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Optics Express
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April 7, 2017
Simplex coded polarization optical time domain reflectometry system
Chaodong 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 sclerosis
Yang 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 Chinese
Yue 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-2
Chaodong Wang, Yanming Xu, Xiuli Feng, et al.
Neurogenetics
|
July 15, 2023
Novel mutations and molecular pathways identified in patients with brain iron accumulation disorders
Lianghao 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 variants
Da-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 study
Yi 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 disease
Na 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 study
Raoli He, Yuqi Zeng, Chaodong Wang, et al.
Frontiers in Molecular Neuroscience
|
June 6, 2022
<i>SCN1A</i>-Related Epilepsy: Novel Mutations and Rare Phenotypes
Rui Ma, Yiran Duan, Liping Zhang, et al.
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Search research articles
Search
Showing results (41-50 of 100) with videos related to
Sort By:
Page
of 10
Optics Express
|
April 7, 2017
Simplex coded polarization optical time domain reflectometry system
Chaodong 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 sclerosis
Yang 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 Chinese
Yue 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-2
Chaodong Wang, Yanming Xu, Xiuli Feng, et al.
Neurogenetics
|
July 15, 2023
Novel mutations and molecular pathways identified in patients with brain iron accumulation disorders
Lianghao 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 variants
Da-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 study
Yi 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 disease
Na 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 study
Raoli He, Yuqi Zeng, Chaodong Wang, et al.
Frontiers in Molecular Neuroscience
|
June 6, 2022
<i>SCN1A</i>-Related Epilepsy: Novel Mutations and Rare Phenotypes
Rui Ma, Yiran Duan, Liping Zhang, et al.
Page
of 10