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Ji-Feng Guo

Showing results (101-110 of 109) with videos related to

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Brain : a Journal of Neurology|November 29, 2011
Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesiasJun-Ling Wang, Li Cao, Xun-Hua Li, et al.
Brain : a Journal of Neurology|December 11, 2019
Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremorQi-Ying Sun, Qian Xu, Yun Tian, et al.
Human Molecular Genetics|January 3, 2018
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 geneXiao-Meng Yin, Jing-Han Lin, Li Cao, et al.
Translational Neurodegeneration|August 5, 2020
GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson's disease: a two-cohort case-control studyHong-Xu Pan, Yu-Wen Zhao, Jun-Pu Mei, et al.
American Journal of Human Genetics|June 11, 2019
Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related DisordersYun Tian, Jun-Ling Wang, Wen Huang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 2, 2022
Sensitivity of Sniffer Dogs for a Diagnosis of Parkinson's Disease: A Diagnostic Accuracy StudyChang-Qing Gao, Shan-Ni Wang, Mei-Mei Wang, et al.
Nature Communications|December 31, 2024
SEAD reference panel with 22,134 haplotypes boosts rare variant imputation and genome-wide association analysis in Asian populationsMeng-Yuan Yang, Jia-Dong Zhong, Xin Li, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 24, 2018
Coding mutations in <i>NUS1</i> contribute to Parkinson's diseaseJi-Feng Guo, Lu Zhang, Kai Li, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 23, 2022
Clinical features of <i>NOTCH2NLC</i>-related neuronal intranuclear inclusion diseaseYun Tian, Lu Zhou, Jing Gao, et al.
Pageof 11

Showing results (101-110 of 109) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 109 results.
Brain : a Journal of Neurology|November 29, 2011
Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesiasJun-Ling Wang, Li Cao, Xun-Hua Li, et al.
Brain : a Journal of Neurology|December 11, 2019
Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremorQi-Ying Sun, Qian Xu, Yun Tian, et al.
Human Molecular Genetics|January 3, 2018
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 geneXiao-Meng Yin, Jing-Han Lin, Li Cao, et al.
Translational Neurodegeneration|August 5, 2020
GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson's disease: a two-cohort case-control studyHong-Xu Pan, Yu-Wen Zhao, Jun-Pu Mei, et al.
American Journal of Human Genetics|June 11, 2019
Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related DisordersYun Tian, Jun-Ling Wang, Wen Huang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 2, 2022
Sensitivity of Sniffer Dogs for a Diagnosis of Parkinson's Disease: A Diagnostic Accuracy StudyChang-Qing Gao, Shan-Ni Wang, Mei-Mei Wang, et al.
Nature Communications|December 31, 2024
SEAD reference panel with 22,134 haplotypes boosts rare variant imputation and genome-wide association analysis in Asian populationsMeng-Yuan Yang, Jia-Dong Zhong, Xin Li, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 24, 2018
Coding mutations in <i>NUS1</i> contribute to Parkinson's diseaseJi-Feng Guo, Lu Zhang, Kai Li, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 23, 2022
Clinical features of <i>NOTCH2NLC</i>-related neuronal intranuclear inclusion diseaseYun Tian, Lu Zhou, Jing Gao, et al.
Pageof 11