Clinical Impact of Lipoprotein (a) and Cumulative Low-Density Lipoprotein Cholesterol Exposure on Coronary Artery Disease in Patients with Heterozygous Familial Hypercholesterolemia. [PDF]
Shishikura D +7 more
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Biochemical and Anthropometric Outcomes in Paediatric Patients with Heterozygous Familial Hypercholesterolemia after COVID-19 Pandemic Lockdowns: An Exploratory Analysis. [PDF]
Peres M +12 more
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Failure of lipid control by PCSK9 inhibitors in compound heterozygous familial hypercholesterolemia complicated with premature myocardial infarction: A case report. [PDF]
Zhang Z +6 more
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† Safety and efficacy of obicetrapib in patients with heterozygous familial hypercholesterolemia
Andy Hsieh +19 more
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Pediatric implications of heterozygous familial hypercholesterolemia
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Heterozygous familial hypercholesterolemia: prevalence and control rates
Expert Review of Endocrinology and Metabolism, 2021Introduction: Heterozygous familial hypercholesterolemia (heFH) is associated with a very high risk for cardiovascular events. Treatment with potent statins substantially reduces cardiovascular morbidity in these patients. Moreover, combination therapy with statins plus ezetimibe and/or proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors ...
Konstantinos Tziomalos +1 more
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Severe xanthomatosis in heterozygous familial hypercholesterolemia
Journal of Clinical Lipidology, 2018Familial hypercholesterolemia is a genetic lipoprotein disorder characterized by elevated plasma low-density lipoprotein cholesterol level, (tendinous xanthomas, xanthelasmas, and premature arcus corneus) and early onset atherosclerotic cardiovascular disease. Familial hypercholesterolemia is caused by mutations in the low-density lipoprotein receptor,
Sumayah Aljenedil, Isabelle Ruel
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