Prevalence of hereditary properdin, C7 and C8 deficiencies in patients with meningococcal infections
Author:
Affiliation:
1. Barzilai Medical Centre, Ashkelon, Israel
2. Ben-Gurion University of the Negev, Beer Sheba, Israel
3. Department of Epidemiology, Ministry of Health, Jerusalem, Israel
4. The Weizmann Institute of Science, Rehovot, Israel
Abstract
Publisher
Oxford University Press (OUP)
Subject
Immunology,Immunology and Allergy
Link
https://academic.oup.com/cei/article-pdf/81/3/423/42217687/j.1365-2249.1990.tb05350.x.pdf
Reference35 articles.
1. Familial properdin deficiency and fatal meningococcemia: correction of the bactericidal effect by vaccination;Densen;N. Eng. J. Med.,1987
2. Complement deficiencies in patients over ten years old with meningococcal disease due to uncommon serogroups;Fijen;Lancet,1989
3. Inherited deficiency of Properdin and C2 in a patient with recurrent bacteremia;Gelfand;Am. J. Med.,1987
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