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dc.contributor.authorBrambati, Simona Maria
dc.contributor.authorTermine, Cristiano
dc.contributor.authorRuffino, Milena
dc.contributor.authorStella, Giacomo
dc.contributor.authorDe Fazio, Francesco
dc.contributor.authorCappa, Stefano F.
dc.contributor.authorPerani, Daniela
dc.date.accessioned2019-05-29T17:15:08Z
dc.date.availableNO_RESTRICTIONfr
dc.date.available2019-05-29T17:15:08Z
dc.date.issued2004
dc.identifier.urihttp://hdl.handle.net/1866/22079
dc.publisherAmerican Academy of Neurologyfr
dc.titleRegional reductions of gray matter volume in familial dyslexiafr
dc.typeArticlefr
dc.contributor.affiliationUniversité de Montréal. Faculté des arts et des sciences. Département de psychologiefr
dc.identifier.doi10.1212/01.wnl.0000134673.95020.ee
dcterms.abstractAn in vivo anatomic study of gray matter volume was performed in a group of familial dyslexic individuals, using an optimized method of voxel-based morphometry. Focal abnormalities in gray matter volume were observed bilaterally in the planum temporale, inferior temporal cortex, and cerebellar nuclei, suggesting that the underlying anatomic abnormalities may be responsible for defective written language acquisition in these subjects.fr
dcterms.isPartOfurn:ISSN:0028-3878fr
dcterms.isPartOfurn:ISSN:1526-632Xfr
dcterms.languageengfr
UdeM.ReferenceFournieParDeposantBrambati, S.M., C. Termine, M. Ruffino, G. Stella, F. Fazio, S.F. Cappa, and D. Perani, Regional reductions of gray matter volume in familial dyslexia Neurology, 2004. 63(4): p. 742-5.fr
UdeM.VersionRioxxVersion publiée / Version of Recordfr
oaire.citationTitleNeurology
oaire.citationVolume63
oaire.citationIssue4
oaire.citationStartPage742
oaire.citationEndPage745


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