Low-density lipoprotein apheresis as long-term treatment for children with homozygous familial hypercholesterolemia
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference36 articles.
1. Familial hypercholesterolemia;Goldstein,1989
2. Lovastatin therapy in receptor-negative homozygous familial hypercholesterolemia: lack of effect on low-density lipoprotein concentrations or turnover;Uauy;J P EDIATR,1988
3. Three different schedules of low-density lipoprotein apheresis compared with plasmapheresis in patients with homozygous familial hypercholesterolemia;Berger;Am J Med,1990
4. Improved survival of patients with homozygous familial hypercholesterolemia treated with plasma exchange;Thompson;Br Med J,1985
5. Liver transplantation to provide low-density-lipoprotein receptors and lower plasma cholesterol in a child with homozygous familial hypercholesterolemia;Bilheimer;N Engl J Med,1984
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1. Clinical practice recommendations on lipoprotein apheresis for children with homozygous familial hypercholesterolaemia: An expert consensus statement from ERKNet and ESPN;Atherosclerosis;2024-05
2. Clinical practice recommendations on lipoprotein apheresis for children with homozygous familial hypercholesterolemia: an expert consensus statement from ERKNet and ESPN;2023-11-15
3. The efficacy of double filtration plasmapheresis in the treatment of homozygous familial hypercholesterolemia: A single-center experience;Transfusion and Apheresis Science;2019-02
4. Case report—Rapid regression of xanthomas under lipoprotein apheresis in a boy with homozygous familial hypercholesterolemia;Journal of Clinical Lipidology;2018-07
5. My Approach to the Patient With Familial Hypercholesterolemia;Mayo Clinic Proceedings;2016-06
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