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JAMA Neurology|January 14, 2020
Ambroxol for the Treatment of Patients With Parkinson Disease With and Without Glucocerebrosidase Gene Mutations: A Nonrandomized, Noncontrolled TrialStephen Mullin, Laura Smith, Katherine Lee, et al.The Journal of Biological Chemistry|December 16, 2014
The H50Q mutation induces a 10-fold decrease in the solubility of α-synucleinRiccardo Porcari, Christos Proukakis, Christopher A Waudby, et al.Journal of Parkinson'S Disease|February 20, 2025
Improving recruitment and retention of people with Parkinson's disease to clinical studies: A scoping reviewRebecca Petty, Veena Agarwal, Jennifer Allison, et al.Neurobiology of Disease|November 5, 2023
Phenotypic effect of GBA1 variants in individuals with and without Parkinson's disease: The RAPSODI studyMarco Toffoli, Harneek Chohan, Stephen Mullin, et al.Movement Disorders : Official Journal of the Movement Disorder Society|April 18, 2025
Treatment Selection and Prioritization for the EJS ACT-PD MAMS Trial PlatformCristina Gonzalez-Robles, Dilan Athauda, Thomas R Barber, et al.Brain : a Journal of Neurology|August 1, 2024
Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson's disease studyAna Westenberger, Volha Skrahina, Tatiana Usnich, et al.Pageof 4