期刊文献+

先天性肝纤维化伴多囊肾一例

原文传递
导出
摘要 患者,女,20岁,因“发现蛋白尿,血肌酐高4个月余”于2011年10月18日入院。患者于4月前体检时发现血肌酐为266μmol/L,24h尿蛋白定量为1.17g,
出处 《中国医师杂志》 CAS 2012年第4期575-576,共2页 Journal of Chinese Physician
  • 相关文献

参考文献8

二级参考文献14

  • 1赵新颜,王宝恩,贾继东.36例先天性肝纤维化的临床病理特点[J].中华消化杂志,2005,25(12):748-749. 被引量:19
  • 2Kerr DNS, Harrison CV, Sherlock S, et al. Congenital hepatic fibrosis[J]. QJ MED, 1961,30(1):91 -117. 被引量:1
  • 3Poddar U, Thapa BR, Vashishta RK, et al. Congenital hepatic fibrosis in Indian children [J]. J Gastroenterol Hepatol, 1999, 14 (12): 1192 -1196. 被引量:1
  • 4Desmet VJ. Ludwig symposium on biliary disorders- part Ⅰ. Pathogenesis of ductal plate abnormalities[ J ]. Mayo Clin Proc, 1998,73 (1):80-89. 被引量:1
  • 5Gunay - Aygun M, Avner ED, Bacallao RL, et al. Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis:summary statement of a first national institutes of health/office of rare diseases conference [ J ]. J Pediatr, 2006,149 ( 2 ) : 159 - 164. 被引量:1
  • 6Turkbey B, Ocak i, Daryanani K,et al. Autosomal recessive polycystic kidney clisease and congenital hepatic fibrosis (ARPKD/CHF) [J]. PediatrRadio, 2009 ,39(2):100-111. 被引量:1
  • 7Nakanuma Y,Harada K, Sato Y, et al. Recent progress in the etiopathogenesis of pediatric biliaty disease, particularly Caroli's disease with congenital hepatic fibrosis and biliary atresia [ J]. Histol Histopathol, 2010,25 ( 2 ) : 223 - 235. 被引量:1
  • 8Gunay- Aygun M. Liver and kidney disease in ciliopathies[ J]. Am J Med Genet C Semin Med Genet, 2009,151C (4) : 296 - 306. 被引量:1
  • 9Desmet VJ.What is congenital hepatic fibrosis? Histopathology,1992,20:465-477. 被引量:1
  • 10Di Bisceglie AM,Befeler AS.Nodular and cystic diseases of the liver//Schiff ER,Sorrell MF,Maddrey WC.Schiff's diseases of the liver.Philadelphia:Lippincott Williams & Wilkins,2003:1160-1162. 被引量:1

共引文献9

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