Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Bei Sha

Showing results (41-50 of 236) with videos related to

Pageof 24
Sort By:
Neuroscience Letters|April 27, 2018
Alzheimer's disease susceptibility genes modify the risk of Parkinson disease and Parkinson's disease-associated cognitive impairmentLu Fang, Bei-Sha Tang, Kuan Fan, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 11, 2011
[The effect of HSPB8 gene mutation on cell viability in Charcot-Marie-Tooth disease type 2L]Shu-jian Li, Bei-sha Tang, Guo-hua Zhao, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 9, 2015
The contribution of GIGYF2 to Parkinson's disease: a meta-analysisYuan Zhang, Qi-Ying Sun, Ren-He Yu, et al.
Chinese Medical Journal|July 22, 2004
Clinical features of hereditary spastic paraplegia with thin corpus callosum: report of 5 Chinese casesBei-sha Tang, Xin Chen, Guo-hua Zhao, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|July 27, 2014
Non-motor symptoms in Chinese Parkinson's disease patients with and without LRRK2 G2385R and R1628P variantsDa-Wei Li, Zhuqin Gu, Chaodong Wang, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|October 23, 2018
Identifying mild-moderate Parkinson's disease using whole-brain functional connectivityYan Tang, Bailin Liu, Yuan Yang, et al.
Zhonghua Nei Ke Za Zhi|July 13, 2005
[The clinical and genetic characteristics of autosomal recessive juvenile Parkinsonism in a Chinese family]Ya-wei Shen, Bei-sha Tang, Xin-xiang Yan, et al.
Chinese Medical Journal|September 14, 2020
Clinical and genetic features of transthyretin-related familial amyloid polyneuropathy in ChinaLei Liu, Xiao-Bo Li, Zheng-Mao Hu, et al.
Neurobiology of Aging|September 6, 2014
Linkage analysis and whole-exome sequencing exclude extra mutations responsible for the parkinsonian phenotype of spinocerebellar ataxia-2Chaodong Wang, Yanming Xu, Xiuli Feng, et al.
Molecular Brain|November 2, 2015
VPS35-deficiency results in an impaired AMPA receptor trafficking and decreased dendritic spine maturationYun Tian, Fu-Lei Tang, XiangDong Sun, et al.
Pageof 24

Showing results (41-50 of 236) with videos related to

Sort By:
Pageof 24
Neuroscience Letters|April 27, 2018
Alzheimer's disease susceptibility genes modify the risk of Parkinson disease and Parkinson's disease-associated cognitive impairmentLu Fang, Bei-Sha Tang, Kuan Fan, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 11, 2011
[The effect of HSPB8 gene mutation on cell viability in Charcot-Marie-Tooth disease type 2L]Shu-jian Li, Bei-sha Tang, Guo-hua Zhao, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 9, 2015
The contribution of GIGYF2 to Parkinson's disease: a meta-analysisYuan Zhang, Qi-Ying Sun, Ren-He Yu, et al.
Chinese Medical Journal|July 22, 2004
Clinical features of hereditary spastic paraplegia with thin corpus callosum: report of 5 Chinese casesBei-sha Tang, Xin Chen, Guo-hua Zhao, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|July 27, 2014
Non-motor symptoms in Chinese Parkinson's disease patients with and without LRRK2 G2385R and R1628P variantsDa-Wei Li, Zhuqin Gu, Chaodong Wang, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|October 23, 2018
Identifying mild-moderate Parkinson's disease using whole-brain functional connectivityYan Tang, Bailin Liu, Yuan Yang, et al.
Zhonghua Nei Ke Za Zhi|July 13, 2005
[The clinical and genetic characteristics of autosomal recessive juvenile Parkinsonism in a Chinese family]Ya-wei Shen, Bei-sha Tang, Xin-xiang Yan, et al.
Chinese Medical Journal|September 14, 2020
Clinical and genetic features of transthyretin-related familial amyloid polyneuropathy in ChinaLei Liu, Xiao-Bo Li, Zheng-Mao Hu, et al.
Neurobiology of Aging|September 6, 2014
Linkage analysis and whole-exome sequencing exclude extra mutations responsible for the parkinsonian phenotype of spinocerebellar ataxia-2Chaodong Wang, Yanming Xu, Xiuli Feng, et al.
Molecular Brain|November 2, 2015
VPS35-deficiency results in an impaired AMPA receptor trafficking and decreased dendritic spine maturationYun Tian, Fu-Lei Tang, XiangDong Sun, et al.
Pageof 24