scholarly article | Q13442814 |
P50 | author | M. Eric Gershwin | Q73297886 |
P2093 | author name string | Raoul Poupon | |
E. Jenny Heathcote | |||
Keith D. Lindor | |||
Marshall Kaplan | |||
Nora V. Bergasa | |||
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P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | primary biliary cholangitis | Q1072420 |
P304 | page(s) | 291-308 | |
P577 | publication date | 2009-02-11 | |
P1433 | published in | Hepatology | Q15724398 |
P1476 | title | Primary biliary cirrhosis | |
P478 | volume | 50 |
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Q51201875 | Anti-centromere antibody is an independent risk factor for chronic kidney disease in patients with primary biliary cirrhosis. |
Q35008069 | Anti-kelch-like 12 and anti-hexokinase 1: novel autoantibodies in primary biliary cirrhosis |
Q36081422 | Anti-mitochondrial M2 antibody-positive autoimmune hepatitis |
Q64095704 | Anti-mitochondrial autoantibodies in systemic lupus erythematosus and their association with disease manifestations |
Q42319828 | Anti-mitochondrial autoantibodies-milestone or byway to primary biliary cholangitis? |
Q33598806 | Apamin suppresses biliary fibrosis and activation of hepatic stellate cells |
Q47770804 | Aquaporin-1 is associated with arterial capillary proliferation and hepatic sinusoidal transformation contributing to portal hypertension in primary biliary cirrhosis. |
Q88599326 | Are Clinicians Ready for Safe Use of Stratified Therapy in Primary Biliary Cholangitis (PBC)? A Study of Educational Awareness |
Q89339335 | Association between STAT4 polymorphisms and risk of primary biliary cholangitis: a meta-analysis |
Q39176767 | Association between serum soluble CD14 and IL-8 levels and clinical outcome in primary biliary cholangitis. |
Q48134030 | Association of autoimmune hepatitis with Src homology 2 adaptor protein 3 gene polymorphisms in Japanese patients |
Q54274187 | Association of genes involved in bile acid synthesis with the progression of primary biliary cirrhosis in Japanese patients. |
Q35990216 | Association of primary biliary cirrhosis with variants in the CLEC16A, SOCS1, SPIB and SIAE immunomodulatory genes. |
Q37750545 | Autoantibodies as prognostic markers in autoimmune liver disease |
Q34827471 | Autoantibodies in Chinese patients with chronic hepatitis B: prevalence and clinical associations |
Q64263911 | Autoantibodies in Systemic Lupus Erythematosus Target Mitochondrial RNA |
Q33751665 | Autoantibodies to GW bodies and other autoantigens in primary biliary cirrhosis |
Q34346124 | Autoimmune hepatitis type 2 associated with an unexpected and transient presence of primary biliary cirrhosis-specific antimitochondrial antibodies: a case study and review of the literature. |
Q35078109 | Autoimmune hepatitis-primary biliary cirrhosis concurrent with biliary stricture after liver transplantation |
Q39010580 | Autoimmune hepatitis: review of histologic features included in the simplified criteria proposed by the international autoimmune hepatitis group and proposal for new histologic criteria |
Q35230369 | Autoimmune liver disease - are there spectra that we do not know? |
Q91788029 | Autoimmune liver disease and the enteric microbiome |
Q30244056 | Autoimmune liver diseases in the Asia-Pacific region: Proceedings of APASL symposium on AIH and PBC 2016. |
Q33825348 | Autoimmunity and environment: am I at risk? |
Q46484331 | B-cell depletion with rituximab in patients with primary biliary cirrhosis refractory to ursodeoxycholic acid |
Q36080972 | BAT117213: Ileal bile acid transporter (IBAT) inhibition as a treatment for pruritus in primary biliary cirrhosis: study protocol for a randomised controlled trial |
Q91431676 | Bezafibrate Improves GLOBE and UK-PBC Scores and Long-Term Outcomes in Patients With Primary Biliary Cholangitis |
Q39145368 | Bile acids and cardiovascular function in cirrhosis. |
Q37666088 | Bile acids reach out to the spinal cord: new insights to the pathogenesis of itch and analgesia in cholestatic liver disease |
Q34108895 | Biliary physiology and disease: reflections of a physician-scientist |
Q42620850 | Biochemical and immunologic effects of rituximab in patients with primary biliary cirrhosis and an incomplete response to ursodeoxycholic acid |
Q33641759 | Biochemical criteria at 1 year are not robust indicators of response to ursodeoxycholic acid in early primary biliary cirrhosis: results from a 29-year cohort study |
Q33723821 | Biochemical response to ursodeoxycholic acid predicts survival in a North American cohort of primary biliary cirrhosis patients. |
Q85345310 | Biochemical responses to bezafibrate improve long-term outcome in asymptomatic patients with primary biliary cirrhosis refractory to UDCA |
Q55324101 | Biomarkers for primary biliary cholangitis: current perspectives. |
Q26766699 | Brazilian society of hepatology recommendations for the diagnosis and management of autoimmune diseases of the liver |
