人类补体蛋白的遗传性缺陷。 - Suppr

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超能文献

Inherited deficiencies of complement proteins in man.

作者信息

Alper C A, Rosen F S

出版信息

Springer Semin Immunopathol. 1984;7(2-3):251-61. doi: 10.1007/BF01893022.

DOI:10.1007/BF01893022

PMID:6238435

Abstract

摘要

相似文献

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.

Inherited deficiencies of complement components in man.人类补体成分的遗传性缺陷。

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Inherited complement component abnormalities.遗传性补体成分异常。

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Inherited deficiencies of complement and complement-related proteins.补体及补体相关蛋白的遗传性缺陷。

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Navigating the maze of complement genetics: a guide for clinicians.探索补体遗传学的迷宫：临床医生指南

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The membrane attack complex.膜攻击复合物

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Defective activation of the alternative pathway of complement in patients with homozygous C2 deficiency: studies in two unrelated families.纯合子C2缺乏症患者补体替代途径的激活缺陷：对两个无关家族的研究。

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Essential hypocomplementemia: report of a case.原发性补体低下血症：一例报告

Blood. 1960 Sep;16:1338-41.

A BIOCHEMICAL ABNORMALITY IN HEREDIATRY ANGIONEUROTIC EDEMA: ABSENCE OF SERUM INHIBITOR OF C' 1-ESTERASE.遗传性血管神经性水肿中的一种生化异常：血清C1酯酶抑制剂缺失

Am J Med. 1963 Jul;35:37-44. doi: 10.1016/0002-9343(63)90162-1.

Hereditary deficiency of the sixth component of complement in man. I. Immunochemical, biologic, and family studies.人类补体第六成分的遗传性缺陷。I. 免疫化学、生物学及家系研究。

J Clin Invest. 1974 Feb;53(2):544-53. doi: 10.1172/JCI107588.

Genetic analysis of C4 deficiency.C4缺乏症的基因分析。

J Clin Invest. 1981 Jan;67(1):260-3. doi: 10.1172/JCI110021.

Homozygous deficiency of the second component of complement presenting with recurrent bacterial meningitis.伴有复发性细菌性脑膜炎的补体第二成分纯合子缺陷。

Arch Dis Child. 1980 Jun;55(6):471-3. doi: 10.1136/adc.55.6.471.

Complement-mediated solubilization in patients with systemic lupus erythematosus, nephritis or vasculitis.系统性红斑狼疮、肾炎或血管炎患者的补体介导溶解作用。

Clin Exp Immunol. 1981 Dec;46(3):557-64.

Properdin deficiency in a family with fulminant meningococcal infections.一个患有暴发性脑膜炎球菌感染的家庭中的备解素缺乏症。

Clin Exp Immunol. 1982 Nov;50(2):291-7.

Deficiency of the eighth component of complement and recurrent meningococcal disease: a case and family study.

Aust N Z J Med. 1982 Dec;12(6):638-41. doi: 10.1111/j.1445-5994.1982.tb02656.x.

Genetic deficiency of C4 presenting with recurrent infections and a SLE-like disease. Genetic and immunologic studies.

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Behavior in vivo of normal and dysfunctional C1 inhibitor in normal subjects and patients with hereditary angioneurotic edema.正常受试者和遗传性血管性水肿患者体内正常和功能失调的C1抑制剂的行为。

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