- ORCID iD
- 0000-0003-1278-6605
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- Journal Article
- A1
- open access
Therapy-induced electrophysiological changes in primary progressive aphasia : a preliminary study
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- Journal Article
- A1
- open access
Mutations in RNU7-1 weaken secondary RNA structure, induce MCP-1 and CXCL10 in CSF, and result in Aicardi-Goutières syndrome with severe end-organ involvement
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Novel mutations in RNU7-1 weaken secondary RNA structure, induce MCP-1 and CXCL10 in CSF and result in Aicardi-Goutières syndrome with severe end-organ involvement
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Proteinopathies of frontotemporal lobar degeneration : investigating the impact of vascular contributions
(2021) -
A case series of verbal semantic processing in primary progressive aphasia : evidence from the N400 effect
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Hippocampal sclerosis in frontotemporal dementia : when vascular pathology meets neurodegeneration
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- Journal Article
- A1
- open access
The electrophysiological correlates of phoneme perception in primary progressive aphasia : a preliminary case series
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- Journal Article
- A1
- open access
End of dose interval symptoms in patients treated with natalizumab : a role for serum cytokines?
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A genetic answer to a neuropsychiatric challenge
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Long lasting trigeminal neuropathy, limbic encephalitis and abdominal ganglionitis without primary cancer : an atypical case of Hu-Antibody syndrome
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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
Amyloid-β1–43 cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations
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Dementia, end of life, and euthanasia : a survey among dementia specialists organized by the Belgian Dementia Council
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- Journal Article
- A1
- open access
Loss of DPP6 in neurodegenerative dementia : a genetic player in the dysfunction of neuronal excitability
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- Journal Article
- A1
- open access
An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's disease
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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
No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients
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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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- Journal Article
- A1
- open access
Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort
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Teenage-onset progressive myoclonic epilepsy due to a familial C9orf72 repeat expansion
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Impaired processing of serial order determines working memory impairments in Alzheimer’s disease
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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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- Miscellaneous
- open access
Bilingualism and cognitive decline : a story of pride and prejudice
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Clinical evidence of disease anticipation in families segregating a 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
Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD
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- Journal Article
- A2
- open access
Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD
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106 FTD cases with refined neuropathological confirmation
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PSP and small vessel disease : more than occasional co-occurence?
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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
Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation
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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
Clinical features of TBKI carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort
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Alzheimer's disease, apolipoprotein E and hormone replacement therapy
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- Miscellaneous
- open access
Dementia : diagnosis, behaviour management, ethical issues
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- Journal Article
- A1
- open access
A 22-single nucleotide polymorphism Alzheimer's disease risk score correlates with family history, onset age, and cerebrospinal fluid Aβ42
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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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- Journal Article
- A1
- open access
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort
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Bilingualism delays clinical manifestation of Alzheimer's disease
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Bilingualism delays clinical manifestation of Alzheimer's disease
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- Journal Article
- A1
- open access
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration
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Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia
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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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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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Late-onset post-irradiation vasculopathy of the posterior cerebral vasculature
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- Journal Article
- A1
- open access
The genetics and neuropathology of frontotemporal lobar degeneration
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- Book Chapter
- open access
Neoplasm related encephalopathies
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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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Repetitive transcranial magnetic stimulation in patients with progressive supranuclear palsy : a pilot study
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Characteristics and outcomes of patients with seizures according to the time of onset in relation to stroke
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A massive extradural cerebrospinal fluid collection
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Preliminary screening results for fabry disease in young stroke patients reveals a new mutation
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Saccadic ping pong gaze in coma
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Deep brain stimulation of the internal pallidum in multiple system atrophy
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Tic reduction in Tourette's disorder with olanzapine