Q35867125 | CXCR5+ CD4+ T follicular helper cells participate in the pathogenesis of primary biliary cirrhosis |
Q36276815 | Cancer and scleroderma: a paraneoplastic disease with implications for malignancy screening |
Q55237166 | Cardiac involvement in patients with primary biliary cholangitis: A 14-year longitudinal survey-based study. |
Q44853838 | Case Report: Ursodeoxycholic acid treatment in Niemann-Pick disease type C; clinical experience in four cases. |
Q90262910 | Changes in the gut microbiota of mice orally exposed to methylimidazolium ionic liquids |
Q55071942 | Changing Nomenclature for PBC: From 'Cirrhosis' to 'Cholangitis'. |
Q93140801 | Changing epidemiology and natural history of primary biliary cirrhosis |
Q34494216 | Changing nomenclature for PBC: From 'cirrhosis' to 'cholangitis'. |
Q55059313 | Changing nomenclature for PBC: from 'cirrhosis' to 'cholangitis'. |
Q33821346 | Characteristics of liver fibrosis with different etiologies using a fully quantitative fibrosis assessment tool |
Q57145981 | Characterization and treatment of persistent hepatocellular secretory failure |
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Q38611759 | Clonal Characteristics of Paired Infiltrating and Circulating B Lymphocyte Repertoire in Patients with Primary Biliary Cholangitis |
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Q48331749 | Complications, symptoms, quality of life and pregnancy in cholestatic liver disease. |
Q91644552 | Concomitant Sjögren's Syndrome Was Not Associated with a Poorer Response or Outcomes in Ursodeoxycholic Acid-Treated Patients with Primary Biliary Cholangitis |
Q48200680 | Concomitant nonalcoholic fatty liver disease does not alter the activity, severity or course of primary biliary cholangitis. |
Q37501384 | Concurrent autoimmune pancreatitis and primary biliary cirrhosis: a rare case report and literature review |
Q37102484 | Connective tissue diseases in primary biliary cirrhosis: a population-based cohort study |
Q46521938 | Cost and health consequences of treatment of primary biliary cirrhosis with ursodeoxycholic acid |
Q36752084 | Current Concepts in Primary Biliary Cirrhosis and Primary Sclerosing Cholangitis |
Q38055205 | Current pharmacotherapy for cholestatic liver disease |
Q92190130 | Cutoff Values of Acoustic Radiation Force Impulse Two-Location Measurements in Different Etiologies of Liver Fibrosis |
Q37993224 | Cytotoxic T-lymphocyte associated antigen-4 gene polymorphisms and primary biliary cirrhosis: a systematic review |
Q33744692 | Deleterious effect of oltipraz on extrahepatic cholestasis in bile duct-ligated mice |
Q33678116 | Detection of AMA-M2 in human saliva: Potentials in diagnosis and monitoring of primary biliary cholangitis |
Q54358503 | Detection of D-3-phosphoglycerate dehydrogenase autoantibodies in patients with autoimmune hepatitis: Clinical significance evaluation. |
Q45932486 | Development of hepatocellular carcinoma in autoimmune hepatitis patients: a case series. |
Q89302981 | Deviations in Peripheral Blood Cell Populations are Associated with the Stage of Primary Biliary Cholangitis and Presence of Itching |
Q28076505 | Diagnosis and Management of Autoimmune Hepatitis: Current Status and Future Directions |
Q44247097 | Diagnosis and Treatment of Autoimmune Liver Diseases in a Tertiary Referral Center in Cuba |
Q38266358 | Diagnosis and management of primary biliary cirrhosis |
Q51726466 | Diagnosis and management of primary sclerosing cholangitis. |
Q39542696 | Diagnostic accuracy of two tests for determination of anti-m2 in the diagnosis of primary biliary cirrhosis: Is it possible to predict the course of the disease? |
Q39424761 | Diagnostic autoantibodies for autoimmune liver diseases |
Q39096610 | Diagnostic considerations for cholestatic liver disease |
Q34776270 | Distinct microRNAs expression profile in primary biliary cirrhosis and evaluation of miR 505-3p and miR197-3p as novel biomarkers. |
Q33731999 | Distinctive HLA-II association with primary biliary cholangitis on the Island of Sardinia |
Q98779028 | Do hepatic artery infusion pumps cause recurrent pleural effusions? |
Q38592916 | Drug treatment of pruritus in liver diseases. |
Q89403871 | Dysbiosis of oral microbiota and its association with salivary immunological biomarkers in autoimmune liver disease |
Q50132221 | Editorial: Itching to Know: Role of Fibrates in PBC. |
Q47440077 | Effect of ileal bile acid transporter inhibitor GSK2330672 on pruritus in primary biliary cholangitis: a double-blind, randomised, placebo-controlled, crossover, phase 2a study. |
Q43004194 | Effect of nalfurafine hydrochloride in patients with chronic liver disease with refractory pruritus on sleep disorders: a study protocol for single-arm, prospective, interventional study |
Q47156253 | Elevated Liver Enzymes in Asymptomatic Patients - What Should I Do? |
Q33962221 | Elevated levels of alanine transaminase and triglycerides within normal limits are associated with fatty liver |
