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Properdin deficiency: molecular basis and disease association.
Fijen CA, van den Bogaard R, Schipper M, Mannens M, Schlesinger M, Nordin FG, Dankert J, Daha MR, Sjöholm AG, Truedsson L, Kuijper EJ. Fijen CA, et al. Among authors: truedsson l. Mol Immunol. 1999 Sep-Oct;36(13-14):863-7. doi: 10.1016/s0161-5890(99)00107-8. Mol Immunol. 1999. PMID: 10698340 Review. No abstract available.
Human properdin deficiency has a heterogeneous genetic background.
Truedsson L, Westberg J, Fredrikson GN, Sjöholm AG, Kuijper EJ, Fijen CA, Späth PJ, Uhlén M. Truedsson L, et al. Immunopharmacology. 1997 Dec;38(1-2):203-6. doi: 10.1016/s0162-3109(97)00087-8. Immunopharmacology. 1997. PMID: 9476131 Review. No abstract available.
Complement deficiency and disease: an update.
Sjöholm AG, Jönsson G, Braconier JH, Sturfelt G, Truedsson L. Sjöholm AG, et al. Among authors: truedsson l. Mol Immunol. 2006 Jan;43(1-2):78-85. doi: 10.1016/j.molimm.2005.06.025. Mol Immunol. 2006. PMID: 16026838 Review.
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 PJ, Sjöholm AG, Fredrikson GN, Misiano G, Scherz R, Schaad UB, Uhring-Lambert B, Hauptmann G, Westberg J, Uhlén M, Wadelius C, Truedsson L. Späth PJ, et al. Among authors: truedsson l. Clin Exp Immunol. 1999 Nov;118(2):278-84. doi: 10.1046/j.1365-2249.1999.01056.x. Clin Exp Immunol. 1999. PMID: 10540191 Free PMC article.
Vaccination responses to capsular polysaccharides of Neisseria meningitidis and Haemophilus influenzae type b in two C2-deficient sisters: alternative pathway-mediated bacterial killing and evidence for a novel type of blocking IgG.
Selander B, Käyhty H, Wedege E, Holmström E, Truedsson L, Söderström C, Sjöholm AG. Selander B, et al. Among authors: truedsson l. J Clin Immunol. 2000 Mar;20(2):138-49. doi: 10.1023/a:1006638631581. J Clin Immunol. 2000. PMID: 10821465
227 results