Primary Biliary Cholangitis: Promising Emerging Innovative Therapies and Their Impact on GLOBE Scores
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[1] H. Yoshiji,et al. Benefit of glucosyl Hesperidin in patients with primary biliary cholangitis: A multicenter, open-label, randomized control study , 2022, Medicine.
[2] R. von Maltzahn,et al. GLIMMER: A randomized Phase 2b dose-ranging trial of linerixibat in primary biliary cholangitis patients with pruritus. , 2022, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.
[3] Changcun Guo,et al. Efficacy and safety of fenofibrate addition therapy in patients with cirrhotic primary biliary cholangitis with incomplete response to ursodeoxycholic acid , 2022, Hepatology communications.
[4] K. Kowdley,et al. Application of the Latest Advances in Evidence-Based Medicine in Primary Biliary Cholangitis , 2022, The American journal of gastroenterology.
[5] F. Nevens,et al. Greater Transplant-free Survival in Patients Receiving Obeticholic Acid for Primary Biliary Cholangitis in a Clinical Trial Setting Compared to Real-World External Controls. , 2022, Gastroenterology.
[6] C. Xi,et al. Efficacy and safety of fenofibrate add-on therapy in patients with primary biliary cholangitis refractory to ursodeoxycholic acid: A retrospective study and updated meta-analysis , 2022, Frontiers in Pharmacology.
[7] K. Kowdley,et al. Farnesoid X receptor agonist tropifexor attenuates cholestasis in a randomised trial in patients with primary biliary cholangitis , 2022, JHEP reports : innovation in hepatology.
[8] C. Mcwherter,et al. 323: SELADELPAR TREATMENT OF PATIENTS WITH PRIMARY BILIARY CHOLANGITIS (PBC) FOR 2 YEARS IMPROVES THE GLOBE PBC SCORE AND PREDICTS IMPROVED TRANSPLANT-FREE SURVIVAL , 2022, Gastroenterology.
[9] Nannan Xu,et al. Setanaxib (GKT137831) Ameliorates Doxorubicin-Induced Cardiotoxicity by Inhibiting the NOX1/NOX4/Reactive Oxygen Species/MAPK Pathway , 2022, Frontiers in Pharmacology.
[10] Rohit Kohli,et al. The Role of FGF19 and MALRD1 in Enterohepatic Bile Acid Signaling , 2022, Frontiers in Endocrinology.
[11] C. Mcwherter,et al. Seladelpar improved measures of pruritus, sleep, and fatigue and decreased serum bile acids in patients with primary biliary cholangitis , 2021, Liver international : official journal of the International Association for the Study of the Liver.
[12] K. Gottlieb,et al. Baricitinib and primary biliary cholangitis , 2021, Journal of translational autoimmunity.
[13] Guangzhi Zhang,et al. Combination antiretroviral therapy improves recurrent primary biliary cholangitis following liver transplantation , 2021, Liver international : official journal of the International Association for the Study of the Liver.
[14] Ying Han,et al. Fenofibrate improves GLOBE and UK-PBC scores and histological features in primary biliary cholangitis. , 2021, Minerva medica.
[15] F. Carrat,et al. Association of bezafibrate with transplant-free survival in patients with primary biliary cholangitis. , 2021, Journal of hepatology.
[16] L. Muñoz-Espinosa,et al. A Multicenter, Open-Label, Single-Arm Study to Evaluate the Efficacy and Safety of Saroglitazar in Patients With Primary Biliary Cholangitis , 2021, Clinical and translational gastroenterology.
[17] Results of a Phase 2, Prospective, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety, Tolerability, and Efficacy of Saroglitazar Magnesium in Patients With Primary Biliary Cholangitis (EPICS). , 2021, Gastroenterology & hepatology.
[18] G. Hirschfield. ENHANCE: Safety and Efficacy of Seladelpar in Patients With Primary Biliary Cholangitis-A Phase 3, International, Randomized, Placebo-Controlled Study. , 2021, Gastroenterology & hepatology.
[19] D. Magrez,et al. A randomized placebo-controlled trial of elafibranor in patients with primary biliary cholangitis and incomplete response to UDCA. , 2021, Journal of hepatology.
[20] N. Shen,et al. Fibrates for the treatment of pruritus in primary biliary cholangitis: a systematic review and meta-analysis. , 2021, Annals of palliative medicine.
