R. Piras

发表

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

G. Remuzzi, E. Daina, P. Iatropoulos, 2016, Molecular immunology.

Fibronectin glomerulopathy: an unusual cause of adult-onset nephrotic syndrome.

N. Kambham, J. Higgins, R. Piras, 2012, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Molecular Studies and an ex vivo Complement Assay on Endothelium Highlight the Genetic Complexity of Atypical Hemolytic Uremic Syndrome: The Case of a Pedigree With a Null CD46 Variant

G. Remuzzi, A. Benigni, P. Iatropoulos, 2020, Frontiers in Medicine.

Rare Functional Variants in Complement Genes and Anti-FH Autoantibodies-Associated aHUS

G. Remuzzi, A. Benigni, A. Amoroso, 2019, Front. Immunol..

Post‐transplant recurrence of atypical hemolytic uremic syndrome in a patient with thrombomodulin mutation

F. Emma, L. Dello Strologo, R. Piras, 2013, Pediatric transplantation.

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.

Mycoplasma pneumoniae Infection Associated with Anti-Factor H Autoantibodies in Atypical Hemolytic Uremic Syndrome.

R. Donadelli, Cristina Bertulli, C. Mele, 2022, Nephron.

Morphofunctional Effects of C5 Convertase Blockade in Immune Complex-Mediated Membranoproliferative Glomerulonephritis: Report of Two Cases with Evidence of Terminal Complement Activation

G. Remuzzi, E. Daina, P. Ruggenenti, 2020, Nephron.

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

G. Remuzzi, A. Benigni, A. Perna, 2019, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Thrombotic microangiopathy without renal involvement: two novel mutations in complement‐regulator genes

M. Noris, L. Lotta, M. Cugno, 2016, Journal of thrombosis and haemostasis : JTH.

Nephrotic-Range Proteinuria and Peripheral Edema in a Child: Not Only Idiopathic Nephrotic Syndrome

F. Emma, M. Vivarelli, M. Colucci, 2016, Case Reports in Nephrology and Dialysis.

Kidney Transplantation From a Donor With Acute Kidney Injury: An Unexpected Outcome

G. Remuzzi, P. Ruggenenti, M. Noris, 2014, American Journal of Transplantation.

Clinical Practice: Case Report

R. Donadelli, Cristina Bertulli, C. Mele, 2022 .

Atypical hemolytic uremic syndrome with MCP mutations preceded by respiratory infection

H. Rakugi, Y. Isaka, Terumasa Hayashi, 2013, CEN Case Reports.

A case of familial glomerulopathy with fibronectin deposits caused by the Y973C mutation in fibronectin.

R. Piras, E. Bresin, A. A. Kutlugun, 2013, American journal of kidney diseases : the official journal of the National Kidney Foundation.

MYO1E mutations and childhood familial focal segmental glomerulosclerosis.

G. Remuzzi, F. Macciardi, A. Benigni, 2011, The New England journal of medicine.

Two Patients With History of STEC‐HUS, Posttransplant Recurrence and Complement Gene Mutations

G. Remuzzi, F. Thaiss, C. Tripodo, 2013, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome.

G. Remuzzi, R. Lifton, Mathieu Lemaire, 2015, Clinical journal of the American Society of Nephrology : CJASN.

Genetic and acquired abnormalities in C3 glomerulopathy and primary immune complex-mediated MPGN

R. Piras, 2018 .

Fibronectin glomerulopathy - A sporadic case with unusual clinical manifestation.

S. Gowrishankar, R. Piras, S. Shrivastava, 2017, Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia.

Eculizumab in patients with severe coronavirus disease 2019 (COVID-19) requiring continuous positive airway pressure ventilator support: Retrospective cohort study

G. Remuzzi, L. Lorini, A. Benigni, 2021, PloS one.

CFH and CFHR Copy Number Variations in C3 Glomerulopathy and Immune Complex-Mediated Membranoproliferative Glomerulonephritis

G. Remuzzi, A. Benigni, P. Iatropoulos, 2021, Frontiers in Genetics.

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

G. Remuzzi, E. Daina, P. Iatropoulos, 2017, Journal of the American Society of Nephrology : JASN.

Unraveling the Molecular Mechanisms Underlying Complement Dysregulation by Nephritic Factors in C3G and IC-MPGN

G. Remuzzi, A. Benigni, P. Iatropoulos, 2018, Front. Immunol..

CFH and CFHR structural variants in atypical Hemolytic Uremic Syndrome: Prevalence, genomic characterization and impact on outcome

G. Remuzzi, A. Benigni, M. Noris, 2023, Frontiers in Immunology.

An ex vivo test to investigate genetic factors conferring susceptibility to atypical haemolytic uremic syndrome

G. Remuzzi, A. Benigni, M. Noris, 2023, Frontiers in Immunology.

Thrombotic microangiopathy without renal involvement: two novel mutations in complement‐regulator genes

M. Noris, L. Lotta, R. Donadelli, 2016, Journal of thrombosis and haemostasis : JTH.