Q51560561 | Elevation of Vδ1 T cells in peripheral blood and livers of patients with primary biliary cholangitis. |
Q38744215 | Emerging drugs for the treatment of Primary Biliary Cholangitis |
Q92864604 | Emerging therapies for PBC |
Q91948597 | Epidemiological survey of antinuclear antibodies in healthy population and analysis of clinical characteristics of positive population |
Q38600118 | Epidemiology and Natural History of Primary Biliary Cholangitis in the Chinese: A Territory-Based Study in Hong Kong between 2000 and 2015. |
Q90269685 | Epidemiology and clinical course of primary biliary cholangitis in the Asia-Pacific region: a systematic review and meta-analysis |
Q60301070 | Epidemiology and liver transplantation burden of primary biliary cholangitis: a retrospective cohort study |
Q51137626 | Epidemiology and natural history of primary biliary cirrhosis in a Canadian health region: a population-based study. |
Q38565478 | Epigenetics and Primary Biliary Cirrhosis: a Comprehensive Review and Implications for Autoimmunity |
Q41361892 | Epigenetics in the Primary Biliary Cholangitis and Primary Sclerosing Cholangitis |
Q52648759 | Evaluation of classical and novel autoantibodies for the diagnosis of Primary Biliary Cholangitis-Autoimmune Hepatitis Overlap Syndrome (PBC-AIH OS). |
Q38183450 | Evaluation of histological staging systems for primary biliary cirrhosis: correlation with clinical and biochemical factors and significance of pathological parameters in prognostication |
Q42263045 | Evaluation of nail fold capillaroscopy findings in patients with primary biliary cirrhosis |
Q91844615 | Evaluation of the United Kingdom-primary biliary cholangitis and global primary biliary cholangitis group prognostic models for primary biliary cholangitis patients treated with ursodeoxycholic acid in the U.S. population |
Q39485889 | Evidence for the association between IgG-antimitochondrial antibody and biochemical response to ursodeoxycholic acid treatment in primary biliary cholangitis |
Q47156128 | Evidence from a familial case suggests maternal inheritance of primary biliary cholangitis |
Q91642039 | Evolving liver inflammation in biochemically normal individuals with anti-mitochondria antibodies |
Q90722135 | Exploration and Development of PPAR Modulators in Health and Disease: An Update of Clinical Evidence |
Q55332862 | External validation of the United Kingdom-primary biliary cholangitis risk scores of patients with primary biliary cholangitis treated with ursodeoxycholic acid. |
Q39177903 | Extrahepatic Manifestations of Primary Biliary Cholangitis |
Q84914116 | Extrahepatic conditions associated with primary biliary cirrhosis |
Q40130719 | Factors that Influence Health-Related Quality of Life in Patients with Primary Sclerosing Cholangitis. |
Q56971225 | Fatigue and pruritus at onset identify a more aggressive subset of primary biliary cirrhosis |
Q38858980 | Finding the cure for primary biliary cholangitis - Still waiting |
Q38313292 | Gene expression profiles of peripheral blood mononuclear cells in primary biliary cirrhosis |
Q37089325 | Genetic Association of PTPN22 Polymorphisms with Autoimmune Hepatitis and Primary Biliary Cholangitis in Japan |
Q37642274 | Genetic Contribution to the Pathogenesis of Primary Biliary Cholangitis. |
Q92229185 | Genetic association of E26 transformation specific sequence 1 polymorphisms with the susceptibility of primary biliary cholangitis in China |
Q43608312 | Genetic association of Fc receptor-like 3 polymorphisms with susceptibility to primary biliary cirrhosis: ethnic comparative study in Japanese and Italian patients |
Q43672317 | Genetic polymorphisms of OCT-1 confer susceptibility to severe progression of primary biliary cirrhosis in Japanese patients |
Q47827554 | Genetics and epigenetics in the pathogenesis of primary biliary cholangitis. |
Q36383011 | Genome-Wide Association Studies in Primary Biliary Cirrhosis |
Q92259854 | Genome-wide Association Studies of Specific Antinuclear Autoantibody Subphenotypes in Primary Biliary Cholangitis |
Q39034887 | Genome-wide association studies identify PRKCB as a novel genetic susceptibility locus for primary biliary cholangitis in the Japanese population |
Q28943429 | Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese population |
Q39213467 | Geoepidemiology and changing mortality in primary biliary cholangitis |
Q47205297 | Geoepidemiology of Primary Biliary Cholangitis: Lessons from Switzerland. |
Q56429943 | Guidelines for the management of primary biliary cirrhosis |
Q38085065 | Gut-liver axis: an immune link between celiac disease and primary biliary cirrhosis |
Q35309953 | Hair dyes as a risk for autoimmunity: from systemic lupus erythematosus to primary biliary cirrhosis |
Q55114620 | Hepatobiliary Manifestations and Complications in Inflammatory Bowel Disease: A Review. |
Q33966083 | Hepatobiliary complications of inflammatory bowel disease |
Q34147508 | Hepatocyte Death: A Clear and Present Danger |
