Primary biliary cirrhosis

Primary biliary cirrhosis is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1002/HEP.22906
P698PubMed publication ID19554543
P5875ResearchGate publication ID26318855

P50authorM. Eric GershwinQ73297886
P2093author name stringRaoul Poupon
E. Jenny Heathcote
Keith D. Lindor
Marshall Kaplan
Nora V. Bergasa
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The true impact of fatigue in primary biliary cirrhosis: a population studyQ40643274
The effect of ursodeoxycholic acid therapy on liver fibrosis progression in primary biliary cirrhosisQ40737262
Combined analysis of randomized controlled trials of ursodeoxycholic acid in primary biliary cirrhosisQ40883127
Natural history of early primary biliary cirrhosisQ41234807
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Effect of oral naltrexone on pruritus in cholestatic patientsQ41808544
Transplantation trends in primary biliary cirrhosis.Q42632785
A prospective trial of colchicine for primary biliary cirrhosisQ42659809
Double blind controlled trial of d-penicillamine in patients with primary biliary cirrhosisQ43214926
Extramural cross-validation of the Mayo primary biliary cirrhosis survival model establishes its generalizabilityQ43475774
Excellent long-term survival in patients with primary biliary cirrhosis and biochemical response to ursodeoxycholic AcidQ43483632
Prevalence and predictors of esophageal varices in patients with primary biliary cirrhosisQ43484548
Induction of primary biliary cirrhosis in guinea pigs following chemical xenobiotic immunizationQ43575984
Hypercholesterolemia and atherosclerosis in primary biliary cirrhosis: what is the risk?Q43676662
Detection of antimitochondrial autoantibodies in immunofluorescent AMA-negative patients with primary biliary cirrhosis using recombinant autoantigensQ43693265
Ten-year combination treatment with colchicine and ursodeoxycholic acid for primary biliary cirrhosis: a double-blind, placebo-controlled trial on symptomatic patients.Q43734578
Incomplete response to ursodeoxycholic acid in primary biliary cirrhosis: is a double dosage worthwhile?Q43807982
Primary biliary cirrhosis with additional features of autoimmune hepatitis: response to therapy with ursodeoxycholic acidQ43875853
Utilization of the Mayo risk score in patients with primary biliary cirrhosis receiving ursodeoxycholic acidQ43893454
Primary biliary cirrhosis: incidence and predictive factors of cirrhosis development in ursodiol-treated patientsQ43903202
Simvastatin in primary biliary cirrhosis: effects on serum lipids and distinct disease markersQ43954071
Randomized trial of chlorambucil for primary biliary cirrhosis.Q44093311
Fenofibrate treatment in patients with primary biliary cirrhosisQ44110727
Long-term survival and impact of ursodeoxycholic acid treatment for recurrent primary biliary cirrhosis after liver transplantationQ44169502
Combined analysis of the effect of treatment with ursodeoxycholic acid on histologic progression in primary biliary cirrhosisQ44487597
Treatment with ursodeoxycholic acid is associated with weight gain in patients with primary biliary cirrhosisQ44517790
Comparison of rifampicin with phenobarbitone for treatment of pruritus in biliary cirrhosis.Q44573504
Recurrence of primary biliary cirrhosis after liver transplantation: Histologic estimate of incidence and natural historyQ44606835
Paroxetine in the treatment of severe non-dermatological pruritus: a randomized, controlled trialQ44679061
When is liver biopsy needed in the diagnosis of primary biliary cirrhosis?Q44797408
Natural history of pruritus in primary biliary cirrhosisQ44797529
Immunosuppression affects the rate of recurrent primary biliary cirrhosis after liver transplantationQ44817502
A randomized controlled trial of colchicine plus ursodiol versus methotrexate plus ursodiol in primary biliary cirrhosis: ten-year resultsQ44825279
Biochemical markers of liver fibrosis and lymphocytic piecemeal necrosis in UDCA-treated patients with primary biliary cirrhosisQ44930578
Diagnostic and therapeutic implications of bile duct injury in autoimmune hepatitisQ45002713
The prognostic importance of clinical and histologic features in asymptomatic and symptomatic primary biliary cirrhosisQ45024371
Quality of life in patients with primary biliary cirrhosisQ45059665
Mucosal immunity and primary biliary cirrhosis: presence of antimitochondrial antibodies in urineQ45168673
The effect of ursodeoxycholic acid therapy on the natural course of primary biliary cirrhosisQ45247238
Epitope mapping and reactivity of autoantibodies to the E2 component of 2-oxoglutarate dehydrogenase complex in primary biliary cirrhosis using recombinant 2-oxoglutarate dehydrogenase complex.Q45948332
Fat-soluble vitamin levels in patients with primary biliary cirrhosisQ34379099
Characterisation of patients with a complete biochemical response to ursodeoxycholic acidQ34408204
Hepatocellular carcinoma in primary biliary cirrhosis and its impact on outcomesQ34445524
Risk factors and comorbidities in primary biliary cirrhosis: a controlled interview-based study of 1032 patientsQ34462959
Portal hypertension in primary biliary cirrhosisQ34474035
Anti-gp210 and anti-centromere antibodies are different risk factors for the progression of primary biliary cirrhosisQ34594429
An open study of modafinil for the treatment of daytime somnolence and fatigue in primary biliary cirrhosisQ34608494
Prevention and management of gastroesophageal varices and variceal hemorrhage in cirrhosisQ34690306
Survival and symptom progression in a geographically based cohort of patients with primary biliary cirrhosis: follow-up for up to 28 yearsQ34932835
Review article: is there an optimal therapeutic regimen for antimitochondrial antibody-negative primary biliary cirrhosis (autoimmune cholangitis)?Q35030826
Natural history of primary biliary cirrhosis.Q35573903
Management of osteoporosis, fat-soluble vitamin deficiencies, and hyperlipidemia in primary biliary cirrhosisQ35573921
Hepatitis and liver dysfunction with rifampicin therapy for pruritus in primary biliary cirrhosis.Q35594405
Hyperlipidaemic state and cardiovascular risk in primary biliary cirrhosisQ35594898
Fatigue and primary biliary cirrhosis: association of globus pallidus magnetisation transfer ratio measurements with fatigue severity and blood manganese levels.Q35596429
Asymptomatic primary biliary cirrhosis: clinical features, prognosis, and symptom progression in a large population based cohortQ35596580
Which patients with primary biliary cirrhosis or primary sclerosing cholangitis should undergo endoscopic screening for oesophageal varices detection?Q35597224
Opioid peptides and primary biliary cirrhosisQ35706319
