IgA nephropathy, initially described in 1968 as a kidney disease with glomerular
“intercapillary deposits of IgA-IgG”, has no disease-specific treatment and is a common …

Background: IgA nephropathy, a frequent cause of end-stage renal disease, is an
autoimmune disease wherein immune complexes consisting of IgA1 with galactose-deficient …

IgA nephropathy, the most common primary glomerulonephritis in the world and a frequent
cause of end-stage renal disease, is characterized by typical mesangial deposits of IgA1, as …

Since its first description more than 40 years ago, IgA nephropathy has become the most
common pattern of primary glomerulonephritis identified in all areas of the world where renal …

IgA nephropathy is an autoimmune disease characterized by IgA1-containing glomerular
immune deposits. We previously proposed a multi-hit pathogenesis model in which patients …

IgA nephropathy, described in 1968 as IgA-IgG immune-complex disease, is an autoimmune
disease. Galactose-deficient IgA1 is recognized by unique autoantibodies, resulting in the …

Immunoglobulin A (IgA) nephropathy (IgAN), the leading cause of primary
glomerulonephritis, is characterized by IgA1‐containing immunodeposits in the glomeruli …

IgA nephropathy (IgAN) is characterized by circulating immune complexes composed of
galactose-deficient IgA1 and a glycan-specific IgG antibody. These immune complexes …

IgA nephropathy (IgAN) is the leading cause of primary glomerulonephritis in the world. The
disease is characterized by the presence of IgA-containing immune complexes in the …

Background IgA nephropathy (IgAN) is the leading primary GN worldwide. The disease is
thought to result from glomerular deposition of circulating immune complexes of IgG bound …