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Haolin Duan

Showing results (11-20 of 19) with videos related to

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Frontiers in Molecular Neuroscience|October 10, 2022
Attention-deficit/hyperactive disorder updatesMiriam Kessi, Haolin Duan, Juan Xiong, et al.
Scientific Reports|June 12, 2026
Assessment of gabapentin efficacy in patients with KCNQ2-developmental epileptic encephalopathyJuan Xiong, Xia You, Huazhen Li, et al.
Frontiers in Neurology|December 5, 2018
Rare Copy Number Variations and Predictors in Children With Intellectual Disability and EpilepsyMiriam Kessi, Juan Xiong, Liwen Wu, et al.
Mitochondrion|December 18, 2025
Biallelic FOXRED1 mutations cause infantile mitochondrial encephalopathy with complex I disassembly and basal ganglia degenerationCunhui Pan, Ruowei Zhu, Xi Huang, et al.
Frontiers in Molecular Neuroscience|June 6, 2022
The Contribution of HCN Channelopathies in Different Epileptic Syndromes, Mechanisms, Modulators, and Potential Treatment Targets: A Systematic ReviewMiriam Kessi, Jing Peng, Haolin Duan, et al.
BMC Medicine|July 2, 2025
The genetic spectrum features of 2261 Chinese children with epilepsy and intellectual disabilityNan Pang, Chen Chen, Lifen Yang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 16, 2025
Gene therapy with covalently closed-end AAV vector for spinal muscular atrophyHaolin Duan, Ciliu Zhang, Zhongliang Zhang, et al.
Epilepsia|January 24, 2026
Integrated genotype-phenotype function analysis reveals distinct pathogenic mechanisms for cognitive impairment in KCNQ2-related disordersJuan Xiong, Haolin Duan, Jun Chen, et al.
Gene|December 11, 2023
Targeted sequencing identifies risk variants in 202 candidate genes for neurodevelopmental disordersNan Pang, Kuokuo Li, Senwei Tan, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Frontiers in Molecular Neuroscience|October 10, 2022
Attention-deficit/hyperactive disorder updatesMiriam Kessi, Haolin Duan, Juan Xiong, et al.
Scientific Reports|June 12, 2026
Assessment of gabapentin efficacy in patients with KCNQ2-developmental epileptic encephalopathyJuan Xiong, Xia You, Huazhen Li, et al.
Frontiers in Neurology|December 5, 2018
Rare Copy Number Variations and Predictors in Children With Intellectual Disability and EpilepsyMiriam Kessi, Juan Xiong, Liwen Wu, et al.
Mitochondrion|December 18, 2025
Biallelic FOXRED1 mutations cause infantile mitochondrial encephalopathy with complex I disassembly and basal ganglia degenerationCunhui Pan, Ruowei Zhu, Xi Huang, et al.
Frontiers in Molecular Neuroscience|June 6, 2022
The Contribution of HCN Channelopathies in Different Epileptic Syndromes, Mechanisms, Modulators, and Potential Treatment Targets: A Systematic ReviewMiriam Kessi, Jing Peng, Haolin Duan, et al.
BMC Medicine|July 2, 2025
The genetic spectrum features of 2261 Chinese children with epilepsy and intellectual disabilityNan Pang, Chen Chen, Lifen Yang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 16, 2025
Gene therapy with covalently closed-end AAV vector for spinal muscular atrophyHaolin Duan, Ciliu Zhang, Zhongliang Zhang, et al.
Epilepsia|January 24, 2026
Integrated genotype-phenotype function analysis reveals distinct pathogenic mechanisms for cognitive impairment in KCNQ2-related disordersJuan Xiong, Haolin Duan, Jun Chen, et al.
Gene|December 11, 2023
Targeted sequencing identifies risk variants in 202 candidate genes for neurodevelopmental disordersNan Pang, Kuokuo Li, Senwei Tan, et al.
Pageof 2