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Results: 1 to 20 of 102

Similar articles for PubMed (Select 17937445)

1.

Comparing phenotypes in patients with idiopathic autism to patients with velocardiofacial syndrome (22q11 DS) with and without autism.

Kates WR, Antshel KM, Fremont WP, Shprintzen RJ, Strunge LA, Burnette CP, Higgins AM.

Am J Med Genet A. 2007 Nov 15;143A(22):2642-50.

PMID:
17937445
2.

Autistic spectrum disorders in velo-cardio facial syndrome (22q11.2 deletion).

Antshel KM, Aneja A, Strunge L, Peebles J, Fremont WP, Stallone K, Abdulsabur N, Higgins AM, Shprintzen RJ, Kates WR.

J Autism Dev Disord. 2007 Oct;37(9):1776-86. Epub 2006 Dec 19.

PMID:
17180713
3.

The neural correlates of non-spatial working memory in velocardiofacial syndrome (22q11.2 deletion syndrome).

Kates WR, Krauss BR, Abdulsabur N, Colgan D, Antshel KM, Higgins AM, Shprintzen RJ.

Neuropsychologia. 2007 Sep 20;45(12):2863-73. Epub 2007 May 24.

4.

Manic symptoms and behavioral dysregulation in youth with velocardiofacial syndrome (22q11.2 deletion syndrome).

Aneja A, Fremont WP, Antshel KM, Faraone SV, AbdulSabur N, Higgins AM, Shprintzen R, Kates WR.

J Child Adolesc Psychopharmacol. 2007 Feb;17(1):105-14.

PMID:
17343558
5.

Temporal lobe anatomy and psychiatric symptoms in velocardiofacial syndrome (22q11.2 deletion syndrome).

Kates WR, Miller AM, Abdulsabur N, Antshel KM, Conchelos J, Fremont W, Roizen N.

J Am Acad Child Adolesc Psychiatry. 2006 May;45(5):587-95.

PMID:
16670653
6.

Microdeletion and microduplication 22q11.2 screening in 295 patients with clinical features of DiGeorge/Velocardiofacial syndrome.

Brunet A, Gabau E, Perich RM, Valdesoiro L, Brun C, CaballĂ­n MR, Guitart M.

Am J Med Genet A. 2006 Nov 15;140(22):2426-32.

PMID:
17041934
7.

Cognition, psychosocial adjustment and coping in familial cases of velocardiofacial syndrome.

Gothelf D, Aviram-Goldring A, Burg M, Steinberg T, Mahajnah M, Frisch A, Fennig S, Zalsman G, Weizman A.

J Neural Transm. 2007;114(11):1495-501. Epub 2007 Jun 8.

PMID:
17557124
8.

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
9.
10.

The velocardiofacial syndrome in older age: dementia and autistic features.

Evers LJ, Vermaak MP, Engelen JJ, Curfs LM.

Genet Couns. 2006;17(3):333-40.

PMID:
17100202
11.

Characteristics of the broader phenotype in autism: a study of siblings using the children's communication checklist-2.

Bishop DV, Maybery M, Wong D, Maley A, Hallmayer J.

Am J Med Genet B Neuropsychiatr Genet. 2006 Mar 5;141B(2):117-22.

PMID:
16389586
12.

Psychiatric disorders and intellectual functioning throughout development in velocardiofacial (22q11.2 deletion) syndrome.

Green T, Gothelf D, Glaser B, Debbane M, Frisch A, Kotler M, Weizman A, Eliez S.

J Am Acad Child Adolesc Psychiatry. 2009 Nov;48(11):1060-8. doi: 10.1097/CHI.0b013e3181b76683.

PMID:
19797984
13.

Temperament in velocardiofacial syndrome.

Antshel KM, Stallone K, Abdulsabur N, Shprintzen R, Roizen N, Higgins AM, Kates WR.

J Intellect Disabil Res. 2007 Mar;51(Pt 3):218-27.

PMID:
17300417
14.

Association of IL-12p70 and IL-6:IL-10 ratio with autism-related behaviors in 22q11.2 deletion syndrome: a preliminary report.

Ross HE, Guo Y, Coleman K, Ousley O, Miller AH.

Brain Behav Immun. 2013 Jul;31:76-81. doi: 10.1016/j.bbi.2012.12.021. Epub 2013 Jan 24.

15.

Velocardiofacial syndrome: is there a neuropsychiatric phenotype?

Jolin EM, Weller EB, Weller RA.

Curr Psychiatry Rep. 2006 Apr;8(2):96-101. Review.

PMID:
16539883
16.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
17.

The MTHFR 677C-->T polymorphism and behaviors in children with autism: exploratory genotype-phenotype correlations.

Goin-Kochel RP, Porter AE, Peters SU, Shinawi M, Sahoo T, Beaudet AL.

Autism Res. 2009 Apr;2(2):98-108. doi: 10.1002/aur.70.

PMID:
19455642
18.

Autism spectrum disorder in fragile X syndrome: communication, social interaction, and specific behaviors.

Kaufmann WE, Cortell R, Kau AS, Bukelis I, Tierney E, Gray RM, Cox C, Capone GT, Stanard P.

Am J Med Genet A. 2004 Sep 1;129A(3):225-34.

PMID:
15326621
19.

Autism in Angelman syndrome: implications for autism research.

Peters SU, Beaudet AL, Madduri N, Bacino CA.

Clin Genet. 2004 Dec;66(6):530-6.

PMID:
15521981
20.

Autistic disorder in patients with Williams-Beuren syndrome: a reconsideration of the Williams-Beuren syndrome phenotype.

Tordjman S, Anderson GM, Botbol M, Toutain A, Sarda P, Carlier M, Saugier-Veber P, Baumann C, Cohen D, Lagneaux C, Tabet AC, Verloes A.

PLoS One. 2012;7(3):e30778. doi: 10.1371/journal.pone.0030778. Epub 2012 Mar 6.

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