Showing results (201-210 of 238) with videos related to

Sort By:
Pageof 24
Movement Disorders : Official Journal of the Movement Disorder Society|April 9, 2019
Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanismsCornelis Blauwendraat, Karl Heilbron, Costanza L Vallerga, et al.
Brain : a Journal of Neurology|August 6, 2026
Defining the underlying pathology of corticobasal syndrome using clinical features and biomarkersDavid P Vaughan, Marte Theilmann Jensen, Raquel Real, et al.
Brain : a Journal of Neurology|July 5, 2014
Parkinson's disease in GTP cyclohydrolase 1 mutation carriersNiccolò E Mencacci, Ioannis U Isaias, Martin M Reich, et al.
Medrxiv : the Preprint Server for Health Sciences|July 17, 2025
The Global Landscape of Genetic Variation in Parkinson's disease: Multi-Ancestry Insights into Established Disease Genes and their Translational RelevanceLara M Lange, Zih-Hua Fang, Mary B Makarious, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 4, 2017
Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteriaGünter U Höglinger, Gesine Respondek, Maria Stamelou, et al.
Brain : a Journal of Neurology|July 29, 2022
Neurofilament light levels predict clinical progression and death in multiple system atrophyViorica Chelban, Elham Nikram, Alexandra Perez-Soriano, et al.
NPJ Parkinson'S Disease|March 30, 2024
Genotype-phenotype correlation in PRKN-associated Parkinson's diseasePoornima Jayadev Menon, Sara Sambin, Baptiste Criniere-Boizet, et al.
Brain : a Journal of Neurology|April 16, 2025
Intronic FGF14 GAA repeat expansions impact progression and survival in multiple system atrophyViorica Chelban, David Pellerin, Nirosen Vijiaratnam, et al.
Plos One|September 7, 2012
Creation of an open-access, mutation-defined fibroblast resource for neurological disease researchSelina Wray, Matthew Self, , et al.
The Lancet. Neurology|July 15, 2026
Parkinson's disease genetics across diverse ancestries: an observational genetic study of causal and risk variants with translational implicationsLara M Lange, Zih-Hua Fang, Mary B Makarious, et al.
Pageof 24