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Lebo Wang

Showing results (11-20 of 22) with videos related to

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Parkinsonism & Related Disorders|January 19, 2025
Unveiling distinct clinical manifestations of primary familial brain calcifications in Asian and European patients: A study based on 10-year individual-level dataDehao Yang, Honghao Huang, Tian Zeng, et al.
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.
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.
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.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Parkinsonism & Related Disorders|January 19, 2025
Unveiling distinct clinical manifestations of primary familial brain calcifications in Asian and European patients: A study based on 10-year individual-level dataDehao Yang, Honghao Huang, Tian Zeng, et al.
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.
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.
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.
Pageof 3