Lipoprotein Deficiency Syndromes (Paperback, Softcover Repri)

One: Lipoprotein Deficiency and Atherosclerosis.- Genetic High Density Lipoprotein Deficiency States and Atherosclerosis.- Metabolic Interrelationships of HDL Subclasses.- Speciation of HDL.- Modifications and Degradation of High Density Lipoproteins.- Effect of Diabetes Mellitus and End-Stage Renal Disease on HDL Metabolism.- HDL Binding to Human Adipocyte Plasma Membranes: Regional Variation in Omental and Subcutaneous Depots.- Clinical, Nutritional and Biochemical Consequences of Apolipoprotein B Deficiency.- Two: Hypoalphalipoproteinemia Syndromes.- Familial Hypoalphalipoproteinemia.- A Family Study of Hypoalphalipoproteinemia.- Apoprotein A-1 and Lecithin: Cholesterol Acyltransferase in a Patient With Tangier Disease.- Severe Hypoalphalipoproteinemia Induced by a Combination of Probucol and Clofibrate.- Control of Plasma HDL Levels After Plasmapheresis.- Clinical Syndrome and Lipid Metabolism in Hereditary Deficiency of Apolipoproteins A-1 and C-III, Variant I.- The Molecular Biology of Human Apo A-1, Apo A-II, Apo C-II and Apo B.- Three: LCAT and Cholesterol Transport.- Lecithin: Cholesterol Acyltransferase, A Review and Immunochemical Studies.- Lecithin: Cholesterol Acyltransferase Deficiency Syndromes.- Cholesterol Efflux: Mechanism and Regulation.- Inhibition and Activation of Cholesteryl Ester Transfer and its Significance in Plasma Cholesterol Metabolism.- Four: Hypertriglyceridemia Secondary to Enzyme or Apoprotein Deficiency.- Apolipoprotein C-II Deficiency.- Primary Lipoprotein Lipase Deficiency.- The Genetics and Molecular Biology of Apolipoprotein C-II.- Familial Hepatic Lipase Deficiency.- The Apo E-System: Genetic Control of Plasma Lipoprotein Concentration.- Type III Hyperlipoproteinemia: A Focus on Lipoprotein Receptor-Apolipoprotein E2 Interactions.- The Role of Apolipoprotein E in Modulating the Metabolism of Apolipoprotein B-48 and Apolipoprotein B-100 Containing Lipoproteins in Humans.