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Hereditary angioedema and "familial" lupus erythematosus in identical twin boys.

作者信息

Kohler P F, Percy J, Campion W M, Smyth C J

出版信息

Am J Med. 1974 Mar;56(3):406-11. doi: 10.1016/0002-9343(74)90623-8.

DOI:10.1016/0002-9343(74)90623-8
PMID:4544343
Abstract
摘要

相似文献

1
Hereditary angioedema and "familial" lupus erythematosus in identical twin boys.同卵双胞胎男孩中的遗传性血管性水肿和“家族性”红斑狼疮。
Am J Med. 1974 Mar;56(3):406-11. doi: 10.1016/0002-9343(74)90623-8.
2
An association between C1 esterase inhibitor deficiency and lupus erythematosus: report of two cases and review of the literature.
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Discoid lupus erythematosus and the variant form of hereditary angioedema.盘状红斑狼疮与遗传性血管性水肿的变异型。
Arch Dermatol. 1977 Mar;113(3):374-5. doi: 10.1001/archderm.1977.01640030120024.
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[Immunoserological follow-up and clinical finding in SLE].
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[Diagnostic value of immunological methods in several chronic skin diseases].[免疫方法在几种慢性皮肤病中的诊断价值]
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C3 metabolism in a patient with deficiency of the second component of complement (C2) and discoid lupus erythematosus.一名补体第二成分（C2）缺乏且患有盘状红斑狼疮患者的C3代谢
Clin Exp Immunol. 1976 May;24(2):238-48.
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[Level of immunoglobulin IgG, IgM and IgA in the serum of patients with chronic discoid lupus erythematosus].[慢性盘状红斑狼疮患者血清中免疫球蛋白IgG、IgM和IgA的水平]
Dermatol Monatsschr. 1973 Sep;159(9):886-91.
8
Genetic deficiencies of the complement system.补体系统的遗传性缺陷
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Discoid lupus erythematosus associated with hereditary angioneurotic oedema.盘状红斑狼疮伴遗传性血管性水肿。
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Interferon production by lymphocytes from patients with systemic lupus erythematosus.
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引用本文的文献

1
Complement and systemic lupus erythematosus.补体与系统性红斑狼疮
Arthritis Res. 2002;4 Suppl 3(Suppl 3):S279-93. doi: 10.1186/ar586. Epub 2002 May 9.
2
Complement deficiency and immune complex disease.补体缺陷与免疫复合物疾病
Springer Semin Immunopathol. 1994;15(4):397-416. doi: 10.1007/BF01837367.
3
Simultaneous occurrence in identical twins of discoid lupus erythematosus and polymorphic light eruption.盘状红斑狼疮和多形性日光疹在同卵双胞胎中的同时发生。
J R Soc Med. 1983 Sep;76(9):791-2. doi: 10.1177/014107688307600918.
4
Family study of the major histocompatibility complex in patients with systemic lupus erythematosus: importance of null alleles of C4A and C4B in determining disease susceptibility.系统性红斑狼疮患者主要组织相容性复合体的家系研究：C4A和C4B无效等位基因在决定疾病易感性中的重要性。
Br Med J (Clin Res Ed). 1983 Feb 5;286(6363):425-8. doi: 10.1136/bmj.286.6363.425.
5
Inherited deficiencies of complement proteins in man.人类补体蛋白的遗传性缺陷。
Springer Semin Immunopathol. 1984;7(2-3):251-61. doi: 10.1007/BF01893022.
6
Heterozygous C2 deficiency associated with angioedema, myasthenia gravis, and systemic lupus erythematosus.与血管性水肿、重症肌无力和系统性红斑狼疮相关的杂合子C2缺乏症。
Ann Rheum Dis. 1986 May;45(5):428-30. doi: 10.1136/ard.45.5.428.
7
Hereditary angioedema and thyroid autoimmunity.遗传性血管性水肿与甲状腺自身免疫
J Clin Pathol. 1987 May;40(5):518-23. doi: 10.1136/jcp.40.5.518.
8
Lupus diseases associated with hereditary and acquired deficiencies of complement.与遗传性和获得性补体缺陷相关的狼疮疾病。
Springer Semin Immunopathol. 1986;9(2-3):161-78. doi: 10.1007/BF02099020.
9
Urticarial vasculitis and syndromes in association with connective tissue diseases.荨麻疹性血管炎及与结缔组织病相关的综合征。
Ann Rheum Dis. 1991 Nov;50(11):743-4. doi: 10.1136/ard.50.11.743.
10
Complete absence of the third component of complement in man.人类补体第三成分完全缺失。
J Clin Invest. 1975 Sep;56(3):703-10. doi: 10.1172/JCI108141.