Results 11 to 20 of about 161,533 (212)
Relapses or de-novo IgA nephropathy following COVID-19 vaccination; a narrative review [PDF]
Journal 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 +3 more sources
Srpski 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
Basta-Jovanović Gordana M. +1 more
core +4 more sources
Predictors of prognosis in IgA nephropathy
Kaohsiung 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
Treatment and practical considerations of IgA nephropathy [PDF]
Frontiers in MedicineIgA nephropathy is a common cause of glomerular disease that may result in kidney failure. Until recently, angiotensin blockade using angiotensin converting enzyme (ACE) inhibitors and angiotensin receptor blockers (ARB) were the main treatment options ...
Hanny Sawaf +4 more
doaj +2 more sources
IgA nephropathy with leucocytoclastic vasculitis
Journal 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]
مجله 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 +2 more sources
KM55 in the evaluation of IgA containing glomerular diseases
Glomerular 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
Frontiers 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
Clinical 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
, 1992 IgA in IgA Nephropathy Lorna Layward IgA nephropathy is a common glomerulonephritis of unknown pathogenesis, characterised by the presence of IgA within the glomerular mesangium.
Lorna. Layward (7628906)
core +5 more sources