Art
J-GLOBAL ID:201302237773437844   Reference number:13A1123052

Biliary atresia type I cyst and choledochal cust: can we differentiate or not?

I cyst型胆道閉鎖症と総胆管嚢胞:鑑別可能か,それとも不可能か?
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Material:
Volume: 20  Issue:Page: 465-471  Publication year: Jun. 2013 
JST Material Number: L4083A  ISSN: 1868-6974  Document type: Article
Article type: 原著論文  Country of issue: Japan (JPN)  Language: ENGLISH (EN)
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Digestive system diagnosis  ,  Diagnostics of congenital diseases, deformities. 
Reference (27):
  • GOLDMAN, M. Biliary disease in children. Curr Gastroenterol Rep. 2011, 13, 193-201
  • KASAI, M. A proposal of new classification of biliary atresia. J Jpn Soc Pediatr Surg. 1976, 12, 327-331
  • RUIZ-ELIZALDE, AR. A practical algorithm for accurate diagnosis and treatment of perinatally identified biliary ductal dilation : three cases that underscore the importance of an individualised approach. J Matern Fetal Neonatal Med. 2009, 22, 622-628
  • OKADA, T. Postnatal management for prenatally diagnosed choledochal cysts. J Pediatr Surg. 2004, 39, 1055-1058
  • ZHOU, LY. Objective differential characteristics of cystic biliary atresia and choledochal cysts in neonates and young infants : sonographic findings. J Ultrasound Med. 2012, 31, 833-841
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