[1] Hays D, Snyder WH. Life-span in untreated biliary atresia. Surgery 1963; 64:373-375
[2] Chardot C, Carton M, Spire-Bendelac N, Le Pommelet C, Golmard J-L, Auvert B. Prognosis of biliary atresia in the era of liver transplantation : French national study from 1986 to 1996. Hepatology 1999; 30(3):606-611
[3] Davenport M, Savage M, Mowat AP, Howard ER. Biliary atresia splenic malformation syndrome : an etiologic and prognostic subgroup. Surgery 1993; 113(6):662-668
[4] Chandra R. Biliary atresia and other structural anomalies in the congenital polysplenia syndrome. J Pediatr 1974; 85(5):649-655
[5] Dimmick J, Bove K, McAdams A. Extrahepatic biliary atresia and the polyslpenia syndrome. J Pediatr 1975; 86(4):644-645
[6] Paddock R, Arensman R. Polysplenia syndrome : spectrum of gastrointestinal congenital anomalies. J Pediatr Surg 1982; 17(5):563-566
[7] Falchetti D, Brandt de Carvalho F, Clapuyt P, Ville de Goyet J, Hemptinne B, Claus D, Otte JB. Liver translantation in children with biliary atresia and polysplenia syndrome. J Pediatr Surg 1991; 26(5):528-531
[8] Sandler A, Azarow K, Superina R. The impact of a previous Kasai procedure on liver transplantation for biliary atresia. J Ped Surg 1997; 32(3):416-419
[9] Karrer F, Lilly J, Stewart B, Hall R. Biliary atresia registry, 1976 to 1989. J Pediatr Surg 1990; 25(10):1076-1081
[10] Rudolph JA, Balistreri WF. Optimal treatment of biliary atresia - « Halfway » there. Hepatology 1999; 30(3):808-810
[11] Ohi R . Surgery for biliary atresia. Liver 2001; 21(3):175-182
[12] Bill A. Biliary atresia_introduction. World J Surg 1978; 2(5):557-559
[13] Mowat A. Biliary atresia into the 21st Century : A historical perspective. Hepatology 1996; 23(6):1693-1695
[14] Holmes JB. Congenital obliteration of the bile ducts. Diagnosis and suggestion of treatment. Am J Dis Child 1916; 11:405-431
[15] Ladd W. Congenital atresia and stenosis of the bile ducts. JAMA 1928; 91(15):1082-1085
[16] Ladd W. Congenital obstruction of the bile ducts. Ann Surg 1935; 102(4):742-751
[17] Ladd W, Gross R. Surgical anastomoses between the biliary and intestinal tracts of the children. Ann Surg 1940; 112(1):51-63
[18] Longmire MD, Sandford MC. Intrahepatic cholangiojejunostomy with partial hepatectomy for biliary obstruction. Surgery 1948; 24:264-276
[19] Hussein M, Howard ER, Mieli-Vergani G, Mowat AP. Jaundice at 14 days of age : exclude biliary atresia. Arch Dis Child 1991; 66(10):1177-1179
[20] Howard ER. Biliary atresia. Liver diseases in childhood.Surgery of the liver and biliary tract. Churchill livinstone Blumgart, second edition, vol 2:835-852
[21] Sterling JA. Long-term survival of infants without extrahepatic bile ducts. Am J Surg 1966; 112(3):382-383
[22] Fonkalsrud EW and al. Hepatic lymphatic drainage to the jejunum of congenital diliary atresia. Am J Surg 1966; 112(2):188-194
[23] Kasai M, Kimura S, Asakura Y, Suzuki H, Taira Y, Ohashi E. Surgical treatment of biliary atresia. J Pediatr Surg 1968; 3(6):665-675
