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遗传性非结合型高胆红素血症 被引量:5

Hereditary non conjugate bilirubinemia
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作者 张新玉 田辉
出处 《肝脏》 2005年第1期51-52,共2页 Chinese Hepatology
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参考文献12

  • 1Kadakol A, Ghosh SS, Sappal BS, et al. Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase ( UGT1A1 ) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype.Hum Mutat, 2000,16: 297-306. 被引量:1
  • 2Monaghan G, Ryan M, Seddon R, et al. Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert' s syndrome.Lancet, 1996,347: 578-581. 被引量:1
  • 3Koiwai O, Aono S, Adachi Y, et al. Crigler-Najjar syndrome type Ⅱ is inherited both as a dominant and as a recessive trait. Hum Mol Genet,1996,5: 645-647. 被引量:1
  • 4Van der Veere CN, Jansen PL, Sinaasappel M, et al. Oral calcium phosphate: a new therapy for Crigler-Najjar disease? Gastroenterology,1997,112:455-462. 被引量:1
  • 5Fox IJ, Chowdhury JR, Kaufman SS, et al. Treatment of the Crigler-Najjar syndrome type I with hepatocyte transplantation. N Engl J Med, 1998,338: 1422-1426. 被引量:1
  • 6Sugatani J, Yamakawa K, Yoshinari K, et al. Identification of a defect in the UGT1A1 gene promoter and its association with hyperbilirubinemia.iochem Biophys Res Commun, 2002,292: 492-497. 被引量:1
  • 7Hall D, Ybazeta G, Destro-Bisol G, et al. Variability at the uridine diphosphate glucuronosyltransferase 1Al promoter in human populations and primates. Pharmacogenetics, 1999,9: 591-599. 被引量:1
  • 8Erdil A, Kadayifci A, Ates Y, et al. Rifampicin test in the diagnosis of Gilbert' s syndrome. Int J Clin Pract ,2001,55: 81-83. 被引量:1
  • 9Mendez-Sanchez N, Martinez M, Gonzalez V, et al. Zinc sulfate inhibits the enterohepatic cycling of unconjugated bilirubin in subjects with Gilbert's syndrome. Ann Hepatol, 2002,1: 40-43. 被引量:1
  • 10Rauchschwalbe SK, Zuhlsdorf MT, Wensing G, et al. Glucuronidation of acetaminophen is independent of UGT1A1 promotor genotype. Int J Clin Pharmacol Ther, 2004,42: 73-77. 被引量:1

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