[1] |
Poupon R. Primary biliary cirrhosis: a 2010 update. J Hepatol, 2010, 52(5):745-758.
|
[2] |
Gautam M, Cheruvattath R, Balan V. Recurrence of autoimmune liver disease after liver transplantation: a systematic review. Liver Transpl, 2006, 12(12):1813-1824.
|
[3] |
Heathcote EJ. Management of primary biliary cirrhosis. the American Association for the Study of Liver Diseases practice guidelines. Hepatology, 2000, 31(4):1005-1013.
|
[4] |
陈规划,陆敏强,何晓顺,等.改良背驮式肝移植69例报告.中国实用外科杂志, 2002, 22(7):405-407.
|
[5] |
Poupon R. Treatment of primary biliary cirrhosis with ursodeoxycholic acid, budesonide and fibrates. Dig Dis, 2011, 29(1):85-88.
|
[6] |
Parés A, Caballería L, Rodés J. Excellent long-term survival in patients with primary biliary cirrhosis and biochemical response to ursodeoxycholic acid. Gastroenterology, 2006, 130(3):715-720.
|
[7] |
Dilger K, Hohenester S, Winkler-Budenhofer U, et al. Effect of ursodeoxycholic acid on bile acid profiles and intestinal detoxification machinery in primary biliary cirrhosis and health. J Hepatol, 2012, 57(1):133-140.
|
[8] |
Jones DE, Al-Rifai A, Frith J, et al. The independent effects of fatigue and UDCA therapy on mortality in primary biliary cirrhosis: results of a 9 year follow-up. J Hepatol, 2010, 53(5):911-917.
|
[9] |
陈国凤,李莉,高君,等.原发性胆汁性肝硬化153例分析.中华医学杂志, 2002, 82(23):1625-1628.
|
[10] |
Tong GD, Tang HH, Wei CS, et al. Efficacy of ursodeoxycholic acid combined with Tongdan Decoction on immunological indices and histopathological changes in primary biliary cirrhosis patients. Chin J Integr Med, 2012, 18(1):16-22.
|
[11] |
Duclos-Vallee JC, Sebagh M. Recurrence of autoimmune disease, primary sclerosing cholangitis, primary biliary cirrhosis, and autoimmune hepatitis after liver transplantation. Liver Transpl, 2009, 15(Suppl 2):S25-S34.
|
[12] |
Kuiper EM, Hansen BE, Metselaar HJ, et al. Trends in liver transplantation for primary biliary cirrhosis in the Netherlands 1988-2008. BMC Gastroenterol, 2010, 10:144.
|
[13] |
Neuberger J. Liver transplantation for primary biliary cirrhosis: indications and risk of recurrence. J Hepatol, 2003, 39(2):142-148.
|
[14] |
Markus BH, Dickson ER, Grambsch PM, et al. Efficiency of liver transplantation in patients with primary biliary cirrhosis. N Engl J Med, 1989, 320(26):1709-1713.
|
[15] |
Momah N, Silveira MG, Jorgensen R, et al. Optimizing biochemical markers as endpoints for clinical trials in primary biliary cirrhosis. Liver Int, 2012, 32(5):790-795.
|
[16] |
Rave S, Schalm SW. The optimal timing of liver transplantation in patients with chronic cholestatic liver disease. Transpl Int, 2005, 18(8):937-940.
|
[17] |
Montano-Loza AJ, Wasilenko S, Bintner J, et al. Cyclosporine A protects against primary biliary cirrhosis recurrence after liver transplantation. Am J Transplant, 2010, 10(4):852-858.
|
[18] |
Nguyen DL, Juran BD, Lazaridis KN. Primary biliary cirrhosis. Best Pract Res Clin Gastroenterol, 2010, 24(5):647-654.
|
[19] |
Charatcharoenwitthaya P, Pimentel S, Talwalkar JA, et al. Long-term survival and impact of ursodeoxycholic acid treatment for recurrent primary biliary cirrhosis after liver transplantation. Liver Transpl, 2007, 13(9):1236-1245.
|
[20] |
Tsuda M, Moritoki Y, Lian ZX, et al. Biochemical and immunologic effects of rituximab in patients with primary biliary cirrhosis and an incomplete response to ursodeoxycholic acid. Hepatology, 2012, 55(2):512-521.
|
[21] |
Silveira MG, Talwalkar JA, Lindor KD, et al. Recurrent primary biliary cirrhosis after liver transplantation. Am J Transplant, 2010, 10(4):720-726.
|