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Zhidong Cen

Showing results (1-10 of 59) 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.
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.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 22, 2024
A novel ATP13A2 variant causing complicated hereditary spastic paraplegiaFan Zhang, Peng Liu, Jiaxiang Li, 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.
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.
Journal of the Neurological Sciences|June 15, 2014
Two cases of dural arteriovenous fistula presenting with parkinsonism and progressive cognitive dysfunctionYong Luo, Jun Qi, Zhidong Cen, et al.
Parkinsonism & Related Disorders|January 29, 2022
Early-onset Parkinson's disease with atypical molecular imaging abnormalities in a patient carrying the de novo PRKCG mutationYueting Chen, Peng Liu, Zhidong Cen, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|December 10, 2014
BSCL2 S90L mutation in a Chinese family with Silver syndrome with a review of the literatureZhidong Cen, Xingjiao Lu, Zhenzhen Wang, et al.
Stem Cell Research|October 27, 2023
Generation of an induced pluripotent stem cell line (ZJUi013-A) from a Familial cortical myoclonic tremor with epilepsy type 1 patient carrying (TTTCA)<sub>n</sub> insertion in the SAMD12 geneFan Zhang, Shuqi Chen, Yiling Chen, et al.
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Showing results (1-10 of 59) with videos related to

Sort By:
Pageof 6
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.
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.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 22, 2024
A novel ATP13A2 variant causing complicated hereditary spastic paraplegiaFan Zhang, Peng Liu, Jiaxiang Li, 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.
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.
Journal of the Neurological Sciences|June 15, 2014
Two cases of dural arteriovenous fistula presenting with parkinsonism and progressive cognitive dysfunctionYong Luo, Jun Qi, Zhidong Cen, et al.
Parkinsonism & Related Disorders|January 29, 2022
Early-onset Parkinson's disease with atypical molecular imaging abnormalities in a patient carrying the de novo PRKCG mutationYueting Chen, Peng Liu, Zhidong Cen, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|December 10, 2014
BSCL2 S90L mutation in a Chinese family with Silver syndrome with a review of the literatureZhidong Cen, Xingjiao Lu, Zhenzhen Wang, et al.
Stem Cell Research|October 27, 2023
Generation of an induced pluripotent stem cell line (ZJUi013-A) from a Familial cortical myoclonic tremor with epilepsy type 1 patient carrying (TTTCA)<sub>n</sub> insertion in the SAMD12 geneFan Zhang, Shuqi Chen, Yiling Chen, et al.
Pageof 6