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- Journal Article
- A1
- open access
Clinical variability and onset age modifiers in an extended Belgian GRN founder family
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- Journal Article
- A1
- open access
Extended FTLD pedigree segregating a Belgian GRN-null mutation : neuropathological heterogeneity in one family
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Teenage-onset progressive myoclonic epilepsy due to a familial C9orf72 repeat expansion
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Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients
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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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- Journal Article
- A1
- open access
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian 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