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Results: 1 to 20 of 130

1.

The early origins of autism.

Rodier PM.

Sci Am. 2000 Feb;282(2):56-63. Review. No abstract available.

PMID:
10710787
[PubMed - indexed for MEDLINE]
2.

No association between HOXA1 and HOXB1 genes and autism spectrum disorders (ASD).

Talebizadeh Z, Bittel DC, Miles JH, Takahashi N, Wang CH, Kibiryeva N, Butler MG.

J Med Genet. 2002 Nov;39(11):e70. No abstract available.

PMID:
12414832
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Development. New hints into the biological basis of autism.

Stokstad E.

Science. 2001 Oct 5;294(5540):34-7. No abstract available.

PMID:
11588233
[PubMed - indexed for MEDLINE]
4.

Early infantile autism in monozygotic twins.

Eshkevari HS.

J Autism Dev Disord. 1979 Mar;9(1):105-9.

PMID:
438110
[PubMed - indexed for MEDLINE]
5.

Minor form of trigonocephaly is an autistic skull shape? A suggestion based on homeobox gene variants and MECP2 mutations.

Ijichi S, Ijichi N.

Med Hypotheses. 2002 Apr;58(4):337-9.

PMID:
12027529
[PubMed - indexed for MEDLINE]
6.

Infantile autism in monozygotic twins.

Salimi-Eshkevari H.

J Am Acad Child Psychiatry. 1985 Sep;24(5):643-6. No abstract available.

PMID:
4045065
[PubMed - indexed for MEDLINE]
7.

[Early infantile autism in twins (review)].

Moskalenko VD.

Zh Nevropatol Psikhiatr Im S S Korsakova. 1979;79(10):1435-41. Review. Russian. No abstract available.

PMID:
386670
[PubMed - indexed for MEDLINE]
8.

Neuroanatomic alterations and social and communication deficits in monozygotic twins discordant for autism disorder.

Mitchell SR, Reiss AL, Tatusko DH, Ikuta I, Kazmerski DB, Botti JA, Burnette CP, Kates WR.

Am J Psychiatry. 2009 Aug;166(8):917-25. doi: 10.1176/appi.ajp.2009.08101538. Epub 2009 Jul 15.

PMID:
19605538
[PubMed - indexed for MEDLINE]
9.

Genetic influences and infantile autism.

Folstein S, Rutter M.

Nature. 1977 Feb 24;265(5596):726-8. No abstract available.

PMID:
558516
[PubMed - indexed for MEDLINE]
10.

Monozygotic twins concordant for infantile autism: follow-up.

Campbell M, Dominijanni C, Schneider B.

Br J Psychiatry. 1977 Dec;131:616-22.

PMID:
563753
[PubMed - indexed for MEDLINE]
11.

Neuroanatomic variation in monozygotic twin pairs discordant for the narrow phenotype for autism.

Kates WR, Burnette CP, Eliez S, Strunge LA, Kaplan D, Landa R, Reiss AL, Pearlson GD.

Am J Psychiatry. 2004 Mar;161(3):539-46.

PMID:
14992981
[PubMed - indexed for MEDLINE]
12.

Lack of association of HOXA1 and HOXB1 variants with autism in the Indian population.

Sen B, Sinha S, Ahmed S, Ghosh S, Gangopadhyay PK, Usha R.

Psychiatr Genet. 2007 Feb;17(1):1. No abstract available.

PMID:
17167333
[PubMed - indexed for MEDLINE]
13.

Lack of association of HOXA1 and HOXB1 mutations and autism in Sicilian (Italian) patients.

Romano V, Calì F, Mirisola M, Gambino G, D' Anna R, Di Rosa P, Seidita G, Chiavetta V, Aiello F, Canziani F, De Leo G, Ayala GF, Elia M.

Mol Psychiatry. 2003 Aug;8(8):716-7. No abstract available.

PMID:
12888798
[PubMed - indexed for MEDLINE]
14.

Autism and epilepsy: organic connections?

Lenti C.

J Am Acad Child Adolesc Psychiatry. 1992 Mar;31(2):370. No abstract available.

PMID:
1564042
[PubMed - indexed for MEDLINE]
15.

A 12Mb deletion at 7q33-q35 associated with autism spectrum disorders and primary amenorrhea.

Rossi E, Verri AP, Patricelli MG, Destefani V, Ricca I, Vetro A, Ciccone R, Giorda R, Toniolo D, Maraschio P, Zuffardi O.

Eur J Med Genet. 2008 Nov-Dec;51(6):631-8. doi: 10.1016/j.ejmg.2008.06.010. Epub 2008 Jul 16.

PMID:
18675947
[PubMed - indexed for MEDLINE]
16.

The HOXA1 A218G polymorphism and autism: lack of association in white and black patients from the South Carolina Autism Project.

Collins JS, Schroer RJ, Bird J, Michaelis RC.

J Autism Dev Disord. 2003 Jun;33(3):343-8.

PMID:
12908836
[PubMed - indexed for MEDLINE]
17.

No association between the EN2 gene and autistic disorder.

Zhong H, Serajee FJ, Nabi R, Huq AH.

J Med Genet. 2003 Jan;40(1):e4. No abstract available.

PMID:
12525552
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families.

Li J, Tabor HK, Nguyen L, Gleason C, Lotspeich LJ, Spiker D, Risch N, Myers RM.

Am J Med Genet. 2002 Jan 8;114(1):24-30.

PMID:
11840501
[PubMed - indexed for MEDLINE]
19.

Expansion of the ARX spectrum.

Wallerstein R, Sugalski R, Cohn L, Jawetz R, Friez M.

Clin Neurol Neurosurg. 2008 Jun;110(6):631-4. doi: 10.1016/j.clineuro.2008.03.007. Epub 2008 May 6.

PMID:
18462864
[PubMed - indexed for MEDLINE]
20.

Discovery of allelic variants of HOXA1 and HOXB1: genetic susceptibility to autism spectrum disorders.

Ingram JL, Stodgell CJ, Hyman SL, Figlewicz DA, Weitkamp LR, Rodier PM.

Teratology. 2000 Dec;62(6):393-405.

PMID:
11091361
[PubMed - indexed for MEDLINE]
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