Q54469701 | High levels of FCγR3A and PRF1 expression in peripheral blood mononuclear cells from patients with primary biliary cirrhosis. |
Q42947254 | High-dose ursodeoxycholic acid therapy for nonalcoholic steatohepatitis: a double-blind, randomized, placebo-controlled trial |
Q52925804 | High-throughput T-cell receptor sequencing across chronic liver diseases reveals distinct disease-associated repertoires. |
Q38554722 | Human autoimmune diseases: a comprehensive update |
Q44980851 | Human intrahepatic biliary epithelial cells engulf blebs from their apoptotic peers |
Q46332063 | Human leucocyte antigen alleles and haplotypes and their associations with antinuclear antibodies features in Chinese patients with primary biliary cirrhosis |
Q85002108 | Human leukocyte antigen class II molecules confer both susceptibility and progression in Japanese patients with primary biliary cirrhosis |
Q35131979 | Human leukocyte antigen in primary biliary cirrhosis: an old story now reviving |
Q33551867 | Human β-Defensin 2 in Primary Sclerosing Cholangitis |
Q36963978 | Humoral autoimmune response heterogeneity in the spectrum of primary biliary cirrhosis. |
Q38957567 | Imaging of autoimmune biliary disease |
Q24617796 | Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants |
Q53019283 | Immunologic derangement preceding clinical autoimmunity. |
Q37877588 | Immunological diseases of the pancreatico-hepatobiliary system: update on etiopathogenesis and cross-sectional imaging findings |
Q35614763 | Immunopathogenesis of primary biliary cirrhosis: an old wives' tale. |
Q37559266 | Immunosuppressive therapy in immune-mediated liver disease in the non-transplanted patient |
Q52925696 | In recurrent primary biliary cirrhosis after liver transplantation, biliary epithelial cells show increased expression of mitochondrial proteins. |
Q38374504 | Incidence and risk factors for hepatocellular carcinoma in primary biliary cirrhosis |
Q38795238 | Incidence of Primary Biliary Cholangitis in a Rural Midwestern Population |
Q49806997 | Increased cholestatic enzymes in two patients with long-term history of ulcerative colitis: consider primary biliary cholangitis not always primary sclerosing cholangitis |
Q45173055 | Increased expression of mitochondrial proteins associated with autophagy in biliary epithelial lesions in primary biliary cirrhosis |
Q36967742 | Increased mean platelet volume is related to histologic severity of primary biliary cirrhosis. |
Q56766238 | Increased numbers of circulating ICOS⁺ follicular helper T and CD38⁺ plasma cells in patients with newly diagnosed primary biliary cirrhosis |
Q60309961 | Increased red cell width distribution to lymphocyte ratio is a predictor of histologic severity in primary biliary cholangitis |
Q48529733 | Inflammatory myopathies associated with anti-mitochondrial antibodies |
Q37017406 | Interleukin-21 plays a critical role in the pathogenesis and severity of type I autoimmune hepatitis |
Q64105140 | Interleukin-33/ST2-Mediated Inflammation Plays a Critical Role in the Pathogenesis and Severity of Type I Autoimmune Hepatitis |
Q53098304 | Investigational drugs in phase II clinical trials for primary biliary cholangitis. |
Q88380162 | Is patient-reported outcome improved by nalfurafine hydrochloride in patients with primary biliary cholangitis and refractory pruritus? A post-marketing, single-arm, prospective study |
Q43155895 | Is there a role for tetrathiomolybdate in the treatment of primary biliary cirrhosis? |
Q38620686 | It is time to change primary biliary cirrhosis (PBC): New nomenclature from "cirrhosis" to "cholangitis", and upcoming treatment based on unveiling pathology |
Q35631405 | Itch and liver: management in primary care. |
Q46640079 | Keratin 19 demonstration of canal of Hering loss in primary biliary cirrhosis: "minimal change PBC"? |
Q39336142 | Large-scale characterization study of patients with antimitochondrial antibodies but nonestablished primary biliary cholangitis |
Q37738636 | Latest and emerging therapies for primary biliary cirrhosis and primary sclerosing cholangitis |
Q50097218 | Less Limb Muscle Involvement in Myositis Patients with Anti-Mitochondrial Antibodies |
Q54254957 | Liver Illness and Psoriatic Patients. |
Q36320523 | Liver Transplantation for Cholestatic Liver Diseases in Adults |
Q37743450 | Liver biopsy diagnosis of hepatitis: clues to clinically-meaningful reporting |
Q37140617 | Liver damage in primary biliary cirrhosis and accompanied by primary Sjögren's syndrome: a retrospective pilot study |
Q37334112 | Liver diseases in pregnancy: diseases not unique to pregnancy |
Q38123133 | Liver transplantation and autoimmune liver diseases |
Q39584105 | Long-Term Fenofibrate Treatment in Primary Biliary Cholangitis Improves Biochemistry but Not the UK-PBC Risk Score |
Q92685166 | Long-term efficacy and safety of obeticholic acid for patients with primary biliary cholangitis: 3-year results of an international open-label extension study |
