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Cerebellum (London, England)|July 15, 2021
Identification of the Largest SCA36 Pedigree in Asia: with Multimodel Neuroimaging Evaluation for the First TimeYue Xie, Zhao Chen, Zhe Long, et al.
Brain : a Journal of Neurology|November 26, 2010
TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencingJun Ling Wang, Xu Yang, Kun Xia, et al.
Nature Medicine|January 19, 2021
Impaired meningeal lymphatic drainage in patients with idiopathic Parkinson's diseaseXue-Bing Ding, Xin-Xin Wang, Dan-Hao Xia, 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.
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.
Brain : a Journal of Neurology|November 29, 2011
Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesiasJun-Ling Wang, Li Cao, Xun-Hua Li, et al.
Brain : a Journal of Neurology|June 15, 2019
Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth diseaseShun-Chang Sun, Di Ma, Mei-Yi Li, et al.
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