The role of complement in C3 glomerulopathy
C3 glomerulopathy describes a spectrum of disorders with glomerular pathology associated
with C3 cleavage product deposition and with defective complement action and regulation …
with C3 cleavage product deposition and with defective complement action and regulation …
C3 glomerulopathy: understanding an ultra‐rare complement‐mediated renal disease
AK Heiderscheit, JJ Hauer… - American Journal of …, 2022 - Wiley Online Library
Abstract C3 glomerulopathy (C3G) describes a pathologic pattern of injury diagnosed by
renal biopsy. It is characterized by the dominant deposition of the third component of …
renal biopsy. It is characterized by the dominant deposition of the third component of …
Incidence and profile of C3 Glomerulopathy: A single center study
C3 glomerulopathy has recently been described as a distinct entity. The underlying
mechanism is unregulated activation of the alternate pathway of the complement system …
mechanism is unregulated activation of the alternate pathway of the complement system …
Novel C3 mutation p. Lys65Gln in aHUS affects complement factor H binding
Background Atypical hemolytic uremic syndrome (aHUS) is associated with mutations
affecting complement proteins and regulators and with autoantibodies against complement …
affecting complement proteins and regulators and with autoantibodies against complement …
A narrative review on C3 glomerulopathy: A rare renal disease
FP Schena, P Esposito, M Rossini - International journal of molecular …, 2020 - mdpi.com
In April 2012, a group of nephrologists organized a consensus conference in Cambridge
(UK) on type II membranoproliferative glomerulonephritis and decided to use a new …
(UK) on type II membranoproliferative glomerulonephritis and decided to use a new …
State of the art: C3 glomerulopathy and membranoproliferative glomerulonephritis: A consensus
B Hohenstein, C Licht, M Wiesener, K Amann… - Der Nephrologe, 2015 - Springer
Based on new pathophysiological discoveries in recent years, a new classification of
glomerulonephritis with dominant or codominant C3 deposits was introduced in 2010, which …
glomerulonephritis with dominant or codominant C3 deposits was introduced in 2010, which …
[PDF][PDF] C3 glomerulopathies: A new category encompassing rare complement mediated glomerulonephritis
F Carvalho, F Nolasco - 2016 - bbg01.com
Disease associated membranoproliferative glomeru‑lonephritis (MPGN) has been well‑
known for decades. Recently, advances in the understanding of the comple‑ment system …
known for decades. Recently, advances in the understanding of the comple‑ment system …
[HTML][HTML] Molecular Studies and an ex vivo Complement Assay on Endothelium Highlight the Genetic Complexity of Atypical Hemolytic Uremic Syndrome: The Case of …
R Piras, P Iatropoulos, E Bresin, M Todeschini… - Frontiers in …, 2020 - frontiersin.org
Atypical hemolytic uremic syndrome (aHUS) is an ultra-rare disease characterized by
microangiopathic hemolysis, thrombocytopenia, and renal impairment and is associated …
microangiopathic hemolysis, thrombocytopenia, and renal impairment and is associated …
C3 glomerulopathy: experience of a pediatric nephrology center
F Yazılıtaş, E Kargın Çakıcı, ED Kurt Şükür… - Acta Clinica …, 2021 - Taylor & Francis
ABSTRACT Background: C3 glomerulopathy (C3G) is an uncommon disease characterized
by the deposition of complement factors in the glomeruli due to overactivation and …
by the deposition of complement factors in the glomeruli due to overactivation and …
[HTML][HTML] Genetic investigation of Nordic patients with complement-mediated kidney diseases
V Rydberg, SS Aradottir, AC Kristoffersson… - Frontiers in …, 2023 - frontiersin.org
Background Complement activation in atypical hemolytic uremic syndrome (aHUS), C3
glomerulonephropathy (C3G) and immune complex-mediated membranoproliferative …
glomerulonephropathy (C3G) and immune complex-mediated membranoproliferative …