Results 11 to 20 of about 94,453 (216)
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 +4 more sources
Colonic Atresia Associated with Biliary Atresia
Journal of Indian Association of Pediatric Surgeons, 2023 Colonic atresia (CA) is an uncommon type of intestinal atresia commonly associated with other anomalies, while biliary atresia (BA) is also rare but usually an isolated anomaly. The pathogenesis for either of the anomalies is unclear. The co-occurrence of both pathologies has not been mentioned in the literature.
Shailesh Solanki +3 more
openaire +4 more sources
Biliary Atresia Associated with Jejunal Atresia and a Review of the Literature in Japan [PDF]
Asian Journal of Surgery, 2005 An unusual case of biliary atresia with jejunal atresia is herein described. Only 12 cases demonstrating biliary atresia associated with a jejunal atresia have been previously reported in Japan.
Koushi Asabe +4 more
doaj +2 more sources
Diagnostic Imaging of Biliary Atresia [PDF]
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 +2 more sources
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 +2 more sources
The Lancet, 2009 Biliary atresia is a rare disease of infancy, which has changed within 30 years from being fatal to being a disorder for which effective palliative surgery or curative liver transplantation, or both, are available. Good outcomes for infants depend on early referral and timely Kasai portoenterostomy, and thus a high index of suspicion is needed for ...
Jane L, Hartley +2 more
core +6 more sources
Alagille Syndrome Mimicking Biliary Atresia in Early Infancy.
PLoS ONE, 2015 Alagille syndrome may mimic biliary atresia in early infancy. Since mutations in JAG1 typical for Alagille syndrome type 1 have also been found in biliary atresia, we aimed to identify JAG1 mutations in newborns with proven biliary atresia (n = 72). Five
Tomáš Dědič +5 more
doaj +2 more sources
Japanese biliary atresia registry
World Journal of Pediatric SurgeryThe Japanese Biliary Atresia Registry (JBAR) was launched in 1989 by the Japanese Biliary Atresia Society (JBAS) to investigate the epidemiology and etiology of biliary atresia and to improve surgical outcomes.
Masaki Nio +3 more
doaj +2 more sources
대한영상의학회지, 2022 Biliary atresia is a progressive, idiopathic, obliterative disease of the extrahepatic biliary tree that presents with biliary obstruction in the neonatal period. It is the most common indication for liver transplantation in children.
Tae Yeon Jeon
doaj +3 more sources
Biliary atresia associated with choledochal cyst
African Journal of Paediatric Surgery, 2009 Choledochal cyst and biliary atresia are rare but important causes of neonatal jaundice. Both present with jaundice and acholic stool in neonatal period. Treatment and prognosis of both entities are very different.
Obaidah Abu +3 more
doaj +3 more sources