Results 31 to 40 of about 222,722 (307)
Abstract Patients with biliary atresia (BA) below 2 years of age in need of a transplantation largely rely on partial grafts from deceased donors (deceased donor liver transplantation [DDLT]) or living donors (living donor liver transplantation [LDLT]).
Hedayatullah Esmati+10 more
wiley +1 more source
The Association Between Biliary Atresia and Cytomegalovirus Infection [PDF]
Perinatal infection of cytomegalovirus (CMV) may cause cholestasis resembling biliary atresia. CMV infection is found in patients with biliary atresia. This simultaneous occurrence of biliary atresia and CMV infection prompted
Kumaheri, M. A. (Meutia)+1 more
core +2 more sources
Biliary Atresia Associated with Jejunal Atresia and a Review of the Literature in Japan
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 +1 more source
The Successful Administration of Steroid in Extrahepatic Cholestasis
Biliary atresia is the most common cause of liver transplantation in children. Kasai surgery is still a bridging therapy for biliary atresia, but patients are often late for treatment.
Anindya Kusuma Winahyu+3 more
doaj +1 more source
Innate Immunity and Pathogenesis of Biliary Atresia
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
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
Biliary atresia (BA) is a cholangiodestructive disease affecting biliary tract, which ultimately leads to cirrhosis, liver failure and death if not treated. The incidence is higher in Asian countries than in Europe. Up to 10% of cases have other congenital anomalies, such as polysplenia, asplenia, situs inversus, absence of inferior vena cava and pre ...
Sinha, C.K., Davenport, Mark
openaire +3 more sources
Live transplantation in children with biliary atresia and vascular anomalies [PDF]
Eight of 29 infants and children undergoing orthotopic liver transplantation for extrahepatic biliary atresia had associated major vascular anomalies.
Lilly, JR, Starzl, TE
core +1 more source
Weaning of immunosuppression in long - Term liver transplant recipients [PDF]
Seventy-two long-surviving liver transplant recipients were evaluated prospectively, including a baseline allograft biopsy for weaning off of immunosuppression.
Abu-Elmagd, K+11 more
core +1 more source
Inflammation, Active Fibroplasia, and End-stage Fibrosis in 172 Biliary Atresia Remnants Correlate Poorly With Age at Kasai Portoenterostomy, Visceral Heterotaxy, and Outcome [PDF]
Published histologic studies of the hilar plate or entire biliary remnant at the time of Kasai portoenterostomy (KHPE) have not provided deep insight into the pathogenesis of biliary atresia, relation to age at surgery, prognosis or the basis for ...
Arva+32 more
core +1 more source