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 …

IgA nephropathy is an autoimmune disease induced by fthe ormation of galactose-deficient
IgA1 and anti-glycans autoantibody. A multi-hit hypothesis was promoted to explain full …

IgA nephropathy (IgAN) is the most common glomerulonephritis worldwide. The classic
manifestation of IgAN is episodic hematuria and proteinuria. Nephrotic syndrome (NS) is not …

Background Hyperuricemia has been reported to be correlated with IgA nephropathy (IgAN).
However, whether hyperuricemia or elevated serum uric acid (SUA) is an independent …

Objective To date, nephrotic syndrome (NS) has not been well characterized in patients with
IgA nephropathy (IgAN). Whether decline in serum albumin is an ominous sign in IgAN …

Abstract Background Both primary IgA nephropathy (IgAN) with and without nephrotic
syndrome (NS) can present massive proteinuria (24-h urinary protein≥ 3.5 g/d). The clinical …

Background: IgA nephropathy (IgAN) has a high degree of heterogeneity in clinical and
pathological features. Among all subsets of IgAN, the pathogenesis of IgAN with minimal …

Aim: Membranous nephropathy and minimal change disease (MCD) have been involved in
mercury-induced nephrotic syndrome. IgA nephropathy is not known to be a common …

Background Few studies have evaluated the treatment of immunoglobulin A nephropathy
(IgAN) patients with nephrotic syndrome (NS) and mesangioproliferative glomerulonephritis …

Purpose To evaluate the differences in clinicopathological features and outcomes of IgA
nephropathy (IgAN) patients with and without nephrotic syndrome. Methods In this …