Publicação
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.author | Keene, CD | |
| dc.contributor.author | Rodrigues, CMP | |
| dc.contributor.author | Eich, T | |
| dc.contributor.author | Linehan-Stieers, C | |
| dc.contributor.author | Abt, A | |
| dc.contributor.author | Kren, BT | |
| dc.contributor.author | Steer, CJ | |
| dc.contributor.author | Low, WC | |
| dc.date.accessioned | 2015-12-30T10:17:24Z | |
| dc.date.available | 2015-12-30T10:17:24Z | |
| dc.date.issued | 2001 | |
| dc.description.abstract | There 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.format | application/pdf | |
| dc.identifier.citation | EXPERIMENTAL NEUROLOGY. - Vol. 171, n. 2 (OCT 2001), p. 351-360 | |
| dc.identifier.doi | http://dx.doi.org/10.1006/exnr.2001.7755 | |
| dc.identifier.issn | 0014-4886 | |
| dc.identifier.uri | http://hdl.handle.net/10451/21050 | |
| dc.language.iso | eng | |
| dc.publisher | ACADEMIC PRESS INC | |
| dc.subject | Neurosciences | |
| dc.title | A bile acid protects against motor and cognitive deficits and reduces striatal degeneration in the 3-nitropropionic acid model of Huntington's disease | |
| dc.type | journal article | |
| dspace.entity.type | Publication | |
| oaire.citation.endPage | 360 | por |
| oaire.citation.startPage | 351 | por |
| oaire.citation.title | EXPERIMENTAL NEUROLOGY | por |
| oaire.citation.volume | Vol. 171 | por |
| rcaap.rights | restrictedAccess | |
| rcaap.type | article |
