Heterozygous familial hypercholesterolaemia in childhood: Cardiovascular risk prevention
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s10545-009-1165-1.pdf
Reference65 articles.
1. Abifadel M, Varret M, Rabes JP et al (2003) Mutations in PCSK9 cause autosomal dominant hypercholesterolemia. Nat Genet 34:154–156
2. Allard D, Amsellem S, Abifadel M et al (2005) Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia. Hum Mutat 26:497
3. American Academy of Pediatrics. Committee on Nutrition (1998) Cholesterol in childhood. Pediatrics 101:141–147
4. Amundsen AL, Ose L, Nenseter MS, Ntanios FY (2002) Plant sterol ester-enriched spread lowers plasma total and LDL cholesterol in children with familial hypercholesterolemia. Am J Clin Nutr 76:338–344
5. Arambepola C, Farmer AJ, Perera R, Neil HA (2007) Statin treatment for children and adolescents with heterozygous familial hypercholesterolaemia: A systematic review and meta-analysis. Atherosclerosis 195:339–347
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