Results 191 to 200 of about 113,982,624 (231)

Advances in Genetics of Immunoglobulin A Nephropathy

open access: yes, 2016
Familial aggregation of IgA nephropathy (IgAN) and variation in prevalence among different ethnicities indicate inherited factors contribute to disease pathogenesis. Studies have also shown that IgAN patients also have an inherited defect in O-glycosylation of IgA1.
Zhang, Hong   +2 more
openaire   +3 more sources

Immunoglobulin A Nephropathy

Pediatrics In Review, 2019
1. Smita Goodman, DO* 2. Jessica Reid-Adam, MD* 1. *Icahn School of Medicine at Mount Sinai, New York, NY Immunoglobulin A nephropathy (IgAN) is the most common form of primary chronic glomerular disease worldwide. First described in 1968 by pathologist Jean Berger, it was regarded for many years as a benign condition.
Smita, Goodman, Jessica, Reid-Adam
  +6 more sources

Immunoglobulin A Nephropathy

Archives of Internal Medicine, 1975
Of 475 renal biopsies examined by immunofluorescence, IgA was seen located selectively in the glomerular mesangium of 18 patients. These patients were generally young men and had hematuria, only minimal proteinuria, and normal renal function. Glomerular lesions consisted of focal segmental capillary hypercellularity or sclerosis and mesangial ...
S W, Zimmerman, P M, Burkholder
openaire   +3 more sources

Pathogenesis of immunoglobulin A nephropathy

Current Opinion in Nephrology and Hypertension, 2013
In this article, we review recent findings on the pathogenesis and genetics of immunoglobulin A (IgA) nephropathy.During the past 2 years, the understanding of the pathogenesis of IgA nephropathy has evolved as a result of progress in technology and new tools that have been developed.
Jan, Novak   +3 more
openaire   +2 more sources

Immunoglobulin A nephropathy

2009
The term immunoglobulin A nephropathy (IgA nephropathy or IgA N) refers to a primary glomerular disease characterized by the dominant or co-dominant, diffuse, and generalized mesangial deposition of IgA, often accompanied by deposition of IgG and the C3 component of complement in a similar distribution (Donadio and Grande, 2004; Barratt and Feehally ...
Richard J. Glassock, Grace Lee
openaire   +2 more sources

Immunoglobulin A nephropathy

Current Opinion in Nephrology and Hypertension, 1996
There is no specific treatment to reduce glomerular IgA deposition in IgA nephropathy. The available controlled trials are restricted to patients with proteinuria and progressive renal failure where mechanisms of injury are common to other chronic glomerular diseases.
openaire   +2 more sources

Pregnancy in immunoglobulin M nephropathy

Journal of Obstetrics and Gynaecology Research, 2017
AbstractImmunoglobulin M nephropathy is an uncommon glomerular disease and a relatively less recognized clinico‐immunopathological entity in the domain of glomerulonephritis, often thought to be a bridge between minimal change disease and focal segmental glomerulosclerosis.
Meryem, Hocaoğlu   +3 more
openaire   +2 more sources

Immunoglobulin A nephropathy: a pathophysiology view

Inflammation Research, 2016
IgA nephropathy is one of the leading causes of primary glomerulonephritis worldwide and an important etiology of renal disease in young adults. IgA nephropathy is considered an immune complex-mediated disease.This review article summarizes recent evidence on the pathophysiology of IgA nephropathy.Current studies indicate an ordered sequence of multi ...
Rafaela Cabral Gonçalves Fabiano   +2 more
openaire   +2 more sources

Serologic study of immunoglobulin A-fibronectin aggregates in immunoglobulin a nephropathy

American Journal of Kidney Diseases, 1996
The immunoglobulin A (IgA)-fibronectin aggregates, detected by enzyme-linked immunosorbent assay using either antifibronectin or collagen I as binding protein, were previously found to be raised in the circulation of patients with IgA nephropathy (IgAN). It has been suggested that IgA-fibronectin aggregates are involved in the pathogenesis and that the
Kar Neng Lai   +4 more
openaire   +4 more sources

Immunoglobulin A nephropathy: insights and progress

Translational Research, 2014
D iseases of the kidney filter, the glomerulus, are generally recognized by clinical signs of hematuria and proteinuria. Many of these diseases can progress to cause kidney dysfunction, hypertension, andmultiple complications. In this issue of Translational Research, investigators from northeastern China present data from a large population of ...
openaire   +2 more sources

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