Results 91 to 100 of about 1,713 (227)

Abstract

open access: yes
JPGN Reports, Volume 6, Issue S2, Page S1-S814, September 2025.
wiley   +1 more source

Common bile duct cysts in neonates, not always a choledochal cyst: A case report

open access: yesJournal of Pediatric Surgery Case Reports
Introduction: Obstructive jaundice in neonates results from disruption of bile drainage from the liver, which may be related to several conditions. Differentiating between these conditions and intervening rapidly is critical, as the success of treatment ...
Josephine Issenman, Kathryn Martin
doaj   +1 more source

Clinical considerations in orthotopic liver transplantation [PDF]

open access: yes, 1987
Three hundred forty (68 per cent) of the 500 patients transplanted with cyclosporine and prednisone are alive, including 197 (66.3 per cent) of the adults and 143 (70.4 per cent) of the children.
Gordon, RD, Makowka, L, Tzakis, AG
core  

UEG Week 2024 Poster Presentations

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

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

open access: yesSiriraj 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   +4 more
doaj  

Emergencies in neonatal management: jaundice and biliary atresia [PDF]

open access: yes, 2016
Biliary atresia is a severe and progressive inflammatory process of unknown cause, which initially involves the extrahepatic bile ducts but which quickly proceeds towards the intrahepatic bile tree leading rapidly to biliary cirrhosis. Biliary atresia is
Clemente, Maria Grazia   +1 more
core  

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

open access: yesTurkish 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   +2 more
doaj   +1 more source

A study on cholangitis after hepatic portoenterostomy for biliary atresia.

open access: yesChinese medical journal, 1998
To investigate the clinical manifestations and factors relating to prognosis in biliary atresia (BA).Twenty-four cases were reviewed on clinical manifestations and bile flow after operation. All patients underwent hepatic portoenterostomy.Twenty-three cases (95%) got bile flow postoperatively. Sixteen (69%) of 23 patients had 27 episodes of cholangitis.
J, Liu, G, Li, B, Lai
openaire   +1 more source

Dynamic changes of gut microbiota and hepatic functions are different among biliary atresia patients after Kasai portoenterostomy

open access: yesClinical and Translational Medicine, 2022
Yingchao Li   +10 more
doaj   +1 more source

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