Four year follow up of fatigue in a geographically defined primary biliary cirrhosis patient cohortQ35760389
Hypercholesterolaemia is not associated with early atherosclerotic lesions in primary biliary cirrhosisQ35760984
Primary biliary cirrhosis: report of a focus study groupQ35894578
Statins and hepatotoxicity: focus on patients with fatty liverQ36079406
Antihistamines in dermatologyQ36193211
The autoepitope of the 74-kD mitochondrial autoantigen of primary biliary cirrhosis corresponds to the functional site of dihydrolipoamide acetyltransferaseQ36357621
Primary biliary cirrhosis, hyperlipidemia, and atherosclerotic risk: a systematic reviewQ36714163
Ursodeoxycholic acid for patients with primary biliary cirrhosis: an updated systematic review and meta-analysis of randomized clinical trials using Bayesian approach as sensitivity analysesQ36801651
Conventional therapy of Sjogren's syndromeQ36997278
Pruritus and fatigue associated with liver disease: is there a role for ondansetron?Q37099029
Identification and precursor frequency analysis of a common T cell epitope motif in mitochondrial autoantigens in primary biliary cirrhosisQ37388003
The pruritus of cholestasis: from bile acids to opiate agonistsQ37879905
Applicability of the IAIHG scoring system to the diagnosis of antimitochondrial/anti-M2 seropositive variant form of autoimmune hepatitis.Q38999540
Characterization of the overlap syndrome of primary biliary cirrhosis (PBC) and autoimmune hepatitis: evidence for it being a hepatitic form of PBC in genetically susceptible individualsQ39225838
Itch in primary biliary cirrhosis: a patients' perspectiveQ39325404
Treatment of pruritus of primary biliary cirrhosis with rifampinQ39511303
Quantitative and functional analysis of PDC-E2-specific autoreactive cytotoxic T lymphocytes in primary biliary cirrhosisQ39737852
Efficacy and safety of oral naltrexone treatment for pruritus of cholestasis, a crossover, double blind, placebo-controlled studyQ78554315
The treatment of pruritus and hypercholesteremia of primary biliary cirrhosis with cholestyramineQ79091520
Plasma separation and anion adsorption transiently relieve intractable pruritus in primary biliary cirrhosisQ79257928
Liver transplantation in precirrhotic biliary tract disease: Portal hypertension is frequently associated with nodular regenerative hyperplasia and obliterative portal venopathyQ79298104
Clinical predictors for hepatocellular carcinoma in patients with primary biliary cirrhosisQ79438224
Overlap syndrome of primary biliary cirrhosis and autoimmune hepatitis: a retrospective study of 115 cases of autoimmune liver diseaseQ79711877
Development of autoimmune hepatitis in patients with typical primary biliary cirrhosisQ79788278
Depression in patients with primary biliary cirrhosis and primary sclerosing cholangitisQ80073128
Rifampin is safe for treatment of pruritus due to chronic cholestasis: a meta-analysis of prospective randomized-controlled trialsQ80215317
Treatment of severe refractory pruritus with fractionated plasma separation and adsorption (Prometheus)Q80311756
Primary biliary cirrhosisQ81246142
Severity of cholestasis and advanced histological stage but not menopausal status are the major risk factors for osteoporosis in primary biliary cirrhosisQ81513622
Increased prevalence of primary biliary cirrhosis near Superfund toxic waste sitesQ82639990
Bone loss and reduced osteoblast function in primary biliary cirrhosisQ93642995
Characterization of antimitochondrial antibodies in health adultsQ46110088
Prognosis in primary biliary cirrhosis: model for decision makingQ46316848
A randomized, controlled crossover trial of ondansetron in patients with primary biliary cirrhosis and fatigueQ46509129
Long-term fibrate treatment for PBC.Q46534026
Alendronate improves bone mineral density in primary biliary cirrhosis: a randomized placebo-controlled trialQ46714065
Modafinil for the treatment of fatigue in primary biliary cirrhosisQ46735291
Methotrexate (MTX) plus ursodeoxycholic acid (UDCA) in the treatment of primary biliary cirrhosisQ46775425
Primary biliary cirrhosis in monozygotic and dizygotic twins: genetics, epigenetics, and environmentQ46795010
Long term outcome and response to therapy of primary biliary cirrhosis-autoimmune hepatitis overlap syndromeQ46852534
Geotherapeutics of primary biliary cirrhosis: bright and sunny around the Mediterranean but still cloudy and foggy in the United KingdomQ46982754
Fatigue in primary biliary cirrhosis is associated with excessive daytime somnolenceQ48496394
Effect of rifampicin treatment on hepatic drug metabolism and serum bile acids in patients with primary biliary cirrhosisQ49323238
Bone disease in primary biliary cirrhosis: independent indicators and rate of progression.Q50684179
Longitudinal bone loss in postmenopausal women with primary biliary cirrhosis and well-preserved liver function.Q50711662
Reduced serum lipoprotein(a) levels in patients with primary biliary cirrhosis.Q51597355
Vitamin E deficiency in primary biliary cirrhosis: gastrointestinal malabsorption, frequency and relationship to other lipid-soluble vitamins.Q51621306
The incidence of pruritus after epidural morphine.Q51748346
Fluoxetine for the treatment of fatigue in primary biliary cirrhosis: a randomized, double-blind controlled trial.Q53221825
Overlap of autoimmune hepatitis and primary biliary cirrhosis: long-term outcomes.Q53241327
Assessment of biliary fibrosis by transient elastography in patients with PBC and PSC.Q53711274
Development of autoimmune hepatitis in primary biliary cirrhosis.Q53713488
Silymarin in the treatment of patients with primary biliary cirrhosis with a suboptimal response to ursodeoxycholic acid.Q54032405
Ursodiol for the long-term treatment of primary biliary cirrhosis. The UDCA-PBC Study Group.Q54118475
Osteoporosis in Primary Biliary Cirrhosis: A Randomized Trial of the Efficacy and Feasibility of Estrogen/ProgestinQ58311495
Fracture risk of women with primary biliary cirrhosis: no increase compared with general population controlsQ58376324
Effect of liver cirrhosis on the systemic availability of naltrexone in humansQ58896381
Sertraline as a first-line treatment for cholestatic pruritusQ61480066
Familial primary biliary cirrhosis reassessed: a geographically-based population studyQ61633902
Oral naltrexone treatment for cholestatic pruritus: A double-blind, placebo-controlled studyQ61854318
Azathioprine and prognosis in primary biliary cirrhosis.Q64903641
A controlled trial of prednisolone treatment in primary biliary cirrhosis. Three-year resultsQ67590480
Topical ciclosporin in the treatment of ocular surface disordersQ24670344
Assessing the quality of reports of randomized clinical trials: is blinding necessary?Q27860973
