6 results match your criteria: "USA. Electronic address: thassanein@livercenters.com.[Affiliation]"
Clin Liver Dis
August 2019
Southern California Liver Centers, 131 Orange Avenue, Suite 101, Coronado, CA 92118, USA. Electronic address:
Clin Liver Dis
August 2019
Southern California Liver Centers, 131 Orange Avenue, Suite 101, Coronado, CA 92118, USA. Electronic address:
Fatty liver prevalence is increasing and becoming a global health burden. Chronic hepatitis B infection (CHB) is one of the most common chronic viral infections. Steatosis in CHB patients increases risk of cirrhosis and hepatocellular carcinoma.
View Article and Find Full Text PDFClin Liver Dis
November 2016
University of California, San Diego School of Medicine, San Diego, CA, USA; Southern California Liver Centers, San Diego, CA, USA; Southern California Research Center, PO Box 181770, Coronado, CA 92178-1770, USA. Electronic address:
Clin Liver Dis
November 2016
Southern California Research Center, Coronado, CA 92118, USA; University of California, San Diego School of Medicine, San Diego, CA, USA. Electronic address:
The goal in patients with immune active hepatitis B virus (HBV) infection is to significantly suppress viral replication and prevent progression of fibrosis to cirrhosis and liver decompensation and decrease the incidence of hepatocellular carcinoma. This is achievable by the highly active antivirals, entecavir and tenofovir, which are considered first-line therapy in most patients with immune active hepatitis C virus and after liver transplantation to prevent HBV recurrence. Patients with decompensated cirrhosis should be referred for liver transplantation and treated with first-line antivirals as early as possible, with the goal of achieving complete viral suppression in the shortest time possible.
View Article and Find Full Text PDFJ Hepatol
October 2016
University of California San Diego and Southern California GI and Liver Centers, USA. Electronic address:
In the current era of therapy with direct-acting antiviral (DAAs) drugs, achievement of a sustained virological response (SVR) is achievable in ⩾90% of hepatitis C-infected patients. SVR benefits are well-recognized with reductions in rates of liver complications, hepatocellular carcinoma and mortality. Additional benefits include reduced morbidity related to extrahepatic and systemic manifestations of hepatitis C such as renal, dermatologic, and metabolic complications.
View Article and Find Full Text PDFJ Hepatol
May 2015
Bristol-Myers Squibb, Hopewell, NJ, USA.