参考文献
[1]MIELI-VERGANI G, VERGANI D. Biliary atresia[J]. Semin Immunopathol, 2009, 31(3): 371-381.
[2]詹江华.我国胆道闭锁早期筛查现状与对策[J].天津医药,2015,43(1):1-3.
[3]詹江华,冯杰雄.胆道闭锁何时完成Kasai手术[J].中华小儿外科杂志,2016,37(5):321-326.
[4]ALTMAN RP, LILLY JR, GREENFIELD J, et al. A multivariable risk factor analysis of the portoenterostomy(Kasai) procedure for biliary atresia: twenty-five years of experience from to centers[J]. Ann Surg, 1997, 226(3): 348-355.
[5]SANTOS JL, CARVALHO E, BEZERRA JA. Advances in biliary atresia: from patient care to research[J]. Brazilian Journal of Medical and Biological Research, 2010, 43(6): 522-527.
[6]KIELING CO, SANTOS JL, VIEIRA SM, et al. Biliary atresia: we still operate too late[J]. J Pediatr, 2008, 84(5): 436-441.
[7]DUCHE M, FABRE M, KRETZSCHMAR B, et al. Prognostic value of portal pressure at the time of Kasai operation in patients with biliary atresia[J]. J Pediatr Gastroenterol Nutr, 2006, 43(5): 640-645.
[8]SOKOL RJ, SHEPHERD RW, SUPERINA R, et al. Screening and outcomes in biliary atresia: summary of a National Institutes of Health workshop[J]. Hepatology, 2007, 46(2): 566-581.
[9]CHITTMITTRAPAP S, CHANDRAKAMOL B, POOVORAWAN Y, et al. Factors influencing outcome after hepatic portoenterostomy for biliary atresia: a logistic regression analysis[J]. J Med Assoc Thai, 2005, 88(8): 1077-1082.
[10]STRINGER MD, DAVISON SM, RAJWAL SR, et al. Kasai portoenterostomy: 12-year experience with a novel adjuvant therapy regimen[J]. J Pediatr Surg, 2007, (42): 1324-1328.
[11]WILDHABER BE, MAJNO P, MAYR J, et al. Biliary atresia: Swiss national study, 1994-2004[J]. J Pediatr Gastroenterol Nutr, 2008, 46(3): 299-307.
[12]SCHREIBER RA, BARKER CC, ROBERTS EA, et al. Biliary atresia: the Canadian experience[J]. J Pediatr, 2007, 151(6): 659-665.
[13]LYKAVIERIS P, CHARDOT C, SOKHN M, et al. Outcome in adulthood of biliary atresia: a study of 63 patients who survived for over 20 years with their native liver. Hepatology, 2005, 41(2): 366-371.
[14]SHEN Z, ZHENG S, DONG R, et al. Saturation of stool color in HSV color model is a promising objective parameter for screening biliary atresia[J]. J Pediatr Surg, 2016, 51(12): 2091-2094.
[15]PAPEL, OLSSON K, PETERSEN C, et al. Prognostic Value of Computerized Quantification of Liver Fibrosis in Children with biliary atresia[J]. Liver transplantation, 2009, 15: 876-882.
[16]SOKOL RJ. Biliary atresia screening: why, when, and how[J]. Pediatrics, 2009, 123(5): 951-952.
[17]HABER BA, ERLICHMAN J, LOOMES KM. Recent advances in biliary atresia: prospects for novel therapies[J]. Expert Opin Investig Drugs, 2008, 17(12): 1911-1924.
[18]MAKI T, SUMAZAKI R, MATSUI A. Mass screening for biliary atresia[J]. Jpn J Pediatr Surg, 1999, 31: 242-246.
[19]CHEN SM, CHANG MH, DU JC, et al. Screening for biliary atresia by infant stool color card in Taiwan[J]. Pediatrics, 2006, 117: 1147-1154.
[20]HSIAO CH, CHANG MH, CHEN HL, et al. Universal screening for biliary atresia using an infant stool color card in Taiwan[J]. Hepatology, 2008, 47(4): 1233-1240.
[21]TYRELL M, HINGLEY S, GILES C, et al. Impact of delayed screening for prolonged jaundice in the newborn[J]. Arch Dis Child Fetal Neonatal Ed, 2009, 94(2): 154.
[22]钟志海,潘静,蒋宏.胆道闭锁患儿早期胆红素变化[J].临床小儿外科杂志,2015,2(14):106-109.
[23]李秋平,封志纯.美国儿科学会最新新生儿黄疸诊疗指南[J].实用儿科临床杂志,2006,21(14):958-960.
[24]CY CHIU, PH CHEN, CF CHAN, et al. Biliary Atresia in Preterm Infants in Taiwan: A Nationwide Survey[J]. J Pediatr, 2013, 163(1): 100-103.
[25]詹江华,管志伟,张辉.重视新生儿胆汁淤积:提高胆道闭锁的早诊率[J].中华实用儿科临床杂志,2014,29(11):803-806.
[26]詹江华,罗喜荣.《胆道闭锁诊疗流程》草案[J].中华小儿外科杂志,2013,34(2):147-149.
[27]孙颖华,郑珊,钱蔷英.超声检查在胆道闭锁鉴别诊断中的运用价值[J].临床小儿外科杂志,2008,7(4):3-6.
[28]苏英姿,袁新宇,张玉林,等.超声检查在新生儿阻塞性肝炎与先天性胆道闭锁鉴别诊断中的应用价值[J].中华妇幼临床医学杂志,2010,6(1):22-24.