Management of homozygous familial hypercholesterolemia in real-world clinical practice: A report of 7 Italian patients treated in Rome with lomitapide and lipoprotein apheresis-Reference-Cited by-同舟云学术

Management of homozygous familial hypercholesterolemia in real-world clinical practice: A report of 7 Italian patients treated in Rome with lomitapide and lipoprotein apheresis

Published:2016-07 Issue:4 Volume:10 Page:782-789
ISSN:1933-2874
Container-title:Journal of Clinical Lipidology
language:en
Short-container-title:Journal of Clinical Lipidology

Author:

Stefanutti Claudia^ORCID,Morozzi Claudia,Di Giacomo Serafina^ORCID,Sovrano Barbara,Mesce Dario,Grossi Alberto

Funder

Aegerion

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Nutrition and Dietetics,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference25 articles.

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2. 2009 Canadian Cardiovascular Society/Canadian guidelines for the diagnosis and treatment of dyslipidemia and prevention of cardiovascular disease in the adult—2009 recommendations;Genest;Can J Cardiol,2009

3. Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: Consensus Statement of the European Atherosclerosis Society;Nordestgaard;Eur Heart J,2013

4. Homozygous familial hypercholesterolemia: current perspectives on diagnosis and treatment;Raal;Atherosclerosis,2012

5. Familial hypercholesterolemia in the Danish general population: prevalence, coronary artery disease, and cholesterol-lowering medication;Benn;J Clin Endocrinol Metab,2012

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4. Case report: Therapy adherence, MTTP variants, and course of atheroma in two patients with HoFH on low-dose, long-term lomitapide therapy;Frontiers in Genetics;2023-01-04

5. Efficacy and Safety of Lomitapide in Homozygous Familial Hypercholesterolaemia: A Systematic Review;Reviews in Cardiovascular Medicine;2022-04-26