How do index patients participating in genetic screening programmes for familial hypercholesterolemia (FH) interpret their DNA results? A UK-based qualitative interview study
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference35 articles.
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1. Genetic testing for familial hypercholesterolemia in a Finnish cohort of patients with premature coronary artery disease and elevated LDL-C levels;Frontiers in Cardiovascular Medicine;2024-07-26
2. The Lipoprotein Profile Evaluated by 1H-NMR Improves the Performance of Genetic Testing in Familial Hypercholesterolemia;The Journal of Clinical Endocrinology & Metabolism;2024-01-23
3. Introducing genetic testing with case finding for familial hypercholesterolaemia in primary care: qualitative study of patient and health professional experience;British Journal of General Practice;2022-03-24
4. Pharmacological treatment with lipid-lowering agents after molecular identification of familial hypercholesterolemia: results from the Hipercol Brasil cohort;Journal of Clinical Lipidology;2022-03
5. Enablers and barriers to treatment adherence in heterozygous familial hypercholesterolaemia: a qualitative evidence synthesis;BMJ Open;2019-07
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