(Q37199782)

18 August 2017

Parkinsonism in FMR1 premutation carriers may be indistinguishable from Parkinson disease (English)

1 reference

18 August 2017

1 reference

parkinsonian syndrome

1 reference

1

Hall DA

1 reference

18 August 2017

2

Howard K

1 reference

18 August 2017

3

Hagerman R

1 reference

18 August 2017

4

Leehey MA

1 reference

18 August 2017

PMC publication ID

2685192

language of work or name

English

0 references

publication date

20 June 2008

1 reference

Parkinsonism and Related Disorders

18 August 2017

4

1 reference

based on heuristic

inferred from page(s)

published in

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18 August 2017

15

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18 August 2017

2

1 reference

18 August 2017

156-159

1 reference

FMR1 CGG repeat length predicts motor dysfunction in premutation carriers.

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2685192

Prevalence of FMR1 repeat expansions in movement disorders. A systematic review

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2685192

Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2685192

Diagnostic criteria for Parkinson disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2685192

Screen for excess FMR1 premutation alleles among males with parkinsonism

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2685192

CGG repeat length correlates with age of onset of motor signs of the fragile X-associated tremor/ataxia syndrome (FXTAS).

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2685192

Parkinsonism, dysautonomia, and intranuclear inclusions in a fragile X carrier: a clinical-pathological study.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2685192

Premutations in the FMR1 gene as a modifying factor in Parkin-associated Parkinson's disease?

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2685192

Evidence for, and a spectrum of, neurological involvement in carriers of the fragile X pre-mutation: FXTAS and beyond.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2685192

Premutation alleles associated with Parkinson disease and essential tremor.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2685192

Parkinsonism, FXTAS, and FMR1 premutations

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2685192

Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2685192

10.1016/J.PARKRELDIS.2008.04.037

3 September 2018

Identifiers

DOI

1 reference

18 August 2017

1 reference

PMC publication ID

2685192

18 August 2017

PubMed publication ID

18565783

1 reference

PMC publication ID

2685192