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Zhongdong Lin

Showing results (11-20 of 24) with videos related to

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Medicine|April 12, 2018
Basal ganglia calcification and novel compound heterozygous mutations in the PANK2 gene in a Chinese boy with classic Pantothenate kinase-associated neurodegeneration: A case reportXulai Shi, Feixia Zheng, Xiuyun Ye, et al.
Frontiers in Neurology|August 29, 2022
Treatment of hyponatremia in children with acute bacterial meningitisFeixia Zheng, Xiaoyan Ye, Yuanyuan Chen, et al.
Optics Express|December 19, 2025
SNR enhancement for low-SNR amplitude-modulated holographic data storage based on deep learningZhongdong Lin, Jianying Hao, Yongkun Lin, et al.
Acta Neurologica Belgica|April 5, 2020
Different experiences of two PRRT2-associated self-limited familial infantile epilepsyQianlei Zhao, Zhenwei Liu, Ying Hu, et al.
Human Genomics|February 3, 2026
Global developmental delay and focal seizures in individuals with de novo truncating MACF1 variantsJianan Xi, Fangyu Deng, Menghui Liang, et al.
Comparative Biochemistry and Physiology. Toxicology & Pharmacology : CBP|December 9, 2023
Mechanisms underlying palmitic acid-induced disruption of locomotor activity and sleep behavior in DrosophilaYumei Huang, Jiaqi Zhang, Dongdong You, et al.
Frontiers in Microbiology|September 29, 2025
Multi-omics integration reveals gut microbiota dysbiosis and metabolic alterations of cerebrospinal fluid in children with epilepsyFeng Li, Dongdong You, Yun Li, et al.
Optics Express|February 20, 2026
Fixed-weight coding method for uniformity processing in holographic data storageHongjie Liu, Shujun Zheng, Xu Zheng, et al.
Frontiers in Genetics|September 7, 2021
Case Report: CNNM2 Mutations Cause Damaged Brain Development and Intractable Epilepsy in a Patient Without HypomagnesemiaXiucui Li, Shijia Bao, Wei Wang, et al.
Seizure|July 23, 2021
PRRT2 variants and effectiveness of various antiepileptic drugs in self-limited familial infantile epilepsyQianlei Zhao, Ying Hu, Zhenwei Liu, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Medicine|April 12, 2018
Basal ganglia calcification and novel compound heterozygous mutations in the PANK2 gene in a Chinese boy with classic Pantothenate kinase-associated neurodegeneration: A case reportXulai Shi, Feixia Zheng, Xiuyun Ye, et al.
Frontiers in Neurology|August 29, 2022
Treatment of hyponatremia in children with acute bacterial meningitisFeixia Zheng, Xiaoyan Ye, Yuanyuan Chen, et al.
Optics Express|December 19, 2025
SNR enhancement for low-SNR amplitude-modulated holographic data storage based on deep learningZhongdong Lin, Jianying Hao, Yongkun Lin, et al.
Acta Neurologica Belgica|April 5, 2020
Different experiences of two PRRT2-associated self-limited familial infantile epilepsyQianlei Zhao, Zhenwei Liu, Ying Hu, et al.
Human Genomics|February 3, 2026
Global developmental delay and focal seizures in individuals with de novo truncating MACF1 variantsJianan Xi, Fangyu Deng, Menghui Liang, et al.
Comparative Biochemistry and Physiology. Toxicology & Pharmacology : CBP|December 9, 2023
Mechanisms underlying palmitic acid-induced disruption of locomotor activity and sleep behavior in DrosophilaYumei Huang, Jiaqi Zhang, Dongdong You, et al.
Frontiers in Microbiology|September 29, 2025
Multi-omics integration reveals gut microbiota dysbiosis and metabolic alterations of cerebrospinal fluid in children with epilepsyFeng Li, Dongdong You, Yun Li, et al.
Optics Express|February 20, 2026
Fixed-weight coding method for uniformity processing in holographic data storageHongjie Liu, Shujun Zheng, Xu Zheng, et al.
Frontiers in Genetics|September 7, 2021
Case Report: CNNM2 Mutations Cause Damaged Brain Development and Intractable Epilepsy in a Patient Without HypomagnesemiaXiucui Li, Shijia Bao, Wei Wang, et al.
Seizure|July 23, 2021
PRRT2 variants and effectiveness of various antiepileptic drugs in self-limited familial infantile epilepsyQianlei Zhao, Ying Hu, Zhenwei Liu, et al.
Pageof 3