scholarly article | Q13442814 |
review article | Q7318358 |
P356 | DOI | 10.1016/S0140-6736(03)13808-1 |
P698 | PubMed publication ID | 12853201 |
P2093 | author name string | Jayant A Talwalkar | |
Keith D Lindor | |||
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The influence of smoking on vitamin D status and calcium metabolism | Q73282911 | ||
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The geographical distribution of primary biliary cirrhosis in a well-defined cohort. | Q39587052 | ||
Phenobarbital Effects in Cholestatic Liver Disease | Q39589574 | ||
Staging of chronic nonsuppurative destructive cholangitis (syndrome of primary biliary cirrhosis) | Q39859200 | ||
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The true impact of fatigue in primary biliary cirrhosis: a population study | Q40643274 | ||
Epidemiology and natural history of primary biliary cirrhosis in a US community | Q40735092 | ||
Combined analysis of randomized controlled trials of ursodeoxycholic acid in primary biliary cirrhosis | Q40883127 | ||
Effects of naloxone infusions in patients with the pruritus of cholestasis. A double-blind, randomized, controlled trial | Q41673941 | ||
Genes within the HLA class II region confer both predisposition and resistance to primary biliary cirrhosis | Q42597329 | ||
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Transplantation for primary biliary cirrhosis: retrospective analysis of 400 patients in a single center | Q43513105 | ||
Ursodeoxycholic acid for primary biliary cirrhosis: lessons from the past--issues for the future | Q43623767 | ||
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 cirrhosis | Q43710194 | ||
Utilization of the Mayo risk score in patients with primary biliary cirrhosis receiving ursodeoxycholic acid | Q43893454 | ||
Tumor necrosis factor-alpha and transforming growth factor-beta reflect severity of liver damage in primary biliary cirrhosis | Q43967448 | ||
Randomized trial of chlorambucil for primary biliary cirrhosis. | Q44093311 | ||
Vitamin E deficiency and psychomotor dysfunction in adults with primary biliary cirrhosis | Q44412633 | ||
The demography of primary biliary cirrhosis in Ontario, Canada | Q44439436 | ||
When is liver biopsy needed in the diagnosis of primary biliary cirrhosis? | Q44797408 | ||
Natural history of pruritus in primary biliary cirrhosis | Q44797529 | ||
Risk factors for primary biliary cirrhosis in a cohort of patients from the united states | Q44933098 | ||
Ursodeoxycholate conjugates protect against disruption of cholesterol-rich membranes by bile salts. | Q45089631 | ||
Prognosis in primary biliary cirrhosis: model for decision making | Q46316848 | ||
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 | ||
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Pathogenesis of steatorrhea in primary biliary cirrhosis | Q68940388 | ||
The Presentation and Diagnosis of 100 Patients with Primary Biliary Cirrhosis | Q69302463 | ||
A pilot, double-blind, controlled 1-year trial of prednisolone treatment in primary biliary cirrhosis: hepatic improvement but greater bone loss | Q69721905 | ||
Prospective evaluation of esophageal varices in primary biliary cirrhosis: development, natural history, and influence on survival | Q69738156 | ||
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P433 | issue | 9377 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | primary biliary cholangitis | Q1072420 |
P304 | page(s) | 53-61 | |
P577 | publication date | 2003-07-01 | |
P1433 | published in | The Lancet | Q939416 |
P1476 | title | Primary biliary cirrhosis | |
P478 | volume | 362 |
Q37207972 | 38-year-old woman with abnormal liver enzymes and hyperlipidemia |
Q33645189 | A case of primary biliary cirrhosis associated with pernicious anemia: a case report |
Q33867374 | A case of primary biliary cirrhosis complicated by Behçet's disease and palmoplantar pustulosis |
Q35837039 | A case of severe osteomalacia caused by Tubulointerstitial nephritis with Fanconi syndrome in asymptomotic primary biliary cirrhosis. |