[24] Mieli-Vergani G, Howard E, Portman B, Mowat A. Late referral for biliary atresia - missed opportunities for effective surgery. The lancet 1989; 25(8635):421-423
[25] Kasai M, Mochizuki N, Chiba T, Ohi R. Surgical limitation for biliary atresia : Indication for liver transplantation. J Ped Surg 1989; 24(9):851-854
[26] Kasai M, Suzuki H, Ohashi E, Ohi R, Chiba T, Okamoto A. Technique and results of operative management of biliary atresia. World J Surg 1978; 2(5):571-579
[27] Starzl T, Gordon R and Todo S. Pediatric liver transplantation. Transpl Proc 1987; 19(4):3230-3235
[28] Starzl T, Marchioro T and al. Homotranplantation of the liver in humans. Surg Gyn Obst 1963; 117(6):659-675
[29] Starzl T, Groth C, and al. Orthotopic homotransplantation of the human liver. Ann Surg 1968; 168(3):393-415
[30] Balistreri WF, Bove KE, Ryckman FC. Biliary atresia and other disorders of extrahepatic biliary ducts. Liver disease in children. Lippincott Williams and Wilkins 2001
[31] Middlesworth W, Altman P. Biliary atresia. Current opinion in Pediatrics 1997; 9(3):265-269
[32] Park WH, Kim SP, Park KK, Choi SO, Lee HJ, Kwon KY. Electron microscopic study of the liver with biliary atresia and neonatal hepatitis. J Pediatr Surg 1996; 31(3):374-376
[33] Balistreri W, Grand R, Hoofnagle J, Suchy F, Ryckman F, Perlmutter D and Sokol R. Biliary atresia : Current concepts and research directions. Hepatology 1996; 23(6):1682-1696
[34] Haas J. Bile duct and liver pathology in biliary atresia. World J Surg 1978; 2(5):561-569
[35] Morecki R, Glaser J, Cho S, Balistreri W and al. Biliary atresia and reovirus type 3 infection. N Eng J Med 1982; 307(8):481-485
[36] Morecki R, Glaser J, Kress J and Y. Detection of reovirus type 3 in the porta hepatis of an infant with extrahepatic biliary atresia: ultrastructural and immonucytochemical study. Hepatology 1984; 4(6):1137-1142
[37] Glaser JH, Balistreri WF, Morecki R. Role of reovirus type 3 in persistent infantile cholestasis. J Pediatr 1984; 105(6):912-915
[38] Dussaix E, Hadchouel M, Tardieu M, Alagille D. Biliary atresia and reovirus type 3 infection. N Engl J Med 1984; 310(10):658
[39] Brown W, Sokol R, Levin M, Silverman A, Tamaru T, Lilly J, Hall R, Cheney M. Lack of correlation between infection with reovirus 3 and extrahepatic biliary atresia or neonatal hepatitis. J Pediatr.1988; 113(4):670-676
[40] Tyler K, Sokol R, Oberhaus S, Le M, Karper F, Narkewicz M, Tyson W, Murohy J, Low J, Brown W. Detection of Reovirus RNA in hepatobiliary tissues from patients with extrahepatic biliary atresia and choledochal cysts. Hepatology 1998; 27(6):1475-1482
[41] Phillips PA, Keast P, Papadimitriou JM, Walters MN, Stanley NF. Chronical obstructive jaunice induce by Reovirus 3 in weanling mice. Pathology 1969; 1(3):193-203
[42] Riepenhoff-Talty M, Schaekel K, Clark F, Muelle W, Uhnoo I, Rossi T, Fisher J, Ogra P. Group A rotavirus produce extrahepatic biliary obstruction in orally inoculated newborn mice. Pediatr Res 1993; 33(4):394-399
