Wei Zhong

[Treatment strategy and prognosis analysis in children with type I( esophageal atresia].

Standardized Indications to Assist in the Safe Thoracoscopic Repair of Congenital Diaphragmatic Hernia in Neonates.

LMO1 gene polymorphisms contribute to decreased neuroblastoma susceptibility in a Southern Chinese population.

Decreased expression of miR-33 in fetal lungs of nitrofen-induced congenital diaphragmatic hernia rat model.

Prenatal diagnosis and early postnatal management of pyriform sinus cyst: experience at a single medical center in mainland China.

[Application of Bishop-Koop stoma in refractory congenital intestinal atresia].

Large-scale replication study identified multiple independent SNPs in synergistically associated with Hirschsprung disease in Southern Chinese population.

Treatment of fetal congenital chylothorax: Report of eight cases at a mainland Chinese medical center.

Neonatal Gastric Perforation: Case Series and Literature Review.

Enhanced expression of SRPK2 contributes to aggressive progression and metastasis in prostate cancer.

The intragenic epistatic association of with biliary atresia in Southern Han Chinese population.

Is the Bishop-Koop procedure useful in severe jejunoileal atresia?

How to make an accurate diagnosis of fetal pyriform sinus fistula in utero: experience at a single medical center in mainland China.

Association between DSCAM polymorphisms and non-syndromic Hirschsprung disease in Chinese population.

The Role of Neonatal Gr-1 Myeloid Cells in a Murine Model of Rhesus-Rotavirus-Induced Biliary Atresia.

Diagnostic value of the acute angle between the prestenotic and poststenotic duodenum in neonatal annular pancreas.

Measuring the common canal of a persistent cloaca: can MRI replace conventional imaging?

Simple and safe thoracoscopic repair of neonatal congenital diaphragmatic hernia by a new modified knot-tying technique.

Associations of genetic polymorphisms with Hirschsprung's disease in a Southern Chinese population.

Efficacy, safety, and biomarker analysis of ensartinib in crizotinib-resistant, ALK-positive non-small-cell lung cancer: a multicentre, phase 2 trial.

Predicting poor outcomes and the need for surgical treatment in neonates with meconium peritonitis.

miR-618 rs2682818 C>A polymorphism decreases Hirschsprung disease risk in Chinese children.

Negative Association Between lncRNA rs3807598 C>G and Hirschsprung Disease.

The value of saline-aided ultrasound in diagnosing congenital duodenal obstruction.

rs1834306 A>G Increases the Risk of Hirschsprung Disease in Southern Chinese Children.

Extracorporeal membrane oxygenation for congenital diaphragmatic hernia: how to begin?

Ultrasonographic diagnosis, classification, and treatment of cervical lymphatic malformation in paediatric patients: a retrospective study.

Association between rs2289030 G>C and susceptibility to Hirschsprung disease in southern Chinese children.

Associations between common genetic variants in microRNAs and Hirschsprung disease susceptibility in Southern Chinese children.

Correlation analysis of IL-11 polymorphisms and Hirschsprung disease subtype susceptibility in Southern Chinese Children.

Decoding the Evolutionary Response to Ensartinib in Patients With ALK-Positive NSCLC by Dynamic Circulating Tumor DNA Sequencing.

Prenatal diagnosis and postnatal management of congenital mesoblastic nephroma: Experience at a single center in China.

Flexible endoscopic identification and catheterization of congenital H-type tracheoesophageal fistula using a laryngeal mask.

Association between ABHD1 and DOK6 polymorphisms and susceptibility to Hirschsprung disease in Southern Chinese children.

T>C polymorphism increases Hirschsprung disease risk: a case-control study of Chinese children.

Prediction of late-onset fetal growth restriction using a combined first- and second-trimester screening model.