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Chaodong Wang

Showing results (41-50 of 100) with videos related to

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Optics Express|April 7, 2017
Simplex coded polarization optical time domain reflectometry systemChaodong Wang, Ruolin Liao, Wenbo Chen, et al.
Neurobiology of Aging|May 8, 2019
Rare, low-frequency and common coding variants of ARHGEF28 gene and their association with sporadic amyotrophic lateral sclerosisYang Song, Feng Lin, Cheng-Hui Ye, et al.
American Journal of Medical Genetics. Part A|July 26, 2024
Clinical, genetic, and neuroimaging profiles of autosomal recessive spinocerebellar ataxia type 4 caused by novel VPS13D variants in ChineseYue Dong, Milan Jia, Shuang Tan, 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.
Neurogenetics|July 15, 2023
Novel mutations and molecular pathways identified in patients with brain iron accumulation disordersLianghao Si, Zhanjun Wang, Xu-Ying Li, 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.
Age and Ageing|October 21, 2024
Development and validation of a functional ability index for older adults: a multicohort studyYi Chang, Suman Sapkota, Bipin Thapa, et al.
Neuroscience|January 1, 2025
Increased α-synuclein phosphorylation and oligomerization and altered enzymes in plasma of patients with Parkinson's diseaseNa Yin, Pengjie Li, Xuran Li, et al.
Frontiers in Aging Neuroscience|April 8, 2024
Associative role of <i>HLA-DRB1</i> as a protective factor for susceptibility and progression of Parkinson's disease: a Chinese cross-sectional and longitudinal studyRaoli He, Yuqi Zeng, Chaodong Wang, et al.
Frontiers in Molecular Neuroscience|June 6, 2022
<i>SCN1A</i>-Related Epilepsy: Novel Mutations and Rare PhenotypesRui Ma, Yiran Duan, Liping Zhang, et al.
Pageof 10

Showing results (41-50 of 100) with videos related to

Sort By:
Pageof 10
Optics Express|April 7, 2017
Simplex coded polarization optical time domain reflectometry systemChaodong Wang, Ruolin Liao, Wenbo Chen, et al.
Neurobiology of Aging|May 8, 2019
Rare, low-frequency and common coding variants of ARHGEF28 gene and their association with sporadic amyotrophic lateral sclerosisYang Song, Feng Lin, Cheng-Hui Ye, et al.
American Journal of Medical Genetics. Part A|July 26, 2024
Clinical, genetic, and neuroimaging profiles of autosomal recessive spinocerebellar ataxia type 4 caused by novel VPS13D variants in ChineseYue Dong, Milan Jia, Shuang Tan, 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.
Neurogenetics|July 15, 2023
Novel mutations and molecular pathways identified in patients with brain iron accumulation disordersLianghao Si, Zhanjun Wang, Xu-Ying Li, 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.
Age and Ageing|October 21, 2024
Development and validation of a functional ability index for older adults: a multicohort studyYi Chang, Suman Sapkota, Bipin Thapa, et al.
Neuroscience|January 1, 2025
Increased α-synuclein phosphorylation and oligomerization and altered enzymes in plasma of patients with Parkinson's diseaseNa Yin, Pengjie Li, Xuran Li, et al.
Frontiers in Aging Neuroscience|April 8, 2024
Associative role of <i>HLA-DRB1</i> as a protective factor for susceptibility and progression of Parkinson's disease: a Chinese cross-sectional and longitudinal studyRaoli He, Yuqi Zeng, Chaodong Wang, et al.
Frontiers in Molecular Neuroscience|June 6, 2022
<i>SCN1A</i>-Related Epilepsy: Novel Mutations and Rare PhenotypesRui Ma, Yiran Duan, Liping Zhang, et al.
Pageof 10