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Items: 1 to 20 of 95

1.

Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia.

Chow EW, Mikulis DJ, Zipursky RB, Scutt LE, Weksberg R, Bassett AS.

Biol Psychiatry. 1999 Nov 15;46(10):1436-42.

2.

Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome.

Chow EW, Zipursky RB, Mikulis DJ, Bassett AS.

Biol Psychiatry. 2002 Feb 1;51(3):208-15.

3.

Schizophrenia and 22q11.2 deletion syndrome.

Bassett AS, Chow EW.

Curr Psychiatry Rep. 2008 Apr;10(2):148-57. Review.

4.

Postmaturity in a genetic subtype of schizophrenia.

Chow EW, Husted J, Weksberg R, Bassett AS.

Acta Psychiatr Scand. 2003 Oct;108(4):260-8.

5.

Low platelet count in a 22q11 deletion syndrome subtype of schizophrenia.

Lazier K, Chow EW, AbdelMalik P, Scutt LE, Weksberg R, Bassett AS.

Schizophr Res. 2001 Jul 1;50(3):177-80.

6.

22q11 deletion syndrome: a genetic subtype of schizophrenia.

Bassett AS, Chow EW.

Biol Psychiatry. 1999 Oct 1;46(7):882-91. Review.

7.

22q11 deletion syndrome in adults with schizophrenia.

Bassett AS, Hodgkinson K, Chow EW, Correia S, Scutt LE, Weksberg R.

Am J Med Genet. 1998 Jul 10;81(4):328-37.

8.

Neurocognitive profile in 22q11 deletion syndrome and schizophrenia.

Chow EW, Watson M, Young DA, Bassett AS.

Schizophr Res. 2006 Oct;87(1-3):270-8. Epub 2006 Jun 6.

9.

Neuropathologic features in adults with 22q11.2 deletion syndrome.

Kiehl TR, Chow EW, Mikulis DJ, George SR, Bassett AS.

Cereb Cortex. 2009 Jan;19(1):153-64. doi: 10.1093/cercor/bhn066. Epub 2008 May 14.

10.

Association of schizophrenia in 22q11.2 deletion syndrome and gray matter volumetric deficits in the superior temporal gyrus.

Chow EW, Ho A, Wei C, Voormolen EH, Crawley AP, Bassett AS.

Am J Psychiatry. 2011 May;168(5):522-9. doi: 10.1176/appi.ajp.2010.10081230. Epub 2011 Mar 1. Erratum in: Am J Psychiatry. 2011 May;168(5):553.

11.

Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study.

Campbell LE, Daly E, Toal F, Stevens A, Azuma R, Catani M, Ng V, van Amelsvoort T, Chitnis X, Cutter W, Murphy DG, Murphy KC.

Brain. 2006 May;129(Pt 5):1218-28. Epub 2006 Mar 28.

12.

Increased basal ganglia volumes in velo-cardio-facial syndrome (deletion 22q11.2).

Eliez S, Barnea-Goraly N, Schmitt JE, Liu Y, Reiss AL.

Biol Psychiatry. 2002 Jul 1;52(1):68-70.

PMID:
12079732
13.

Phenotype of adults with the 22q11 deletion syndrome: A review.

Cohen E, Chow EW, Weksberg R, Bassett AS.

Am J Med Genet. 1999 Oct 8;86(4):359-65. Review.

14.

Structural brain abnormalities associated with deletion at chromosome 22q11: quantitative neuroimaging study of adults with velo-cardio-facial syndrome.

van Amelsvoort T, Daly E, Robertson D, Suckling J, Ng V, Critchley H, Owen MJ, Henry J, Murphy KC, Murphy DG.

Br J Psychiatry. 2001 May;178:412-9.

15.

Midline brain anomalies and schizophrenia in people with CATCH 22 syndrome.

Vataja R, Elomaa E.

Br J Psychiatry. 1998 Jun;172:518-20.

PMID:
9828993
16.

The schizophrenia phenotype in 22q11 deletion syndrome.

Bassett AS, Chow EW, AbdelMalik P, Gheorghiu M, Husted J, Weksberg R.

Am J Psychiatry. 2003 Sep;160(9):1580-6.

17.

Velocardiofacial syndrome in childhood-onset schizophrenia.

Usiskin SI, Nicolson R, Krasnewich DM, Yan W, Lenane M, Wudarsky M, Hamburger SD, Rapoport JL.

J Am Acad Child Adolesc Psychiatry. 1999 Dec;38(12):1536-43.

PMID:
10596254
18.

Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: preliminary results of a structural magnetic resonance imaging study.

van Amelsvoort T, Daly E, Henry J, Robertson D, Ng V, Owen M, Murphy KC, Murphy DG.

Arch Gen Psychiatry. 2004 Nov;61(11):1085-96.

PMID:
15520356
19.

Neuropsychological profile and neuroimaging in patients with 22Q11.2 Deletion Syndrome: a review.

Zinkstok J, van Amelsvoort T.

Child Neuropsychol. 2005 Feb;11(1):21-37. Review.

PMID:
15823981
20.

Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndrome.

Weksberg R, Stachon AC, Squire JA, Moldovan L, Bayani J, Meyn S, Chow E, Bassett AS.

Hum Genet. 2007 Feb;120(6):837-45. Epub 2006 Oct 7.

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