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C3 glomerulopathy [version 1; referees: 4 approved] [PDF]

open access: yesF1000Research, 2017
C3 glomerulopathy is a recently defined entity that encompasses a group of kidney diseases caused by abnormal control of complement activation with deposition of complement component C3 in glomeruli leading to variable glomerular inflammation. Before the
H. Terence Cook
doaj   +6 more sources

Pathology of C3 Glomerulopathy [PDF]

open access: yesChildhood Kidney Diseases, 2019
C3 glomerulopathy is a renal disorder involving dysregulation of alternative pathway complement activation. In most instances, a membranoproliferative pattern of glomerular injury with a prevalence of C3 deposition is observed by immunofluorescence ...
Su-Jin Shin, Yoonje Seong, Beom Jin Lim
doaj   +7 more sources

Diagnostic Problems in C3 Glomerulopathy

open access: yesBiomedicines, 2023
Background: C3 glomerulopathies (C3GN) are a group of rare kidney diseases associated with impaired complement regulation. The effects of this disease include the accumulation of complement C3 in the kidneys. Based on the clinical data, as well as light,
Leszek Niepolski   +11 more
doaj   +4 more sources

Acquired drivers of C3 glomerulopathy. [PDF]

open access: yesClin Kidney J
C3 glomerulopathy (C3G) is a group of heterogeneous ultrarare kidney diseases characterized by dysregulated activation of the complement alternative pathway (AP) leading to excessive C3 cleavage.
Welsh SJ, Zhang Y, Smith RJH.
europepmc   +4 more sources

Pregnancy outcomes in C3 glomerulopathy: a retrospective review [PDF]

open access: yesBMC Nephrology
Background C3 Glomerulopathy (C3G) is an ultra-rare glomerular disease driven by dysregulation of the alternative pathway of complement. 30–50% of adult patients progress to end stage kidney disease (ESKD) within 10 years of diagnosis. Little is known of
Lauren O. Fergus   +9 more
doaj   +3 more sources

Clinical characteristics and short term outcomes of childhood immune complex membranoproliferative glomerulonephritis and C3 glomerulopathy: a single centre retrospective study [PDF]

open access: yesBMC Nephrology
Background Membranoproliferative glomerulonephritis, with its immune complex variety and C3 glomerulopathy, is a rare glomerular disease in children. The objective of this study was to determine the clinical features and short-term outcomes in children ...
Irshad Ali Bajeer   +5 more
doaj   +3 more sources

Updates on C3 Glomerulopathy in Kidney Transplantation: Pathogenesis and Treatment Options [PDF]

open access: yesInt J Mol Sci
C3 glomerulopathy is a rare disease, characterized by an abnormal activation of the complement’s alternative pathway that leads to the accumulation of the C3 component in the kidney.
Bartoli G   +3 more
europepmc   +3 more sources

Iptacopan Reduces Proteinuria and Stabilizes Kidney Function in C3 Glomerulopathy [PDF]

open access: yesKidney Int Rep
C3 glomerulopathy; Iptacopan; TransplantationGlomerulopatia C3; Iptacopan; TrasplantamentGlomerulopatía C3; Iptacopan; TrasplanteIntroduction C3 glomerulopathy (C3G) is a complex, chronic, ultra rare, progressive primary glomerulonephritis, resulting ...
Nester C   +15 more
europepmc   +3 more sources

An Interdisciplinary Diagnostic Approach to Guide Therapy in C3 Glomerulopathy [PDF]

open access: yesFrontiers in Immunology, 2022
Since the re-classification of membranoproliferative glomerulonephritis the new disease entity C3 glomerulopathy is diagnosed if C3 deposition is clearly dominant over immunoglobulins in immunohistochemistry or immunofluorescence.
Tilman Schmidt   +9 more
doaj   +2 more sources

Kidney transplant in patients with C3 glomerulopathy. [PDF]

open access: yesClin Kidney J
Complement protein 3 (C3) glomerulopathy (C3G) is a rare and progressive kidney disease primarily affecting young individuals and frequently advancing to end-stage kidney disease (ESKD).
Attieh RM   +5 more
europepmc   +2 more sources

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