Xing-guang Ye

Foshan, China

Last Updated: 09/26/2026

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Found 11 publications

Self-limited epilepsy with centrotemporal spikes (SeLECTS) with spike-and-wave activation in sleep (SWAS): clinical characteristics and electroencephalogram outcomes at the 2-year follow-up.

Self-limited epilepsy with centrotemporal spikes (SeLECTS) with spike-and-wave activation in sleep (SWAS): clinical characteristics and electroencephalogram outcomes at the 2-year follow-up.

Journal: Seizure

Published: March 08, 2026

Increased expression of proinflammatory cytokines in the cerebrospinal fluid of patients with a history of electrical status epilepticus in sleep.

Increased expression of proinflammatory cytokines in the cerebrospinal fluid of patients with a history of electrical status epilepticus in sleep.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: March 21, 2025

ARHGAP4 variants are associated with X-linked early-onset temporal lobe epilepsy.

ARHGAP4 variants are associated with X-linked early-onset temporal lobe epilepsy.

Journal: World journal of pediatrics : WJP

Published: December 19, 2023

SZT2 variants associated with partial epilepsy or epileptic encephalopathy and the genotype-phenotype correlation.

SZT2 variants associated with partial epilepsy or epileptic encephalopathy and the genotype-phenotype correlation.

Journal: Frontiers in molecular neuroscience

Published: February 09, 2023

Increased expression of NLRP3 associated with elevated levels of HMGB1 in children with febrile seizures: a case-control study.

Increased expression of NLRP3 associated with elevated levels of HMGB1 in children with febrile seizures: a case-control study.

Journal: BMC pediatrics

Published: November 14, 2022

Nitrogen Permease Regulator Like-2 (NPRL2 ) truncating mutation causes Ohtahara syndrome with incomplete penetrance: expanding the genotype-phenotype correlations.

Nitrogen Permease Regulator Like-2 (NPRL2 ) truncating mutation causes Ohtahara syndrome with incomplete penetrance: expanding the genotype-phenotype correlations.

Journal: Clinical dysmorphology

Published: June 22, 2022

YWHAZ variation causes intellectual disability and global developmental delay with brain malformation.

YWHAZ variation causes intellectual disability and global developmental delay with brain malformation.

Journal: Human molecular genetics

Published: May 16, 2022

Recessive LAMA5 Variants Associated With Partial Epilepsy and Spasms in Infancy.

Recessive LAMA5 Variants Associated With Partial Epilepsy and Spasms in Infancy.

Journal: Frontiers in molecular neuroscience

Published: November 30, 2021

YWHAG Mutations Cause Childhood Myoclonic Epilepsy and Febrile Seizures: Molecular Sub-regional Effect and Mechanism.

YWHAG Mutations Cause Childhood Myoclonic Epilepsy and Febrile Seizures: Molecular Sub-regional Effect and Mechanism.

Journal: Frontiers in genetics

Published: November 23, 2020

Association of LPP and TAGAP Polymorphisms with Celiac Disease Risk: A Meta-Analysis.

Association of LPP and TAGAP Polymorphisms with Celiac Disease Risk: A Meta-Analysis.

Journal: International journal of environmental research and public health

Published: December 01, 2016

Meta-Analysis on Associations of RGS1 and IL12A Polymorphisms with Celiac Disease Risk.

Meta-Analysis on Associations of RGS1 and IL12A Polymorphisms with Celiac Disease Risk.

Journal: International journal of molecular sciences

Published: February 16, 2016

Showing 1-11 of 11

Last Updated: 09/26/2026