F. Castelletti

Mutations in FN1 cause glomerulopathy with fibronectin deposits

G. Remuzzi, P. Zipfel, C. Skerka, 2008, Proceedings of the National Academy of Sciences.

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

G. Remuzzi, J. Atkinson, M. Noris, 2006, Blood.

Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype.

G. Remuzzi, P. Zipfel, I. M. van der Meer, 2010, Clinical journal of the American Society of Nephrology : CJASN.

Complement factor H mutation in familial thrombotic thrombocytopenic purpura with ADAMTS13 deficiency and renal involvement.

G. Remuzzi, M. Noris, M. Galbusera, 2005, Journal of the American Society of Nephrology : JASN.

Hemolytic uremic syndrome in an infant following Bordetella pertussis infection

A. Caprioli, A. Giammanco, F. Castelletti, 2006, European Journal of Clinical Microbiology and Infectious Diseases.

Outcome of renal transplantation in patients with non-Shiga toxin-associated hemolytic uremic syndrome: prognostic significance of genetic background.

R. Stefanov, G. Remuzzi, E. Daina, 2005, Clinical journal of the American Society of Nephrology : CJASN.

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.

G. Remuzzi, E. Daina, M. Noris, 2003, Human molecular genetics.

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

G. Remuzzi, J. Atkinson, M. Noris, 2013 .

Fast Track Complement Factor H Mutation in Familial Thrombotic Thrombocytopenic Purpura with ADAMTS 13 Deficiency and Renal Involvement

G. Remuzzi, M. Noris, M. Galbusera, 2005 .

Assessing Humoral Immuno-Inflammatory Pathways Associated with Respiratory Failure in COVID-19 Patients

L. Malatino, B. Stancanelli, Alessandra Sorce, 2023, Journal of clinical medicine.