Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/11684

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dc.contributor.authorPinheiro, Ana P.-
dc.contributor.authorGaldo-Álvarez, Santiago-
dc.contributor.authorSampaio, Adriana-
dc.contributor.authorNiznikiewicz, Margaret-
dc.contributor.authorGonçalves, Óscar F.-
dc.date.accessioned2011-02-08T11:16:59Z-
dc.date.available2011-02-08T11:16:59Z-
dc.date.issued2010-
dc.identifier.citation"Research in Developmental Disabilities". ISSN 0891-4222. 31 (2010) 1412–1425.por
dc.identifier.issn0891-4222por
dc.identifier.urihttp://hdl.handle.net/1822/11684-
dc.description.abstractWilliams syndrome (WS), a genetic neurodevelopmental disorder due to microdeletion in chromosome 7, has been described as a syndrome with an intriguing socio-cognitive phenotype. Cognitively, the relative preservation of language and face processing abilities coexists with severe deficits in visual-spatial tasks, as well as in tasks involving abstract reasoning. However, in spite of early claims of the independence of language from general cognition in WS, a detailed investigation of language subcomponents has demonstrated several abnormalities in lexical-semantic processing. Nonetheless, the neurobiological processes underlying language processing in Williams syndrome remain to be clarified. The aim of this study was to examine the electrophysiological correlates of semantic processing in WS, taking typical development as a reference. A group of 12 individuals diagnosed with Williams syndrome, with age range between 9 and 31 years, was compared with a group of typically developing participants, individually matched in chronological age, gender and handedness. Participants were presented with sentences that ended with words incongruent (50%) with the previous sentence context or with words judged to be its best completion (50%), and they were asked to decide if the sentence made sense or not. Results in WS suggest atypical sensory ERP components (N100 and P200), preserved N400 amplitude, and abnormal P600 in WS, with the latter being related to late integration and re-analysis processes. These results may represent a physiological signature of underlying impaired on-line language processing in this disorderpor
dc.description.sponsorshipThis research was supported by a Doctoral Grant (SFRH/BD/35882/2007) awarded to the first author, as well as by the grant PIC/IC/83290/2007, both from FCT (Fundação para a Cieˆncia e a Tecnologia), in Portugal.por
dc.language.isoengpor
dc.publisherElsevierpor
dc.rightsrestrictedAccesspor
dc.subjectWilliams syndromepor
dc.subjectLanguagepor
dc.subjectSemantic processingpor
dc.subjectEvent-related potentialspor
dc.subjectNeurodevelopmentpor
dc.titleElectrophysiological correlates of semantic processing in Williams syndromepor
dc.typearticlepor
dc.peerreviewedyespor
dc.relation.publisherversiondoi:10.1016/j.ridd.2010.06.017por
sdum.pagination1412–1425por
sdum.publicationstatuspublishedpor
sdum.volume31por
oaire.citationStartPage1412por
oaire.citationEndPage1425por
oaire.citationIssue6por
oaire.citationVolume31por
dc.identifier.doi10.1016/j.ridd.2010.06.017por
dc.identifier.pmid20674263por
dc.subject.wosSocial Sciencespor
dc.subject.wosScience & Technologypor
sdum.journalResearch in Developmental Disabilitiespor
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