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Hyperlipoproteinemia Type I

Known as: Familial Chylomicronemia, Familial LPL Deficiencies, LPL DEFICIENCY 
An inherited condition due to a deficiency of either LIPOPROTEIN LIPASE or APOLIPOPROTEIN C-II (a lipase-activating protein). The lack of lipase… 
National Institutes of Health

Related topics

Related topics

20 relations

Narrower (2)

Apolipoprotein C-II Deficiency (disorder)Familial hyperchylomicronemia syndrome

Broader (2)

Enzyme DeficiencyHyperlipoproteinemias
Hypercholesterolemia, FamilialHyperlipoproteinemia Type IIIHyperlipoproteinemia Type IVHyperlipoproteinemia Type V

Papers overview

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2004
2004
Temporal changes in nitrogen and phosphorus codeficiency of plankton in lakes of coastal and interior British Columbia
Plankton nutrient limitation and deficiency were assessed in six coastal and four interior lakes and reservoirs in British… 
1984
1984
Genetic and environmental sources of familial aggregation of body mass in Tecumseh, Michigan.
1981
1981
Familial lecithin:cholesterol acyltransferase deficiency - a new metabolic disease with renal involvement.
1980
1980
Effects of diet on apoprotein E levels and on the apoprotein E subspecies in human plasma lipoproteins.
Type III hyperlipoproteinemia is characterized by a marked deficiency of the apoprotein E (ApoE)-3 subspecies of ApoE in very low… 
1980
1980
Familial combined hyperlipoproteinemia. Evidence for a role of growth hormone deficiency in effecting its manifestation.
Hyperlipidemia associated with an isolated deficiency of growth hormone was investigated in 10 subjects with hypercholesterolemia… 
1978
1978
Enzyme immunoassay for human apolipoprotein B, the major protein moiety in low-density- and very-low-density lipoproteins.
We used enzyme immunoassay to measure apolipoprotein B concentration in human plasma. Pure lipoprotein B was isolated from serum… 
1971
1971
Differences Between Metabolic Responses to Fasting in Obese Diabetic and Obese Nondiabetic Subjects
The metabolic response to two weeks' fasting and the influence of starvation on glucose tolerance have been studied in obese… 
Review
1971
Review
1971
Orthopaedic defects in familial dysautonomia. A review of sixty-five cases.
Familial dysautonomia is a rare autosomal disorder of the central nervous system characterized by many abnormalities, several of… 
Highly Cited
1953
Highly Cited
1953
Myoclonus epilepsy as a symptom of diffuse neuronal disease.
UNVERRICHT 1 and Lundborg 2 described a progressive familial syndrome of myoclonus epilepsy, the fully developed form of which… 
Review
1933
Review
1933
FAMILIAL SPASTIC PARALYSIS: REPORT OF THREE CASES IN ONE FAMILY AND OBSERVATION AT NECROPSY
Familial spastic paralysis is characterized clinically by the hereditary or familial occurrence of spastic paralysis, which is…