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Items: 1 to 20 of 93

1.

A multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children.

Simon TJ, Bish JP, Bearden CE, Ding L, Ferrante S, Nguyen V, Gee JC, McDonald-McGinn DM, Zackai EH, Emanuel BS.

Dev Psychopathol. 2005 Summer;17(3):753-84. Review.

2.

Visuospatial and numerical cognitive deficits in children with chromosome 22q11.2 deletion syndrome.

Simon TJ, Bearden CE, Mc-Ginn DM, Zackai E.

Cortex. 2005 Apr;41(2):145-55.

4.

Performance on the Modified Card Sorting Test and its relation to psychopathology in adolescents and young adults with 22q11.2 deletion syndrome.

Rockers K, Ousley O, Sutton T, Schoenberg E, Coleman K, Walker E, Cubells JF.

J Intellect Disabil Res. 2009 Jul;53(7):665-76. doi: 10.1111/j.1365-2788.2009.01178.x. Epub 2009 May 12.

PMID:
19460069
5.

Clues to the foundations of numerical cognitive impairments: evidence from genetic disorders.

Simon TJ.

Dev Neuropsychol. 2011;36(6):788-805. doi: 10.1080/87565641.2010.549879. Review.

6.

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.

Specific cerebellar reductions in children with chromosome 22q11.2 deletion syndrome.

Bish JP, Pendyal A, Ding L, Ferrante H, Nguyen V, McDonald-McGinn D, Zackai E, Simon TJ.

Neurosci Lett. 2006 May 22;399(3):245-8. Epub 2006 Mar 3.

PMID:
16517069
9.

Domain specific attentional impairments in children with chromosome 22q11.2 deletion syndrome.

Bish JP, Chiodo R, Mattei V, Simon TJ.

Brain Cogn. 2007 Aug;64(3):265-73. Epub 2007 May 11.

10.

22q11.2 deletion syndrome: genetics, neuroanatomy and cognitive/behavioral features keywords.

Antshel KM, Kates WR, Roizen N, Fremont W, Shprintzen RJ.

Child Neuropsychol. 2005 Feb;11(1):5-19. Review.

PMID:
15823980
11.

Maladaptive conflict monitoring as evidence for executive dysfunction in children with chromosome 22q11.2 deletion syndrome.

Bish JP, Ferrante SM, McDonald-McGinn D, Zackai E, Simon TJ.

Dev Sci. 2005 Jan;8(1):36-43.

PMID:
15647065
12.

Atypical neuropsychological profile in a boy with 22q11.2 Deletion Syndrome.

Stiers P, Swillen A, De Smedt B, Lagae L, Devriendt K, D'Agostino E, Sunaert S, Fryns AP.

Child Neuropsychol. 2005 Feb;11(1):87-108.

PMID:
15823985
13.

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
14.

Altered functioning of the cingulate gyrus in two cases of chromosome 22q11 deletion syndrome.

Reif A, Fallgatter AJ, Ehlis AC, Lesch KP.

Psychiatry Res. 2004 Dec 30;132(3):273-8.

PMID:
15664798
15.

Behavior and corpus callosum morphology relationships in velocardiofacial syndrome (22q11.2 deletion syndrome).

Antshel KM, Conchelos J, Lanzetta G, Fremont W, Kates WR.

Psychiatry Res. 2005 Apr 30;138(3):235-45.

PMID:
15854791
16.
17.

Cognitive characteristics of children with genetic syndromes.

Simon TJ.

Child Adolesc Psychiatr Clin N Am. 2007 Jul;16(3):599-616. Review.

18.

Eye gaze during face processing in children and adolescents with 22q11.2 deletion syndrome.

Glaser B, Debbané M, Ottet MC, Vuilleumier P, Zesiger P, Antonarakis SE, Eliez S.

J Am Acad Child Adolesc Psychiatry. 2010 Jul;49(7):665-74. doi: 10.1016/j.jaac.2010.04.004. Epub 2010 Jun 2.

PMID:
20610136
19.

Atypical cortical connectivity and visuospatial cognitive impairments are related in children with chromosome 22q11.2 deletion syndrome.

Simon TJ, Wu Z, Avants B, Zhang H, Gee JC, Stebbins GT.

Behav Brain Funct. 2008 Jun 17;4:25. doi: 10.1186/1744-9081-4-25.

20.
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