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Parkinsonism & Related Disorders|October 28, 2008
Haplotype analysis of Lrrk2 R1441H carriers with parkinsonismOwen A Ross, Cleanthe Spanaki, Alida Griffith, et al.NPJ Parkinson'S Disease|December 13, 2023
Mendelian randomization reveals association between retinal thickness and non-motor symptoms of Parkinson's diseaseHang Zhou, Bibiao Shen, Zifeng Huang, et al.NPJ Parkinson'S Disease|October 30, 2022
An integrated biometric voice and facial features for early detection of Parkinson's diseaseWee Shin Lim, Shu-I Chiu, Meng-Ciao Wu, et al.Scientific Reports|November 29, 2025
Intraarterial microbubble delivery enhances focused ultrasound induced blood brain barrier opening in the murine substantia nigraHsun Li, Yung-Han Lee, Xiao Zen, et al.Neurology|April 24, 2025
Investigating Plasma Metabolomics and Gut Microbiota Changes Associated With Parkinson Disease: A Focus on Caffeine MetabolismChieh-Chang Chen, Jian-Ying Chiu, Ai Huey Tan, et al.Molecular Cell|February 20, 2018
PINK1 Phosphorylates MIC60/Mitofilin to Control Structural Plasticity of Mitochondrial Crista JunctionsPei-I Tsai, Chin-Hsien Lin, Chung-Han Hsieh, et al.Journal of Parkinson'S Disease|February 20, 2025
Subcortical tau burden correlates with regional brain atrophy and plasma markers in four-repeat tauopathy parkinsonismCheng-Hsuan Li, Sung-Pin Fan, Ming-Chieh Shih, et al.Journal of Movement Disorders|June 9, 2023
Historical and More Common Nongenetic Movement Disorders From AsiaNorlinah Mohamed Ibrahim, Priya Jagota, Pramod Kumar Pal, et al.Movement Disorders Clinical Practice|June 19, 2023
Genetic Movement Disorders Commonly Seen in AsiansPriya Jagota, Shen-Yang Lim, Pramod Kumar Pal, et al.NPJ Parkinson'S Disease|January 15, 2026
UQCRC1 deficiency impairs mitophagy via PINK1-dependent mechanisms in Parkinson's diseaseJeng-Lin Li, Shu-Yi Huang, Po-Yu Huang, et al.Pageof 23