Veille | CBP

Derniers articles listés par Medworm sur la CBP (en anglais)

MedWorm: Primary Biliary Cirrhosis

Primary biliary cirrhosis: a multi‐faced interactive disease involving genetics, environment and the immune response
Deletion of IL‐12p35 induces liver fibrosis in dominant negative transforming growth factor β receptor type II mice
Classical HLA-DRB1 and DPB1 alleles account for HLA associations with primary biliary cirrhosis
Is primary biliary cirrhosis a steroid‐sensitive autoimmune disease?
Cutting-edge Issues in Autoimmunity and Allergy of the Digestive System
Living‐donor liver transplantation for autoimmune hepatitis and autoimmune hepatitis–primary biliary cirrhosis overlap syndrome
Epitope-specific anti-nuclear antibodies are expressed in a mouse model of primary biliary cirrhosis and are cytokine-dependent.
The role of natural killer (NK) and NK T cells in the loss of tolerance in murine primary biliary cirrhosis.
Assessment of metabolic syndrome in patients with primary biliary cirrhosis.
Herbal medicines: Liver injury (first report with Melissa officinalis) mimicking primary biliary cirrhosis in an elderly patient: case report
Epitope‐specific anti‐nuclear antibodies are expressed in a mouse model of primary biliary cirrhosis and are cytokine‐dependent
The role of natural killer (NK) and NK T cells in the loss of tolerance in murine primary biliary cirrhosis
The Promise and Pitfalls of Serologic Testing in Inflammatory Bowel Disease
Living donor liver transplantation for autoimmune hepatitis and autoimmune hepatitis‐primary biliary cirrhosis overlap syndrome
Comparative analysis of portal cell infiltrates in antimitochondrial autoantibody–positive versus antimitochondrial autoantibody–negative primary biliary cirrhosis
Survival Data Analysis with Time-Dependent Covariates Using Generalized Additive Models
Primary biliary cirrhosis and cancer risk: a systematic review and meta‐analysis
Primary biliary cirrhosis and the nuclear pore complex.
Antimitochondrial antibody ‐M2 positive autoimmune hepatitis during standard of care for chronic hepatitis C
Sleep Disorders in Chronic Liver Disease
Efficacy of fenofibrate in Chinese patients with primary biliary cirrhosis partially responding to ursodeoxycholic acid therapy
Etiopathogenesis of primary biliary cirrhosis: an overview of recent developments
The human IL-7 receptor gene: Deletions, polymorphisms and mutations.
Unexplained Findings of Kayser-Fleischer-Like Rings in a Patient with Cryptogenic Cirrhosis
Pathogenesis and Management of Pruritus in Cholestatic Liver Disease
Cytotoxic T‐lymphocyte associated antigen‐4 gene polymorphisms and Primary Biliary Cirrhosis: A Systematic Review
Prevalence and associated factors with esophageal varices in early primary biliary cirrhosis
Pathogenesis and Management of Pruritus in Cholestatic Liver Disease
Prevalence and associated factors with esophageal varices in early primary biliary cirrhosis
Cytotoxic T‐lymphocyte associated antigen‐4 gene polymorphisms and Primary Biliary Cirrhosis: A Systematic Review
Unusual binding of ursodeoxycholic acid to ileal bile acid binding protein: role in activation of FXR{alpha} [Research Articles]
Characterization of Ursodeoxycholic and Norursodeoxycholic Acid as Substrates of the Hepatic Uptake Transporters OATP1B1, OATP1B3, OATP2B1 and NTCP
On the covariate-adjusted estimation for an overall treatment difference with data from a randomized comparative clinical trial
Influence of liver‐disease etiology on long‐term quality of life and employment after liver transplantation
Etiological factors in primary hepatic B-cell lymphoma
The Role of NK and NKT cells in the Loss of Tolerance in Murine Primary Biliary Cirrhosis
Upregulation of mir‐506 leads to decreased AE2 expression in biliary epithelium of patients with primary biliary cirrhosis
The Role of NK and NKT cells in the Loss of Tolerance in Murine Primary Biliary Cirrhosis
Upregulation of mir‐506 leads to decreased AE2 expression in biliary epithelium of patients with primary biliary cirrhosis
Investigation of Histological Vascular Invasion From Preoperative Evaluation in Patients with Hepatocellular Carcinoma Who Underwent Living Donor Liver Transplantation
Model for End-stage Liver Disease and Model for End-stage Liver Disease-Na Scores Predict Both Before-Listing and Wait-List Mortality
Distribution‐free inference on contrasts of arbitrary summary measures of survival
The current endeavors to understand the pathogenesis of intractable liver diseases.
Epitope‐specific Antinuclear Antibodies are Expressed in a Mouse Model of Primary Biliary Cirrhosis and are Cytokine‐dependent
Extended quasi‐likelihood with fractional polynomials in the frame of the accelerated failure time model
High prevalence of primary biliary cirrhosis and disease-associated autoantibodies in Japanese patients with systemic sclerosis
