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Brain : a Journal of Neurology
|
November 29, 2011
Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias
Jun-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 tremor
Qi-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 gene
Xiao-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 study
Hong-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 Disorders
Yun 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 Study
Chang-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 populations
Meng-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 disease
Ji-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 disease
Yun Tian, Lu Zhou, Jing Gao, et al.
Page
of 11
Search research articles
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Showing results (101-110 of 109) with videos related to
Sort By:
Page
of 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 dyskinesias
Jun-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 tremor
Qi-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 gene
Xiao-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 study
Hong-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 Disorders
Yun 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 Study
Chang-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 populations
Meng-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 disease
Ji-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 disease
Yun Tian, Lu Zhou, Jing Gao, et al.
Page
of 11