Renaming primary biliary cirrhosis—clarity or confusion?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Gastroenterology,Hepatology
Link
http://www.nature.com/articles/nrgastro.2015.187.pdf
Reference10 articles.
1. Trivedi, P. J. et al. Optimising risk stratification in primary biliary cirrhosis: AST/platelet ratio index predicts outcome independent of ursodeoxycholic acid response. J. Hepatol. 60, 1249–1258 (2014).
2. Lammers, W. J. et al. Development and validation of a scoring system to predict outcomes of patients with primary biliary cirrhosis receiving ursodeoxycholic acid therapy. Gastroenterology http://dx.doi.org/10.1053/j.gastro.2015.07.061 .
3. Carbone, M. et al. Sex and age are determinants of the clinical phenotype of primary biliary cirrhosis and response to ursodeoxycholic acid. Gastroenterology 144, 560–569 (2013).
4. Sherlock, S. & Scheuer, P. J. The presentation and diagnosis of 100 patients with primary biliary cirrhosis. N. Engl. J. Med. 289, 674–678 (1973).
5. Beuers, U. et al. Changing nomenclature for PBC: from 'cirrhosis' to 'cholangitis'. Hepatology http://dx.doi.org/10.1002/hep.28140 .
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