Rossella Piras

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

Marina Noris, Jessica Caprioli, Elena Bresin et al. · Clinical Journal of the American Society of Nephrology · 2010 · 1K citations · Full text

<i>MYO1E</i>Mutations and Childhood Familial Focal Segmental Glomerulosclerosis

Caterina Mele, Paraskevas Iatropoulos, Roberta Donadelli et al. · New England Journal of Medicine · 2011 · 245 citations · Full text

Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcome

Paraskevas Iatropoulos, Marina Noris, Caterina Mele et al. · Molecular Immunology · 2016 · 177 citations

Glomerular Disease, Renal Pathology, Genetic Epidemiology +19

Cluster Analysis Identifies Distinct Pathogenetic Patterns in C3 Glomerulopathies/Immune Complex–Mediated Membranoproliferative GN

Paraskevas Iatropoulos, Erica Daina, Manuela Curreri et al. · Journal of the American Society of Nephrology · 2017 · 131 citations · Full text

Glomerular Disease, Immunology, Pathology +20

An Ex Vivo Test of Complement Activation on Endothelium for Individualized Eculizumab Therapy in Hemolytic Uremic Syndrome

Miriam Galbusera, Marina Noris, Sara Gastoldi et al. · American Journal of Kidney Diseases · 2019 · 92 citations

Complement System, Autoimmune Disease, Hematology +6