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Exhausted natural killer cells in adult IgA vasculitis. [PDF]
Bajželj M +10 more
europepmc +1 more source
Durvalumab-Associated Crescentic Glomerulonephritis With IgA Vasculitis-Like Features. [PDF]
Zhao T, Zhang X, Li Y, Su T.
europepmc +1 more source
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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 ...
E. Nüsken, L. Weber
semanticscholar +3 more sources
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 ...
E. Nüsken, L. Weber
semanticscholar +3 more sources
Geospatial clustering of childhood IgA vasculitis and IgA vasculitis-associated nephritis
Annals of the Rheumatic Diseases, 2021Research 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, 2021Immunoglobulin 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
Interventions for preventing and treating kidney disease in IgA vasculitis.
Cochrane Database of Systematic Reviews, 2023BACKGROUND IgA vasculitis (IgAV), previously known as Henoch-Schönlein purpura, is the most common vasculitis of childhood but may also occur in adults.
D. Hahn, E. Hodson, J. Craig
semanticscholar +1 more source
Seminars in Arthritis & Rheumatism, 2023
OBJECTIVE IgA vasculitis (IgAV) (formerly Henoch-Schönlein Purpura, HSP) rarely causes severe skin lesions in children. The purpose of the research was to determine whether severe skin manifestations were associated with a more severe disease course ...
M. Šestan +24 more
semanticscholar +1 more source
OBJECTIVE IgA vasculitis (IgAV) (formerly Henoch-Schönlein Purpura, HSP) rarely causes severe skin lesions in children. The purpose of the research was to determine whether severe skin manifestations were associated with a more severe disease course ...
M. Šestan +24 more
semanticscholar +1 more source
IgA vasculitis induced by acenocoumarol
Reumatología Clínica (English Edition), 2020We present the case of a 73-year-old man with IgA vasculitis after administration of acenocoumarol, confirmed by anatomopathological study. He had cutaneous, joint and renal involvement. With the reintroduction of the drug, the clinical manifestations worsened. They were completely resolved with its suspension, without additional maintenance treatment.
Sara, Esteban Terradillos +5 more
openaire +2 more sources
Multisystemic manifestations of IgA vasculitis
Clinical Rheumatology, 2020Immunoglobulin A vasculitis (IgAV), also known as Henoch-Schönlein Purpura, is one of the most common kind of systemic vasculitis in children, and due to the involvement of small blood vessels throughout the body, this disease can cause a variety of symptoms in different organs. Our aim was to review the data on various systemic manifestations of IgAV.
Lina Du +5 more
openaire +2 more sources

