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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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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In-vitro and in-vivo consequences of mutations in the von Willebrand factor cleaving protease ADAMTS13 in thrombotic thrombocytopenic purpura von Donadelli, Roberta, Banterla, Federica, Galbusera, Miriam, Capoferri, Cristina, Bucchioni, Sara, Gastoldi, Sara, Nosari, Silvia, Monteferrante, Giuseppe, Ruggeri, Zaverio M, Bresin, Elena, Scheiflinger, Friedrich, Rossi, Edoardo, Martinez, Constantino, Coppo, Rosanna, Remuzzi, Giuseppe, Noris, Marina

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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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In-vitro and in-vivo consequences of mutations in the von Willebrand factor cleaving protease ADAMTS13 in thrombotic thrombocytopenic purpura von Donadelli, Roberta, Banterla, Federica, Galbusera, Miriam, Capoferri, Cristina, Bucchioni, Sara, Gastoldi, Sara, Nosari, Silvia, Monteferrante, Giuseppe, Ruggeri, Zaverio M., Bresin, Elena, Scheiflinger, Friedrich, Rossi, Edoardo, Martinez, Constantino, Coppo, Rosanna, Remuzzi, Giuseppe, Noris, Marina

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Hemolytic Uremic Syndrome: A Fatal Outcome after Kidney and Liver Transplantation Performed to Correct Factor H Gene Mutation von Remuzzi, Giuseppe, Ruggenenti, Piero, Colledan, Michele, Gridelli, Bruno, Bertani, Alessandro, Bettinaglio, Paola, Bucchioni, Sara, Sonzogni, Aurelio, Bonanomi, Ezio, Sonzogni, Valter, Platt, Jeffrey L., Perico, Norberto, Noris, Marina

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In-vitro and in-vivo consequences of mutations in the von Willebrand factor cleaving protease ADAMTSI3 in thrombotic thrombocytopenic purpura von DONADELLI, Roberta, BANTERLA, Federica, SCHEIFLINGER, Friedrich, ROSSI, Edoardo, MARTINEZ, Constantino, COPPO, Rosanna, REMUZZI, Giuseppe, NORIS, Marina, GALBUSERA, Miriam, CAPOFERRI, Cristina, BUCCHIONI, Sara, GASTOLDI, Sara, NOSARI, Silvia, MONTEFERRANTE, Giuseppe, RUGGERI, Zaverio M, BRESIN, Elena

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Diverse Functional Implications of ADAMTS13 Gene Mutations in Patients with TTP and Congenital Deficiency von Donadelli, Roberta, Banterla, Federica, Capoferri, Cristina, Galbusera, Miriam, Ruggeri, Zaverio M., Bucchioni, Sara, Noris, Marina, Remuzzi, Giuseppe

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Single strand conformation polymorphism (SSCP) as a quick and reliable method to genotype M235T polymorphism of angiotensinogen gene von Bettinaglio, Paola, Galbusera, Andrea, Caprioli, Jessica, Orisio, Silvia, Perna, Annalisa, Arnoldi, Federica, Bucchioni, Sara, Noris, Marina

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