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David Crosiers
David Crosiers
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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
4662013
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study
OA Ross, AI Soto-Ortolaza, MG Heckman, JO Aasly, N Abahuni, G Annesi, ...
The Lancet Neurology 10 (10), 898-908, 2011
3382011
Large-scale replication and heterogeneity in Parkinson disease genetic loci
M Sharma, JPA Ioannidis, JO Aasly, G Annesi, A Brice, ...
Neurology 79 (7), 659-667, 2012
1572012
A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants
M Sharma, JPA Ioannidis, JO Aasly, G Annesi, A Brice, L Bertram, M Bozi, ...
Journal of medical genetics 49 (11), 721-726, 2012
1162012
Parkinson disease: insights in clinical, genetic and pathological features of monogenic disease subtypes
D Crosiers, J Theuns, P Cras, C Van Broeckhoven
Journal of chemical neuroanatomy 42 (2), 131-141, 2011
1082011
DLB and PDD: a role for mutations in dementia and Parkinson disease genes?
B Meeus, A Verstraeten, D Crosiers, S Engelborghs, M Van den Broeck, ...
Neurobiology of aging 33 (3), 629. e5-629. e18, 2012
1002012
Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population
K Nuytemans, B Meeus, D Crosiers, N Brouwers, D Goossens, ...
Human mutation 30 (7), 1054-1061, 2009
802009
Juvenile dystonia-parkinsonism and dementia caused by a novel ATP13A2 frameshift mutation
D Crosiers, B Ceulemans, B Meeus, K Nuytemans, P Pals, ...
Parkinsonism & related disorders 17 (2), 135-138, 2011
722011
Mindfulness training among individuals with Parkinson’s disease: neurobehavioral effects
B Pickut, S Vanneste, MA Hirsch, W Van Hecke, E Kerckhofs, P Mariën, ...
Parkinson’s disease 2015, 2015
702015
Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease
J Theuns, A Verstraeten, K Sleegers, E Wauters, I Gijselinck, S Smolders, ...
Neurology 83 (21), 1906-1913, 2014
682014
Mutated ATP10B increases Parkinson’s disease risk by compromising lysosomal glucosylceramide export
S Martin, S Smolders, C Van den Haute, B Heeman, S van Veen, ...
Acta Neuropathologica 139, 1001-1024, 2020
502020
Myoclonus and cerebellar ataxia following COVID‐19
F Dijkstra, T Van den Bossche, B Willekens, P Cras, D Crosiers
Movement disorders clinical practice 7 (8), 974, 2020
472020
Non-motor symptoms in a Flanders-Belgian population of 215 Parkinson’s disease patients as assessed by the Non-Motor Symptoms Questionnaire
D Crosiers, B Pickut, J Theuns, PP De Deyn, C Van Broeckhoven, ...
American Journal of Neurodegenerative Disease 1 (2), 160, 2012
452012
Impulse control disorders in Parkinson’s disease: an overview from neurobiology to treatment
E Maréchal, B Denoiseux, E Thys, D Crosiers, B Pickut, P Cras
Journal of Neurology 262, 7-20, 2015
382015
Mutations in glucocerebrosidase are a major genetic risk factor for Parkinson’s disease and increase susceptibility to dementia in a Flanders-Belgian cohort
D Crosiers, A Verstraeten, E Wauters, S Engelborghs, K Peeters, ...
Neuroscience letters 629, 160-164, 2016
312016
GIGYF2 has no major role in Parkinson genetic etiology in a Belgian population
B Meeus, K Nuytemans, D Crosiers, S Engelborghs, P Pals, B Pickut, ...
Neurobiology of aging 32 (2), 308-312, 2011
302011
Contribution of VPS35 genetic variability to LBD in the Flanders-Belgian population
A Verstraeten, E Wauters, D Crosiers, B Meeus, E Corsmit, E Elinck, ...
Neurobiology of aging 33 (8), 1844. e11-1844. e13, 2012
292012
Using global team science to identify genetic Parkinson’s disease worldwide
EJ Vollstedt, M Kasten, C Klein
Annals of neurology 86 (2), 153, 2019
282019
Large-scale assessment of polyglutamine repeat expansions in Parkinson disease
L Wang, JO Aasly, G Annesi, S Bardien, M Bozi, A Brice, J Carr, SJ Chung, ...
Neurology 85 (15), 1283-1292, 2015
282015
Natural history study of STXBP1-developmental and epileptic encephalopathy into adulthood
H Stamberger, D Crosiers, G Balagura, CM Bonardi, A Basu, G Cantalupo, ...
Neurology 99 (3), e221-e233, 2022
262022
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Artikelen 1–20