Hepatology Digest: This next question in on primary biliary cirrhosis.
国际肝病：下一个问题是关于原发性胆汁性肝硬化的。
A cases with biliary cirrhosis and sclerotic cholangitis underwent the liver transplantation.
肝移植治疗一例胆汁性肝硬变，硬化性胆管炎。
Objective To study the diagnosis and treatment of portal hypertension in secondary biliary cirrhosis(PHSBC).
目的探讨继发性胆汁性肝硬变门脉高压症的诊断和治疗。
Micronodular cirrhosis may also be seen with Wilson's disease, primary biliary cirrhosis, and hemochromatosis.
小结节型肝硬化也可见于Wilson病、原发性胆汁硬化和血色素沉着症。
The advanced patients often possess severe jaundice, severe liver dysfunction, biliary cirrhosis, portal hypertension.
晚期病人常有重度黄疸、严重肝功效损害、胆汁性肝硬变、门静脉高压症的表现。
Background Current survival models for primary biliary cirrhosis have limited precision for medium and long-term survival.
当前对原发性胆汁性肝硬化患者生存模式的预测，多局限在预测其中期和长期得生存率。
To explore the correlation of adenine nucleotide translocator 3(ANT3) gene expression level with primary biliary cirrhosis(PBC).
目的探讨腺嘌呤易位体3（ANT 3）基因表达水平与原发性胆汁性肝硬化（PBC）的相关性。
Primary biliary cirrhosis (PBC) is a chronic, progressive cholestatic liver disease of unknown cause that usually affects middle-aged women.
原发性胆汁淤积性肝硬化(PBC)是一种多发于中年女性、不明原因导致的慢性进行性胆汁淤积性肝脏疾病。
Aim to describe a prognostic model for the advent of complications in primary biliary cirrhosis as the first approach to a staged prognostic model.
目的：描述一种可以预测原发性胆汁性肝硬化患者并发症出现的模型，并把其作为一种阶段化预测模式的第一方法。
Objective: to investigate the surgical treatment of 15 patients with portal hypertension of secondary biliary cirrhosis due to hepatolithiasis (PHSBCH).
目的：探讨15例因肝胆管结石至胆管狭窄合并胆汁性肝硬变门脉高压症(PHSBCH)的外科治疗。
Needle biopsies of the liver from 4 patients with primary biliary cirrhosis were studied ultrastructurally with special reference to intrahepatic bile ducts.
本文对4例原发性胆汁性肝硬化肝穿组织肝内小胆管进行了光镜和电镜观察。
Primary biliary cirrhosis (PBC), which is an early form of liver cirrhosis, is a long term progressive autoimmune disease, in which environmental factors are thought to play a part.
原发性胆汁性肝硬化(PBC)的，是肝硬化的早期形式，是一项长期的渐进自身免疫性疾病，在这过程中环境因素被认为是发挥作用的。
Objective To study the association between the polymorphisms of vitamin D receptor (VDR) gene and autoimmune liver diseases and (AIH) and primary biliary cirrhosis (PBC) in Chinese.
目的探讨维生素D受体（VDR）基因多态性与中国人自身免疫性肝炎（AIH）和原发性胆汁性肝硬化（PBC）发病的相关性。
Newborn pigs lacking CFTR showed defective chloride transport and developed meconium ileus, exocrine pancreatic destruction, and focal biliary cirrhosis, which are all hallmark of CF disease.
新生的缺乏CFTR基因的猪表现出氯化物转移缺陷，胎粪性肠梗阻，胰腺外分泌缺陷和局限性胆道硬化，而这些症状正是人类CF疾病的主要症状。
A small number of patients possess positive anti-nuclear antibody and anti-smooth muscle antibody and negative anti-mitochondrial antibody, which can be distinguished from primary biliary cirrhosis.
少数病人抗核抗体及抗不随意肌抗体可为阳性，但抗线粒体抗体阴性，这可与原发性胆汁性肝硬化区别。
The results of biopsy showed 2 chronic rejections, 1 biliary stasis hepatic cirrhosis and 1 hepatic focal necrosis.
活检病理结果慢性排斥反应2例，胆汁淤积性肝硬化1例，肝脏局灶性坏死1例。
Postoperative pathological analysis revealed biliary liver cirrhosis.
术后病理结果为胆汁性肝硬化。
Postoperative pathological analysis revealed biliary liver cirrhosis.
术后病理结果为胆汁性肝硬化。
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