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chronic viral hepatitis, auto-immune chronic edema hepatitis, primary biliary edema cirrhosis or genetic liver disease such as Wilson’s disease, hemochromatosis, alpha-1 antitrypsin deficiency, biliary obstruction); b) complications of liver disease such as recurrent variceal bleeding, resistant ascites, spontaneous portosystemic encephalopathy or bacterial peritonitis; c) concurrent medical illness contra-indicating a liver edema biopsy, history of unexplained bleeding, hemophilia or abnormal coagulation results as per routine laboratory work-up or other reason judged by the hepatologist to contra-indicate a percutaneous liver biopsy; d) medications known to precipitate steatohepatitis (corticosteroids, high dose estrogens, methotrexate, amiodarone, calcium channel blockers, spironolactone, sulfasalazine, naproxen, oxacillin or ampinovire) in the 6 months prior to entry; e) antioxidant vitamin supplementation, ursodeoxycholic acid or any other experimental drug 6 months prior to study entry; f) pregnant or lactating Location and Contact Information Please refer to this study by ClinicalTrials.gov
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