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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.
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
Increased fragmentation of von Willebrand factor, due to abnormal cleavage of the subunit, parallels disease activity in recurrent hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and discloses predisposition in families. The Italian Registry of Familial and Recurrent HUS/TTP.
Galbusera M, Noris M, Rossi C, Orisio S, Caprioli J, Ruggeri ZM, Amadei B, Ruggenenti P, Vasile B, Casari G, Remuzzi G. Galbusera M, et al. Among authors: remuzzi g. Blood. 1999 Jul 15;94(2):610-20. Blood. 1999. PMID: 10397728 Free article.
1,532 results