Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jingbin Du"'
Autor:
Dayan sun, Chuanping Xie, Yong Zhao, Junmin Liao, Shuangshuang Li, Yanan Zhang, Dingding Wang, Kaiyun Hua, Yichao Gu, Jingbin Du, Guoxian Huang, Jinshi Huang
Publikováno v:
Molecular Medicine, Vol 30, Iss 1, Pp 1-16 (2024)
Abstract Cholestatic liver diseases (CLD) are characterized by impaired normal bile flow, culminating in excessive accumulation of toxic bile acids. The majority of patients with CLD ultimately progress to liver cirrhosis and hepatic failure, necessi
Externí odkaz:
https://doaj.org/article/bec822a5f6ad4295afcfc57946bd54c3
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundWe aimed to evaluate the function of the reconstructed anal canal in postoperative anorectal malformations (ARMs) patients through three dimension (3D) high-definition anorectal manometry.MethodsFrom January 2015 to December 2019, 3D manome
Externí odkaz:
https://doaj.org/article/b36c01d4f6f94550a152b8045571f4aa
Autor:
Shen Yang, Ruizhe Yang, Xiaofan Ma, Shuangfeng Yang, Yun Peng, Qiang Tao, Kuai Chen, Junfeng Tao, Yanan Zhang, Jingbin Du, Jinshi Huang, Xiaoxia Peng, Peifang Wei
Publikováno v:
Chinese Medical Journal, Vol 135, Iss 4, Pp 485-487 (2022)
Externí odkaz:
https://doaj.org/article/dce1f5344d5e4d94bf327489d5375f12
Autor:
Wenjun Mou, Shen Yang, Ruolan Guo, Libing Fu, Li Zhang, Weihong Guo, Jingbin Du, Jianxin He, Qinghua Ren, Chanjuan Hao, Jingang Gui, Jinshi Huang
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Rare autosomal-recessive variants in tetratricopeptide repeat domain 7A (TTC7A) gene have been shown to cause intestinal and immune disorders of variable severity. Missense mutations in TTC7A gene, usually retaining most of the functional motifs, is
Externí odkaz:
https://doaj.org/article/714461f1dec74823a529e7e63e8e2dec
Autor:
Zhaozhou Liu, Yanan Zhang, Shuangshuang Li, Shen Yang, Jiawei Zhao, Ting Yang, Siqi Li, Yongwei Chen, Weihong Guo, Dawei Hou, Jingbin Du, Yingzi Li, Jinshi Huang
Publikováno v:
International Journal of Colorectal Disease. 37:1127-1132
Purpose To explore the risk factors of enterostomy in neonates with Hirschsprung disease (HD) to provide reference for clinicians to make treatment decisions. Methods The medical records of 284 patients who were diagnosed with HD during the neonatal
Publikováno v:
Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility SocietyREFERENCES. 34(10)
We aimed to evaluate anorectal function of normal infants and children through three dimension high-definition anorectal manometry (3D ARM) to fill the research blank in this area.From November 2014 to January 2019, 104 normal infants and children am
Autor:
Wenjun, Mou, Shen, Yang, Ruolan, Guo, Libing, Fu, Li, Zhang, Weihong, Guo, Jingbin, Du, Jianxin, He, Qinghua, Ren, Chanjuan, Hao, Jingang, Gui, Jinshi, Huang
Publikováno v:
Frontiers in Immunology
Rare autosomal-recessive variants in tetratricopeptide repeat domain 7A (TTC7A) gene have been shown to cause intestinal and immune disorders of variable severity. Missense mutations in TTC7A gene, usually retaining most of the functional motifs, is
Publikováno v:
Annals of Laparoscopic and Endoscopic Surgery. 4:90-90
Esophageal atresia (EA) is a rare and complicated congenital malformation. Since it was first reported, it has had a long history. Nowadays, standard treatment options consist of open procedure and thoracoscopic surgery. Each procedure has its benefi