Primary biliary cirrhosis

scientific article published on 01 July 2003

Primary biliary cirrhosis is …
instance of (P31):
scholarly articleQ13442814
review articleQ7318358

External links are
P356DOI10.1016/S0140-6736(03)13808-1
P698PubMed publication ID12853201

P2093author name stringJayant A Talwalkar
Keith D Lindor
P2860cites workEtidronate 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
Does antimitochondrial antibody status affect response to treatment in patients with primary biliary cirrhosis? Outcomes of ursodeoxycholic acid therapy and liver transplantationQ73491973
The combination of ursodeoxycholic acid and methotrexate for primary biliary cirrhosis is not better than ursodeoxycholic acid aloneQ73574823
Long-term effects of ursodeoxycholic acid in primary biliary cirrhosis: results of a double-blind controlled multicentric trial. UDCA-Cooperative Group from the Spanish Association for the Study of the LiverQ73715566
An exploratory population-based case-control study of primary biliary cirrhosisQ73746110
The pathology of primary biliary cirrhosis and autoimmune cholangitisQ74280817
Pruritus and fatigue in primary biliary cirrhosisQ74280848
Open-label trial of oral nalmefene therapy for the pruritus of cholestasisQ74310569
Fatigue in primary biliary cirrhosisQ77586211
Triple therapy with ursodeoxycholic acid, prednisone and azathioprine in primary biliary cirrhosis: a 1-year randomized, placebo-controlled studyQ77619532
Expression of pyruvate-dehydrogenase complex PDC-E2 on biliary epithelial cells induced by lymph nodes from primary biliary cirrhosisQ77647596
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
Cholestatic syndromesQ79216771
Overlap of autoimmune hepatitis and primary biliary cirrhosis: an evaluation of a modified scoring systemQ94054254
A multicenter, controlled trial of ursodiol for the treatment of primary biliary cirrhosis. UDCA-PBC Study GroupQ28243457
Membrane dihydrolipoamide acetyltransferase (E2) on human biliary epithelial cells in primary biliary cirrhosisQ31167633
Anticentromere antibody in primary biliary cirrhosisQ33553886
Incidence of cancer in primary biliary cirrhosis: the Mayo experienceQ33601440
Randomised controlled trials of ursodeoxycholic-acid therapy for primary biliary cirrhosis: a meta-analysisQ33745849
Mitochondrial membrane perturbations in cholestasis.Q33836633
Primary biliary cirrhosis: an orchestrated immune response against epithelial cellsQ33916633
PBC: an infectious disease?Q34032141
Effect of stanozolol on itching in primary biliary cirrhosisQ34166986
Positive antimitochondrial antibody but normal alkaline phosphatase: is this primary biliary cirrhosis?Q34190802
Hepatic retransplantation in cholestatic liver disease: impact of the interval to retransplantation on survival and resource utilizationQ34210591
Primary biliary cirrhosis and primary sclerosing cholangitisQ34210604
Susceptibility to primary biliary cirrhosis is associated with the HLA-DR8-DQB1*0402 haplotypeQ34245122
SEROLOGICAL TESTS IN DIAGNOSIS OF PRIMARY BILIARY CIRRHOSISQ34259351
Fat-soluble vitamin levels in patients with primary biliary cirrhosisQ34379099
Low prevalence of primary biliary cirrhosis in Victoria, Australia. Melbourne Liver GroupQ34408189
Breast cancer in women with primary biliary cirrhosisQ34491081
Serum bilirubin: a prognostic factor in primary biliary cirrhosisQ34494336
Primary biliary cirrhosis: new thoughts on pathophysiology and treatmentQ34515652
Rationale for trials of long-term mycophenolate mofetil therapy for primary biliary cirrhosisQ34516425
Hepatic osteodystrophy: vitamin D metabolism in patients with liver diseaseQ34530672
The association between gravidity and primary biliary cirrhosisQ35143021
Characterisation of patients with primary biliary cirrhosis responding to long term ursodeoxycholic acid treatmentQ35358467
