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Dehao Yang

Showing results (61-70 of 72) with videos related to

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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.
Medicine|April 14, 2017
Low serum levels of uric acid and albumin in patients with Guillain-Barre syndromeZhongqian Su, Zhibo Chen, Yian Xiang, et al.
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.
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|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.
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.
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.
Pageof 8

Showing results (61-70 of 72) with videos related to

Sort By:
Pageof 8
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.
Medicine|April 14, 2017
Low serum levels of uric acid and albumin in patients with Guillain-Barre syndromeZhongqian Su, Zhibo Chen, Yian Xiang, et al.
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.
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|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.
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.
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.
Pageof 8