Results 161 to 170 of about 123,589 (210)

IgA Vasculitis: Etiology, Treatment, Biomarkers and Epigenetic Changes

open access: yesInternational Journal of Molecular Sciences, 2021
IgA, previously called Henoch-Schönlein vasculitis, is an essential immune component that drives the host immune response to the external environment.
Yu Sawada, Hitomi Sugino
exaly   +2 more sources

IgA vasculitis

open access: yesSeminars in Immunopathology, 2021
IgA vasculitis (IgAV) is an inflammation of small vessels caused by perivascular deposition of IgA and activation of neutrophils. It may present as systemic vasculitis (IgAV - Henoch-Schönlein purpura) or as a variant restricted to the skin (skin-limited IgAV), while IgA nephropathy presents a variant restricted to the kidneys.
Évangéline Pillebout   +1 more
exaly   +4 more sources

IgA vasculitis nephritis

Current Opinion in Pediatrics, 2022
Purpose of review The purpose of this update is to summarize current knowledge on the pathophysiology of immunglobulin A (IgA) vasculitis nephritis (IgAVN) as well as to critically review evidence for established therapeutic regimes and available biomarkers. An additional purpose is to raise the discussion what could be done to
Eva, Nüsken, Lutz T, Weber
openaire   +2 more sources

Geospatial clustering of childhood IgA vasculitis and IgA vasculitis-associated nephritis

Annals of the Rheumatic Diseases, 2021
Research on spatial variability of the incidence of IgA vasculitis (IgAV) in children and its potential implications for elucidation of the multifactorial aetiology and pathogenesis is limited. We intended to observe spatial variability of the incidence of IgAV and IgA vasculitis-associated nephritis (IgAVN) using modern geostatistical methods, and ...
Matej Sapina   +10 more
openaire   +3 more sources

Management of IgA Vasculitis with Nephritis

Pediatric Drugs, 2021
Immunoglobulin A (IgA) vasculitis (IgAV), previously called Henoch-Schönlein purpura, is characterized by IgA-dominant immune deposits affecting small vessels and often involves the skin, gastrointestinal tract, joints, and kidneys. IgAV is the most common cause of systemic vasculitis in children.
Jean-Daniel, Delbet   +4 more
openaire   +2 more sources

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