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Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains
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- Journal Article
- A1
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Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration
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Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia
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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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Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort
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Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patients
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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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Ataxin-2 polyQ expansions in FTLD-ALS spectrum disorders in Flanders-Belgian cohorts
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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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- Journal Article
- A1
- open access
The genetics and neuropathology of frontotemporal lobar degeneration