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Sclerosing cholangitis in ulcerative colitis.
In a 5-year period 48 (14%) of 336 patients with ulcerative colitis were found to have hepatobiliary disease. The bile ducts were examined in 35 of these patients, and optimal visualization of bothExpand
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Familial serum-cholesterol esterification failure. A new inborn error of metabolism.
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Primary sclerosing cholangitis: a long-term follow-up study.
During the 10-year period from 1 January 1975 to 31 December 1984, primary sclerosing cholangitis (PSC) was diagnosed in 45 patients. Twelve of the patients have died (26.7%), 10 of them of causesExpand
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A study of the small spherical high density lipoproteins of patients afflicted with familial lecithin: cholesterol acyltransferase deficiency.
We studied the effects of the lecithin:cholesterol acyltransferase reaction on the size and composition of the small spherical high density lipoproteins of patients afflicted with familialExpand
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Thrombocytosis in ulcerative colitis and Crohn's disease.
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Measurement of two plasma triglyceride lipases by an immunochemical method: studies in patients with hypertriglyceridemia.
Postheparin plasma lipolytic activity consists of two hydrolytic activities, hepatic triglyceride lipase and lipoprotein lipase. These two enzymes were separated and partially purified by means ofExpand
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Epidemiology of ulcerative colitis and regional enterocolitis (Crohn's disease) in Norway.
Individual reports from the paediatric, surgical and medical departments and from non-specialized hospitals showed that the incidence of cases with ulcerative colitis for the years 1964–69 was 32.9Expand
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Crohn's disease. Clinical manifestations.
Two hundred and fourteen patients with Crohn's disease (CD) consecutively admitted during a 5-year period were observed for a mean of 9 years (range, 0-35 years). Sixty-five per cent had theirExpand
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Familial serum cholesterol ester deficiency. Clinical study of a patient with a new syndrome.
Three adult sisters with only traces of esterified cholesterol in serum are reported. All had proteinuria and anemia. Elevated total cholesterol, triglyceride and phospholipid concentrations wereExpand
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Familial Plasma Lecithin:Cholesterol Acyltransferase Deficiency
A woman with familial plasma lecithin: cholesterol acyltransferase (L.C.A.T.) deficiency showed, like the other reported cases, obvious corneal opacity, proteinuria, and moderate anaemia with aExpand
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