For Patients With Primary Biliary Cirrhosis, Rituximab A Possible Treatment Option
Rituximab possible treatment option for patients with primary biliary cirrhosis
Bezafibrate for primary biliary cirrhosis
Rituximab possible treatment option for patients with primary biliary cirrhosis
[Herbal drugs mimicking primary biliary cirrhosis].
Characterization of Ursodeoxycholic and Norursodeoxycholic Acid as Substrates of the Hepatic Uptake Transporters OATP1B1, OATP1B3, OATP2B1 and NTCP
Antinuclear Antibodies as Markers in Biliary CirrhosisAntinuclear Antibodies as Markers in Biliary Cirrhosis
Biochemical and immunologic effects of rituximab in patients with primary biliary cirrhosis and an incomplete response to ursodeoxycholic acid
Bezafibrate for primary biliary cirrhosis.
CD8+ T-Cell Deficiency, Epstein-Barr Virus Infection, Vitamin D Deficiency, and Steps to Autoimmunity: A Unifying Hypothesis
Frequent detection of IgM anti‐herpes simplex viral antibody in patients with primary biliary cirrhosis
Noninvasive elastography‐based assessment of liver fibrosis progression and prognosis in primary biliary cirrhosis
Frequent detection of IgM anti‐herpes simplex viral antibody in patients with primary biliary cirrhosis
Association of primary biliary cirrhosis with variants in the CLEC16A, SOCS1, SPIB and SIAE immunomodulatory genes
Histamine regulation of biliary proliferation
Epidemiology of primary sclerosing cholangitis and primary biliary cirrhosis: A systematic review
Primary Biliary Cirrhosis: Bad Genes, Bad Luck
Primary Sjögren's syndrome as a systemic disease: A study of participants enrolled in an international Sjögren's syndrome registry
Generation of a cholangiocyte‐specific cDNA expression library for the identification of B and T cell autoantigens in murine biliary disease
The efficacy of fenofibrate in Chinese patients with primary biliary cirrhosis partially responding to ursodeoxycholic acid therapy
Low incidence of positive smooth muscle antibody and high incidence of isolated IgM elevation in Chinese patients with autoimmune hepatitis and primary biliary cirrhosis overlap syndrome: a retrospective study
Bisphosphonates for osteoporosis in primary biliary cirrhosis
Fibrosis distribution in explanted cirrhotic livers
Excellent posttransplant survival for patients with nonalcoholic steatohepatitis in the United States
Bisphosphonates for osteoporosis in primary biliary cirrhosis.
Hormone replacement for osteoporosis in women with primary biliary cirrhosis.
Hepatobiliary membrane transporters in primary biliary cirrhosis
Primary biliary cirrhosis and Sjögren's syndrome: Autoimmune epithelitis.
Low incidence and prevalence of primary biliary cirrhosis in Canterbury, New Zealand: a population-based study
Metabolomic profiling of 17 bile acids in serum from patients with primary biliary cirrhosis and primary sclerosing cholangitis: A pilot study
IgM predominance in autoimmune disease: Genetics and gender.
Possible interaction between opioidergic and cholinergic systems of CA1 in cholestasis-induced amnesia in mice.
Cumulative risk of cardiovascular events following orthotopic liver transplantation
Optimizing biochemical markers as endpoints for clinical trials in primary biliary cirrhosis
Sex differences in spontaneous versus induced animal models of autoimmunity.
The X chromosome and the sex ratio of autoimmunity.
Immunopathogenesis of Primary biliary cirrhosis: An old wives' tale
Comparative analysis of portal cell infiltrates in antimitochondrial autoantibody–positive versus antimitochondrial autoantibody–negative primary biliary cirrhosis
Autoimmune liver disease
Diagnosis of primary biliary cirrhosis
Liver transplantation in autoimmune liver diseases
Comparative analysis of portal cell infiltrates in AMA positive versus AMA negative PBC
Seasonal variation in the patient diagnosis of primary biliary cirrhosis: Further evidence for an environmental component to etiology
De novo autoimmune hepatitis associated with PTH(1–34) and PTH(1–84) administration for severe osteoporosis in a liver transplant patient
Cytotoxic T‐lymphocyte antigen 4 gene +49A/G polymorphism significantly associated with susceptibility to primary biliary cirrhosis: A meta‐analysis
Severe outflow block syndrome caused by compression by the swollen caudate lobe after living donor liver transplantation: report of a case
AASLD: Drug for Autoimmune Liver Disease Promising (CME/CE)
Effect of the aetiology and severity of liver disease on oral health and dental treatment prior to transplantation
Primary biliary cirrhosis in a rheumatoid arthritis patient treated with rituximab, a case-based review
Toll-Like Receptors in Secondary Obstructive Cholangiopathy
Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis
Plasma cells and the chronic nonsuppurative destructive cholangitis of primary biliary cirrhosis
Biochemical and immunologic effects of rituximab in primary biliary cirrhosis patients with an incomplete response to ursodeoxycholic acid
Towards common denominators in primary biliary cirrhosis: The role of IL-12
Integrative role of MRI in the evaluation of primary biliary cirrhosis
Mortality and the risk of malignancy in autoimmune liver diseases: A population‐based study in Canterbury, New Zealand
Autophagy May Precede Cellular Senescence of Bile Ductular Cells in Ductular Reaction in Primary Biliary Cirrhosis
Prevalence of non-organ-specific autoantibodies in a rural community from northeastern Brazil: a population-based study.
Pathological vertebra fracture in a man with primary biliary cirrhosis
Long-term Outcomes of Patients With Primary Biliary Cirrhosis and Hepatocellular Carcinoma
Recurrent and De Novo Autoimmune Liver Diseases
Fine phenotypic and functional characterization of effector cluster of differentiation 8 positive T cells in human patients with primary biliary cirrhosis
NovImmune commences primary biliary cirrhosis drug study
A possible involvement of p62/sequestosome‐1 in the process of biliary epithelial autophagy and senescence in primary biliary cirrhosis
HLA class II molecules confer both susceptibility and progression in Japanese patients with primary biliary cirrhosis
Human leukocyte antigen class II molecules confer both susceptibility and progression in japanese patients with primary biliary cirrhosis
Primary biliary cirrhosis
Bezafibrate in Patients With Primary Biliary CirrhosisBezafibrate in Patients With Primary Biliary Cirrhosis
Long-term ursodeoxycholate improves circulating redox changes in primary biliary cirrhotic patients.
Excellent post‐transplantation survival in patients with non‐alcoholic steatohepatitis in the united states
Hypothesis for a new method to measure the dynamic patterns of tissue injury
Long‐term outcome of living donor liver transplantation for primary biliary cirrhosis
The multi-hit hypothesis of primary biliary cirrhosis: polyinosinic-polycytidylic acid (poly I:C) and murine autoimmune cholangitis.
Primary Biliary Cirrhosis-related Autoantibodies in a Large Cohort of Italian Patients with Systemic Sclerosis.
Meta‐analysis: Cytotoxic T‐lymphocyte antigen 4 gene +49A/G polymorphism significantly associates with susceptibility to Primary Biliary Cirrhosis
The multi‐hit hypothesis of primary biliary cirrhosis: polyinosinic‐polycytidylic acid (poly I:C) and murine autoimmune cholangitis
Autoimmune liver disease - Are there spectra that we do not know?
Relevance of the inner mitochondrial membrane enzyme F1F0‐ATPase as an autoantigen in autoimmune liver disorders
Elastography-based assessment of primary biliary cirrhosis staging
The diagnosis and treatment of primary biliary cirrhosis.
Autoimmune hepatitis from the paediatric perspective
Primary biliary cirrhosis – Autoimmune hepatitis overlap syndrome: A rationale for corticosteroids use based on a nation‐wide retrospective study in Japan
No more pilots, a phase III trial of fibrates in primary biliary cirrhosis is long overdue!
An increased risk of Urinary Tract Infection precedes development of Primary Biliary Cirrhosis.
Outcomes of orthotopic liver transplantation for hepatic sarcoidosis: An analysis of the United Network for organ sharing/organ Procurement and Transplantation Network data files for a comparative study with cholestatic liver diseases
Anti-CENPI autoantibodies in scleroderma patients with features of autoimmune liver diseases.
Immunoglobulin M levels inversely correlate with CD40 ligand promoter methylation in patients with primary biliary cirrhosis
IgM levels inversely correlate with cd40l promoter methylation in patients with primary biliary cirrhosis Hepatology‐Ana lleo library 4‐26
Endoscopic naso-pancreatic drainage for the treatment of pancreatic fistula occurring after LDLT.
The impact of biopsychosocial factors on quality of life: Women with primary biliary cirrhosis on waiting list and post liver transplantation.
Seasonal variation in the diagnosis of primary biliary cirrhosis: Further evidence for an environmental component to etiology
Performance and utility of transient elastography and noninvasive markers of liver fibrosis in primary biliary cirrhosis
NKT cells in liver fibrosis: Controversies or complexities
Electrophile-modified lipoic derivatives of PDC-E2 elicits anti-mitochondrial antibody reactivity.
Fine phenotypic and functional characterization of effector CD8+ T cells in patients with primary biliary cirrhosis
[No Complaints, but Constantly Elevated Cholestatic Serum Liver Tests.]

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Sommaire de cette partie : veille & bibliographie

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