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Neurobiology of Aging
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September 8, 2015
Mutation analysis of CHCHD2 gene in Chinese familial Parkinson's disease
Zhenhua Liu, Jifeng Guo, Kai Li, et al.
Frontiers in Genetics
|
November 16, 2020
A Novel Potentially Pathogenic Rare Variant in the <i>DNAJC7</i> Gene Identified in Amyotrophic Lateral Sclerosis Patients From Mainland China
Mengli Wang, Zhen Liu, Yanchun Yuan, et al.
Human Genetics
|
January 23, 2018
Identification of rare RTN3 variants in Alzheimer's disease in Han Chinese
Yongyi Zou, Wanxia He, Kangli Wang, et al.
Molecular Neurodegeneration
|
October 1, 2021
METTL3-dependent RNA m<sup>6</sup>A dysregulation contributes to neurodegeneration in Alzheimer's disease through aberrant cell cycle events
Fanpeng Zhao, Ying Xu, Shichao Gao, et al.
Clinical Genetics
|
May 10, 2019
A novel WARS mutation (p.Asp314Gly) identified in a Chinese distal hereditary motor neuropathy family
Binghao Wang, Xiaobo Li, Shunxiang Huang, et al.
Frontiers in Aging Neuroscience
|
March 27, 2023
Characteristics of fatigue in Parkinson's disease: A longitudinal cohort study
Xiaoxia Zhou, Yaqin Xiang, Tingwei Song, et al.
Nature Communications
|
May 24, 2020
Truncation of mutant huntingtin in knock-in mice demonstrates exon1 huntingtin is a key pathogenic form
Huiming Yang, Su Yang, Liang Jing, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 15, 2025
Dysfunctional Alternative Polyadenylation Modifies the Penetrance of LRRK2 Variants in Parkinson's Disease
Songyu Yang, Yixiao Zhu, Pei Yu, et al.
Brain and Behavior
|
February 10, 2025
Nonmotor Symptoms Differ Between Essential Tremor and Tremor-Dominant Parkinson's Disease
Mingqiang Li, Runcheng He, Xun Zhou, et al.
NPJ Parkinson'S Disease
|
February 24, 2025
Early detection of Parkinson's disease through multiplex blood and urine biomarkers prior to clinical diagnosis
Shuo Gao, Zheng Wang, Yuanfeng Huang, et al.
Page
of 52
Search research articles
Search
Showing results (331-340 of 514) with videos related to
Sort By:
Page
of 52
Neurobiology of Aging
|
September 8, 2015
Mutation analysis of CHCHD2 gene in Chinese familial Parkinson's disease
Zhenhua Liu, Jifeng Guo, Kai Li, et al.
Frontiers in Genetics
|
November 16, 2020
A Novel Potentially Pathogenic Rare Variant in the <i>DNAJC7</i> Gene Identified in Amyotrophic Lateral Sclerosis Patients From Mainland China
Mengli Wang, Zhen Liu, Yanchun Yuan, et al.
Human Genetics
|
January 23, 2018
Identification of rare RTN3 variants in Alzheimer's disease in Han Chinese
Yongyi Zou, Wanxia He, Kangli Wang, et al.
Molecular Neurodegeneration
|
October 1, 2021
METTL3-dependent RNA m<sup>6</sup>A dysregulation contributes to neurodegeneration in Alzheimer's disease through aberrant cell cycle events
Fanpeng Zhao, Ying Xu, Shichao Gao, et al.
Clinical Genetics
|
May 10, 2019
A novel WARS mutation (p.Asp314Gly) identified in a Chinese distal hereditary motor neuropathy family
Binghao Wang, Xiaobo Li, Shunxiang Huang, et al.
Frontiers in Aging Neuroscience
|
March 27, 2023
Characteristics of fatigue in Parkinson's disease: A longitudinal cohort study
Xiaoxia Zhou, Yaqin Xiang, Tingwei Song, et al.
Nature Communications
|
May 24, 2020
Truncation of mutant huntingtin in knock-in mice demonstrates exon1 huntingtin is a key pathogenic form
Huiming Yang, Su Yang, Liang Jing, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 15, 2025
Dysfunctional Alternative Polyadenylation Modifies the Penetrance of LRRK2 Variants in Parkinson's Disease
Songyu Yang, Yixiao Zhu, Pei Yu, et al.
Brain and Behavior
|
February 10, 2025
Nonmotor Symptoms Differ Between Essential Tremor and Tremor-Dominant Parkinson's Disease
Mingqiang Li, Runcheng He, Xun Zhou, et al.
NPJ Parkinson'S Disease
|
February 24, 2025
Early detection of Parkinson's disease through multiplex blood and urine biomarkers prior to clinical diagnosis
Shuo Gao, Zheng Wang, Yuanfeng Huang, et al.
Page
of 52