Transcription of BSG and UKPBC Primary Biliary Cholangitis Treatment and ...
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1 HirschfieldflGM, et al. Gut 2018;0:1 27. British Society of Gastroenterology/UK-PBC Primary Biliary Cholangitis Treatment and management guidelinesGideon M Hirschfield,1,2,3 Jessica K Dyson,4,5,6 Graeme J M Alexander,7,8 Michael H Chapman,9 Jane Collier,10 Stefan H bscher,3,11 Imran Patanwala,12,13 Stephen P Pereira,7,8,9 Collette Thain,14 Douglas Thorburn,7,8 Dina Tiniakos,5 Martine Walmsley,15 George Webster,9 David E J Jones4,5,6 ABSTRACTP rimary Biliary Cholangitis (formerly known as Primary Biliary cirrhosis, PBC) is an autoimmune liver disease in which a cycle of immune mediated Biliary epithelial cell injury, cholestasis and progressive fibrosis can culminate over time in an end-stage Biliary cirrhosis.
Primary biliary cholangitis (formerly known as primary biliary cirrhosis, PBC), is a life-long autoimmune cholestatic liver disease that is a rare but important cause of chronic liver disease. More than 15000 individuals in the UK live with the risks and consequences of chronic biliary inflammation. New advances in
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EASL Clinical Practice Guidelines: The diagnosis, Primary Biliary, Primary bil-iary, 2021 Coding & Payment Quick Reference, Boston Scientific, Biliary, Primary, Newborn Care Summary Checklist for, Newborn Care Summary Checklist for Primary Care Providers, ICD-10 Diagnosis Codes Unacceptable as Primary Diagnosis, Primary Biliary Cholangitis: 2018 Practice Guidance, American Association for the Study, DIAGNOSTICS: RECOVERY AND RENEWAL