受强制性开放获取政策约束的文章 - Carles Vilarino-Guell了解详情
无法在其他位置公开访问的文章：14 篇
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Alpha‐synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease
S Appel‐Cresswell, C Vilarino‐Guell, M Encarnacion, H Sherman, I Yu, ...
Movement disorders 28 (6), 811-813, 2013
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research …
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Defining neurodegeneration on Guam by targeted genomic sequencing
JC Steele, I Guella, C Szu‐Tu, MK Lin, C Thompson, DM Evans, ...
Annals of neurology 77 (3), 458-468, 2015
强制性开放获取政策： Canadian Institutes of Health Research, UK Medical Research Council
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A Novel DCTN1 mutation with late‐onset parkinsonism and frontotemporal atrophy
E Araki, Y Tsuboi, J Daechsel, A Milnerwood, C Vilarino‐Guell, N Fujii, ...
Movement Disorders 29 (9), 1201-1204, 2014
强制性开放获取政策： Genome Canada
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SNCA, MAPT, and GSK3B in Parkinson disease: a gene–gene interaction study
C Wider, C Vilariño‐Güell, MG Heckman, B Jasinska‐Myga, ...
European journal of neurology 18 (6), 876-881, 2011
强制性开放获取政策： Swiss National Science Foundation, US National Institutes of Health …
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Reported mutations in GIGYF2 are not a common cause of Parkinson's disease
C Vilariño‐Güell, OA Ross, AI Soto, MJ Farrer, K Haugarvoll, JO Aasly, ...
Movement Disorders 24 (4), 619-620, 2009
强制性开放获取政策： US National Institutes of Health
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Alpha‐synuclein polymorphisms are associated with Parkinson's disease in a Saskatchewan population
A Rajput, C Vilariño‐Güell, ML Rajput, OA Ross, AI Soto‐Ortolaza, ...
Movement disorders 24 (16), 2411-2414, 2009
强制性开放获取政策： US National Institutes of Health, National Institute of Health and Medical …
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Mitochondrial translation initiation factor 3 polymorphism and Parkinson's disease
B Behrouz, C Vilariño-Güell, MG Heckman, AI Soto-Ortolaza, JO Aasly, ...
Neuroscience letters 486 (3), 228-230, 2010
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research
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Teneurin transmembrane protein 4 is not a cause for essential tremor in a Canadian population
G Houle, JF Schmouth, CS Leblond, A Ambalavanan, D Spiegelman, ...
Movement Disorders 32 (2), 292-295, 2017
强制性开放获取政策： Canadian Institutes of Health Research
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Genetic analysis of nucleotide-binding leucine-rich repeat (NLR) receptors in multiple sclerosis
LF Popplewell, M Encarnacion, CQ Bernales, AD Sadovnick, ...
Immunogenetics 72, 381-385, 2020
强制性开放获取政策： Canadian Institutes of Health Research, Michael Smith Foundation for Health …
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The role of SNCA and MAPT in Parkinson disease and LRRK2 parkinsonism in the Tunisian Arab-Berber population.
J Trinh, EK Gustavsson, I Guella, C Vilariño‐Güell, D Evans, ...
European Journal of Neurology 21 (11), 2014
强制性开放获取政策： Canadian Institutes of Health Research, Genome Canada
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Death‐associated protein kinase 1 variation and Parkinson’s disease
JC Dachsel, C Wider, C Vilariño‐Güell, JO Aasly, A Rajput, AH Rajput, ...
European Journal of Neurology 18 (8), 1090-1093, 2011
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research
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Enhanced expression of complement and microglial-specific genes prior to clinical progression in the MOG-experimental autoimmune encephalomyelitis model of multiple sclerosis
P Becquart, C Vilariño-Güell, JA Quandt
Brain Research Bulletin 165, 63-69, 2020
强制性开放获取政策： Michael Smith Foundation for Health Research, Multiple Sclerosis Society of …
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Elevated levels of serum CD5 antigen-like protein distinguish secondary progressive multiple sclerosis from other disease subtypes
E Kamma, P Becquart, A Traboulsee, A Schabas, IM Vavasour, C Laule, ...
Multiple Sclerosis and Related Disorders 56, 103269, 2021
强制性开放获取政策： Multiple Sclerosis Society of Canada
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Analysis of Canadian multiple sclerosis patients does not support a role for FKBP6 in disease
C Vilariño-Güell, M Encarnacion, CQ Bernales, AD Sadovnick
Multiple Sclerosis Journal 25 (7), 1011-1013, 2019
强制性开放获取政策： Canadian Institutes of Health Research, Michael Smith Foundation for Health …
可在其他位置公开访问的文章：88 篇
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VPS35 mutations in Parkinson disease
C Vilariño-Güell, C Wider, OA Ross, JC Dachsel, JM Kachergus, ...
The American Journal of Human Genetics 89 (1), 162-167, 2011
强制性开放获取政策： US National Institutes of Health, Genome Canada
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Translation initiator EIF4G1 mutations in familial Parkinson disease
MC Chartier-Harlin, JC Dachsel, C Vilariño-Güell, SJ Lincoln, F Leprêtre, ...
The American Journal of Human Genetics 89 (3), 398-406, 2011
强制性开放获取政策： US National Institutes of Health, Genome Canada, National Institute of …
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DNAJC13 mutations in Parkinson disease
C Vilariño-Güell, A Rajput, AJ Milnerwood, B Shah, C Szu-Tu, J Trinh, I Yu, ...
Human molecular genetics 23 (7), 1794-1801, 2014
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research …
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DCTN1 mutations in Perry syndrome
MJ Farrer, MM Hulihan, JM Kachergus, JC Dächsel, AJ Stoessl, ...
Nature genetics 41 (2), 163-165, 2009
强制性开放获取政策： US National Institutes of Health
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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
强制性开放获取政策： US National Institutes of Health, Research Foundation (Flanders), Genome …
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Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12. 1
J Winkelmann, D Czamara, B Schormair, F Knauf, EC Schulte, ...
PLoS genetics 7 (7), e1002171, 2011
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research …
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