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Zhidong Cen

Showing results (41-50 of 59) with videos related to

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NPJ Parkinson'S Disease|January 20, 2025
Long-read sequencing revealed complex biallelic pentanucleotide repeat expansions in RFC1-related Parkinson's diseasePeng Liu, Fan Zhang, Xinhui Chen, et al.
European Journal of Neurology|February 11, 2022
The role of NOTCH2NLC in Parkinson's disease: A clinical, neuroimaging, and pathological studyPeng Liu, Dehao Yang, Fan Zhang, et al.
European Journal of Neurology|November 9, 2021
Neuronal intranuclear inclusion disease tremor-dominant subtype: A mimicker of essential tremorDehao Yang, Zhidong Cen, Lebo Wang, et al.
European Journal of Human Genetics : EJHG|March 12, 2024
Origin and evolution of pentanucleotide repeat expansions at the familial cortical myoclonic tremor with epilepsy type1 - SAMD12 locusXinhui Chen, Fan Zhang, Yihua Shi, et al.
Annals of Clinical and Translational Neurology|December 7, 2023
Seizures and electrophysiological features in familial cortical myoclonic tremor with epilepsy 1Yao Ding, Zhidong Cen, Yang Zheng, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 8, 2025
RRP12 Variants Are Associated With Autosomal Recessive Brain CalcificationsEdoardo Monfrini, Paola Rinchetti, Mathieu Anheim, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 5, 2020
Altered Cerebello-Motor Network in Familial Cortical Myoclonic Tremor With Epilepsy Type 1Bo Wang, Jue Wang, Zhidong Cen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 21, 2024
(TTTCA)exp Drives the Genotype-Phenotype Correlation and Genetic Anticipation in FCMTE1Xinhui Chen, Bo Wang, Haibin Xia, et al.
Brain : a Journal of Neurology|June 26, 2018
Intronic pentanucleotide TTTCA repeat insertion in the SAMD12 gene causes familial cortical myoclonic tremor with epilepsy type 1Zhidong Cen, Zhengwen Jiang, You Chen, et al.
Cell|April 25, 2025
SLC7A11 is an unconventional H<sup>+</sup> transporter in lysosomesNan Zhou, Jingzhi Chen, Meiqin Hu, et al.
Pageof 6

Showing results (41-50 of 59) with videos related to

Sort By:
Pageof 6
NPJ Parkinson'S Disease|January 20, 2025
Long-read sequencing revealed complex biallelic pentanucleotide repeat expansions in RFC1-related Parkinson's diseasePeng Liu, Fan Zhang, Xinhui Chen, et al.
European Journal of Neurology|February 11, 2022
The role of NOTCH2NLC in Parkinson's disease: A clinical, neuroimaging, and pathological studyPeng Liu, Dehao Yang, Fan Zhang, et al.
European Journal of Neurology|November 9, 2021
Neuronal intranuclear inclusion disease tremor-dominant subtype: A mimicker of essential tremorDehao Yang, Zhidong Cen, Lebo Wang, et al.
European Journal of Human Genetics : EJHG|March 12, 2024
Origin and evolution of pentanucleotide repeat expansions at the familial cortical myoclonic tremor with epilepsy type1 - SAMD12 locusXinhui Chen, Fan Zhang, Yihua Shi, et al.
Annals of Clinical and Translational Neurology|December 7, 2023
Seizures and electrophysiological features in familial cortical myoclonic tremor with epilepsy 1Yao Ding, Zhidong Cen, Yang Zheng, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 8, 2025
RRP12 Variants Are Associated With Autosomal Recessive Brain CalcificationsEdoardo Monfrini, Paola Rinchetti, Mathieu Anheim, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 5, 2020
Altered Cerebello-Motor Network in Familial Cortical Myoclonic Tremor With Epilepsy Type 1Bo Wang, Jue Wang, Zhidong Cen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 21, 2024
(TTTCA)exp Drives the Genotype-Phenotype Correlation and Genetic Anticipation in FCMTE1Xinhui Chen, Bo Wang, Haibin Xia, et al.
Brain : a Journal of Neurology|June 26, 2018
Intronic pentanucleotide TTTCA repeat insertion in the SAMD12 gene causes familial cortical myoclonic tremor with epilepsy type 1Zhidong Cen, Zhengwen Jiang, You Chen, et al.
Cell|April 25, 2025
SLC7A11 is an unconventional H<sup>+</sup> transporter in lysosomesNan Zhou, Jingzhi Chen, Meiqin Hu, et al.
Pageof 6