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Association of Parkinson disease to PARK16 in a Chilean sample
(Elsevier, 2011-01)
HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin
(WILEY-LISS, DIV JOHN WILEY & SONS, 2006-09)
Inverse Association between Cancer and Dementia of the Alzheimer’s Type
(Nova Science Publishers, Inc., 2008)
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase
(NATURE PUBLISHING GROUP, 2006-10)
Effects of ATP, Mg2+, and redox agents on the Ca2+ dependence of RyR channels from rat brain cortex
(AMER PHYSIOLOGICAL SOC, 2007-07)
ATP13A2 variants in early-onset Parkinson's disease patients and controls
(John Wiley and Sons Inc., 2009)