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Zhidong Cen

Showing results (51-60 of 59) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2025
Primary Brain Calcification: An International Consensus on Nomenclature, Diagnosis, Evaluation, and ManagementWei Luo, Zhidong Cen, Huiberdina Koek, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 4, 2024
A Homozygous Variant in NAA60 Is Associated with Primary Familial Brain CalcificationXinhui Chen, Yihua Shi, Feng Fu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 5, 2019
Intronic (TTTGA)<sub>n</sub> insertion in SAMD12 also causes familial cortical myoclonic tremor with epilepsyZhidong Cen, You Chen, Dehao Yang, et al.
Brain : a Journal of Neurology|December 19, 2019
Biallelic loss-of-function mutations in JAM2 cause primary familial brain calcificationZhidong Cen, You Chen, Si Chen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 18, 2020
MYORG Mutation Heterozygosity Is Associated With Brain CalcificationYou Chen, Zhidong Cen, Xinhui Chen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 24, 2025
A Complex FGF14 (TTC)/(TGC) Repeat Expansion in Parkinson's DiseaseXiaosheng Zheng, Zhidong Cen, Xinhui Chen, et al.
Parkinsonism & Related Disorders|April 21, 2019
Underestimated disease prevalence and severe phenotypes in patients with biallelic variants: A cohort study of primary familial brain calcification from ChinaSi Chen, Zhidong Cen, Feng Fu, et al.
NPJ Parkinson'S Disease|February 23, 2025
Clinical and functional evidence for the pathogenicity of the LRRK2 p.Arg1067Gln variantShen-Yang Lim, Tzi Shin Toh, Jia Wei Hor, et al.
Cell Discovery|November 28, 2022
Loss of function of CMPK2 causes mitochondria deficiency and brain calcificationMiao Zhao, Hui-Zhen Su, Yi-Heng Zeng, et al.
Pageof 6

Showing results (51-60 of 59) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 59 results.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2025
Primary Brain Calcification: An International Consensus on Nomenclature, Diagnosis, Evaluation, and ManagementWei Luo, Zhidong Cen, Huiberdina Koek, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 4, 2024
A Homozygous Variant in NAA60 Is Associated with Primary Familial Brain CalcificationXinhui Chen, Yihua Shi, Feng Fu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 5, 2019
Intronic (TTTGA)<sub>n</sub> insertion in SAMD12 also causes familial cortical myoclonic tremor with epilepsyZhidong Cen, You Chen, Dehao Yang, et al.
Brain : a Journal of Neurology|December 19, 2019
Biallelic loss-of-function mutations in JAM2 cause primary familial brain calcificationZhidong Cen, You Chen, Si Chen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 18, 2020
MYORG Mutation Heterozygosity Is Associated With Brain CalcificationYou Chen, Zhidong Cen, Xinhui Chen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 24, 2025
A Complex FGF14 (TTC)/(TGC) Repeat Expansion in Parkinson's DiseaseXiaosheng Zheng, Zhidong Cen, Xinhui Chen, et al.
Parkinsonism & Related Disorders|April 21, 2019
Underestimated disease prevalence and severe phenotypes in patients with biallelic variants: A cohort study of primary familial brain calcification from ChinaSi Chen, Zhidong Cen, Feng Fu, et al.
NPJ Parkinson'S Disease|February 23, 2025
Clinical and functional evidence for the pathogenicity of the LRRK2 p.Arg1067Gln variantShen-Yang Lim, Tzi Shin Toh, Jia Wei Hor, et al.
Cell Discovery|November 28, 2022
Loss of function of CMPK2 causes mitochondria deficiency and brain calcificationMiao Zhao, Hui-Zhen Su, Yi-Heng Zeng, et al.
Pageof 6