Jeong-Tak Oh
Yonsei University · Medicine
About the Lab
Professor Jeong-Tak Oh's research lab specializes in pediatric surgical diseases, with a focus on congenital anomalies of the biliary and gastrointestinal tracts, including biliary atresia, choledochal cysts, and Hirschsprung disease. The lab emphasizes advanced imaging techniques such as MR cholangiopancreatography and innovative surgical approaches, including laparoscopic and robot-assisted resections, to improve diagnostic accuracy and surgical outcomes. Research also extends to short bowel syndrome, exploring surgical interventions like STEP to enhance nutritional status and intestinal function.
Research Overview
Research Output Trend
Figures are computed from collected data and may differ slightly.
Selected Papers
15The presence of hepatic subcapsular flow is useful for differentiating between BA and other causes of neonatal jaundice.
OBJECTIVE: The purpose of this study was to determine whether MR cholangiopancreatography can accurately depict anomalous pancreaticobiliary ductal union in children with choledochal cysts. SUBJECTS AND METHODS: Twenty children (age range, 1 month-13 years; mean age, 4.6 years; all girls) who were diagnosed with choledochal cyst by sonography underwent MR cholangiopancreatography with a single-shot fast spin-echo sequence. The type of choledochal cyst and anomalous pancreaticobiliary ductal unio
STEP improves weight retention, nutritional status, intestinal absorptive capacity, and serum citrulline levels in a porcine short bowel model. A salutary effect upon bacterial overgrowth was also noted. These data support the use of this operation in short bowel syndrome.
The objective of this study is to define optimal diagnosis and treatment strategies for patients with urachal anomalies in the pediatric age group. The medical records of 21 children who had undergone surgery for urachal anomalies at Severance Hospital, Yonsei University College of Medicine from January 1990 to April 2005 were reviewed. The subjects included 14 males and 7 females (M:F 2:1). The four types of urachal anomalies confirmed were a urachal cyst in 10 patients (47.6%), a patent urachu
PURPOSE: The laparoscopic surgery for a choledochal cyst in children is technically challenging because of its high degree of complexity despite its possibility. In an attempt to overcome this laparoscopic weakness and to facilitate the difficult steps in the minimally invasive surgery for choledochal cyst resection in children, we have performed the robot-assisted resection of the choledochal cyst. The aim of this study is to report lessons and tips obtained from our experience of the robot-ass
Hirschsprung disease (HSCR) is a congenital and heterogeneous disorder characterized by the absence of intramural nervous plexuses along variable lengths of the hindgut. Although RET is a well-established risk factor, a recent genome-wide association study (GWAS) of HSCR has identified NRG1 as an additional susceptibility locus. To discover additional risk loci, we performed a GWAS of 123 sporadic HSCR patients and 432 unaffected controls using a large-scale platform with coverage of over 1 mill
Research Areas
Dive deeper into Jeong-Tak Oh's research on Nubint
Open this lab's papers in the app to read with AI, summarize, and cite in your writing.