[43] Riepenhoff-Talty M, Gouvea V, Evans MJ and al. Detection of group C rotavirus in infants with extrahepatic biliary atresia. JID 1996; 174:8-15
[44] Strickland AD, Shannon K. Studies in the etiology of extrahepatic biliary atresia : Time-space clustering. J Pediatr 1982; 100(5):749-753
[45] Cocjin J, Rosenthal P, Buslon V, Luk L, Barajas L, Geller S, Ruebner B, French S. Bile ductule formation in fetal, neonatal, and infant livers compared with extrahepatic biliary atresia. Hepatology 1996; 24(3):568-574
[46] Tagge DU, Tagge EP, Drongowski RA, Oldham KT, Coran AG. A long-term experience with biliary atresia. Reassessment of pronostic factors. Ann Surg 1991; 214(5):590-598
[47] Schweizer MHJ. Prospektive klinische und histologische Studie zur Pathogenese, Therapie und Prognose der Extrahepatischen Gallengangsatresie. Tettnang.2000
[48] Tan C, Davenport M, Driver M, Howard ER. Does the morphology of the extrahepatic biliary remnants in biliary atresia influence survival ? A review of 205 cases. J Pediatr Surg 1994; 29(11):1459-1464
[49] Yokoyama T, Copeland N, Jenkins N, Montgomery C, Elder F, Overbeek P. Reversal of left-right asymmetry : a situs inversus mutation. Science 1993; 260:679-682
[50] Mazziotti M, Willis L, Heuckeroth R, La Regina M, Swanson P, Overbeek P, Perlmutter D. Anomalous development of hepatobiliary sytem in the inv mouse. Hepatology 1999; 30(2):372-378
[51] Ando K, Miyano T, Kimura K, Shimomura H, Ohya T. Congenital biliary atresia and congenital biliary dilatation in siblings.J Pediatr Surg 1991; 26(12):1399-1400
[52] Funaki N, Sasano H, Shizawa S, Nio M, Iwami D, Ohi R, Nagura H. Apoptosis and cell proliferation in biliary atresia. J Pathol 1998; 186:429-433
[53] Davenport M, Gonde C, Redkar R, Koukoulis G, Tredger M, Mieli-Vergani G, Portmann B, Howard E.R. Immunohistochimie of the liver and biliary tree in extrahepatic biliary atresia. J Pediatr Surg 2001; 36(7):1017-1025
[54] Kobayashi H, Puri P, O'Brian DS, Surana R, Miyano T. Hepatic overexpression of MHC class 2 antigens and macrophage-associated antigens (CD68) in patients with biliary atresia of poor prognosis. J Pediatr Surg 1997; 32(4):590-593
[55] Silveira TR, Salzano FM, Donaldson PT, Mieli-Vergani G, Howard ER, Mowat AP. Association between HLA and extrahepatic biliary atresia. J Pediatr Surg 1993; 16(2):114-117
[56] Dillon P, Belchis D, Tracy T, Cilley R, Hafer L, Krummel T. Increased expression of intercellular adhesion molecules in biliary atresia Am J Pathol 1994; 145(2):263-267
[57] Broomé U, Nemeth A, Hlutcrantz R, Schneynius A. Different expression of HLA-DR and ICAM-1 in livers from patients with biliary atresia and Byler's disease. J Hepatol 1997; 26:857-862
[58] Urushihara N,, Iwagaki H, Yagi T, Kohka H, Kobashi K, Morimoto Y, Yoshino T, Tanimoto T, Kurimoto M, Tanaka N. Elevation of serum interleukin-18 levels and activation of kupffer cells in biliary atresia. J Pediatr Surg 2000; 35(3):446-449
[59] Strazzabosco M, Spirli C, Okolicsanyi L. Pathophysiology of the intrahepatic biliary epithelium. J Gastroenterology and Hepatology 2000; 15:244-253
