Developing and applying clinically useful approaches to identify individuals with familial hypercholesterolemia in the UK
Author:
Affiliation:
1. NIHR School of Primary Care Research, Division Public Health & Primary Health Care, University of Oxford, UK
Publisher
Informa UK Limited
Subject
Cardiology and Cardiovascular Medicine,Endocrinology, Diabetes and Metabolism
Link
https://www.tandfonline.com/doi/pdf/10.2217/clp.10.39
Reference48 articles.
1. Marks D, Thorogood M, Neil HA, Humphries SE: A review on the diagnosis, natural history, and treatment of familial hypercholesterolaemia. Atherosclerosis 168(1), 1–14 (2003).
2. Slack J: Risks of ischaemic heart-disease in familial hyperlipoproteinaemic states. Lancet 2(7635), 1380–1382 (1969).
3. Patterson D, Slack J: Lipid abnormalities in male and female survivors of myocardial infarction and their first-degree relatives. Lancet 1(7747), 393–399 (1972).
4. Scientific Steering Committee on behalf of The Simon Broome Register Group: The risk of fatal coronary heart disease in familial hypercholesterolaemia. BMJ 303(6807), 893–896 (1991).
5. DeMott K, Nherera L, Shaw EJ et al.: Clinical Guidelines and Evidence Review for Familial Hypercholesterolaemia: the Identification and Management of Adults and Children with Familial Hypercholesterolaemia. National Collaborating Centre for Primary Care and Royal College of General Practitioners, London, UK (2008).
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