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Parkinsonism & Related Disorders
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September 15, 2022
Analysis of GIPC1 CGG repeat expansions in essential tremor
Xun Zhou, Hong-Yan Huang, Run-Cheng He, et al.
Neuroscience Letters
|
November 13, 2020
Assessment of the association between NUS1 variants and essential tremor
Hong-Lan Yang, Li Jiang, Hong-Xu Pan, et al.
Parkinsonism & Related Disorders
|
February 6, 2021
Contribution of coding/non-coding variants in NUS1 to late-onset sporadic Parkinson's disease
Li Jiang, Hong-Xu Pan, Yu-Wen Zhao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
August 9, 2005
Mutation analysis of small heat-shock protein 22 gene in Chinese patients with Charcot-Marie-Tooth disease
Fu-feng Zhang, Bei-sha Tang, Guo-hua Zhao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
October 11, 2005
[Detection of duplications or deletions of the PMP22 gene using real-time quantitative PCR]
Fu-feng Zhang, Bei-sha Tang, Yan Shen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 13, 2009
Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: genetic, clinical, and positron emission tomography findings
Jun-Ling Wang, Bin Xiao, Xiang-Xiang Cui, et al.
Oxidative Medicine and Cellular Longevity
|
March 29, 2017
BAG5 Interacts with DJ-1 and Inhibits the Neuroprotective Effects of DJ-1 to Combat Mitochondrial Oxidative Damage
Li-Xia Qin, Jie-Qiong Tan, Hai-Nan Zhang, et al.
Neurobiology of Aging
|
October 12, 2021
Low-frequency and rare coding variants of NUS1 contribute to susceptibility and phenotype of Parkinson's disease
Li Jiang, Jun-Pu Mei, Yu-Wen Zhao, et al.
European Journal of Medical Genetics
|
May 14, 2013
Exome sequencing released a case of X-linked adrenoleukodystrophy mimicking recessive hereditary spastic paraplegia
Zi-Xiong Zhan, Xin-Xin Liao, Juan Du, et al.
Neurobiology of Aging
|
April 30, 2022
PSEN1 G417S mutation in a Chinese pedigree causing early-onset parkinsonism with cognitive impairment
Li Jiang, Yan Qin, Yu-Wen Zhao, et al.
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of 24
Search research articles
Search
Showing results (181-190 of 236) with videos related to
Sort By:
Page
of 24
Parkinsonism & Related Disorders
|
September 15, 2022
Analysis of GIPC1 CGG repeat expansions in essential tremor
Xun Zhou, Hong-Yan Huang, Run-Cheng He, et al.
Neuroscience Letters
|
November 13, 2020
Assessment of the association between NUS1 variants and essential tremor
Hong-Lan Yang, Li Jiang, Hong-Xu Pan, et al.
Parkinsonism & Related Disorders
|
February 6, 2021
Contribution of coding/non-coding variants in NUS1 to late-onset sporadic Parkinson's disease
Li Jiang, Hong-Xu Pan, Yu-Wen Zhao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
August 9, 2005
Mutation analysis of small heat-shock protein 22 gene in Chinese patients with Charcot-Marie-Tooth disease
Fu-feng Zhang, Bei-sha Tang, Guo-hua Zhao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
October 11, 2005
[Detection of duplications or deletions of the PMP22 gene using real-time quantitative PCR]
Fu-feng Zhang, Bei-sha Tang, Yan Shen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 13, 2009
Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: genetic, clinical, and positron emission tomography findings
Jun-Ling Wang, Bin Xiao, Xiang-Xiang Cui, et al.
Oxidative Medicine and Cellular Longevity
|
March 29, 2017
BAG5 Interacts with DJ-1 and Inhibits the Neuroprotective Effects of DJ-1 to Combat Mitochondrial Oxidative Damage
Li-Xia Qin, Jie-Qiong Tan, Hai-Nan Zhang, et al.
Neurobiology of Aging
|
October 12, 2021
Low-frequency and rare coding variants of NUS1 contribute to susceptibility and phenotype of Parkinson's disease
Li Jiang, Jun-Pu Mei, Yu-Wen Zhao, et al.
European Journal of Medical Genetics
|
May 14, 2013
Exome sequencing released a case of X-linked adrenoleukodystrophy mimicking recessive hereditary spastic paraplegia
Zi-Xiong Zhan, Xin-Xin Liao, Juan Du, et al.
Neurobiology of Aging
|
April 30, 2022
PSEN1 G417S mutation in a Chinese pedigree causing early-onset parkinsonism with cognitive impairment
Li Jiang, Yan Qin, Yu-Wen Zhao, et al.
Page
of 24