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Neurobiology of Aging|April 30, 2022
PSEN1 G417S mutation in a Chinese pedigree causing early-onset parkinsonism with cognitive impairmentLi Jiang, Yan Qin, Yu-Wen Zhao, et al.
Neurobiology of Aging|September 17, 2021
Evaluating the role of ARSA in Chinese patients with Parkinson's diseaseHong-Xu Pan, Yi-Ge Wang, Yu-Wen Zhao, et al.
Frontiers in Aging Neuroscience|December 6, 2021
The Association Between Lysosomal Storage Disorder Genes and Parkinson's Disease: A Large Cohort Study in Chinese Mainland PopulationYu-Wen Zhao, Hong-Xu Pan, Zhenhua Liu, et al.
The Plant Cell|April 12, 2026
MdARF16/17 Link Auxin Signaling to Ma1-Independent Control of Vacuolar Malate Transport in AppleChu-Kun Wang, Meng-Meng Wei, Fan Xiao, et al.
Annals of Neurology|April 7, 2025
Biallelic Variants in EPG5 Gene Are Associated with Parkinson's DiseaseQi-Ying Sun, Fu-Liang Tang, Yao Zhou, et al.
Translational Neurodegeneration|August 5, 2020
GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson's disease: a two-cohort case-control studyHong-Xu Pan, Yu-Wen Zhao, Jun-Pu Mei, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 24, 2018
Coding mutations in NUS1 contribute to Parkinson's diseaseJi-Feng Guo, Lu Zhang, Kai Li, et al.
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