Bing-mei K. Li

Key Laboratory Of Neurogenetics And Channelopathies Of Guangdong Province, The Ministry Of Education Of China
Guangzhou, China

Last Updated: 09/26/2026

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Found 38 publications

Perampanel in Chinese patients with Dravet syndrome: Efficacy and tolerability assessed via a multicenter, prospective, real-world observational study.

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

RLIM variant associated with X-linked epilepsy with neurodevelopmental disorders and the molecular sub-regional effects.

RLIM variant associated with X-linked epilepsy with neurodevelopmental disorders and the molecular sub-regional effects.

Journal: Seizure

Published: February 28, 2026

De novo SRCAP variants cause developmental and epileptic encephalopathy and the phenotypic spectrum.

De novo SRCAP variants cause developmental and epileptic encephalopathy and the phenotypic spectrum.

Journal: Epilepsia

Published: June 26, 2025

Variants in CSMD2 and CSMD3, genes involved in synaptogenesis, are associated with epilepsies.

Variants in CSMD2 and CSMD3, genes involved in synaptogenesis, are associated with epilepsies.

Journal: Epilepsia

Published: March 17, 2025

Identification of MACF1 as a causative gene of generalised epilepsy.

Identification of MACF1 as a causative gene of generalised epilepsy.

Journal: Journal of medical genetics

Published: February 09, 2025

Epilepsy in NHS actin remodeling regulator gene (NHS) and genotype-phenotype correlations.

Epilepsy in NHS actin remodeling regulator gene (NHS) and genotype-phenotype correlations.

Journal: Pediatric research

Published: October 21, 2024

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

Efficacy and safety of Bacteroides fragilis BF839 for pediatric autism spectrum disorder: a randomized clinical trial.

Efficacy and safety of Bacteroides fragilis BF839 for pediatric autism spectrum disorder: a randomized clinical trial.

Journal: Frontiers in nutrition

Published: June 11, 2024

Missense variants in SLC9A6 cause partial epilepsy without neurodevelopmental delay.

Missense variants in SLC9A6 cause partial epilepsy without neurodevelopmental delay.

Journal: Orphanet journal of rare diseases

Published: May 10, 2024

RYR3 Variants Are Potentially Associated With Idiopathic (Non-Lesional) Partial Epilepsy/Susceptibility of Seizures, Toward Understanding the Gene-Disease Association by Genetic Dependent Nature.

RYR3 Variants Are Potentially Associated With Idiopathic (Non-Lesional) Partial Epilepsy/Susceptibility of Seizures, Toward Understanding the Gene-Disease Association by Genetic Dependent Nature.

Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics

Published: March 30, 2024

Heterozygous variants in USP25 cause genetic generalized epilepsy.

Heterozygous variants in USP25 cause genetic generalized epilepsy.

Journal: Brain : a journal of neurology

Published: January 24, 2024

ZFHX3 variants cause childhood partial epilepsy and infantile spasms with favourable outcomes.

ZFHX3 variants cause childhood partial epilepsy and infantile spasms with favourable outcomes.

Journal: Journal of medical genetics

Published: November 01, 2023

Showing 1-12 of 38

Last Updated: 09/26/2026