Sheng Luo

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 51 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

Clinical and genetic characteristics of CSF1R-related leukoencephalopathy: a retrospective analysis of three cases.

Clinical and genetic characteristics of CSF1R-related leukoencephalopathy: a retrospective analysis of three cases.

Journal: Neurogenetics

Published: January 20, 2026

Biological Context-Informed and Population-Stratified Strategies Improve Genetic Diagnosis of CCDC22-Related Disorder.

Biological Context-Informed and Population-Stratified Strategies Improve Genetic Diagnosis of CCDC22-Related Disorder.

Journal: Genetics research

Published: December 10, 2025

Correction: Generalized tonic-clonic seizures as the initial symptom of late-onset Krabbe disease: a Case Report.

Correction: Generalized tonic-clonic seizures as the initial symptom of late-onset Krabbe disease: a Case Report.

Journal: Frontiers in behavioral neuroscience

Published: November 06, 2025

Reply: USP25 in genetic generalized epilepsy: a gene under scrutiny.

Reply: USP25 in genetic generalized epilepsy: a gene under scrutiny.

Journal: Brain : a journal of neurology

Published: August 15, 2025

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

De novo truncating variant in the FBRSL1 gene caused neurodevelopmental disorders, epilepsy, congenital heart disease, and facial dysmorphism.

De novo truncating variant in the FBRSL1 gene caused neurodevelopmental disorders, epilepsy, congenital heart disease, and facial dysmorphism.

Journal: Experimental neurology

Published: March 20, 2025

Quercetin promotes angiogenesis and protects the blood-spinal cord barrier structure after spinal cord injury by targeting the PI3K/Akt signaling pathway.

Quercetin promotes angiogenesis and protects the blood-spinal cord barrier structure after spinal cord injury by targeting the PI3K/Akt signaling pathway.

Journal: Journal of translational medicine

Published: March 18, 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

Generalized tonic-clonic seizures as the initial symptom of late-onset Krabbe disease: a Case Report.

Generalized tonic-clonic seizures as the initial symptom of late-onset Krabbe disease: a Case Report.

Journal: Frontiers in behavioral neuroscience

Published: January 23, 2025

Showing 1-12 of 51

Last Updated: 09/26/2026