Myocardial infarction in the familial forms of hypertriglyceridemia.
about
Next-generation gene discovery for variants of large impact on lipid traitsFamilial combined hyperlipidemia is associated with alterations in the cholesterol synthesis pathway.FABP4 plasma levels are increased in familial combined hyperlipidemia.Plasma lipoproteins, lipid transport, and atherosclerosis: recent developmentsEffects of low dose oral contraceptives on very low density and low density lipoprotein metabolism.Cholesterol metabolism in manDietary carbohydrate's effects on lipogenesis and the relationship of lipogenesis to blood insulin and glucose concentrations.Impaired activation of adipocyte lipolysis in familial combined hyperlipidemiaDrug therapy of hypercholesterolaemia in children and adolescents.Bile acid metabolism in hereditary forms of hypertriglyceridemia: evidence for an increased synthesis rate in monogenic familial hypertriglyceridemia.A mutation in the promoter of the lipoprotein lipase (LPL) gene in a patient with familial combined hyperlipidemia and low LPL activityDNA polymorphisms in and around the Apo-A1-CIII genes and genetic hyperlipidemiasPlasma low density lipoprotein transport kinetics in noninsulin-dependent diabetes mellitus.Genetic epidemiology of low-density lipoprotein subclass phenotypes.Association of coronary atherosclerosis with hyperapobetalipoproteinemia [increased protein but normal cholesterol levels in human plasma low density (beta) lipoproteins]Apo B versus cholesterol in estimating cardiovascular risk and in guiding therapy: report of the thirty-person/ten-country panel.Genetics of apolipoprotein B and apolipoprotein AI and premature coronary artery disease.Prevention of coronary heart disease: the role of high density lipoproteinsCombined hyperlipidemia in relation to race/ethnicity, obesity, and insulin resistance in the Multi-Ethnic Study of Atherosclerosis.A diagnostic algorithm for the atherogenic apolipoprotein B dyslipoproteinemias.Study of 100 patients with bilateral sensorineural hearing loss for lipid abnormalities.Triglyceride turnover in health and disease.Triglyceride-rich lipoproteins and atherosclerosis, from fast to feast.Lipoprotein(a) as a risk factor for maternal cardiovascular disease mortality in kindreds with familial combined hyperlipidemia or familial hypertriglyceridemia.Genome-wide scan for quantitative trait loci influencing LDL size and plasma triglyceride in familial hypertriglyceridemia.Overexpression and accumulation of apolipoprotein E as a cause of hypertriglyceridemia.Decreased adiponectin levels in familial combined hyperlipidemia patients contribute to the atherogenic lipid profile.Endothelial function in familial combined hyperlipidaemia.Treatment of familial hypertriglyceridaemia with acarbose.Association of serum lipids and obesity with cardiovascular mortality.Increased risk for endogenous hypertriglyceridaemia is associated with an apolipoprotein C3 haplotype specified by the SstI polymorphism
P2860
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P2860
Myocardial infarction in the familial forms of hypertriglyceridemia.
description
1976 nî lūn-bûn
@nan
1976年の論文
@ja
1976年学术文章
@wuu
1976年学术文章
@zh-cn
1976年学术文章
@zh-hans
1976年学术文章
@zh-my
1976年学术文章
@zh-sg
1976年學術文章
@yue
1976年學術文章
@zh
1976年學術文章
@zh-hant
name
Myocardial infarction in the familial forms of hypertriglyceridemia.
@en
Myocardial infarction in the familial forms of hypertriglyceridemia.
@nl
type
label
Myocardial infarction in the familial forms of hypertriglyceridemia.
@en
Myocardial infarction in the familial forms of hypertriglyceridemia.
@nl
prefLabel
Myocardial infarction in the familial forms of hypertriglyceridemia.
@en
Myocardial infarction in the familial forms of hypertriglyceridemia.
@nl
P2093
P1433
P1476
Myocardial infarction in the familial forms of hypertriglyceridemia.
@en
P2093
Bierman EL
Brunzell JD
Motulsky AG
Schrott HG
P304
P356
10.1016/0026-0495(76)90089-5
P577
1976-03-01T00:00:00Z