Cholestyramine therapy in patients homozygous for familial hypercholesterolemia (familial hypercholesterolemic xanthomatosis)
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference19 articles.
1. Plasma-cholesterol-lowering action of bile acid binding polymers in experimental animals;Tennent;J. Lipid Res.,1960
2. Cholestyramine resin therapy for hypercholesteremia;Hashim;J. Amer. med. Ass.,1965
3. Fat transport in lipoproteins—an integrated approach to mechanisms and disorders;Fredrickson;New Engl. J. Med.,1967
4. The inheritance of essential familial hypercholesterolemia;Khachadurian;Amer. J. Med.,1964
5. ‘Juvenile’ xanthomatosis—a recessive inherited disease?;Nitter-Hauge;Acta med. scand.,1966
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1. Clinical Utility of Bile Acid Sequestrants in the Treatment of Dyslipidemia: A Scientific Review;Southern Medical Journal;2006-03
2. The genetic determinants of plasma cholesterol and response to diet;Baillière's Clinical Endocrinology and Metabolism;1995-10
3. Effectiveness of cascade filtration plasmapheresis in two patients affected by familial hypercholesterolemia;Journal of Clinical Apheresis;1995
4. The Molecular Genetics of Pediatric Lipid Disorders: Recent Progress and Future Research Directions;Pediatric Research;1993-10
5. Ex Vivo Gene Therapy of Familial Hypercholesterolemia. Howard Hughes Medical Institute, University of Michigan;Human Gene Therapy;1992-04
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