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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: caprioli j. Int Immunopharmacol. 2001 Mar;1(3):461-8. doi: 10.1016/s1567-5769(00)00047-3. Int Immunopharmacol. 2001. PMID: 11367530 Review.
The hemolytic uremic syndromes.
Caprioli J, Peng L, Remuzzi G. Caprioli J, et al. Curr Opin Crit Care. 2005 Oct;11(5):487-92. doi: 10.1097/01.ccx.0000176688.10810.30. Curr Opin Crit Care. 2005. PMID: 16175037 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: caprioli j. J Am Soc Nephrol. 1999 Feb;10(2):281-93. doi: 10.1681/ASN.V102281. J Am Soc Nephrol. 1999. PMID: 10215327
Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype.
Bresin E, Rurali E, Caprioli J, Sanchez-Corral P, Fremeaux-Bacchi V, Rodriguez de Cordoba S, Pinto S, Goodship TH, Alberti M, Ribes D, Valoti E, Remuzzi G, Noris M; European Working Party on Complement Genetics in Renal Diseases. Bresin E, et al. Among authors: caprioli j. J Am Soc Nephrol. 2013 Feb;24(3):475-86. doi: 10.1681/ASN.2012090884. Epub 2013 Feb 21. J Am Soc Nephrol. 2013. PMID: 23431077 Free PMC article.
392 results