Hong-jun Yan
Guangzhou, China
Last Updated: 09/26/2026
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Found 8 publications
Perampanel in Chinese patients with Dravet syndrome: Efficacy and tolerability assessed via a multicenter, prospective, real-world observational study.
Journal: Epileptic disorders : international epilepsy journal with videotape
Published: April 03, 2026
Variants in EP400, encoding a chromatin remodeler, cause epilepsy with neurodevelopmental disorders.
Variants in EP400, encoding a chromatin remodeler, cause epilepsy with neurodevelopmental disorders.
Journal: American journal of human genetics
Published: June 18, 2024
De Novo ACTB Variant Associated With Juvenile-Onset Temporal Lobe Epilepsy With Favorable Outcomes.
Journal: Human mutation
Published: April 08, 2024
DLG3 variants caused X-linked epilepsy with/without neurodevelopmental disorders and the genotype-phenotype correlation.
Journal: Frontiers in molecular neuroscience
Published: October 11, 2023
NEXMIF variants are associated with epilepsy with or without intellectual disability.
Journal: Seizure
Published: May 09, 2023
SZT2 variants associated with partial epilepsy or epileptic encephalopathy and the genotype-phenotype correlation.
Journal: Frontiers in molecular neuroscience
Published: February 09, 2023
Expanding the phenotypic spectrum of KCNK4: From syndromic neurodevelopmental disorder to rolandic epilepsy.
Journal: Frontiers in molecular neuroscience
Published: October 26, 2022
Showing 1-8 of 8
Last Updated: 09/26/2026