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Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
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The molecular genetics of early-onset Alzheimer's disease
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Neuropathological and biochemical characterization of a familial FTD patient carrying PS1 GLY183VAL
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Novel German APP V715A mutation associated with presenile Alzheimer's disease
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In vitro analysis of Alzheimer's disease-related presenilin 1 and 2 mutations: effect on beta-amyloid processing
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Systematic analysis of the effect of novel Alzheimer disease PS1/2 mutations on A beta secretion
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Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutation
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Transforming growth factor-β, basement membrane components and heparan sulphate proteoglycans in experimental hepatic schistosomiasis mansoni