Results 81 to 90 of about 1,679 (231)

Surgical complications in human orthotopic liver transplantation. [PDF]

, 1987
Between March 1, 1980 and December 31, 1984, 393 orthotopic liver transplantations (OLT) were performed in 313 consecutive recipients. Technical complications were responsible for a substantial morbidity (41/393 allograft loss--10.4%) and mortality (26 ...
Gordon, RD, Iwatsuki, S, Lerut, J, Starzl, TE   +3 more
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Maternal microchimerism in the livers of patients with Biliary atresia [PDF]

, 2004
Background Biliary atresia (BA) is a neonatal cholestatic disease of unknown etiology. It is the leading cause of liver transplantation in children. Many similarities exist between BA and graft versus host disease suggesting engraftment of maternal cells
David L Suskind, Philip Rosenthal, Melvin B Heyman, Denice Kong, Greg Magrane, Lee-Ann Baxter-Lowe, Marcus O Muench, M Hollander, M Hollander, JA Sterling, B Fischler, R Ohi, B Fischler, FM Karrer, F Amersi, VJ Desmet, JM Ben-Ezra, U Broome, NJ Chao, JL Ferrara, A Nonomura, J Schroder, YM Lo, SM Müller, W Reed, EL Assche, JG Ocejo-Vinyals, T Ohya, JA Bezerra, HZ Hu, PW Dillon, M Nakada, C Shimazaki, J., Chang M., Lee H., Muench M.O. Chen   +33 more
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Patient complexity and genotype-phenotype correlations in biliary atresia: a cross-sectional analysis [PDF]

, 2017
published_or_final_versio
Chan, EKW, Cheng, G, Cherny, SS, Chung, HY, Garcia-Barcelo, MM, Sham, PC, So, MT, Tam, PKH   +7 more
core   +1 more source

Bile duct matrix metalloproteinase-7 expression: a new modality for diagnosis of biliary atresia

Egyptian Liver Journal
Background Biliary atresia (BA) is an obliterative cholangiopathy of infancy that results in cholestasis and liver fibrosis. This fibrosis is due to an imbalance in extracellular matrix (ECM) breakdown and deposition.
Alif Abdelhakim Allam, Mohammed Ahmed Khedr, Shimaa Saad Elkholy, Takwa Abd El Rahman Yassin, Ola Ahmed Fouad   +4 more
doaj   +1 more source

A histopathological study of liver and biliary remnants in the long-term survivors (>10 years) of cases of biliary atresia

Indian Journal of Pathology and Microbiology, 2014
Context: Biliary atresia (BA) is a destructive process affecting both extra- and intra-hepatic bile ducts leading to fibrosis and obliteration of the biliary tree and cirrhosis usually within 2 years.
Sabuj Ghana Mukhopadhyay, Paromita Roy, Uttara Chatterjee, Chhanda Datta, Mala Banerjee, Sugato Banerjee, Ashoke Kumar Basu, Manojit Ganguli   +7 more
doaj   +1 more source

Atresia de vias biliares: análise de 28 casos. [PDF]

, 2007
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina. Curso de Medicina.
Souza, Wanessa Pereira de
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A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1 [PDF]

, 2018
Biliary atresia (BA) is a rare pediatric cholangiopathy characterized by fibrosclerosing obliteration of the extrahepatic bile ducts, leading to cholestasis, fibrosis, cirrhosis, and eventual liver failure.
Bailey-Wilson, Joan E, Chen, Ying, Devoto, Marcella, Gilbert, Melissa A, Grochowski, Christopher M, Hakonarson, Hakon, Llewellyn, Jessica, Loomes, Kathleen M, Mceldrew, Deborah, Russo, Pierre, Spinner, Nancy B, Waisbourd-Zinman, Orith, Wells, Rebecca G   +12 more
core   +2 more sources

Role of CD56-expressing immature biliary epithelial cells in biliary atresia [PDF]

, 2016
published_or_final_versio
Chen, Y, Lamb, JR, Liu, HY, Lui, VCH, Nicholls, JM, Peng, J, Tam, PKH, Wang, FH, Xia, HM, Yu, JK, Zhang, RZ   +10 more
core   +1 more source

Abstract

JPGN Reports, Volume 6, Issue S2, Page S1-S814, September 2025.
wiley   +1 more source

Emergencies in neonatal management: jaundice and biliary atresia [PDF]

, 2016
Biliary atresia is a severe and progressive inflammatory process of unknown cause, which initially involves the extrahepatic bile ducts but which quickly proceeds towards the intrahepatic bile tree leading rapidly to biliary cirrhosis. Biliary atresia is
Clemente, Maria Grazia, Dessanti, Antonio   +1 more
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