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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.
The hemolytic uremic syndrome.
Remuzzi G, Ruggenenti P. Remuzzi G, et al. Kidney Int. 1995 Jul;48(1):2-19. doi: 10.1038/ki.1995.261. Kidney Int. 1995. PMID: 7564079 Free article. Review. No abstract available.
The hemolytic uremic syndrome.
Remuzzi G, Ruggenenti P. Remuzzi G, et al. Kidney Int Suppl. 1998 May;66:S54-7. Kidney Int Suppl. 1998. PMID: 9573574 Review. No abstract available.
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
1,536 results