FAQ

Hyperlipoproteinemia Type IV

Known as: Fredrickson Type IV hyperlipoproteinemia, Hyperprebetalipoproteinemia, Very-low-density-lipoid-type hyperlipoproteinemia 
A hypertriglyceridemia disorder, often with autosomal dominant inheritance. It is characterized by the persistent elevations of plasma TRIGLYCERIDES… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1969-2017
0246819692017

Related topics

Related topics

13 relations
Hyperlipoproteinemia Type IHyperlipoproteinemia Type IIIHypertriglyceridemiaIn Blood
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Broader (2)

congenital deficiencyfamilial hyperlipoproteinemia

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
Hyperlipoproteinemia Type IV
radiotherapeutic
prevention & control
Hypertriglyceridemia
LIPOPROTEIN LIPASE
Microbiological

Papers overview

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2004
2004
Dyslipidemia management in adults with diabetes.
PREVALENCE OF DYSLIPIDEMIA IN TYPE 2 DIABETES — The most common pattern of dyslipidemia in patients with type 2 diabetes patients… (More)
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Highly Cited
2003
Highly Cited
2003
Coronary artery disease risk in familial combined hyperlipidemia and familial hypertriglyceridemia: a case-control comparison from the National Heart, Lung, and Blood Institute Family Heart Study.
BACKGROUND Conventional wisdom suggests that a diagnosis of familial combined hyperlipidemia (FCHL) carries a substantially… (More)
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Highly Cited
2000
Highly Cited
2000
Cardiovascular disease mortality in familial forms of hypertriglyceridemia: A 20-year prospective study.
BACKGROUND Familial combined hyperlipidemia (FCHL) and familial hypertriglyceridemia (FHTG) are 2 of the most common familial… (More)
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Highly Cited
1992
Highly Cited
1992
Mechanism of hypertriglyceridemia in human apolipoprotein (apo) CIII transgenic mice. Diminished very low density lipoprotein fractional catabolic rate associated with increased apo CIII and reduced…
Hypertriglyceridemia is common in the general population, but its mechanism is largely unknown. In previous work human apo CIII… (More)
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1990
1990
Phenotypic expression of heterozygous lipoprotein lipase deficiency in the extended pedigree of a proband homozygous for a missense mutation.
Familial lipoprotein lipase (LPL) deficiency is a rare genetic disorder accompanied by well-characterized manifestations. The… (More)
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Highly Cited
1983
Highly Cited
1983
Plasma lipoproteins in familial combined hyperlipidemia and monogenic familial hypertriglyceridemia.
Plasma lipoprotein concentration, composition, and size were evaluated in two common familial forms of hypertriglyceridemia and… (More)
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Highly Cited
1981
Highly Cited
1981
Integrated regulation of very low density lipoprotein triglyceride and apolipoprotein-B kinetics in man: normolipemic subjects, familial hypertriglyceridemia and familial combined hyperlipidemia.
Turnover kinetics of triglycerides (TG) and apolipoprotein-B (apo-B) of plasma very low density lipoprotein (VLDL) and their… (More)
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Highly Cited
1976
Highly Cited
1976
Myocardial infarction in the familial forms of hypertriglyceridemia.
Among 74 hypertriglyceridemic patients who were referred for study because of hypertriglyceridemia, family investigations… (More)
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1975
1975
The biochemical, clinical, and genetic features of type III hyperlipoproteinemia.
The clinical and biochemical features of type III hyperlipoproteinemia are described in 49 patients from 23 to 70 years of age… (More)
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Highly Cited
1973
Highly Cited
1973
Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia.
To assess the genetics of hyperlipidemia in coronary heart disease, family studies were carried out in 2520 relatives and spouses… (More)
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