Effect of distal splenorenal shunt on survival of patients with primary biliary cirrhosisQ28242047
A multicenter, controlled trial of ursodiol for the treatment of primary biliary cirrhosis. UDCA-PBC Study GroupQ28243457
Modafinil for excessive sleepiness associated with shift-work sleep disorderQ28265627
Long-term follow-up of antimitochondrial antibody-positive autoimmune hepatitisQ28289028
A sensitive bead assay for antimitochondrial antibodies: Chipping away at AMA-negative primary biliary cirrhosisQ28290430
Rifampin-induced selective serotonin reuptake inhibitor withdrawal syndrome in a patient treated with sertralineQ28369455
Management of hepatocellular carcinomaQ29616230
Antimitochondrial antibody negative primary biliary cirrhosis in Japan: utilization of clinical data when patients applied to receive public financial aid.Q31027142
Consecutive occurrence of primary biliary cirrhosis and autoimmune hepatitis: a case report and review of the literatureQ32090723
The efficacy and safety of bile Acid binding agents, opioid antagonists, or rifampin in the treatment of cholestasis-associated pruritusQ33280833
Incidence of cancer in primary biliary cirrhosis: the Mayo experienceQ33601440
Randomised controlled trials of ursodeoxycholic-acid therapy for primary biliary cirrhosis: a meta-analysisQ33745849
International Autoimmune Hepatitis Group Report: review of criteria for diagnosis of autoimmune hepatitisQ33784003
Long-term outcome after partial external biliary diversion for intractable pruritus in patients with intrahepatic cholestasisQ33851658
Primary biliary cirrhosis: an orchestrated immune response against epithelial cellsQ33916633
Role of hyperbilirubinemia in the impairment of osteoblast proliferation associated with cholestatic jaundiceQ34223451
Extracorporeal albumin dialysis: a procedure for prolonged relief of intractable pruritus in patients with primary biliary cirrhosisQ34324928
Antimitochondrial antibody negative primary biliary cirrhosis: a distinct syndrome of autoimmune cholangitisQ34377943
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 subjectsQ67928582
Fat-Soluble Vitamin Nutriture in primary Biliary CirrhosisQ68450012
A controlled trial of cyclosporine in the treatment of primary biliary cirrhosisQ68505504
Pathogenesis of steatorrhea in primary biliary cirrhosisQ68940388
Prospective evaluation of esophageal varices in primary biliary cirrhosis: development, natural history, and influence on survivalQ69738156
Naltrexone and hepatotoxicityQ69880968
Trial of penicillamine in advanced primary biliary cirrhosisQ69887093
Primary biliary cirrhosis: clinical features and outcome, with special reference to asymptomatic diseaseQ69971289
Vitamin E deficiency and its clinical significance in adults with primary biliary cirrhosis and other forms of chronic liver diseaseQ70183282
Cyclosporin A treatment in primary biliary cirrhosis: results of a long-term placebo controlled trialQ70542319
Time course of histological progression in primary biliary cirrhosisQ70869710
Effects of ursodeoxycholic acid on survival in patients with primary biliary cirrhosisQ71035932
Increased incidence of hypothyroidism in primary biliary cirrhosisQ71065625
A placebo-controlled trial of primary biliary cirrhosis treatment with colchicine and ursodeoxycholic acidQ72189521
Improvement of cholestatic pruritus by ondansetronQ72218628
Primary biliary cirrhosis. Sole presentation with rampant dental cariesQ72241874
Ondansetron for pruritus due to cholestasisQ72379137
American Gastroenterological Association policy statement on the use of medical practice guidelines by managed care organizations and insurance carriersQ72590133
Major histocompatibility complex class-II alleles in primary biliary cirrhosisQ72664892
Primary biliary cirrhosis: survival of a large cohort of symptomatic and asymptomatic patients followed for 24 yearsQ72727069
Effect of ursodeoxycholic acid on serum lipids of patients with primary biliary cirrhosisQ72736523
Autoimmune cholangiopathy: the result of consecutive primary biliary cirrhosis and autoimmune hepatitis?Q72800622
Vitamin D-receptor genotypes as independent genetic predictors of decreased bone mineral density in primary biliary cirrhosisQ73302312
Comparison of the clinical features and clinical course of antimitochondrial antibody-positive and -negative primary biliary cirrhosisQ73319901
Etidronate for osteoporosis in primary biliary cirrhosis: a randomized trialQ73330566
Oral budesonide in the treatment of patients with primary biliary cirrhosis with a suboptimal response to ursodeoxycholic acidQ73401694
Primary biliary cirrhosis, sicca complex, and dysphagiaQ73430902
Pain as a complication of use of opiate antagonists for symptom control in cholestasisQ73735616
Bioavailability of four ursodeoxycholic acid preparationsQ74260266
Open-label trial of oral nalmefene therapy for the pruritus of cholestasisQ74310569
Long-term ursodeoxycholic acid delays histological progression in primary biliary cirrhosisQ74529900
Histopathological study of primary biliary cirrhosis and the effect of ursodeoxycholic acid treatment on histology progressionQ74645177
Primary biliary cirrhosis-autoimmune hepatitis overlap syndrome: clinical features and response to therapyQ77058192
Liver transplantation for intractable pruritus is contraindicated before an adequate trial of opiate antagonist therapyQ77113445
Clinical and biochemical expression of the histopathological lesions of primary biliary cirrhosis. UDCA-PBC GroupQ77221662
Naltrexone in the treatment of alcohol dependenceQ77347366
Ten-year survival in ursodeoxycholic acid-treated patients with primary biliary cirrhosis. The UDCA-PBC Study GroupQ77807948
Comparison of three doses of ursodeoxycholic acid in the treatment of primary biliary cirrhosis: a randomized trialQ77872001
Low-dose methotrexate is ineffective in primary biliary cirrhosis: long-term results of a placebo-controlled trialQ78039888
Relief from profound fatigue associated with chronic liver disease by long-term ondansetron therapyQ78100086
Oral nalmefene therapy reduces scratching activity due to the pruritus of cholestasis: a controlled studyQ78163535
P433issue1
P407language of work or nameEnglishQ1860
P921main subjectprimary biliary cholangitisQ1072420
P304page(s)291-308
P577publication date2009-02-11
P1433published inHepatologyQ15724398
P1476titlePrimary biliary cirrhosis
P478volume50

Reverse relations

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Q47440077Effect of ileal bile acid transporter inhibitor GSK2330672 on pruritus in primary biliary cholangitis: a double-blind, randomised, placebo-controlled, crossover, phase 2a study.
