نتایج جستجو برای: hypercholesterolemia
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Abstract Background and objectives: Familial hypercholesterolemia (FH) is an autosomal disorder characterized by increased levels of total cholesterol and low density lipoprotein cholesterol. The FH clinical phenotype has been associated with increased risk of coronary heart disease and premature death. The mutation in LDLR gene in most cases is responsible for FH phenotype. Furthermore, other ...
Vol.31, No. 4, 1985 649 tecting hypercholesterolemia must have the best possible analytical performance. We suggest that, in screening a population for hypercholesterolemia, serum or plasma samples are preferable to blood spots on fiter paper. Instruments such as the Cobas-Bio centrifugal analyzer require less than 50 L of sample and the typical overall CV is 4% for assays of cholesterol in pla...
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