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In-depth phenotypic description of TBK1 mutations ; a frequent cause of FTD and ALS in the Flanders-Belgian population
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Extensive genetic and phenotypic description of MAPT p.R406W in the Flanders-Belgian population
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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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Status update and interim results from the Asymptomatic Carotid Surgery Trial-2 (ACST-2)
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Organisation of inhospital acute stroke care and minimum criteria for stroke care units: recommendations of the Belgian Stroke Council
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Case-control study of environmental risk factors for Parkinson's disease in Belgium
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Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutation
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Experimental gerontology in Belgium: from model organisms to age-related pathologies.