Q43004194Effect of nalfurafine hydrochloride in patients with chronic liver disease with refractory pruritus on sleep disorders: a study protocol for single-arm, prospective, interventional study
Q47156253Elevated Liver Enzymes in Asymptomatic Patients - What Should I Do?
Q33962221Elevated levels of alanine transaminase and triglycerides within normal limits are associated with fatty liver
Q51560561Elevation of Vδ1 T cells in peripheral blood and livers of patients with primary biliary cholangitis.
Q38744215Emerging drugs for the treatment of Primary Biliary Cholangitis
Q92864604Emerging therapies for PBC
Q91948597Epidemiological survey of antinuclear antibodies in healthy population and analysis of clinical characteristics of positive population
Q38600118Epidemiology and Natural History of Primary Biliary Cholangitis in the Chinese: A Territory-Based Study in Hong Kong between 2000 and 2015.
Q90269685Epidemiology and clinical course of primary biliary cholangitis in the Asia-Pacific region: a systematic review and meta-analysis
Q60301070Epidemiology and liver transplantation burden of primary biliary cholangitis: a retrospective cohort study
Q51137626Epidemiology and natural history of primary biliary cirrhosis in a Canadian health region: a population-based study.
Q38565478Epigenetics and Primary Biliary Cirrhosis: a Comprehensive Review and Implications for Autoimmunity
Q41361892Epigenetics in the Primary Biliary Cholangitis and Primary Sclerosing Cholangitis
Q52648759Evaluation of classical and novel autoantibodies for the diagnosis of Primary Biliary Cholangitis-Autoimmune Hepatitis Overlap Syndrome (PBC-AIH OS).
Q38183450Evaluation of histological staging systems for primary biliary cirrhosis: correlation with clinical and biochemical factors and significance of pathological parameters in prognostication
Q42263045Evaluation of nail fold capillaroscopy findings in patients with primary biliary cirrhosis
Q91844615Evaluation 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
Q39485889Evidence for the association between IgG-antimitochondrial antibody and biochemical response to ursodeoxycholic acid treatment in primary biliary cholangitis
Q47156128Evidence from a familial case suggests maternal inheritance of primary biliary cholangitis
Q91642039Evolving liver inflammation in biochemically normal individuals with anti-mitochondria antibodies
Q90722135Exploration and Development of PPAR Modulators in Health and Disease: An Update of Clinical Evidence
Q55332862External validation of the United Kingdom-primary biliary cholangitis risk scores of patients with primary biliary cholangitis treated with ursodeoxycholic acid.
Q39177903Extrahepatic Manifestations of Primary Biliary Cholangitis
Q84914116Extrahepatic conditions associated with primary biliary cirrhosis
Q40130719Factors that Influence Health-Related Quality of Life in Patients with Primary Sclerosing Cholangitis.
Q56971225Fatigue and pruritus at onset identify a more aggressive subset of primary biliary cirrhosis
Q38858980Finding the cure for primary biliary cholangitis - Still waiting
Q38313292Gene expression profiles of peripheral blood mononuclear cells in primary biliary cirrhosis
Q37089325Genetic Association of PTPN22 Polymorphisms with Autoimmune Hepatitis and Primary Biliary Cholangitis in Japan
Q37642274Genetic Contribution to the Pathogenesis of Primary Biliary Cholangitis.
Q92229185Genetic association of E26 transformation specific sequence 1 polymorphisms with the susceptibility of primary biliary cholangitis in China
Q43608312Genetic association of Fc receptor-like 3 polymorphisms with susceptibility to primary biliary cirrhosis: ethnic comparative study in Japanese and Italian patients
Q43672317Genetic polymorphisms of OCT-1 confer susceptibility to severe progression of primary biliary cirrhosis in Japanese patients
Q47827554Genetics and epigenetics in the pathogenesis of primary biliary cholangitis.
Q36383011Genome-Wide Association Studies in Primary Biliary Cirrhosis
Q92259854Genome-wide Association Studies of Specific Antinuclear Autoantibody Subphenotypes in Primary Biliary Cholangitis
Q39034887Genome-wide association studies identify PRKCB as a novel genetic susceptibility locus for primary biliary cholangitis in the Japanese population
Q28943429Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese population
Q39213467Geoepidemiology and changing mortality in primary biliary cholangitis
Q47205297Geoepidemiology of Primary Biliary Cholangitis: Lessons from Switzerland.
Q56429943Guidelines for the management of primary biliary cirrhosis
Q38085065Gut-liver axis: an immune link between celiac disease and primary biliary cirrhosis
Q35309953Hair dyes as a risk for autoimmunity: from systemic lupus erythematosus to primary biliary cirrhosis
Q55114620Hepatobiliary Manifestations and Complications in Inflammatory Bowel Disease: A Review.
Q33966083Hepatobiliary complications of inflammatory bowel disease
Q34147508Hepatocyte Death: A Clear and Present Danger
Q54469701High levels of FCγR3A and PRF1 expression in peripheral blood mononuclear cells from patients with primary biliary cirrhosis.
Q42947254High-dose ursodeoxycholic acid therapy for nonalcoholic steatohepatitis: a double-blind, randomized, placebo-controlled trial
Q52925804High-throughput T-cell receptor sequencing across chronic liver diseases reveals distinct disease-associated repertoires.
Q38554722Human autoimmune diseases: a comprehensive update
Q44980851Human intrahepatic biliary epithelial cells engulf blebs from their apoptotic peers
Q46332063Human leucocyte antigen alleles and haplotypes and their associations with antinuclear antibodies features in Chinese patients with primary biliary cirrhosis
Q85002108Human leukocyte antigen class II molecules confer both susceptibility and progression in Japanese patients with primary biliary cirrhosis
Q35131979Human leukocyte antigen in primary biliary cirrhosis: an old story now reviving
Q33551867Human β-Defensin 2 in Primary Sclerosing Cholangitis
Q36963978Humoral autoimmune response heterogeneity in the spectrum of primary biliary cirrhosis.
