Combined Complement Gene Mutations in Atypical Hemolytic Uremic Syndrome Influence Clinical Phenotype von BRESIN, Elena, RURALI, Erica, VALOTI, Elisabetta, REMUZZI, Giuseppe, NORIS, Marina, CAPRIOLI, Jessica, SANCHEZ-CORRAL, Pilar, FREMEAUX-BACCHI, Veronique, DE CORDOBA, Santiago Rodriguez, PINTO, Sheila, GOODSHIP, Timothy H. J, ALBERTI, Marta, RIBES, David

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Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotype von Noris, Marina, Caprioli, Jessica, Bresin, Elena, Mossali, Chiara, Pianetti, Gaia, Gamba, Sara, Daina, Erica, Fenili, Chiara, Castelletti, Federica, Sorosina, Annalisa, Piras, Rossella, Donadelli, Roberta, Maranta, Ramona, van der Meer, Irene, Conway, Edward M, Zipfel, Peter F, Goodship, Timothy H, Remuzzi, Giuseppe

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Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome von Caprioli, Jessica, Noris, Marina, Brioschi, Simona, Pianetti, Gaia, Castelletti, Federica, Bettinaglio, Paola, Mele, Caterina, Bresin, Elena, Cassis, Linda, Gamba, Sara, Porrati, Francesca, Bucchioni, Sara, Monteferrante, Giuseppe, Fang, Celia J., Liszewski, M.K., Kavanagh, David, Atkinson, John P., Remuzzi, Giuseppe

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Familial haemolytic uraemic syndrome and an MCP mutation von Noris, Marina, Brioschi, Simona, Caprioli, Jessica, Todeschini, Marta, Bresin, Elena, Porrati, Francesca, Gamba, Sara, Remuzzi, Giuseppe

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Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome von Manuelian, Tamara, Hellwage, Jens, Meri, Seppo, Caprioli, Jessica, Noris, Marina, Heinen, Stefan, Jozsi, Mihaly, Neumann, Hartmut P H, Remuzzi, Giuseppe, Zipfel, Peter F

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Mutations in FN1 cause glomerulopathy with fibronectin deposits von Castelletti, Federica, Donadelli, Roberta, Banterla, Federica, Hildebrandt, Friedhelm, Zipfel, Peter F, Bresin, Elena, Otto, Edgar, Skerka, Christine, Renieri, Alessandra, Todeschini, Marta, Caprioli, Jessica, Caruso, Rosa Maria, Artuso, Rosangela, Remuzzi, Giuseppe, Noris, Marina

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von Willebrand factor cleaving protease (ADAMTS13) is deficient in recurrent and familial thrombotic thrombocytopenic purpura and hemolytic uremic syndrome von Remuzzi, Giuseppe, Galbusera, Miriam, Noris, Marina, Canciani, Maria Teresa, Daina, Erica, Bresin, Elena, Contaretti, Silvia, Caprioli, Jessica, Gamba, Sara, Ruggenenti, Piero, Perico, Norberto, Mannucci, Pier Mannuccio

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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 von Caprioli, Jessica, Castelletti, Federica, Bucchioni, Sara, Bettinaglio, Paola, Bresin, Elena, Pianetti, Gaia, Gamba, Sara, Brioschi, Simona, Daina, Erica, Remuzzi, Giuseppe, Noris, Marina

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Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome von Manuelian, T, Hellwage, J, Meri, S, Caprioli, J, Noris, M, Heinen, S, Jozsi, M, Neumann, HPH, Remuzzi, G, Zipfel, P F

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Complement factor H mutation in familial thrombotic thrombocytopenic purpura with ADAMTS13 deficiency and renal involvement von NORIS, Marina, BUCCHIONI, Sara, GALBUSERA, Miriam, DONADELLI, Roberta, BRESIN, Elena, CASTELLETTI, Federica, CAPRIOLI, Jessica, BRIOSCHI, Simona, SCHEIFLINGER, Friedrich, REMUZZI, Giuseppe

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The molecular basis of Familial hemolytic uremic syndrome : Mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20 von CAPRIOLI, Jessica, BETTINAGLIO, Paola, ZIPFEL, Peter F, AMADEI, Barbara, DAINA, Erica, GAMBA, Sara, SKERKA, Christine, MARZILIANO, Nicola, REMUZZI, Giuseppe, NORIS, Marina

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Combined kidney and liver transplantation for familial haemolytic uraemic syndrome von Remuzzi, Giuseppe, Ruggenenti, Piero, Codazzi, Daniela, Noris, Marina, Caprioli, Jessica, Locatelli, Giuseppe, Gridelli, Bruno

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Complement hyperactivation may cause atypical haemolytic uraemic syndrome— gain-of-function mutations in factor B von Caprioli, Jessica, Remuzzi, Giuseppe

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A mouse model of non-Shiga toxin-associated haemolytic uraemic syndrome von Caprioli, Jessica, Remuzzi, Giuseppe

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The hemolytic uremic syndromes von Caprioli, Jessica, Peng, Li, Remuzzi, Giuseppe

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Hypocomplementemia discloses genetic predisposition to hemolytic uremic syndrome and thrombotic thrombocytopenic purpura : Role of factor H abnormalities von NORIS, M, RUGGENENTI, P, PERNA, A, ORISIO, S, CAPRIOLI, J, SKERKA, C, VASILE, B, ZIPFEL, P. F, REMUZZI, G

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Results for C3 and CFB genetic screening in atypical-HUS von Mossali, Chiara, Fenili, Chiara, Castelletti, Federica, Caprioli, Jessica, Pianetti, Gaia, Bresin, Elena, Remuzzi, Giuseppe, Noris, Marina

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A retrospective analysis on disease onset, number of episodes and final outcome in CFH mutated non-Stx-HUS patients von Noris, Marina, Mossali, Chiara, Bresin, Elena, Castelletti, Federica, Pianetti, Gaia, Remuzzi, Giuseppe, Caprioli, Jessica

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Thrombotic Microangiopathies: From Animal Models to Human Disease and Cure von Caprioli, Jessica, Remuzzi, Giuseppe, Noris, Marina

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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 thromboc... von GALBUSERA, M, NORIS, M, REMUZZI, G, ROSSI, C, ORISIO, S, CAPRIOLI, J, RUGGERI, Z. M, AMADEI, B, RUGGENENTI, P, VASILE, B, CASARI, G

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