Incidence, prevalence, and outcome of primary biliary cholangitis in a nationwide Swedish population-based cohort
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-019-47890-2.pdf
Reference30 articles.
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2. Beuers, U. et al. Changing nomenclature for PBC: From ‘cirrhosis’ to ‘cholangitis’. J. Hepatol. 63, 1285–1287, https://doi.org/10.1016/j.jhep.2015.06.031 (2015).
3. Liver, E. A. F. T. S. O. T. EASL Clinical Practice Guidelines: The diagnosis and management of patients with primary biliary cholangitis. J. Hepatol. 67, 145–172, https://doi.org/10.1016/j.jhep.2017.03.022 (2017).
4. Dyson, J. K. et al. Novel therapeutic targets in primary biliary cirrhosis. Nat. Rev. Gastroenterol. Hepatol. 12, 147–158, https://doi.org/10.1038/nrgastro.2015.12 (2015).
5. Pares, A., Caballeria, L. & Rodes, J. Excellent long-term survival in patients with primary biliary cirrhosis and biochemical response to ursodeoxycholic Acid. Gastroenterology 130, 715–720, https://doi.org/10.1053/j.gastro.2005.12.029 (2006).
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