Familial Hypercholesterolaemia in the Malaysian Community: Prevalence, Under-Detection and Under-Treatment
Author:
Affiliation:
1. Institute of Pathology, Laboratory and Forensic Medicine (I-PPerForM), Universiti Teknologi MARA, Sungai Buloh
Publisher
Japan Atherosclerosis Society
Subject
Biochemistry (medical),Cardiology and Cardiovascular Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/jat/28/10/28_57026/_pdf
Reference78 articles.
1. 1) Defesche JC, Gidding SS, Harada-Shiba M, Hegele RA, Santos RD, and Wierzbicki AS: Familial hypercholesterolaemia. Nat Rev Dis Primers, 2017; 3: 17093
2. 2) Truong PK, Lao TD, and Le THA: The Major Molecular Causes of Familial Hypercholesterolemia. Asian J Pharma Res Health Care, 2018; 10: 60-68
3. 3) Austin MA, Hutter CM, Zimmern RL, and Humphries SE: Genetic causes of monogenic heterozygous familial hypercholesterolemia: a HuGE prevalence review. Am J Epidemiol, 2004; 160: 407-420
4. 4) Mabuchi H: Half a century tales of familial hypercholesterolemia (FH) in Japan. J Atheroscler Thromb, 2017; 24: 189-207
5. 5) Goldstein JL and Brown MS: A century of cholesterol and coronaries: from plaques to genes to statins. Cell, 2015; 161: 161-172
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5. Reducing Premature Coronary Artery Disease in Malaysia by Early Identification of Familial Hypercholesterolemia Using the Familial Hypercholesterolemia Case Ascertainment Tool (FAMCAT): Protocol for a Mixed Methods Evaluation Study (Preprint);2023-04-05
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