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Results: 1 to 20 of 102

Similar articles for PubMed (Select 24353423)

1.

22q11 deletion syndrome: a review of the neuropsychiatric features and their neurobiological basis.

Squarcione C, Torti MC, Di Fabio F, Biondi M.

Neuropsychiatr Dis Treat. 2013;9:1873-84. doi: 10.2147/NDT.S52188. Epub 2013 Dec 4. Review.

2.

COMT implication in cognitive and psychiatric symptoms in chromosome 22q11 microdeletion syndrome: a selective review.

Armando M, Papaleo F, Vicari S.

CNS Neurol Disord Drug Targets. 2012 May;11(3):273-81. Review.

PMID:
22483289
3.

[Neurocognitive and psychiatric management of the 22q11.2 deletion syndrome].

Demily C, Rossi M, Schneider M, Edery P, Leleu A, d'Amato T, Franck N, Eliez S.

Encephale. 2015 Jun;41(3):266-73. doi: 10.1016/j.encep.2014.10.005. Epub 2014 Dec 16. French.

PMID:
25523123
4.

Analyses of the associations between the genes of 22q11 deletion syndrome and schizophrenia.

Arinami T.

J Hum Genet. 2006;51(12):1037-45. Epub 2006 Sep 13. Review.

PMID:
16969581
5.

[Microdeletion 22q11: apropos of case of schizophrenia in an adolescent].

Pinquier C, Héron D, de Carvalho W, Lazar G, Mazet P, Cohen D.

Encephale. 2001 Jan-Feb;27(1):45-50. French.

PMID:
11294038
6.

COMT Val108/158 Met modifies mismatch negativity and cognitive function in 22q11 deletion syndrome.

Baker K, Baldeweg T, Sivagnanasundaram S, Scambler P, Skuse D.

Biol Psychiatry. 2005 Jul 1;58(1):23-31.

PMID:
15935994
7.

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
8.

Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.

Prasad SE, Howley S, Murphy KC.

Dev Disabil Res Rev. 2008;14(1):26-34. doi: 10.1002/ddrr.5. Review.

PMID:
18636634
9.

Is there a core neuropsychiatric phenotype in 22q11.2 deletion syndrome?

Baker K, Vorstman JA.

Curr Opin Neurol. 2012 Apr;25(2):131-7. doi: 10.1097/WCO.0b013e328352dd58. Review.

PMID:
22395003
10.

[22q11.2 microdeletion].

Schneider M, Eliez S.

Arch Pediatr. 2010 Apr;17(4):431-4. doi: 10.1016/j.arcped.2009.10.010. Epub 2009 Nov 25. Review. French.

PMID:
19942416
11.

Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome.

Gothelf D, Schaer M, Eliez S.

Dev Disabil Res Rev. 2008;14(1):59-68. doi: 10.1002/ddrr.9. Review.

PMID:
18636637
12.

Neuroimaging correlates of 22q11.2 deletion syndrome: implications for schizophrenia research.

Boot E, van Amelsvoort TA.

Curr Top Med Chem. 2012;12(21):2303-13. Review.

PMID:
23279171
13.

Structural abnormalities in cortical volume, thickness, and surface area in 22q11.2 microdeletion syndrome: Relationship with psychotic symptoms.

Jalbrzikowski M, Jonas R, Senturk D, Patel A, Chow C, Green MF, Bearden CE.

Neuroimage Clin. 2013 Oct 14;3:405-15. doi: 10.1016/j.nicl.2013.09.013. eCollection 2013.

14.

Adolescents at ultra-high risk for psychosis with and without 22q11 deletion syndrome: a comparison of prodromal psychotic symptoms and general functioning.

Armando M, Girardi P, Vicari S, Menghini D, Digilio MC, Pontillo M, Saba R, Mazzone L, Lin A, Klier CM, Schäfer MR, Amminger GP.

Schizophr Res. 2012 Aug;139(1-3):151-6. doi: 10.1016/j.schres.2012.04.020. Epub 2012 May 23.

PMID:
22627123
15.

A longitudinal examination of the psychoeducational, neurocognitive, and psychiatric functioning in children with 22q11.2 deletion syndrome.

Hooper SR, Curtiss K, Schoch K, Keshavan MS, Allen A, Shashi V.

Res Dev Disabil. 2013 May;34(5):1758-69. doi: 10.1016/j.ridd.2012.12.003. Epub 2013 Mar 16.

16.

[Spectrum of neuropsychiatric features associated with velocardiofacial syndrome (Deletion 22q11.2)].

Sieberer M, Runte I, Wilkening A, Pabst B, Ziegenbein M, Haltenhof H.

Fortschr Neurol Psychiatr. 2006 May;74(5):263-74. Review. German.

PMID:
16758538
17.

The 22q11.2 deletion syndrome.

Yamagishi H.

Keio J Med. 2002 Jun;51(2):77-88. Review.

18.

Molecular mechanisms in 22q11 deletion syndrome.

Williams NM.

Schizophr Bull. 2011 Sep;37(5):882-9. doi: 10.1093/schbul/sbr095. Review.

19.

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome.

Paylor R, Glaser B, Mupo A, Ataliotis P, Spencer C, Sobotka A, Sparks C, Choi CH, Oghalai J, Curran S, Murphy KC, Monks S, Williams N, O'Donovan MC, Owen MJ, Scambler PJ, Lindsay E.

Proc Natl Acad Sci U S A. 2006 May 16;103(20):7729-34. Epub 2006 May 9.

20.

Neuroanatomy in adolescents and young adults with 22q11 deletion syndrome: comparison to an IQ-matched group.

Baker K, Chaddock CA, Baldeweg T, Skuse D.

Neuroimage. 2011 Mar 15;55(2):491-9. doi: 10.1016/j.neuroimage.2010.12.041. Epub 2010 Dec 22.

PMID:
21184831
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