Management of homozygous familial hypercholesterolaemia in two brothers
Author:
Publisher
BMJ
Subject
General Medicine
Reference21 articles.
1. Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society;Cuchel;Eur Heart J,2014
2. Homozygous familial hypercholesterolemia in spain: prevalence and phenotype-genotype relationship;Sánchez-Hernández;Circ Cardiovasc Genet,2016
3. Homozygous familial hypercholesterolemia: current perspectives on diagnosis and treatment;Raal;Atherosclerosis,2012
4. Homozygous autosomal dominant hypercholesterolaemia in the Netherlands: prevalence, genotype-phenotype relationship, and clinical outcome;Sjouke;Eur Heart J,2015
5. Clinical experience of lomitapide therapy in patients with homozygous familial hypercholesterolaemia;Cuchel;Atheroscler Suppl,2014
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1. Efficacy and safety of lomitapide in homozygous familial hypercholesterolaemia: the pan-European retrospective observational study;European Journal of Preventive Cardiology;2021-12-31
2. Pharmacogenomics Variability of Lipid-Lowering Therapies in Familial Hypercholesterolemia;Journal of Personalized Medicine;2021-08-31
3. Novel therapeutic targets and agents for pediatric dyslipidemia;Therapeutic Advances in Endocrinology and Metabolism;2021-01
4. Lomitapide–a Microsomal Triglyceride Transfer Protein Inhibitor for Homozygous Familial Hypercholesterolemia;Current Atherosclerosis Reports;2020-06-18
5. Lomitapide: a review of its clinical use, efficacy, and tolerability;Core Evidence;2019-07
Lomitapide: a review of its clinical use, efficacy, and tolerability
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