| Atypical hemolytic–uremic syndrome M Noris, G Remuzzi New England Journal of Medicine 361 (17), 1676-1687, 2009 | 1628 | 2009 |
| Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype M Noris, J Caprioli, E Bresin, C Mossali, G Pianetti, S Gamba, E Daina, ... Clinical Journal of the American Society of Nephrology 5 (10), 1844-1859, 2010 | 1250 | 2010 |
| Overview of complement activation and regulation M Noris, G Remuzzi Seminars in nephrology 33 (6), 479-492, 2013 | 933 | 2013 |
| Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome J Caprioli, M Noris, S Brioschi, G Pianetti, F Castelletti, P Bettinaglio, ... Blood 108 (4), 1267-1279, 2006 | 887 | 2006 |
| Hemolytic uremic syndrome M Noris, G Remuzzi Journal of the American Society of Nephrology 16 (4), 1035-1050, 2005 | 756 | 2005 |
| Nitric oxide synthesis by cultured endothelial cells is modulated by flow conditions M Noris, M Morigi, R Donadelli, S Aiello, M Foppolo, M Todeschini, ... Circulation research 76 (4), 536-543, 1995 | 713 | 1995 |
| Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura P Ruggenenti, M Noris, G Remuzzi Kidney international 60 (3), 831-846, 2001 | 701 | 2001 |
| Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes”(KDIGO) Controversies Conference THJ Goodship, HT Cook, F Fakhouri, FC Fervenza, V Frémeaux-Bacchi, ... Kidney international 91 (3), 539-551, 2017 | 669 | 2017 |
| Thrombomodulin mutations in atypical hemolytic–uremic syndrome M Delvaeye, M Noris, A De Vriese, CT Esmon, NL Esmon, G Ferrell, ... New England Journal of Medicine 361 (4), 345-357, 2009 | 640 | 2009 |
| Pretransplant infusion of mesenchymal stem cells prolongs the survival of a semiallogeneic heart transplant through the generation of regulatory T cells F Casiraghi, N Azzollini, P Cassis, B Imberti, M Morigi, D Cugini, ... The Journal of Immunology 181 (6), 3933-3946, 2008 | 555 | 2008 |
| Mechanisms of disease: pre-eclampsia M Noris, N Perico, G Remuzzi Nature clinical practice Nephrology 1 (2), 98-114, 2005 | 491 | 2005 |
| STEC-HUS, atypical HUS and TTP are all diseases of complement activation M Noris, F Mescia, G Remuzzi Nature Reviews Nephrology 8 (11), 622-633, 2012 | 483 | 2012 |
| Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype E Bresin, E Rurali, J Caprioli, P Sanchez-Corral, V Fremeaux-Bacchi, ... Journal of the American Society of Nephrology 24 (3), 475-486, 2013 | 417 | 2013 |
| Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome T Manuelian, J Hellwage, S Meri, J Caprioli, M Noris, S Heinen, M Jozsi, ... The Journal of clinical investigation 111 (8), 1181-1190, 2003 | 407 | 2003 |
| The case of complement activation in COVID-19 multiorgan impact M Noris, A Benigni, G Remuzzi Kidney international 98 (2), 314-322, 2020 | 377 | 2020 |
| Familial haemolytic uraemic syndrome and an MCP mutation M Noris, S Brioschi, J Caprioli, M Todeschini, E Bresin, F Porrati, ... The Lancet 362 (9395), 1542-1547, 2003 | 373 | 2003 |
| Autologous mesenchymal stromal cells and kidney transplantation: a pilot study of safety and clinical feasibility N Perico, F Casiraghi, M Introna, E Gotti, M Todeschini, RA Cavinato, ... Clinical Journal of the American Society of Nephrology 6 (2), 412-422, 2011 | 368 | 2011 |
| Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease J Caprioli, F Castelletti, S Bucchioni, P Bettinaglio, E Bresin, G Pianetti, ... Human molecular genetics 12 (24), 3385-3395, 2003 | 348 | 2003 |
| Dynamics of complement activation in aHUS and how to monitor eculizumab therapy M Noris, M Galbusera, S Gastoldi, P Macor, F Banterla, E Bresin, ... Blood, The Journal of the American Society of Hematology 124 (11), 1715-1726, 2014 | 336 | 2014 |
| The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20 J Caprioli, P Bettinaglio, PF Zipfel, B Amadei, E Daina, S Gamba, ... Journal of the American Society of Nephrology 12 (2), 297-307, 2001 | 331 | 2001 |
Benigni ArielaIstituto di Ricerche Farmacologiche Mario Negri 在 marionegri.it 的电子邮件经过验证
Benigni ArielaIstituto di Ricerche Farmacologiche Mario Negri 在 marionegri.it 的电子邮件经过验证