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Li-ping Zou

Showing results (161-170 of 181) with videos related to

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Mitochondrial DNA|January 31, 2013
Heterogeneity of six children and their mothers with mitochondrial DNA 3243 A>G mutationYan-Yan Ma, Tong-Fei Wu, Yu-Peng Liu, et al.
Frontiers in Psychiatry|January 11, 2021
The Efficacy of Fecal Microbiota Transplantation for Children With Tourette Syndrome: A Preliminary StudyHui-Jun Zhao, Xi Luo, Yi-Chao Shi, et al.
Seizure|January 10, 2022
Efficacy of levetiracetam in STXBP1 encephalopathy with different phenotypic and genetic spectraQiu-Hong Wang, Jia-Jie Cao, Yang-Yang Wang, et al.
Zhonghua Yi Xue Za Zhi|January 13, 2011
[Analysis of clinical phenotype in 42 nuclear pedigrees carrying mitochondrial DNA A3243G mutation]Yi-nan Ma, Fang Fang, Yan-yan Cao, et al.
Annals of Clinical and Translational Neurology|October 31, 2014
Febrile seizure recurrence reduced by intermittent oral levetiracetamLin-Yan Hu, Li-Ping Zou, Jian-Min Zhong, et al.
Therapeutic Advances in Neurological Disorders|January 5, 2023
Vigabatrin-associated brain abnormalities on MRI in tuberous sclerosis complex patients with infantile spasms: are they preventable?Lin Wan, Wen He, Yang-Yang Wang, et al.
Microbiology Spectrum|April 25, 2022
Postnatal Cytomegalovirus Infection May Increase the Susceptibility of Tuberous Sclerosis Complex to Autism Spectrum DisordersXiao-Yan Yang, Yang-Yang Wang, Yue-Peng Zhou, et al.
Seizure|March 14, 2022
Sirolimus treatment for tuberous sclerosis complex prior to epilepsy: Evidence from a registry-based real-world studyYan-Wen Shen, Yang-Yang Wang, Meng-Na Zhang, et al.
Epilepsia|June 2, 2026
Neurodevelopmental trajectories and clinical outcomes following ultra-early epilepsy surgery in infants: A matched cohort studyHai-Qing Zhao, Feng-Peng Wang, Yang-Yang Wang, et al.
Brain & Development|July 16, 2013
Two compound frame-shift mutations in succinate dehydrogenase gene of a Chinese boy with encephalopathyYan-Yan Ma, Tong-Fei Wu, Yu-Peng Liu, et al.
Pageof 19

Showing results (161-170 of 181) with videos related to

Sort By:
Pageof 19
Mitochondrial DNA|January 31, 2013
Heterogeneity of six children and their mothers with mitochondrial DNA 3243 A>G mutationYan-Yan Ma, Tong-Fei Wu, Yu-Peng Liu, et al.
Frontiers in Psychiatry|January 11, 2021
The Efficacy of Fecal Microbiota Transplantation for Children With Tourette Syndrome: A Preliminary StudyHui-Jun Zhao, Xi Luo, Yi-Chao Shi, et al.
Seizure|January 10, 2022
Efficacy of levetiracetam in STXBP1 encephalopathy with different phenotypic and genetic spectraQiu-Hong Wang, Jia-Jie Cao, Yang-Yang Wang, et al.
Zhonghua Yi Xue Za Zhi|January 13, 2011
[Analysis of clinical phenotype in 42 nuclear pedigrees carrying mitochondrial DNA A3243G mutation]Yi-nan Ma, Fang Fang, Yan-yan Cao, et al.
Annals of Clinical and Translational Neurology|October 31, 2014
Febrile seizure recurrence reduced by intermittent oral levetiracetamLin-Yan Hu, Li-Ping Zou, Jian-Min Zhong, et al.
Therapeutic Advances in Neurological Disorders|January 5, 2023
Vigabatrin-associated brain abnormalities on MRI in tuberous sclerosis complex patients with infantile spasms: are they preventable?Lin Wan, Wen He, Yang-Yang Wang, et al.
Microbiology Spectrum|April 25, 2022
Postnatal Cytomegalovirus Infection May Increase the Susceptibility of Tuberous Sclerosis Complex to Autism Spectrum DisordersXiao-Yan Yang, Yang-Yang Wang, Yue-Peng Zhou, et al.
Seizure|March 14, 2022
Sirolimus treatment for tuberous sclerosis complex prior to epilepsy: Evidence from a registry-based real-world studyYan-Wen Shen, Yang-Yang Wang, Meng-Na Zhang, et al.
Epilepsia|June 2, 2026
Neurodevelopmental trajectories and clinical outcomes following ultra-early epilepsy surgery in infants: A matched cohort studyHai-Qing Zhao, Feng-Peng Wang, Yang-Yang Wang, et al.
Brain & Development|July 16, 2013
Two compound frame-shift mutations in succinate dehydrogenase gene of a Chinese boy with encephalopathyYan-Yan Ma, Tong-Fei Wu, Yu-Peng Liu, et al.
Pageof 19