[21] A. Tanaka. Current understanding of primary biliary cholangitis , 2020, Clinical and molecular hepatology.
[22] J. Jia,et al. Regional variation and temporal trend of primary biliary cholangitis epidemiology: A systematic review and meta‐analysis , 2020, Journal of gastroenterology and hepatology.
[23] A. Floreani,et al. Obeticholic acid is associated with improvements in AST-to-platelet ratio index and GLOBE score in patients with primary biliary cholangitis , 2020, JHEP reports : innovation in hepatology.
[24] J. Trotter,et al. Efficacy and Safety of Aldafermin, an Engineered FGF19 Analog, in a Randomized, Double-Blind, Placebo-Controlled Trial of Patients With Nonalcoholic Steatohepatitis. , 2020, Gastroenterology.
[25] M. Avila,et al. S-adenosyl-L-methionine (SAMe) halts the autoimmune response in patients with primary biliary cholangitis (PBC) via antioxidant and S-glutathionylation processes in cholangiocytes. , 2020, Biochimica et biophysica acta. Molecular basis of disease.
[26] P. Kamath,et al. Liver Injury in Patients With Cholestatic Liver Disease Treated With Obeticholic Acid , 2020, Hepatology.
[27] V. Wong,et al. Cilofexor, a Nonsteroidal FXR Agonist, in Patients With Noncirrhotic NASH: A Phase 2 Randomized Controlled Trial , 2020, Hepatology.
[28] J. Drenth,et al. Elafibranor: a potential drug for the treatment of nonalcoholic steatohepatitis (NASH) , 2020, Expert opinion on investigational drugs.
[29] M. Wagner,et al. Drug Therapies for Chronic Cholestatic Liver Diseases. , 2020, Annual review of pharmacology and toxicology.
[30] B. Neuschwander‐Tetri,et al. Impact of Obeticholic Acid on the Lipoprotein Profile in Patients with Nonalcoholic Steatohepatitis. , 2020, Journal of hepatology.
[31] H. Yoshiji,et al. Bezafibrate Improves GLOBE and UK‐PBC Scores and Long‐Term Outcomes in Patients With Primary Biliary Cholangitis , 2019, Hepatology.
[32] A. Quaas,et al. Sex differences in clinical presentation and prognosis in patients with primary biliary cholangitis , 2019, Scandinavian journal of gastroenterology.
[33] F. Nevens,et al. Ursodeoxycholic acid therapy and liver transplant-free survival in patients with primary biliary cholangitis. , 2019, Journal of hepatology.
[34] M. Gershwin,et al. Therapeutic trials of biologics in primary biliary cholangitis: An open label study of abatacept and review of the literature. , 2019, Journal of autoimmunity.
[35] K. Kowdley,et al. The Nonsteroidal Farnesoid X Receptor Agonist Cilofexor (GS‐9674) Improves Markers of Cholestasis and Liver Injury in Patients With Primary Sclerosing Cholangitis , 2019, Hepatology.
[36] M. Karsdal,et al. Effect of NGM282, an FGF19 analogue, in primary sclerosing cholangitis: A multicenter, randomized, double-blind, placebo-controlled phase II trial. , 2019, Journal of hepatology.
[37] G. Hirschfield,et al. A Practical Review of Primary Biliary Cholangitis for the Gastroenterologist. , 2019, Gastroenterology & hepatology.
[38] S. Medendorp,et al. A Randomized, Controlled, Phase 2 Study of Maralixibat in the Treatment of Itching Associated With Primary Biliary Cholangitis , 2019, Hepatology communications.
[39] J. Boyer,et al. Primary Biliary Cholangitis: 2018 Practice Guidance from the American Association for the Study of Liver Diseases , 2018, Hepatology.
[40] Y. Kim,et al. Prognostic Value of Biochemical Response Models for Primary Biliary Cholangitis and the Additional Role of the Neutrophil-to-Lymphocyte Ratio , 2018, Gut and liver.
[41] M. Krawczyk,et al. Effect of S-adenosyl-L-methionine on liver biochemistry and quality of life in patients with primary biliary cholangitis treated with ursodeoxycholic acid. A prospective, open label pilot study. , 2018, Journal of gastrointestinal and liver diseases : JGLD.
