Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/13811

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Campo DCValorIdioma
dc.contributor.authorCapitão, Liliana-
dc.contributor.authorSampaio, Adriana-
dc.contributor.authorSampaio, Cassandra-
dc.contributor.authorVasconcelos, Cristiana-
dc.contributor.authorFérnandez, Montse-
dc.contributor.authorGarayzábal Heinze, Elena-
dc.contributor.authorShenton, Martha E.-
dc.contributor.authorGonçalves, Óscar F.-
dc.date.accessioned2011-10-10T12:31:36Z-
dc.date.available2011-10-10T12:31:36Z-
dc.date.issued2011-
dc.date.submitted2011-
dc.identifier.issn0891-4222por
dc.identifier.urihttps://hdl.handle.net/1822/13811-
dc.description.abstractOne of the most intriguing characteristics of Williams Syndrome individuals is their hypersociability. The amygdala has been consistently implicated in the etiology of this social profile, particularly given its role in emotional and social behavior. This study examined amygdala volume and symmetry in WS individuals and in age and sex matched controls. Magnetic resonance imaging scans were obtained on a GE 1.5-T magnet with 1.5- mm contiguous slices and were used to measure whole gray matter, white matter and cerebrospinal fluid volumes, as well as amygdala volume (right and left). Results revealed significantly reduced intracranial volume in individuals with WS, compared with controls. There were no differences between groups in absolute amygdalae volume, although there was a relative increase in amygdalae volumes, when adjusted for total intracranial content. There were no inter-hemispheric differences in amygdalae volumes in both groups. These results suggest a relative increase in amygdala volume in WS compared with healthy controls that likely reflects abnormal neurodevelopmental processes of midline brain structures.por
dc.description.sponsorshipThis research was supported by the grants PIC/IC/83290/2007 from Fundac¸a˜o para a Cieˆncia e Tecnologia (Portugal) and Fundacio´n Alicia Koplowitz. (V convocatoria de 2009. Ayudas a la investigacio´n en psiquiatrı´a de la infancia y adolescencia enfermedades neurodegenerativas tempranas)por
dc.language.isoengpor
dc.publisherElsevier 1por
dc.rightsopenAccesspor
dc.subjectWilliams syndromepor
dc.subjectHypersociabilitypor
dc.subjectAmygdalapor
dc.subjectNeurodevelopmentpor
dc.titleMRI amygdala volume in Williams syndromepor
dc.typearticlepor
dc.peerreviewedyespor
sdum.publicationstatuspublishedpor
oaire.citationStartPage2767por
oaire.citationEndPage2772por
oaire.citationIssue6por
oaire.citationTitleResearch in Developmental Disabilitiespor
oaire.citationVolume32por
dc.identifier.doi10.1016/j.ridd.2011.05.033por
dc.identifier.pmid21752593por
dc.subject.wosSocial Sciencespor
dc.subject.wosScience & Technologypor
sdum.journalResearch in Developmental Disabilitiespor
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