Membrane cofactor protein mutations in atypical hemolytic uremic syndrome (aHUS), fatal Stx-HUS, C3 glomerulonephritis, and the HELLP syndrome

Por Fang, Celia J., Fremeaux-Bacchi, Veronique, Liszewski, M. Kathryn, Pianetti, Gaia, Noris, Marina, Goodship, Timothy H. J., Atkinson, John P.
Publicado em 2008

The Complement Factor H R1210C Mutation Is Associated With Atypical Hemolytic Uremic Syndrome

Por Martinez-Barricarte, Ruben, Pianetti, Gaia, Gautard, Ruxandra, Misselwitz, Joachim, Strain, Lisa, Fremeaux-Bacchi, Veronique, Skerka, Christine, Zipfel, Peter F., Goodship, Tim, Noris, Marina, Remuzzi, Giuseppe, de Cordoba, Santiago Rodriguez
Publicado em 2008

Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome

Por 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
Publicado em 2006

Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotype

Por 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
Publicado em 2010