IGA Glomerulonephritis

IgA glomerulonephritis is a chronic form of glomerulonephritis characterized by deposits of predominantly Iimmunoglobin A in the mesangial area. Discover the latest research on IgA glomerulonephritis here.

July 19, 2020
Open Access

GWAS-Based Discoveries in IgA Nephropathy, Membranous Nephropathy, and Steroid Sensitive Nephrotic Syndrome

Clinical Journal of the American Society of Nephrology : CJASN
Elena Sanchez-RodriguezKrzysztof Kiryluk
July 4, 2020

External Validation of the International IgA Nephropathy Prediction Tool

Clinical Journal of the American Society of Nephrology : CJASN
Junjun ZhangJingjing Ren
July 28, 2020

Neutrophil-to-lymphocyte ratio as an independent inflammatory indicator of poor prognosis in IgA nephropathy

International Immunopharmacology
Qianqian LiHong Zhang
July 6, 2020

Value of electron microscopy in the pathological diagnosis of native kidney biopsies in children

Pediatric Nephrology : Journal of the International Pediatric Nephrology Association
Xu ZhangSuxia Wang
July 28, 2020

Detection of microRNA Expression in the Kidneys of Immunoglobulin a Nephropathic Mice

Journal of Visualized Experiments : JoVE
Shohei KanekoYoshiyuki Morishita
July 15, 2020
Open Access

Utility of transjugular renal biopsy as an alternative to percutaneous biopsy

Nefrología : publicación oficial de la Sociedad Española Nefrologia
Mónica BoluferMaría José Soler
July 8, 2020
Review
Open Access

Monoclonal Gammopathies of Renal Significance: Renal Biopsy and Beyond

Cancers
Paolo MenèAntonella Stoppacciaro
July 6, 2020
Review

Practical management of C3 glomerulopathy and immunoglobulin-mediated MPGN: facts and uncertainties

Kidney International
Fadi FakhouriVéronique Frémeaux-Bacchi
July 30, 2020
Open Access

Pathological application of carbocyanine dye-based multicolour imaging of vasculature and associated structures

Scientific Reports
Alu KonnoShigetoshi Okazaki
July 10, 2020

Adult-onset IgA vasculitis (Henoch-Schönlein): Update on therapy

La Presse médicale
Federica MaritatiAugusto Vaglio
July 9, 2020

Clinical impact of urinary CD11b and CD163 on the renal outcomes of anti-neutrophil cytoplasmic antibody-associated glomerulonephritis

Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association
Yuki YokoeSeiichi Matsuo
July 18, 2020
Open Access

ST6Gal1 is up-regulated and associated with aberrant IgA1 glycosylation in IgA nephropathy: An integrated analysis of the transcriptome

Journal of Cellular and Molecular Medicine
Youxia LiuTiekun Yan
July 30, 2020
Open Access

Renal Survival in Children with Glomerulonephritis with Crescents: A Pediatric Nephrology Research Consortium Cohort Study

Journal of Clinical Medicine
Joseph G MaliakkalScott E Wenderfer
July 28, 2020
Case Report

Immunoglobulin-Negative DNAJB9-Associated Fibrillary Glomerulonephritis: A Report of 9 Cases

American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
Samar M SaidSamih H Nasr

Sign up to follow this feed and discover related papers.

Related Feeds

Acute Disseminated Encephalomyelitis

Acute disseminated encephalomyelitis (ADEM) is a rare inflammatory demyelinating disease of the central nervous system. Discover the latest research on acute disseminated encephalomyelitis here.

Addison Disease

Addison's disease, also known as primary adrenal insufficiency and hypocortisolism, is a long-term endocrine disorder in which the adrenal glands do not produce enough steroid hormones. Discover the latest research on Addison's disease here.

Adult-Onset Still's Disease

Adult-onset Still's disease (AOSD) is a form of Still's disease, a rare systemic autoinflammatory disease characterized by the classic triad of persistent high spiking fevers, joint pain, and a distinctive salmon-colored bumpy rash. Discover the latest research on AOSD here.

Anti-N-Methyl-D-Aspartate Receptor Encephalitis

Anti-N-Methyl-D-Aspartate (NMDA) receptor encephalitis is a form of of brain inflammation due to antibodies against NMDA receptors. Discover the latest research on anti-NMDA receptor encephalitis here.

Antiphospholipid Syndrome

Antiphospholipid syndrome or antiphospholipid antibody syndrome (APS or APLS), is an autoimmune, hypercoagulable state caused by the presence of antibodies directed against phospholipids.

Autoimmune Diabetes & Tolerance

Patients with type I diabetes lack insulin-producing beta cells due to the loss of immunological tolerance and autoimmune disease. Discover the latest research on targeting tolerance to prevent diabetes.

Autoimmune Disease Therapy

In autoimmune diseases, the immune system responds and attacks self-antigens and damages or impairs the function of the tissues. The treatment for autoimmune diseases often involves immunosuppressive agents, but newer treatments are being investigated. Discover the latest research on autoimmune disease therapy here.

Autoimmune Diseases

Autoimmune diseases occur as a result of an attack by the immune system on the body’s own tissues resulting in damage and dysfunction. There are different types of autoimmune diseases, in which there is a complex and unknown interaction between genetics and the environment. Discover the latest research on autoimmune diseases here.

Autoimmune Hemolytic Anemia

Autoimmune hemolytic anemia (AIHA) occurs when antibodies directed against the person's own red blood cells (RBCs) cause them to burst (lyse), leading to an insufficient number of oxygen-carrying red blood cells in the circulation. Discover the latest research on AIHA here.

Autoimmune Hepatitis

Autoimmune hepatitis formerly called lupoid hepatitis, is a chronic, autoimmune disease of the liver that occurs when the body's immune system attacks liver cells causing the liver to be inflamed. Discover the latest research on autoimmune hepatitis here.

© 2020 Meta ULC. All rights reserved
/feed-previews/iga-glomerulonephritis/ae5ab7a6-6820-4f1f-86d3-f340d34b4a48