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Dietary Therapy for Children with Hypercholesterolemia In persons with familial hypercholesterolemia, The recommendation in the original NCEP guidelines is
The National Lipid Association Expert Panel on Familial Hypercholesterolemia Guidelines usually recommend apheresis every week or every 2 weeks.
Hypercholesterolemia, also called high cholesterol, is the presence of high levels of cholesterol in the blood. It is a form of high blood lipids and
Familial hypercholesterolemia Professional guidelines recommend that the decision to treat a person with FH with statins should not be based on the usual risk
This collection features AFP content on hyperlipidemia and related issues, including dyslipidemia, hypercholesterolemia, hypertriglyceridemia, kidney disease, lipid
Familial hypercholesterolemia affects the way the body processes Expert panel on integrated guidelines for cardiovascular health and risk reduction in
Familial combined hyperlipidemia is a disorder that is passed down through families. It causes high cholesterol and high blood triglycerides.
Familial hypercholesterolemia (FH) is an autosomal dominant disorder that causes severe elevations in total cholesterol and low-density lipoprotein
Familial hypercholesterolemia (FH) is a genetic condition that causes high low-density lipoprotein (LDL) cholesterol (sometimes referred to as bad cholesterol) from
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Familial Hypercholesterolemia: This report goes beyond previously published guidelines by providing specific clinical guidance for the primary care clinician
Familial Hypercholesterolemia: This report goes beyond previously published guidelines by providing specific clinical guidance for the primary care clinician
Familial hypercholesterolemia results from gene mutations approximately halving the number of functional LDL receptors in heterozygotes and a greater lack in
Familial hypercholesterolemia (FH) is a genetic disorder of lipoprotein metabolism characterized by very high plasma concentrations of low density lipoprotein
INTRODUCTION. Familial hypercholesterolemia (FH) is the most common autosomal dominant genetic disease. The clinical syndrome (phenotype) is characterized by

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March 2018