[42] J. Jia,et al. Efficacy and safety of fenofibrate add-on therapy for patients with primary biliary cholangitis and a suboptimal response to UDCA. , 2018, Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva.
[43] A. Parés. Primary biliary cholangitis. , 2018, Medicina clinica.
[44] B. Leggett,et al. NGM282 for Treatment of Patients With Primary Biliary Cholangitis: A Multicenter, Randomized, Double‐Blind, Placebo‐Controlled Trial , 2018, Hepatology communications.
[45] A. Goel,et al. Natural History of Primary Biliary Cholangitis in the Ursodeoxycholic Acid Era: Role of Scoring Systems. , 2018, Clinics in liver disease.
[46] V. de Lédinghen,et al. A Placebo‐Controlled Trial of Bezafibrate in Primary Biliary Cholangitis , 2018, The New England journal of medicine.
[47] M. Carbone,et al. Risk stratification and prognostic modelling in primary biliary cholangitis. , 2018, Best practice & research. Clinical gastroenterology.
[48] R. Chapman,et al. NI‐0801, an anti‐chemokine (C‐X‐C motif) ligand 10 antibody, in patients with primary biliary cholangitis and an incomplete response to ursodeoxycholic acid , 2018, Hepatology communications.
[49] Yasunori Sato,et al. An impaired biliary bicarbonate umbrella may be involved in dysregulated autophagy in primary biliary cholangitis , 2018, Laboratory Investigation.
[50] D. Aschenbrenner. Excessive Dosing of Obeticholic Acid May Increase Risk of Liver Damage. , 2018, The American journal of nursing.
[51] R. Chapman,et al. A randomized trial of obeticholic acid monotherapy in patients with primary biliary cholangitis , 2018, Hepatology.
[52] W. Wahli,et al. Dual PPARα/γ agonist saroglitazar improves liver histopathology and biochemistry in experimental NASH models , 2017, Liver international : official journal of the International Association for the Study of the Liver.
[53] Robert L. Martin,et al. Seladelpar (MBX-8025), a selective PPAR-δ agonist, in patients with primary biliary cholangitis with an inadequate response to ursodeoxycholic acid: a double-blind, randomised, placebo-controlled, phase 2, proof-of-concept study. , 2017, The lancet. Gastroenterology & hepatology.
[54] Xiaoli Fan,et al. Underestimated Male Prevalence of Primary Biliary Cholangitis in China: Results of a 16-yr cohort study involving 769 patients , 2017, Scientific Reports.
[55] G. Hirschfield,et al. EASL Clinical Practice Guidelines: The diagnosis and management of patients with primary biliary cholangitis. , 2017, Journal of hepatology.
[56] S. Kersten,et al. The role and regulation of the peroxisome proliferator activated receptor alpha in human liver. , 2017, Biochimie.
[57] Ying-Qiu Huang. Recent advances in the diagnosis and treatment of primary biliary cholangitis , 2016, World journal of hepatology.
[58] J. Reguła,et al. A Placebo-Controlled Trial of Obeticholic Acid in Primary Biliary Cholangitis. , 2016, The New England journal of medicine.
[59] A. Khanna,et al. Long-Term Fenofibrate Treatment in Primary Biliary Cholangitis Improves Biochemistry but Not the UK-PBC Risk Score , 2016, Digestive Diseases and Sciences.
[60] K. Lindor,et al. Ustekinumab for patients with primary biliary cholangitis who have an inadequate response to ursodeoxycholic acid: A proof‐of‐concept study , 2016, Hepatology.
[61] C. Bowlus,et al. Management of symptom complexes in primary biliary cholangitis , 2016, Current opinion in gastroenterology.
[62] C. Paulusma,et al. Soluble Adenylyl Cyclase Regulates Bile Salt‐Induced Apoptosis in Human Cholangiocytes , 2016, Hepatology.
[63] D. Brenner,et al. The Role of NADPH Oxidases (NOXs) in Liver Fibrosis and the Activation of Myofibroblasts , 2016, Front. Physiol..
[64] A. Burroughs,et al. University of Birmingham Development and Validation of a Scoring System to Predict Outcomes of Patients With Primary Biliary Cirrhosis Receiving Ursodeoxycholic Acid Therapy , 2022 .
