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Hdl Deficiency, Type 2

Known as: Low Serum Hdl Cholesterol, Primary Hypoalphalipoproteinemia 
National Institutes of Health

Related topics

Related topics

3 relations

Broader (1)

Familial HDL deficiency
Hypoalphalipoproteinemia, FamilialHypoalphalipoproteinemias

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2011
Review
2011
[LCAT deficiency: a nephrological diagnosis].
A genetic mendelian autosomal recessive condition of deficiency of lecithin- cholesterol acyltransferase (LCAT) can produce two… 
2005
2005
C-reactive protein levels and prevalence of chronic infections in subjects with hypoalphalipoproteinemia.
2005
2005
Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes.
2003
2003
Early vascular damage in primary hypoalphalipoproteinemia.
The relationship between hypoalphalipoproteinemia (hypoalpha), a metabolic disorder characterized by reduced high-density… 
1992
1992
Relationship of triglycerides and HDL cholesterol in hypertriglyceridemia.
1992
1992
Postprandial lipoprotein(a) response to a single meal containing either saturated or omega-3 polyunsaturated fatty acids in subjects with hypoalphalipoproteinemia.
1992
1992
Postprandial lipemia in subjects with primary hypoalphalipoproteinemia and hypoalphalipoproteinemia associated with diabetes
El acumulo durante el postprandio (PP) de lipoproteinas de muy baja densidad y sus remanentes, se considera potencialmente… 
1992
1992
[Postprandial lipemia in subjects with primary hypoalphalipoproteinemia and hypoalphalipoproteinemia associated with diabetes].
The postprandial (PP) elevations in triglyceride rich lipoproteins (TRL) are potentially atherogenic. We compared PP lipemia in… 
1989
1989
[The relationship between high-density lipoproteins, thromboxane B2 and arteriosclerosis in a case of primary hypoalphalipoproteinemia].
Data in the literature suggest that cases of hypoalphalipoproteinemia involve an increase in thromboxane B2 (TXB2) together with… 
1986
1986
A major gene for primary hypoalphalipoproteinemia.
Sixteen kindreds were ascertained through probands clinically determined to have primary hypoalphalipoproteinemia, characterized… 
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