The association of auditory integration training in children with autism spectrum disorders among Chinese: a meta-analysis

por Li, Ning, Li, Ling, Li, Guimei, Gai, Zhongtao
Publicado 2018

Great Expectations: Induced pluripotent stem cell technologies in neurodevelopmental impairments

por Zhang, Xue, Li, Zilong, Liu, Yi, Gai, Zhongtao
Publicado 2021

A case series report of hospitalized children with severe acute respiratory syndrome coronavirus-2 infection in Jinan, China

por Li, Jian, Geng, Jin, Su, Liang, Yang, Bo, Gai, Zhongtao
Publicado 2020

Association of the ACE, GSTM1, IL-6, NOS3, and CYP1A1 polymorphisms with susceptibility of mycoplasma pneumoniae pneumonia in Chinese children

por Zhao, Jie, Zhang, Wen, Shen, Li, Yang, Xiaomeng, Liu, Yi, Gai, Zhongtao
Publicado 2017

Do children need a longer time to shed SARS-CoV-2 in stool than adults?

por Ma, Xiang, Su, Liang, Zhang, Yunkui, Zhang, Xiuzhen, Gai, Zhongtao, Zhang, Zhongfa
Publicado 2020

Comparison of Laparoscopic-Assisted Operations and Laparotomy Operations for the Treatment of Hirschsprung Disease: Evidence From a Meta-Analysis

por Zhang, Shisong, Li, Juan, Wu, Yurui, Hu, Yuanjun, Duan, Chunhong, Wang, Meiyun, Gai, Zhongtao
Publicado 2015

Pathogenic Triad in Bacterial Meningitis: Pathogen Invasion, NF-κB Activation, and Leukocyte Transmigration that Occur at the Blood-Brain Barrier

por Wang, Shifu, Peng, Liang, Gai, Zhongtao, Zhang, Lehai, Jong, Ambrose, Cao, Hong, Huang, Sheng-He
Publicado 2016

Evaluation of a Viral Microarray Based on Simultaneous Extraction and Amplification of Viral Nucleotide Acid for Detecting Human Herpesviruses and Enteroviruses

por Liu, Yi, Duan, Chunhong, Zhang, Chunxiu, Yang, Xiaomeng, Zhao, Yan, Dong, Rui, Zhou, Jiajing, Gai, Zhongtao
Publicado 2015

Clinical Application of an Innovative Multiplex-Fluorescent-Labeled STRs Assay for Prader-Willi Syndrome and Angelman Syndrome

por Zhang, Kaihui, Liu, Shu, Feng, Bing, Yang, Yali, Zhang, Haiyan, Dong, Rui, Liu, Yi, Gai, Zhongtao
Publicado 2016

Correction to: Familial intellectual disability as a result of a derivative chromosome 22 originating from a balanced translocation (3;22) in a four generation family

por Zhang, Kaihui, Huang, Yan, Dong, Rui, Yang, Yali, Wang, Ying, Zhang, Haiyan, Zhang, Yufeng, Gai, Zhongtao, Liu, Yi
Publicado 2018

Novel Neonatal Variants of the Carbamoyl Phosphate Synthetase 1 Deficiency: Two Case Reports and Review of Literature

por Yan, Beibei, Wang, Chao, Zhang, Kaihui, Zhang, Haiyan, Gao, Min, Lv, Yuqiang, Li, Xiaoying, Liu, Yi, Gai, Zhongtao
Publicado 2019

Expression of circulating angiotensin‐converting enzyme 2 in children with asthma and the effects of inhaled corticosteroids

por Ma, Xiang, Liu, Lesen, Sun, Jing, Zhang, Yun, Liu, Yanqin, Liu, Miao, Wang, Bing, Chang, Yuna, Han, Yuling, Gai, Zhongtao
Publicado 2023

Molecular Genetics Analysis of 70 Chinese Families With Muscular Dystrophy Using Multiplex Ligation-Dependent Probe Amplification and Next-Generation Sequencing

por Wang, Dong, Gao, Min, Zhang, Kaihui, Jin, Ruifeng, Lv, Yuqiang, Liu, Yong, Ma, Jian, Wan, Ya, Gai, Zhongtao, Liu, Yi
Publicado 2019

Mutational Characteristics of Causative Genes in Chinese Hereditary Spherocytosis Patients: a Report on Fourteen Cases and a Review of the Literature

por Wang, Dong, Song, Li, Shen, Li, Zhang, Kaihui, Lv, Yuqiang, Gao, Min, Ma, Jian, Wan, Ya, Gai, Zhongtao, Liu, Yi
Publicado 2021

Genotypic and phenotypic characteristics of 12 chinese children with glycogen storage diseases

por Dong, Rui, Wei, Xuxia, Zhang, Kaihui, Song, Fengling, Lv, Yuqiang, Gao, Min, Wang, Dong, Ma, Jian, Gai, Zhongtao, Liu, Yi
Publicado 2022

A potential pathogenic hypoxia-related gene HK2 in necrotizing enterocolitis (NEC) of newborns

por Han, Yujie, Liu, Xianghong, Kang, Lili, Chen, Dong, Li, Yongqing, Zhang, Huiping, Sun, Mingying, Gao, Hui, Gai, Zhongtao, Li, Xiaoying
Publicado 2022

Phenotype and genotype analyses of Chinese patients with autosomal dominant mental retardation type 5 caused by SYNGAP1 gene mutations

por Wang, Yanxin, Lv, Yuqiang, Li, Zilong, Gao, Min, Yang, Xiaomeng, Li, Yue, Shi, Jianguo, Gao, Zaifen, Liu, Yi, Gai, Zhongtao
Publicado 2022

Diagnostic application of exome sequencing in Chinese children with suspected inherited kidney diseases

por Gao, Min, Yu, Fengling, Dong, Rui, Zhang, Kaihui, Lv, Yuqiang, Ma, Jian, Wang, Dong, Zhang, Hongxia, Gai, Zhongtao, Liu, Yi
Publicado 2023

DCX variants in two unrelated Chinese families with subcortical band heterotopia: Two case reports and review of literature

por Gao, Chunlai, Liu, Ning, Ma, Jian, Zhao, Jianshe, Zhao, Bing, Song, Fengling, Dong, Rui, Li, Zilong, Lv, Yuqiang, Liu, Yi, Gai, Zhongtao
Publicado 2023

Group B Streptococcus colonization induces Prevotella and Megasphaera abundance-featured vaginal microbiome compositional change in non-pregnant women

por Mu, Xiaofeng, Zhao, Changying, Yang, Junjie, Wei, Xiaofang, Zhang, Jiaming, Liang, Cheng, Gai, Zhongtao, Zhang, Chunling, Zhu, Dequan, Wang, Ye, Zhang, Lei
Publicado 2019