Q38957567Imaging of autoimmune biliary disease
Q24617796Immunochip 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
Q53019283Immunologic derangement preceding clinical autoimmunity.
Q37877588Immunological diseases of the pancreatico-hepatobiliary system: update on etiopathogenesis and cross-sectional imaging findings
Q35614763Immunopathogenesis of primary biliary cirrhosis: an old wives' tale.
Q37559266Immunosuppressive therapy in immune-mediated liver disease in the non-transplanted patient
Q52925696In recurrent primary biliary cirrhosis after liver transplantation, biliary epithelial cells show increased expression of mitochondrial proteins.
Q38374504Incidence and risk factors for hepatocellular carcinoma in primary biliary cirrhosis
Q38795238Incidence of Primary Biliary Cholangitis in a Rural Midwestern Population
Q49806997Increased cholestatic enzymes in two patients with long-term history of ulcerative colitis: consider primary biliary cholangitis not always primary sclerosing cholangitis
Q45173055Increased expression of mitochondrial proteins associated with autophagy in biliary epithelial lesions in primary biliary cirrhosis
Q36967742Increased mean platelet volume is related to histologic severity of primary biliary cirrhosis.
Q56766238Increased numbers of circulating ICOS⁺ follicular helper T and CD38⁺ plasma cells in patients with newly diagnosed primary biliary cirrhosis
Q60309961Increased red cell width distribution to lymphocyte ratio is a predictor of histologic severity in primary biliary cholangitis
Q48529733Inflammatory myopathies associated with anti-mitochondrial antibodies
Q37017406Interleukin-21 plays a critical role in the pathogenesis and severity of type I autoimmune hepatitis
Q64105140Interleukin-33/ST2-Mediated Inflammation Plays a Critical Role in the Pathogenesis and Severity of Type I Autoimmune Hepatitis
Q53098304Investigational drugs in phase II clinical trials for primary biliary cholangitis.
Q88380162Is patient-reported outcome improved by nalfurafine hydrochloride in patients with primary biliary cholangitis and refractory pruritus? A post-marketing, single-arm, prospective study
Q43155895Is there a role for tetrathiomolybdate in the treatment of primary biliary cirrhosis?
Q38620686It is time to change primary biliary cirrhosis (PBC): New nomenclature from "cirrhosis" to "cholangitis", and upcoming treatment based on unveiling pathology
Q35631405Itch and liver: management in primary care.
Q46640079Keratin 19 demonstration of canal of Hering loss in primary biliary cirrhosis: "minimal change PBC"?
Q39336142Large-scale characterization study of patients with antimitochondrial antibodies but nonestablished primary biliary cholangitis
Q37738636Latest and emerging therapies for primary biliary cirrhosis and primary sclerosing cholangitis
Q50097218Less Limb Muscle Involvement in Myositis Patients with Anti-Mitochondrial Antibodies
Q54254957Liver Illness and Psoriatic Patients.
Q36320523Liver Transplantation for Cholestatic Liver Diseases in Adults
Q37743450Liver biopsy diagnosis of hepatitis: clues to clinically-meaningful reporting
Q37140617Liver damage in primary biliary cirrhosis and accompanied by primary Sjögren's syndrome: a retrospective pilot study
Q37334112Liver diseases in pregnancy: diseases not unique to pregnancy
Q38123133Liver transplantation and autoimmune liver diseases
Q39584105Long-Term Fenofibrate Treatment in Primary Biliary Cholangitis Improves Biochemistry but Not the UK-PBC Risk Score
Q92685166Long-term efficacy and safety of obeticholic acid for patients with primary biliary cholangitis: 3-year results of an international open-label extension study
Q38699595Long-term outcomes in antimitochondrial antibody negative primary biliary cirrhosis.
Q35745075Low Serum Hepcidin in Patients with Autoimmune Liver Diseases
Q40808835Low incidence of primary biliary cirrhosis (PBC) in the first-degree relatives of PBC probands after 8 years of follow-up
Q54980590Low risk of hepatotoxicity from rifampicin when used for cholestatic pruritus: a cross-disease cohort study.
Q50142593Lymphocytes contribute to biliary injury and fibrosis in experimental xenobiotic-induced cholestasis
Q55498617Magnetic resonance imaging evidence of hippocampal structural changes in patients with primary biliary cholangitis.
Q47787189Major Hepatic Complications in Ursodeoxycholic Acid-Treated Patients With Primary Biliary Cholangitis: Risk Factors and Time Trends in Incidence and Outcome
Q40623611Management of pruritus in patients with cholestatic liver disease.
Q89285900Managing PBC: Expanding the Provider Comfort Zone
Q36009282Membranous Nephropathy Associated With Immunological Disorder-Related Liver Disease: A Retrospective Study of 10 Cases
Q33882608Meta-analysis assessment of GP210 and SP100 for the diagnosis of primary biliary cirrhosis
Q43013514Methotrexate in patients with primary biliary cirrhosis who respond incompletely to treatment with ursodeoxycholic acid
Q36144748MiR-139-5p is associated with inflammatory regulation through c-FOS suppression, and contributes to the progression of primary biliary cholangitis.
Q41492969MicroRNA-223 and microRNA-21 in peripheral blood B cells associated with progression of primary biliary cholangitis patients
Q47567609Milder disease stage in patients with primary biliary cholangitis over a 44-year period: A changing natural history.
Q50130002Modern treatment of primary biliary cholangitis
Q37631707Modulation of the Unfolded Protein Response by Tauroursodeoxycholic Acid Counteracts Apoptotic Cell Death and Fibrosis in a Mouse Model for Secondary Biliary Liver Fibrosis
Q36086498Molecular diagnostic testing for primary biliary cholangitis
Q57119171Molecular magnetic resonance imaging accurately measures the antifibrotic effect of EDP-305, a novel farnesoid X receptor agonist
Q88035378Monoclonal gammopathy in rheumatic diseases
Q46186395Mouse model of primary biliary cirrhosis with progressive fibrosis: are we there yet?
Q35038847Multiple autoimmune propensity and B-non-hodgkin lymphoma: cause or effect?
