Publications by authors named "Elisabetta Valoti"

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A GWAS in the pandemic epicenter highlights the severe COVID-19 risk locus introgressed by Neanderthals.
Matteo Breno, Marina Noris, Nadia Rubis, Aneliya Ilieva Parvanova, Davide Martinetti, Elisabetta Valoti

iScience· October 2023

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and structural variants in atypical Hemolytic Uremic Syndrome: Prevalence, genomic characterization and impact on outcome.
Rossella Piras, Elisabetta Valoti, Marta Alberti, Elena Bresin, Caterina Mele

Front Immunol· February 2023

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Mycoplasma pneumoniae Infection Associated with Anti-Factor H Autoantibodies in Atypical Hemolytic Uremic Syndrome.
Elisabetta Valoti, Rossella Piras, Caterina Mele, Marta Alberti, Lucia Liguori

Nephron· December 2022

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and Copy Number Variations in C3 Glomerulopathy and Immune Complex-Mediated Membranoproliferative Glomerulonephritis.
Rossella Piras, Matteo Breno, Elisabetta Valoti, Marta Alberti, Paraskevas Iatropoulos

Front Genet· June 2021

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Molecular Studies and an Complement Assay on Endothelium Highlight the Genetic Complexity of Atypical Hemolytic Uremic Syndrome: The Case of a Pedigree With a Null CD46 Variant.
Rossella Piras, Paraskevas Iatropoulos, Elena Bresin, Marta Todeschini, Sara Gastoldi, Elisabetta Valoti

Front Med (Lausanne)· November 2020

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Rare Functional Variants in Complement Genes and Anti-FH Autoantibodies-Associated aHUS.
Elisabetta Valoti, Marta Alberti, Paraskevas Iatropoulos, Rossella Piras, Caterina Mele

Front Immunol· September 2020

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Hemolytic Uremic Syndrome in an Infant with Primary Hyperoxaluria Type II: An Unreported Clinical Association.
Elisabetta Valoti, Marta Alberti, Camillo Carrara, Matteo Breno, Ebru Yilmaz Keskin

Nephron· June 2020

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More about Factor H Autoantibodies in Membranous Nephropathy.
Elisabetta Valoti, Marina Noris, Giuseppe Remuzzi

N Engl J Med· October 2019

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Unraveling the Molecular Mechanisms Underlying Complement Dysregulation by Nephritic Factors in C3G and IC-MPGN.
Roberta Donadelli, Patrizia Pulieri, Rossella Piras, Paraskevas Iatropoulos, Elisabetta Valoti

Front Immunol· September 2019

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An Ex Vivo Test of Complement Activation on Endothelium for Individualized Eculizumab Therapy in Hemolytic Uremic Syndrome.
Miriam Galbusera, Marina Noris, Sara Gastoldi, Elena Bresin, Caterina Mele, Elisabetta Valoti

Am J Kidney Dis· July 2019

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Impact of a Complement Factor H Gene Variant on Renal Dysfunction, Cardiovascular Events, and Response to ACE Inhibitor Therapy in Type 2 Diabetes.
Elisabetta Valoti, Marina Noris, Annalisa Perna, Erica Rurali, Giulia Gherardi

Front Genet· July 2019

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Cluster Analysis Identifies Distinct Pathogenetic Patterns in C3 Glomerulopathies/Immune Complex-Mediated Membranoproliferative GN.
Paraskevas Iatropoulos, Erica Daina, Manuela Curreri, Rossella Piras, Elisabetta Valoti

J Am Soc Nephrol· January 2018

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Association of CFHR1 homozygous deletion with acute myelogenous leukemia in the European population.
Maddalena Fratelli, Marco Bolis, Mami Kurosaki, Martina Dori, Valeria Guarnaccia, Elisabetta Valoti

Leuk Lymphoma· May 2016

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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, Rossella Piras, Elisabetta Valoti

Mol Immunol· March 2016

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Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome.
Caterina Mele, Mathieu Lemaire, Paraskevas Iatropoulos, Rossella Piras, Elena Bresin, Elisabetta Valoti

Clin J Am Soc Nephrol· June 2015

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Mapping interactions between complement C3 and regulators using mutations in atypical hemolytic uremic syndrome.
Elizabeth C Schramm, Lubka T Roumenina, Tania Rybkine, Sophie Chauvet, Paula Vieira-Martins, Elisabetta Valoti

Blood· April 2015

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A novel atypical hemolytic uremic syndrome-associated hybrid CFHR1/CFH gene encoding a fusion protein that antagonizes factor H-dependent complement regulation.
Elisabetta Valoti, Marta Alberti, Agustin Tortajada, Jesus Garcia-Fernandez, Sara Gastoldi

J Am Soc Nephrol· January 2015

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Dynamics of complement activation in aHUS and how to monitor eculizumab therapy.
Marina Noris, Miriam Galbusera, Sara Gastoldi, Paolo Macor, Federica Banterla, Elisabetta Valoti

Blood· September 2014

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Atypical haemolytic uraemic syndrome with underlying glomerulopathies. A case series and a review of the literature.
Lucio Manenti, Elisa Gnappi, Augusto Vaglio, Landino Allegri, Marina Noris, Elisabetta Valoti

Nephrol Dial Transplant· September 2013

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Posttransplant recurrence of atypical hemolytic uremic syndrome.
Elisabetta Valoti, Marta Alberti, Marina Noris

J Nephrol· May 2013

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Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype.
Elena Bresin, Erica Rurali, Jessica Caprioli, Pilar Sanchez-Corral, Veronique Fremeaux-Bacchi, Elisabetta Valoti

J Am Soc Nephrol· February 2013

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