Zobrazeno 1 - 10
of 154
pro vyhledávání: '"antineutrophil cytoplasm antibodies"'
Autor:
Ciaran Twomey Brenner, Sujit Saha, Kate Bramham, Katie Vinen, Catherine Horsfield, Eirini Lioudaki
Publikováno v:
Case Reports in Nephrology and Dialysis, Vol 14, Iss 1, Pp 110-115 (2024)
Introduction: Anti-glomerular basement membrane (GBM) disease is a rare cause of glomerulonephritis usually mediated by IgG antibodies and is associated with ANCA-associated glomerulonephritis in up to 50% of cases. IgA-mediated anti-GBM disease is e
Externí odkaz:
https://doaj.org/article/fe0577beab2841209989c4a0a55618d2
Autor:
O V Blagova, I N Aliyeva, A V Nedostup, E A Kogan, R N Komarov, S V Chernyavsky, V V Seslavinskaya, P A Shelukha, V P Sedov, N V Gagarina, E A Mershina, V E Sinitsyn, V V Fomin
Publikováno v:
Терапевтический архив, Vol 91, Iss 4, Pp 99-106 (2019)
Loeffler's endocarditis remains is a very rare disease, develops due to eosinophilic inflammation predominantly of the endocardium with an outcome in fibrosis and massive thrombus formation and. He is generally characterized by an unfavorable prognos
Externí odkaz:
https://doaj.org/article/1485daf6e0e042b6bca6186faa6865b5
Akademický článek
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Autor:
N V Gagarina, Olga Blagova, V V Seslavinskaya, E A Kogan, V V Fomin, V P Sedov, S V Chernyavsky, I N Aliyeva, Nedostup Av, Elena Mershina, Roman Komarov, P A Shelukha, Valentin Sinitsyn
Publikováno v:
Терапевтический архив, Vol 91, Iss 4, Pp 99-106 (2019)
Loeffler's endocarditis remains is a very rare disease, develops due to eosinophilic inflammation predominantly of the endocardium with an outcome in fibrosis and massive thrombus formation and. He is generally characterized by an unfavorable prognos
Publikováno v:
Indian Journal of Medical and Paediatric Oncology. 40:598-600
Publikováno v:
Joint Bone Spine
Joint Bone Spine, 2018, 85 (1), pp.9--14. ⟨10.1016/j.jbspin.2017.05.022⟩
Joint Bone Spine, 2018, 85 (1), pp.9--14. ⟨10.1016/j.jbspin.2017.05.022⟩
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6557ff57ccdee05cca0052fb85179b30
https://www.hal.inserm.fr/hal-01881143
https://www.hal.inserm.fr/hal-01881143
Autor:
Caroline O. S. Savage, Rachel B. Jones
Publikováno v:
Medicine. 42:134-137
Systemic vasculitides comprise a collection of disorders characterized by the presence of fibrinoid necrosis and inflammation of blood vessels. This article provides an overview for small, medium and large vessel vasculitides.
Akademický článek
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Autor:
David Jayne
Publikováno v:
Current Opinion in Rheumatology. 20:3-9
Microscopic polyangiitis is defined within the context of primary systemic vasculitis. The presentation and management of renal involvement in microscopic polyangiitis is discussed, with emphasis on prognosis and outcomes. Potential roles of newer th