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Podocyte dysfunction in atypical haemolytic uraemic syndrome.
Noris M, Mele C, Remuzzi G. Noris M, et al. Nat Rev Nephrol. 2015 Apr;11(4):245-52. doi: 10.1038/nrneph.2014.250. Epub 2015 Jan 20. Nat Rev Nephrol. 2015. PMID: 25599621 Review.
Urinary excretion of platelet-activating factor in haemolytic uraemic syndrome.
Benigni A, Boccardo P, Noris M, Remuzzi G, Siegler RL. Benigni A, et al. Lancet. 1992 Apr 4;339(8797):835-6. doi: 10.1016/0140-6736(92)90281-7. Lancet. 1992. PMID: 1347859
Renal prostacyclin biosynthesis is reduced in children with hemolytic-uremic syndrome in the context of systemic platelet activation.
Noris M, Benigni A, Siegler R, Gaspari F, Casiraghi F, Mancini ML, Remuzzi G. Noris M, et al. Am J Kidney Dis. 1992 Aug;20(2):144-9. doi: 10.1016/s0272-6386(12)80542-7. Am J Kidney Dis. 1992. PMID: 1496967
Evidence for a role of nitric oxide in hypertension and in renal disease in man.
Noris M, Remuzzi G. Noris M, et al. Contrib Nephrol. 1996;119:8-15. doi: 10.1159/000425441. Contrib Nephrol. 1996. PMID: 8783584 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. J Am Soc Nephrol. 1999 Feb;10(2):281-93. 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. Blood. 1999 Jul 15;94(2):610-20. Blood. 1999. PMID: 10397728
The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20.
Caprioli J, Bettinaglio P, Zipfel PF, Amadei B, Daina E, Gamba S, Skerka C, Marziliano N, Remuzzi G, Noris M; Itaslian Registry of Familial and Recurrent HUS/TTP. Caprioli J, et al. J Am Soc Nephrol. 2001 Feb;12(2):297-307. J Am Soc Nephrol. 2001. PMID: 11158219
Pathogenesis of Takayasu's arteritis.
Noris M. Noris M. J Nephrol. 2001 Nov-Dec;14(6):506-13. J Nephrol. 2001. PMID: 11783607 Review.
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