Zhefeng Yuan

Hangzhou, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 20 publications

Salience network hub dysfunction is associated with cognitive impairment in self-limited epilepsy with centrotemporal spikes: An OPM-MEG study.

Salience network hub dysfunction is associated with cognitive impairment in self-limited epilepsy with centrotemporal spikes: An OPM-MEG study.

Journal: Epilepsia open

Published: February 28, 2026

Thyroid disease burden among individuals aged 0-19 years in low-SDI countries, 1990-2035: a systematic analysis of the Global Burden of Disease Study 2023.

Thyroid disease burden among individuals aged 0-19 years in low-SDI countries, 1990-2035: a systematic analysis of the Global Burden of Disease Study 2023.

Journal: Translational pediatrics

Published: February 27, 2026

Characterization of the plasma metabolomic profile in infantile epileptic spasms syndrome.

Characterization of the plasma metabolomic profile in infantile epileptic spasms syndrome.

Journal: Translational pediatrics

Published: December 29, 2025

Research trends on herpes simplex encephalitis in children: a bibliometric analysis from 1975 to 2024.

Research trends on herpes simplex encephalitis in children: a bibliometric analysis from 1975 to 2024.

Journal: Translational pediatrics

Published: June 19, 2025

Cognitive Impairment in Temporal Lobe Epilepsy: Alterations in the Basal Forebrain Cholinergic System.

Cognitive Impairment in Temporal Lobe Epilepsy: Alterations in the Basal Forebrain Cholinergic System.

Journal: Brain and behavior

Published: June 06, 2025

INTS11-related neurodevelopmental disorder: a case report and literature review.

INTS11-related neurodevelopmental disorder: a case report and literature review.

Journal: Journal of human genetics

Published: March 19, 2024

Novel compound heterozygous mutation and phenotype in the tetratricopeptide repeat-like domain of the GEMIN5 gene in two Chinese families.

Novel compound heterozygous mutation and phenotype in the tetratricopeptide repeat-like domain of the GEMIN5 gene in two Chinese families.

Journal: Journal of human genetics

Published: April 01, 2023

Phenotypic characteristics of myelin oligodendrocyte glycoprotein antibody-associated disease in children: a single-center, retrospective study.

Phenotypic characteristics of myelin oligodendrocyte glycoprotein antibody-associated disease in children: a single-center, retrospective study.

Journal: Frontiers in neurology

Published: March 17, 2023

Case report: Pediatric anti-gamma aminobutyric acid-B receptor encephalitis with benign prognosis.

Case report: Pediatric anti-gamma aminobutyric acid-B receptor encephalitis with benign prognosis.

Journal: Frontiers in pediatrics

Published: November 21, 2022

Hutchinson-Gilford progeria syndrome complicated with stroke: A report of 2 cases and literature review.

Hutchinson-Gilford progeria syndrome complicated with stroke: A report of 2 cases and literature review.

Journal: Frontiers in pediatrics

Published: September 28, 2022

Expanding the Phenotypic and Genotypic Spectrum of ARFGEF1-Related Neurodevelopmental Disorder.

Expanding the Phenotypic and Genotypic Spectrum of ARFGEF1-Related Neurodevelopmental Disorder.

Journal: Frontiers in molecular neuroscience

Published: January 25, 2022

A novel SCN9A gene variant identified in a Chinese girl with paroxysmal extreme pain disorder (PEPD): a rare case report.

A novel SCN9A gene variant identified in a Chinese girl with paroxysmal extreme pain disorder (PEPD): a rare case report.

Journal: BMC medical genomics

Published: December 18, 2021

Showing 1-12 of 20

Last Updated: 09/26/2026