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Usefulness of genetic characterization of narcolepsy and hypersomnia on phenotype definition: a study in Portuguese patients

dc.contributor.authorMartins-da-Silva, António
dc.contributor.authorLopes, João
dc.contributor.authorRamalheira, João
dc.contributor.authorCarvalho, Cláudia
dc.contributor.authorCunha, Daniela
dc.contributor.authorCosta, Paulo P
dc.contributor.authorSilva, M Berta
dc.date.accessioned2015-11-02T13:39:26Z
dc.date.available2015-11-02T13:39:26Z
dc.date.issued2014-01-16
dc.description.abstractThe determination of human leukocyte antigen (HLA) class II genotype is widely used to confirm the diagnosis of narcolepsy with or without cataplexy. The HLA genotyping is reliable, easy to perform and reassures the clinician. It is also less invasive than other methodologies and is in accordance with the autoimmune hypothesis for the origin of narcolepsy. AIM. To assess the usefulness of genetic markers (HLA) in the differential diagnosis between different sleep disorders and their relevance in the context of our population.pt_PT
dc.identifier.citationRev Neurol 2014; 58 (2): 49-54pt_PT
dc.identifier.issn0210-0010
dc.identifier.urihttp://hdl.handle.net/10400.16/1875
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherRevista De Neurologiapt_PT
dc.relation.publisherversionhttp://www.revneurol.com/sec/resumen.php?or=pubmed&id=2013361#pt_PT
dc.subjectHLA-DQB1*06:02pt_PT
dc.subjectHypocretinpt_PT
dc.subjectIdiopathic hypersomniapt_PT
dc.subjectNarcolepsypt_PT
dc.subjectNarcolepsy with cataplexypt_PT
dc.subjectSleep disorderspt_PT
dc.titleUsefulness of genetic characterization of narcolepsy and hypersomnia on phenotype definition: a study in Portuguese patientspt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlaceSpainpt_PT
oaire.citation.endPage54pt_PT
oaire.citation.startPage49pt_PT
oaire.citation.titleRevista de neurologiapt_PT
oaire.citation.volume58(2)pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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