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先天性胆道闭锁的外科治疗 被引量:18

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作者 夏强 李齐根
出处 《临床外科杂志》 2007年第4期222-223,共2页 Journal of Clinical Surgery
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参考文献10

  • 1Nio M,Ohi R,Miyano T,et al.Five and 10-year survival rates after surgery for biliary atresia:a report from the Japanese Biliar Atresia Registry[J].J Pediatr Surg,2003,38(7):997-1000.
  • 2McKiernan PJ,Baker AJ,Kelly DA.The frequency and outcome of biliary atresia in the UK and Ireland[J].Lancet,2000,355(9197):25-29.
  • 3Davenport M.Biliary atresia:outcome and management[J].Indian J Pediatr,2006,73(9):825-828.
  • 4Hung PY,Chen CC,Chen WJ,et al.Long-term prognosis of patient with biliary atresia:a 25 year summary[J].J Pediatr Gastrol Nutr,2006,42:190-195.
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  • 6Chardot C,Carton M,Spire-Bendelac N,et al.Prognosis of biliary atresia in the era of liver transplantation:French national study from 1986 to 1996[J].Hepatology,1999,30(3):606-611.
  • 7Altman RP,Lilly JR,Greenfeld J,et al.A multivariable risk factor analysis of the portoenterostomy (Kasai) procedure for biliary atresia:25 years of experience from two centers[J].Ann Surg,1997,226(3):348-353.
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