[60] Vasquez J, Lopez Gutierrez JC, Gamez M, Lopez-Santamaria M, Murcia J, Larrauri J, Diaz MC, Jara P, Tovar JA. Biliary atresia and polysplenia syndrome: its impact on final outcome. J Pediatr Surg 1995; 30(3):485-487
[61] Karrer F, Hall R, Lilly J. Biliary atresia and the polysplenia syndrome. J Pediatr Surg 1991; 26(5):524-527
[62] Hoffman MA, Celli S, Ninkov P, Rolles K, Calme RY. Orthotopic transplantation of the liver in children with biliary atresia and polysplenia syndrome : report of two cases. J.Pediatr.Surg 1998; 24(10):1020-1022
[63] Varela-Faschinetto G, Castaldo P, Fox I, Sudan D, Heffron T, Shaw B, Langnas A. Biliary atresia-Polysplenia syndrome. Surgical and clinical relevance in liver transplantation.Ann Surg 1998; 227(4):583-589
[64] Desmet V. Congenital diseases of intrahepatic bile ducts : variations on the theme « ductal plate malformation ». Hepatology 1992; 16(4):1069-1083
[65] Lilly J, Chandra R. Surgical hazards of co-existing anomalies in biliary atresia. Surg,Gyn,Obst 1974; 139(1):49-54
[66] Lilly J, Starzl T. Liver transplantation in children with biliary atresia and vascular anomalies. J Pediatr Surg 1974 ;9(5):707-714
[67] Lilly J, Karrer F, Hall R, Stellin G, Vasquez-Estevez J, Greenholz S, Wanek E, Schroter G. The Surgery of biliary atresia. Ann Surg 1989; 210(3):289-296
[68] Otte J-B, De Ville De Goyet J, Reding R, Hausleithner V, Sokal E, Chardot C, Debande B. Sequential treatment of biliary atresia with Kasai portoenterostomy and liver transplantation : A review. Hepatology 1994 jul ;20(1 Pt 2):41S-48S
[69] Ohi R, Hanamatsu M, Mochizuki I, Chiba T and Kasai M. Progress in the treatment of biliary atresia. World J Surg 1985; 9(2):285-293
[70] Schweizer P, Kirschner HV, Schittenhelm C. Anatomy of the porta hepatis as rational basis for the hepatoporto-enterostomy. Eur J Pediatr Surg 1999 ;9(1):13-18
[71] Miyano T, Fujimoto T, Ohya T, Shimomura H. Current concept of the treatment of biliary atresia. World J Surg 1993; 17(3):332-336
[72] Ohi R. Surgical treatment of biliary atresia in the liver transplantation era. Jpn J Surg 1998; 28:1229-1232
[73] Wood P, Langnas A, Stratta R, Pillen T, Williams L, Lindsay S, Meiergerd D, Shaw B. Optimal therapy for patients with biliary atresia :portoenterostomy (« Kasai » procedures) versus primary transplantation. J Ped Surg 1990; 25(1):153-162
[74] Maksoud J, Fauza D, Silva M, Porta G, Miura I and Zerbini M. Management of biliary atresia in the liver transplantation era : A 15 years, single-center experience. J Ped Surg 1998; 33(1):115-118
[75] Smith E, Carson J, Tunell W, Hitch D, Pysher T. Improved results with hepatic portoenterostomy. Ann Surgery 1982; 195(6):746-755
[76] Okazaki T, Kobayashi H, Yamataka A, Lane GJ, Miyano T. Long-term post surgical outcome of biliairy atresia. J Pediatr Surg 1999; 34(2):312-315
[77] Lawrence D, Howard E, Tzannatos C and Mowat A. Hepatic portoenterostomy for biliary atresia. Archives Disease Childhood 1981; 56(6):460-463
