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dc.contributor.authorGenro, Júlia Pasqualinipt_BR
dc.contributor.authorRoman, Tatianapt_BR
dc.contributor.authorRohde, Luis Augusto Paimpt_BR
dc.contributor.authorHutz, Mara Helenapt_BR
dc.date.accessioned2014-02-28T01:50:56Zpt_BR
dc.date.issued2012pt_BR
dc.identifier.issn1415-4757pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/87999pt_BR
dc.description.abstractAttention-Deficit/Hyperactivity Disorder (ADHD) is a common psychiatric condition of children worldwide. This disorder is defined by a combination of symptoms of inattention and hyperactivity/impulsivity. Diagnosis is based on a sufficient number of symptoms causing impairment in these two domains determining several problems in personal and academic life. Although genetic and environmental factors are important in ADHD etiology, how these factors influence the brain and consequently behavior is still under debate. It seems to be consensus that a fronto-subcortical dysfunction is responsible, at least in part, for the ADHD phenotype spectrum. The main results from association and pharmacogenetic studies performed in Brazil are discussed. The investigations performed so far on ADHD genetics in Brazil and elsewhere are far from conclusive. New plausible biological hypotheses linked to neurotransmission and neurodevelopment, as well as new analytic approaches are needed to fully disclose the genetic component of the disorder.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofGenetics and molecular biology. Ribeirão Preto. Vol. 35, n. 4 supl (Dec. 2012), p. 932-938pt_BR
dc.rightsOpen Accessen
dc.subjectTranstorno do déficit de atenção com hiperatividadept_BR
dc.subjectADHDen
dc.subjectcandidate genesen
dc.subjectGenéticapt_BR
dc.subjectPatologia molecularpt_BR
dc.subjectpharmacogeneticsen
dc.subjectCriançapt_BR
dc.subjectAdolescentept_BR
dc.titleThe brazilian contribution to attention-deficit/hyperactivity disorder molecular genetics in children and adolescentspt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb000876356pt_BR
dc.type.originNacionalpt_BR


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