(Q51934788)

English

FMR1 premutation as a rare cause of late onset ataxia--evidence for FXTAS in female carriers.

scientific article published in November 2004

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scholarly article

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15592745

FMR1 premutation as a rare cause of late onset ataxia--evidence for FXTAS in female carriers. (English)

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15592745

author name string

Ch Zühlke

1

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15592745

A Budnik

2

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15592745

U Gehlken

3

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15592745

A Dalski

4

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15592745

S Purmann

5

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15592745

M Naumann

6

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15592745

M Schmidt

7

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15592745

K Bürk

8

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15592745

E Schwinger

9

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15592745

publication date

1 November 2004

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15592745

Journal of Neurology

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15592745

251

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15592745

11

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15592745

1418-1419

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15592745

https://scigraph.springernature.com/pub.10.1007/s00415-004-0558-1

0 references

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/15592745

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The fragile X premutation: into the phenotypic fold

1 reference

https://pubmed.ncbi.nlm.nih.gov/15592745

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/15592745

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/15592745

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/15592745

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/15592745

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X premutation carriers: characteristic MR imaging findings of adult male patients with progressive cerebellar and cognitive dysfunction.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15592745

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Observation of an excess of fragile-X premutations in a population of males referred with spinocerebellar ataxia

1 reference

https://pubmed.ncbi.nlm.nih.gov/15592745

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/15592745

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00415-004-0558-1

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15592745

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15592745

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