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血清病原学阴性病毒性肝炎误诊为Gilbert综合征40例分析 被引量:1

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出处 《中国实用内科杂志》 CAS CSCD 北大核心 2000年第6期377-377,共1页 Chinese Journal of Practical Internal Medicine
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  • 1沈红章,严正,朱家沂.Gilbert综合症8例误诊原因分析[J].中原医刊,1995,22(3):133-134. 被引量:1
  • 2吴锦荣,陈剑峰.Gilbert综合征69例临床分析[J].新医学,1995,26(12):635-636. 被引量:9
  • 3魏元明 郭允希 孙克坚.Gilbert综合征一家7例.中华医学遗传学杂志,1994,11(5):302-302.
  • 4YAMAMOTO K,SATO H,FUJIAMA Y,et al. Contribution of two missens mutations(G71R and Y486D)of the bilirubin UDP-glyeosyhransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type Ⅱ[J].Biophys Aeta, 1998,1406(3) : 267-273.
  • 5BREIMER L H,WANNAMETHEE G,EBRAHIM S,et al.Serum bilirubin and risk of ischemic heart disease in middleaged British men[J]. Clin ehem, 1995,41(10) : 1504-1508.
  • 6DEBINSKI H S, LEE C S, DHILLEN A P, et al. UDP-glucuronosyltransfase in Gilbert's syndrome[J]. Patohology,1996,28 (3) : 238-241.
  • 7GUTLER V, PARKIN J D, MAYALL B C. Use of double gradient denaturating gradient gel eleetrophoresis to deteet(AT) n polymorphisms in the UDP-glucuronosyltransferase 1 gene promoter assoeiated with Gilbert's syndrome[J].Eleetrophoresis, 1999,20(14): 2841-2843.
  • 8BOSMA P J, CHOWDHURY J R, BAKKER C,et al . The genetic basis of the reduced expression of bilirubin UDP-glucuronosyhransferase 1 in Gilbert's syndrome[J]. N Engl J Med,1995,333(18) :1171-1175.
  • 9MONAGHAN G, RYAN M, SEDDON R, et al. Genetic variation in bilirubin UDP-glucuronosyhransferase gene promoter and Gilbert' s syndrome [J]. Lancet, 1996, 347(9001) : 578-581.
  • 10STRASSBURG C P,NGUYEN N,MANNS M P,et al. UDP-glucuronosyltransferase activity in human liver and colon [J].Gastroenterology, 1999,116(1) : 149-160.

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