Q38699595 | Long-term outcomes in antimitochondrial antibody negative primary biliary cirrhosis. |
Q35745075 | Low Serum Hepcidin in Patients with Autoimmune Liver Diseases |
Q40808835 | Low incidence of primary biliary cirrhosis (PBC) in the first-degree relatives of PBC probands after 8 years of follow-up |
Q54980590 | Low risk of hepatotoxicity from rifampicin when used for cholestatic pruritus: a cross-disease cohort study. |
Q50142593 | Lymphocytes contribute to biliary injury and fibrosis in experimental xenobiotic-induced cholestasis |
Q55498617 | Magnetic resonance imaging evidence of hippocampal structural changes in patients with primary biliary cholangitis. |
Q47787189 | Major Hepatic Complications in Ursodeoxycholic Acid-Treated Patients With Primary Biliary Cholangitis: Risk Factors and Time Trends in Incidence and Outcome |
Q40623611 | Management of pruritus in patients with cholestatic liver disease. |
Q89285900 | Managing PBC: Expanding the Provider Comfort Zone |
Q36009282 | Membranous Nephropathy Associated With Immunological Disorder-Related Liver Disease: A Retrospective Study of 10 Cases |
Q33882608 | Meta-analysis assessment of GP210 and SP100 for the diagnosis of primary biliary cirrhosis |
Q43013514 | Methotrexate in patients with primary biliary cirrhosis who respond incompletely to treatment with ursodeoxycholic acid |
Q36144748 | MiR-139-5p is associated with inflammatory regulation through c-FOS suppression, and contributes to the progression of primary biliary cholangitis. |
Q41492969 | MicroRNA-223 and microRNA-21 in peripheral blood B cells associated with progression of primary biliary cholangitis patients |
Q47567609 | Milder disease stage in patients with primary biliary cholangitis over a 44-year period: A changing natural history. |
Q50130002 | Modern treatment of primary biliary cholangitis |
Q37631707 | Modulation of the Unfolded Protein Response by Tauroursodeoxycholic Acid Counteracts Apoptotic Cell Death and Fibrosis in a Mouse Model for Secondary Biliary Liver Fibrosis |
Q36086498 | Molecular diagnostic testing for primary biliary cholangitis |
Q57119171 | Molecular magnetic resonance imaging accurately measures the antifibrotic effect of EDP-305, a novel farnesoid X receptor agonist |
Q88035378 | Monoclonal gammopathy in rheumatic diseases |
Q46186395 | Mouse model of primary biliary cirrhosis with progressive fibrosis: are we there yet? |
Q35038847 | Multiple autoimmune propensity and B-non-hodgkin lymphoma: cause or effect? |
Q41615335 | Multiple genetic variants associated with primary biliary cirrhosis in a Han Chinese population |
Q38388403 | Mycobacteria and autoimmunity |
Q57110523 | NGM282 for Treatment of Patients With Primary Biliary Cholangitis: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial |
Q37355843 | Natural history and management of primary biliary cirrhosis |
Q26824664 | Network meta-analysis of randomized controlled trials: efficacy and safety of UDCA-based therapies in primary biliary cirrhosis |
Q48218121 | New simple prognostic score for primary biliary cirrhosis: Albumin-bilirubin score |
Q46182874 | New therapeutics in primary biliary cirrhosis: will there ever be light? |
Q38261577 | New therapies for primary biliary cirrhosis |
Q58708624 | Non-alcoholic steatohepatitis-like pattern in liver biopsy of rheumatoid arthritis patients with persistent transaminitis during low-dose methotrexate treatment |
Q41042363 | Non-invasive assessment of liver fibrosis using two-dimensional shear wave elastography in patients with autoimmune liver diseases |
Q44966935 | Noninvasive elastography-based assessment of liver fibrosis progression and prognosis in primary biliary cirrhosis |
Q26748613 | Novel bile acid therapeutics for the treatment of chronic liver diseases |
Q42375647 | Novel strategies and therapeutic options for the management of primary biliary cholangitis |
Q38342107 | Novel therapeutic targets in primary biliary cirrhosis |
Q89910702 | Nutritional Management of Cholestasis |
Q55165714 | Obeticholic Acid: A Farnesoid X Receptor Agonist for Primary Biliary Cholangitis. |
Q38911238 | Obeticholic acid for the treatment of primary biliary cholangitis |
Q28072209 | Obeticholic acid for the treatment of primary biliary cholangitis in adult patients: clinical utility and patient selection |
Q38628470 | Obeticholic acid for the treatment of primary biliary cirrhosis |
Q38626000 | Obeticholic acid, a selective farnesoid X receptor agonist, regulates bile acid homeostasis in sandwich-cultured human hepatocytes. |
Q50155645 | Occurrence of Jaundice Following Simultaneous Ursodeoxycholic Acid Cessation and Obeticholic Acid Initiation |
Q39216355 | Old and new treatments for primary biliary cholangitis |
Q34415757 | Ongoing activation of autoantigen-specific B cells in primary biliary cirrhosis |
Q28087211 | Optimal drug regimens for primary biliary cirrhosis: a systematic review and network meta-analysis |
Q37963978 | Optimizing biochemical markers as endpoints for clinical trials in primary biliary cirrhosis |
