C1q levels in hereditary angioedema
- 1 March 1977
- journal article
- research article
- Published by Elsevier in Journal of Allergy and Clinical Immunology
- Vol. 59 (3) , 263-265
- https://doi.org/10.1016/0091-6749(77)90160-9
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Hereditary Angioedema: the Clinical Syndrome and Its ManagementAnnals of Internal Medicine, 1976
- Complement component analysis in angiodema. Diagnostic valueArchives of Dermatology, 1975
- Acquired inhibitor deficiency in lymphosarcomaClinical Immunology and Immunopathology, 1972
- The Complement System of ManNew England Journal of Medicine, 1972
- Metabolism of Human C1q STUDIES IN HYPOGAMMAGLOBULINEMIA, MYELOMA, AND SYSTEMIC LUPUS ERYTHEMATOSUSJournal of Clinical Investigation, 1972
- Genetically determined heterogeneity of the C1 esterase inhibitor in patients with hereditary angioneurotic edemaJournal of Clinical Investigation, 1971
- Complement metabolism in man: hypercatabolism of the fourth (C4) and third (C3) components in patients with renal allograft rejection and hereditary angioedema (HAE)Journal of Clinical Investigation, 1969
- Immunochemical quantitation of antigens by single radial immunodiffusionImmunochemistry, 1965
- Hereditary Angioneurotic Edema: Two Genetic VariantsScience, 1965
- Action of Complement in Hereditary Angioneurotic Edema: The Role of C′1-Esterase *Journal of Clinical Investigation, 1964