Wei Zhong

Provincial Key Laboratory of Research in Structure Birth Defect Disease and Department of Pediatric Surgery, Guangzhou Medical University

Affiliated withGuangzhou Medical University Guangzhou Medical University

Research Area

Medicine

Biography

Wei Zhong has not added Biography.
If you are Wei Zhong and would like to personalize this page please email our Author Liaison for assistance.

JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 4	2021

Other Publications

Article	Year
[Treatment strategy and prognosis analysis in children with type I( esophageal atresia]. Zhonghua wei chang wai ke za zhi = Chinese journal of gastrointestinal surgery\| PubMed ID: 24061994	2013
Standardized Indications to Assist in the Safe Thoracoscopic Repair of Congenital Diaphragmatic Hernia in Neonates. Journal of laparoendoscopic & advanced surgical techniques. Part A\| PubMed ID: 26989924	2016
LMO1 gene polymorphisms contribute to decreased neuroblastoma susceptibility in a Southern Chinese population. Oncotarget\| PubMed ID: 27009839	2016
Decreased expression of miR-33 in fetal lungs of nitrofen-induced congenital diaphragmatic hernia rat model. Journal of pediatric surgery\| PubMed ID: 27041227	2016
Prenatal diagnosis and early postnatal management of pyriform sinus cyst: experience at a single medical center in mainland China. Prenatal diagnosis\| PubMed ID: 27669366	2016
[Application of Bishop-Koop stoma in refractory congenital intestinal atresia]. Zhonghua wei chang wai ke za zhi = Chinese journal of gastrointestinal surgery\| PubMed ID: 27781254	2016
Large-scale replication study identified multiple independent SNPs in synergistically associated with Hirschsprung disease in Southern Chinese population. Aging\| PubMed ID: 28930629	2017
Treatment of fetal congenital chylothorax: Report of eight cases at a mainland Chinese medical center. Taiwanese journal of obstetrics & gynecology\| PubMed ID: 29241937	2017
Neonatal Gastric Perforation: Case Series and Literature Review. World journal of surgery\| PubMed ID: 29392435	2018
Enhanced expression of SRPK2 contributes to aggressive progression and metastasis in prostate cancer. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie\| PubMed ID: 29587239	2018
The intragenic epistatic association of with biliary atresia in Southern Han Chinese population. Bioscience reports\| PubMed ID: 29685956	2018
Is the Bishop-Koop procedure useful in severe jejunoileal atresia? Journal of pediatric surgery\| PubMed ID: 29709288	2018
How to make an accurate diagnosis of fetal pyriform sinus fistula in utero: experience at a single medical center in mainland China. European journal of obstetrics, gynecology, and reproductive biology\| PubMed ID: 29909267	2018
Association between DSCAM polymorphisms and non-syndromic Hirschsprung disease in Chinese population. BMC medical genetics\| PubMed ID: 30005639	2018
The Role of Neonatal Gr-1 Myeloid Cells in a Murine Model of Rhesus-Rotavirus-Induced Biliary Atresia. The American journal of pathology\| PubMed ID: 30201498	2018
Diagnostic value of the acute angle between the prestenotic and poststenotic duodenum in neonatal annular pancreas. European radiology\| PubMed ID: 30617479	2019
Measuring the common canal of a persistent cloaca: can MRI replace conventional imaging? Clinical radiology\| PubMed ID: 30905379	2019
Simple and safe thoracoscopic repair of neonatal congenital diaphragmatic hernia by a new modified knot-tying technique. Hernia : the journal of hernias and abdominal wall surgery\| PubMed ID: 31317290	2019
Associations of genetic polymorphisms with Hirschsprung's disease in a Southern Chinese population. Bioscience reports\| PubMed ID: 31358688	2019
Efficacy, safety, and biomarker analysis of ensartinib in crizotinib-resistant, ALK-positive non-small-cell lung cancer: a multicentre, phase 2 trial. The Lancet. Respiratory medicine\| PubMed ID: 31628085	2020
Predicting poor outcomes and the need for surgical treatment in neonates with meconium peritonitis. Prenatal diagnosis\| PubMed ID: 31713898	2020
miR-618 rs2682818 C>A polymorphism decreases Hirschsprung disease risk in Chinese children. Bioscience reports\| PubMed ID: 32364585	2020
Negative Association Between lncRNA rs3807598 C>G and Hirschsprung Disease. Pharmacogenomics and personalized medicine\| PubMed ID: 32440194	2020
The value of saline-aided ultrasound in diagnosing congenital duodenal obstruction. Pediatric surgery international\| PubMed ID: 32715324	2020
rs1834306 A>G Increases the Risk of Hirschsprung Disease in Southern Chinese Children. Pharmacogenomics and personalized medicine\| PubMed ID: 32848443	2020
Extracorporeal membrane oxygenation for congenital diaphragmatic hernia: how to begin? Minerva pediatrica\| PubMed ID: 32881475	2020
Ultrasonographic diagnosis, classification, and treatment of cervical lymphatic malformation in paediatric patients: a retrospective study. BMC pediatrics\| PubMed ID: 32950065	2020
Association between rs2289030 G>C and susceptibility to Hirschsprung disease in southern Chinese children. The Journal of international medical research\| PubMed ID: 33103535	2020
Associations between common genetic variants in microRNAs and Hirschsprung disease susceptibility in Southern Chinese children. The journal of gene medicine\| PubMed ID: 33294994	2021
Correlation analysis of IL-11 polymorphisms and Hirschsprung disease subtype susceptibility in Southern Chinese Children. BMC medical genomics\| PubMed ID: 33468134	2021
Decoding the Evolutionary Response to Ensartinib in Patients With ALK-Positive NSCLC by Dynamic Circulating Tumor DNA Sequencing. Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer\| PubMed ID: 33588113	2021
Prenatal diagnosis and postnatal management of congenital mesoblastic nephroma: Experience at a single center in China. Prenatal diagnosis\| PubMed ID: 33782977	2021
Flexible endoscopic identification and catheterization of congenital H-type tracheoesophageal fistula using a laryngeal mask. Digestive endoscopy : official journal of the Japan Gastroenterological Endoscopy Society\| PubMed ID: 34432913	2021
Association between ABHD1 and DOK6 polymorphisms and susceptibility to Hirschsprung disease in Southern Chinese children. Journal of cellular and molecular medicine\| PubMed ID: 34545688	2021
T>C polymorphism increases Hirschsprung disease risk: a case-control study of Chinese children. Personalized medicine\| PubMed ID: 34761964	2021
Prediction of late-onset fetal growth restriction using a combined first- and second-trimester screening model. Journal of gynecology obstetrics and human reproduction\| PubMed ID: 34813940	2021