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Zhongdong Lin

Showing results (1-10 of 24) with videos related to

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Medicine|February 3, 2018
Unusual brain images of a boy with adolescent cerebral X-linked adrenoleukodystrophy presenting with exhibitionism: A CARE-compliant case reportFeixia Zheng, Zhongdong Lin, Xiuyun Ye, et al.
Frontiers in Neurology|March 10, 2018
Management of Refractory Orofacial Dyskinesia Caused by Anti-<i>N</i>-methyl-d-aspartate Receptor Encephalitis Using Botulinum ToxinFeixia Zheng, Xiuyun Ye, Xulai Shi, et al.
Frontiers in Neurology|May 23, 2019
Hyponatremia in Children With Bacterial MeningitisFeixia Zheng, Xiuyun Ye, Xulai Shi, et al.
Molecular Neurobiology|April 8, 2017
Identification of De Novo DNMT3A Mutations That Cause West Syndrome by Using Whole-Exome SequencingZhenwei Liu, Zhongshan Li, Xiao Zhi, et al.
Journal of Clinical Medicine|January 21, 2023
Identification of a Novel Non-Canonical Splice-Site Variant in <i>ABCD1</i>Feixia Zheng, Zhongdong Lin, Ying Hu, et al.
Optics Express|March 18, 2026
Optimal unequal-interval phase encoding method for phase modulated holographic data storageZhongdong Lin, Hongjie Liu, Shujun Zheng, et al.
Cytokine|June 19, 2024
The ROS/TXNIP/NLRP3 pathway mediates LPS-induced microglial inflammatory responseQianlei Zhao, Guanhao Liu, Qiang Ding, et al.
Nucleic Acids Research|October 18, 2014
EpilepsyGene: a genetic resource for genes and mutations related to epilepsyXia Ran, Jinchen Li, Qianzhi Shao, et al.
Frontiers in Cellular Neuroscience|April 11, 2022
Sulforaphane Attenuates Chronic Intermittent Hypoxia-Induced Brain Damage in Mice <i>via</i> Augmenting Nrf2 Nuclear Translocation and AutophagyXiucui Li, Huiya Ying, Zilong Zhang, et al.
Scientific Reports|March 23, 2017
Whole-exome sequencing identifies a novel de novo mutation in DYNC1H1 in epileptic encephalopathiesZhongdong Lin, Zhenwei Liu, Xiucui Li, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Medicine|February 3, 2018
Unusual brain images of a boy with adolescent cerebral X-linked adrenoleukodystrophy presenting with exhibitionism: A CARE-compliant case reportFeixia Zheng, Zhongdong Lin, Xiuyun Ye, et al.
Frontiers in Neurology|March 10, 2018
Management of Refractory Orofacial Dyskinesia Caused by Anti-<i>N</i>-methyl-d-aspartate Receptor Encephalitis Using Botulinum ToxinFeixia Zheng, Xiuyun Ye, Xulai Shi, et al.
Frontiers in Neurology|May 23, 2019
Hyponatremia in Children With Bacterial MeningitisFeixia Zheng, Xiuyun Ye, Xulai Shi, et al.
Molecular Neurobiology|April 8, 2017
Identification of De Novo DNMT3A Mutations That Cause West Syndrome by Using Whole-Exome SequencingZhenwei Liu, Zhongshan Li, Xiao Zhi, et al.
Journal of Clinical Medicine|January 21, 2023
Identification of a Novel Non-Canonical Splice-Site Variant in <i>ABCD1</i>Feixia Zheng, Zhongdong Lin, Ying Hu, et al.
Optics Express|March 18, 2026
Optimal unequal-interval phase encoding method for phase modulated holographic data storageZhongdong Lin, Hongjie Liu, Shujun Zheng, et al.
Cytokine|June 19, 2024
The ROS/TXNIP/NLRP3 pathway mediates LPS-induced microglial inflammatory responseQianlei Zhao, Guanhao Liu, Qiang Ding, et al.
Nucleic Acids Research|October 18, 2014
EpilepsyGene: a genetic resource for genes and mutations related to epilepsyXia Ran, Jinchen Li, Qianzhi Shao, et al.
Frontiers in Cellular Neuroscience|April 11, 2022
Sulforaphane Attenuates Chronic Intermittent Hypoxia-Induced Brain Damage in Mice <i>via</i> Augmenting Nrf2 Nuclear Translocation and AutophagyXiucui Li, Huiya Ying, Zilong Zhang, et al.
Scientific Reports|March 23, 2017
Whole-exome sequencing identifies a novel de novo mutation in DYNC1H1 in epileptic encephalopathiesZhongdong Lin, Zhenwei Liu, Xiucui Li, et al.
Pageof 3