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A pan-European study of the C9orf72 repeat associated with FTLD : geographic prevalence, genomic instability, and intermediate repeats
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Genetic variant in the HSPB1 promoter region impairs the HSP27 stress response
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Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family
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Mean age-of-onset of familial Alzheimer disease caused by presenilin mutations correlates with both increased Aβ42 and decreased Aβ40
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- Journal Article
- A1
- open access
Tau is central in the genetic Alzheimer-frontotemporal dementia spectrum
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Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sample
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A novel presenilin 1 mutation (gly183val) is associated with Pick's disease in the absence of β-amyloid plaques
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A novel presenilin 1 mutation associated with Pick's disease but not β-amyloid plaques
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The gene encoding nicastrin, a major γ-secretase component, modifies risk for familial early-onset Alzheimer disease in a Dutch population-based sample
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The TNFRSF6 gene is not implicated in familial early-onset Alzheimer's disease
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Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression