Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12530/27400
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dc.contributor.authorPulido-Valdeolivas, Irene
dc.contributor.authorGómez-Andrés, David
dc.contributor.authorSanz-Gallego, Irene
dc.contributor.authorRausell, Estrella
dc.contributor.authorArpa, Javier
dc.date.accessioned2019-06-28T15:15:22Z-
dc.date.available2019-06-28T15:15:22Z-
dc.date.issued2016
dc.identifier.citationCerebellum Ataxias.2016;(3):4
dc.identifier.issn2053-8871
dc.identifier.urihttps://hdl.handle.net/20.500.12530/27400-
dc.description.abstractSpinocerebellar ataxia type 3 (SCA3) is a neurodegenerative disorder that affects the cerebellar system and other subcortical regions of the brain. As for other cerebellar diseases, the severity of this type of ataxia can be assessed with the Scale for Assessment and Rating of Ataxia (SARA) which gives a total score that reflects functional impairment out of 8 cerebellar function tests. SCA3 patients score profile is heterogeneous on at the start of follow up. This study investigates possible patterns in those profiles and analyses the impact of other usually concurrent signs of impairment of extracerebellar motor systems in that profile variability by means of multivariate statistical approaches.
dc.language.isoeng
dc.rightsopenAccess-
dc.subjectAtaxia
dc.subjectMachado-Joseph disease
dc.subjectMultivariate analysis
dc.subjectNetwork analysis
dc.subjectSARA scale
dc.subjectSPECT
dc.titlePatterns of motor signs in spinocerebellar ataxia type 3 at the start of follow-up in a reference unit.
dc.typeArtículo
dc.identifier.pubmedID26909158
dc.format.volume3
dc.format.page4
dc.identifier.journalCerebellum & ataxias
dc.identifier.doi10.1186/s40673-016-0042-6
dc.identifier.pmcPMC4763420
dc.pubmedtypeJournal Article
Appears in Collections:Fundaciones e Institutos de Investigación > IIS H. U. La Paz > Artículos
Hospitales > H. U. Infanta Sofía > Artículos
Hospitales > H. U. La Paz > Artículos

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