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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Detalhes bibliográficos
Main Authors: Maria Mytilinaiou, Ioannis Kyrou, Mike Khan, Dimitris K. Grammatopoulos, Harpal S. Randeva
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2018-07-01
Colecção:Frontiers in Pharmacology
Assuntos:
familial hypercholesterolemia (FH)
heterozygous FH (HeFH)
homozygous FH (HoFH)
atherosclerotic cardiovascular disease (ASCVD)
low density lipoprotein (LDL)
statins
Acesso em linha:https://www.frontiersin.org/article/10.3389/fphar.2018.00707/full
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