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SHR Neuro Krebs Kardio Lipid Stoffw Microb

Trauner, M; Halilbasic, E; Baghdasaryan, A; Moustafa, T; Krones, E; Fickert, P; Hofer, H; Penner, E.
Primary sclerosing cholangitis: new approaches to diagnosis, surveillance and treatment.
Dig Dis. 2012; 30 Suppl 1(6):39-47 Doi: 10.1159/000341123
Web of Science PubMed FullText FullText_MUG

 

Führende Autor*innen der Med Uni Graz
Trauner Michael
Co-Autor*innen der Med Uni Graz
Baghdasaryan Anna
Fickert Peter
Halilbasic Emina
Moustafa Tarek
Tatscher Elisabeth
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Abstract:
Primary sclerosing cholangitis (PSC) is a chronic inflammatory bile duct disease of unknown etiology, frequently associated with inflammatory bowel disease and leading to end-stage liver disease requiring liver transplantation. Moreover, PSC is a premalignant condition associated with an increased risk for hepatobiliary and colorectal malignancy. Since effective medical therapy for PSC is still lacking, this disorder represents a potentially fatal disease with poor prognosis. This article is a summary of an overview given at the 5th Falk Gastro Conference in Munich 2012 and reviews the challenges associated with diagnosis, surveillance and therapy of PSC. Copyright © 2012 S. Karger AG, Basel.
Find related publications in this database (using NLM MeSH Indexing)
Cholangitis, Sclerosing - diagnosis Cholangitis, Sclerosing - drug therapy Cholangitis, Sclerosing - epidemiology Cholangitis, Sclerosing - therapy
Humans -
Population Surveillance -
Ursodeoxycholic Acid - therapeutic use

Find related publications in this database (Keywords)
Cholestasis
Cholangiocellular carcinoma
Bile acids
Nuclear receptors
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