Export 191 results:
Filters: Author is Dupré, Nicolas [Clear All Filters]
Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis. JAMA Neurol. 2022;79(2):185-193..
CAPTURE ALS: the comprehensive analysis platform to understand, remedy and eliminate ALS. Amyotroph Lateral Scler Frontotemporal Degener. 2022;:1-7..
Distinct patterns of progressive gray and white matter degeneration in amyotrophic lateral sclerosis. Hum Brain Mapp. 2022;43(5):1519-1534..
Environmental risk factors for amyotrophic lateral sclerosis: a case-control study in Canada and France. Amyotroph Lateral Scler Frontotemporal Degener. 2022;:1-9..
Goal management training and psychoeducation / mindfulness for treatment of executive dysfunction in Parkinson's disease: A feasibility pilot trial. PLoS One. 2022;17(2):e0263108..
Moyamoya Disease Susceptibility Gene Regulates Endothelial Barrier Function. Stroke. 2022;53(4):1263-1275..
Recessive cerebellar and afferent ataxias - clinical challenges and future directions. Nat Rev Neurol. 2022;..
Chemosensory Dysfunctions Induced by COVID-19 Can Persist up to 7 Months: A Study of Over 700 Healthcare Workers. Chem Senses. 2021;46..
Clinical perception and management of Parkinson's disease during the COVID-19 pandemic: A Canadian experience. Parkinsonism Relat Disord. 2021;91:66-76..
Genetic testing for amyotrophic lateral sclerosis in Canada - an assessment of current practices. Amyotroph Lateral Scler Frontotemporal Degener. 2021;:1-8..
Analysis of common and rare variants in late-onset Parkinson disease. Neurol Genet. 2020;6(1):385..
Clinical and genetic analysis of ATP13A2 in hereditary spastic paraplegia expands the phenotype. Mol Genet Genomic Med. 2020;:e1052..
Fine-Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies. Ann Neurol. 2020;..
The Quebec Parkinson Network: A Researcher-Patient Matching Platform and Multimodal Biorepository. J Parkinsons Dis. 2020;10(1):301-313..
Common and rare GCH1 variants are associated with Parkinson's disease. Neurobiol Aging. 2019;73:231.e1-231.e6..
Goal management training ® home-based approach for mild cognitive impairment in Parkinson's disease: a multiple baseline case report. Neurocase. 2019;:1-11..
Portrait of blood-derived extracellular vesicles in patients with Parkinson's disease. Neurobiol Dis. 2019;124:163-175..
SMPD1 mutations, activity, and α-synuclein accumulation in Parkinson's disease. Mov Disord. 2019;34(4):526-535..
Absence of Mutation Enrichment for Genes Phylogenetically Conserved in the Olivocerebellar Motor Circuitry in a Cohort of Canadian Essential Tremor Cases. Mol Neurobiol. 2018;..
Association study of essential tremor genetic loci in Parkinson's disease. Neurobiol Aging. 2018;66:178.e13-178.e15..
Current and Promising Therapies in Autosomal Recessive Ataxias. CNS Neurol Disord Drug Targets. 2018;17(3):161-171..
Effects of Antiparkinson Medication on Cognition in Parkinson's Disease: A Systematic Review. Can J Neurol Sci. 2018;45(4):375-404..
Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder. Mov Disord. 2018;33(6):1016-1020..
Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population. Sci Rep. 2018;8(1):4356..
Misfolded SOD1 pathology in sporadic Amyotrophic Lateral Sclerosis. Sci Rep. 2018;8(1):14223..