Jia W. Zhang

No. 20, South Renmin Road
Chengdu, 610041, China

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 23 publications

Correction: Analysis of treatment outcome variations in infantile epileptic spasms syndrome.

Correction: Analysis of treatment outcome variations in infantile epileptic spasms syndrome.

Journal: Frontiers in neurology
Published: April 16, 2026

Clinical Analysis of SYNGAP1 Variant-Related Neurodevelopmental Disorders in Chinese Children.

Clinical Analysis of SYNGAP1 Variant-Related Neurodevelopmental Disorders in Chinese Children.

Journal: Clinical genetics
Published: January 22, 2026

Research progress in SYNGAP1-related neurodevelopmental disorders: from pathogenesis to therapeutic strategies.

Research progress in SYNGAP1-related neurodevelopmental disorders: from pathogenesis to therapeutic strategies.

Journal: Frontiers in neurology
Published: December 22, 2025

Analysis of treatment outcome variations in infantile epileptic spasms syndrome.

Analysis of treatment outcome variations in infantile epileptic spasms syndrome.

Journal: Frontiers in neurology
Published: November 19, 2025

Clinical Characteristics and Treatment Outcomes in Children With Non-Acquired Epilepsy: A Cohort Study Based on Genetic Findings.

Clinical Characteristics and Treatment Outcomes in Children With Non-Acquired Epilepsy: A Cohort Study Based on Genetic Findings.

Journal: Clinical genetics
Published: October 24, 2025

Modeling epilepsy by loss-of-function of the CUG-binding protein Elav-like family member 2 in zebrafish with multi-omics analysis.

Modeling epilepsy by loss-of-function of the CUG-binding protein Elav-like family member 2 in zebrafish with multi-omics analysis.

Journal: Chinese medical journal
Published: April 17, 2024

Analysis of a child featuring global developmental delay and autism due to variant of TBR1 gene and a literature review

Analysis of a child featuring global developmental delay and autism due to variant of TBR1 gene and a literature review

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: March 06, 2024

Analysis of clinical characteristics and ATP7A gene variants in a Chinese pedigree affected with Menkes disease

Analysis of clinical characteristics and ATP7A gene variants in a Chinese pedigree affected with Menkes disease

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: November 23, 2023

Analysis of clinical features and PAK1 gene variant in a child with epilepsy and global developmental delay

Analysis of clinical features and PAK1 gene variant in a child with epilepsy and global developmental delay

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: April 27, 2023

Anti-NMDAR encephalitis secondary to acute necrotizing encephalopathy caused by herpes simplex virus infection in infants: Case series.

Anti-NMDAR encephalitis secondary to acute necrotizing encephalopathy caused by herpes simplex virus infection in infants: Case series.

Journal: Clinical neurology and neurosurgery
Published: April 24, 2023

Genetic mechanisms in generalized epilepsies.

Genetic mechanisms in generalized epilepsies.

Journal: Acta epileptologica
Published: October 01, 2022

De novo variant of CSNK2B causes Poirier-Bienvenu neurodevelopmental syndrome: two case report

De novo variant of CSNK2B causes Poirier-Bienvenu neurodevelopmental syndrome: two case report

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: May 22, 2022
Showing 1-12 of 23

Last Updated: 09/26/2026