Results 21 to 30 of about 150,371 (141)
Prevalence of IgA Antibodies to Endomysium and Tissue Transglutaminase in Primary Biliary Cirrhosis
Canadian Journal of Gastroenterology and Hepatology, Volume 14, Issue 8, Page 672-675, 2000., 2000 The association between celiac disease and primary biliary cirrhosis has been described in several case reports and small screening studies, with varying prevalence rates. Stored sera from 378 patients with primary biliary cirrhosis were tested for immunoglobulin (Ig) A endomysium and tissue transglutaminase antibodies.
Helen R Gillett +3 more
wiley +1 more source
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
Primitive polynomials with prescribed second coefficient [PDF]
, 2006 The Hansen-Mullen Primitivity Conjecture (HMPC) (1992) asserts that, with some (mostly obvious) exceptions, there exists a primitive polynomial of degree n over any finite fieldwith any coefficient arbitrarily prescribed.
Cohen, Stephen D. +3 more
core +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
Kyste du cholédoque compliqué d’une cirrhose biliaire secondaire chez un nourrisson de 12 mois [PDF]
Le kyste du cholédoque est une anomalie congénitale rare. Son diagnostic est difficile en l’absence de signes évocateurs et son évolution peut aboutir à des complications parmi lesquelles la cirrhose biliaire secondaire.
Boume, Missoki Azanledji +7 more
core +1 more source
Acquisitions thérapeutiques 1999 : Syndrômes cholestatiques
, 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.
Spahr, L. +4 more
core +1 more source