Results 81 to 90 of about 1,713 (227)

Pregnancy after liver transplantation: a case series and review of the literature [PDF]

, 2019
Objective: To evaluate maternal and perinatal outcomes in pregnant women after liver transplantation with a case series and literature systematic review.
Berghella, Vincenzo, Donnarumma, Laura, Guida, Maurizio, Marino, Ignazio, Saccone, Gabriele, Zullo, Fabrizio   +5 more
core   +1 more source

A case of biliary atresia with pancreaticobiliary maljunction

Surgical Case Reports, 2017
Background The pathogenesis of biliary atresia (BA) is still unknown. There are several reports on the etiology of BA, including pancreaticobiliary maljunction (PBM).
Kosuke Endo, Akiko Yokoi, Yasuhiko Mishima, Akihiko Tamaki, Keiichi Morita, Yuichi Okata, Chieko Hisamatsu, Hiroaki Fukuzawa, Makiko Yoshida, Yoshinobu Akasaka, Kosaku Maeda   +10 more
doaj   +1 more source

Relationship Between Early Feeding and Communication Development in Infants: Birth To 12 Months [PDF]

, 2004
Introduction: Anecdotal reports suggest that infants experiencing early feeding difficulties may have delays in communication development. Methods: The first stage of the study involved the development of a theoretically based assessment protocol to test
Hird, Kathryn, Massey, S J, Simmer, K
core   +1 more source

Identification of PKD1L1 Gene Variants in Children with the Biliary Atresia Splenic Malformation Syndrome [PDF]

, 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.
Alonso, Estella M, Berauer, John‐Paul, Bezerra, Jorge A, Bull, Laura N, Chopra, Pankaj, Cutler, David J, Finegold, Milton J, Gibbs, Richard A, Guthery, Stephen L, Harpavat, Sanjiv, Hegde, Madhuri R, Kamath, Binita M, Karpen, Saul J, Loomes, Kathleen M, Magee, John C, Mezina, Anya I, Molleston, Jean P, Moore, Barry, Murray, Karen F, Muzny, Donna M, Network, for the Childhood Liver Disease Research, Okou, David T, Perlmutter, David H, Rajagopalan, Ramakrishnan, Rosenthal, Philip, Russo, Pierre, Sabo, Aniko, Sherker, Averell H, Sokol, Ronald J, Spinner, Nancy B, Squires, Robert H, Thompson, Richard J, Wang, Kasper S, Yandell, Mark   +33 more
core   +2 more sources

Changing perspectives on liver transplantation in 1988. [PDF]

, 1988
After liver transplantation for cancer, there is a high incidence of disease recurrence within 18 to 36 months for most tumors, although there are a small number of long-term survivors.
Gordon, RD, Starzl, TE
core  

Choosing a pediatric recipient for orthotopic liver transplantation [PDF]

, 1987
Between March 3, 1981, and June 1, 1984, 216 children were evaluated for orthotopic liver transplantation. Of the 216 patients, 117 (55%) had recelved at least one liver transplant by June 1, 1985. Fifty-five (25%) died before transplantation.
Andrew H. Urbach, Atkin, Basil J. Zitelli, Borel, Byar, Byar, Byers W. Shaw, Cox, Cutler, Daniel J. Schaid, Fallon, Gartner, Gartner, Gartner, Gordon, Houssin, Howard Rockette, J. Carlton Gartner, J. Jeffrey Malatack, John Fischer, Lachin, Lee, Mantel, National Institutes of Health Consensus Development Conference statement, Perrin, Sabbeth, Shaw, Shunzaburo Iwatsuki, Starzl, Starzl, Thomas E. Starzl, Zitelli   +31 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

Predictors of clinical outcome in children undergoing orthotopic liver transplantation for acute and chronic liver disease. [PDF]

, 2006
The current United Network for Organ Sharing (UNOS) policy is to allocate liver grafts to pediatric patients with chronic liver disease based on the pediatric end-stage liver disease (PELD) scoring system, while children with fulminant hepatic failure ...
Engelhardt, Rita, Martín, Martín G, Molina, Ricardo A, Narsinh, Kiran, Nga, Visal, Rhee, Chris, Venick, Robert S   +6 more
core   +1 more source

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