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Items: 15

1.

Mitochondrial dysfunction in autistic patients with 15q inverted duplication.

Filipek PA, Juranek J, Smith M, Mays LZ, Ramos ER, Bocian M, Masser-Frye D, Laulhere TM, Modahl C, Spence MA, Gargus JJ.

Ann Neurol. 2003 Jun;53(6):801-4.

2.

The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders.

Bolton PF, Dennis NR, Browne CE, Thomas NS, Veltman MW, Thompson RJ, Jacobs P.

Am J Med Genet. 2001 Dec 8;105(8):675-85. Review.

PMID:
11803514
3.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

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

PMID:
15121991
4.

Syndromic autism: causes and pathogenetic pathways.

Benvenuto A, Moavero R, Alessandrelli R, Manzi B, Curatolo P.

World J Pediatr. 2009 Aug;5(3):169-76. doi: 10.1007/s12519-009-0033-2. Epub 2009 Aug 20. Review.

PMID:
19693459
5.

Autism and 15q11-q13 disorders: behavioral, genetic, and pathophysiological issues.

Dykens EM, Sutcliffe JS, Levitt P.

Ment Retard Dev Disabil Res Rev. 2004;10(4):284-91. Review.

PMID:
15666333
6.

Toward a developmental neurobiology of autism.

Polleux F, Lauder JM.

Ment Retard Dev Disabil Res Rev. 2004;10(4):303-17. Review.

PMID:
15666334
7.

Duplication of the distal long arm of chromosome 15: report of three new patients and review of the literature.

Roggenbuck JA, Mendelsohn NJ, Tenenholz B, Ladda RL, Fink JM.

Am J Med Genet A. 2004 May 1;126A(4):398-402. Review.

PMID:
15098238
8.

Epigenetics of autism spectrum disorders.

Schanen NC.

Hum Mol Genet. 2006 Oct 15;15 Spec No 2:R138-50. Review.

PMID:
16987877
9.

Nuclear and mitochondrial genome defects in autisms.

Smith M, Spence MA, Flodman P.

Ann N Y Acad Sci. 2009 Jan;1151:102-32. doi: 10.1111/j.1749-6632.2008.03571.x. Review.

PMID:
19154520
10.

Molecular genetics of autism spectrum disorder.

Veenstra-VanderWeele J, Cook EH Jr.

Mol Psychiatry. 2004 Sep;9(9):819-32. Review.

PMID:
15197396
11.

Autistic-like symptomatology in Prader-Willi syndrome: a review of recent findings.

Dimitropoulos A, Schultz RT.

Curr Psychiatry Rep. 2007 Apr;9(2):159-64. Review.

PMID:
17389128
12.

Autism and cytogenetic abnormalities: solving autism one chromosome at a time.

Martin CL, Ledbetter DH.

Curr Psychiatry Rep. 2007 Apr;9(2):141-7. Review.

PMID:
17389126
13.

Shared susceptibility region on chromosome 15 between autism and catatonia.

Chagnon YC.

Int Rev Neurobiol. 2006;72:165-78. Review.

PMID:
16697297
14.

The inv dup(15) or idic(15) syndrome: a clinically recognisable neurogenetic disorder.

Battaglia A.

Brain Dev. 2005 Aug;27(5):365-9. Epub 2005 Apr 22. Review.

PMID:
16023554
15.

[Humanized mouse model of autism].

Tamada K, Nakai N, Takumi T.

Seikagaku. 2011 Sep;83(9):841-5. Review. Japanese. No abstract available.

PMID:
22111376

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