Метаболизм билирубина и гипербилирубинемия: литература


Доброкачественный рецидивирующий внутрипеченочный холестаз

Depagter AGF et al: Familial benign intrahepatic cholestasis. Gastroenterology 71:202, 1976

Endo T et al: Bile acid metabolism in benign recurrent intrahepatic cholestasis. Gastroenterology 76:1002, 1979

Синдромы Дубина-Джонсона и Ротора

Paulusma CC et al: Congenital jaundice in rats with a mutation in a multidrug resistance-associated protein gene. Science 271:1126, 1996

Rosenthal P et al: Homozygous Dubin-Johnson syndrome exhibits a characteristic serum bilirubin pattern. Hepatology 1:540, 1981

Swartz HM et al: On the nature and excretion of the hepatic pigment in the Dubin-Johnson syndrome. Gastroenterology 76:958, 1979

Wolpert E et al: Abnormal sulfobromophthalein metabolism in Rotor's syndrome and obligate heterozygotes. N Engl J Med 206:1099, 1977

Заболевания, обусловленные недостаточностью глюкуронилтрансферазы

Aono S et al: Analysis of genes for bilirubin UDP- glucuronosyltransferase in Gilbert's syndrome. Lancet 345:958, 1995

Bosma PJ et al: The genetic basis of the reduced expression of UDP-glucuronosyltransferase 1 in Gilbert's syndrome. N Engl J Med 333:1171, 1995

Burchell В et al: Function and regulation of UDP-glucuronosyltransferase genes in health and liver disease. Hepatology 20:1622, 1994

Chowdury JR et al: Hereditary jaundice and disorders of bilirubin metabolism, in The Metabolic and Molecular Bases of Inherited Disease, 7th ed. CR Scriver et al. (eds). New York, McGraw-Hill, 1995, pp 2161-2208

Chowdury JR, Chowdury NR: Unveiling the mysteries of inherited disorders of bilirubin glucuronidation. Gastroenterology 105:288, 1993

Monaghan G et al: Genetic variation in bilirubin UDP-glucuronosyltransferase gene promotor and Gilbert's syndrome. Lancet 347:578, 1996

Ritter JK et al: Identification of a genetic alteration in the code for bilirubin UDP-glucuronosyltransferase in the UGT1 gene complex of a Crigler-Najjartype I patient. J Clin Invest 90:150, 1992

Seppen J et al: Discrimination between Crigler-Najjar type I and II by expression of mutant bilirubin uridine diphosphat-glucuronosyltransferase. J Clin Invest 94:2385, 1994

Soeda Y et al: Predicted homozygous missence mutation in Gilbert's syndrome. Lancet 346:1494, 1995

Van der Veere CN et al: Current therapy for Crigler-Najjar syndrome Type 1: Report of a world registry. Hepatology 24:311, 1996

Послеоперационная желтуха

Hootegem PV et al: Serum bilirubins in hepatobiliary disease: Comparison with other liver function tests and changes in the postobstractive period. Hepatology 5:112, 1985

Lamont JT, Isselbacher KJ: Postoperative jaundice, in Wright's Liver and Biliary Disease, 3ded., GH Millward-Sadleretal. (eds). Philadelphia, Saunders, 1992, pp 1372-1380

Смотрите также:

  • МЕТАБОЛИЗМ БИЛИРУБИНА И ГИПЕРБИЛИРУБИНЕМИЯ