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Factor H family proteins: on complement, microbes and human diseases.
Zipfel PF, Skerka C, Hellwage J, Jokiranta ST, Meri S, Brade V, Kraiczy P, Noris M, Remuzzi G. Zipfel PF, et al. Among authors: remuzzi g. Biochem Soc Trans. 2002 Nov;30(Pt 6):971-8. doi: 10.1042/bst0300971. Biochem Soc Trans. 2002. PMID: 12440956 Review.
Complement factor H and hemolytic uremic syndrome.
Zipfel PF, Skerka C, Caprioli J, Manuelian T, Neumann HH, Noris M, Remuzzi G. Zipfel PF, et al. Among authors: remuzzi g. Int Immunopharmacol. 2001 Mar;1(3):461-8. doi: 10.1016/s1567-5769(00)00047-3. Int Immunopharmacol. 2001. PMID: 11367530 Review.
Hypocomplementemia discloses genetic predisposition to hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: role of factor H abnormalities. Italian Registry of Familial and Recurrent Hemolytic Uremic Syndrome/Thrombotic Thrombocytopenic Purpura.
Noris M, Ruggenenti P, Perna A, Orisio S, Caprioli J, Skerka C, Vasile B, Zipfel PF, Remuzzi G. Noris M, et al. Among authors: remuzzi g. J Am Soc Nephrol. 1999 Feb;10(2):281-93. doi: 10.1681/ASN.V102281. J Am Soc Nephrol. 1999. PMID: 10215327
Thrombotic microangiopathy after kidney transplantation.
Noris M, Remuzzi G. Noris M, et al. Among authors: remuzzi g. Am J Transplant. 2010 Jul;10(7):1517-23. doi: 10.1111/j.1600-6143.2010.03156.x. Am J Transplant. 2010. PMID: 20642678 Free article.
Are HUS and TTP genetically determined?
Noris M, Remuzzi G. Noris M, et al. Among authors: remuzzi g. Kidney Int. 1998 Apr;53(4):1085-6. doi: 10.1111/j.1523-1755.1998.00860.x. Kidney Int. 1998. PMID: 9551421 Free article. No abstract available.
1,537 results