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A bile acid protects against motor and cognitive deficits and reduces striatal degeneration in the 3-nitropropionic acid model of Huntington's disease

dc.contributor.authorKeene, CD
dc.contributor.authorRodrigues, CMP
dc.contributor.authorEich, T
dc.contributor.authorLinehan-Stieers, C
dc.contributor.authorAbt, A
dc.contributor.authorKren, BT
dc.contributor.authorSteer, CJ
dc.contributor.authorLow, WC
dc.date.accessioned2015-12-30T10:17:24Z
dc.date.available2015-12-30T10:17:24Z
dc.date.issued2001
dc.description.abstractThere is currently no effective treatment for Huntington's disease (HD), a progressive, fatal, neurodegenerative disorder characterized by motor and cognitive deterioration. It is well established that HD is associated with perturbation of mitochondrial e
dc.formatapplication/pdf
dc.identifier.citationEXPERIMENTAL NEUROLOGY. - Vol. 171, n. 2 (OCT 2001), p. 351-360
dc.identifier.doihttp://dx.doi.org/10.1006/exnr.2001.7755
dc.identifier.issn0014-4886
dc.identifier.urihttp://hdl.handle.net/10451/21050
dc.language.isoeng
dc.publisherACADEMIC PRESS INC
dc.subjectNeurosciences
dc.titleA bile acid protects against motor and cognitive deficits and reduces striatal degeneration in the 3-nitropropionic acid model of Huntington's disease
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage360por
oaire.citation.startPage351por
oaire.citation.titleEXPERIMENTAL NEUROLOGYpor
oaire.citation.volumeVol. 171por
rcaap.rightsrestrictedAccess
rcaap.typearticle

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