(Q51734072)

English

FXTAS in spanish patients with ataxia: support for female FMR1 premutation screening.

scientific article published in June 2007

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17917121

FXTAS in spanish patients with ataxia: support for female FMR1 premutation screening. (English)

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17917121

6

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17917121

Dolores Jimenez

object named as

Dolores Jiménez

4

0 references

Montserrat Milà

object named as

Montserrat Milà

9

0 references

author name string

Laia Rodriguez-Revenga

1

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17917121

Beatriz Gómez-Anson

2

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17917121

Esteban Muñoz

3

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17917121

Monica Santos

5

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17917121

Gisela Martín

7

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17917121

Luis Brieva

8

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17917121

publication date

1 June 2007

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17917121

Molecular Neurobiology

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17917121

35

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17917121

3

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17917121

324-328

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17917121

https://scigraph.springernature.com/pub.10.1007/s12035-007-0020-3

0 references

FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia.

1 reference

https://api.crossref.org/works/10.1007%2FS12035-007-0020-3

21 January 2018

FXTAS, SCA10, and SCA17 in American patients with movement disorders.

1 reference

https://api.crossref.org/works/10.1007%2FS12035-007-0020-3

21 January 2018

The fragile-X premutation: a maturing perspective

1 reference

https://pubmed.ncbi.nlm.nih.gov/17917121

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17917121

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myotonic syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17917121

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence of expression of the FMR-1 gene in fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17917121

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17917121

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/17917121

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/17917121

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

1 reference

https://pubmed.ncbi.nlm.nih.gov/17917121

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Should we screen for FMR1 premutations in female subjects presenting with ataxia?

1 reference

https://pubmed.ncbi.nlm.nih.gov/17917121

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17917121

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incidence of fragile X in 5,000 consecutive newborn males.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17917121

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/17917121

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/17917121

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for FMR-1 premutations in 122 older Flemish males presenting with ataxia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17917121

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Noninvasive test for fragile X syndrome, using hair root analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17917121

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/17917121

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S12035-007-0020-3

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17917121

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17917121

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