Primär biliäre Cholangitis – Response-Kriterien der Erstlinientherapie und Perspektiven der Zweitlinientherapie
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s00108-024-01674-7.pdf
Reference25 articles.
1. Colapietro F et al (2023) PPAR agonists for the treatment of primary biliary cholangitis: old and new tales. J Transl Autoimmun 6:100188. https://doi.org/10.1016/J.JTAUTO.2023.100188
2. Corpechot C et al (2018) A placebo-controlled trial of bezafibrate in primary biliary cholangitis. N Engl J Med 378(23):2171–2181. https://doi.org/10.1056/NEJMOA1714519/SUPPL_FILE/NEJMOA1714519_DISCLOSURES.PDF
3. Corpechot C et al (2023) Adequate versus deep response to ursodeoxycholic acid in primary biliary cholangitis: To what extent and under what conditions is normal alkaline phosphatase level associated with complication-free survival gain? Hepatology. https://doi.org/10.1097/HEP.0000000000000529
4. Corpechot C et al (2011) Early primary biliary cirrhosis: biochemical response to treatment and prediction of long-term outcome. J Hepatol 55(6):1361–1367. https://doi.org/10.1016/J.JHEP.2011.02.031
5. Harms MH et al (2020) Number needed to treat with ursodeoxycholic acid therapy to prevent liver transplantation or death in primary biliary cholangitis. Gut 69(8):1502–1509. https://doi.org/10.1136/GUTJNL-2019-319057
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