Q89538006 | Osteoporosis in Primary Biliary Cholangitis: Prevalence, Impact and Management Challenges |
Q57168372 | Osteoporosis in primary biliary cholangitis |
Q37824300 | Overcoming a "probable" diagnosis in antimitochondrial antibody negative primary biliary cirrhosis: study of 100 sera and review of the literature |
Q59384428 | Overlap syndrome: A real syndrome? |
Q36442097 | Overlapping of primary biliary cirrhosis and small duct primary sclerosing cholangitis: first case report |
Q87561627 | Oxidative stress and antioxidant status in patients with autoimmune liver diseases |
Q39782708 | PML nuclear body component Sp140 is a novel autoantigen in primary biliary cirrhosis |
Q37993126 | Pathogenesis and management of pruritus in cholestatic liver disease |
Q34623557 | Pathogenesis of Cholestatic Liver Disease and Therapeutic Approaches |
Q93140232 | Pathological patterns of biliary disease |
Q37191674 | Pathway-based analysis of primary biliary cirrhosis genome-wide association studies |
Q82719034 | Performance parameters of the conventional serological markers for autoimmune hepatitis |
Q38738566 | Pharmacological interventions for primary biliary cholangitis: an attempted network meta-analysis. |
Q37681567 | Pharmacological treatment of biliary cirrhosis with ursodeoxycholic acid |
Q24186852 | Pharmacological treatments for primary biliary cirrhosis: a network meta-analysis |
Q51636366 | Pilot study: fenofibrate for patients with primary biliary cirrhosis and an incomplete response to ursodeoxycholic acid |
Q50003369 | Platelet count to spleen thickness ratio is related to histologic severity of primary biliary cholangitis |
Q38162283 | Polymorphisms in the vitamin D receptor gene and risk of primary biliary cirrhosis: a meta-analysis |
Q35309882 | Popular and unpopular infectious agents linked to primary biliary cirrhosis. |
Q48312123 | Possible involvement of chemokine C-C receptor 7- programmed cell death-1+ follicular helper T-cell subset in the pathogenesis of autoimmune hepatitis. |
Q38063171 | Potential Roles for Infectious Agents in the Pathophysiology of Primary Biliary Cirrhosis: What's New? |
Q64230889 | Practical strategies for pruritus management in the obeticholic acid-treated patient with PBC: proceedings from the 2018 expert panel |
Q35309854 | Predicting and preventing autoimmunity: the case of anti-mitochondrial antibodies |
Q47114292 | Prediction of hepatocellular carcinoma development by aminotransferase to platelet ratio index in primary biliary cholangitis |
Q33978160 | Pregnancy with portal hypertension |
Q89070694 | Prevalence of and Factors Associated With Minimal Hepatic Encephalopathy in Patients With Cirrhosis of Liver |
Q40055616 | Prevalence of pruritus in patients with chronic liver disease: a multicenter study |
Q89639221 | Preventative care in cholestatic liver disease: Pearls for the specialist and subspecialist |
Q38998320 | Primary Biliary Cholangitis Associated with Skin Disorders: A Case Report and Review of the Literature |
Q57114658 | Primary Biliary Cholangitis in Medicare Population: The Impact on Mortality and Resource Utilization |
Q39047912 | Primary Biliary Cholangitis: Disease Pathogenesis and Implications for Established and Novel Therapeutics |
Q26781780 | Primary Biliary Cirrhosis and Primary Sclerosing Cholangitis: a Review Featuring a Women's Health Perspective |
Q50954296 | Primary biliary cholangitis associated with warm autoimmune hemolytic anemia. |
Q90014773 | Primary biliary cholangitis presenting as acute ischemic stroke: A rare association |
Q64286582 | Primary biliary cholangitis with contemporary presence of anti-mithocondrial and anti-rods and rings autoantibodies: literature first case |
Q54390436 | Primary biliary cholangitis: new treatments for an old disease. |
Q56428272 | Primary biliary cirrhosis |
Q57141930 | Primary biliary cirrhosis |
Q85213554 | Primary biliary cirrhosis |
Q36599248 | Primary biliary cirrhosis and Sjögren's syndrome: autoimmune epithelitis |
Q38058979 | Primary biliary cirrhosis and bile acids |
Q34637500 | Primary biliary cirrhosis and cancer risk: a systematic review and meta-analysis |
Q26853145 | Primary biliary cirrhosis and liver transplantation |
Q37266330 | Primary biliary cirrhosis in HBV and HCV patients: Clinical characteristics and outcome |
Q38192045 | Primary biliary cirrhosis in adults |
Q50631086 | Primary biliary cirrhosis-autoimmune hepatitis overlap syndrome: simplified criteria may be effective in the diagnosis in Chinese patients. |
Q84773471 | Primary biliary cirrhosis/autoimmune hepatitis overlap syndrome developing in a patient with systemic lupus erythematosus: a case report and review of the literature |
Q26799419 | Primary biliary cirrhosis: From bench to bedside |
Q26853649 | Primary biliary cirrhosis: Pathophysiology, clinical presentation and therapy |
Q35038800 | Primary biliary cirrhosis: family stories |
Q43987255 | Primary biliary cirrhosis: proposal for a new simple histological scoring system |
