Results 101 to 110 of about 613,875 (232)

UEG Week 2024 Poster Presentations

United European Gastroenterology Journal, Volume 12, Issue S8, Page 665-1360, October 2024.
wiley   +1 more source

Biliary Atresia

, 2011
Biliary atresia (BA) is an infantile cholestatic disease of progressive obliterative cholangiopathy with varying degrees of damage to both extra and intrahepatic bile ducts due to unknown causes.
한석주
core  

Hepatic fibrosis scan for liver stiffness score measurement: a useful preendoscopic screening test for the detection of varices in postoperative patients with biliary atresia

, 2009
OBJECTIVE: Even after successful Kasai portoenterostomy, progressive hepatic fibrosis in postoperative patients with biliary atresia (BA) can be associated with portal hypertension and esophageal or gastric varices.
오정탁, 한석주, 정기섭, 고홍, 김성민, 장혜경   +5 more
core   +1 more source

Correlation of Transient Elastography and Progression of Cirrhosis in Longterm Survivors of Biliary Atresia

Siriraj Medical Journal, 2020
Objective: This study aimed to use transient elastography (TE) to evaluate the correlation between liver stiffness measure (LSM) and functional status of native liver in longterm follow-up of pediatric patients with biliary atresia (BA). Methods: Twenty
Witsanee Srisuwan, Wison Laochareonsuk, Panu Wetwittayakhlang, Supika Kritsaneepaiboon, Surasak Sangkhathat   +4 more
doaj  

Biomarkers in Biliary Atresia Following Successful Portoenterostomy Surgery

, 2023
Biliary atresia (BA) is a rare pediatric liver disease characterized by fibrotic, inflammatory and obliterative damage of the bile ducts and obstruction of the bile flow.
Godbole, Nimish
core  

Are Medical Students and Primary Health-care Professionals Aware of Neonatal Cholestasis and Acholic Stool

Turkish Archives of Pediatrics
Objective: Early diagnosis of biliary atresia (BA) and the timing of Kasai hepatic portoenterostomy are associated with improved survival rates of the native liver. Acholic stool is a major and earliest sign of BA.
Neslihan Gürcan Kaya, Sinan Sarı, Buket Dalgıç   +2 more
doaj   +1 more source

The management of biliary atresia in the era of liver transplantation

, 2003
Biliary atresia is the commonest cause of pathological jaundice in infants. The aetiology and pathogenesis are largely unknown despite advances in molecular science.
Tam, PKH, Wong, KKY, Fan, ST, Chan, KL, Saing, H   +4 more
core  

[Hepatic portoenterostomy and primary liver transplantation in the treatment of biliary atresia].

Lijecnicki vjesnik, 2002
Results show that the use of sequential surgical treatment, employing Kasai portoenterostomy in infancy, followed by selective liver transplantation for children with progressive hepatic deterioration yields improved overall survival. All children with successful Kasai portoenterostomy procedures who do not require orthotopic liver transplantation are ...
S, Batinica, J, Vuković, L, Popović
openaire   +1 more source

Liver mobilization during Kasai portoenterostomy: retrospective multicentre analysis. [PDF]

BJS Open
Uecker M, Holweg M, Hukkinen M, Moratilla-Lapeña L, Dräger K, Domasch A, Nickel K, Wiesner S, van Beekum CJ, Fuchs J, Herden U, Hernández F, Pakarinen M, Superina R, Kuebler JF, Slavetinsky C, Madadi-Sanjani O.   +16 more
europepmc   +1 more source

Comparison of short-term outcomes of open, laparoscopic, and robotic surgery for Kasai portoenterostomy in biliary atresia: a 10-year single center study. [PDF]

Front Surg
Jiang Y, Zhu M, Chen J, Zhu Z, Zhao H, Wang Q, Wang Z, Zhu J, Cai P.   +8 more
europepmc   +1 more source