Results 11 to 20 of about 31,703 (224)

Relapses or de-novo IgA nephropathy following COVID-19 vaccination; a narrative review [PDF]

open access: yesJournal of Nephropathology, 2023
Immunoglobulin A (IgA) nephropathy is the most common type of glomerulonephritis worldwide characterized by excessive serum levels of glycosylated which triggers the generation of glycan-specific IgG and IgA autoantibodies.
Masoud Hafizi   +5 more
doaj   +2 more sources

IgA nephropathy [PDF]

open access: yesNature Reviews Disease Primers, 2016
Globally, IgA nephropathy (IgAN) is the most common primary glomerulonephritis that can progress to renal failure. The exact pathogenesis of IgAN is not well defined, but current biochemical and genetic data implicate overproduction of aberrantly glycosylated IgA1.
Sydney C W Tang   +2 more
exaly   +9 more sources

IgA nephropathy

open access: yesNature Reviews Disease Primers, 2023
Immunoglobulin A nephropathy (IgAN) is the most common glomerulonephritis in the world. The etiology is unknown but a dysregulated T-cell immune response to viral, bacterial, and food antigens activating mucosal plasma cells to produce polymeric IgA has been proposed. No serological test exists to diagnosis IgAN.
Eleni Stamellou   +2 more
exaly   +6 more sources

Urinary IL-18 predicts progression of IgA nephropathy [PDF]

open access: yesBMC Nephrology
Background There is currently a lack of noninvasive biomarkers that effectively predict the progression of IgA nephropathy. We investigated the value of urinary IL-18 in predicting the progression of IgA nephropathy and whether its combination with ...
Yuhong Tang   +8 more
doaj   +2 more sources

IgA nephropathy – new insights into IgA nephropathy [PDF]

open access: yesLiječnički vjesnik : glasilo Hrvatskoga liječničkog zbora, 2022
. Uvod: IgA nefropatija je najčešći oblik primarnog glomerulonefritisa u svijetu i značajno doprinosi nastanku kronične bolesti bubrega i završnog stadija bubrežnog zatajenja. Cilj: Prikazati nove spoznaje o IgA nefropatiji. Metode: Napravljen je pregled objavljene literature.
Arapović, Adela
core   +4 more sources

Predictors of prognosis in IgA nephropathy

open access: yesKaohsiung Journal of Medical Sciences, 2012
IgA nephropathy (nephropathy with mesangial IgA and IgG deposits, so-called Berger's disease) is the most common primary chronic glomerulonephritis worldwide, and was first described in 1968.
Yasuhiko Tomino
doaj   +2 more sources

Iga nephropathy

open access: yesSrpski arhiv za celokupno lekarstvo, 2004
IgA nephropathy is glomerular disease first described in 1968 by Berger, named after him Morbus Berger. The disease is characterized by the presence of IgA dominant or codominant imunoglobuline deposits in glomerular mesangium which can be demostrated by immunofluorescence.
Basta-Jovanović Gordana M.   +1 more
openaire   +4 more sources

IgA nephropathy with leucocytoclastic vasculitis

open access: yesJournal of International Medical Research, 2018
Leucocytoclastic vasculitis is a rare type of allergic disease caused by immune complexes. IgA nephropathy is a glomerulopathy characterized by recurrent episodes of gross haematuria or microscopic haematuria and IgA deposition in the glomerular ...
Lin-Yan Wei   +3 more
doaj   +2 more sources

Hyperuricemia Aggravates IgA Nephropathy [PDF]

open access: yesمجله دانشکده پزشکی اصفهان, 2013
It is well documented that hyperuricemia is an independent risk factor for IgA nephropathy, and appropriate treatment by allopurinol is a reasonable modality in the patients.
Mahmoud Rafieian-Kopaei   +2 more
doaj   +1 more source

IgA Nephropathy [PDF]

open access: yesClinical Journal of the American Society of Nephrology, 2017
IgA nephropathy (IgAN) is a leading cause of CKD and renal failure. Recent international collaborative efforts have led to important discoveries that have improved our understanding of some of the key steps involved in the immunopathogenesis of IgAN. Furthermore, establishment of multicenter networks has contributed to rigorous design and execution of ...
Jennifer C, Rodrigues   +2 more
openaire   +4 more sources

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