[65] David C. Jones,et al. Changing nomenclature for PBC: from ‘cirrhosis’ to ‘cholangitis’ , 2015, Gut.
[66] B. Neuschwander‐Tetri. Targeting the FXR nuclear receptor to treat liver disease. , 2015, Gastroenterology.
[67] M. Yamada,et al. A Prospective Randomized Controlled Study of Long-Term Combination Therapy Using Ursodeoxycholic Acid and Bezafibrate in Patients With Primary Biliary Cirrhosis and Dyslipidemia , 2015, The American Journal of Gastroenterology.
[68] A. Burroughs,et al. Levels of alkaline phosphatase and bilirubin are surrogate end points of outcomes of patients with primary biliary cirrhosis: an international follow-up study. , 2014, Gastroenterology.
[69] Q. Han,et al. Allogeneic bone marrow mesenchymal stem cell transplantation in patients with UDCA-resistant primary biliary cirrhosis. , 2014, Stem cells and development.
[70] S. Lens,et al. Bezafibrate normalizes alkaline phosphatase in primary biliary cirrhosis patients with incomplete response to ursodeoxycholic acid , 2014, Liver international : official journal of the International Association for the Study of the Liver.
[71] Ying Sun,et al. A pilot study of umbilical cord‐derived mesenchymal stem cell transfusion in patients with primary biliary cirrhosis , 2013, Journal of gastroenterology and hepatology.
[72] A. Burroughs,et al. Impact of primary biliary cirrhosis on perceived quality of life: The UK‐PBC national study , 2013, Hepatology.
[73] M. Swain,et al. B-Cell Depletion With Rituximab in Patients With Primary Biliary Cirrhosis Refractory to Ursodeoxycholic Acid , 2013, The American Journal of Gastroenterology.
[74] Y. Nakanuma,et al. PPARγ ligand attenuates portal inflammation in the MRL-lpr mouse: a new strategy to restrain cholangiopathy in primary biliary cirrhosis , 2013, Medical Molecular Morphology.
[75] J. Gustafsson,et al. Liver X receptor β and peroxisome proliferator‐activated receptor δ regulate cholesterol transport in murine cholangiocytes , 2012, Hepatology.
[76] K. Lindor,et al. Biochemical and immunologic effects of rituximab in patients with primary biliary cirrhosis and an incomplete response to ursodeoxycholic acid , 2012, Hepatology.
[77] J. Prieto,et al. Ursodeoxycholic Acid Is Conjugated with Taurine to Promote Secretin-Stimulated Biliary Hydrocholeresis in the Normal Rat , 2011, PloS one.
[78] O. Chazouilleres,et al. Early primary biliary cirrhosis: biochemical response to treatment and prediction of long-term outcome. , 2011, Journal of hepatology.
[79] S. Kliewer,et al. FGF15/19 regulates hepatic glucose metabolism by inhibiting the CREB-PGC-1α pathway. , 2011, Cell metabolism.
[80] U. Beuers,et al. Pathophysiology and current management of pruritus in liver disease. , 2011, Clinics and research in hepatology and gastroenterology.
[81] K. Lindor,et al. Pilot study: fenofibrate for patients with primary biliary cirrhosis and an incomplete response to ursodeoxycholic acid , 2011, Alimentary pharmacology & therapeutics.
[82] T. Arenovich,et al. Baseline Ductopenia and Treatment Response Predict Long-Term Histological Progression in Primary Biliary Cirrhosis , 2010, The American Journal of Gastroenterology.
[83] G. Gores,et al. Biliary apotopes and anti-mitochondrial antibodies activate innate immune responses in primary biliary cirrhosis. , 2010, Hepatology.
[84] A. Chawla. Control of macrophage activation and function by PPARs. , 2010, Circulation research.
[85] M. Elisaf,et al. Fenofibrate in Primary Biliary Cirrhosis: A Pilot Study , 2010, The open cardiovascular medicine journal.
[86] B. Lemon,et al. FGF19-induced Hepatocyte Proliferation Is Mediated through FGFR4 Activation , 2009, The Journal of Biological Chemistry.
[87] Lawrence Steinman,et al. PPAR-δ senses and orchestrates clearance of apoptotic cells to promote tolerance , 2009, Nature Medicine.
