Results 21 to 30 of about 31,703 (224)

KM55 in the evaluation of IgA containing glomerular diseases

open access: yesGlomerular Diseases, 2021
Introduction: Mucosal derived galactose deficient IgA is central to the pathogenesis of primary IgA nephropathy. Recent reports suggest similar pathogenesis in Henoch Schonlein purpura and secondary IgA nephropathy.
Rahul Raj   +7 more
doaj   +1 more source

Diagnostic Potential of Plasma IgA1 O-Glycans in Discriminating IgA Nephropathy From Other Glomerular Diseases and Healthy Participants

open access: yesFrontiers in Molecular Biosciences, 2022
Background: Aberrant O-glycosylation of IgA1 plays an important role in IgA nephropathy pathogenesis. Previous proteomic studies analyzed O-glycans of the circulating IgA1 hinge region and found that the N-acetylgalactosamine (GalNAc) and galactose ...
Shuyu Zhang   +8 more
doaj   +1 more source

Histological Features of IgA Nephropathy in Pediatrics and the Magnitude of the Disease in Saudi Children

open access: yesInternational Journal of Pediatrics, 2023
Objectives. This review addresses the microscopic features of immunoglobulin A nephropathy (IgA nephropathy), its prognostic variables in children, and measures to which extent these features and variables differ from adults.
Reem A. Al Zahrani
doaj   +1 more source

COVID-19 Hyperinflammation: What about Neutrophils?

open access: yesmSphere, 2020
COVID-19 is often related to hyperinflammation that drives lung or multiorgan injury. The immunopathological mechanisms that cause excessive inflammation are under investigation and constantly updated.
Athanasios Didangelos
doaj   +1 more source

Urinary exosomal miRNA signature of IgA nephropathy: a case–control study

open access: yesScientific Reports, 2023
IgA nephropathy is the most common primary glomerulonephritis worldwide and can progress to end-stage kidney disease (ESKD). The current “gold standard” for diagnosis is kidney biopsy, which is invasive and associated with morbidity.
Mythri Shankar   +5 more
doaj   +1 more source

Serum galactose-deficient-IgA1 and IgG autoantibodies correlate in patients with IgA nephropathy. [PDF]

open access: yesPLoS ONE, 2018
IgA nephropathy is an autoimmune disease characterized by IgA1-containing glomerular immune deposits. We previously proposed a multi-hit pathogenesis model in which patients with IgA nephropathy have elevated levels of circulatory IgA1 with some O ...
William J Placzek   +8 more
doaj   +1 more source

Current knowledge of targeted-release budesonide in immunoglobulin A nephropathy: A comprehensive review

open access: yesFrontiers in Immunology, 2023
Immunoglobulin A (IgA) nephropathy is a common autoimmune kidney disease. Accumulating studies showed that IgA nephropathy may be partially correlated with mucosal immune system dysfunction.
Jian Liao   +9 more
doaj   +1 more source

Lack of serologic evidence to link IgA nephropathy with celiac disease or immune reactivity to gluten. [PDF]

open access: yesPLoS ONE, 2014
IgA nephropathy is the most common form of primary glomerulonephritis worldwide. Mucosal infections and food antigens, including wheat gluten, have been proposed as potential contributing environmental factors.
Sina Moeller   +7 more
doaj   +1 more source

IgA Nephropathy [PDF]

open access: yesJournal of the American Society of Nephrology, 2005
14863
Barratt, J, Feehally, J
openaire   +3 more sources

Serological Measurement of Poly-IgA Immune Complex Levels in IgA Nephropathy and IgA Vasculitis

open access: yesBio-Protocol, 2022
Both IgA nephropathy and IgA vasculitis, formerly known as Henoch-Schӧnlein purpura, are immune deposition diseases. IgA nephropathy is caused by the deposition of aberrantly formed poly-IgA complexes from blood circulation to the kidney glomerulus; IgA ...
Xue Zhang   +6 more
doaj   +1 more source

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