[1] 陈婧,何卫平,胡瑾华,等. 先天性肝纤维化-附12例临床分析[J]. 肝脏,2009,14(1):14-16. [2] 赵新颜,王宝恩,贾继东. 36例先天性肝纤维化的临床病理特点[J]. 中华消化杂志,2005,25(12):748-749. [3] 赵新颜,王泰龄,贾继东. 先天性肝纤维化14例临床病理特点[J]. 临床肝胆病杂志,2010,26(2):191-193. [4] YONEM O,BAYRAKTARR Y. Clinical characteristics of Caroli’s syndrome[J]. World J Gastroenterol,2007,13(13): 1934-1937. [5] DESMET VJ. What is congenital hepatic fibrosis[J]. Histopathology,1992,20(6):465-477. [6] DE KONING TJ,NIKKELS PG,DORLAND L,et al. Congenital hepatic fibrosis in 3 siblings with phosphomannose isomerase deficiency[J]. Virchows Arch, 2000,437(1):101-105. [7] YONEM O,BAYRAKTAR Y. Is portal vein cavernous transformation a component of congenital hepatic fibrosis[J]. World J Gastroenterol,2007,13(13):1928-1929. [8] SHORBAGI A,BAYRAKTAR Y. Experience of a single center with congenital hepatic fibrosis:a review of the literature[J]. World J Gastroenterol,2010,16(6):683-690. [9] LING SC. Congenital cholestatic syndromes:what happens when children grow up[J]. Can J Gastroenterol, 2007,21(11):743-751. |