Primary hyperbetalipoproteinemia (type II hyperlipoproteinemia) is a common disorder associated with premature vascular disease. It is frequently due to genetic abnormalities, some of which are expressed in childhood. We have examined the manner in which that form of hyperbetalipoproteinemia known as familial hypercholesterolemia may be expressed in 236 children aged 1-19 born of 90 matings in which one parent had hyperbetalipoproteinemia of this variety and one parent did not.
Peter O. Kwiterovich Jr., Donald S. Fredrickson, Robert I. Levy
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Nutrition, the Child and Atherosclerosis
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Diagnosis and Management of Familial Dyslipoproteinemia in Children and Adolescents
PO Kwiterovich |
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Ineffectiveness of Ascorbic Acid Therapy in Nephropathic Cystinosis
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GE Andersen |
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The Lipoprotein Molecule
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1978 | |
DOSE-EFFECT RELATION OF CHOLESTYRAMINE IN CHILDREN AND YOUNG ADULTS WITH FAMILIAL HYPERCHOLESTEROLÆMIA
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The Lancet | 1977 |
Diagnosing familial hypercholesterolaemia in childhood by measuring serum cholesterol
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British medical journal | 1977 |
Characterization of serum lipids and lipoproteins of prairie dogs fed a chow diet or cholesterol-supplemented diet
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Inheritance of xanthomatosis and hyper-β-lipoproteinaemia: A study of 7 large kind reds
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1976 | |
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CORONARY DISEASE-A CHILDHOOD MALADY
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British heart journal | 1975 |
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Prospects for genetic screening
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The Journal of Pediatrics | 1975 |
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1975 | |
Lipids, Lipoproteins, and Drugs
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1975 | |
Abnormal induction of 3-hydroxy-3-methylglutaryl coenzyme A reductase in leukocytes from subjects with heterozygous familial hypercholesterolemia
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The Journal of biological chemistry | 1975 |