Q38554677 | Primary biliary cirrhosis: safety and benefits of established and emerging therapies |
Q49712375 | Primary cutaneous amyloidosis associated with autoimmune hepatitis-primary biliary cirrhosis overlap syndrome and Sjögren syndrome: A case report |
Q37799533 | Primary sclerosing cholangitis: overview and update |
Q33920325 | Prognostic Factors for Transplant-Free Survival and Validation of Prognostic Models in Chinese Patients with Primary Biliary Cholangitis Receiving Ursodeoxycholic Acid |
Q40311999 | Prognostic Models for Survival in Patients with Stable Cirrhosis: A Multicenter Cohort Study |
Q83627142 | Prognostic factors and survival analysis of antimitochondrial antibody-positive primary biliary cirrhosis in Chinese patients |
Q37072380 | Proposed therapies in primary biliary cholangitis |
Q46933007 | Prospective evaluation of ursodeoxycholic acid withdrawal in patients with primary sclerosing cholangitis |
Q38210112 | Pruritus in cholestasis: facts and fiction. |
Q36134061 | Quantitation of the Rank-Rankl Axis in Primary Biliary Cholangitis |
Q35998928 | RITPBC: B-cell depleting therapy (rituximab) as a treatment for fatigue in primary biliary cirrhosis: study protocol for a randomised controlled trial |
Q34464043 | Recent advances in the development of farnesoid X receptor agonists |
Q28076353 | Recent advances in the diagnosis and treatment of primary biliary cholangitis |
Q33719935 | Recent advances in the management of pruritus in chronic liver diseases |
Q26748537 | Recent advances in understanding and managing cholestasis |
Q93140872 | Recurrence of autoimmune hepatitis, primary biliary cirrhosis, and primary sclerosing cholangitis after transplantation |
Q36822889 | Red Blood Cell Distribution Width to Platelet Ratio is Related to Histologic Severity of Primary Biliary Cirrhosis |
Q33911547 | Reduced coffee consumption among individuals with primary sclerosing cholangitis but not primary biliary cirrhosis. |
Q43940290 | Reduced hepatitis B and D viral entry using clinically applied drugs as novel inhibitors of the bile acid transporter NTCP. |
Q90126673 | Reduction and stabilization of bilirubin with obeticholic acid treatment in patients with primary biliary cholangitis |
Q37314381 | Refractory pruritus in primary biliary cirrhosis |
Q38974002 | Reversal of liver cirrhosis: current evidence and expectations |
Q38174167 | Review article: controversies in the management of primary biliary cirrhosis and primary sclerosing cholangitis |
Q26864272 | Review article: the management of autoimmune hepatitis beyond consensus guidelines |
Q36369284 | Rheumatoid arthritis and primary biliary cirrhosis: cause, consequence, or coincidence? |
Q55395737 | Risk of Cardiovascular Events in Patients with Primary Biliary Cholangitis - Systematic Review. |
Q42363647 | Risk of liver disease in methotrexate treated patients |
Q26796355 | Risk stratification in autoimmune cholestatic liver diseases: Opportunities for clinicians and trialists |
Q88780685 | Rituximab Is Ineffective for Treatment of Fatigue in Primary Biliary Cholangitis: A Phase 2 Randomized Controlled Trial |
Q36248162 | Role for mycobacterial infection in pathogenesis of primary biliary cirrhosis? |
Q95942116 | Roles of trained immunity in the pathogenesis of cholangiopathies: a novel therapeutic target |
Q41702160 | S100A12 expression in patients with primary biliary cirrhosis |
Q38837130 | SP140L, an Evolutionarily Recent Member of the SP100 Family, Is an Autoantigen in Primary Biliary Cirrhosis |
Q37598572 | STAT4 gene polymorphisms are associated with susceptibility and ANA status in primary biliary cirrhosis |
Q34644916 | Sarcoidosis and primary biliary cirrhosis association: report of a new case |
Q38390677 | Scandinavian epidemiological research in gastroenterology and hepatology |
Q46651249 | Scratching the surface of cholestatic itch treatments |
Q94326725 | Serological tests for primary biliary cholangitis |
Q55009231 | Serum Autotaxin Is a Useful Disease Progression Marker in Patients with Primary Biliary Cholangitis. |
Q37725466 | Serum Golgi protein 73 is not a suitable diagnostic marker for hepatocellular carcinoma |
Q36151445 | Serum IgG subclasses in autoimmune diseases |
Q41933128 | Serum Wisteria Floribunda Agglutinin-Positive Mac-2 Binding Protein Could Not Always Predict Early Cirrhosis in Non-Viral Liver Diseases |
Q41009473 | Serum Wisteria floribunda Agglutinin-Positive Mac-2-Binding Protein Level Predicts Liver Fibrosis and Prognosis in Primary Biliary Cirrhosis |
Q35674098 | Serum cell death biomarkers for prediction of liver fibrosis and poor prognosis in primary biliary cirrhosis |
Q48145461 | Serum levels of a cell death biomarker predict the development of cirrhosis-related conditions in primary biliary cholangitis. |
Q34944763 | Serum metabolic signatures of primary biliary cirrhosis and primary sclerosing cholangitis. |
Q34408701 | Serum microRNAs as potential biomarkers of primary biliary cirrhosis |
