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1.
Hypomorphic variants of cationic amino acid transporter 3 in males with autism spectrum disorders.
Amino Acids
; 47(12): 2647-58, 2015 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-26215737
2.
Acute behavioral crises in psychiatric inpatients with autism spectrum disorder (ASD): recognition of concomitant medical or non-ASD psychiatric conditions predicts enhanced improvement.
Res Dev Disabil
; 38: 242-55, 2015 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-25575287
3.
Are there cultural differences in parental interest in early diagnosis and genetic risk assessment for autism spectrum disorder?
Front Pediatr
; 2: 32, 2014.
Artículo
en Inglés
| MEDLINE | ID: mdl-24795872
4.
A scoring strategy combining statistics and functional genomics supports a possible role for common polygenic variation in autism.
Front Genet
; 5: 33, 2014.
Artículo
en Inglés
| MEDLINE | ID: mdl-24600472
5.
Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders.
Eur J Hum Genet
; 22(1): 71-8, 2014 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-23632794
6.
Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?
Mol Autism
; 4(1): 47, 2013 Dec 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-24289166
7.
Risk factors of acute behavioral regression in psychiatrically hospitalized adolescents with autism.
J Can Acad Child Adolesc Psychiatry
; 19(2): 100-8, 2010 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-20467546
8.
Epilepsy in simplex autism pedigrees is much lower than the rate in multiplex autism pedigrees.
Biol Psychiatry
; 74(3): e3-4, 2013 Aug 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-23507000
9.
Epilepsy in autism is associated with intellectual disability and gender: evidence from a meta-analysis.
Biol Psychiatry
; 64(7): 577-82, 2008 Oct 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-18565495
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