Q41615335Multiple genetic variants associated with primary biliary cirrhosis in a Han Chinese population
Q38388403Mycobacteria and autoimmunity
Q57110523NGM282 for Treatment of Patients With Primary Biliary Cholangitis: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial
Q37355843Natural history and management of primary biliary cirrhosis
Q26824664Network meta-analysis of randomized controlled trials: efficacy and safety of UDCA-based therapies in primary biliary cirrhosis
Q48218121New simple prognostic score for primary biliary cirrhosis: Albumin-bilirubin score
Q46182874New therapeutics in primary biliary cirrhosis: will there ever be light?
Q38261577New therapies for primary biliary cirrhosis
Q58708624Non-alcoholic steatohepatitis-like pattern in liver biopsy of rheumatoid arthritis patients with persistent transaminitis during low-dose methotrexate treatment
Q41042363Non-invasive assessment of liver fibrosis using two-dimensional shear wave elastography in patients with autoimmune liver diseases
Q44966935Noninvasive elastography-based assessment of liver fibrosis progression and prognosis in primary biliary cirrhosis
Q26748613Novel bile acid therapeutics for the treatment of chronic liver diseases
Q42375647Novel strategies and therapeutic options for the management of primary biliary cholangitis
Q38342107Novel therapeutic targets in primary biliary cirrhosis
Q89910702Nutritional Management of Cholestasis
Q55165714Obeticholic Acid: A Farnesoid X Receptor Agonist for Primary Biliary Cholangitis.
Q38911238Obeticholic acid for the treatment of primary biliary cholangitis
Q28072209Obeticholic acid for the treatment of primary biliary cholangitis in adult patients: clinical utility and patient selection
Q38628470Obeticholic acid for the treatment of primary biliary cirrhosis
Q38626000Obeticholic acid, a selective farnesoid X receptor agonist, regulates bile acid homeostasis in sandwich-cultured human hepatocytes.
Q50155645Occurrence of Jaundice Following Simultaneous Ursodeoxycholic Acid Cessation and Obeticholic Acid Initiation
Q39216355Old and new treatments for primary biliary cholangitis
Q34415757Ongoing activation of autoantigen-specific B cells in primary biliary cirrhosis
Q28087211Optimal drug regimens for primary biliary cirrhosis: a systematic review and network meta-analysis
Q37963978Optimizing biochemical markers as endpoints for clinical trials in primary biliary cirrhosis
Q89538006Osteoporosis in Primary Biliary Cholangitis: Prevalence, Impact and Management Challenges
Q57168372Osteoporosis in primary biliary cholangitis
Q37824300Overcoming a "probable" diagnosis in antimitochondrial antibody negative primary biliary cirrhosis: study of 100 sera and review of the literature
Q59384428Overlap syndrome: A real syndrome?
Q36442097Overlapping of primary biliary cirrhosis and small duct primary sclerosing cholangitis: first case report
Q87561627Oxidative stress and antioxidant status in patients with autoimmune liver diseases
Q39782708PML nuclear body component Sp140 is a novel autoantigen in primary biliary cirrhosis
Q37993126Pathogenesis and management of pruritus in cholestatic liver disease
Q34623557Pathogenesis of Cholestatic Liver Disease and Therapeutic Approaches
Q93140232Pathological patterns of biliary disease
Q37191674Pathway-based analysis of primary biliary cirrhosis genome-wide association studies
Q82719034Performance parameters of the conventional serological markers for autoimmune hepatitis
Q38738566Pharmacological interventions for primary biliary cholangitis: an attempted network meta-analysis.
Q37681567Pharmacological treatment of biliary cirrhosis with ursodeoxycholic acid
Q24186852Pharmacological treatments for primary biliary cirrhosis: a network meta-analysis
Q51636366Pilot study: fenofibrate for patients with primary biliary cirrhosis and an incomplete response to ursodeoxycholic acid
Q50003369Platelet count to spleen thickness ratio is related to histologic severity of primary biliary cholangitis
Q38162283Polymorphisms in the vitamin D receptor gene and risk of primary biliary cirrhosis: a meta-analysis
Q35309882Popular and unpopular infectious agents linked to primary biliary cirrhosis.
Q48312123Possible involvement of chemokine C-C receptor 7- programmed cell death-1+ follicular helper T-cell subset in the pathogenesis of autoimmune hepatitis.
Q38063171Potential Roles for Infectious Agents in the Pathophysiology of Primary Biliary Cirrhosis: What's New?
Q64230889Practical strategies for pruritus management in the obeticholic acid-treated patient with PBC: proceedings from the 2018 expert panel
Q35309854Predicting and preventing autoimmunity: the case of anti-mitochondrial antibodies
Q47114292Prediction of hepatocellular carcinoma development by aminotransferase to platelet ratio index in primary biliary cholangitis
Q33978160Pregnancy with portal hypertension
Q89070694Prevalence of and Factors Associated With Minimal Hepatic Encephalopathy in Patients With Cirrhosis of Liver
Q40055616Prevalence of pruritus in patients with chronic liver disease: a multicenter study
Q89639221Preventative care in cholestatic liver disease: Pearls for the specialist and subspecialist
Q38998320Primary Biliary Cholangitis Associated with Skin Disorders: A Case Report and Review of the Literature
Q57114658Primary Biliary Cholangitis in Medicare Population: The Impact on Mortality and Resource Utilization
Q39047912Primary Biliary Cholangitis: Disease Pathogenesis and Implications for Established and Novel Therapeutics
Q26781780Primary Biliary Cirrhosis and Primary Sclerosing Cholangitis: a Review Featuring a Women's Health Perspective
Q50954296Primary biliary cholangitis associated with warm autoimmune hemolytic anemia.
Q90014773Primary biliary cholangitis presenting as acute ischemic stroke: A rare association
Q64286582Primary biliary cholangitis with contemporary presence of anti-mithocondrial and anti-rods and rings autoantibodies: literature first case
Q54390436Primary biliary cholangitis: new treatments for an old disease.
Q56428272Primary biliary cirrhosis
Q57141930Primary biliary cirrhosis
Q85213554Primary biliary cirrhosis
Q36599248Primary biliary cirrhosis and Sjögren's syndrome: autoimmune epithelitis
Q38058979Primary biliary cirrhosis and bile acids
Q34637500Primary biliary cirrhosis and cancer risk: a systematic review and meta-analysis
Q26853145Primary biliary cirrhosis and liver transplantation
Q37266330Primary biliary cirrhosis in HBV and HCV patients: Clinical characteristics and outcome
Q38192045Primary biliary cirrhosis in adults
Q50631086Primary biliary cirrhosis-autoimmune hepatitis overlap syndrome: simplified criteria may be effective in the diagnosis in Chinese patients.
