Results 11 to 20 of about 149,546 (225)
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 immunofluorescence.
Basta-Jovanović Gordana M. +1 more
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IgA nephropathy – new insights into IgA nephropathy [PDF]
Liječnički 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
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Predictors of prognosis in IgA nephropathy [PDF]
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
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
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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
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, 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)
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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
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Lack of serologic evidence to link IgA nephropathy with celiac disease or immune reactivity to gluten. [PDF]
PLoS 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
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Journal of the American Society of Nephrology, 2005 14863
Barratt, J, Feehally, J
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Serological Measurement of Poly-IgA Immune Complex Levels in IgA Nephropathy and IgA Vasculitis
Bio-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
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