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Pooled analysis of patients with inherited prion disease caused by two- to twelve-octapeptide repeat insertions in the prion protein gene (PRNP)
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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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Proteinopathies of frontotemporal lobar degeneration : investigating the impact of vascular contributions
(2021) -
- Journal Article
- A1
- open access
The electrophysiological correlates of phoneme perception in primary progressive aphasia : a preliminary case series
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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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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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Long lasting trigeminal neuropathy, limbic encephalitis and abdominal ganglionitis without primary cancer : an atypical case of Hu-Antibody syndrome
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De diagnostische toepassing van taalgerelateerde potentialen in de non-fluente variant van primair progressieve afasie : een gevalsstudie