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Bei Sha

Showing results (201-210 of 236) with videos related to

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Neurology. Genetics|April 29, 2016
Paroxysmal hypnogenic dyskinesia is associated with mutations in the PRRT2 geneXiao-Rong Liu, Dan Huang, Jie Wang, et al.
Neuroscience Letters|February 25, 2010
Novel GIGYF2 gene variants in patients with Parkinson's disease in Chinese populationLei Wang, Ji-feng Guo, Wen-wen Zhang, et al.
Neurobiology of Aging|January 28, 2015
Polygenic determinants of Parkinson's disease in a Chinese populationJi-Feng Guo, Kai Li, Ri-Li Yu, et al.
Frontiers in Aging Neuroscience|August 15, 2022
Associations of multiple visual rating scales based on structural magnetic resonance imaging with disease severity and cerebrospinal fluid biomarkers in patients with Alzheimer's diseaseMei-Dan Wan, Hui Liu, Xi-Xi Liu, et al.
Neurology|October 9, 2015
Paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 110 patientsXiao-Jun Huang, Tian Wang, Jun-Ling Wang, et al.
Neurobiology of Aging|September 17, 2021
Evaluating the role of ARSA in Chinese patients with Parkinson's diseaseHong-Xu Pan, Yi-Ge Wang, Yu-Wen Zhao, et al.
Clinical and Translational Medicine|May 11, 2022
Identification of clinically actionable secondary genetic variants from whole-genome sequencing in a large-scale Chinese populationPei-Kuan Cong, Saber Khederzadeh, Cheng-Da Yuan, et al.
Journal of the Neurological Sciences|October 7, 2008
Novel mutations of the SPG11 gene in hereditary spastic paraplegia with thin corpus callosumShu-sheng Liao, Lu Shen, Juan Du, et al.
Autophagy|June 17, 2020
NRBF2 is a RAB7 effector required for autophagosome maturation and mediates the association of APP-CTFs with active form of RAB7 for degradationCui-Zan Cai, Chuanbin Yang, Xu-Xu Zhuang, et al.
Neurobiology of Aging|June 4, 2013
Using next-generation sequencing as a genetic diagnostic tool in rare autosomal recessive neurologic Mendelian disordersZhao Chen, Jun-Ling Wang, Bei-Sha Tang, et al.
Pageof 24

Showing results (201-210 of 236) with videos related to

Sort By:
Pageof 24
Neurology. Genetics|April 29, 2016
Paroxysmal hypnogenic dyskinesia is associated with mutations in the PRRT2 geneXiao-Rong Liu, Dan Huang, Jie Wang, et al.
Neuroscience Letters|February 25, 2010
Novel GIGYF2 gene variants in patients with Parkinson's disease in Chinese populationLei Wang, Ji-feng Guo, Wen-wen Zhang, et al.
Neurobiology of Aging|January 28, 2015
Polygenic determinants of Parkinson's disease in a Chinese populationJi-Feng Guo, Kai Li, Ri-Li Yu, et al.
Frontiers in Aging Neuroscience|August 15, 2022
Associations of multiple visual rating scales based on structural magnetic resonance imaging with disease severity and cerebrospinal fluid biomarkers in patients with Alzheimer's diseaseMei-Dan Wan, Hui Liu, Xi-Xi Liu, et al.
Neurology|October 9, 2015
Paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 110 patientsXiao-Jun Huang, Tian Wang, Jun-Ling Wang, et al.
Neurobiology of Aging|September 17, 2021
Evaluating the role of ARSA in Chinese patients with Parkinson's diseaseHong-Xu Pan, Yi-Ge Wang, Yu-Wen Zhao, et al.
Clinical and Translational Medicine|May 11, 2022
Identification of clinically actionable secondary genetic variants from whole-genome sequencing in a large-scale Chinese populationPei-Kuan Cong, Saber Khederzadeh, Cheng-Da Yuan, et al.
Journal of the Neurological Sciences|October 7, 2008
Novel mutations of the SPG11 gene in hereditary spastic paraplegia with thin corpus callosumShu-sheng Liao, Lu Shen, Juan Du, et al.
Autophagy|June 17, 2020
NRBF2 is a RAB7 effector required for autophagosome maturation and mediates the association of APP-CTFs with active form of RAB7 for degradationCui-Zan Cai, Chuanbin Yang, Xu-Xu Zhuang, et al.
Neurobiology of Aging|June 4, 2013
Using next-generation sequencing as a genetic diagnostic tool in rare autosomal recessive neurologic Mendelian disordersZhao Chen, Jun-Ling Wang, Bei-Sha Tang, et al.
Pageof 24