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Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|January 27, 2021
Frequency of spinocerebellar ataxia mutations in patients with multiple system atrophyAnna I Wernick, Ronald L Walton, Alexandra I Soto-Beasley, et al.
Parkinsonism & Related Disorders|August 7, 2013
Novel A18T and pA29S substitutions in α-synuclein may be associated with sporadic Parkinson's diseaseDorota Hoffman-Zacharska, Dariusz Koziorowski, Owen A Ross, et al.
American Journal of Human Genetics|June 12, 2010
Principal-component analysis for assessment of population stratification in mitochondrial medical geneticsAlessandro Biffi, Christopher D Anderson, Michael A Nalls, et al.
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.
Cells|September 27, 2024
Structural and Functional Characterization of the Most Frequent Pathogenic PRKN Substitution p.R275WBernardo A Bustillos, Liam T Cocker, Mathew A Coban, et al.
Medrxiv : the Preprint Server for Health Sciences|February 20, 2025
Polygenic scores for disease risk are not associated with clinical outcomes in Parkinson's diseaseManuela Mx Tan, Hirotaka Iwaki, Sara Bandres-Ciga, et al.
Science Advances|May 2, 2025
Characterizing the expression profile of 3R tau pathology in Pick's diseaseNicole Tamvaka, Alexandra I Soto-Beasley, Marios Gavrielatos, et al.
Parkinsonism & Related Disorders|October 19, 2024
Taxonomic intestinal microbiota differences in Lewy body spectrum disease and cohabitant controlsLevi M Teigen, Stuart J McCarter, Zachary Ziegert, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|May 1, 2025
Genome-wide association analysis identifies APOE as a mitophagy modifier in Lewy body diseaseXu Hou, Michael G Heckman, Fabienne C Fiesel, et al.
Medrxiv : the Preprint Server for Health Sciences|October 31, 2023
Genome-wide association study identifies APOE and ZMIZ1 variants as mitophagy modifiers in Lewy body diseaseXu Hou, Michael G Heckman, Fabienne C Fiesel, et al.
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