Utilize este identificador para referenciar este registo:
https://hdl.handle.net/1822/17404
Registo completo
Campo DC | Valor | Idioma |
---|---|---|
dc.contributor.author | Garayzábal Heinze, Elena | - |
dc.contributor.author | Capo, Magdalena | - |
dc.contributor.author | Moruno Lopéz, Esther | - |
dc.contributor.author | Gonçalves, Óscar F. | - |
dc.contributor.author | Férnandez, Montserrat | - |
dc.contributor.author | Lens, María | - |
dc.contributor.author | Sampaio, Adriana | - |
dc.date.accessioned | 2012-02-24T14:12:54Z | - |
dc.date.available | 2012-02-24T14:12:54Z | - |
dc.date.issued | 2012 | - |
dc.identifier.issn | 2047-3877 | por |
dc.identifier.uri | https://hdl.handle.net/1822/17404 | - |
dc.description.abstract | This study compares narrative production among three syndromes with genetic microdeletions: Williams syndrome (WS), Smith-Magenis syndrome (SMS), and Prader-Willi syndrome (PWS), characterized by intellectual disabilities and relatively spared language abilities. Our objective is to study the quality of narrative production in the context of a common intellectual disability. To elicit a narrative production, the task Frog! Where Are You was used. Then, structure, process, and content of the narrative process were analysed in the three genetic disorders:WS (n52), SMS (n52), and PWS (n52). Data show evidence of an overall low narrative quality in these syndromes, despite a high variability within different measures of narrative production. Results support the hypothesis that narrative is a highly complex cognitive process and that, in a context of intellectual disability, there is no evidence of particular ‘hypernarrativity’ in these syndromes. | por |
dc.description.sponsorship | This research was supported by the grants FEDER – 1 | por |
dc.language.iso | eng | por |
dc.publisher | Maney Publishing | por |
dc.rights | openAccess | por |
dc.subject | Williams syndrome | por |
dc.subject | Smith-Magenis syndrome | por |
dc.subject | Prader-Willi syndrome | por |
dc.subject | Narrative abilities | por |
dc.title | Uncommon genetic syndromes and narrative production - Case Studies with Williams, Smith-Magenis and Prader- Willi Syndromes | por |
dc.type | article | por |
dc.peerreviewed | yes | por |
sdum.publicationstatus | published | por |
oaire.citationStartPage | 48 | por |
oaire.citationEndPage | 65 | por |
oaire.citationIssue | 1 | por |
oaire.citationTitle | international journal of developmental disabilities | por |
oaire.citationVolume | 58 | por |
dc.identifier.doi | 10.1179/2047387711Y.0000000008 | por |
dc.subject.wos | Social Sciences | por |
dc.subject.wos | Science & Technology | por |
sdum.journal | international journal of developmental disabilities | por |
Aparece nas coleções: | CIPsi - Artigos (Papers) |
Ficheiros deste registo:
Ficheiro | Descrição | Tamanho | Formato | |
---|---|---|---|---|
JDD intersindromic narrative comparison.pdf | 192,81 kB | Adobe PDF | Ver/Abrir |