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。 - Suppr

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超能文献

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

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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。

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引用本文的文献

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.

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.

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.

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.

Inherited deficiencies of complement proteins in man.人类补体蛋白的遗传性缺陷。

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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。

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Hereditary angioedema and thyroid autoimmunity.遗传性血管性水肿与甲状腺自身免疫

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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。

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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.

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.

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