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Xuerong Leng

Showing results (1-10 of 9) with videos related to

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Seizure|November 18, 2022
Genotype and phenotype analysis of epilepsy caused by ADGRV1 mutations in Chinese childrenXuerong Leng, Tiantian Zhang, Yanping Guan, et al.
Frontiers in Neurology|February 12, 2026
Resting-state MEG of whole-brain functional network in cingulate gyrus epilepsyXuerong Leng, Xue Yang, Jing Xiang, et al.
Human Brain Mapping|February 26, 2020
Frequency-specific changes in the default mode network in patients with cingulate gyrus epilepsyXuerong Leng, Jing Xiang, Yingxue Yang, et al.
Frontiers in Neurology|April 26, 2021
The Correlation of ELP4-PAX6 With Rolandic Spike Sources in Idiopathic Rolandic Epilepsy SyndromesYiran Duan, Xuerong Leng, Chunyan Liu, et al.
Brain & Development|December 3, 2015
Endoplasmic reticulum stress intolerance in EIF2B3 mutant oligodendrocytes is modulated by depressed autophagyNa Chen, Lifang Dai, Yuwu Jiang, et al.
Journal of Human Genetics|January 23, 2009
Identification of novel EIF2B mutations in Chinese patients with vanishing white matter diseaseYe Wu, Yanxia Pan, Li Du, et al.
Plos One|March 12, 2015
Fifteen novel EIF2B1-5 mutations identified in Chinese children with leukoencephalopathy with vanishing white matter and a long term follow-upHaihua Zhang, Lifang Dai, Na Chen, et al.
Journal of Human Genetics|February 11, 2011
Functional analysis of recently identified mutations in eukaryotic translation initiation factor 2Bɛ (eIF2Bɛ) identified in Chinese patients with vanishing white matter diseaseXuerong Leng, Ye Wu, Xuemin Wang, et al.
Epilepsia Open|October 6, 2025
Simultaneous tDCS-rTMS stimulation to regulate the language network and improve language ability in Landau-Kleffner syndromeRunze Chen, Xinyan Liu, Xiaohong Qi, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Seizure|November 18, 2022
Genotype and phenotype analysis of epilepsy caused by ADGRV1 mutations in Chinese childrenXuerong Leng, Tiantian Zhang, Yanping Guan, et al.
Frontiers in Neurology|February 12, 2026
Resting-state MEG of whole-brain functional network in cingulate gyrus epilepsyXuerong Leng, Xue Yang, Jing Xiang, et al.
Human Brain Mapping|February 26, 2020
Frequency-specific changes in the default mode network in patients with cingulate gyrus epilepsyXuerong Leng, Jing Xiang, Yingxue Yang, et al.
Frontiers in Neurology|April 26, 2021
The Correlation of ELP4-PAX6 With Rolandic Spike Sources in Idiopathic Rolandic Epilepsy SyndromesYiran Duan, Xuerong Leng, Chunyan Liu, et al.
Brain & Development|December 3, 2015
Endoplasmic reticulum stress intolerance in EIF2B3 mutant oligodendrocytes is modulated by depressed autophagyNa Chen, Lifang Dai, Yuwu Jiang, et al.
Journal of Human Genetics|January 23, 2009
Identification of novel EIF2B mutations in Chinese patients with vanishing white matter diseaseYe Wu, Yanxia Pan, Li Du, et al.
Plos One|March 12, 2015
Fifteen novel EIF2B1-5 mutations identified in Chinese children with leukoencephalopathy with vanishing white matter and a long term follow-upHaihua Zhang, Lifang Dai, Na Chen, et al.
Journal of Human Genetics|February 11, 2011
Functional analysis of recently identified mutations in eukaryotic translation initiation factor 2Bɛ (eIF2Bɛ) identified in Chinese patients with vanishing white matter diseaseXuerong Leng, Ye Wu, Xuemin Wang, et al.
Epilepsia Open|October 6, 2025
Simultaneous tDCS-rTMS stimulation to regulate the language network and improve language ability in Landau-Kleffner syndromeRunze Chen, Xinyan Liu, Xiaohong Qi, et al.
Pageof 1