(Q48918586)

16 February 2018

title

Predisposition to epilepsy in fragile X syndrome: does the Val66Met polymorphism in the BDNF gene play a role? (English)

1 reference

16 February 2018

1 reference

Mireia Tondo

1

1 reference

16 February 2018

Pilar Poo

2

1 reference

16 February 2018

Montserrat Naudó

3

1 reference

16 February 2018

Teresa Ferrando

4

1 reference

16 February 2018

Jordi Genovés

5

1 reference

16 February 2018

Marta Molero

6

1 reference

16 February 2018

Loreto Martorell

7

1 reference

16 February 2018

publication date

3 September 2011

1 reference

16 February 2018

published in

Epilepsy Behavior

1 reference

16 February 2018

volume

22

1 reference

16 February 2018

issue

3

1 reference

16 February 2018

page(s)

581-583

1 reference

16 February 2018

The Fragile X premutation: new insights and clinical consequences

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.08.003

Partial seizures with focal epileptogenic electroencephalographic patterns in three related female patients with fragile-X syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.08.003

Epilepsy and EEG findings in 18 males with fragile X syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.08.003

The Val66Met polymorphism in the BDNF gene is associated with epilepsy in fragile X syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.08.003

Brain-derived neurotrophic factor Val66Met and psychiatric disorders: meta-analysis of case-control studies confirm association to substance-related disorders, eating disorders, and schizophrenia.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.08.003

Impact of genetic variant BDNF (Val66Met) on brain structure and function

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.08.003

The p.Val66Met polymorphism in the BDNF gene protects against early seizures in Rett syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.08.003

The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.08.003

A simple salting out procedure for extracting DNA from human nucleated cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.08.003

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.08.003

Autoimmune disease in mothers with the FMR1 premutation is associated with seizures in their children with fragile X syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.08.003

10.1016/J.YEBEH.2011.08.003

7 January 2021

Identifiers

DOI

1 reference

16 February 2018

1 reference

16 February 2018