Show
Sort by
-
- Journal Article
- A1
- open access
CRISPR/Cas9 screen in human iPSC-derived cortical neurons identifies NEK6 as a novel disease modifier of C9orf72 poly(PR) toxicity
-
- Journal Article
- A1
- open access
Acquired pedophilia : international Delphi-method-based consensus guidelines
-
- Journal Article
- A1
- open access
No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriers
-
Hippocampal sclerosis in frontotemporal dementia : when vascular pathology meets neurodegeneration
-
GAD65 autoimmune encephalitis : a cause of rapidly evolving frontotemporal atrophy
-
- Journal Article
- A1
- open access
No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients
-
- Journal Article
- A1
- open access
Clinical variability and onset age modifiers in an extended Belgian GRN founder family
-
- Journal Article
- A1
- open access
Extended FTLD pedigree segregating a Belgian GRN-null mutation : neuropathological heterogeneity in one family
-
Teenage-onset progressive myoclonic epilepsy due to a familial C9orf72 repeat expansion
-
- Journal Article
- A1
- open access
Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort