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- Journal Article
- A1
- open access
Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD
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- Journal Article
- A1
- open access
The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter
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A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD
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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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Mutation analysis of candidate genes for chromosome 17-linked tau-negative FTD
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Possible association of nicastrin polymorphisms and Alzheimer disease in the Finnish population
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Octapeptide repeat insertions in the prion protein gene and early onset dementia
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Tau (MAPT) mutation Arg406Trp presenting clinically with Alzheimer disease does not share a common founder in western Europe
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Prospective Belgian study of neurodegenerative and vascular dementia: APOE genotype effects