Results 11 to 20 of about 222,722 (307)
Identification of Polycystic Kidney Disease 1 Like 1 Gene Variants in Children With Biliary Atresia Splenic Malformation Syndrome [PDF]
Hepatology, 2019 Biliary atresia (BA) is the most common cause of end‐stage liver disease in children and the primary indication for pediatric liver transplantation, yet underlying etiologies remain unknown.
John-Paul Berauer +32 more
semanticscholar +4 more sources
Biliary atresia: Potential for a new decade.
Seminars in Pediatric Surgery, 2020 Biliary atresia is characterised as an obliterative cholangiopathy of both extra-and intra-hepatic bile ducts. There is marked aetiological heterogeneity with a number of different variants, some syndromic and others perhaps virally-mediated.
F. Scottoni, M. Davenport
semanticscholar +2 more sources
Medisur, 2005 Biliary atresia is an obstructive and progressive process of unknown etiology that affects intra and/or extrahepatics biliary tracts and cause neonatal jaundice by serious obstruction of the biliary flow.
Miurkis Endis Miranda +2 more
doaj +7 more sources
Orphanet Journal of Rare Diseases, 2006 Biliary atresia (BA) is a rare disease characterised by a biliary obstruction of unknown origin that presents in the neonatal period. It is the most frequent surgical cause of cholestatic jaundice in this age group. BA occurs in approximately 1/18,000 live births in Western Europe.
Garret S, Zallen +4 more
openaire +7 more sources
Serum FGF19 predicts outcomes of Kasai portoenterostomy in biliary atresia
Hepatology, 2023 Background and Aims: Outcomes after Kasai portoenterostomy (KPE) for biliary atresia remain highly variable for unclear reasons. As reliable early biomarkers predicting KPE outcomes are lacking, we studied the prognostic value of FGF19.
I. Nyholm +13 more
semanticscholar +1 more source
Biliary Atresia in 2021: Epidemiology, Screening and Public Policy
Journal of Clinical Medicine, 2022 Biliary atresia (BA) is a rare newborn liver disease with significant morbidity and mortality, especially if not recognized and treated early in life.
R. Schreiber +3 more
semanticscholar +1 more source
Genetic Factors and Their Role in the Pathogenesis of Biliary Atresia
Frontiers in Pediatrics, 2022 Biliary Atresia, a common basis for neonatal cholestasis and primary indication for Liver Transplantation, accounts for 60% of pediatric Liver Transplantations.
Li-Na Wu +7 more
doaj +1 more source
Biliatresone: progress in biliary atresia study
World Journal of Pediatrics, 2022 Background Biliary atresia (BA) is one of the main causes of neonatal end-stage liver disease. Without timely diagnosis and treatment, most children with BA will develop irreversible liver fibrosis within the first two months.
Jiajie Zhu +3 more
semanticscholar +1 more source
Clinical Case Reports, 2023 Key Clinical Message A newborn with a rare form of biliary atresia had posterior fossa bleed and subarachnoid hemorrhage despite vitamin K prophylaxis, indicating biliary atresia is a causality rather than chance.
Susmin Karki +5 more
doaj +1 more source
Hepatology, EarlyView., 2022 Natural history of liver disease in a large international cohort of children with Alagille syndrome: Results from the GALA study. Abstract Background and Aims Alagille syndrome (ALGS) is a multisystem disorder, characterized by cholestasis. Existing outcome data are largely derived from tertiary centers, and real‐world data are lacking.
Shannon M. Vandriel +93 more
wiley +1 more source