Properdin deficiency associated with recurrent otitis media and pneumonia, and identification of male carrier with Klinefelter syndrome-Reference-Cited by-同舟云学术

Properdin deficiency associated with recurrent otitis media and pneumonia, and identification of male carrier with Klinefelter syndrome

Published:2009-06 Issue:3 Volume:131 Page:456-462
ISSN:1521-6616
Container-title:Clinical Immunology
language:en
Short-container-title:Clinical Immunology

Author:

Schejbel Lone,Rosenfeldt Vibeke,Marquart Hanne,Valerius Niels Henrik,Garred Peter

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference40 articles.

1. Properdin, a positive regulator of complement activation, is expressed in human T cell lines and peripheral blood T cells;Schwaeble;J. Immunol.,1993

2. Expression of properdin in human monocytes;Schwaeble;Eur. J. Biochem.,1994

3. Properdin, a positive regulator of complement activation, is released from secondary granules of stimulated peripheral blood neutrophils;Wirthmueller;J. Immunol.,1997

4. Properdin deficiency in a large Swiss family: identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G2m(n);Späth;Clin. Exp. Immunol.,1999

5. Assessment of complement deficiency in patients with meningococcal disease in The Netherlands;Fijen;Clin. Infect. Dis.,1999

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