Results 191 to 200 of about 24,135 (222)
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IgA vasculitis with severe renal manifestation
BMJ Case Reports, 2022IgA vasculitis is a rare systemic vasculitis in adults, frequently more severe than in paediatric age. It manifests with cutaneous, articular, gastrointestinal and renal involvement. We present a case of a man in his 40s diagnosed with IgA vasculitis with cutaneous, joint, gastrointestinal and renal disease.
Joana, Marques Dias +3 more
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Current Treatment Options in Rheumatology, 2018
Immunoglobulin A vasculitis (IgAV) is a small vessel vasculitis with skin, joint, gastrointestinal and renal manifestations. Our understanding of the natural history of this disease is limited due to the overall low incidence of IgAV in adults and a lack of consensus regarding diagnostic criteria.
Sarah M. Moran, Heather N. Reich
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Immunoglobulin A vasculitis (IgAV) is a small vessel vasculitis with skin, joint, gastrointestinal and renal manifestations. Our understanding of the natural history of this disease is limited due to the overall low incidence of IgAV in adults and a lack of consensus regarding diagnostic criteria.
Sarah M. Moran, Heather N. Reich
openaire +1 more source
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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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
IgA Vasculitis: Etiology, Treatment, Biomarkers and Epigenetic Changes
International Journal of Molecular Sciences, 2021Yu Sawada
exaly
Pathogenesis of IgA Vasculitis: An Up-To-Date Review
Frontiers in Immunology, 2021Jianjun Qiao, Jun Cheng, Jianghua Chen
exaly