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Xiaosheng Zheng

Showing results (1-10 of 26) with videos related to

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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|November 9, 2019
[Genetic analysis of a pedigree affected with X-linked adrenoleukodystrophy]Qinqing Pan, Xiaosheng Zheng, Zhidong Cen, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 11, 2019
[Analysis of a patient with early-onset Parkinson's disease and PARK7 gene variation]Fei Xie, Xiaosheng Zheng, Zhidong Cen, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 24, 2025
[A case report of a family with Primary familial brain calcification caused by a novel MYORG gene variants]Enkui Xia, Yixin Kang, Xiaosheng Zheng, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|June 10, 2024
Careful Phenotypic Characterization of Tremor Phenomenology in a Patient with Spinocerebellar Ataxia Type 12-Tremor Features Do Not Match Those of Essential TremorWeili Luo, Xiaosheng Zheng, Zhiru Lin, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 30, 2025
Novel SPR mutation in first Chinese patient with sepiapterin reductase deficiency: urinary biomarker validation in oldest treated caseXiaosheng Zheng, Chenxin Ying, Fei Xie, et al.
World Neurosurgery|April 28, 2025
Investigation of the Impact of Deep Brain Stimulation of the Subthalamic Nucleus on Parkinson Disease Patients with Genetic Risk Factors/CausesSheng Wu, Zhidong Cen, Xiaosheng Zheng, et al.
Neuroscience Letters|June 30, 2016
Genetic analysis of the CHCHD2 gene in a cohort of Chinese patients with Parkinson diseaseHongwei Wu, Xingjiao Lu, Fei Xie, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 1, 2026
Biallelic SYNJ1 Variants in a patient with multiple system atrophy mimic syndromeYiying Zhang, Yixin Kang, Xiaosheng Zheng, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 5, 2018
[Genetic study of a Parkinson's disease pedigree caused by compound heterozygous mutations in PARK2 gene]Meihong Chen, Zhidong Cen, You Chen, et al.
Neuroscience Letters|November 7, 2016
Genetic analysis of the CHCHD2 gene in Chinese patients with familial essential tremorHongwei Wu, Xingjiao Lu, Zhidong Cen, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|November 9, 2019
[Genetic analysis of a pedigree affected with X-linked adrenoleukodystrophy]Qinqing Pan, Xiaosheng Zheng, Zhidong Cen, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 11, 2019
[Analysis of a patient with early-onset Parkinson's disease and PARK7 gene variation]Fei Xie, Xiaosheng Zheng, Zhidong Cen, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 24, 2025
[A case report of a family with Primary familial brain calcification caused by a novel MYORG gene variants]Enkui Xia, Yixin Kang, Xiaosheng Zheng, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|June 10, 2024
Careful Phenotypic Characterization of Tremor Phenomenology in a Patient with Spinocerebellar Ataxia Type 12-Tremor Features Do Not Match Those of Essential TremorWeili Luo, Xiaosheng Zheng, Zhiru Lin, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 30, 2025
Novel SPR mutation in first Chinese patient with sepiapterin reductase deficiency: urinary biomarker validation in oldest treated caseXiaosheng Zheng, Chenxin Ying, Fei Xie, et al.
World Neurosurgery|April 28, 2025
Investigation of the Impact of Deep Brain Stimulation of the Subthalamic Nucleus on Parkinson Disease Patients with Genetic Risk Factors/CausesSheng Wu, Zhidong Cen, Xiaosheng Zheng, et al.
Neuroscience Letters|June 30, 2016
Genetic analysis of the CHCHD2 gene in a cohort of Chinese patients with Parkinson diseaseHongwei Wu, Xingjiao Lu, Fei Xie, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 1, 2026
Biallelic SYNJ1 Variants in a patient with multiple system atrophy mimic syndromeYiying Zhang, Yixin Kang, Xiaosheng Zheng, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 5, 2018
[Genetic study of a Parkinson's disease pedigree caused by compound heterozygous mutations in PARK2 gene]Meihong Chen, Zhidong Cen, You Chen, et al.
Neuroscience Letters|November 7, 2016
Genetic analysis of the CHCHD2 gene in Chinese patients with familial essential tremorHongwei Wu, Xingjiao Lu, Zhidong Cen, et al.
Pageof 3