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Results: 1 to 20 of 29

References for PMC Articles for PubMed (Select 18925666)

1.

Aicardi syndrome in monozygotic twins.

Pons ME, Garcia CA.

Ophthalmic Genet. 2008 Jun;29(2):87-8. doi: 10.1080/13816810801968669. No abstract available.

PMID:
18484315
2.

Screening of subtle copy number changes in Aicardi syndrome patients with a high resolution X chromosome array-CGH.

Yilmaz S, Fontaine H, Brochet K, Grégoire MJ, Devignes MD, Schaff JL, Philippe C, Nemos C, McGregor JL, Jonveaux P.

Eur J Med Genet. 2007 Sep-Oct;50(5):386-91. Epub 2007 Jun 7.

PMID:
17625997
3.

Cerebral developmental disorders.

Lian G, Sheen V.

Curr Opin Pediatr. 2006 Dec;18(6):614-20. Review.

PMID:
17099359
4.

Aicardi syndrome: chorioretinal lacunae without corpus callosum agenesis.

Iturralde D, Meyerle CB, Yannuzzi LA.

Retina. 2006 Oct;26(8):977-8. No abstract available.

PMID:
17031307
5.

Aicardi syndrome: presentation at onset in Swedish children born in 1975-2002.

Palmér L, Zetterlund B, Hård AL, Steneryd K, Kyllerman M.

Neuropediatrics. 2006 Jun;37(3):154-8.

PMID:
16967367
6.

A developmental and genetic classification for malformations of cortical development.

Barkovich AJ, Kuzniecky RI, Jackson GD, Guerrini R, Dobyns WB.

Neurology. 2005 Dec 27;65(12):1873-87. Epub 2005 Sep 28. Review.

PMID:
16192428
7.

Facial and physical features of Aicardi syndrome: infants to teenagers.

Sutton VR, Hopkins BJ, Eble TN, Gambhir N, Lewis RA, Van den Veyver IB.

Am J Med Genet A. 2005 Oct 15;138A(3):254-8.

PMID:
16158440
8.

Oculocerebrocutaneous syndrome: the brain malformation defines a core phenotype.

Moog U, Jones MC, Bird LM, Dobyns WB.

J Med Genet. 2005 Dec;42(12):913-21. Epub 2005 May 6. Erratum in: J Med Genet. 2006 Mar;43(3):243.

9.

Aicardi syndrome.

Aicardi J.

Brain Dev. 2005 Apr;27(3):164-71. Review.

PMID:
15737696
10.

Aicardi syndrome in a girl with mild developmental delay, absence of epilepsy and normal EEG.

Matlary A, Prescott T, Tvedt B, Lindberg K, Server A, Aicardi J, Strømme P.

Clin Dysmorphol. 2004 Oct;13(4):257-60.

PMID:
15365465
11.

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
13.

A locus for bilateral perisylvian polymicrogyria maps to Xq28.

Villard L, Nguyen K, Cardoso C, Martin CL, Weiss AM, Sifry-Platt M, Grix AW, Graham JM Jr, Winter RM, Leventer RJ, Dobyns WB.

Am J Hum Genet. 2002 Apr;70(4):1003-8. Epub 2002 Jan 29.

14.

Callosal agenesis with cyst: a better understanding and new classification.

Barkovich AJ, Simon EM, Walsh CA.

Neurology. 2001 Jan 23;56(2):220-7.

PMID:
11160959
15.

Aicardi's syndrome in a male child: an unusual presentation.

Aggarwal KC, Aggarwal A, Prasad MS, Salhan RN, Upadhaya A.

Indian Pediatr. 2000 May;37(5):542-5. No abstract available.

PMID:
10820550
16.

Characterization of a novel chromo domain gene in xp22.3 with homology to Drosophila msl-3.

Prakash SK, Van den Veyver IB, Franco B, Volta M, Ballabio A, Zoghbi HY.

Genomics. 1999 Jul 1;59(1):77-84.

PMID:
10395802
17.

Characterization and physical mapping in human and mouse of a novel RING finger gene in Xp22.

Van den Veyver IB, Cormier TA, Jurecic V, Baldini A, Zoghbi HY.

Genomics. 1998 Jul 15;51(2):251-61.

PMID:
9722948
19.

Magnetic resonance imaging of the brain in Aicardi's syndrome. Report of 20 patients.

Smith CD, Ryan SJ, Hoover SL, Baumann RJ.

J Neuroimaging. 1996 Oct;6(4):214-21.

PMID:
8903072
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