Anatomically based guidelines for systematic investigation of the central somatosensory system and their application to a spinocerebellar ataxia type 2 (SCA2) patient

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

SCA2 and SCA3 mutations in young-onset dopa-responsive parkinsonism

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

Thalamic involvement in a spinocerebellar ataxia type 2 (SCA2) and a spinocerebellar ataxia type 3 (SCA3) patient, and its clinical relevance

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

SCA2 may present as levodopa-responsive parkinsonism

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

SCA8 repeat expansion: large CTA/CTG repeat alleles are more common in ataxic patients, including those with SCA6

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

Spinocerebellar ataxia type 3 phenotypically resembling parkinson disease in a black family

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

The wide clinical spectrum and nigrostriatal dopaminergic damage in spinocerebellar ataxia type 6.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington's disease-like phenotype.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

Role of SCA2 mutations in early- and late-onset dopa-responsive parkinsonism

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

Azorean disease of the nervous system.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

Dopa-responsive parkinsonism phenotype of Machado-Joseph disease: Confirmation of 14q CAG expansion

2 June 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

SCA-2 presenting as parkinsonism in an Alberta family: clinical, genetic, and PET findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

The parkinsonian phenotype of spinocerebellar ataxia type 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Presence of spinocerebellar ataxia type 2 gene mutation in a patient with apparently sporadic Parkinson's disease: clinical implications.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

SCA2 presenting as levodopa-responsive parkinsonism in a young patient from the United Kingdom: a case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Parkinsonism and nigrostriatal dysfunction are associated with spinocerebellar ataxia type 6 (SCA6).

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Dopamine transporter positron emission tomography in spinocerebellar ataxias type 1, 2, 3, and 6.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

The SCA17 phenotype can include features of MSA-C, PSP and cognitive impairment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Spinocerebellar ataxia type 17 mutation as a causative and susceptibility gene in parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

PET and MRI reveal early evidence of neurodegeneration in spinocerebellar ataxia type 17.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Prevalence of spinocerebellar ataxia type 2 mutation among Italian Parkinsonian patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: genetic, clinical, and positron emission tomography findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Importance of low-range CAG expansion and CAA interruption in SCA2 Parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Relative contribution of SCA2, SCA3 and SCA17 in Korean patients with parkinsonism and ataxia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Dopa-responsive parkinsonism phenotype of spinocerebellar ataxia type 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17).

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Case of spinocerebellar ataxia type 17 (SCA17) associated with only 41 repeats of the TATA-binding protein (TBP) gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Late onset ataxia: MSA-C or SCA 17? A gene penetrance dilemma

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Ethnic differences in the expression of neurodegenerative disease: Machado-Joseph disease in Africans and Caucasians

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Genetic analysis of SCA 2 and 3 repeat expansions in essential tremor and atypical Parkinsonism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Dopaminergic response in Parkinsonian phenotype of Machado-Joseph disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Spinocerebellar ataxia type 3 (SCA3): thalamic neurodegeneration occurs independently from thalamic ataxin-3 immunopositive neuronal intranuclear inclusions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Multiple system atrophy in a patient with the spinocerebellar ataxia 3 gene mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Frequency analysis and clinical characterization of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Korean patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

SCA6 presenting with young-onset parkinsonism without ataxia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Autosomal dominant cerebellar ataxia (SCA6): clinical, genetic and neuropathological study in a family.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Spinocerebellar ataxia type 8: clinical features in a large family.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Non-Ataxic Phenotypes of SCA8 Mimicking Amyotrophic Lateral Sclerosis and Parkinson Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Expanded ATXN2 CAG repeat size in ALS identifies genetic overlap between ALS and SCA2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Intergenerational instability and marked anticipation in SCA-17

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Behavioral Disorder, Dementia, Ataxia, and Rigidity in a Large Family With TATA Box-Binding Protein Mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Glucocerebrosidase gene variants in parkinsonian patients with Machado Joseph/spinocerebellar ataxia 3

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Are interruptedSCA2CAG repeat expansions responsible for parkinsonism?

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Mutation at the SCA17 locus is not a common cause of parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

Searching for mutation in the JPH3, ATN1 and TBP genes in Polish patients suspected of Huntington's disease and without mutation in the IT15 gene.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

SCA 1, SCA 2 & SCA 3/MJD mutations in ataxia syndromes in southern India.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

Molecular analysis of Spinocerebellar ataxias in Koreans: frequencies and reference ranges of SCA1, SCA2, SCA3, SCA6, and SCA7.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383270

Association of Long ATXN2 CAG Repeat Sizes With Increased Risk of Amyotrophic Lateral Sclerosis

27 November 2018

1 reference

https://api.crossref.org/works/10.1155%2F2015%2F125273

SCA2 trinucleotide expansion in German SCA patients

21 January 2018

1 reference

12 December 2020

[A case of spinocerebellar ataxia type 6 with hypochondriasis and severe parkinsonism]

1 reference

12 December 2020

[Autopsy case of SCA2 with Parkinsonian phenotype]

1 reference

12 December 2020

1 reference

12 December 2020

Identification of a novel 45 repeat unstable allele associated with a disease phenotype at the MJD1/SCA3 locus

1 reference

12 December 2020

CAG repeats containing CAA interruptions form branched hairpin structures in spinocerebellar ataxia type 2 transcripts

1 reference

12 December 2020

Spinocerebellar ataxia type 2 presenting as familial levodopa-responsive parkinsonism

1 reference

12 December 2020

Spinocerebellar ataxia type 2 with Levodopa-responsive parkinsonism culminating in motor neuron disease

1 reference

12 December 2020

[Neuropathological study of autosomal dominant ataxia linked to loci on chromosome 6p (SCA 1)]

1 reference

12 December 2020

The spinocerebellar ataxias

1 reference

12 December 2020

Genetic analysis of SCA2, 3 and 17 in idiopathic Parkinson's disease

1 reference

12 December 2020

Spinocerebellar ataxias

1 reference

12 December 2020

Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (ethnic Chinese) cohort of familial and early-onset parkinsonism

1 reference

12 December 2020

An interrupted 34-CAG repeat SCA-2 allele in patients with sporadic spinocerebellar ataxia

1 reference

12 December 2020

Identifiers

DOI

10.1155/2015/125273

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

553921

OpenCitations bibliographic resource ID

553921

1 reference