Results 101 to 110 of about 6,839 (215)
Frontiers in ImmunologyC3 glomerulopathy encompasses a group of glomerular diseases characterized by the predominant deposition of complement component C3 on kidney biopsy without significant immunoglobulin staining.
Wenjing Cai +13 more
doaj +1 more source
Zdorovʹe RebenkaBackground. IF-negative acute proliferative glomerulonephritis (APIGN) represents a significant diagnostic pitfall, particularly when complement levels are normal and serological markers are inconclusive.
Tiffany Wongsodiharjo +5 more
doaj +1 more source
A Compendium of Urinary Biomarkers Indicative of Glomerular Podocytopathy [PDF]
, 2013 It is well known that glomerular podocyte injury and loss are present in numerous nephropathies and that the pathophysiologic consecution of disease hinges upon the fate of the podocyte.
Pichler Sekulic, Simona +1 more
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Factor B and C4b2a Autoantibodies in C3 Glomerulopathy
Frontiers in Immunology, 2019 C3 Glomerulopathy (C3G) is a renal disease mediated primarily by dysregulation of the alternative pathway of complement. Complement is the cornerstone of innate immunity.
Jill J. Hauer +4 more
doaj +1 more source
Clinicopathological study of renal biopsies after liver transplantation [PDF]
, 2013 published_or_final_versio
Chan, GSW +5 more
core
Immune complexes in chronic Chagas disease patients are formed by exovesicles from Trypanosoma cruzi carrying the conserved MASP N-terminal region [PDF]
, 2017 The exovesicles (EVs) are involved in pathologic host-parasite immune associations and have been recently used as biomarkers for diagnosis of infectious diseases.
De Pablos, Luis Miguel +5 more
core +3 more sources
Dense Deposit Disease and C3 Glomerulopathy
Seminars in Nephrology, 2013 C3 glomerulopathy refers to those renal lesions characterized histologically by predominant C3 accumulation within the glomerulus, and pathogenetically by aberrant regulation of the alternative pathway of complement. Dense deposit disease is distinguished from other forms of C3 glomerulopathy by its characteristic appearance on electron microscopy. The
Barbour, Thomas D. +2 more
openaire +2 more sources
Anticoagulant-Related Nephropathy in a Patient with IgA Nephropathy [PDF]
, 2017 Anticoagulant-related nephropathy is a type of acute kidney injury caused by overcoagulation. We describe a case of an 84-year-old man with arterial hypertension, coronary heart disease and atrial fibrillation treated with acenocoumarol, who presented ...
Azevedo, A +3 more
core +1 more source
Pauci-immune glomerulonephritis in individuals with disease associated with levamisole-adulterated cocaine: a series of 4 cases. [PDF]
, 2014 Exposure to levamisole-adulterated cocaine can induce a distinct clinical syndrome characterized by retiform purpura and/or agranulocytosis accompanied by an unusual constellation of serologic abnormalities including antiphospholipid antibodies, lupus ...
Butcher, Brad +6 more
core +2 more sources
The many faces of C3 glomerulopathy [PDF]
Kidney International, 2012 To the Editor: The recent article by Sethi et al., ‘Membranoproliferative glomerulonephritis and C3 glomerulopathy: resolving the confusion’, made me revisit a 12-year-old publication. In ‘Apparent progression of acute glomerulonephritis to dense deposit disease’ we described an 8-year-old boy with hypocomplementemia and meningococcemia.
openaire +2 more sources