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Ji-Feng Guo

Showing results (71-80 of 109) with videos related to

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Frontiers in Cellular Neuroscience|September 27, 2013
C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in ChinaBin Jiao, Ji-Feng Guo, Ya-Qin Wang, et al.
Scientific Reports|October 4, 2016
RAB39B gene mutations are not linked to familial Parkinson's disease in ChinaJi-Feng Kang, Yang Luo, Bei-Sha Tang, et al.
Frontiers in Neurology|March 7, 2019
Clinical Features and Correlates of Excessive Daytime Sleepiness in Parkinson's DiseaseYa-Qin Xiang, Qian Xu, Qi-Ying Sun, et al.
Frontiers in Neurology|December 23, 2021
Constructing Prediction Models for Freezing of Gait by Nomogram and Machine Learning: A Longitudinal StudyKun Xu, Xiao-Xia Zhou, Run-Cheng He, et al.
Journal of Neurology|March 1, 2023
Neuroimaging uncovers distinct relationships of glymphatic dysfunction and motor symptoms in Parkinson's diseaseYan Qin, Runcheng He, Juan Chen, et al.
Neurobiology of Aging|January 4, 2016
Relationship between Alzheimer's disease GWAS-linked top hits and risk of Parkinson's disease with or without cognitive decline: a Chinese population-based studyYa-qin Wang, Bei-sha Tang, Yang Yang, et al.
Zhonghua Yi Xue Za Zhi|September 24, 2005
[Mutation analysis of PINK1 gene in Chinese patients with autosomal recessive early-onset parkinsonism type 6]Yu-hu Zhang, Bei-sha Tang, Ji-feng Guo, et al.
The International Journal of Neuroscience|July 10, 2014
The BAG2 and BAG5 proteins inhibit the ubiquitination of pathogenic ataxin3-80QXiang-Qian Che, Bei-Sha Tang, Hong-Feng Wang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 12, 2008
Mutation analysis of Parkin, PINK1, DJ-1 and ATP13A2 genes in Chinese patients with autosomal recessive early-onset ParkinsonismJi-Feng Guo, Bin Xiao, Bing Liao, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|November 26, 2011
Follow-up study of variants of the GIGYF2 gene in Chinese patients with Parkinson’s diseaseLei Wang, Ji-Feng Guo, Wen-Wen Zhang, et al.
Pageof 11

Showing results (71-80 of 109) with videos related to

Sort By:
Pageof 11
Frontiers in Cellular Neuroscience|September 27, 2013
C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in ChinaBin Jiao, Ji-Feng Guo, Ya-Qin Wang, et al.
Scientific Reports|October 4, 2016
RAB39B gene mutations are not linked to familial Parkinson's disease in ChinaJi-Feng Kang, Yang Luo, Bei-Sha Tang, et al.
Frontiers in Neurology|March 7, 2019
Clinical Features and Correlates of Excessive Daytime Sleepiness in Parkinson's DiseaseYa-Qin Xiang, Qian Xu, Qi-Ying Sun, et al.
Frontiers in Neurology|December 23, 2021
Constructing Prediction Models for Freezing of Gait by Nomogram and Machine Learning: A Longitudinal StudyKun Xu, Xiao-Xia Zhou, Run-Cheng He, et al.
Journal of Neurology|March 1, 2023
Neuroimaging uncovers distinct relationships of glymphatic dysfunction and motor symptoms in Parkinson's diseaseYan Qin, Runcheng He, Juan Chen, et al.
Neurobiology of Aging|January 4, 2016
Relationship between Alzheimer's disease GWAS-linked top hits and risk of Parkinson's disease with or without cognitive decline: a Chinese population-based studyYa-qin Wang, Bei-sha Tang, Yang Yang, et al.
Zhonghua Yi Xue Za Zhi|September 24, 2005
[Mutation analysis of PINK1 gene in Chinese patients with autosomal recessive early-onset parkinsonism type 6]Yu-hu Zhang, Bei-sha Tang, Ji-feng Guo, et al.
The International Journal of Neuroscience|July 10, 2014
The BAG2 and BAG5 proteins inhibit the ubiquitination of pathogenic ataxin3-80QXiang-Qian Che, Bei-Sha Tang, Hong-Feng Wang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 12, 2008
Mutation analysis of Parkin, PINK1, DJ-1 and ATP13A2 genes in Chinese patients with autosomal recessive early-onset ParkinsonismJi-Feng Guo, Bin Xiao, Bing Liao, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|November 26, 2011
Follow-up study of variants of the GIGYF2 gene in Chinese patients with Parkinson’s diseaseLei Wang, Ji-Feng Guo, Wen-Wen Zhang, et al.
Pageof 11