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SHR Neuro Krebs Kardio Lipid Stoffw Microb

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 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Führende Autor*innen der Med Uni Graz
Odler Balazs
Co-Autor*innen der Med Uni Graz
Dejaco Christian
Eller Kathrin
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)
Humans - administration & dosage
Microscopic Polyangiitis - diagnosis, therapy
Nephrology - administration & dosage
Rheumatology - administration & dosage
Austria - administration & dosage
Consensus - administration & dosage
Granulomatosis with Polyangiitis - diagnosis, therapy
Intercellular Signaling Peptides and Proteins - administration & dosage

Find related publications in this database (Keywords)
ANCA-associated vasculitides (AAV)
Diagnostics
Therapy
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