(Q48685551)

English

Mutation in filamin A causes periventricular heterotopia, developmental regression, and West syndrome in males

scientific article published in January 2006

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

Mutation in filamin A causes periventricular heterotopia, developmental regression, and West syndrome in males (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

developmental regression

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Christopher A. Walsh

14

object named as

Christopher Walsh

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

author name string

Marcelo R Masruha

1

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

Luis O S F Caboclo

2

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

Henrique Carrete

3

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

Iscia L Cendes

4

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

Murilo G Rodrigues

5

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

Eliana Garzon

6

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

Elza M T Yacubian

7

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

Américo C Sakamoto

8

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

Volney Sheen

9

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

Megan Harney

10

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

Jason Neal

11

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

R Sean Hill

12

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

Adria Bodell

13

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

Luiz C P Vilanova

15

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

publication date

1 January 2006

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Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

47

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Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

1

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

211-214

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Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

Gray matter heterotopias: MR characteristics and correlation with developmental and neurologic manifestations

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2006.00390.X

21 January 2018

Periventricular nodular heterotopia in patients with filamin-1 gene mutations: neuroimaging findings

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2006.00390.X

21 January 2018

Familial periventricular heterotopia: missense and distal truncating mutations of the FLN1 gene

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2006.00390.X

21 January 2018

Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interact

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2006.00390.X

21 January 2018

Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2006.00390.X

21 January 2018

Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2006.00390.X

21 January 2018

Identifiers

10.1111/J.1528-1167.2006.00390.X

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/16417552

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