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Items: 1 to 20 of 103

1.

Septo-optic dysplasia plus bilateral perisylvian polymicrogyria: a case report.

Labate A, Gambardella A, Quattrone A.

Neurol Sci. 2013 Aug;34(8):1479-80. doi: 10.1007/s10072-012-1227-2. Epub 2012 Nov 4. No abstract available.

PMID:
23124487
2.

Voxel-based morphometry and intellectual assessment in patients with congenital bilateral perisylvian syndrome.

Yasuda CL, Guimarães CA, Guerreiro MM, Boscariol M, Oliveira EP, Teixeira KC, Costa AL, Beltramini GC, Cendes F.

J Neurol. 2014 Jul;261(7):1374-80. doi: 10.1007/s00415-014-7356-1. Epub 2014 Apr 30.

PMID:
24781839
3.

Septo-optic dysplasia with encephalocele.

Periakaruppan A, Pendharkar HS, Gupta AK, Thomas B, Kesavdas C.

J Clin Neurosci. 2009 Dec;16(12):1665-7. doi: 10.1016/j.jocn.2009.03.018. Epub 2009 Sep 18.

PMID:
19766496
4.

Bilateral perisylvian ulegyria: an under-recognized, surgically remediable epileptic syndrome.

Schilling LP, Kieling RR, Pascoal TA, Kim HI, Lee MC, Kim YH, Paglioli E, Neto PR, Costa JC, Palmini A.

Epilepsia. 2013 Aug;54(8):1360-7. doi: 10.1111/epi.12160. Epub 2013 Apr 15.

5.

A case of Bilateral Perisylvian Syndrome with reading disability.

Eckert MA, Berninger VW, Hoeft F, Vaden KI Jr; Dyslexia Data Consortium.

Cortex. 2016 Mar;76:121-4. doi: 10.1016/j.cortex.2016.01.004. Epub 2016 Jan 19. No abstract available.

6.

Septo-optic dysplasia plus: a patient with diabetes insipidus.

Carman KB, Yarar C, Yakut A, Adapinar B.

Pediatr Neurol. 2010 Jul;43(1):76-8. doi: 10.1016/j.pediatrneurol.2010.03.001.

PMID:
20682211
7.

Septo-optic dysplasia syndrome with schizencephaly and sudden visual loss. A new observation.

Masri AT, Abu-Libdeh AM, Ababneh OH, Al-Hadidy AM.

Neurosciences (Riyadh). 2011 Jul;16(3):281-2. No abstract available.

PMID:
21677624
8.

Prenatal diagnosis of schizencephaly with septo-optic dysplasia by ultrasound and magnetic resonance imaging.

Hung JH, Shen SH, Guo WY, Chen CY, Chao KC, Yang MJ, Hung CY.

J Obstet Gynaecol Res. 2008 Aug;34(4 Pt 2):674-9. doi: 10.1111/j.1447-0756.2008.00905.x.

PMID:
18840179
9.

Two cases of septo-optic dysplasia-plus syndrome with epilepsy and mirror hand movements.

Karatas H, Saygi S.

Epilepsy Behav. 2009 Jun;15(2):245-8. doi: 10.1016/j.yebeh.2009.02.046. Epub 2009 Mar 5.

PMID:
19268717
10.

Bilateral perisylvian polymicrogyria with cerebellar dysplasia and ectopic neurohypophysis.

Toldo I, Calderone M, Sartori S, Mardari R, Gatta M, Boniver C, Guerrini R, Battistella PA.

J Child Neurol. 2011 Mar;26(3):361-5. doi: 10.1177/0883073810381447. Epub 2011 Jan 27.

PMID:
21273507
11.

Type IV intestinal atresia, congenital bilateral perisylvian syndrome, and chronic pulmonary hypertension secondary to multiple vascular disruption syndrome in a monochorionic twin.

Shue EH, Soares B, Courtier J, Hogue J, Shimotake T, MacKenzie TC.

J Pediatr Surg. 2012 Oct;47(10):1938-42. doi: 10.1016/j.jpedsurg.2012.08.021.

PMID:
23084212
12.

Bilateral agenesis of arcuate fasciculus demonstrated by fiber tractography in congenital bilateral perisylvian syndrome.

Kilinc O, Ekinci G, Demirkol E, Agan K.

Brain Dev. 2015 Mar;37(3):352-5. doi: 10.1016/j.braindev.2014.05.003. Epub 2014 May 20.

PMID:
24852949
13.

The subclassification of schizencephaly and its clinical characterization.

Maeda T, Akaishi M, Shimizu M, Sekiguchi K, Anan A, Takano T, Imai K, Suenobu S, Korematsu S, Izumi T.

Brain Dev. 2009 Oct;31(9):694-701. doi: 10.1016/j.braindev.2008.10.004. Epub 2008 Nov 26.

PMID:
19038511
14.

Septo-optic dysplasia and associations with amyoplasia and gastroschisis.

Kamien B, Zankl A, Gabbett M.

Birth Defects Res A Clin Mol Teratol. 2010 Jun;88(6):497-501. doi: 10.1002/bdra.20663.

PMID:
20589918
15.

Septo-optic dysplasia, limb anomalies and cutis aplasia: further evidence for overlap between Pagon and Adams-Oliver syndromes.

Pottinger CC, Joshi H, Rowe SA, Fryer AE.

Clin Dysmorphol. 2009 Oct;18(4):228-31. doi: 10.1097/MCD.0b013e32832dc33a. No abstract available.

PMID:
19623038
16.

Candidate gene sequencing of LHX2, HESX1, and SOX2 in a large schizencephaly cohort.

Mellado C, Poduri A, Gleason D, Elhosary PC, Barry BJ, Partlow JN, Chang BS, Shaw GM, Barkovich AJ, Walsh CA.

Am J Med Genet A. 2010 Nov;152A(11):2736-42. doi: 10.1002/ajmg.a.33684.

17.

[Congenital mydriasis as an initial sign of septo-optic dysplasia].

Carrascosa-Romero MC, Ruiz-Cano R, Martínez-López F, Alfaro-Ponce B, Pérez-Pardo A.

Arch Soc Esp Oftalmol. 2013 Oct;88(10):398-402. doi: 10.1016/j.oftal.2012.05.005. Epub 2012 Aug 4. Spanish.

PMID:
24060304
18.

Septo-optic dysplasia and amniotic bands: further evidence for a vascular pathogenesis.

Stevens CA, Dobyns WB.

Am J Med Genet A. 2004 Feb 15;125A(1):12-6. Review.

PMID:
14755460
19.

Septo-optic dysplasia complex: a heterogeneous malformation syndrome.

Polizzi A, Pavone P, Iannetti P, Manfré L, Ruggieri M.

Pediatr Neurol. 2006 Jan;34(1):66-71.

PMID:
16376284
20.

Perisylvian polymicrogyria, infantile spasms and arthrogryposis: the severe end of the spectrum of congenital bilateral perisylvian polymicrogyria.

De Coene A, Van Coster R, Verhelst H.

Eur J Paediatr Neurol. 2010 May;14(3):270-3. doi: 10.1016/j.ejpn.2009.05.005. Epub 2009 Jun 25.

PMID:
19559633

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