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Beisha Tang

Showing results (311-320 of 514) with videos related to

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Journal of Human Genetics|January 11, 2003
A novel locus for autosomal dominant nonsyndromic hearing loss identified at 5q31.1-32 in a Chinese pedigreeJiahui Xia, Hao Deng, Yong Feng, et al.
Journal of the Peripheral Nervous System : JPNS|April 11, 2025
Genetic and Clinical Features of 10 Families With Hereditary Sensory NeuropathiesKe Xu, Zhongzheng Li, Mengli Wang, et al.
Neuroreport|October 1, 2019
TOMM40 polymorphism is associated with resting-state functional MRI results in patients with Alzheimer's diseaseXuewen Xiao, Jingya Wei, Weiwei Zhang, et al.
Neurology India|March 1, 2021
Preliminary Study of hsa-mir-626 Change in the Cerebrospinal Fluid in Parkinson's DiseaseLi-Xia Qin, Jie-Qiong Tan, Hai-Nan Zhang, et al.
Neurogastroenterology and Motility|January 21, 2025
Disrupted Paraventricular Hypothalamic Nucleus Functional Connectivity in Parkinson's Disease With ConstipationXiaorong Hou, Hongfei Zhou, Qiugui Zhou, et al.
CNS Neuroscience & Therapeutics|September 22, 2023
The prevalence and risk factors study of cognitive impairment: Analysis of the elderly population of Han nationality in Hunan province, ChinaTianyan Xu, Guiwen Bu, Li Yuan, et al.
Journal of Neurology|June 26, 2023
The genetic and clinical spectrum in a cohort of 39 families with complex inherited peripheral neuropathiesMengli Wang, Honglan Yang, Zhiqiang Lin, et al.
Journal of Advanced Research|February 19, 2026
TCF4 intronic CAG repeat length modulates the effect of ATXN3 on age at onset in spinocerebellar ataxia type 3Na Wan, Qi Wu, Linlin Wan, et al.
Plos One|June 18, 2015
Analysis of the GGGGCC Repeat Expansions of the C9orf72 Gene in SCA3/MJD Patients from ChinaChunrong Wang, Zhao Chen, Fang Yang, et al.
Archives of Neurology|August 10, 2005
Mutation analysis of the small heat shock protein 27 gene in chinese patients with Charcot-Marie-Tooth diseaseBeisha Tang, Xiaomin Liu, Guohua Zhao, et al.
Pageof 52

Showing results (311-320 of 514) with videos related to

Sort By:
Pageof 52
Journal of Human Genetics|January 11, 2003
A novel locus for autosomal dominant nonsyndromic hearing loss identified at 5q31.1-32 in a Chinese pedigreeJiahui Xia, Hao Deng, Yong Feng, et al.
Journal of the Peripheral Nervous System : JPNS|April 11, 2025
Genetic and Clinical Features of 10 Families With Hereditary Sensory NeuropathiesKe Xu, Zhongzheng Li, Mengli Wang, et al.
Neuroreport|October 1, 2019
TOMM40 polymorphism is associated with resting-state functional MRI results in patients with Alzheimer's diseaseXuewen Xiao, Jingya Wei, Weiwei Zhang, et al.
Neurology India|March 1, 2021
Preliminary Study of hsa-mir-626 Change in the Cerebrospinal Fluid in Parkinson's DiseaseLi-Xia Qin, Jie-Qiong Tan, Hai-Nan Zhang, et al.
Neurogastroenterology and Motility|January 21, 2025
Disrupted Paraventricular Hypothalamic Nucleus Functional Connectivity in Parkinson's Disease With ConstipationXiaorong Hou, Hongfei Zhou, Qiugui Zhou, et al.
CNS Neuroscience & Therapeutics|September 22, 2023
The prevalence and risk factors study of cognitive impairment: Analysis of the elderly population of Han nationality in Hunan province, ChinaTianyan Xu, Guiwen Bu, Li Yuan, et al.
Journal of Neurology|June 26, 2023
The genetic and clinical spectrum in a cohort of 39 families with complex inherited peripheral neuropathiesMengli Wang, Honglan Yang, Zhiqiang Lin, et al.
Journal of Advanced Research|February 19, 2026
TCF4 intronic CAG repeat length modulates the effect of ATXN3 on age at onset in spinocerebellar ataxia type 3Na Wan, Qi Wu, Linlin Wan, et al.
Plos One|June 18, 2015
Analysis of the GGGGCC Repeat Expansions of the C9orf72 Gene in SCA3/MJD Patients from ChinaChunrong Wang, Zhao Chen, Fang Yang, et al.
Archives of Neurology|August 10, 2005
Mutation analysis of the small heat shock protein 27 gene in chinese patients with Charcot-Marie-Tooth diseaseBeisha Tang, Xiaomin Liu, Guohua Zhao, et al.
Pageof 52