Q84773471Primary biliary cirrhosis/autoimmune hepatitis overlap syndrome developing in a patient with systemic lupus erythematosus: a case report and review of the literature
Q26799419Primary biliary cirrhosis: From bench to bedside
Q26853649Primary biliary cirrhosis: Pathophysiology, clinical presentation and therapy
Q35038800Primary biliary cirrhosis: family stories
Q43987255Primary biliary cirrhosis: proposal for a new simple histological scoring system
Q38554677Primary biliary cirrhosis: safety and benefits of established and emerging therapies
Q49712375Primary cutaneous amyloidosis associated with autoimmune hepatitis-primary biliary cirrhosis overlap syndrome and Sjögren syndrome: A case report
Q37799533Primary sclerosing cholangitis: overview and update
Q33920325Prognostic Factors for Transplant-Free Survival and Validation of Prognostic Models in Chinese Patients with Primary Biliary Cholangitis Receiving Ursodeoxycholic Acid
Q40311999Prognostic Models for Survival in Patients with Stable Cirrhosis: A Multicenter Cohort Study
Q83627142Prognostic factors and survival analysis of antimitochondrial antibody-positive primary biliary cirrhosis in Chinese patients
Q37072380Proposed therapies in primary biliary cholangitis
Q46933007Prospective evaluation of ursodeoxycholic acid withdrawal in patients with primary sclerosing cholangitis
Q38210112Pruritus in cholestasis: facts and fiction.
Q36134061Quantitation of the Rank-Rankl Axis in Primary Biliary Cholangitis
Q35998928RITPBC: B-cell depleting therapy (rituximab) as a treatment for fatigue in primary biliary cirrhosis: study protocol for a randomised controlled trial
Q34464043Recent advances in the development of farnesoid X receptor agonists
Q28076353Recent advances in the diagnosis and treatment of primary biliary cholangitis
Q33719935Recent advances in the management of pruritus in chronic liver diseases
Q26748537Recent advances in understanding and managing cholestasis
Q93140872Recurrence of autoimmune hepatitis, primary biliary cirrhosis, and primary sclerosing cholangitis after transplantation
Q36822889Red Blood Cell Distribution Width to Platelet Ratio is Related to Histologic Severity of Primary Biliary Cirrhosis
Q33911547Reduced coffee consumption among individuals with primary sclerosing cholangitis but not primary biliary cirrhosis.
Q43940290Reduced hepatitis B and D viral entry using clinically applied drugs as novel inhibitors of the bile acid transporter NTCP.
Q90126673Reduction and stabilization of bilirubin with obeticholic acid treatment in patients with primary biliary cholangitis
Q37314381Refractory pruritus in primary biliary cirrhosis
Q38974002Reversal of liver cirrhosis: current evidence and expectations
Q38174167Review article: controversies in the management of primary biliary cirrhosis and primary sclerosing cholangitis
Q26864272Review article: the management of autoimmune hepatitis beyond consensus guidelines
Q36369284Rheumatoid arthritis and primary biliary cirrhosis: cause, consequence, or coincidence?
Q55395737Risk of Cardiovascular Events in Patients with Primary Biliary Cholangitis - Systematic Review.
Q42363647Risk of liver disease in methotrexate treated patients
Q26796355Risk stratification in autoimmune cholestatic liver diseases: Opportunities for clinicians and trialists
Q88780685Rituximab Is Ineffective for Treatment of Fatigue in Primary Biliary Cholangitis: A Phase 2 Randomized Controlled Trial
Q36248162Role for mycobacterial infection in pathogenesis of primary biliary cirrhosis?
Q95942116Roles of trained immunity in the pathogenesis of cholangiopathies: a novel therapeutic target
Q41702160S100A12 expression in patients with primary biliary cirrhosis
Q38837130SP140L, an Evolutionarily Recent Member of the SP100 Family, Is an Autoantigen in Primary Biliary Cirrhosis
Q37598572STAT4 gene polymorphisms are associated with susceptibility and ANA status in primary biliary cirrhosis
Q34644916Sarcoidosis and primary biliary cirrhosis association: report of a new case
Q38390677Scandinavian epidemiological research in gastroenterology and hepatology
Q46651249Scratching the surface of cholestatic itch treatments
Q94326725Serological tests for primary biliary cholangitis
Q55009231Serum Autotaxin Is a Useful Disease Progression Marker in Patients with Primary Biliary Cholangitis.
Q37725466Serum Golgi protein 73 is not a suitable diagnostic marker for hepatocellular carcinoma
Q36151445Serum IgG subclasses in autoimmune diseases
Q41933128Serum Wisteria Floribunda Agglutinin-Positive Mac-2 Binding Protein Could Not Always Predict Early Cirrhosis in Non-Viral Liver Diseases
Q41009473Serum Wisteria floribunda Agglutinin-Positive Mac-2-Binding Protein Level Predicts Liver Fibrosis and Prognosis in Primary Biliary Cirrhosis
Q35674098Serum cell death biomarkers for prediction of liver fibrosis and poor prognosis in primary biliary cirrhosis
Q48145461Serum levels of a cell death biomarker predict the development of cirrhosis-related conditions in primary biliary cholangitis.
Q34944763Serum metabolic signatures of primary biliary cirrhosis and primary sclerosing cholangitis.
Q34408701Serum microRNAs as potential biomarkers of primary biliary cirrhosis
Q43230366Severe coagulopathy caused by rifampicin in patients with primary sclerosing cholangitis and refractory pruritus
Q36014535Sex differences associated with primary biliary cirrhosis.
Q38190931Shear wave elastography for liver stiffness measurement in clinical sonographic examinations: evaluation of intraobserver reproducibility, technical failure, and unreliable stiffness measurements
Q48218731Skin Manifestations Associated with Autoimmune Liver Diseases: a Systematic Review
Q33419647Stratification of hepatocellular carcinoma risk in primary biliary cirrhosis: a multicentre international study
Q34303048Study of liver cirrhosis over ten consecutive years in Southern China
Q33647458Subtle presentation of active primary biliary cirrhosis in chronic hepatitis B: a case report
Q54936764Suitability of the simplified autoimmune hepatitis score for the diagnosis of autoimmune hepatitis in a German cohort.
