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Journal of Neurology|July 10, 2016
The heterozygous A53T mutation in the alpha-synuclein gene in a Chinese Han patient with Parkinson disease: case report and literature reviewWei-Xi Xiong, Yi-Min Sun, Rong-Yuan Guan, et al.Frontiers in Neuroscience|August 29, 2022
Serum metabolomic characterization of PLA2G6-associated dystonia-parkinsonism: A case-control biomarker studyChen Chen, Min-Min Lou, Yi-Min Sun, et al.Neurobiology of Aging|July 20, 2014
Common GSAP promoter variant contributes to Alzheimer's disease liabilityMin Zhu, Yu Tao, Qin He, et al.Clinical Interventions in Aging|February 13, 2015
Associations between apolipoprotein E gene polymorphisms and Alzheimer's disease risk in a large Chinese Han populationPing Wu, Hong-Lei Li, Zhi-Jun Liu, et al.Annals of Translational Medicine|April 6, 2016
Objective and quantitative assessment of motor function in Parkinson's disease-from the perspective of practical applicationsKe Yang, Wei-Xi Xiong, Feng-Tao Liu, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 28, 2014
A variant within FGF1 is associated with Alzheimer's disease in the Han Chinese populationQing-Qing Tao, Yi-Min Sun, Zhi-Jun Liu, et al.Acta Neurologica Scandinavica|May 25, 2022
Dopamine transporter imaging in progressive supranuclear palsy: Severe but nonspecific to subtypesQi-Si Chen, Xin-Yi Li, Ling Li, et al.Psychiatric Genetics|December 3, 2014
Common variants at Bin1 are associated with sporadic Alzheimer's disease in the Han Chinese populationHong-Lei Li, Ping Yang, Zhi-Jun Liu, et al.Journal of Proteome Research|June 10, 2008
Novel high-throughput profiling of human transcription factors and its use for systematic pathway mappingJi-Ying Qiao, Wei Shao, Hua-Jiang Wei, et al.Molecular Genetics & Genomic Medicine|January 24, 2019
Association of the TBK1 mutation p.Ile334Thr with frontotemporal dementia and literature reviewHuiling Yu, Wenbo Yu, Su-Shan Luo, et al.Pageof 9