Serum antibodies to Helicobacter hepaticus and Helicobacter pylori in patients with chronic liver diseaseQ35359468
Hepatitis and liver dysfunction with rifampicin therapy for pruritus in primary biliary cirrhosis.Q35594405
Hyperlipidaemic state and cardiovascular risk in primary biliary cirrhosisQ35594898
Molecular mimicry in primary biliary cirrhosis. Evidence for biliary epithelial expression of a molecule cross-reactive with pyruvate dehydrogenase complex-E2Q35610980
Incidence and prevalence of primary biliary cirrhosis in the city of Newcastle upon Tyne, EnglandQ39452020
Serum bile acids in primary biliary cirrhosis: effect of ursodeoxycholic acid therapyQ70670255
Does primary biliary cirrhosis in men differ from primary biliary cirrhosis in women?Q71428839
Ursodeoxycholic acid and prednisolone versus ursodeoxycholic acid and placebo in the treatment of early stages of primary biliary cirrhosisQ71605603
A randomized trial comparing colchicine and ursodeoxycholic acid combination to ursodeoxycholic acid in primary biliary cirrhosis. UDCA-PBC Study GroupQ71748735
Effects of bile acids and cholestasis on major histocompatibility complex class I in human and rat hepatocytesQ72164376
Antibodies to carbonic anhydrase in patients with immune cholangiopathiesQ72281881
Autoimmune cholangitis: a variant of primary biliary cirrhosis. Clinicopathologic and serologic correlations in 200 casesQ72313586
Prediction of prognosis of primary biliary cirrhosis in JapanQ72336290
Ursodeoxycholic acid in the treatment of primary biliary cirrhosisQ72401649
Immunohistochemical characterization of hepatic lymphocytes in primary biliary cirrhosis in comparison with primary sclerosing cholangitis and autoimmune chronic active hepatitisQ72582427
Soluble intercellular adhesion molecule-1 in primary biliary cirrhosis: relationship with disease stage, immune activity and cholestasisQ72719827
Effect of ursodeoxycholic acid on serum lipids of patients with primary biliary cirrhosisQ72736523
Oral budesonide and ursodeoxycholic acid for treatment of primary biliary cirrhosis: results of a prospective double-blind trialQ73026352
Is fatigue associated with cholestasis mediated by altered central neurotransmission?Q73043135
Bezafibrate in the treatment of primary biliary cirrhosis: comparison with ursodeoxycholic acidQ73122828
The influence of smoking on vitamin D status and calcium metabolismQ73282911
Vitamin D-receptor genotypes as independent genetic predictors of decreased bone mineral density in primary biliary cirrhosisQ73302312
The geographical distribution of primary biliary cirrhosis in a well-defined cohort.Q39587052
Phenobarbital Effects in Cholestatic Liver DiseaseQ39589574
Staging of chronic nonsuppurative destructive cholangitis (syndrome of primary biliary cirrhosis)Q39859200
Familial primary biliary cirrhosisQ40634968
The true impact of fatigue in primary biliary cirrhosis: a population studyQ40643274
Epidemiology and natural history of primary biliary cirrhosis in a US communityQ40735092
Combined analysis of randomized controlled trials of ursodeoxycholic acid in primary biliary cirrhosisQ40883127
Effects of naloxone infusions in patients with the pruritus of cholestasis. A double-blind, randomized, controlled trialQ41673941
Genes within the HLA class II region confer both predisposition and resistance to primary biliary cirrhosisQ42597329
A prospective trial of colchicine for primary biliary cirrhosisQ42659809
Transplantation for primary biliary cirrhosis: retrospective analysis of 400 patients in a single centerQ43513105
Ursodeoxycholic acid for primary biliary cirrhosis: lessons from the past--issues for the futureQ43623767
Hypercholesterolemia and atherosclerosis in primary biliary cirrhosis: what is the risk?Q43676662
Immunoreactivity of organic mimeotopes of the E2 component of pyruvate dehydrogenase: connecting xenobiotics with primary biliary cirrhosisQ43710194
