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Bei Sha

Showing results (221-230 of 236) with videos related to

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Brain : a Journal of Neurology|November 29, 2011
Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesiasJun-Ling Wang, Li Cao, Xun-Hua Li, et al.
Brain : a Journal of Neurology|June 15, 2019
Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth diseaseShun-Chang Sun, Di Ma, Mei-Yi Li, et al.
Stroke and Vascular Neurology|August 19, 2022
Temporal trends and rural-urban disparities in cerebrovascular risk factors, in-hospital management and outcomes in ischaemic strokes in China from 2005 to 2015: a nationwide serial cross-sectional surveyChun-Juan Wang, Hong-Qiu Gu, Xin-Miao Zhang, et al.
Clinical and Translational Medicine|June 2, 2023
HCFC1 variants in the proteolysis domain are associated with X-linked idiopathic partial epilepsy: Exploring the underlying mechanismNa He, Bao-Zhu Guan, Jie Wang, et al.
Brain : a Journal of Neurology|December 11, 2019
Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremorQi-Ying Sun, Qian Xu, Yun Tian, et al.
Nature Communications|May 26, 2022
Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot projectPei-Kuan Cong, Wei-Yang Bai, Jin-Chen Li, et al.
Brain : a Journal of Neurology|April 1, 2021
PSAP variants in Parkinson's disease: a large cohort study in Chinese mainland populationYu-Wen Zhao, Hong-Xu Pan, Qian Zeng, et al.
Human Molecular Genetics|January 3, 2018
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 geneXiao-Meng Yin, Jing-Han Lin, Li Cao, et al.
Human Molecular Genetics|January 20, 2018
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 geneXiao-Meng Yin, Jing-Han Lin, Li Cao, et al.
Translational Neurodegeneration|August 5, 2020
GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson's disease: a two-cohort case-control studyHong-Xu Pan, Yu-Wen Zhao, Jun-Pu Mei, et al.
Pageof 24

Showing results (221-230 of 236) with videos related to

Sort By:
Pageof 24
Brain : a Journal of Neurology|November 29, 2011
Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesiasJun-Ling Wang, Li Cao, Xun-Hua Li, et al.
Brain : a Journal of Neurology|June 15, 2019
Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth diseaseShun-Chang Sun, Di Ma, Mei-Yi Li, et al.
Stroke and Vascular Neurology|August 19, 2022
Temporal trends and rural-urban disparities in cerebrovascular risk factors, in-hospital management and outcomes in ischaemic strokes in China from 2005 to 2015: a nationwide serial cross-sectional surveyChun-Juan Wang, Hong-Qiu Gu, Xin-Miao Zhang, et al.
Clinical and Translational Medicine|June 2, 2023
HCFC1 variants in the proteolysis domain are associated with X-linked idiopathic partial epilepsy: Exploring the underlying mechanismNa He, Bao-Zhu Guan, Jie Wang, et al.
Brain : a Journal of Neurology|December 11, 2019
Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremorQi-Ying Sun, Qian Xu, Yun Tian, et al.
Nature Communications|May 26, 2022
Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot projectPei-Kuan Cong, Wei-Yang Bai, Jin-Chen Li, et al.
Brain : a Journal of Neurology|April 1, 2021
PSAP variants in Parkinson's disease: a large cohort study in Chinese mainland populationYu-Wen Zhao, Hong-Xu Pan, Qian Zeng, et al.
Human Molecular Genetics|January 3, 2018
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 geneXiao-Meng Yin, Jing-Han Lin, Li Cao, et al.
Human Molecular Genetics|January 20, 2018
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 geneXiao-Meng Yin, Jing-Han Lin, Li Cao, et al.
Translational Neurodegeneration|August 5, 2020
GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson's disease: a two-cohort case-control studyHong-Xu Pan, Yu-Wen Zhao, Jun-Pu Mei, et al.
Pageof 24