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Odler, B; Windpessl, M; Eller, K; Säemann, MD; Lhotta, K; Neumann, I; Öberseder, G; Duftner, C; Dejaco, C; Rudnicki, M; Gauckler, P; Hintenberger, R; Zwerina, J; Thiel, J; Kronbichler, A.
[Diagnosis and therapy of granulomatosis with polyangiitis and microscopic polyangiitis-2023: consensus of the Austrian society of nephrology (ÖGN) and Austrian society of rheumatology (ÖGR)].
Wien Klin Wochenschr. 2023; 135(Suppl 5): 656-674.
Doi: 10.1007/s00508-023-02262-9
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- Führende Autor*innen der Med Uni Graz
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Odler Balazs
- Co-Autor*innen der Med Uni Graz
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Dejaco Christian
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Eller Kathrin
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Thiel Jens
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- Abstract:
- ANCA-associated vasculitides (AAV) are rare, complex systemic diseases that are often difficult to diagnose, because of unspecific clinical symptoms at presentation. However, the clinical course may be very dramatic and even life-threatening, necessitating prompt diagnosis and treatment.Therefore, it is important to increase disease awareness among physicians and support colleagues who are not confronted with these rare diseases on a regular basis. Here, the Austrian Society of Nephrology (ÖGN) and the Austrian Society of Rheumatology (ÖGR) provide a joint consensus on how to best diagnose and manage patients with granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA).
- Find related publications in this database (using NLM MeSH Indexing)
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Humans - administration & dosage
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Microscopic Polyangiitis - diagnosis, therapy
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Nephrology - administration & dosage
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Rheumatology - administration & dosage
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Austria - administration & dosage
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Consensus - administration & dosage
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Granulomatosis with Polyangiitis - diagnosis, therapy
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Intercellular Signaling Peptides and Proteins - administration & dosage
- Find related publications in this database (Keywords)
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ANCA-associated vasculitides (AAV)
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Diagnostics
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Therapy