Keene, CDRodrigues, CMPEich, TLinehan-Stieers, CAbt, AKren, BTSteer, CJLow, WC2015-12-302015-12-302001EXPERIMENTAL NEUROLOGY. - Vol. 171, n. 2 (OCT 2001), p. 351-3600014-4886http://hdl.handle.net/10451/21050There 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 eapplication/pdfengNeurosciencesA bile acid protects against motor and cognitive deficits and reduces striatal degeneration in the 3-nitropropionic acid model of Huntington's diseasejournal articlehttp://dx.doi.org/10.1006/exnr.2001.7755