[78] Vacanti J, Shamberger R, Eraklis A and Lillehei C. The therapy of biliary atresia combining the Kasai portoenterostomy with liver transplantation : A single center experience. J Ped Surg 1990; 25(1):149-152
[79] Carceller A, Blanchard H, Alvarez F, St-Vil D, Bensoussan A, Di Lorenzo M. Past and futur of biliary atresia. J Pediatr Surg 2000; 35(1):717-720
[80] Schweizer P, Lunzmann K. Extrahepatic bile duct atresia : how efficient is the hepatoportoenterostomy ?. Eur J Pediatr Surg 1998; 8(3):150-154
[81] Valayer J. Conventional treatment of biliary atresia: long-term results. J Pediatr Surg 1996; 31(11):1546-1551
[82] Alagille D. Extrahepatic biliary atresia. Hepatology 1984; 4(1S):7S-10S
[83] Azarow K, Phillips M, Sandler A, Hagerstrand I, Superina R. Biliary atresia : Should all patients undergo a portoenterostomy ? Ped Surg 1997; 32(2):168-174
[84] Ohi R and Ibrahim M. Biliary atresia. Seminars Ped Surg 1992; 1:115-124
[85] Schweizer P, Schweizer M, Schellinger K, Kirschner H. J, Schittenhelm C. Prognosis of extrahepatic bile-duct atresia after hepatoportoenterostomy. Pediatr Surg Int 2000; 16(5-6):351-355
[86] Houwen RHJ, Zwiersta RP, Severijnen RSVM, Bouquet J, Madern G, Vos A, Bax NMA, Heymans HSA and Bijleveld CMA. Prognostic of extrahepatic biliary atresia. Arch Dis Child 1989; 64:214-218
[87] Valayer J, Gauthier F, Yandza T, Lababidi A, De Dreuzy O and Hamada H. Biliary atresia : Result of long-term conservative treatment and of liver transplantation. Transplant Proceedings 1993; 25(6):3290-3292
[88] Davenport M, Kerkar N, Mieli-Vergani G, Mowat A and Howard R. Biliary atresia : The King's College Hospital Experience. J Ped Surg 1997; 32(3):479-485
[89] Bernard O. Diagnostic précoce des ictères cholestatiques chez le nouveau-né. Archives Pédiatrie 1998; 5(9):1031-1035
[90] Grigorescu J, Marinescu LE, Ionescu I. Atresie der äusseren Gallengänge. Hepatogastrostomie. Anhaltende Heilung noch nach 12 monaten. Zentralblatt Chirurg 1958; 9:597-604
[91] Schweizer P, Kirschner H, Schittenhelm C. Anatomy of the porta hepatis as a basis for extended hepatoporto-enterostomy for extrahepatic biliary atresia - A new surgical technique. Eur J Pediatr Surg 2001; 11(1):15-18
[92] Toyosaka A, Okamoto E, Okasora T, Nose K, Tomimoto Y, Seki Y. Extensive dissection at the porta hepatis for biliary atresia. J Pediatr Surg 1994; 29(7):896-899
[93] Ando H, Seo T, Ito F, Kaneko K, Watanabe Y, Harada T, Ito T. A new portoenterostomy with division of the ligamentum venosum for treatment of biliary atresia: a preliminar report. J Pediatr Surg 1997; 32(11):1552-1554
[94] Hasegawa T, Fukui Y, Tanano H, Kobayashi T, Fukuzawa M, Okada A. Factor influencing the outcome of liver transplantation for biliary atresia. J Ped Surg 1997; 32(11):1548-1551
[95] Ohi R. A history of the Kasai operation: hepatic portoenterostomy for biliary atresia. World J Surg 1988; 12(6):871-874
[96] Matory Y, Miyano T, Suruga K. Hepaticportoenterostomy as surgical therapy for biliary atresia. Surg, Gyn. and Obst. 1985; 161(16):541-544.
