Abstract: Journal of Pediatric Gastroenterology and NutritionVolume 37, Issue 4 p. 407-408 Editorial Treatment for Biliary Atresia in 2003 Christophe Chardot, Christophe Chardot French Observatory of Biliary Atresia, Centre Hospitalier Universitaire de Bicêtre, Service de Chirurgie Pédiatrique, Le Kremlin Bicêtre, FranceSearch for more papers by this author Christophe Chardot, Christophe Chardot French Observatory of Biliary Atresia, Centre Hospitalier Universitaire de Bicêtre, Service de Chirurgie Pédiatrique, Le Kremlin Bicêtre, FranceSearch for more papers by this author First published: 01 October 2003 https://doi.org/10.1002/j.1536-4801.2003.tb12029.xCitations: 2Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. REFERENCES 1.Thomson J. Congenital Obliteration of the Bile Ducts. Edinburgh: Oliver & Boyd; 1892. Google Scholar 2.Kasai M, Suzuki S. A new operation for `non correctable' biliary atresia: portoenterostomy. Shijitsu 1959; 13: 457–81. Google Scholar 3.Kasai M, Kimura S, Asakura Y, et al. Surgical treatment of biliary atresia. J Pediatr Surg 1968; 3: 665–75. 10.1016/0022-3468(68)90897-X Google Scholar 4.Caccia G, Dessanti A, Alberti D, et al. More than 10 year survival after surgery for biliary atresia. In: R Ohi, ed. Biliary Atresia. Tokyo: ICOM Associates INC; 1991: 246–9. Google Scholar 5.Karrer FM, Price MR, Bensard DD, et al. Long-term results with the Kasai operation for biliary atresia. Arch Surg 1996; 131(5): 493–6. 10.1001/archsurg.1996.01430170039006 CASPubMedWeb of Science®Google Scholar 6.Howard ER, Davenport M. The treatment of biliary atresia in Europe 1969-1995. Tohoku J Exp Med 1997; 181(1): 75–83. 10.1620/tjem.181.75 CASPubMedWeb of Science®Google Scholar 7.Valayer J. Conventional treatment of biliary atresia: long-term results. J Pediatr Surg 1996; 31(11): 1546–51. 10.1016/S0022-3468(96)90174-8 CASPubMedWeb of Science®Google Scholar 8.Starzl TE, Groth CG, Brettschneider L, et al. Orthotopic homotransplantation of the human liver. Ann Surg 1968; 168(3): 392–415. 10.1097/00000658-196809000-00009 CASPubMedWeb of Science®Google Scholar 9.National Institutes of Health Consensus Development Conference Statement: liver transplantation--June 20-23, 1983. Hepatology 1984; 4(1 Suppl): 107S–10S. PubMedWeb of Science®Google Scholar 10.Otte JB, de Ville de Goyet J, Alberti D, et al. Liver transplantation in children: University of Louvain Medical School (Brussels) experience with the first 139 patients. In: P Terasaki, ed. Clinical Transplants. Los Angeles, CA: UCLA Tissue Typing Laboratory; 1989: 143–52. Google Scholar 11.Starzl TE, Esquivel C, Gordon R, et al. Pediatric liver transplantation. Transplant Proc 1987; 29: 3230–5. Google Scholar 12.Otte JB, de Ville de Goyet J, Reding R, et al. Sequential treatment of biliary atresia with Kasai portoenterostomy and liver transplantation: a review. Hepatology 1994; 20(1 Pt 2): 41S–8S. 10.1002/hep.1840200711 CASPubMedWeb of Science®Google Scholar 13.Chardot 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. Hepatology 1999; 30(3): 606–11. 10.1002/hep.510300330 CASPubMedWeb of Science®Google Scholar 14.Nio M, Ohi R, Hayashi Y, et al. Current status of 21 patients who have survived more than 20 years since undergoing surgery for biliary atresia. J Pediatr Surg 1996; 31(3): 381–4. 10.1016/S0022-3468(96)90742-3 CASPubMedWeb of Science®Google Scholar 15.Okazaki T, Kobayashi H, Yamataka A, et al. Long-term postsurgical outcome of biliary atresia. J Pediatr Surg 1999; 34(2): 312–5. 10.1016/S0022-3468(99)90198-7 CASPubMedWeb of Science®Google Scholar 16.Howard ER, MacLean G, Nio M, et al. Survival patterns in biliary atresia and comparison of quality of life of long-term survivors in Japan and England. J Pediatr Surg 2001; 36(6): 892–7. 10.1053/jpsu.2001.23965 CASPubMedWeb of Science®Google Scholar 17.Hadzic N, Davenport M, Tizzard S, et al. Long-term survival following Kasai portoenterostomy: is chronic liver disease inevitable? J Pediatr Gastroenterol Nutr 2003; 37: 430–433. 10.1002/j.1536-4801.2003.tb12033.x PubMedWeb of Science®Google Scholar 18.Chardot C, Carton M, Spire-Bendelac N, et al. Is the Kasai operation still indicated in children older than 3 months diagnosed with biliary atresia? J Pediatr 2001; 138(2): 224–8. 10.1067/mpd.2001.111276 CASPubMedWeb of Science®Google Scholar 19.McKiernan PJ, Baker AJ, Kelly DA. The frequency and outcome of biliary atresia in the UK and Ireland. Lancet 2000; 355: 25–9. 10.1016/S0140-6736(99)03492-3 CASPubMedWeb of Science®Google Scholar 20.McKiernan P, Baker A, Mieli-Vergani G, et al. The BPSU study of biliary atresia after 8 years. J Pediatr Gastroenterol Nutr 2003; 36(4): 529. Google Scholar 21.Inomata Y, Oike F, Okamoto S, et al. Impact of the development of a liver transplant program on the treatment of biliary atresia in an institution in Japan. J Pediatr Surg 1997; 32(8): 1201–5. 10.1016/S0022-3468(97)90682-5 CASPubMedWeb of Science®Google Scholar Citing Literature Volume37, Issue4October 2003Pages 407-408 ReferencesRelatedInformation
Publication Year: 2003
Publication Date: 2003-10-01
Language: en
Type: article
Indexed In: ['crossref']
Access and Citation
Cited By Count: 1
AI Researcher Chatbot
Get quick answers to your questions about the article from our AI researcher chatbot