Results 61 to 70 of about 1,679 (231)

Correlation of the Expression Profile of Peripheral Leukocyte and Liver Tissue Immune Markers With Serum Liver Injury Indices in Children With Biliary Atresia

open access: yesMediators of Inflammation, Volume 2025, Issue 1, 2025.
The aim of the study was to find associations between the levels of liver injury serum markers and the selected liver, peripheral leukocytes, and plasma immune characteristics in biliary atresia (BA) children. Twenty‐five newly diagnosed BA children aged 4–30 weeks and 12 age‐matched controls were included (for leukocytes characteristics) and 19 BA ...
Anna Helmin-Basa   +8 more
wiley   +1 more source

Nutritional status of children with biliary atresia and the role of portoenterostomy to improve nutrition

open access: yesJournal of Indian Association of Pediatric Surgeons, 2020
Background: Nutritional depletion and growth stunting are present in patients with biliary atresia; “normal” nutrient and vitamin supplementation fail to correct these deficiencies.
Shailesh Solanki   +5 more
doaj   +1 more source

Improved Results with Hepatic Portoenterostomy

open access: yesAnnals of Surgery, 1982
As reported in 1974, the initial experience at the Oklahoma Children's Memorial Hospital with the Kasai procedure for biliary atresia was unsatisfactory. A subsequent series of 20 patients, in which 50% of the patients are alive and improved and 25% jaundice-free, is described.
E I, Smith   +4 more
openaire   +3 more sources

Extrahepatic biliary atresia and normal‐range serum gamma‐glutamyltranspeptidase activity: A case report

open access: yesJPGN Reports, Volume 5, Issue 4, Page 533-537, November 2024.
Abstract An infant with biliary atresia had normal‐range (‘low’) serum gamma‐glutamyltranspeptidase (GGT) activity, exceptional because GGT generally is elevated in biliary atresia. Mechanisms underlying low‐GGT cholestasis in biliary atresia are not defined, but the phenomenon is associated with worse clinical outcome.
Benno Kohlmaier   +5 more
wiley   +1 more source

P53 Mutation at Codon 249 is Uncommon in Neonatal Kotb Disease Biliary Atresia [PDF]

open access: yesPediatric Sciences Journal
Background: Hepatocellular carcinoma (HCC) is known to result from aflatoxin B1 that induces p53 mutation at codon 249. Aflatoxins are also known to cause The Kotb disease Biliary atresia (BA) variant which is characterized by congenital aflatoxicosis B1
Magd A. Kotb   +7 more
doaj   +1 more source

Diagnostic and Prognostic Significance of Various Histopathological Features in Extrahepatic Biliary Atresia [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2016
Introduction: Extrahepatic biliary atresia is a progressive disorder characterised by fibroinflammatory obliteration or stenosis of the extrahepatic biliary tree leading to obstruction of bile flow and cholestatic jaundice.
Shenbagam Jeevakarunyam Muthukanagarajan   +4 more
doaj   +1 more source

A histopathological study of liver and biliary remnants with clinical outcome in cases of extrahepatic biliary atresia

open access: yesIndian Journal of Pathology and Microbiology, 2010
Context: The indicators of poor prognosis in cases of extrahepatic biliary atresia (EHBA) continue to remain controversial. Aims: To correlate the histopathological findings of wedge biopsy from liver and tissue obtained from the shaving at the porta ...
Roy Paromita   +5 more
doaj  

Correlation of pre- and post-operative liver function, duct diameter at porta hepatis, and portal fibrosis with surgical outcomes in biliary atresia

open access: yesJournal of Indian Association of Pediatric Surgeons, 2015
Background and Aims: Extrahepatic biliary atresia is one of the most challenging conditions in pediatric surgery. The definition of prognostic factors is controversial. Surgical outcomes after bilioenteric drainage procedures are variable.
Rajib Ray Baruah   +3 more
doaj   +1 more source

Pregnancy after liver transplantation: a case series and review of the literature [PDF]

open access: yes, 2019
Objective: To evaluate maternal and perinatal outcomes in pregnant women after liver transplantation with a case series and literature systematic review.
Berghella, Vincenzo   +5 more
core   +1 more source

Awareness, referral and age at Kasai surgery for biliary atresia in Europe: A survey of the Quality‐of‐Care Task Force of ESPGHAN

open access: yesJournal of Pediatric Gastroenterology and Nutrition, Volume 78, Issue 6, Page 1374-1382, June 2024.
Abstract Objectives To identify infants with biliary atresia (BA), European Society of Paediatric Gastroenteroloy and Nutrition (ESPGHAN)/North American Society of Pediatric Gastroenteroloy and Nutrition (NASPGHAN) guidelines recommend measurement of conjugated/direct bilirubin in infants with prolonged jaundice and using a stool colour card (SCC). The
Florence Lacaille   +6 more
wiley   +1 more source

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