Article
Longitudinal analysis of the electroencephalogram and sleep phenotype in the R6/2 mouse model of Huntington's disease.
Brain : a journal of neurology - 1 Jul 2013
Fisher Simon P, Black Sarah W, Schwartz Michael D, Wilk Alan J, Chen Tsui-Ming, Lincoln Webster U, Liu Helen W, Kilduff Thomas S, Morairty Stephen R
Abstract excerpt
Deficits in sleep and circadian organization have been identified as common early features in patients with Huntington's disease that correlate with symptom severity and may be instrumental in disease progression. Studies in Huntington's disease gene carriers suggest that alterations in the electroencephalogram may reflect underlying neuronal dysfunction that is present in the premanifest stage. We conducted a...
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