Sara Bucchioni

Single Strand Conformation Polymorphism (SSCP) as a quick and reliable method to genotype M235T polymorphism of angiotensinogen gene.

A. Perna, M. Noris, S. Orisio, 2002, Clinical biochemistry.

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.

In-vitro and in-vivo consequences of mutations in the von Willebrand factor cleaving protease ADAMTS 13 in thrombotic thrombocytopenic purpura

G. Remuzzi, R. Coppo, M. Noris, 2018 .

Hemolytic Uremic Syndrome: A Fatal Outcome after Kidney and Liver Transplantation Performed to Correct Factor H Gene Mutation

N. Perico, G. Remuzzi, J. Platt, 2005, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

In-vitro and in-vivo consequences of mutations in the von Willebrand factor cleaving protease ADAMTS13 in thrombotic thrombocytopenic purpura

G. Remuzzi, R. Coppo, M. Noris, 2006, Thrombosis and Haemostasis.

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.

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 .