Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/62190

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dc.contributor.authorSampaio, Adrianapor
dc.contributor.authorBouix, Sylvainpor
dc.contributor.authorSousa, Nunopor
dc.contributor.authorVasconcelos, Cristianapor
dc.contributor.authorFérnandez, Montsepor
dc.contributor.authorShenton, Martha E.por
dc.contributor.authorGonçalves, Óscar F.por
dc.date.accessioned2019-11-18T12:26:51Z-
dc.date.issued2013-05-
dc.identifier.citationSampaio, A., Bouix, S., Sousa, N., Vasconcelos, C., Férnandez, M., Shenton, M. E., & Gonçalves, O. F. (2013). Morphometry of corpus callosum in Williams syndrome: shape as an index of neural development. Brain Structure and Function, 218(3), 711-720.por
dc.identifier.issn1863-2653-
dc.identifier.urihttps://hdl.handle.net/1822/62190-
dc.description.abstractBrain abnormalities in Williams syndrome (WS) have been consistently reported, despite few studies have devoted attention to connectivity between different brain regions in WS. In this study, we evaluated corpus callosum (CC) morphometry: bending angle, length, thickness and curvature of CC using a new shape analysis method in a group of 17 individuals with WS matched with a typically developing group. We used this multimethod approach because we hypothesized that neurodevelopmental abnormalities might result in both volume changes and structure deformation. Overall, we found reduced absolute CC cross-sectional area and volume in WS (mean CC and subsections). In parallel, we observed group differences regarding CC shape and thickness. Specifically, CC of WS is morphologically different, characterized by a larger bending angle and being more curved in the posterior part. Moreover, although CC in WS is shorter, a larger relative thickness of CC was found in all callosal sections. Finally, groups differed regarding the association between CC measures, age, white matter volume and cognitive performance. In conclusions, abnormal patterns of CC morphology and shape may be implicated in WS cognitive and behavioural phenotype.por
dc.description.sponsorshipPIC/IC/83290/2007 and PTDC/PSI-PCL/115316/2009 from Fundação para a Ciência e Tecnologia (Portugal). This study was also supported, in part, by grants from the National Institutes of Health (K05 MH070047)por
dc.language.isoengpor
dc.publisherSpringer Heidelbergpor
dc.rightsrestrictedAccesspor
dc.subjectAdolescentpor
dc.subjectAdultpor
dc.subjectCase-Control Studiespor
dc.subjectChildpor
dc.subjectCognition Disorderspor
dc.subjectCorpus Callosumpor
dc.subjectElectroencephalographypor
dc.subjectFemalepor
dc.subjectHumanspor
dc.subjectImage Processing, Computer-Assistedpor
dc.subjectMagnetic Resonance Imagingpor
dc.subjectMalepor
dc.subjectModels, Neurologicalpor
dc.subjectNeural Pathwayspor
dc.subjectNeuropsychological Testspor
dc.subjectStatistics as Topicpor
dc.subjectWilliams Syndromepor
dc.subjectYoung Adultpor
dc.subjectBrain Mappingpor
dc.subjectMRIpor
dc.subjectNeurodevelopmentpor
dc.titleMorphometry of corpus callosum in Williams syndrome: shape as an index of neural developmentpor
dc.typearticlepor
dc.peerreviewedyespor
dc.relation.publisherversionhttps://link.springer.com/article/10.1007/s00429-012-0423-4por
oaire.citationStartPage711por
oaire.citationEndPage720por
oaire.citationIssue3por
oaire.citationVolume218por
dc.identifier.eissn1863-2661-
dc.identifier.doi10.1007/s00429-012-0423-4por
dc.date.embargo10000-01-01-
dc.identifier.pmid22648762por
dc.subject.fosCiências Médicas::Medicina Básicapor
dc.subject.wosScience & Technologypor
sdum.journalBrain Structure & Functionpor
Aparece nas coleções:ICVS - Artigos em revistas internacionais / Papers in international journals

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