Treatment of Homozygous Familial Hypercholesterolemia with Low Density Lipoprotein Apheresis: A 4 Year Follow-Up Study
Author:
Publisher
Wiley
Subject
Biomedical Engineering,General Medicine,Biomaterials,Medicine (miscellaneous),Bioengineering
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1525-1594.1997.tb00732.x/fullpdf
Reference20 articles.
1. Molecular basis of familial hypercholesterolemia;Russell;Arteriosclerosis,1989
2. Familial hypercholesterolemia. A genetic defect in the LDL-receptor;Brown;N Engl J Med,1976
3. Relation of high-density lipoprotein cholesterol and triglycerides to incidence of atherosclerotic coronary heart disease. The PROCAM experience;Assmann;Am J Cardiol,1992
4. Apolipoprotein (a) and ischaemic heart disease in familial hypercholesterolemia;Wiklund;Lancet,1990
5. Lipoprotein (a) and atherosclerosis;Scanu;Ann Intern Med,1991
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1. Effect of Lipoprotein Apheresis on Oxidative Stress and Antioxidant Status in Familial Hypercholesterolemic Patients;The International Journal of Artificial Organs;2004-12
2. Effect of Lipoprotein Apheresis on Oxidative Stress and Antioxidant Status in Familial Hypercholesterolemic Patients;The International Journal of Artificial Organs;2003-11
3. Familial hypercholesterolemia—Improving treatment and meeting guidelines;International Journal of Cardiology;2003-05
4. Therapeutic efficiency of lipoprotein(a) reduction by low-density lipoprotein immunoapheresis;Metabolism;1998-09
5. Identification of complement activators and elucidation of the fate of complement activation products during extracorporeal plasma purification therapy;Journal of Clinical Apheresis;1998
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