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Hypoalphalipoproteinemia
Commonly Used Lipidcentric ICD-10 (ICD-9) Codes
Evaluation and Treatment of Hypertriglyceridemia: an Endocrine Society Clinical Practice Guideline
ABCA1) in Human Disease
ATP III Report on High Blood Cholesterol
Efficacy of Polyphenols in the Management of Dyslipidemia
Rare Dyslipidaemias, from Phenotype to Genotype to Management: a European Atherosclerosis Society Task Force Consensus Statement
Supplementary Materials Table S1. List of 63 Evaluated Genes Related to Dyslipidemia and Premature Atherosclerosis with Associated Phenotypes
Metabolic Studies in an Unusual Case of Asymptomatic Familial Hypobetalipoproteinemia with Hypoalphalipoproteinemia and Fasting Chylomicronemia
Primary Disorders of LDL-Cholesterol Metabolism
Management of Hypertriglyceridemia: Common Questions and Answers
Familial Hypercholesterolemia Associated with Severe Hypoalphalipoproteinemia in a Moroccan Family
Familial Hypobetalipoproteinemia (FHBL) Is a Disorder That Impairs the Body's Ability to Absorb and Transport Fats, Causing Low Levels of Cholesterol in the Blood
Central and Bioanalytical Labs for Cardiovascular Download
32 Dyslipidemias
Phenotypes of Dyslipidemia Disclosures
Hypertriglyceridemia: a Strategic Approach
Other Forms of Primary Hypercholesterolemia. Familial Combined Hyperlipidemia and Polygenic Or Common Hypercholesterolemia
Familial Hypercholesterolemia
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Novel Missense Variants in LCAT and APOB Genes in an Italian Kindred with Familial Lecithin:Cholesterol Acyltransferase Deficien