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No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriers
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Processing of laser-evoked potentials in patients with chronic whiplash-associated disorders, chronic fatigue syndrome, and healthy controls : a case–control study
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- Journal Article
- A1
- open access
Does motor cortex engagement during movement preparation differentially inhibit nociceptive processing in patients with chronic whiplash associated disorders, chronic fatigue syndrome and healthy controls? An experimental study
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Practices and opinions about disclosure of the diagnosis of Alzheimer’s disease to patients with MCI or dementia : a survey among Belgian medical experts in the field of dementia
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- Miscellaneous
- open access
Homozygous and compound heterozygous rare variants in VPS13C contribute to Lewy body diseases
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- Journal Article
- A1
- open access
Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide export
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- Journal Article
- A1
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Loss of DPP6 in neurodegenerative dementia : a genetic player in the dysfunction of neuronal excitability
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Medische zorg toegediend door de arts in verband met toxicomanie : risico’s, gevolgen en mogelijke oplossingen
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- Journal Article
- A1
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An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's disease
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- Journal Article
- A1
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Extended FTLD pedigree segregating a Belgian GRN-null mutation : neuropathological heterogeneity in one family
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- Journal Article
- A1
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Clinical variability and onset age modifiers in an extended Belgian GRN founder family
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- Journal Article
- A1
- open access
No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients
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Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients
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Clinical evidence of disease anticipation in families segregating a C9orf72 repeat expansion
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Alzheimer’s disease and driving : review of the literature and consensus guideline from Belgian dementia experts and the Belgian road safety institute endorsed by the Belgian Medical Association
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- Journal Article
- A1
- open access
TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis
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What is in a name? : comparing diagnostic criteria for chronic fatigue syndrome with or without fibromyalgia
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PSP and small vessel disease : more than occasional co-occurence?
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- Journal Article
- A2
- open access
Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD
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- Journal Article
- A1
- open access
Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation
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- Journal Article
- A1
- open access
Clinical features of TBKI carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort
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- Journal Article
- A1
- open access
A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease
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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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- 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
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Recovery of peripheral muscle function from fatiguing exercise and daily physical activity level in patients with multiple sclerosis: a case-control study
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Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia
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- Journal Article
- A1
- open access
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration
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Management of chronic sensitization, from drugs to physical therapy
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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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Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort
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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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- Journal Article
- A1
- open access
The genetics and neuropathology of frontotemporal lobar degeneration
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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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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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Evaluatie en behandeling van patiënten met chronische whiplashgeassocieerde aandoeningen: recente ontwikkelingen
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Neoplastic meningitis: a rare presentation of bronchial adenocarcinoma
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- Journal Article
- A1
- open access
Assessment of prosodic communicative efficiency in Parkinson's disease as judged by professional listeners
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Long-term functioning following whiplash injury : the role of social support and personality traits
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Recruitment bias in chronic pain research : whiplash as a model
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TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort
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Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family
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A novel presenilin 1 mutation associated with Pick's disease but not β-amyloid plaques
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Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt-Jakob disease phenotype
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Familial Creutzfeldt-Jakob disease in a patient carrying both a presenilin 1 missense substitution and a prion protein gene insertion