Q43230366 | Severe coagulopathy caused by rifampicin in patients with primary sclerosing cholangitis and refractory pruritus |
Q36014535 | Sex differences associated with primary biliary cirrhosis. |
Q38190931 | Shear wave elastography for liver stiffness measurement in clinical sonographic examinations: evaluation of intraobserver reproducibility, technical failure, and unreliable stiffness measurements |
Q48218731 | Skin Manifestations Associated with Autoimmune Liver Diseases: a Systematic Review |
Q33419647 | Stratification of hepatocellular carcinoma risk in primary biliary cirrhosis: a multicentre international study |
Q34303048 | Study of liver cirrhosis over ten consecutive years in Southern China |
Q33647458 | Subtle presentation of active primary biliary cirrhosis in chronic hepatitis B: a case report |
Q54936764 | Suitability of the simplified autoimmune hepatitis score for the diagnosis of autoimmune hepatitis in a German cohort. |
Q58722495 | Symptoms and health-related quality of life in Japanese patients with primary biliary cholangitis |
Q52955409 | Synthesis of diastereomerically pure Lys(Nε-lipoyl) building blocks and their use in Fmoc/tBu solid phase synthesis of lipoyl-containing peptides for diagnosis of primary biliary cirrhosis. |
Q36413970 | Tauroursodeoxycholic acid dampens oncogenic apoptosis induced by endoplasmic reticulum stress during hepatocarcinogen exposure |
Q37526157 | Tauroursodeoxycholic acid reduces ER stress by regulating of Akt-dependent cellular prion protein |
Q52624982 | The British Society of Gastroenterology/UK-PBC primary biliary cholangitis treatment and management guidelines. |
Q46847997 | The Challenges of Nutritional Assessment in Cirrhosis |
Q35942610 | The Cholangiopathies |
Q47278009 | The Clinical Significance of GP73 in Immunologically Mediated Chronic Liver Diseases: Experimental Data and Literature Review |
Q59384433 | The Diagnosis and Classification of Immune-Mediated Biliary Diseases |
Q91790202 | The Enlargement of Abdominal Lymph Nodes Is a Characteristic of Autoimmune Liver Disease |
Q41303819 | The Natural History and Prognosis of Primary Biliary Cirrhosis with Clinical Features of Autoimmune Hepatitis |
Q40681087 | The UK-PBC risk scores: Derivation and validation of a scoring system for long-term prediction of end-stage liver disease in primary biliary cholangitis. |
Q26830032 | The X-factor in primary biliary cirrhosis: monosomy X and xenobiotics |
Q34438127 | The association between bile salt export pump single-nucleotide polymorphisms and primary biliary cirrhosis susceptibility and ursodeoxycholic acid response |
Q38355697 | The coexistence of Sjögren's syndrome and primary biliary cirrhosis: a comprehensive review |
Q35833175 | The diagnosis and treatment of primary biliary cirrhosis |
Q26829493 | The diagnosis of primary biliary cirrhosis |
Q53237682 | The dynamic and clinical significance of autoantibodies and immunoglobulins in liver transplant recipients. |
Q37317828 | The dynamic biliary epithelia: molecules, pathways, and disease |
Q39284642 | The emerging role of mast cells in liver disease |
Q90293731 | The expression and clinical significance of serum IL-17 in patients with primary biliary cirrhosis |
Q35939141 | The expression of miR-125b-5p is increased in the serum of patients with chronic hepatitis B infection and inhibits the detection of hepatitis B virus surface antigen. |
Q36573783 | The immunopathology of liver granulomas in primary biliary cirrhosis |
Q38017976 | The immunophysiology and apoptosis of biliary epithelial cells: primary biliary cirrhosis and primary sclerosing cholangitis |
Q47285348 | The impact of biopsychosocial factors on quality of life: women with primary biliary cirrhosis on waiting list and post liver transplantation |
Q37371109 | The inter-relationship of symptom severity and quality of life in 2055 patients with primary biliary cholangitis. |
Q38622370 | The management of autoimmunity in patients with cholestatic liver diseases |
Q37714640 | The modulation of co-stimulatory molecules by circulating exosomes in primary biliary cirrhosis |
Q38037392 | The overlap syndromes of autoimmune hepatitis |
Q46813053 | The risk predictive values of UK-PBC and GLOBE scoring system in Chinese patients with primary biliary cholangitis: the additional effect of anti-gp210. |
Q43589988 | The specificity of fatigue in primary biliary cirrhosis: evaluation of a large clinic practice |
Q88164317 | The utility of IgG, IgM, and CD138 immunohistochemistry in the evaluation of autoimmune liver diseases |
Q35187219 | The value of MRI in the diagnosis of primary biliary cirrhosis and assessment of liver fibrosis |
Q90599038 | Therapeutic Effects of Apamin as a Bee Venom Component for Non-Neoplastic Disease |
Q39816216 | Therapeutic Equivalence of Ursodeoxycholic Acid Tablets and Ursodeoxycholic Acid Capsules for the Treatment of Primary Biliary Cirrhosis |
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