Results 21 to 30 of about 179 (145)
Update on Primary Biliary Cirrhosis
Canadian Journal of Gastroenterology and Hepatology, Volume 14, Issue 1, Page 43-48, 2000., 2000 The diagnosis of primary biliary cirrhosis (PBC) is most often made in the asymptomatic phase, sometimes before the development of abnormal liver biochemistry. The antimitochondrial antibody remains the predominant hallmark, although not all patients test positive, even when the most sensitive techniques are used.
Jenny Heathcote
wiley +1 more source
Primary Biliary Cirrhosis and Type II Autoimmune Polyglandular Syndrome
Canadian Journal of Gastroenterology and Hepatology, Volume 13, Issue 9, Page 767-770, 1999., 1999 A 45‐year‐old female was diagnosed with Hashimoto’s thyroiditis in 1976 and Addison’s disease in 1979. At that time, her antimitochondrial antibody (AMA) level was elevated at 1:32. She subsequently developed premature ovarian failure and type I diabetes mellitus. In 1996, she became jaundiced with a cholestatic enzyme pattern.
Mark Ram Borgaonkar +1 more
wiley +1 more source
Hepatobiliary Tract and Pancreatic Disorders in Celiac Disease
Canadian Journal of Gastroenterology and Hepatology, Volume 11, Issue 1, Page 77-81, 1997., 1997 A number of hepatobiliary tract and pancreatic disorders have been documented in patients with celiac disease. Some disorders have shared immunological or genetic factors, including chronic hepatitis, primary biliary cirrhosis and sclerosing cholangitis. Other hepatic or pancreatic pathological changes in celiac disease have been documented with severe
Hugh J Freeman
wiley +1 more source
Descriptive Epidemiology of Primary Biliary Cirrhosis in the Province of Quebec
Canadian Journal of Gastroenterology and Hepatology, Volume 5, Issue 5, Page 174-178, 1991., 1991 Primary biliary cirrhosis (PBC) is a rare disease, but is usually recognized because of the characteristic clinical picture and the diagnostic specificity of antimitochondrial antibody (AMA) determination. Information on the epitlemiology of PBC is limited.
Jean-Pierre Villeneuve +2 more
wiley +1 more source
Antibodies to Cardiolipin in Patients with Primary Biliary Cirrhosis
Canadian Journal of Gastroenterology and Hepatology, Volume 3, Issue 3, Page 98-102, 1989., 1989 Antibodies to cardiolipin have been recognized in up to 65% of patients with systemic lupus erythematosus. It has been claimed that they are significantly associated with intravascular thrombosis and with obstetrical complications. Thus far they have been found to be less prevalent in other diseases.
John Verrier Jones +6 more
wiley +1 more source
, 2002 Canadian Journal of Gastroenterology and Hepatology, Volume 16, Issue 10, Page 727-732, 2002.
Richard N Fedorak, Desmond J Leddin
wiley +1 more source
Atteintes pulmonaires au cours de la cirrhose biliaire primitive [PDF]
, 2004 La cirrhose biliaire primitive (CBP) est une hépatopathie auto-immune. Des atteintes de l'appareil respiratoire ont été décrites au cours de la maladie.
CRESTANI, Bruno, BORIE, Raphaël
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Acquisitions thérapeutiques 1999 : Syndrômes cholestatiques [PDF]
, 2000 Les syndromes cholestatiques principaux sont la cirrhose biliaire primitive et la cholangite primaire sclérosante. L'acide ursodésoxycholique reste le traitement de choix pour la cirrhose biliaire primitive.
Gonvers, J.J. +4 more
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Hépatopathies autoimmunes [PDF]
, 1998 La cirrhose biliaire primitive, l'hépatite autoimmune et la cholangite sclérosante primitive sont des causes d'hépatopathies chroniques ou aiguës dont nous revoyons l'approche diagnostique immunologique: IgG, IgM et différents autoanticorps ...
Mantegani, A., Spertini, F.
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Primary biliary cirrhosis and hepatocellular carcinoma : are the two directly correlated ? Report upon a case [PDF]
, 1996 Les auteurs rapportent un cas de carcinome hépatocellulaire (CHC) chez un patient d'abord diagnostiqué comme porteur d'une cirrhose biliaire primitive (CBP) mais qui, après révision de l'observation, a été classée comme cirrhose post nécrotique ...
Cecchetto A. +7 more
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