Primary Biliary Cholangitis: 2018 Practice Guidance from the American Association for the Study of Liver Diseases

Cites (263)

Items 201–275 of 275

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10. Clinical predictors for hepatocellular carcinoma in patients with primary biliary cirrhosis
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16. Treatment of severe refractory pruritus with fractionated plasma separation and adsorption (Prometheus)
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18. Mycophenolate Mofetil for the Treatment of Primary Biliary Cirrhosis in Patients with an Incomplete Response to Ursodeoxycholic Acid
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19. Plasma separation and anion adsorption transiently relieve intractable pruritus in primary biliary cirrhosis
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20. Varices in early histological stage primary biliary cirrhosis
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21. Effect of Ursodeoxycholic Acid on Serum Lipids of Patients With Primary Biliary Cirrhosis
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22. Biochemical markers of liver fibrosis and lymphocytic piecemeal necrosis in UDCA-treated patients with primary biliary cirrhosis
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23. Long-term outcomes in antimitochondrial antibody negative primary biliary cirrhosis
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25. Assessment of health related quality of life in polish patients with primary biliary cirrhosis
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26. A 2-year multicenter, double-blind, randomized, placebo-controlled study of bezafibrate for the treatment of primary biliary cholangitis in patients with inadequate biochemical response to ursodeoxycholic acid therapy (Bezurso)
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27. Low specificity of anti‐tissue transglutaminase antibodies in patients with primary biliary cirrhosis
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28. The incidence of pruritus after epidural morphine
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29. Applicability of the IAIHG scoring system to the diagnosis of antimitochondrial/anti‐M2 seropositive variant form of autoimmune hepatitis
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30. Antimitochondrial antibody negative primary biliary cirrhosis in Japan: utilization of clinical data when patients applied to receive public financial aid
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31. Changing nomenclature for PBC: From 'cirrhosis' to 'cholangitis'
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32. Treatment with ursodeoxycholic acid is associated with weight gain in patients with primary biliary cirrhosis
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33. Questionnaire based assessment of risk factors for primary biliary cirrhosis
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34. Clinical and pathological characteristics of the autoimmune hepatitis and primary biliary cirrhosis overlap syndrome
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38. Comparative analysis of portal cell infiltrates in antimitochondrial autoantibody–positive versus antimitochondrial autoantibody–negative primary biliary cirrhosis
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39. Geoepidemiology and space–time analysis of Primary biliary cirrhosis in Crete, Greece
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40. Coronary artery disease in primary biliary cirrhosis: A systematic review and meta‐analysis of observational studies
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41. Rifampin‐induced selective serotonin reuptake inhibitor withdrawal syndrome in a patient treated with sertraline
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42. Autoreactive monoclonal antibodies from patients with primary biliary cholangitis recognize environmental xenobiotics
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43. Paradoxical elevation of serum cholesterol by clofibrate in patients with primary biliary cirrhosis
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47. Long‐term fibrate treatment for PBC
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48. Geotherapeutics of primary biliary cirrhosis
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49. Primary biliary cirrhosis–autoimmune hepatitis overlap syndrome: Simplified criteria may be effective in the diagnosis in <scp>C</scp>hinese patients
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52. A brief review on prognostic models of primary biliary cholangitis
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53. Bioavailability of four ursodeoxycholic acid preparations
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54. Utility of Noninvasive Markers of Fibrosis in Cholestatic Liver Diseases
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55. Right liver lobe diameter:albumin ratio: a new non-invasive parameter for prediction of oesophageal varices in patients with liver cirrhosis (preliminary report).
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56. Clinical implications of antimitochondrial antibody seropositivity in autoimmune hepatitis: a multicentre study
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57. Lipoprotein pattern and plasma lipoprotein lipase activities in patients with primary biliary cirrhosis: Relationship with increase of HDL2 fraction in Lp-X-positive and Lp-X-Negative subjects
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58. Consecutive occurrence of primary biliary cirrhosis and autoimmune hepatitis: a case report and review of the literature
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59. Association between fatigue and decreased survival in primary biliary cirrhosis.
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61. Azathioprine and prognosis in primary biliary cirrhosis
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67. Optimizing Biochemical Markers as Endpoints for Clinical Trials in Primary Biliary Cirrhosis
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