Zhihong H. Zhuo

Zhengzhou, China

Last Updated: 09/26/2026

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Found 22 publications

Clinical features and genetic analysis of a child with Christianson syndrome due to variant of SLC9A6 gene

Clinical features and genetic analysis of a child with Christianson syndrome due to variant of SLC9A6 gene

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

Published: June 24, 2025

The impact of Vav1 on epileptogenesis and neuronal apoptosis: insights from Sirt1 activation.

The impact of Vav1 on epileptogenesis and neuronal apoptosis: insights from Sirt1 activation.

Journal: Biochemical pharmacology

Published: June 10, 2025

Clinical phenotypic and genetic analysis of three children with Paroxysmal kinesigenic dyskinesia and Self-limited familial infantile epilepsy caused by PRRT2 gene mutation

Clinical phenotypic and genetic analysis of three children with Paroxysmal kinesigenic dyskinesia and Self-limited familial infantile epilepsy caused by PRRT2 gene mutation

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

Published: May 15, 2025

Biomarkers for diagnosis and prognosis of myelin oligodendrocyte glycoprotein antibody-associated disease - review article.

Biomarkers for diagnosis and prognosis of myelin oligodendrocyte glycoprotein antibody-associated disease - review article.

Journal: Frontiers in immunology

Published: March 17, 2025

Clinical and genetic analysis of a child with X-linked mental retardation due to variant of SLC9A7 gene

Clinical and genetic analysis of a child with X-linked mental retardation due to variant of SLC9A7 gene

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

Published: May 31, 2024

Variants of TSC1 are associated with developmental and epileptic encephalopathy and focal epilepsy without tuberous sclerosis : For the China Epilepsy Gene 1.0 Project.

Variants of TSC1 are associated with developmental and epileptic encephalopathy and focal epilepsy without tuberous sclerosis : For the China Epilepsy Gene 1.0 Project.

Journal: Acta epileptologica

Published: May 07, 2024

A case report of anti-GAD65 antibody-positive autoimmune encephalitis in children associated with autoimmune polyendocrine syndrome type-II and literature review.

A case report of anti-GAD65 antibody-positive autoimmune encephalitis in children associated with autoimmune polyendocrine syndrome type-II and literature review.

Journal: Frontiers in immunology

Published: August 08, 2023

Maturation of the gut metabolome during the first year of life in humans.

Maturation of the gut metabolome during the first year of life in humans.

Journal: Gut microbes

Published: July 10, 2023

Crosstalk between Breast Milk N-Acetylneuraminic Acid and Infant Growth in a Gut Microbiota-Dependent Manner.

Crosstalk between Breast Milk N-Acetylneuraminic Acid and Infant Growth in a Gut Microbiota-Dependent Manner.

Journal: Metabolites

Published: June 14, 2023

Epilepsy, gut microbiota, and circadian rhythm.

Epilepsy, gut microbiota, and circadian rhythm.

Journal: Frontiers in neurology

Published: February 02, 2023

GKLF, a transcriptional activator of Txnip, drives microglia activation in kainic acid-induced murine models of epileptic seizures.

GKLF, a transcriptional activator of Txnip, drives microglia activation in kainic acid-induced murine models of epileptic seizures.

Journal: International immunopharmacology

Published: January 23, 2023

Effect of Breastmilk Microbiota and Sialylated Oligosaccharides on the Colonization of Infant Gut Microbial Community and Fecal Metabolome.

Effect of Breastmilk Microbiota and Sialylated Oligosaccharides on the Colonization of Infant Gut Microbial Community and Fecal Metabolome.

Journal: Metabolites

Published: October 20, 2022

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Last Updated: 09/26/2026