[97] Hirsig J, Kara O, Rickham PP. Experimental investigations into etiology of cholangitis following operation for biliary atresia. J Pediatr Surg 1978; 13(1):55-57
[98] Lilly JR, Altman RP. Hepatic portoenterostomy (the Kasai operation) for biliary atresia. Surg 1975; 78(1):76-86
[99] Chiba T, Ohi R, Nio M, Ibrahim M. Late complications in long-term survivors of biliary atresia. Eur J Pediatr Surg 1992; 2(1):22-25
[100] Grosfeld J, Fitzgerald J, Predaina R, West K, Vane D and Rescorla F. The efficacy of hepatoportoenterostomy in biliary atresia. Surgery 1989; 106(4):692-701
[101] Lally KP, Kanegaye J, Matsumura M, Rosenthal P, Sinatra F and Atkinson J. Perioperative factors affecting the outcome following repair of biliary atresia. Pediatrics 1989; 83:723-726
[102] Endo M, Katsuma K, Yokohama J, Morikawa Y, Ikawa H, Kamagata S, Nakano M, Nirasawa Y, Ueno S. Extended dissection of the portahepatis and creation of an intussuscepted ileocolic conduit for biliary atresia. J Pediatr Surg 1983; 18(6):784-793
[103] Laurent J, Gauthier F, Bernard O, Hadchouel M, Odièvre M, Valayer J, Alagille D. Long-term outcome after surgery for biliary atresia. Gastroenterology 1990; 99:1793-1797
[104] Schoen B, Lee H, Sullivan K, Ricketts R. The Kasai Portoenterostomy : When is it too late ?. J Pediatr Surg 2001; 36(1):97-99
[105] Lowell JA, Shenoy S, Molleston J, Howard TK. Long-term results with the Kasai operation for biliary atresia.
Arch Surg 1996; 131(5):493-496
[106] Chardot C, Carton M, Spire-Bendelac N, Le Pommelet C, Golmard JL, Reding R, Auvert B. Is the Kasai operation still indicated in children older than 3 months diagnosed with biliary atresia ?. J. Pediatr 2001; 138(2):224-227
[107] Oh M, Hobeldin M, Chen T, Thomas DW, Atkinson JB. The Kasai procedure in the treatment of biliary atresia. J Pediatr Surg 1995; 30(7):1077-1080; discussion 1080-1081.
[108] Nio M, Ohi R, Hayashi Y, Endo N, Ibrahim M and Iwami D. Current status of 21 patients who have survived more than 20 years since undergoing surgery for biliary atresia. J Ped Surg 1996; 31(3):381-384
[109] Matsuo S, Suita S, Kubota M, Shono K. Long-term results and cllinical problems after portoenterostomy in patients with biliary atresia. Eur J Pediatr Surg 1998; 8(3):142-145
[110] Ryckmann F, Fisher R, Pedersen S, Dittrich V, Heubi J, Farrell M, Balistreri W, Ziegler M. Improved survival in bilary atresia patients in the present era of liver transplantation. J Pediatr Surg 1993 ;28(3):382-386
[111] Wu E.-T, Chen H.-L, Ni Y.-H, Lee P.-I, Hsu H.-Y, Lai H.-S, Chang M.-H. Bacterial cholangitis in patients with biliary atresia: impact on short-term outcome. Pediatr Surg Int 2001; 17(5-6):390-395
[112] Gottrand F, Bernard O, Hadchouel M, Pariente D, Gauthier F, Alagille D. Late cholangitis after successful surgical repair of biliary atresia. ADJC 1991; 145(2):213-215
[113] Lunzmann K, Schweizer P. The influence of cholangitis on the prognosis of extrahepatic biliary atresia.
