Zobrazeno 1 - 10
of 112
pro vyhledávání: '"E. R. Dickson"'
Autor:
Tousif M. Pasha, E R Dickson, Pavla Kasparova, Fátima A. F. Figueiredo, Terry M. Therneau, Sara R. DiCecco, Michael Charlton, Nickie Francisco-Ziller, Michael Malinchoc
Publikováno v:
Transplantation. 70:1347-1352
BACKGROUND Poor preoperative nutritional status has been reported to be associated with adverse outcomes after liver transplantation. Published data are, however, conflicting, with methods of preoperative nutritional assessment and postoperative outc
Autor:
E R Dickson, W R Kim
Publikováno v:
Seminars in Liver Disease. 20:451-464
Under the current environment of liver transplantation, there are several factors to be considered in the timing of liver transplantation. These include expected patient survival with and without liver transplantation, patient's morbidity and quality
Autor:
John J. Poterucha, Terry M. Therneau, Nicholas F. LaRusso, E R Dickson, Keith D. Lindor, Janice L. Petz, Michael Malinchoc, Russell H. Wiesner, W. R. Kim
Publikováno v:
Hepatology. 29:1643-1648
The Child-Pugh classification is a simple, convenient prognostic measure in patients with liver cirrhosis. We investigated the relative role of the Child-Pugh classification and the Mayo model in the assessment of survival in patients with primary sc
Autor:
Keith D. Lindor, A. F. Hofmann, E. R. Dickson, Gerald Salen, S. S. Rossi, Roberta A. Jorgensen, Carolee K. DeSotel, Marco A. Lacerda, Ashok K. Batta
Publikováno v:
American Journal of Gastroenterology. 93:1498-1504
Objective: Ursodeoxycholic acid (UDCA) improves liver biochemistries and enriches the bile with UDCA in patients with primary biliary cirrhosis. The aim of this study was to determine whether the degree of enrichment of bile correlated with that of s
Publikováno v:
American Journal of Gastroenterology. 93:958-961
Objectives A variety of autoimmune conditions occur in association with primary biliary cirrhosis. Among these conditions are sicca syndrome, Raynaud's phenomenon, arthritis, and Hashimoto's thyroiditis. Information is sparse regarding the prevalence
Autor:
Renée E. Poupon, E. R. Dickson, Keith D. Lindor, E. J. Heathcote, K Cauch-Dudek, Raoul Poupon
Publikováno v:
Gastroenterology. 113:884-890
Long-term ursodeoxycholic acid (UDCA) therapy slows the progression of primary biliary cirrhosis. This study examined the effect of UDCA therapy on survival free of liver transplantation in a large group of patients.Data from three clinical trials we
Autor:
Henry A. Homburger, Keith D. Lindor, M. E. Gershwin, E. R. Dickson, Terry M. Therneau, Patrick S.C. Leung, Michael Malinchoc, Michael D. Van Norstrand
Publikováno v:
Hepatology. 25:6-11
We examined the clinical usefulness of measurements of antimitochondrial autoantibodies (AMA) in predicting disease progression in patients with primary biliary cirrhosis (PBC). We determined the relationships between AMA levels measured by indirect
Autor:
E. R. Dickson, Michael K. Porayko, Jeffery L. Steers, W. R. Kim, John J. Poterucha, Russell H. Wiesner
Publikováno v:
Transplantation. 62:1802-1805
Patients with nonalcoholic steatohepatitis (NASH) may develop progressive liver dysfunction necessitating liver transplantation (OLT). We report the incidence of recurrent disease and outcome in patients undergoing OLT for NASH. Patients transplanted
Autor:
Patrick S.C. Leung, M. E. Gershwin, S. Moteki, Ross L. Coppel, E. R. Dickson, M. M. Kaplan, S. Munoz
Publikováno v:
Hepatology. 24:97-103
The detection of antimitochondrial autoantibodies (AMAs) is critical in the diagnosis of primary biliary cirrhosis (PBC). However, conventional laboratory assays to detect AMA are dependent on the time-consuming method of immunofluorescence microscop
Autor:
Thorsten Buch, D. Alarcon-Segovia, K. Kawano, Patrick S.C. Leung, D. Kershenobich, S. Moteki, E. R. Dickson, D. H. Van Thiel, Claudio Galperin, Ross L. Coppel, S. Matuda, M. E. Gershwin
Publikováno v:
Hepatology. 23:436-444
Five different target mitochondrial autoantigens recognized by sera from patients with primary biliary cirrhosis (PBC) have been identified as subunits of the following 2-oxo acid dehydrogenase complexes: the pyruvate dehydrogenase complex (PDC), the