Results 221 to 230 of about 84,856 (259)

Sclerosing cholangitis in children

The Journal of Pediatrics, 1994
We report on 56 children with sclerosing cholangitis (SC) seen between 1972 and 1992. The first symptoms occurred at a mean age of 3.7 years; 15 infants had neonatal cholestatic jaundice. At diagnosis, cholestatic jaundice was present in 25 children, hepatomegaly in 54, splenomegaly in 41, and ascites in 12.
Michelle Hadchouel, Danièle Pariente, Dominique Debray, Olivier Bernard, E. Urvoas   +4 more
openaire   +3 more sources

The microbiota and the gut–liver axis in primary sclerosing cholangitis

Nature reviews: Gastroenterology & hepatology, 2022
J. Hov, T. Karlsen
semanticscholar   +1 more source

Primary Sclerosing Cholangitis

Endoscopy, 1985
Primary sclerosing cholangitis was diagnosed in 6 patients (4 men and 2 women), with ages ranging from 33 to 71 years. Four of them had ulcerative colitis, with an evolution from 8 to 21 years, the other two had Crohn's disease with 2 and 3 years of evolution.
A D Jorge, C Esley
openaire   +6 more sources

Increase trend in the prevalence and male‐to‐female ratio of primary biliary cholangitis, autoimmune hepatitis, and primary sclerosing cholangitis in Japan

Hepatology Research, 2019
Autoimmune liver diseases (AILD) including autoimmune hepatitis (AIH), primary biliary cholangitis (PBC), and primary sclerosing cholangitis (PSC) impose a significant burden on public health, and it is important to estimate their prevalence.
A. Tanaka, Mitsuru Mori, Kosuke Matsumoto, H. Ohira, S. Tazuma, H. Takikawa   +5 more
semanticscholar   +1 more source

Reporting standards for primary sclerosing cholangitis using MRI and MR cholangiopancreatography: guidelines from MR Working Group of the International Primary Sclerosing Cholangitis Study Group

European Radiology, 2021
S. Venkatesh, Christopher L. Welle, F. Miller, K. Jhaveri, K. Ringe, J. Eaton, H. Bungay, L. Arrivé, A. Ba-Ssalamah, Aristeidis Grigoriadis, C. Schramm, A. Fulcher   +11 more
semanticscholar   +1 more source

Primary Sclerosing Cholangitis

Inflammatory Bowel Diseases, 2005
Primary sclerosing cholangitis (PSC) is a chronic cholestatic liver disease characterized by inflammation and fibrosis of the intra- and extrahepatic bile ducts. An estimated 80% of patients in North America and Europe have coexistent inflammatory bowel disease (IBD). The underlying pathophysiology of PSC remains poorly understood.
Keith D. Lindor, Jayant A. Talwalkar
openaire   +2 more sources

Primary sclerosing cholangitis

The American Journal of Surgery, 1987
Primary sclerosing cholangitis was seen in only 7 of 6,494 biliary operations performed between 1948 and 1979. Fifteen more cases were seen in 1,467 biliary operations performed over a recent 5 year period. Surgery was directed primarily towards the differential diagnosis between cholangiocarcinoma and primary sclerosing cholangitis of the upper bile ...
Thomas Taylor White, Michael J. Hart
openaire   +3 more sources

Primary Sclerosing Cholangitis

2011
Primary sclerosing cholangitis (PSC) is a chronic liver condition which may affect both intra and extrahepatic biliary tree. Etiology of PSC remains to be fully elucidated but genetic, autoimmune, inflammatory and possibly infective factors could all contribute to its development.
Piotr Milkiewicz, Ewa Wunsch
openaire   +3 more sources

Primary Sclerosing Cholangitis

Archives of Internal Medicine, 1982
Recent investigations have clarified the clinical, radiologic, and pathologic features of primary sclerosing cholangitis, a chronic fibrosing disorder affecting the biliary tree. This progressive, cholestatic biliary disease is diagnosed when an elevated serum alkaline phosphatase level and stricturing and beading of bile ducts on cholangiography are ...
openaire   +3 more sources

Sclerosing Cholangitis

Archives of Surgery, 1972
B W, Thompson, R C, Read, H J, White
openaire   +2 more sources