Showing results (101-110 of 210) with videos related to

Sort By:
Pageof 21
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 8, 2010
Clinical features and [11C]-CFT PET analysis of PARK2, PARK6, PARK7-linked autosomal recessive early onset ParkinsonismJi-feng Guo, Lei Wang, Dan He, et al.
Neuroscience Letters|September 19, 2012
Spinocerebellar ataxia type 23 is an uncommon SCA subtype in the Chinese Han populationYu-Tao Liu, Bei-Sha Tang, Jun-Ling Wang, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|November 16, 2012
Genetic association study of glucocerebrosidase gene L444P mutation in essential tremor and multiple system atrophy in mainland ChinaQi-ying Sun, Ji-feng Guo, Wei-wei Han, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|February 15, 2011
Case-control study of the UCH-L1 S18Y variant in sporadic Parkinson's disease in the Chinese populationLei Wang, Ji-feng Guo, Li-luo Nie, et al.
Neuroscience Letters|October 19, 2013
The relationship between the phenotype of Parkinson's disease and levodopa-induced dyskinesiaYu-Han Zhang, Bei-Sha Tang, Chen-Yuan Song, et al.
Journal of the Neurological Sciences|January 27, 2016
C9ORF72 repeat expansion is not detected in sporadic ataxia patients in mainland ChinaMiao He, Wei-Qian Yan, Sheng Zeng, et al.
Journal of Alzheimer'S Disease : JAD|October 10, 2019
Analysis of Salivary Microbiome in Patients with Alzheimer's DiseaseXi-Xi Liu, Bin Jiao, Xin-Xin Liao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 4, 2006
[Genotype and phenotype analyses of three families with autosomal recessive juvenile parkinsonism]Ji-feng Guo, Bei-sha Tang, Yu-hu Zhang, et al.
BMC Neurology|April 27, 2013
Analysis of EIF4G1 in ethnic ChineseKai Li, Bei-sha Tang, Ji-feng Guo, et al.
Pageof 21