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Journal Abstract Search

546 related items for PubMed ID: 8185474

  • 1. The spectrum of biliary tract disorders in infants and children. Experience with 300 cases.
    Grosfeld JL, Rescorla FJ, Skinner MA, West KW, Scherer LR.
    Arch Surg; 1994 May; 129(5):513-8; discussion 518-20. PubMed ID: 8185474
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  • 4. Effect of repeat Kasai hepatic portoenterostomy on pediatric live-donor liver graft for biliary atresia.
    Urahashi T, Ihara Y, Sanada Y, Wakiya T, Yamada N, Okada N, Mizuta K.
    Exp Clin Transplant; 2013 Jun; 11(3):259-63. PubMed ID: 23530849
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  • 5. [Diagnosis and treatment of biliary tract obstruction in children with biliary atresia].
    Krivchenia DIu, Iurchenko NI, Almashiĭ GG, Iaremenko VV.
    Khirurgiia (Mosk); 1990 Aug; (8):7-12. PubMed ID: 2259178
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  • 7. The Roux-en-Y procedure in congenital hepato-biliary disorders.
    Gardikis S, Antypas S, Kambouri K, Lainakis N, Panagidis A, Deftereos S, Polychronidis A, Dolatzas T, Simopoulos C.
    Rom J Gastroenterol; 2005 Jun; 14(2):135-40. PubMed ID: 15990932
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  • 9. Surgical experience in children with biliary atresia treated with portoenterostomy.
    Bittmann S.
    Curr Surg; 2005 Jun; 62(4):439-43. PubMed ID: 15964472
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  • 13. Long-term results with the Kasai operation for biliary atresia.
    Karrer FM, Price MR, Bensard DD, Sokol RJ, Narkewicz MR, Smith DJ, Lilly JR.
    Arch Surg; 1996 May; 131(5):493-6. PubMed ID: 8624194
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  • 16. Complications in pediatric hepatobiliary surgery.
    Grisotti G, Cowles RA.
    Semin Pediatr Surg; 2016 Dec; 25(6):388-394. PubMed ID: 27989363
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  • 18. Survival with the native liver after laparoscopic versus conventional kasai portoenterostomy in infants with biliary atresia: a prospective trial.
    Ure BM, Kuebler JF, Schukfeh N, Engelmann C, Dingemann J, Petersen C.
    Ann Surg; 2011 Apr; 253(4):826-30. PubMed ID: 21475026
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  • 19. The robotic approach to complex hepatobiliary anomalies in children: preliminary report.
    Meehan JJ, Elliott S, Sandler A.
    J Pediatr Surg; 2007 Dec; 42(12):2110-4. PubMed ID: 18082719
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