Q58722495Symptoms and health-related quality of life in Japanese patients with primary biliary cholangitis
Q52955409Synthesis 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.
Q36413970Tauroursodeoxycholic acid dampens oncogenic apoptosis induced by endoplasmic reticulum stress during hepatocarcinogen exposure
Q37526157Tauroursodeoxycholic acid reduces ER stress by regulating of Akt-dependent cellular prion protein
Q52624982The British Society of Gastroenterology/UK-PBC primary biliary cholangitis treatment and management guidelines.
Q46847997The Challenges of Nutritional Assessment in Cirrhosis
Q35942610The Cholangiopathies
Q47278009The Clinical Significance of GP73 in Immunologically Mediated Chronic Liver Diseases: Experimental Data and Literature Review
Q59384433The Diagnosis and Classification of Immune-Mediated Biliary Diseases
Q91790202The Enlargement of Abdominal Lymph Nodes Is a Characteristic of Autoimmune Liver Disease
Q41303819The Natural History and Prognosis of Primary Biliary Cirrhosis with Clinical Features of Autoimmune Hepatitis
Q40681087The UK-PBC risk scores: Derivation and validation of a scoring system for long-term prediction of end-stage liver disease in primary biliary cholangitis.
Q26830032The X-factor in primary biliary cirrhosis: monosomy X and xenobiotics
Q34438127The association between bile salt export pump single-nucleotide polymorphisms and primary biliary cirrhosis susceptibility and ursodeoxycholic acid response
Q38355697The coexistence of Sjögren's syndrome and primary biliary cirrhosis: a comprehensive review
Q35833175The diagnosis and treatment of primary biliary cirrhosis
Q26829493The diagnosis of primary biliary cirrhosis
Q53237682The dynamic and clinical significance of autoantibodies and immunoglobulins in liver transplant recipients.
Q37317828The dynamic biliary epithelia: molecules, pathways, and disease
Q39284642The emerging role of mast cells in liver disease
Q90293731The expression and clinical significance of serum IL-17 in patients with primary biliary cirrhosis
Q35939141The 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.
Q36573783The immunopathology of liver granulomas in primary biliary cirrhosis
Q38017976The immunophysiology and apoptosis of biliary epithelial cells: primary biliary cirrhosis and primary sclerosing cholangitis
Q47285348The impact of biopsychosocial factors on quality of life: women with primary biliary cirrhosis on waiting list and post liver transplantation
Q37371109The inter-relationship of symptom severity and quality of life in 2055 patients with primary biliary cholangitis.
Q38622370The management of autoimmunity in patients with cholestatic liver diseases
Q37714640The modulation of co-stimulatory molecules by circulating exosomes in primary biliary cirrhosis
Q38037392The overlap syndromes of autoimmune hepatitis
Q46813053The risk predictive values of UK-PBC and GLOBE scoring system in Chinese patients with primary biliary cholangitis: the additional effect of anti-gp210.
Q43589988The specificity of fatigue in primary biliary cirrhosis: evaluation of a large clinic practice
Q88164317The utility of IgG, IgM, and CD138 immunohistochemistry in the evaluation of autoimmune liver diseases
Q35187219The value of MRI in the diagnosis of primary biliary cirrhosis and assessment of liver fibrosis
Q90599038Therapeutic Effects of Apamin as a Bee Venom Component for Non-Neoplastic Disease
Q39816216Therapeutic Equivalence of Ursodeoxycholic Acid Tablets and Ursodeoxycholic Acid Capsules for the Treatment of Primary Biliary Cirrhosis
Q38543052Therapeutic Potential of IL-17-Mediated Signaling Pathway in Autoimmune Liver Diseases
Q90013058Therapeutic and immunological interventions in primary biliary cholangitis: from mouse models to humans
Q89509897Tight Junction Proteins and the Biology of Hepatobiliary Disease
Q55387422Toward solving the etiological mystery of primary biliary cholangitis.
Q59384465Toward the molecular dissection of primary biliary cirrhosis
Q54310426Towards the serological diagnosis of primary biliary cirrhosis.
Q34342199Treatment of autoimmune liver disease: current and future therapeutic options
Q39314534Treatment of primary biliary cholangitis ursodeoxycholic acid non-responders: A systematic review.
Q64991757Treatment of primary biliary cirrhosis: Is there more to offer than ursodeoxycholic acid?
Q37777156Treatment options for primary sclerosing cholangitis
Q90607266Trends in liver transplantation for primary biliary cholangitis in Europe over the past three decades
Q33932461Triglyceride is strongly associated with nonalcoholic fatty liver disease among markers of hyperlipidemia and diabetes
Q36417949Tuberculosis is not a risk factor for primary biliary cirrhosis: a review of the literature
Q36449565Twelve-year-old girl with primary biliary cirrhosis
Q56934656UEG Week 2015 Poster Presentations
Q48542369Unmet challenges in immune-mediated hepatobiliary diseases
Q55190939Update on New Drugs and Those in Development for the Treatment of Primary Biliary Cholangitis.
Q55333522Update on pharmacotherapies for cholestatic liver disease.
Q37358534Ursodeoxycholic Acid in Treatment of Non-cholestatic Liver Diseases: A Systematic Review.
Q59810022Use of Obeticholic Acid in Patients With Primary Biliary Cholangitis
Q46226926Using the Icelandic Genealogical Database to define the familial risk of primary biliary cholangitis
Q33547476Validation of coding algorithms for the identification of patients with primary biliary cirrhosis using administrative data
Q82344181Validation of the simplified criteria for diagnosis of autoimmune hepatitis in Chinese patients
Q34087671Variants at IRF5-TNPO3, 17q12-21 and MMEL1 are associated with primary biliary cirrhosis
Q26745766Vitamin D deficiency in patients with liver cirrhosis
Q37960398Vitamin d deficiency in patients with chronic liver disease and cirrhosis
Q33840969Why Doesn't Primary Biliary Cholangitis Respond to Immunosuppressive Medications?
Q38252904Women and primary biliary cirrhosis
Q37249179X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome
Q83330062[Anesthesia in the patient with impaired liver function]
Q88019229[Extracorporeal therapies in hepatic diseases]
Q49999392microRevolution in understanding primary biliary cholangitis pathophysiology
Q86258230β1 integrin is a long-sought sensor for tauroursodeoxycholic acid

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