Q46872722 | AMA production in primary biliary cirrhosis is promoted by the TLR9 ligand CpG and suppressed by potassium channel blockers |
Q46745228 | Altered monocyte responses to defined TLR ligands in patients with primary biliary cirrhosis |
Q84476629 | American Association for the Study of Liver Diseases endpoints conference: design and endpoints for clinical trials in primary biliary cirrhosis |
Q36300105 | Antimitochondrial antibodies in patients with chronic hepatitis C virus infection: description of 18 cases and review of the literature |
Q35926418 | Approach to a patient with elevated serum alkaline phosphatase |
Q34993666 | Asymptomatic primary biliary cirrhosis is not associated with increased frequency of cardiovascular disease |
Q33866371 | Autoimmune liver disease and the Canadian First Nations Aboriginal Communities of British Columbia's Pacific Northwest. |
Q36166941 | B cell depletion in treating primary biliary cirrhosis: pros and cons |
Q46484331 | B-cell depletion with rituximab in patients with primary biliary cirrhosis refractory to ursodeoxycholic acid |
Q35769888 | Can the laboratory affect the investigation and diagnosis of primary biliary cirrhosis? |
Q54573681 | Chenodeoxycholic acid and taurochenodexycholic acid induce anti-apoptotic cIAP-1 expression in human hepatocytes. |
Q24235780 | Chlorambucil for primary biliary cirrhosis |
Q36567737 | Cholestatic liver disease. Recognizing the clinical signs |
Q56907597 | Circulating auto-antibodies against nuclear and non-nuclear antigens in primary Sjögren's syndrome |
Q37182934 | Clinical features and management of primary biliary cirrhosis. |
Q55041843 | Correlation of initial autoantibody profile and clinical outcome in primary biliary cirrhosis. |
Q43114906 | Current and emerging surrogate markers of hepatic fibrosis in primary biliary cirrhosis |
Q37993224 | Cytotoxic T-lymphocyte associated antigen-4 gene polymorphisms and primary biliary cirrhosis: a systematic review |
Q37194433 | Diagnosing and treating a patient with primary biliary cirrhosis |
Q38266358 | Diagnosis and management of primary biliary cirrhosis |
Q33612198 | Diagnostic utility of IgG and IgM immunohistochemistry in autoimmune liver disease |
Q37699257 | Disappearance of Oral Lichen Planus After Liver Transplantation for Primary Biliary Cirrhosis and Immunosuppressive Therapy in a 63-year-Old Japanese Woman |
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Q43457417 | Falls and fall-related injury are common in older people with chronic liver disease. |
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Q55038191 | Frequency of monosomy X in women with primary biliary cirrhosis. |
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Q28268456 | Generalized morphea and primary biliary cirrhosis coexisting in a male patient |
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Q37642274 | Genetic Contribution to the Pathogenesis of Primary Biliary Cholangitis. |
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Q28235162 | Human leukocyte antigen class II alleles in Caucasian women with primary biliary cirrhosis |
Q35760984 | Hypercholesterolaemia is not associated with early atherosclerotic lesions in primary biliary cirrhosis |
Q34012609 | Hyperhomocysteinemia and hypercoagulability in primary biliary cirrhosis. |
Q38957567 | Imaging of autoimmune biliary disease |
Q53019283 | Immunologic derangement preceding clinical autoimmunity. |
Q40186249 | Increased prevalence of antimitochondrial antibodies in first-degree relatives of patients with primary biliary cirrhosis |
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Q43155895 | Is there a role for tetrathiomolybdate in the treatment of primary biliary cirrhosis? |
Q37372660 | Keratin variants are overrepresented in primary biliary cirrhosis and associate with disease severity |
Q43419136 | Lack of PBC-specific antimitochondrial antibodies in patients with Chlamydia pneumoniae infection |
Q53136628 | Lack of association between vitamin D receptor gene ApaI, BsmI, and TaqI polymorphisms and primary biliary cirrhosis risk: a meta-analysis. |
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