[88] D. Vergani,et al. New ELISA for detecting primary biliary cirrhosis-specific antimitochondrial antibodies. , 2009, Clinical chemistry.
[89] K. V. van Erpecum,et al. Improved prognosis of patients with primary biliary cirrhosis that have a biochemical response to ursodeoxycholic acid. , 2009, Gastroenterology.
[90] I. Fabregat,et al. Upregulation of the NADPH oxidase NOX4 by TGF-beta in hepatocytes is required for its pro-apoptotic activity. , 2008, Journal of hepatology.
[91] I. Mackay,et al. CD4 T-cell autoreactivity to the mitochondrial autoantigen PDC-E2 in AMA-negative primary biliary cirrhosis. , 2008, Journal of autoimmunity.
[92] Y. Chrétien,et al. Biochemical response to ursodeoxycholic acid and long‐term prognosis in primary biliary cirrhosis , 2008, Hepatology.
[93] I. Mackay,et al. Autoimmune liver serology: current diagnostic and clinical challenges. , 2008, World journal of gastroenterology.
[94] S. Kaneko,et al. The efficacy of ursodeoxycholic acid and bezafibrate combination therapy for primary biliary cirrhosis: A prospective, multicenter study , 2008, Hepatology research : the official journal of the Japan Society of Hepatology.
[95] Liang Zhu,et al. Long-Term Effects of Mid-Dose Ursodeoxycholic Acid in Primary Biliary Cirrhosis: A Meta-analysis of Randomized Controlled Trials , 2006, The American Journal of Gastroenterology.
[96] Shinichiro Yamamoto,et al. Long-term effect of bezafibrate on parameters of hepatic fibrosis in primary biliary cirrhosis , 2006, Journal of Gastroenterology.
[97] J. Prieto,et al. Bicarbonate-rich choleresis induced by secretin in normal rat is taurocholate-dependent and involves AE2 anion exchanger. , 2006, Hepatology.
[98] K. Tsuneyama,et al. Liver‐targeted and peripheral blood alterations of regulatory T cells in primary biliary cirrhosis , 2006, Hepatology.
[99] J. Rodés,et al. Excellent long-term survival in patients with primary biliary cirrhosis and biochemical response to ursodeoxycholic Acid. , 2006, Gastroenterology.
[100] K. Isse,et al. Th1 cytokine–induced downregulation of PPARγ in human biliary cells relates to cholangitis in primary biliary cirrhosis , 2005, Hepatology.
[101] J. Neuberger,et al. Pilot Studies of Single and Combination Antiretroviral Therapy in Patients with Primary Biliary Cirrhosis , 2004, The American Journal of Gastroenterology.
[102] J. Talwalkar,et al. Natural history of pruritus in primary biliary cirrhosis. , 2003, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.
[103] T. Sauerbruch,et al. Pharmacokinetics and pharmacodynamic action of budesonide in early‐ and late‐stage primary biliary cirrhosis , 2003, Hepatology.
[104] N. LaRusso,et al. Cholangiocyte biology , 2003, Current opinion in gastroenterology.
[105] U. Beuers,et al. Ursodeoxycholic acid in cholestatic liver disease: Mechanisms of action and therapeutic use revisited , 2002, Hepatology.
[106] T. Ueno,et al. Fenofibrate treatment in patients with primary biliary cirrhosis , 2002, American Journal of Gastroenterology.
[107] T. Willson,et al. 6alpha-ethyl-chenodeoxycholic acid (6-ECDCA), a potent and selective FXR agonist endowed with anticholestatic activity. , 2002, Journal of medicinal chemistry.
[108] J. Neuberger,et al. Defective regulation of cholangiocyte Cl−/HCO−3 and Na+/H+ exchanger activities in primary biliary cirrhosis , 2002, Hepatology.
[109] G. Gores,et al. Ursodeoxycholic acid 'mechanisms of action and clinical use in hepatobiliary disorders'. , 2001, Journal of hepatology.
[110] T M Therneau,et al. A model to predict survival in patients with end‐stage liver disease , 2001, Hepatology.
[111] T M Therneau,et al. Adaptation of the mayo primary biliary cirrhosis natural history model for application in liver transplant candidates , 2000, Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.
[112] S. Iwasaki. Bezafibrate may have a beneficial effect in pre-cirrhotic primary biliary cirrhosis , 1999 .
