Familial Hypercholesterolemia: New Horizons for Diagnosis and Effective Management

Familial hypercholesterolemia (FH) is a common genetic cause of premature cardiovascular disease (CVD). The reported prevalence rates for both heterozygous FH (HeFH) and homozygous FH (HoFH) vary significantly, and this can be attributed, at least in part, to the variable diagnostic criteria used ac...

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Detalles Bibliográficos
Autores principales: Mytilinaiou, Maria, Kyrou, Ioannis, Khan, Mike, Grammatopoulos, Dimitris K., Randeva, Harpal S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Pharmacology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6052892/
https://www.ncbi.nlm.nih.gov/pubmed/30050433
http://dx.doi.org/10.3389/fphar.2018.00707

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6052892/
https://www.ncbi.nlm.nih.gov/pubmed/30050433
http://dx.doi.org/10.3389/fphar.2018.00707

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