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

Bằng Fang, Celia J., Fremeaux-Bacchi, Veronique, Liszewski, M. Kathryn, Pianetti, Gaia, Noris, Marina, Goodship, Timothy H. J., Atkinson, John P.
Được phát hành 2008

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

Bằng 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
Được phát hành 2008

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

Bằng 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
Được phát hành 2006

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

Bằng 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
Được phát hành 2010