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IgA nephropathy: A vasculitis?
Nephrology, 1997Summary: Vasculitis is an inflammation of blood vessels which leads to necrosis and infarction of the endorgans involved. IgA nephropathy (IgAN) is the kidney‐limited expression of a single disease with Henoch‐Schonlei purpura as the systemic vasculitic form.
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[IgA vasculitis - similarities and differences to IgA nephropathy].
Therapeutische Umschau. Revue therapeutique, 2022IgA vasculitis - similarities and differences to IgA nephropathy Abstract. IgA vasculitis (IgAV), formerly called Henoch-Schönlein Purpura (HSP) is an immune complex-mediated vasculitis of small vessels typically affecting the skin, gastrointestinal tract, and the kidneys. Based on distinct histopathological and pathophysiological commonalities of IgAV
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Gastrointestinal involvement and its association with the risk for nephritis in IgA vasculitis
Therapeutic Advances in Musculoskeletal Disease, 2021Martina Held, Sasa Srsen, Marijana Coric
exaly
Pathogenesis of IgA Vasculitis: An Up-To-Date Review
Frontiers in Immunology, 2021Jun Cheng, Jianghua Chen, Jian-Yong Wu
exaly
Post-COVID-19 vaccination IgA vasculitis in an adult
Journal of Cutaneous Pathology, 2022Alicia Little +2 more
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La Revue du praticien
ADULT IGA VASCULITIS. IgA vasculitis previously named rheumatoid purpura is a rare systemic vasculitis in adults involving small vessels and associated with the presence of immunoglobulin A deposits. IgA vasculitis is often triggerd by infections, taking medication and vaccination. It is characterised by the presence of vascular purpura associated with
Antoine, Hankard +1 more
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ADULT IGA VASCULITIS. IgA vasculitis previously named rheumatoid purpura is a rare systemic vasculitis in adults involving small vessels and associated with the presence of immunoglobulin A deposits. IgA vasculitis is often triggerd by infections, taking medication and vaccination. It is characterised by the presence of vascular purpura associated with
Antoine, Hankard +1 more
openaire +1 more source

