Case Report: Severe Complement-Mediated Thrombotic Microangiopathy in IgG4-Related Disease Secondary to Anti-Factor H IgG4 Autoantibodies.
第一作者:
Gautier,Breville
第一单位:
Department of Medicine, Division of Immunology and Allergy, Geneva University Hospitals, Geneva, Switzerland.;Department of Clinical Neurosciences, Division of Neurology, Geneva University Hospitals, Geneva, Switzerland.
作者:
医学主题词
载脂蛋白类(Apolipoproteins);自身抗体(Autoantibodies);补体C3b灭活蛋白质类(Complement C3b Inactivator Proteins);补体因子H(Complement Factor H);女(雌)性(Female);基因缺失(Gene Deletion);疾病遗传易感性(Genetic Predisposition to Disease);人类(Humans);免疫球蛋白G(Immunoglobulin G);中年人(Middle Aged);血栓性微血管病(Thrombotic Microangiopathies)
DOI
10.3389/fimmu.2020.604759
PMID
33643292
发布时间
2021-03-10
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Frontiers in immunology
604759页
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