Eur J Pediatr Surg 1999; 9(1):19-23
[114] Burnweit C, Coln D. Influence of diversion on the development of cholangitis after hepatoportoenterostomy for biliary atresia. J Ped Surg 1986; 21(12):1143-1146
[115] Juncheng L, Giusheng L and Bingyao L. A Study on cholangitis after hepatic portoenterostomy for biliary atresia. Chinese Med J 1997; 110(5):335-337
[116] Gauthier F. Atrésie des voies biliaires. Chirurgie digestive de l'enfant. Doin
[117] Lilly JR, Hitch DC. Postoperative ascending cholangitis following portoenterostomy for biliary atresia: Measures for control. World J Surg 1978; 2(5):581-587
[118] Howard ER, Davenport M. The treatment of biliary atresia in Europe 1969-1995. Tohoku J Exp Med 1997; 181(1):75-83
[119] Muraji T, Higashimoto Y. The improved outlook for biliary atresia with corticosteroid therapy. J Ped Surg 1997; 32(7):1103-1107
[120] Miner P, Gaito J. Bile flow in response to pharmacologic agents. Bioch Pharma 1979; 28(7):1063-1066
[121] Karrer FM, Lilly JR. Corticosteroid therapy in biliary atresia. J Pediatr Surg 1985; 20(6):693-695
[122] McKiernan P, Baker A, Kelly D. The frequency and outcome of biliary atresia in the UK and Ireland. The Lancet 2000; 355(1):25-29
[123] Biliary atreasia: Lessons from the japanese experience. The Lancet 1980; 13:1283-1284
[124] Gartner J, Jaffe R, Malatack J, Zitelli B and Urbach A. Hepatic infarction and acute liver failure in children with extrahepatic biliary atresia and cirrhosis. J Ped Surg 1987; 22(4):360-362
[125] Howard E.R, MacLean G, Nio M, Donaldson N, Singer J, Ohi R. 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):892-897
[126] Laurent J, Valayer J, Bernard O. Devenir après 10 ans de l'atrésie des vois biliaires initialement opérée selon la technique de Kasai. Atrésie des voies biliaires.
[127] Odièvre M. Long-term results of surgical treatement of biliary atresia. World J Surg 1978; 2(5):589-593
Bernard O. L'atrésie des voies biliaires: aspects médicaux. Chirurgie hépato-biliare de l'enfant. Sauramps medical 1994
129 Kasai M. Treatment of biliary atresia with special reference to hepato-porto-enterostomy and its modifications. Prog.ped.Surg.1974; 6:5-52
Kasai M, Suzuki S. A new operation for " non-correctable" biliary atresia: Hepatic porto-enterostomy.Shujutsu 1959; 13:733 ( en japonais)
131 Genin B, McLin V, Belli D, Bugmann P, Mentha G, LeCoultre C. Atrésie des voies biliaires: une urgence médico-chirurgicale néonatale. Med Hyg 1999; 57:366-369
132 Redkar R, Davenport M, Howard E. Antenatal diagnosis of congenital anomalies of the biliary tract. J Ped Surg 1998; 33(5):700-704
133 LeCoultre C, Battaglin C, Bugmann P. and al: Biliary atresia ant orthotopic liver transplantation.11 year experience in Geneva. Swiss Surg 2001; 7:199-204
134 Chuang JH, Chen WJ, Lee SY, Chang NK. Prompt colonization of the hepaticojejunostomy and translocation of bacteria to liver after bile duct reconstruction. J Pediatr Surg 1998; 33(8):1215-1218
Park W, Choi S, Lee H, Kim S, Zeon S, Lee S. A new diagnostic approach to biliary atresia with emphasis on the ultrasonographic triangular cord sign: comparison of ultrasonography, hepatobiliary scintigraphy, and liver needle biopsy in the evaluation of infantile cholestasis. J Pediatr Surg 1997; 32(11):1555-1559
Gauthier F. L'atrésie des voies bilaires: aspects chirugicaux. Chirugie hépato-biliaire de l'enfant. Ed. Sauramps medical 1994
Chandra R, Altman P. Ductal remnants in extrahepatic biliary atresia : a histopathologic study with clinical correlation. J Pediatr 1978; 93(2):196-200
138 Dillon P, Owings E, Cilley R, Field D, Curnow A, Georgeson K. Immunosuppression as adjuvant therapy for biliary atresia. J Pediatr Surg 2001; 36(1):80-85
139 Gautier M, Jehan P, Odièvre M. Histologic study of biliary fibrous remnants in 48 cases of extrahepatic biliary atresia: correlation with postoperative bile flow restoration. J pediatr 1976; 89(5):704-709