(Q51934789)

English

No association between FMR1 premutations and multiple system atrophy.

scientific article published in November 2004

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15592742

No association between FMR1 premutations and multiple system atrophy. (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15592742

author name string

Ichiro Yabe

1

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15592742

Hiroyuki Soma

2

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15592742

Asako Takei

3

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15592742

Naoto Fujik

4

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15592742

Hidenao Sasaki

5

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15592742

publication date

1 November 2004

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15592742

Journal of Neurology

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15592742

251

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15592742

11

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15592742

1411-1412

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15592742

https://scigraph.springernature.com/pub.10.1007/s00415-004-0546-5

0 references

Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy-Drager syndrome).

1 reference

https://pubmed.ncbi.nlm.nih.gov/15592742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotypic involvement in females with the FMR1 gene mutation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15592742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15592742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

1 reference

https://pubmed.ncbi.nlm.nih.gov/15592742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15592742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The fragile X premutation presenting as essential tremor

1 reference

https://pubmed.ncbi.nlm.nih.gov/15592742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Data on the CGG repeat at the fragile X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutate

1 reference

https://pubmed.ncbi.nlm.nih.gov/15592742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glial cytoplasmic inclusions in white matter oligodendrocytes of multiple system atrophy brains contain insoluble alpha-synuclein.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15592742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates

1 reference

https://pubmed.ncbi.nlm.nih.gov/15592742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Consensus statement on the diagnosis of multiple system atrophy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15592742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spinocerebellar degenerations in Japan: a nationwide epidemiological and clinical study

1 reference

https://pubmed.ncbi.nlm.nih.gov/15592742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Learning-disabled males with a fragile X CGG expansion in the upper premutation size range.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15592742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15592742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00415-004-0546-5

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15592742

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/15592742

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