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The Lancet. Neurology|December 20, 2020
Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association studyEdwin Jabbari, Shunsuke Koga, Rebecca R Valentino, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 23, 2018
Developing and validating Parkinson's disease subtypes and their motor and cognitive progressionMichael Lawton, Yoav Ben-Shlomo, Margaret T May, et al.
Neurology. Genetics|January 14, 2025
Global Perspectives on Returning Genetic Research Results in Parkinson DiseaseAi Huey Tan, Paula Saffie-Awad, Artur F Schumacher Schuh, et al.
Brain : a Journal of Neurology|November 9, 2022
Association between the LRP1B and APOE loci and the development of Parkinson's disease dementiaRaquel Real, Alejandro Martinez-Carrasco, Regina H Reynolds, et al.
Medrxiv : the Preprint Server for Health Sciences|January 2, 2026
Identification of common variants influencing risk of the three-repeat tauopathy Pick's disease: a genome wide association studyWilliam J Scotton, Rebecca R Valentino, Alejandro Martinez-Carrasco, et al.
Brain : a Journal of Neurology|July 21, 2019
Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease studyManuela M X Tan, Naveed Malek, Michael A Lawton, et al.
Research Square|October 7, 2024
The LRRK2 p.L1795F variant causes Parkinson's disease in the European populationLara M Lange, Kristin Levine, Susan H Fox, et al.
Journal of Parkinson'S Disease|September 26, 2015
Precompetitive Data Sharing as a Catalyst to Address Unmet Needs in Parkinson's DiseaseDiane Stephenson, Michele T Hu, Klaus Romero, et al.
NPJ Parkinson'S Disease|September 12, 2023
Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2)Clodagh Towns, Madeleine Richer, Simona Jasaityte, et al.
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