Erhu Wei
Zhengzhou, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 12 publications
Acute diquat poisoning in children: a single-center retrospective observational study.
Journal: Frontiers in pediatrics
Published: April 01, 2026
Metagenomic next-generation sequencing could play a pivotal role in validating the diagnosis of invasive mold disease of the central nervous system.
Journal: Frontiers in cellular and infection microbiology
Published: February 28, 2024
Clinical features of pediatric mucormycosis: role of metagenomic next generation sequencing in diagnosis.
Journal: Frontiers in cellular and infection microbiology
Published: January 10, 2024
Interplay between mitochondrial dysfunction and lysosomal storage: challenges in genetic metabolic muscle diseases with a focus on infantile onset Pompe disease.
Journal: Frontiers in cardiovascular medicine
Published: January 08, 2024
Analysis of OTC gene variants in four children with delayed onset Ornithine transcarbamylase deficiency
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: February 28, 2023
Clinical features and diagnostic value of metagenomic next -generation sequencing in five cases of non-HIV related Pneumocystis jirovecii pneumonia in children.
Journal: Frontiers in cellular and infection microbiology
Published: December 27, 2022
Metagenomic next-generation sequencing may assist diagnosis of cat-scratch disease.
Journal: Frontiers in cellular and infection microbiology
Published: May 18, 2022
Genetic Characterization of Enterobacter hormaechei Co-Harboring bla NDM-1 and mcr-9 Causing Upper Respiratory Tract Infection.
Journal: Infection and drug resistance
Published: March 19, 2022
Genetic analysis and identification of novel variations in Chinese patients with pediatric epilepsy by whole-exome sequencing.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: December 08, 2021
A de novo and novel nonsense variants in ASXL2 gene is associated with Shashi-Pena syndrome.
Journal: European journal of medical genetics
Published: October 27, 2021
Showing 1-12 of 12
Last Updated: 09/26/2026