Serum complement and familial combined hyperlipidemia
- 21 March 1997
- journal article
- Published by Elsevier in Atherosclerosis
- Vol. 129 (2) , 271-277
- https://doi.org/10.1016/s0021-9150(96)06054-6
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Impaired fatty acid metabolism in familial combined hyperlipidemia. A mechanism associating hepatic apolipoprotein B overproduction and insulin resistance.Journal of Clinical Investigation, 1993
- Stable isotopes show a direct relation between VLDL apoB overproduction and serum triglyceride levels and indicate a metabolically and biochemically coherent basis for familial combined hyperlipidemia.Arteriosclerosis and Thrombosis: A Journal of Vascular Biology, 1993
- Simvastatin improves chylomicron remnant removal in familial combined hyperlipidemia without changing chylomicron conversionMetabolism, 1993
- Familial lipoprotein disorders in patients with premature coronary artery disease.Circulation, 1992
- Isolation and characterization of a complement-activating lipid extracted from human atherosclerotic lesions.The Journal of Experimental Medicine, 1990
- Association of serum IgA and C4 with severe atherosclerosisAtherosclerosis, 1988
- Activation of the human terminal complement pathway in atherosclerosisClinical Immunology and Immunopathology, 1987
- Hyperlipidemia in Coronary Heart Disease II. GENETIC ANALYSIS OF LIPID LEVELS IN 176 FAMILIES AND DELINEATION OF A NEW INHERITED DISORDER, COMBINED HYPERLIPIDEMIAJournal of Clinical Investigation, 1973
- FAMILY STUDY OF SERUM LIPIDS AND LIPOPROTEINS IN CORONARY HEART-DISEASEThe Lancet, 1973
- Inheritance of combined hyperlipoproteinemia: Evidence for a new lipoprotein phenotypeThe American Journal of Medicine, 1973