[113] T. Therneau,et al. Utilization of the Mayo risk score in patients with primary biliary cirrhosis receiving ursodeoxycholic acid. , 1999, Liver.
[114] M. Strazzabosco,et al. Transport systems in cholangiocytes: their role in bile formation and cholestasis. , 1997, The Yale journal of biology and medicine.
[115] J. Prieto,et al. Decreased anion exchanger 2 immunoreactivity in the liver of patients with primary biliary cirrhosis , 1997, Hepatology.
[116] P. Grambsch,et al. Primary biliary cirrhosis: Prediction of short‐term survival based on repeated patient visits , 1994, Hepatology.
[117] J. Medina,et al. Immunohistochemical detection of chloride/bicarbonate anion exchangers in human liver , 1994, Hepatology.
[118] D G Altman,et al. Updating prognosis in primary biliary cirrhosis using a time-dependent Cox regression model. PBC1 and PBC2 trial groups. , 1993, Gastroenterology.
[119] P. Grambsch,et al. Prognosis in primary biliary cirrhosis: Model for decision making , 1989, Hepatology.
[120] A. Ryrfeldt,et al. Liver metabolism of budesonide in rat, mouse, and man. Comparative aspects. , 1987, Drug metabolism and disposition: the biological fate of chemicals.
[121] D. Altman,et al. Beneficial effect of azathioprine and prediction of prognosis in primary biliary cirrhosis. Final results of an international trial. , 1985, Gastroenterology.
[122] J. Boyer,et al. The prognostic importance of clinical and histologic features in asymptomatic and symptomatic primary biliary cirrhosis. , 1983, The New England journal of medicine.
[123] L. Hellman,et al. REDUCTION OF CHOLESTEROL AND LIPIDS IN MAN BY ETHYL P-CHLOROPHENOXYISOBUTYRATE. , 1963, Annals of internal medicine.
[124] A. Parés,et al. Effects of Bezafibrate on Outcome and Pruritus in Primary Biliary Cholangitis With Suboptimal Ursodeoxycholic Acid Response , 2018, The American Journal of Gastroenterology.
[125] F. Nevens,et al. Time-dependent factors associated with diminished transplant-free survival in patients with primary biliary cholangitis and an optimal response to ursodeoxycholic acid after one year of treatment , 2017 .
[126] K. Tsuneyama,et al. Primary Biliary Cholangitis: Its Pathological Characteristics and Immunopathological Mechanisms. , 2017, The journal of medical investigation : JMI.
[127] F. Nevens,et al. The GLOBE score identifies PBC patients at increased risk of liver transplantation or death in different age-categories over time , 2017 .
[128] F. Nevens,et al. The GLOBE score identifies PBC patients at increased risk of liver transplantation or death during follow-up , 2016 .
[129] C. Selmi,et al. Experimental evidence on the immunopathogenesis of primary biliary cirrhosis , 2010, Cellular and Molecular Immunology.
[130] T. Kurihara,et al. Investigation into the efficacy of bezafibrate against primary biliary cirrhosis, with histological references from cases receiving long term monotherapy , 2002, American Journal of Gastroenterology.
[131] M. Kaplan,et al. Identification of HLA-A2-restricted CD8(+) cytotoxic T cell responses in primary biliary cirrhosis: T cell activation is augmented by immune complexes cross-presented by dendritic cells. , 2002, The Journal of experimental medicine.
[132] T. Kurihara,et al. Bezafibrate in the treatment of primary biliary cirrhosis: comparison with ursodeoxycholic acid , 2000, American Journal of Gastroenterology.
[133] T. Masaki,et al. Combination therapy of bezafibrate and ursodeoxycholic acid in primary biliary cirrhosis: a preliminary study , 2000, American Journal of Gastroenterology.
[134] M. Manns,et al. Is there a serological difference between men and women with primary biliary cirrhosis? , 1999, American Journal of Gastroenterology.
[135] A. Hofmann,et al. Pharmacology of ursodeoxycholic acid, an enterohepatic drug. , 1994, Scandinavian journal of gastroenterology. Supplement.
[136] J. Senior,et al. Effect of long-term treatment with ursodiol on clinical and biochemical features and biliary bile acid metabolism in patients with primary biliary cirrhosis. , 1993, The American journal of gastroenterology.