The Role of Genetic Counselors for Patients with Familial Hypercholesterolemia
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s40142-014-0036-8.pdf
Reference49 articles.
1. •• Nordestgaard BG, Chapman MJ, Humphries SE et al. Familial hypercholesterolemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: consensus statement of the European Atherosclerosis Society. Eur Heart J. 2013;34(45):3478–3490a. Recent consensus statement that provides in-depth review of FH prevalence, screening strategies, diagnosis and treatment with multiple informative figures and tables.
2. Alonso R, Mata P, Zambon D, Mata N, Fuentes-Jimenez F. Early diagnosis and treatment of familial hypercholesterolemia: improving patient outcomes. Exp Rev Cardiovasc Ther. 2013;11(3):327–42.
3. Slack J. Risks of ischaemic heart-disease in familial hyperlipoproteinaemic states. Lancet. 1969;2(7635):1380–2.
4. Williams RR, Hunt SC, Schumacher MC, et al. Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics. Am J Cardiol. 1993;72(2):171–6.
5. Organization WHO. Familial hypercholesterolemia. Report of a second WHO consultation. 1999.
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