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Complement and the atypical hemolytic uremic syndrome in children.
Loirat C, Noris M, Fremeaux-Bacchi V. Loirat C, et al. Among authors: noris m. Pediatr Nephrol. 2008 Nov;23(11):1957-72. doi: 10.1007/s00467-008-0872-4. Epub 2008 Jul 2. Pediatr Nephrol. 2008. PMID: 18594873 Free PMC article. 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. Among authors: noris m. 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
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. Among authors: noris m. 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. Among authors: noris m. J Am Soc Nephrol. 2001 Feb;12(2):297-307. J Am Soc Nephrol. 2001. PMID: 11158219
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: noris m. Int Immunopharmacol. 2001 Mar;1(3):461-8. doi: 10.1016/s1567-5769(00)00047-3. Int Immunopharmacol. 2001. PMID: 11367530 Review.
Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura.
Ruggenenti P, Noris M, Remuzzi G. Ruggenenti P, et al. Among authors: noris m. Kidney Int. 2001 Sep;60(3):831-46. doi: 10.1046/j.1523-1755.2001.060003831.x. Kidney Int. 2001. PMID: 11532079 Review.
Familial and recurrent forms of hemolytic uremic syndrome/thrombotic thrombocytopenic purpura.
Noris M, Remuzzi G. Noris M, et al. Contrib Nephrol. 2001;(136):125-39. doi: 10.1159/000060183. Contrib Nephrol. 2001. PMID: 11688376 Review. No abstract available.
Combined kidney and liver transplantation for familial haemolytic uraemic syndrome.
Remuzzi G, Ruggenenti P, Codazzi D, Noris M, Caprioli J, Locatelli G, Gridelli B. Remuzzi G, et al. Among authors: noris m. Lancet. 2002 May 11;359(9318):1671-2. doi: 10.1016/S0140-6736(02)08560-4. Lancet. 2002. PMID: 12020532
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