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Results: 11

1.

Lung disease in FLNA mutation: confirmatory report.

de Wit MC, Tiddens HA, de Coo IF, Mancini GM.

Eur J Med Genet. 2011 May-Jun;54(3):299-300. doi: 10.1016/j.ejmg.2010.12.009. Epub 2010 Dec 29.

PMID:
21194575
[PubMed - indexed for MEDLINE]
2.

Familial cardiac valvulopathy due to filamin A mutation.

Bernstein JA, Bernstein D, Hehr U, Hudgins L.

Am J Med Genet A. 2011 Sep;155A(9):2236-41. doi: 10.1002/ajmg.a.34132. Epub 2011 Aug 3. Review.

PMID:
21815255
[PubMed - indexed for MEDLINE]
3.

Trouble making the first move: interpreting arrested neuronal migration in the cerebral cortex.

Sarkisian MR, Bartley CM, Rakic P.

Trends Neurosci. 2008 Feb;31(2):54-61. doi: 10.1016/j.tins.2007.11.009. Epub 2008 Jan 16. Review.

PMID:
18201775
[PubMed - indexed for MEDLINE]
4.

Presence of filamin in the astrocytic inclusions of Aicardi syndrome.

Van den Veyver IB, Panichkul PP, Antalffy BA, Sun Y, Hunter JV, Armstrong DD.

Pediatr Neurol. 2004 Jan;30(1):7-15. Review.

PMID:
14738943
[PubMed - indexed for MEDLINE]
5.

[Epileptogenic brain malformations: radiological and clinical presentation and indications for genetic testing].

Bahi-Buisson N, Boddaert N, Saillour Y, Souville I, Poirier K, Léger PL, Castelnau L, Plouin P, Carion N, Beldjord C, Chelly J.

Rev Neurol (Paris). 2008 Dec;164(12):995-1009. doi: 10.1016/j.neurol.2008.04.006. Epub 2008 Jun 9. Review. French.

PMID:
18808783
[PubMed - indexed for MEDLINE]
6.

Periventricular heterotopia and the genetics of neuronal migration in the cerebral cortex.

Fox JW, Walsh CA.

Am J Hum Genet. 1999 Jul;65(1):19-24. Review. No abstract available.

PMID:
10364512
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Epilepsy and genetic malformations of the cerebral cortex.

Guerrini R, Carrozzo R.

Am J Med Genet. 2001 Summer;106(2):160-73. Review.

PMID:
11579436
[PubMed - indexed for MEDLINE]
8.

Filamins in cardiovascular development.

Zhou X, Borén J, Akyürek LM.

Trends Cardiovasc Med. 2007 Oct;17(7):222-9. Review.

PMID:
17936203
[PubMed - indexed for MEDLINE]
9.

The many faces of filamin: a versatile molecular scaffold for cell motility and signalling.

Feng Y, Walsh CA.

Nat Cell Biol. 2004 Nov;6(11):1034-8. Review.

PMID:
15516996
[PubMed - indexed for MEDLINE]
10.

[Heterotopia as the cause of seizures. A case report of familial periependymal heterotopia].

Navarro-Cantarero E, Pina-Leita JI, Lasierra-Díaz R.

Rev Neurol. 2005 Jul 16-31;41(2):86-90. Review. Spanish.

PMID:
16028186
[PubMed - indexed for MEDLINE]
Free Article
11.

Filamin A: phenotypic diversity.

Robertson SP.

Curr Opin Genet Dev. 2005 Jun;15(3):301-7. Review.

PMID:
15917206
[PubMed - indexed for MEDLINE]

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