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Results: 1 to 20 of 179

1.

A new autosomal recessive disorder of bilateral frontotemporal pachygyria without microcephaly: report of a case and review of literature.

Phadke SR, Girisha KM, Phadke RV.

Neurol India. 2007 Jan-Mar;55(1):57-60. Review.

PMID:
17272902
[PubMed - indexed for MEDLINE]
Free Article
2.

Autosomal recessive frontotemporal pachygyria.

Ramirez D, Lammer EJ, Johnson CB, Peterson CD.

Am J Med Genet A. 2004 Jan 30;124A(3):231-8. Review.

PMID:
14708094
[PubMed - indexed for MEDLINE]
3.

An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21.

Piao X, Basel-Vanagaite L, Straussberg R, Grant PE, Pugh EW, Doheny K, Doan B, Hong SE, Shugart YY, Walsh CA.

Am J Hum Genet. 2002 Apr;70(4):1028-33. Epub 2002 Feb 13.

PMID:
11845408
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

A new autosomal recessive syndrome of pachygyria.

Straussberg R, Gross S, Amir J, Gadoth N.

Clin Genet. 1996 Dec;50(6):498-501.

PMID:
9147882
[PubMed - indexed for MEDLINE]
5.

Bilateral frontoparietal polymicrogyria and epilepsy.

Sztriha L, Nork M.

Pediatr Neurol. 2000 Mar;22(3):240-3.

PMID:
10734259
[PubMed - indexed for MEDLINE]
6.

Frontotemporal abnormal gyration with infantile spasms in identical twins.

Saito Y, Yokoyama A, Shiraishi H, Maegaki Y, Ohno K.

Brain Dev. 2007 Oct;29(9):595-9. Epub 2007 Apr 9.

PMID:
17416476
[PubMed - indexed for MEDLINE]
7.

Autosomal recessive type I lissencephaly.

Garg A, Sridhar MR, Gulati S.

Indian J Pediatr. 2007 Feb;74(2):199-201.

PMID:
17337836
[PubMed - indexed for MEDLINE]
8.

Genetic malformations of the cerebral cortex and epilepsy.

Guerrini R.

Epilepsia. 2005;46 Suppl 1:32-7. Review.

PMID:
15816977
[PubMed - indexed for MEDLINE]
9.

Non-progressive leukoencephalopathy with bilateral anterior temporal cysts: a case report and review of the literature.

Grosso S, Cerase A, De Stefano N, Marco LD, Galluzzi P, Galimberti D, Morgese G, Balestri P.

Brain Dev. 2005 Jan;27(1):73-7. Review.

PMID:
15626547
[PubMed - indexed for MEDLINE]
10.

Characterization of brain malformations in the Baraitser-Winter syndrome and review of the literature.

Rossi M, Guerrini R, Dobyns WB, Andria G, Winter RM.

Neuropediatrics. 2003 Dec;34(6):287-92. Review.

PMID:
14681753
[PubMed - indexed for MEDLINE]
11.

Cardiomyopathy with renal anomalies in two siblings: a new recessive syndrome?

Leask KM, Kerr B, Ladusans E.

Clin Dysmorphol. 2007 Jan;16(1):51-3.

PMID:
17159516
[PubMed - indexed for MEDLINE]
12.

Familial neuronal migration disorder: subcortical laminar heterotopia in a mother and pachygyria in the son.

Toyama J, Kasuya H, Higuchi S, Kondo H, Naganuma Y, Uchiyama M.

Am J Med Genet. 1998 Feb 17;75(5):481-4.

PMID:
9489790
[PubMed - indexed for MEDLINE]
13.

Agyria-pachygyria and agenesis of the corpus callosum: autosomal recessive inheritance with neonatal death.

Sztriha L, Al-Gazali L, Dawodu A, Bakir M, Chandran P.

Neurology. 1998 May;50(5):1466-9.

PMID:
9596009
[PubMed - indexed for MEDLINE]
14.

Cystic leukoencephalopathy without megalencephaly: a distinct disease entity in 15 children.

Henneke M, Preuss N, Engelbrecht V, Aksu F, Bertini E, Bibat G, Brockmann K, Hübner C, Mayer M, Mejaski-Bosnjak V, Naidu S, Neumaier-Probst E, Rodriguez D, Weisz W, Kohlschütter A, Gärtner J.

Neurology. 2005 Apr 26;64(8):1411-6.

PMID:
15851732
[PubMed - indexed for MEDLINE]
15.

Posterior agyria-pachygyria with polymicrogyria: evidence for an inherited neuronal migration disorder.

Ferrie CD, Jackson GD, Giannakodimos S, Panayiotopoulos CP.

Neurology. 1995 Jan;45(1):150-3.

PMID:
7824106
[PubMed - indexed for MEDLINE]
16.

Microcephaly with simplified gyral pattern in six related children.

Peiffer A, Singh N, Leppert M, Dobyns WB, Carey JC.

Am J Med Genet. 1999 May 21;84(2):137-44.

PMID:
10323739
[PubMed - indexed for MEDLINE]
17.

Clinical features of 21 patients with lissencephaly type I (agyria-pachygyria).

Ozmen M, Yilmaz Y, Calişkan M, Minareci O, Aydinli N.

Turk J Pediatr. 2000 Jul-Sep;42(3):210-4.

PMID:
11105619
[PubMed - indexed for MEDLINE]
18.

Neonatal hepatitis in 2 siblings with Seckel syndrome.

Deniz K, Kontaş O, akçakuş M.

Pediatr Dev Pathol. 2006 Jan-Feb;9(1):81-5. Epub 2006 Apr 4.

PMID:
16808631
[PubMed - indexed for MEDLINE]
19.

Frontotemporal pachygyria-two new patients.

Avela K, Toiviainen-Salo S, Karttunen-Lewandowski P, Kauria L, Valanne L, Salonen-Kajander R.

Eur J Med Genet. 2012 Dec;55(12):753-7. doi: 10.1016/j.ejmg.2012.09.007. Epub 2012 Sep 27.

PMID:
23022981
[PubMed - indexed for MEDLINE]
20.

Autosomal recessive nonsyndromal microcephaly with normal intelligence.

Teebi AS, Al-Awadi SA, White AG.

Am J Med Genet. 1987 Feb;26(2):355-9.

PMID:
3812587
[PubMed - indexed for MEDLINE]

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