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Primary biliary cirrhosis associated with features of systemic lupus erythematosus.

作者信息

Iliffe G D, Naidoo S, Hunter T

出版信息

Dig Dis Sci. 1982 Mar;27(3):274-8. doi: 10.1007/BF01296928.

DOI:10.1007/BF01296928
PMID:7042250
Abstract
摘要

相似文献

1
Primary biliary cirrhosis associated with features of systemic lupus erythematosus.
Dig Dis Sci. 1982 Mar;27(3):274-8. doi: 10.1007/BF01296928.
2
Primary biliary cirrhosis and systemic lupus erythematosus. A new case report.原发性胆汁性肝硬化与系统性红斑狼疮。一例新病例报告。
Rev Rhum Engl Ed. 1998 Jul-Sep;65(7-9):504-7.
3
Shared autoimmunity: a concept for which the time has come.共享自身免疫：一个时机已至的概念。
Autoimmunity. 2005 May;38(3):201-3. doi: 10.1080/08916930500050285.
4
Case report: a rare association of primary biliary cirrhosis and systemic lupus erythematosus and review of the literature.病例报告：原发性胆汁性肝硬化与系统性红斑狼疮的罕见关联及文献综述
J Gastroenterol Hepatol. 1999 May;14(5):431-5. doi: 10.1046/j.1440-1746.1999.01883.x.
5
Primary biliary cirrhosis and systemic lupus erythematosus. A rare association.
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6
[Primary biliary cirrhosis and minimal change glomerulonephritis].
Nefrologia. 2001;21(6):609-10.
7
[Primary biliary cirrhosis and systemic lupus erythematosus. Association or succession? (author's transl)].
Gastroenterol Clin Biol. 1981 Nov;5(11):1047-51.
8
Unusual coexistence of systemic lupus erythematosus and primary biliary cirrhosis.系统性红斑狼疮与原发性胆汁性肝硬化的罕见共存。
Dermatology. 1994;188(4):313-7. doi: 10.1159/000247174.
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Systemic lupus erythematosus developing in patients with primary biliary cirrhosis.原发性胆汁性肝硬化患者中发生的系统性红斑狼疮。
Ann Intern Med. 1984 Mar;100(3):388-9. doi: 10.7326/0003-4819-100-3-388.
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Visceral leishmaniasis mimicking autoimmune hepatitis, primary biliary cirrhosis, and systemic lupus erythematosus overlap.内脏利什曼病酷似自身免疫性肝炎、原发性胆汁性肝硬化和系统性红斑狼疮重叠综合征。
Korean J Parasitol. 2012 Jun;50(2):133-6. doi: 10.3347/kjp.2012.50.2.133. Epub 2012 May 24.

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Pathological findings with vacuoles in anti-mitochondrial antibody-positive inflammatory myopathy.抗线粒体抗体阳性的炎性肌病中的空泡性病理改变。
BMC Musculoskelet Disord. 2024 Apr 2;25(1):257. doi: 10.1186/s12891-023-06941-6.
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Extrahepatic Manifestations of Primary Biliary Cholangitis.原发性胆汁性胆管炎的肝外表现。
Gut Liver. 2017 Nov 15;11(6):771-780. doi: 10.5009/gnl16365.
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Clinical Characteristics of Concomitant Systemic Lupus Erythematosus and Primary Biliary Cirrhosis: A Literature Review.系统性红斑狼疮合并原发性胆汁性肝硬化的临床特征：文献综述

本文引用的文献

1
Primary or secondary sicca complex? Investigation in primary biliary cirrhosis by histocompatibility testing.原发性或继发性干燥综合征？通过组织相容性检测对原发性胆汁性肝硬化的研究。
Br Med J. 1980 Aug 9;281(6237):425-6. doi: 10.1136/bmj.281.6237.425.
2
Complement metabolism in chronic liver disease: catabolism of C1q in chronic active liver disease and primary biliary cirrhosis.慢性肝病中的补体代谢：慢性活动性肝病和原发性胆汁性肝硬化中C1q的分解代谢
Gastroenterology. 1980 May;78(5 Pt 1):1034-40.
3
Primary biliary cirrhosis and cold autoimmune hemolytic anemia: effect of partial plasma exchange.
J Immunol Res. 2015;2015:713728. doi: 10.1155/2015/713728. Epub 2015 May 18.
原发性胆汁性肝硬化与冷凝集素型自身免疫性溶血性贫血：部分血浆置换的疗效
Gastroenterology. 1980 Mar;78(3):576-8.
4
Adverse effects of D-penicillamine in rheumatoid arthritis.青霉胺在类风湿关节炎中的不良反应。
Ann Intern Med. 1980 Jan;92(1):24-9. doi: 10.7326/0003-4819-92-1-24.
5
Clinical pattern and course of disease in primary biliary cirrhosis based on an analysis of 236 patients.基于236例患者分析的原发性胆汁性肝硬化的临床模式与病程
Gastroenterology. 1980 Feb;78(2):236-46.
6
HLA-DRw3 and systemic lupus erythematosus.人类白细胞抗原-DRw3与系统性红斑狼疮
Arthritis Rheum. 1980 Aug;23(8):954-7. doi: 10.1002/art.1780230815.
7
[Primary biliary cirrhosis associated with acute disseminated lupus erythematosus (author's transl)].
Nouv Presse Med. 1980 Jan 5;9(1):31-4.
8
Primary biliary cirrhosis: the prevalence of hypothyroidism and its relationship to thyroid autoantibodies and sicca syndrome.原发性胆汁性肝硬化：甲状腺功能减退症的患病率及其与甲状腺自身抗体和干燥综合征的关系。
Gastroenterology. 1980 Jun;78(6):1437-41.
9
Suppressor cell activity in primary biliary cirrhosis.原发性胆汁性肝硬化中的抑制细胞活性。
Dig Dis Sci. 1980 Feb;25(2):104-7. doi: 10.1007/BF01308306.
10
Primary biliary cirrhosis and graft-versus-hjost disease.
Lancet. 1980 Jul 26;2(8187):207. doi: 10.1016/s0140-6736(80)90098-7.