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Lista de obras de Elisabetta Valoti

A novel atypical hemolytic uremic syndrome-associated hybrid CFHR1/CFH gene encoding a fusion protein that antagonizes factor H-dependent complement regulation

artículo científico publicado en 2014

Association of CFHR1 homozygous deletion with acute myelogenous leukemia in the European population

artículo científico publicado en 2015

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

artículo científico publicado en 2015

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

artículo científico publicado en 2017

Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype

artículo científico publicado en 2013

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

artículo científico publicado en 2016

Dynamics of complement activation in aHUS and how to monitor eculizumab therapy

artículo científico publicado en 2014

Impact of a Complement Factor H Gene Variant on Renal Dysfunction, Cardiovascular Events, and Response to ACE Inhibitor Therapy in Type 2 Diabetes

scientific article published on 26 July 2019

Mapping interactions between complement C3 and regulators using mutations in atypical hemolytic uremic syndrome

artículo científico publicado en 2015

Posttransplant recurrence of atypical hemolytic uremic syndrome

artículo científico publicado en 2012

Two patients with history of STEC-HUS, posttransplant recurrence and complement gene mutations

artículo científico publicado en 2013

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