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Results: 1 to 20 of 171

Similar articles for PubMed (Select 11226724)

1.

Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteria.

Vivarelli R, Grosso S, Cioni M, Galluzzi P, Monti L, Morgese G, Balestri P.

Brain Dev. 2001 Mar;23(1):18-23.

PMID:
11226724
2.
3.

Autosomal recessive congenital intrauterine infection-like syndrome of microcephaly, intracranial calcification, and CNS disease.

Reardon W, Hockey A, Silberstein P, Kendall B, Farag TI, Swash M, Stevenson R, Baraitser M.

Am J Med Genet. 1994 Aug 1;52(1):58-65.

PMID:
7977464
4.

Microcephaly, malformation of brain development and intracranial calcification in sibs: pseudo-TORCH or a new syndrome.

Abdel-Salam GM, Zaki MS, Saleem SN, Gaber KR.

Am J Med Genet A. 2008 Nov 15;146A(22):2929-36. doi: 10.1002/ajmg.a.32549.

PMID:
18925673
5.

Two brothers with findings resembling congenital intrauterine infection-like syndrome (pseudo-TORCH syndrome).

Knoblauch H, Tennstedt C, Brueck W, Hammer H, Vulliamy T, Dokal I, Lehmann R, Hanefeld F, Tinschert S.

Am J Med Genet A. 2003 Jul 15;120A(2):261-5.

PMID:
12833411
6.

Band-like intracranial calcification with simplified gyration and polymicrogyria: a distinct "pseudo-TORCH" phenotype.

Briggs TA, Wolf NI, D'Arrigo S, Ebinger F, Harting I, Dobyns WB, Livingston JH, Rice GI, Crooks D, Rowland-Hill CA, Squier W, Stoodley N, Pilz DT, Crow YJ.

Am J Med Genet A. 2008 Dec 15;146A(24):3173-80. doi: 10.1002/ajmg.a.32614.

PMID:
19012351
7.

Fetal intracranial calcification: pseudo-TORCH phenotype and discussion of related phenotypes.

Kulkarni AM, Baskar S, Kulkarni ML, Kulkarni AJ, Mahuli AV, Vittalrao S, Kulkarni PM.

Am J Med Genet A. 2010 Apr;152A(4):930-7. doi: 10.1002/ajmg.a.33358.

PMID:
20358603
8.

Chorioretinal dysplasia, hydranencephaly, and intracranial calcifications: pseudo-TORCH or a new syndrome?

Watts P, Kumar N, Ganesh A, Sastry P, Pilz D, Levin AV, Chitayat D.

Eye (Lond). 2008 May;22(5):730-3. Epub 2007 Dec 14.

PMID:
18084237
9.

Intracranial calcifications, microcephaly, and seizure. If not congenital infection, what could it be?

Eyaid W, Al-Tassan RS, Al-Nouri DM.

Neurosciences (Riyadh). 2012 Jul;17(3):248-52.

PMID:
22772931
10.

[Genetic syndromes that mimic congenital infections: report of 2 cases].

Thibault M, Leydet J, Tournier-Lasserve E, Crow YJ, Rivier F, Echenne B, Langlois C, Daudet H, Sarda P, Roubertie A.

Arch Pediatr. 2011 Dec;18(12):1297-1301. doi: 10.1016/j.arcped.2011.08.009. Epub 2011 Oct 2. French.

PMID:
21963371
11.

Syndrome of microcephaly, microphthalmia, cataracts, and intracranial calcification.

Slee J, Lam G, Walpole I.

Am J Med Genet. 1999 Jun 4;84(4):330-3.

PMID:
10340646
12.

Magnetic resonance imaging of brain abnormalities in patients with the Nijmegen breakage syndrome.

Bekiesińska-Figatowska M, Chrzanowska KH, Jurkiewicz E, Wakulińska A, Rysiewskis H, Gładkowska-Dura M, Walecki J.

Acta Neurobiol Exp (Wars). 2004;64(4):503-9.

13.

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
14.

Recurrent pseudo-TORCH appearances of the brain presenting as "Dandy-Walker" malformation.

Cohen MC, Karaman I, Squier W, Farrel T, Whitby EH.

Pediatr Dev Pathol. 2012 Jan-Feb;15(1):45-9. doi: 10.2350/10-01-0783-CR.1. Epub 2011 Jul 15.

PMID:
21762029
15.

Aicardi-Goutières syndrome: clinical and neuroradiological findings of 10 new cases.

Abdel-Salam GM, Zaki MS, Lebon P, Meguid NA.

Acta Paediatr. 2004 Jul;93(7):929-36.

PMID:
15303808
16.

Lissencephaly-pachygyria associated with congenital cytomegalovirus infection.

Hayward JC, Titelbaum DS, Clancy RR, Zimmerman RA.

J Child Neurol. 1991 Apr;6(2):109-14.

PMID:
1646253
17.

Spectrum of congenital CNS malformations in pediatric epilepsy.

Sanghvi JP, Rajadhyaksha SB, Ursekar M.

Indian Pediatr. 2004 Aug;41(8):831-8.

18.

Lack of progression of brain atrophy in Aicardi-Goutières syndrome.

Polizzi A, Pavone P, Parano E, Incorpora G, Ruggieri M.

Pediatr Neurol. 2001 Apr;24(4):300-2.

PMID:
11377106
19.

Genetic malformations of the cerebral cortex and epilepsy.

Guerrini R.

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

PMID:
15816977
20.

Sporadic neonatal schizencephaly associated with brain calcification.

al-Alawi AM, al-Tawil KI, al-Hathal MM, Amir I.

Ann Trop Paediatr. 2001 Mar;21(1):34-7; discussion 37-8.

PMID:
11284244
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