Results 31 to 40 of about 21,381 (225)
Complement membrane attack (MAC) in idiopathic IgA-glomerulonephritis [PDF]
, 1987 Complement membrane attack (MAC) in idiopathic IgA-glomerulonephritis. Antigens of the membrane attack complex of complement (MAC), such as C5, C6, C9 and MAC-related neoantigen(s), were demonstrated in the mesangium of 23 cases with IgA ...
Ritz, Eberhard +3 more
core +1 more source
Linchuang shenzangbing zazhi, 2022 ObjectiveTo explore the distribution characteristics and disease spectrum changes of pathological types in patients with renal puncture biopsy.MethodsFrom January，2005 to December，2019，clinicopathological data were retrospectively reviewed for 1703 renal
Huang Chun-lin +7 more
doaj
Critical Role of Kupffer Cell CD89 Expression in Experimental IgA Nephropathy. [PDF]
PLoS ONE, 2016 Although IgA nephropathy (IgAN) is the most common primary glomerulonephritis worldwide, its etiology remains only partly understood. It is clear that the pathogenesis of IgAN involves the formation of macromolecular IgA1 complexes and increased levels ...
Lijun Xu +7 more
doaj +1 more source
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 +1 more source
A Case Report of Systemic Lupus Erythematosus With IgA Nephropathy and Crescentic Nephritis
Annals of Internal Medicine: Clinical Cases, 2023 We report a case of systemic lupus erythematosus with IgA nephropathy and acute progressive glomerulonephritis. Renal function failed to recover after the administration of glucocorticoid and cyclophosphamide pulse therapy, which shows that systemic ...
Zhifeng Jiang, Aiqiao Feng
doaj +1 more source
Inflammatory markers and the progression of IgA glomerulonephritis [PDF]
Nephrology Dialysis Transplantation, 2007 IgA glomerulonephritis (IgAGN) composes a variable prognosis with 15-40% of the patients eventually progressing to end-stage renal failure. Known risk factors for progressive course of IgAGN include hypertension, proteinuria and renal insufficiency. Although markers of inflammation such as serum or urinary interleukin-6 (IL-6) and serum albumin have ...
Kati, Kaartinen +7 more
openaire +2 more sources
IgA-Dominant Postinfectious Glomerulonephritis: A New Twist on an Old Disease [PDF]
, 2011 IgA-dominant acute postinfectious glomerulonephritis (APIGN) is an increasingly recognized morphologic variant of APIGN, particularly in the elderly. In contrast to classic APIGN, in which there is typically glomerular deposition of IgG and C3 or C3 only,
Vivette D. D’Agati, Samih H. Nasr
core +1 more source
BMC Nephrology, 2018 Background Despite the development of biomarkers and noninvasive imaging tools, biopsy remains the only method for correctly diagnosing patients with unexplained hematuria, proteinuria and renal failure.
Hsien-Fu Chiu +4 more
doaj +1 more source
Insulin resistance and the progression of IgA glomerulonephritis [PDF]
Nephrology Dialysis Transplantation, 2007 IgA glomerulonephritis (IgAGN) has a highly variable prognosis with 15-40% of patients progressing to end-stage renal disease. Hypertension, proteinuria and renal insufficiency are risk factors associated with poor prognosis. The role of insulin resistance is unclear in IgAGN.From a retrospective cohort of IgAGN patients, a total of 174 patients (104 ...
Kati, Kaartinen +7 more
openaire +2 more sources
Case Reports in Nephrology and DialysisIntroduction: Anti-glomerular basement membrane (GBM) disease is a rare cause of glomerulonephritis usually mediated by IgG antibodies and is associated with ANCA-associated glomerulonephritis in up to 50% of cases.
Ciaran Twomey Brenner +5 more
doaj +1 more source