[1] 孔祥璐, 郭晓霞. 中药联合熊去氧胆酸胶囊治疗原发性胆汁性肝硬化疗效系统评价. 实用肝脏病杂志, 2015, 18(4): 379-382. [2] Guo J, Shi J, Wang H, et al. Emerging gram-positive bacteria and drug resistance in cirrhosis patients with spontaneous bacterial peritonitis: a retrospective study. Exp Ther Med, 2019, 17(6): 4568-4576. [3] 秦维, 陈宇萍, 杨昭, 等 原发性胆汁性肝硬化患者肝组织转化生长因子β-1表达水平变化. 实用肝脏病杂志, 2018, 21(2): 237-240. [4] 陶明玲, 张世斌, 吴燕京, 等. 原发性胆汁性肝硬化患者食管静脉曲张特点及其无创预测指标研究. 实用肝脏病杂志, 2017, 20(4): 439-442. [5] Zhang J, Wen XY, Gao RP. Hepatitis B virus-related liver cirrhosis complicated with dermatomyositis: A case report. World J Clin Cases, 2019, 7(10): 1206-1212. [6] de Liso F, Matinato C, Ronchi M, et al. The diagnostic accuracy of biomarkers for diagnosis of primary biliary cholangitis (PBC) in anti-mitochondrial antibody (AMA)-negative PBC patients: a review of literature. Clin Chem Lab Med, 2017, 56(1): 25-31. [7] Marzorati S, Lleo A, Carbone M, et al. The epigenetics of PBC: the link between genetic susceptibility and environment. Clin Res Hepatol Gastroenterol, 2016, 40(6): 650-659. [8] Yang F, Yang Y, Wang Q, et al. The risk predictive values of UK-PBC and GLOBE scoring system in Chinese patients with primary biliary cholangitis: the additional effect of anti-gp210. Aliment Pharmacol Ther, 2017, 45(5): 733-743. [9] Peng Y, Qi X, Guo X. Child-Pugh versus meld score for the assessment of prognosis in liver cirrhosis: a systematic review and meta-analysis of observational studies. Medicine (Baltimore), 2016, 95(8): e2877. [10] Fawaz R, Baumann U, Ekong U, et al. Guideline for the evaluation of cholestatic jaundice in infants: joint recommendations of the north american society for pediatric gastroenterology, hepatology, and nutrition and the european society for pediatric gastroenterology, hepatology, and nutrition. J Pediatr Gastroenterol Nutr, 2017, 64(1): 154-168. [11] Voiosu AM, Wiese S, Voiosu TA, et al. Total bile acid levels are associated with left atrial volume and cardiac output in patients with cirrhosis. Eur J Gastroenterol Hepatol, 2018, 30(4): 392-397. [12] Gulamhusein AF, Juran BD, Atkinson EJ, et al. Low incidence of primary biliary cirrhosis (PBC) in the first-degree relatives of PBC probands after 8 years of follow-up. Liver Int, 2016, 36(9): 1378-1382. [13] Shimoda S, Tanaka A. It is time to change primary biliary cirrhosis (PBC): New nomenclature from "cirrhosis" to "cholangitis", and upcoming treatment based on unveiling pathology. Hepatol Res, 2016, 46(5): 407- 415. [14] Van den B, Hindryckx P, Devisscher L, et al. Ursodeoxycholic acid and its taurine- or glycine-conjugated species reduce colitogenic dysbiosis and equally suppress experimental colitis in mice. Appl Environ Microbiol, 2017, 83(7): e02766-2776. [15] Woodhouse CA, Patel VC, Singanayagam A, et al. The gut microbiome as a therapeutic target in the pathogenesis and treatment of chronic liver disease. Aliment Pharmacol Ther, 2018, 47(2): 192-202. [16] Cusin F, Fernandes Azevedo L, Bonnaventure P, et al. Hepatocyte concentrations of indocyanine green reflect transfer rates across membrane transporters. Basic Clin Pharmacol Toxicol, 2017, 120(2): 171-178. [17] Nakagawa R, Muroyama R, Saeki C, et al. Mir-425 regulates inflammatory cytokine production in CD4+ t cells via N-Ras upregulation in primary biliary cholangitis. J Hepatol, 2017, 66(6): 1223-1230. [18] Dokmak S, Aussilhou B, Ragot E, et al. Reconstruction of bile duct injury and defect with the round ligament. J Gastrointest Surg, 2017, 21(9): 1540-1543. [19] Vancamelbeke M, Vermeire S. The intestinal barrier: a fundamental role in health and disease. Expert Rev Gastroenterol Hepatol, 2017, 11(9): 821-834. [20] Halilbasic E, Steinacher D. Nor-ursodeoxycholic acid as a novel therapeutic approach for cholestatic and metabolic liver diseases. Dig Dis, 2017, 35(3): 288-292. |