Showing results (81-90 of 103) with videos related to
Sort By:
Pageof 11
Parkinsonism & Related Disorders|October 26, 2010
Glucocerebrosidase mutations in diffuse Lewy body diseaseKenya Nishioka, Owen A Ross, Carles Vilariño-Güell, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 13, 2009
FGF20 and Parkinson's disease: no evidence of association or pathogenicity via alpha-synuclein expressionChristian Wider, Justus C Dachsel, Alexandra I Soto, et al.Biorxiv : the Preprint Server for Biology|April 17, 2026
WDR44 drives de novo α-synuclein aggregation at the lysosomal membrane and promotes neuronal dysfunction in Parkinson's DiseaseMaxime Teixeira, Razan Sheta, Morgan Bérard, et al.Brain : a Journal of Neurology|December 8, 2022
Mitochondrial DNA heteroplasmy distinguishes disease manifestation in PINK1/PRKN-linked Parkinson's diseaseJoanne Trinh, Andrew A Hicks, Inke R König, et al.Iscience|September 20, 2019
Rewiring of the Human Mitochondrial Interactome during Neuronal Reprogramming Reveals Regulators of the Respirasome and NeurogenesisMohamed Taha Moutaoufik, Ramy Malty, Shahreen Amin, et al.Tremor and Other Hyperkinetic Movements (New York, N.Y.)|February 16, 2026
Copy Number Variant Duplications Associated with Essential TremorMiranda Medeiros, Calwing Liao, Allison A Dilliott, et al.Canada Communicable Disease Report = Releve Des Maladies Transmissibles Au Canada|February 15, 2024
Resource use and disease severity of children hospitalized for COVID-19 versus multisystem inflammatory syndrome in children (MIS-C) in CanadaDaniel Farrar, Charlotte Moore Hepburn, Olivier Drouin, et al.Pediatric Research|June 5, 2023
Paediatric inflammatory multisystem syndrome in Canada: population-based surveillance and role of SARS-CoV-2 linkageTala El Tal, Marie-Paule Morin, Shaun K Morris, et al.Parkinsonism & Related Disorders|December 6, 2020
Exome-wide rare variant analysis in familial essential tremorMonica Diez-Fairen, Gabrielle Houle, Sara Ortega-Cubero, et al.American Journal of Human Genetics|July 19, 2011
VPS35 mutations in Parkinson diseaseCarles Vilariño-Güell, Christian Wider, Owen A Ross, et al.Pageof 11