Show
Sort by
-
- Journal Article
- A1
- open access
Extended FTLD pedigree segregating a Belgian GRN-null mutation : neuropathological heterogeneity in one family
-
- Journal Article
- A1
- open access
Clinical variability and onset age modifiers in an extended Belgian GRN founder family
-
- Journal Article
- A1
- open access
Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort
-
Clinical evidence of disease anticipation in families segregating a C9orf72 repeat expansion
-
- Journal Article
- A1
- open access
TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis
-
- Journal Article
- A1
- open access
Clinical features of TBKI carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort
-
- Journal Article
- A1
- open access
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort
-
- Journal Article
- A1
- open access
Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains
-
Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia
-
- Journal Article
- A1
- open access
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration
-
Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patients
-
Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort
-
A pan-European study of the C9orf72 repeat associated with FTLD : geographic prevalence, genomic instability, and intermediate repeats
-
- Journal Article
- A1
- open access
The genetics and neuropathology of frontotemporal lobar degeneration
-
Identification of novel causal genes for frontotemporal lobar degeneration using whole genome sequencing
-
Ataxin-2 polyQ expansions in FTLD-ALS spectrum disorders in Flanders-Belgian cohorts
-
Distinct clinical characteristics of C9orf72 expansion carriers compared to GRN, MAPT and non-mutation carries in a Flanders-Belgian FTLD cohort
-
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
-
TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort
-
Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS