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Frontiers in Molecular Neuroscience|March 13, 2018
Integrated Genetic Analysis of Racial Differences of Common GBA Variants in Parkinson's Disease: A Meta-AnalysisYuan Zhang, Li Shu, Qiying Sun, et al.
Parkinson'S Disease|January 12, 2019
Gastrointestinal Dysfunctions Are Associated with IL-10 Variants in Parkinson's DiseaseLi Shu, Dongxiao Liang, Hongxu Pan, et al.
Molecular Neurobiology|December 7, 2018
Conditional Haploinsufficiency of β-Catenin Aggravates Neuronal Damage in a Paraquat-Based Mouse Model of Parkinson DiseaseFanpeng Zhao, Sandra L Siedlak, Sandy L Torres, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|March 29, 2005
[ATM gene mutations in Chinese patients with ataxia telangiectasia]Hong Jiang, Beisha Tang, Zhengmao Hu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 10, 2008
[Study on the single-nucleotide substitution (c.-16C to T) of the PURATROPHIN-1 gene in Chinese patients with spinocerebellar ataxia]Yafang Zhou, Xingwang Song, Jiping Yi, et al.
Journal of Neurochemistry|February 1, 2012
Hypoxia regulation of ATP13A2 (PARK9) gene transcriptionQian Xu, Hongling Guo, Xiaojie Zhang, et al.
The International Journal of Neuroscience|November 28, 2014
SNP rs11931074 of the SNCA gene may not be associated with multiple system atrophy in Chinese populationZhanFang Sun, XiaoShuang Xiang, BeiSha Tang, et al.
Frontiers in Aging Neuroscience|October 5, 2018
Clinical Heterogeneity Among LRRK2 Variants in Parkinson's Disease: A Meta-AnalysisLi Shu, Yuan Zhang, Hongxu Pan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 23, 2026
Association Analysis of HSF1 Variable Number Tandem Repeat Expansion and Coding Variants with Essential Tremor Risk in a Large CohortSheng Zeng, Yuwen Zhao, Dong Chang, et al.
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