Xiao-rong S. Liu

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 48 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

STXBP1 Variants Associated With Epilepsy With Variable Severity.

STXBP1 Variants Associated With Epilepsy With Variable Severity.

Journal: CNS neuroscience & therapeutics

Published: October 29, 2025

CACNA1C variants associated with focal epilepsy and their correlations with arrhythmias and developmental disorders.

CACNA1C variants associated with focal epilepsy and their correlations with arrhythmias and developmental disorders.

Journal: Journal of medical genetics

Published: May 20, 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

De novo TANC2 variants caused developmental and epileptic encephalopathy and epilepsy.

De novo TANC2 variants caused developmental and epileptic encephalopathy and epilepsy.

Journal: Epilepsia

Published: October 28, 2024

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

Association of LONP1 gene with epilepsy and the sub-regional effect.

Association of LONP1 gene with epilepsy and the sub-regional effect.

Journal: Scientific reports

Published: April 25, 2024

IFIH1 variants are associated with generalised epilepsy preceded by febrile seizures.

IFIH1 variants are associated with generalised epilepsy preceded by febrile seizures.

Journal: Journal of medical genetics

Published: February 27, 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 48

Last Updated: 09/26/2026