Abstract
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Christopher L. Bowlus, Gideon M. Hirschfield, Alejandra M. Villamil, Kris V. Kowdley, Hany Elbeshbeshy, Christophe Corpechot, Andreas E. Kremer, Palak J. Trivedi, Yiannis Kallis, Sook-Hyang Jeong, Kyung min Kwon, Victor de Ledinghen, Daria B. Crittenden, Cynthia Levy
Abstract
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Primary biliary cholangitis
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Goals of Treatment for Improved Survival in Primary Biliary Cholangitis: Treatment Target Should Be Bilirubin Within the Normal Range and Normalization of Alkaline Phosphatase
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Noninvasive elastography-based assessment of liver fibrosis progression and prognosis in primary biliary cirrhosis
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Dynamics of Liver Stiffness Measurement and Clinical Course of Primary Biliary Cholangitis
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Selective PPARδ agonist seladelpar suppresses bile acid synthesis by reducing hepatocyte CYP7A1 via the fibroblast growth factor 21 signaling pathway
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Selective PPARδ Agonist GW501516 Protects Against LPS-Induced Macrophage Inflammation and Acute Liver Failure in Mice via Suppressing Inflammatory Mediators
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Long-Term Efficacy and Safety of Selective PPARδ Agonist Seladelpar in Primary Biliary Cholangitis: ASSURE Interim Study Results
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Effects of Age and Sex of Response to Ursodeoxycholic Acid and Transplant-free Survival in Patients With Primary Biliary Cholangitis
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Fibrosis stage is an independent predictor of outcome in primary biliary cholangitis despite biochemical treatment response
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A Placebo-Controlled Trial of Bezafibrate in Primary Biliary Cholangitis
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Noninvasive Assessment of Portal Hypertension in Patients With Primary Biliary Cholangitis Is Affected by Severity of Cholestasis
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