Recurrent systemic bacterial infections in homozygous C2 deficiency
- 1 October 1990
- journal article
- Published by Wiley in Pediatric Allergy and Immunology
- Vol. 1 (1) , 46-49
- https://doi.org/10.1111/j.1399-3038.1990.tb00008.x
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- C2 Deficiency, Moderately Low lgG2 Concentrations and Lack of the G2m(23) Allotype Marker in a Child with Repeated Bacterial InfectionsActa Paediatrica, 1987
- Inherited deficiency of properdin and C2 in a patient with recurrent bacteremiaThe American Journal of Medicine, 1987
- Complement, membrane glycoproteins, and complement receptors: Their role in regulation of the immune responseClinical Immunology and Immunopathology, 1986
- Complement Deficiency States and InfectionMedicine, 1984
- Increased susceptibility to severe pyogenic infections in patients with an inherited deficiency of the second component of complementThe Journal of Pediatrics, 1981
- Homozygous deficiency of the second component of complement presenting with recurrent bacterial meningitis.Archives of Disease in Childhood, 1980
- Recurrent Septicemia Associated with Congenital Deficiency of C2 and Partial Deficiency of Factor B and the Alternative Complement PathwayNew England Journal of Medicine, 1978
- Influence of a deficiency of the second component of complement on the bactericidal activity of neutrophils in vitro.Journal of Clinical Investigation, 1977
- C2 Deficiency DEVELOPMENT OF LUPUS ERYTHEMATOSUSJournal of Clinical Investigation, 1973
- THE ENHANCEMENT OF BACTERIAL PHAGOCYTOSIS BY SERUMThe Journal of Experimental Medicine, 1969