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Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort
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Clinical evidence of disease anticipation in families segregating a C9orf72 repeat expansion
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- Journal Article
- A1
- open access
TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis
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- Journal Article
- A1
- open access
Clinical features of TBKI carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort
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- Journal Article
- A1
- open access
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort
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Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia
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Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort
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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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Identification of novel causal genes for frontotemporal lobar degeneration using whole genome sequencing
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Distinct clinical characteristics of C9orf72 expansion carriers compared to GRN, MAPT and non-mutation carries in a Flanders-Belgian FTLD cohort
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A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum : a gene identification study
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Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS
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Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS
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Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia
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Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family
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Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region