Wenxiong F. Chen
Foshan Key Laboratory For Precision Diagnosis Of Birth Defects
Foshan, 528000, China
Foshan, 528000, China
Last Updated: 09/26/2026
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Found 26 publications
Newborn screening and early disease-modifying therapy for spinal muscular atrophy in the Foshan region
Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: May 14, 2026
Efficacy and Safety of Extended-Release Clonidine Hydrochloride for Attention Deficit Hyperactivity Disorder in Chinese Children and Adolescents: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial.
Journal: Journal of child and adolescent psychopharmacology
Published: April 07, 2026
Comprehensive multi-omics mapping of immune perturbations in autism spectrum disorder.
Journal: Clinical and translational medicine
Published: May 09, 2025
Chinese Expert Consensus on Integrated Chinese and Western Medicine for the Treatment of Tic Disorders.
Journal: Journal of evidence-based medicine
Published: August 17, 2024
Correlation between clinical phenotypes and genotypes among 46 children with SCN1A-related developmental epileptic encephalopathy
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: April 02, 2024
Postoperative EEG abnormalities in relation to neurodevelopmental outcomes after pediatric cardiac surgery.
Journal: Pediatric research
Published: December 21, 2023
A Post-Marketing Surveillance Study of Nusinersen for Spinal Muscular Atrophy in Routine Medical Practice in China: Interim Results.
Journal: Advances in therapy
Published: November 20, 2023
Analysis of NR2F1 gene variant in a child with optic atrophy and global developmental delay
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: September 20, 2023
Clinical and genetic analysis of 18 patients with KCNQ2 mutations from South China.
Journal: The Turkish journal of pediatrics
Published: July 26, 2023
Modified nusinersen intrathecal injection method: inclusion of a septal needle-free closed infusion connector.
Journal: Frontiers in neurology
Published: June 04, 2023
Clinical and genetic analysis of a child with Mental retardation autosomal dominant 51
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: May 22, 2023
Last Updated: 09/26/2026