Utilization of the Mayo risk score in patients with primary biliary cirrhosis receiving ursodeoxycholic acidQ43893454
Tumor necrosis factor-alpha and transforming growth factor-beta reflect severity of liver damage in primary biliary cirrhosisQ43967448
Randomized trial of chlorambucil for primary biliary cirrhosis.Q44093311
Vitamin E deficiency and psychomotor dysfunction in adults with primary biliary cirrhosisQ44412633
The demography of primary biliary cirrhosis in Ontario, CanadaQ44439436
When is liver biopsy needed in the diagnosis of primary biliary cirrhosis?Q44797408
Natural history of pruritus in primary biliary cirrhosisQ44797529
Risk factors for primary biliary cirrhosis in a cohort of patients from the united statesQ44933098
Ursodeoxycholate conjugates protect against disruption of cholesterol-rich membranes by bile salts.Q45089631
Prognosis in primary biliary cirrhosis: model for decision makingQ46316848
A 3-year pilot study with 1,25-dihydroxyvitamin D, calcium, and calcitonin for severe osteodystrophy in primary biliary cirrhosis.Q50623946
Cost-effectiveness of ursodeoxycholic acid therapy in primary biliary cirrhosis.Q50636830
Bone disease in primary biliary cirrhosis: independent indicators and rate of progression.Q50684179
Reduced serum lipoprotein(a) levels in patients with primary biliary cirrhosis.Q51597355
Optimal timing of liver transplantation for primary biliary cirrhosis.Q52240035
Validation of a fatigue impact score in primary biliary cirrhosis: towards a standard for clinical and trial use.Q52920374
Flumecinol for the treatment of pruritus associated with primary biliary cirrhosis.Q53662990
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
Multicentre randomized placebo-controlled trial of ursodeoxycholic acid with or without colchicine in symptomatic primary biliary cirrhosisQ58803462
Molecular mimicry in liver diseaseQ59072748
Familial primary biliary cirrhosis reassessed: a geographically-based population studyQ61633902
Thalidomide as therapy for primary biliary cirrhosis: a double-blind placebo controlled pilot study.Q64974270
A controlled trial of prednisolone treatment in primary biliary cirrhosis. Three-year resultsQ67590480
Sodium fluoride prevents bone loss in primary biliary cirrhosisQ67590482
Immunomodulatory effects of ursodeoxycholic acid on immune responsesQ68225187
A controlled trial of cyclosporine in the treatment of primary biliary cirrhosisQ68505504
Sjögren's syndrome in patients with primary biliary cirrhosisQ68802525
Primary biliary cirrhosis: associations with class II major histocompatibility complex antigensQ68829231
Pathogenesis of steatorrhea in primary biliary cirrhosisQ68940388
The Presentation and Diagnosis of 100 Patients with Primary Biliary CirrhosisQ69302463
A pilot, double-blind, controlled 1-year trial of prednisolone treatment in primary biliary cirrhosis: hepatic improvement but greater bone lossQ69721905
Prospective evaluation of esophageal varices in primary biliary cirrhosis: development, natural history, and influence on survivalQ69738156
Primary biliary cirrhosis and Graves' diseaseQ69805652
Trial of penicillamine in advanced primary biliary cirrhosisQ69887093
Cyclosporin A treatment in primary biliary cirrhosis: results of a long-term placebo controlled trialQ70542319
The results of a randomized double blind controlled trial evaluating malotilate in primary biliary cirrhosis. A European multicentre study groupQ70590270
P433issue9377
P407language of work or nameEnglishQ1860
P921main subjectprimary biliary cholangitisQ1072420
P304page(s)53-61
P577publication date2003-07-01
P1433published inThe LancetQ939416
P1476titlePrimary biliary cirrhosis
P478volume362

Reverse relations

cites work (P2860)
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