Patrick Cras
Patrick Cras
University of Antwerp
Geverifieerd e-mailadres voor uza.be
Geciteerd door
Geciteerd door
Fmr1 knockout mice: a model to study fragile X mental retardation
TDBFX Consorthium, CE Bakker, C Verheij, R Willemsen, R van der Helm, ...
Cell 78 (1), 23-33, 1994
Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the β–amyloid precursor protein gene
L Hendriks, CM van Duijn, P Cras, M Cruts, W Van Hul, F van Harskamp, ...
Nature genetics 1 (3), 218-221, 1992
10-year stroke prevention after successful carotid endarterectomy for asymptomatic stenosis (ACST-1): a multicentre randomised trial
A Halliday, M Harrison, E Hayter, X Kong, A Mansfield, J Marro, H Pan, ...
The Lancet 376 (9746), 1074-1084, 2010
Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease
I Zerr, K Kallenberg, DM Summers, C Romero, A Taratuto, U Heinemann, ...
Brain 132 (10), 2659-2668, 2009
Improved discrimination of AD patients using β-amyloid(1-42) and tau levels in CSF
F Hulstaert, K Blennow, A Ivanoiu, HC Schoonderwaldt, ...
Neurology 52 (8), 1555-1555, 1999
Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile‐X syndrome: a quantitative examination
SA Irwin, B Patel, M Idupulapati, JB Harris, RA Crisostomo, BP Larsen, ...
American journal of medical genetics 98 (2), 161-167, 2001
A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene†…
I Gijselinck, T Van Langenhove, J van der Zee, K Sleegers, S Philtjens, ...
The Lancet Neurology 11 (1), 54-65, 2012
European Society for Swallowing Disorders–European Union Geriatric Medicine Society white paper: oropharyngeal dysphagia as a geriatric syndrome
LWJ Baijens, P Clavť, P Cras, O Ekberg, A Forster, GF Kolb, JC Leners, ...
Clinical interventions in aging, 1403-1428, 2016
Detection of proteins in normal and Alzheimer's disease cerebrospinal fluid with a sensitive sandwich enzyme‐linked immunosorbent assay
M Vandermeeren, M Mercken, E Vanmechelen, J Six, A Van de Voorde, ...
Journal of neurochemistry 61 (5), 1828-1834, 1993
The abnormal phosphorylation of tau protein at Ser-202 in Alzheimer disease recapitulates phosphorylation during development.
M Goedert, R Jakes, RA Crowther, J Six, U LŁbke, M Vandermeeren, ...
Proceedings of the National Academy of Sciences 90 (11), 5066-5070, 1993
A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies
MA Nalls, R Duran, G Lopez, M Kurzawa-Akanbi, IG McKeith, ...
JAMA neurology 70 (6), 727-735, 2013
Mapping of a gene predisposing to early–onset Alzheimer's disease to chromosome 14q24. 3
C Van Broeckhoven, H Backhovens, M Cruts, G De Winter, M Bruyland, ...
Nature genetics 2 (4), 335-339, 1992
Epitope mapping of monoclonal antibodies to the paired helical filaments of Alzheimer's disease: identification of phosphorylation sites in tau protein
M Goedert, R Jakes, RA Crowther, P Cohen, E Vanmechelen, ...
Biochemical Journal 301 (3), 871-877, 1994
Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European families
CV Broeckhoven, AM Genthe, A Vandenberghe, B Horsthemke, ...
Nature 329 (6135), 153-155, 1987
The genetics and neuropathology of frontotemporal lobar degeneration
A Sieben, T Van Langenhove, S Engelborghs, JJ Martin, P Boon, P Cras, ...
Acta neuropathologica 124, 353-372, 2012
Senile plaque neurites in Alzheimer disease accumulate amyloid precursor protein.
P Cras, M Kawai, D Lowery, P Gonzalez-DeWhitt, B Greenberg, G Perry
Proceedings of the National Academy of Sciences 88 (17), 7552-7556, 1991
Diagnostic performance of a CSF-biomarker panel in autopsy-confirmed dementia
S Engelborghs, K De Vreese, T Van de Casteele, H Vanderstichele, ...
Neurobiology of aging 29 (8), 1143-1159, 2008
A Pan‐European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats
J van der Zee, I Gijselinck, L Dillen, T Van Langenhove, J Theuns, ...
Human mutation 34 (2), 363-373, 2013
The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter
I Gijselinck, S Van Mossevelde, J van der Zee, A Sieben, S Engelborghs, ...
Molecular psychiatry 21 (8), 1112-1124, 2016
Incidence and spectrum of sporadic Creutzfeldt–Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification
P Parchi, R Strammiello, S Notari, A Giese, JPM Langeveld, A Ladogana, ...
Acta neuropathologica 118, 659-671, 2009
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