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Oxford Medical Case Reports|November 28, 2025
Focal dystonia attributed to secondary Nigrostriatal pathway disruption following brainstem Hemorrhage: a case reportLingyan Zhou, Cheng Zhao, Zhanfang Sun, et al.
IEEE Transactions on Neural Systems and Rehabilitation Engineering : a Publication of the IEEE Engineering in Medicine and Biology Society|September 11, 2023
An Interpretable Deep Learning Optimized Wearable Daily Detection System for Parkinson's DiseaseMin Chen, Zhanfang Sun, Tao Xin, et al.
IEEE Transactions on Neural Systems and Rehabilitation Engineering : a Publication of the IEEE Engineering in Medicine and Biology Society|August 10, 2022
An Auxiliary Diagnostic System for Parkinson's Disease Based on Wearable Sensors and Genetic Algorithm Optimized Random ForestMin Chen, Zhanfang Sun, Fei Su, et al.
Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences|July 13, 2015
[1H-proton magnetic resonance spectroscopy in patients with multiple system atrophy and 
cognitive dysfunction]Xiaoshuang Xiang, Xuan Hou, Zhanfang Sun, et al.
Cell & Bioscience|April 28, 2021
Galectin-3: a key player in microglia-mediated neuroinflammation and Alzheimer's diseaseYinyin Tan, Yanqun Zheng, Daiwen Xu, 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.
International Journal of Biological Macromolecules|March 1, 2020
Astragalus polysaccharide exerts anti-Parkinson via activating the PI3K/AKT/mTOR pathway to increase cellular autophagy level in vitroYinyin Tan, Ling Yin, Zhanfang Sun, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|March 27, 2026
Depression in Parkinson's disease: prevalence and impact on oculomotor featuresLingyan Zhou, Meng Guan, Bo Zhang, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|May 2, 2013
A deletion mutation of the VHL gene associated with a patient with sporadic von Hippel-Lindau diseaseDandan Jia, Beisha Tang, Yuting Shi, et al.
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