Hongjun Fang

Changsha, China

Last Updated: 09/26/2026

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Found 18 publications

A novel de novo QRICH1 variant causing Ververi-Brady syndrome with infantile epileptic spasms syndrome: clinical and genetic analysis.

A novel de novo QRICH1 variant causing Ververi-Brady syndrome with infantile epileptic spasms syndrome: clinical and genetic analysis.

Journal: Frontiers in neuroscience

Published: April 06, 2026

A single-center retrospective analysis of autoimmune glial fibrillary acidic protein astrocytopathy with seizures in children.

A single-center retrospective analysis of autoimmune glial fibrillary acidic protein astrocytopathy with seizures in children.

Journal: Frontiers in neurology

Published: March 13, 2025

Breath-holding spells comorbidity with epileptic seizures in children: VEEG and clinical outcomes.

Breath-holding spells comorbidity with epileptic seizures in children: VEEG and clinical outcomes.

Journal: Medicine

Published: September 03, 2024

Video-electroencephalographic findings and clinical characteristics of bathing seizures in children.

Video-electroencephalographic findings and clinical characteristics of bathing seizures in children.

Journal: Frontiers in neurology

Published: January 05, 2024

Clinical characteristics and genetic analysis of pediatric patients with sodium channel gene mutation-related childhood epilepsy: a review of 94 patients.

Clinical characteristics and genetic analysis of pediatric patients with sodium channel gene mutation-related childhood epilepsy: a review of 94 patients.

Journal: Frontiers in neurology

Published: October 09, 2023

Genetic analysis of a child with early onset neurodevelopmental disorder with involuntary movement and a literature review

Genetic analysis of a child with early onset neurodevelopmental disorder with involuntary movement and a literature review

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: March 27, 2023

Analysis of clinical phenotype and genetic variants in a child with mitochondrial F-S disease due to variants of FDXR gene

Analysis of clinical phenotype and genetic variants in a child with mitochondrial F-S disease due to variants of FDXR gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: March 27, 2023

Clinical analysis of 173 pediatric patients with antibody-mediated autoimmune diseases of the central nervous system: a single-center cohort study.

Clinical analysis of 173 pediatric patients with antibody-mediated autoimmune diseases of the central nervous system: a single-center cohort study.

Journal: Frontiers in immunology

Published: January 09, 2023

Clinical spectrum of contactin-associated protein 2 autoimmune encephalitis in children.

Clinical spectrum of contactin-associated protein 2 autoimmune encephalitis in children.

Journal: Frontiers in neuroscience

Published: November 23, 2022

Clinical and genetic analyses of premature mitochondrial encephalopathy with epilepsia partialis continua caused by novel biallelic NARS2 mutations.

Clinical and genetic analyses of premature mitochondrial encephalopathy with epilepsia partialis continua caused by novel biallelic NARS2 mutations.

Journal: Frontiers in neuroscience

Published: October 21, 2022

Nabais Sa-de Vries syndrome in a Chinese infant associated with a novel SPOP mutation: A clinical study and genetic report.

Nabais Sa-de Vries syndrome in a Chinese infant associated with a novel SPOP mutation: A clinical study and genetic report.

Journal: Molecular genetics & genomic medicine

Published: August 23, 2022

CASPR2 antibody associated neurological syndromes in children.

CASPR2 antibody associated neurological syndromes in children.

Journal: Scientific reports

Published: July 10, 2022

Showing 1-12 of 18

Last Updated: 09/26/2026