Patrick Santens
Patrick Santens
Ghent University and Ghent University Hospital
Geverifieerd e-mailadres voor telenet.be
Geciteerd door
Geciteerd door
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
M Cruts, I Gijselinck, J Van Der Zee, S Engelborghs, H Wils, D Pirici, ...
Nature 442 (7105), 920-924, 2006
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
Treatment of Parkinson's disease with pergolide and relation to restrictive valvular heart disease
G Van Camp, A Flamez, B Cosyns, C Weytjens, L Muyldermans, ...
The Lancet 363 (9416), 1179-1183, 2004
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
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
Bilingualism delays clinical manifestation of Alzheimer's disease
EVY Woumans, P Santens, A Sieben, JAN Versijpt, M Stevens, W Duyck
Bilingualism: Language and Cognition 18 (3), 568-574, 2015
Dystonia in neurodegeneration with brain iron accumulation: outcome of bilateral pallidal stimulation
L Timmermann, KAM Pauls, K Wieland, R Jech, G Kurlemann, N Sharma, ...
Brain 133 (3), 701-712, 2010
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort
I Gijselinck, S Van Mossevelde, J Van Der Zee, A Sieben, S Philtjens, ...
Neurology 85 (24), 2116-2125, 2015
Characterization and functional studies of lipoproteins, lipid transfer proteins, and lecithin: cholesterol acyltransferase in CSF of normal individuals and patients with …
N Demeester, G Castro, C Desrumaux, C De Geitere, JC Fruchart, ...
Journal of lipid research 41 (6), 963-974, 2000
CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro
J van der Zee, H Urwin, S Engelborghs, M Bruyland, R Vandenberghe, ...
Human molecular genetics 17 (2), 313-322, 2008
Assessment of Neuroinflammation and Microglial Activation in Alzheimer’s Disease with Radiolabelled PK11195 and Single Photon Emission Computed TomographyA Pilot Study
JJ Versijpt, F Dumont, KJ Van Laere, D Decoo, P Santens, K Audenaert, ...
European neurology 50 (1), 39-47, 2003
Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family
N Brouwers, K Nuytemans, J van der Zee, I Gijselinck, S Engelborghs, ...
Archives of neurology 64 (10), 1436-1446, 2007
Mutations in SACS cause atypical and late-onset forms of ARSACS
J Baets, T Deconinck, K Smets, D Goossens, P Van den Bergh, K Dahan, ...
Neurology 75 (13), 1181-1188, 2010
Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia
J van der Zee, I Le Ber, S Maurer‐Stroh, S Engelborghs, I Gijselinck, ...
Human mutation 28 (4), 416-416, 2007
TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort
J van der Zee, T Van Langenhove, G Kleinberger, K Sleegers, ...
Brain 134 (3), 808-815, 2011
Task preparation processes related to reward prediction precede those related to task-difficulty expectation
H Schevernels, RM Krebs, P Santens, MG Woldorff, CN Boehler
NeuroImage 84, 639-647, 2014
Multisubject learning for common spatial patterns in motor‐imagery BCI
D Devlaminck, B Wyns, M Grosse-Wentrup, G Otte, P Santens
Computational intelligence and neuroscience 2011 (1), 217987, 2011
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration
J Van Der Zee, T Van Langenhove, GG Kovacs, L Dillen, W Deschamps, ...
Acta neuropathologica 128, 397-410, 2014
Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort
T Van Langenhove, J Van Der Zee, I Gijselinck, S Engelborghs, ...
JAMA neurology 70 (3), 365-373, 2013
Lateralized effects of subthalamic nucleus stimulation on different aspects of speech in Parkinson’s disease
P Santens, M De Letter, J Van Borsel, J De Reuck, J Caemaert
Brain and language 87 (2), 253-258, 2003
Het systeem kan de bewerking nu niet uitvoeren. Probeer het later opnieuw.
Artikelen 1–20