[1] 李盼.遗传代谢性婴儿胆汁淤积性肝病精准诊断的初步研究.中国医科大学,2017.
[2] 张婧,王晓红,叶颖子,等.白蛋白在诊断Citrin缺陷导致的新生儿肝内胆汁淤积症的价值.中华肝脏病杂志,2016,24:755-760.
[3] 李宝鑫,叶峻杰.希特林缺乏所致新生儿肝内胆汁淤积症的研究进展.检验医学与临床,2016,13:362-364.
[4] 高源.希特林蛋白缺陷症致婴儿胆汁淤积性肝炎四例临床分析.中国综合临床,2016,32:467-470.
[5] 卢春婷,李佳萦,冯烈,等.Citrin缺陷导致的新生儿肝内胆汁淤积症患儿SLC25A13基因突变与生化指标的相关性研究.中国病理生理杂志,2014,30:859-863.
[6] 宫磊,朱延玲,胡卫华,等.妊娠期肝内胆汁淤积症中ABCB4基因外显子12突变的研究.中国优生与遗传杂志,2007,15:17-18,20.
[7] 周轶红,谢玲玫,洪娟,等.总胆汁酸测定在妊娠期肝内胆汁淤积症中应用重要性的探讨.中国优生与遗传杂志,2007,15:68-68.
[8] Russo P, Magee JC, Anders RA, et al. Key Histopathologic Features of Liver Biopsies That Distinguish Biliary Atresia From Other Causes of Infantile Cholestasis and Their Correlation With Outcome: A Multicenter Study.Am J Surg Pathol,2016,40:1601-1615.
[9] Wada K, Kobayashi H, Moriyama A, et al. A case of an infant with congenital combined pituitary hormone deficiency and normalized liver histology of infantile cholestasis after hormone replacement therapy.Clin Pediatr Endocrinol,2017,26:251-257.
[10] Sangkhathat S, Laochareonsuk W, Maneechay W, et al. Variants associated with infantile cholestatic syndromes detected in extrahepatic biliary atresia by whole exome studies: A 20-case series from Thailand.J Pediatr Genet,2018,7:67-73. |
