Inherited complement deficiency states: implications for immunity and immunological disease
Author:
Publisher
Wiley
Subject
Microbiology (medical),General Medicine,Immunology and Allergy,Pathology and Forensic Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1699-0463.1990.tb05008.x/fullpdf
Reference108 articles.
1. Lupus diseases associated with hereditary and acquired deficiencies of complement;Agnello;Springer Semin. Immunopathol.,1986
2. Hereditary C2 deficiency with some manifestations of systemic lupus erythematosus;Agnello;J. Immunol.,1972
3. Increased susceptibility to infection associated with abnormalities of complement-mediated functions and of the third component of complement (C3);Alper;N. Engl. J. Med.,1970
4. Increased susceptibility to infection in a patient with type II essential hypercatabolism of C3;Alper;N. Engl. J. Med.,1973
5. Homozygous deficiency of C3 in a patient with repeated infections;Alper;Lancet,1972
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