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Dragon-Durey MA, Frémeaux-Bacchi V. Atypical haemolytic uraemic syndrome and mutations in complement regulator genes. „Springer Semin. Immunopathol.”. 27 (3), s. 359–74, 2005. DOI: 10.1007/s00281-005-0003-2. PMID: 16189652.
Zipfel PF, Misselwitz J, Licht C, Skerka C. The role of defective complement control in hemolytic uremic syndrome. „Semin. Thromb. Hemost.”. 32 (2), s. 146–54, 2006. DOI: 10.1055/s-2006-939770. PMID: 16575689.
SP. Mooijaart, KM. Koeijvoets, EJ. Sijbrands, MR. Daha i inni. Complement Factor H polymorphism Y402H associates with inflammation, visual acuity, and cardiovascular mortality in the elderly population at large. „Exp Gerontol”. 42 (11), s. 1116-22, Nov 2007. DOI: 10.1016/j.exger.2007.08.001. PMID: 17869048.
Molly S.M.S.BolgerMolly S.M.S. i inni, Complement Levels and Activity in the Normal and LPS-Injured Lung, „American Journal of Physiology: Lung Cellular and Molecular Physiology”, 292 (3), 2006, s. L748-L759, DOI: 10.1152/ajplung.00127.2006, PMID: 17071722.
P.K.P.K.DattaP.K.P.K., J.J.RappaportJ.J., HIV and Complement: Hijacking an immune defence, „Biomedicine & Pharmacotherapy”, 60 (9), 2006, s. 561-568, DOI: 10.1016/j.biopha.2006.07.087, PMID: 16978830.a?