期刊文献+

Gilbert综合征二例报告

下载PDF
导出
作者 马英 孔丽
出处 《华北国防医药》 2007年第5期46-46,共1页 Medical Journal of Beijing Military Region
  • 相关文献

参考文献5

二级参考文献16

  • 1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
  • 2江绍基.肝脏免疫.临床肝胆病学[M].上海:上海科技出版社,1994.66-68.
  • 3李仕梅.简明内科学[M].北京:人民卫生出版社,1987.51.
  • 4[4]全汉珍,黄德珉,官希志,主编.实用新生儿学[M].第2版.北京:人民卫生出版社,1997.222.
  • 5Vitek L,Jirsa M, Brodanova M, et al. Gilbert syndrome and ischemic heart disease:a protective effect of elevated bilirubin levels [J]. Atherosclerosis, 2002,160:449-456.
  • 6Clarke DJ, Moghrabi N, Monaghan G,et al. Genetic defects of the UDP-glucuronosyltransferase-1 ( UGT1 ) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias[J]. Clin Chim Acta, 1997,266:63-74.
  • 7Kohle C, Mohrle B, Munzel PA,et al. Frequent co-occurrence of the TATA box mutation associated with Gilbert's syndrome(UGT1A1"28)with other polymorphisms of the UDP-glucuronosyltransferase-1 locus( UGT1A6'2 and UGT1A7'3) in Caucasians and Egyptians [ J ]. Biochem Pharmacol, 2003,65:1521-1527.
  • 8Sugatani J, Yamakawa K, Yoshinari K, et al. Identification of a defect in the UGT1A1 gene promoter and its association with hyperbilirubinemia [ J ]. Biochem Biophys Res Commun,2002.292:492 -497.
  • 9Yamamoto K, Sato H, Fujiyama Y, et al. Contribution of two missense mutations (GT1R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-rqajjar syndrome type Ⅱ [J].Biochim Biophys Acta, 1998,1406:267-273.
  • 10王德炳 主译.哈里森内科学[M](第15版)[M].北京:人民卫生出版社,2003.312-318,2107-2144.

共引文献24

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部