Results 51 to 60 of about 226,924 (326)
Innate Immunity and Pathogenesis of Biliary Atresia
Frontiers in Immunology, 2020 Biliary atresia (BA) is a devastating fibro-inflammatory disease characterized by the obstruction of extrahepatic and intrahepatic bile ducts in infants that can have fatal consequences, when not treated in a timely manner.
Ana Ortiz‐Perez +5 more
semanticscholar +1 more source
Hepatology, 2021 Biliary atresia (BA) is a devastating cholangiopathy of infancy. Upon diagnosis, surgical reconstruction by Kasai hepatoportoenterostomy (HPE) restores biliary drainage in a subset of patients, but most patients develop fibrosis and progress to end‐stage
S. Mohanty +13 more
semanticscholar +1 more source
Diagnostic Imaging of Biliary Atresia
대한영상의학회지, 2022 Biliary atresia is a rare but significant cause of neonatal cholestasis. An early and accurate diagnosis is important for proper management and prognosis.
Haesung Yoon +3 more
doaj +1 more source
Indications for pediatric liver transplantation [PDF]
, 1987 Two hundred fifty pediatric (
Andreas G. Tzakis +21 more
core +1 more source
Majalah Kedokteran Andalas, 2009 AbstrakAtresia bilier merupakan penyakit yang jarang terjadi dan penyababnya belum diketahui secara pasti. Karakteristik dari penyakit ini adalah terjadinya inflamasi progresif pada duktus bilier sehingga terjadi obstruksi ekstrahepatal yang akhirnya ...
Julinar Julinar +2 more
doaj +1 more source
The incidence of portal vein thrombosis at liver transplantation [PDF]
, 1992 The incidence of portal vein thrombosis was examined in 885 patients who received orthotopic liver transplantations for various end‐stage liver diseases between 1989 and 1990. The thrombosis was classified into four grades.
Iwatsuki, S +3 more
core +1 more source
Correctable biliary atresia and cholangiocarcinoma: a case report of a 63-year-old patient
Surgical Case Reports, 2019 Background Although cancer occurrence following surgery for biliary atresia has gradually increased, the development of cholangiocarcinoma in a native liver survivor of biliary atresia is extremely rare.
Masaki Nio +5 more
doaj +1 more source
What to measure in biliary atresia research: study protocol for developing a core outcome set
BMJ Open, 2021 Aim Extrahepatic biliary atresia is a rare disorder. This creates challenges in the quality and quantity of research conducted. This issue is exacerbated by the potential heterogeneity in the reported outcomes in research examining the management of ...
Roy M Kimble +6 more
doaj +1 more source
Hepatolithiasis in a 52-year-old native liver survivor with postoperative biliary atresia
Journal of Pediatric Surgery Case Reports, 2023 Hepatolithiasis is well known to be a late complication after biliary reconstruction. However, there were few reports regarding hepatolithiasis in late complications of long-term, native liver survivors in postoperative patients of biliary atresia. Here,
Kazuki Shirane +5 more
doaj +1 more source
Current Concepts of Biliary Atresia and Matrix Metalloproteinase-7: A Review of Literature
Frontiers in Medicine, 2020 Biliary atresia (BA) is a rare cholangiopathy of infancy in which the bile ducts obliterate, leading to profound cholestasis and liver fibrosis. BA is hypothesized to be caused by a viral insult that leads to over-activation of the immune system ...
M. Nomden +4 more
semanticscholar +1 more source