Genetic causes of monogenic familial hypercholesterolemia in the Greek population: Lessons, mistakes, and the way forward
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine,Nutrition and Dietetics,Endocrinology, Diabetes and Metabolism,Internal Medicine
Reference44 articles.
1. Familial hypercholesterolemia;Goldstein,2001
2. Familial hypercholesterolaemia in children and adolescents: gaining decades of life by optimizing detection and treatment;Wiegman;Eur Heart J,2015
3. Lipid abnormalities in male and female survivors of myocardial infarction and their first-degree relatives;Patterson;Lancet,1972
4. Genetic causes of monogenic heterozygous familial hypercholesterolemia: a HuGE prevalence review;Austin;Am J Epidemiol,2004
5. Molecular genetics of the LDL receptor gene in familial hypercholesterolemia;Hobbs;Hum Mutat,1992
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1. Exploring the Landscape of Familial Hypercholesterolemia: Unraveling Genetic Complexity and Clinical Implications;European Journal of Internal Medicine;2024-05
2. Prevalent Variants in the LDLR Gene Impair Responsiveness to Rosuvastatin among Family Members of Patients with Premature Myocardial Infarction;Journal of Personalized Medicine;2023-12-18
3. An update on the first recorded case of familial hypercholesterolaemia: The Charioteer of Delphi;Journal of Clinical Lipidology;2023-07
4. The LDLR c.501C>A is a disease-causing variant in familial hypercholesterolemia;Lipids in Health and Disease;2021-09-12
5. Comparison of the mutation spectrum and association with pre and post treatment lipid measures of children with heterozygous familial hypercholesterolaemia (FH) from eight European countries;Atherosclerosis;2021-02
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