LDL-Apheresis in Homozygous LDL-Receptor-Defective Familial Hypercholesterolemia: The Munich Experience
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine,General Medicine,Internal Medicine
Reference19 articles.
1. Plasma exchange in the management of homozygous familial hypercholesterolaemia;Thompson;Lancet,1975
2. Improved survival of patients with homozygous familial hypercholesterolemia treated with plasma exchange;Thompson;BMJ,1985
3. Formes homozygotes cutanéo-tendineuses de xanthomatose hypercholestérolique dans une observation familiale exemplaire – essai de plasmaphérèse à titre de traitement héroique;De Gennes;Soc Med Hop Paris,1967
4. Effect of plasma exchange with and without concomitant drug treatment on lipids and lipoproteins in patients with familial hypercholesterolemia confirmed by tissue culture;Keller;Atherosclerosis,1985
5. Mutations in the low-density-lipoprotein receptor gene in German patients with FH;Weiss;J Inher Metabol Dis,2000
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1. Cardiovascular outcomes in patients with homozygous familial hypercholesterolaemia on lipoprotein apheresis initiated during childhood: long-term follow-up of an international cohort from two registries;The Lancet Child & Adolescent Health;2024-07
2. Dyslipidaemia as a target for atherosclerotic cardiovascular disease prevention in children with type 1 diabetes: lessons learned from familial hypercholesterolaemia;Diabetologia;2023-11-30
3. Homozygous Familial Hypercholesterolemia in Canada;JACC: Advances;2023-05
4. Aortic stenosis in homozygous familial hypercholesterolaemia: a paradigm shift over a century;European Heart Journal;2022-07-01
5. Use of apheresis in the age of new therapies for familial hypercholesterolaemia;Current Opinion in Lipidology;2021-09-22
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