familial hypercholesterolemia (fh) is an autosomal co-dominant disorder of lipid metabolism, caused by mutations in ldl receptor gene. the penetrance of fh is almost 100%, meaning that half of the offspring of affected parents born with disease. the patients are at risk of premature coronary heart disease (chd). there is no report about the molecular basis of fh in iran. identification of mutat...

objective(s) oxidized low-density lipoproteins (ox-ldls) appear to play a significant role in atherogenesis. in fact, circulating ox-ldl concentrations have been recognized as a risk factor for cardiovascular disease (cvd). the main objectives of this study were to assess the effects of antioxidant vitamins on ox-ldl as a biomarker of cvd in male subjects with cvd risk factors. materials and me...

conclusions this study provides evidence indicating high prevalence of metabolic syndrome in children with t1dm in southern iran. preventive programs aimed towards decreasing the risk factors of metabolic syndrome and interpretation of a healthier diet and physical activity for children with t1dm should be considered in our country. results in this study, 87 children with diabetes (48 females a...

We compared the results obtained by a micromethod for the determination of plasma lipoprotein cholesterol, in which electrophoresis is used to separate the lipoprotein fractions (beta-, pre-beta-, and alpha-lipoproteins), with those determinations with ultracentrifugation (low-density, very-low-density, and high-density lipoproteins). Precision of determination (coefficient of variation, CV, %)...

Familial hyperalphalipoproteinemia is determined by a major gene and is characterized by high levels of high density lipoprotein cholesterol and longevity. To describe the plasma lipoproteins in this condition more completely, a kindred consisting of the proband, her affected father, add her two affected brothers was studied. Fasting plasmas were analyzed for lipoprotein lipids by combined prep...