Atorvastatin: a review of its pharmacological properties and use in familial hypercholesterolemia
Author:
Affiliation:
1. Atlanta Vascular Research Foundation, Emory University School of Medicine, Atlanta, GA 30084, USA
Publisher
Informa UK Limited
Subject
Cardiology and Cardiovascular Medicine,Endocrinology, Diabetes and Metabolism
Link
https://www.tandfonline.com/doi/pdf/10.2217/clp.10.55
Reference71 articles.
1. Bourbon M, Alves AC, Medeiros AM, Silva S, Soutar AK; Investigators of Portuguese FH Study: Familial hypercholesterolaemia in Portugal. Atherosclerosis 196(2), 633–642 (2008).
2. Identification of a recurrent insertion mutation in the LDLR gene in a Pakistani family with autosomal dominant hypercholesterolemia
3. 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).
4. ▪▪ Essential for a comprehensive overview of familial hypercholesterolemia (FH).
5. Yang KC, Su YN, Shew JY et al.: LDLR and APOB are major genetic causes of autosomal dominant hypercholesterolemia in a Taiwanese population. J. Formos. Med. Assoc. 106(10), 799–807 (2007).
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