Clinical and biochemical expression of the histopathological lesions of primary biliary cirrhosis. UDCA-PBC Group

scientific article published on 01 March 1999

Clinical and biochemical expression of the histopathological lesions of primary biliary cirrhosis. UDCA-PBC Group is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/S0168-8278(99)80098-1
P698PubMed publication ID10190722

P2093author name stringB Balkau
O Chazouillères
R Poupon
R E Poupon
P2860cites workA multicenter, controlled trial of ursodiol for the treatment of primary biliary cirrhosis. UDCA-PBC Study GroupQ28243457
The pruritus of cholestasis and the opioid systemQ34239166
Histopathological features in mixed types of chronic aggressive hepatitis and primary biliary cirrhosis. Correlations of liver histology with mitochondrial antibodies of different specificityQ39809553
The control of pain in peripheral tissue by opioids.Q40531445
A 33-year-old woman with an autoimmune syndromeQ43550973
The problem of histologic evaluation of primary biliary cirrhosisQ66841743
Chronic active hepatitis with histological features of primary biliary cirrhosisQ68822637
Sequential and diagnostic features in primary biliary cirrhosis based on serial histologic study in 209 patientsQ70109771
Primary biliary cirrhosisQ71742524
Primary biliary cirrhosis-autoimmune hepatitis overlap syndrome. Corticoresistance and effective treatment by cyclosporine AQ72188593
Autoimmune cholangiopathy: the result of consecutive primary biliary cirrhosis and autoimmune hepatitis?Q72800622
Sustained biochemical and histologic remission of primary biliary cirrhosis in response to medical treatmentQ73316077
Primary biliary cirrhosis-autoimmune hepatitis overlap syndrome: clinical features and response to therapyQ77058192
P433issue3
P921main subjectprimary biliary cholangitisQ1072420
P304page(s)408-412
P577publication date1999-03-01
P1433published inJournal of HepatologyQ15724402
P1476titleClinical and biochemical expression of the histopathological lesions of primary biliary cirrhosis. UDCA-PBC Group
P478volume30

Reverse relations

cites work (P2860)
Q64077115A Practical Review of Primary Biliary Cholangitis for the Gastroenterologist
Q73419940Aberrant expression of cytokeratin 7 as a histological marker of progression in primary biliary cirrhosis
Q34594429Anti-gp210 and anti-centromere antibodies are different risk factors for the progression of primary biliary cirrhosis
Q90443379Apoptosis induced by ursodeoxycholic acid in human melanoma cells through the mitochondrial pathway
Q34746158Autoimmune hepatitis and overlap syndromes
Q35573912Autoimmune overlapping syndromes
Q36193470Case-control study on prednisolone combined with ursodeoxycholic acid and azathioprine in pure primary biliary cirrhosis with high levels of immunoglobulin G and transaminases: efficacy and safety analysis
Q91795125Clinical Updates in Primary Biliary Cholangitis: Trends, Epidemiology, Diagnostics, and New Therapeutic Approaches
Q24247122Colchicine for primary biliary cirrhosis
Q44487597Combined analysis of the effect of treatment with ursodeoxycholic acid on histologic progression in primary biliary cirrhosis
Q27333658Inhibition of the Unfolded Protein Response Mechanism Prevents Cardiac Fibrosis
Q38738566Pharmacological interventions for primary biliary cholangitis: an attempted network meta-analysis.
Q89639221Preventative care in cholestatic liver disease: Pearls for the specialist and subspecialist
Q90707736Primary Biliary Cholangitis: 2018 Practice Guidance from the American Association for the Study of Liver Diseases
Q56428273Primary biliary cirrhosis
Q26853649Primary biliary cirrhosis: Pathophysiology, clinical presentation and therapy
Q35573894Primary biliary cirrhosis—presentation and diagnosis
Q35573916Pruritus and fatigue in primary biliary cirrhosis
Q35628089Pruritus in chronic liver disease: mechanisms and treatment
Q44797516Studying pruritus in the 21st century
Q52624982The British Society of Gastroenterology/UK-PBC primary biliary cholangitis treatment and management guidelines.
Q35833175The diagnosis and treatment of primary biliary cirrhosis
Q24202184Ursodeoxycholic acid for primary biliary cirrhosis
Q33866782Ursodeoxycholic acid treatment of vanishing bile duct syndromes

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