Results 121 to 130 of about 222,722 (307)

Primary Healthcare Providers' Knowledge on the Early Detection of Biliary Atresia

open access: yesFolia Medica Indonesiana
Highlights: 1. An evaluation is necessary to verify that the knowledge of healthcare providers is sufficient for the early detection of biliary atresia. 2.
Rendi Aji Prihaningtyas   +5 more
doaj   +1 more source

Nutritional status of patients with biliary atresia and autoimmune hepatitis related to serum levels of vitamins A, D and E Estado nutricional de pacientes com atresia biliar e hepatite autoimune e relação com os níveis séricos de vitaminas A, D e E

open access: yesArquivos de Gastroenterologia, 2009
CONTEXT: Chronic liver disease may induce to malabsorption of lipids and fat-soluble vitamins, leading to injury of nutritional status. OBJECTIVES: To evaluate the nutritional status of pediatric-age patients with autoimmune hepatitis and biliary atresia
Margareth L. G. Saron   +2 more
doaj   +1 more source

Update on pediatric liver transplantation in Europe 2022: An ELITA‐ESPGHAN report

open access: yesJournal of Pediatric Gastroenterology and Nutrition, Volume 81, Issue 1, Page 82-90, July 2025.
Abstract Objectives The European Liver Transplant Registry (ELTR) has been collecting data on liver transplantation (LT) in Europe since 1968. The aim of this report is to outline the number, techniques utilized, indications for, and outcomes of pediatric LT (pLT) in Europe, focusing on the Year 2022 in comparison to the preceding 5 years. Methods Data
Norman Junge   +28 more
wiley   +1 more source

Gene Expression Signatures Associated With Survival Times of Pediatric Patients With Biliary Atresia Identify Potential Therapeutic Agents.

open access: yesGastroenterology, 2019
BACKGROUND & AIMS Little is known about the factors that affect outcomes of patients with biliary atresia and there are no medical therapies that increase biliary drainage.
Zhenhua Luo   +4 more
semanticscholar   +1 more source

Clinical Utility of Non‐Invasive Tests for Liver Fibrosis in People Living With Alpha‐1 Antitrypsin Deficiency

open access: yesLiver International, Volume 45, Issue 7, July 2025.
ABSTRACT Severe alpha‐1 antitrypsin deficiency (AATD) is a rare genetic condition characterised by low systemic levels of alpha‐1 antitrypsin due to its retention in the liver. Consequently, it predisposes individuals to the development of chronic obstructive pulmonary disease and liver cirrhosis.
Joost Boeckmans   +4 more
wiley   +1 more source

Alterations of gut microbiota in infants with biliary atresia identified by 16S rRNA-sequencing

open access: yesBMC Pediatrics
Background Biliary atresia (BA) is a severe neonatal disease with progressive intra- and extra-hepatic bile ducts inflammation and hepatic fibrosis.
Fei Liu   +6 more
doaj   +1 more source

ALFA-FETOPROTEIN /AFP/, A1-ANTITRYPSIN ACTIVITY AND HBsAg IN NEONATAL HEPATITIS AND BILIARY ATRESIA [PDF]

open access: bronze, 1975
C. Kattamis   +3 more
openalex   +1 more source

Biliary Atresia – emerging diagnostic and therapy opportunities

open access: yesEBioMedicine, 2021
U. Lendahl, V. Lui, P. Chung, P. Tam
semanticscholar   +1 more source

Biliary Atresia as a Disease Starting In Utero: Implications for Treatment, Diagnosis, and Pathogenesis.

open access: yesJournal of Pediatric Gastroenterology and Nutrition - JPGN, 2019
Biliary atresia (BA) is the most common reason for pediatric liver transplant. BA's varied presentation, natural history, and treatment with the KP have been well described; however, when BA starts relative to birth has not been clearly defined.
K. Mysore, B. Shneider, S. Harpavat
semanticscholar   +1 more source

Pediatric liver transplantation [PDF]

open access: yes, 1987
Liver transplantation, which once was an experimental procedure of no practical interest, has become the preferred treatment for infants and children dying of almost all non-neoplastic end-stage liver diseases. Liver replacement is being provided by many
Esquivel, C   +3 more
core  

Home - About - Disclaimer - Privacy