Microscopic Polyangiitis

Microscopic polyangiitis is a primary systemic vasculitis of small- and some medium-sized vessels. It is characterized by a tropism for kidneys and lungs, positive association with anti-neutrophil cytoplasmic antibodies (ANCA), and a paucity of immunoglobulin deposits in vessel walls. Discover the latest research on microscopic polyangiitis here.

August 9, 2020
Open Access

Crescentic glomerulonephritis: what's different in South Asia? A single center observational cohort study

Wellcome Open Research
Suceena AlexanderSantosh Varughese
August 10, 2020

Mild COVID-19 in ANCA-associated vasculitis treated with rituximab

Annals of the Rheumatic Diseases
Silvia Suárez-DíazLuis Caminal-Montero
August 10, 2020

Presence of purpura is related to active inflammation in association with IL-5 in eosinophilic granulomatosis with polyangiitis

Rheumatology International
Hiroshi KataokaMasaya Mukai
August 4, 2020

Risk factors, etiology, and outcome of ischemic stroke in young adults: A Japanese multicenter prospective study

Journal of the Neurological Sciences
Yu KonoYoshitaka Murakami
August 3, 2020

New therapeutic strategies in lung vasculitis

Current Opinion in Pulmonary Medicine
Mouhamad Nasser, Vincent Cottin
August 10, 2020

MMP-9 Inhibitor GM6001 Prevents the Development of ssTBI-Induced Parkinson's Disease via the Autophagy Pathway

Cellular and Molecular Neurobiology
Chao LinNing Liu
August 10, 2020

Update to the ASFA guidelines on the use of therapeutic apheresis in ANCA-associated vasculitis

Journal of Clinical Apheresis
Rasheed A BalogunNancy M Dunbar
August 7, 2020

Mid to Late Life Hypertension Trends and Cerebral Small Vessel Disease in the Framingham Heart Study

Rodica Elena PetreaJose Rafael Romero
August 4, 2020
Case Report
Open Access

Hydralazine-Induced Dual Antineutrophil Cytoplasmic Antibody Positive Vasculitis and Nephritis

Sandeep A PadalaStanley Nahman
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
Open Access

Cerebral Small-Vessel Disease and Risk of Incidence of Depression: A Meta-Analysis of Longitudinal Cohort Studies

Journal of the American Heart Association
Yuanyuan FangMinghuan Wang
August 1, 2020
Open Access

Broad phenotype of cysteine altering NOTCH3 variants in UK Biobank: CADASIL to non-penetrance

Julie W RuttenSaskia A J Lesnik Oberstein

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