Articles with "glomerulopathy" as a keyword



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Immunosuppressive Treatment in C3 Glomerulopathy: Is it Really Effective?

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Published in 2017 at "American Journal of Nephrology"

DOI: 10.1159/000479012

Abstract: Background: C3 glomerulopathy (C3GP) is a recently identified and described disease that has a high risk of progressing into end-stage renal disease. We aimed to evaluate the effects of various immunosuppressive regimens on C3GP progression… read more here.

Keywords: primary outcome; glomerulopathy; treatment; mmf based ... See more keywords
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A case of immunotactoid glomerulopathy with false-negative IgG staining

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Published in 2018 at "BMC Nephrology"

DOI: 10.1186/s12882-018-0931-4

Abstract: BackgroundImmunotactoid glomerulopathy (ITG) is a rare glomerulonephritis characterized by microtubular deposits. Immunofluorescence findings are necessary to differentiate ITG from other proliferative glomerular diseases. The characteristic tubular structure on electron microscopy is essential for a definitive… read more here.

Keywords: igg; glomerulopathy; false negative; case ... See more keywords
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Comparative analysis of hypertensive nephrosclerosis in animal models of hypertension and its relevance to human pathology. Glomerulopathy

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Published in 2022 at "PLoS ONE"

DOI: 10.1371/journal.pone.0264136

Abstract: Current research on hypertension utilizes more than fifty animal models that rely mainly on stable increases in systolic blood pressure. In experimental hypertension, grading or scoring of glomerulopathy in the majority of studies is based… read more here.

Keywords: analysis; animal models; human pathology; glomerulopathy ... See more keywords
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Large-Scale Whole-Genome Sequencing Reveals the Genetic Architecture of Primary Membranoproliferative GN and C3 Glomerulopathy.

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Published in 2020 at "Journal of the American Society of Nephrology : JASN"

DOI: 10.1681/asn.2019040433

Abstract: BACKGROUND Primary membranoproliferative GN, including complement 3 (C3) glomerulopathy, is a rare, untreatable kidney disease characterized by glomerular complement deposition. Complement gene mutations can cause familial C3 glomerulopathy, and studies have reported rare variants in… read more here.

Keywords: primary membranoproliferative; whole genome; complement gene; complement ... See more keywords
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C3 glomerulopathy.

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Published in 2023 at "Cleveland Clinic journal of medicine"

DOI: 10.3949/ccjm.90.e-s1.01

Abstract: C3 glomerulopathy (C3G) is a rare kidney disease that causes kidney dysfunction as a result of dysregulation of the complement system alternate pathway (AP). C3G encompasses 2 separate disorders, C3 glomerulonephritis and dense deposit disease.… read more here.

Keywords: c3g; disease; kidney; glomerulopathy ... See more keywords
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Collagenofibrotic Glomerulopathy

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Published in 2017 at "Indian Journal of Nephrology"

DOI: 10.4103/ijn.ijn_227_16

Abstract: Background: Collagenofibrotic glomerulopathy is a rare renal disease of unknown etiology that is secondary to deposition of type III collagen within the glomerulus. Only rare case series exist in the literature. Methods: Renal biopsies diagnosed… read more here.

Keywords: renal disease; etiology; glomerulopathy; pathology ... See more keywords