Familial hypercholesterolemia (FH) is a hereditary condition caused by mutations in the lipid pathway. The goal in managing FH is to reduce circulating low‐density lipoprotein cholesterol and, therefore, reduce the risk of developing atherosclerotic cardiovascular disease (ASCVD). Because FH patients were considered high risk groups due to an increased susceptible for contracting COVID‐19 infection, we hypothesized whether the effects of the pandemic hindered access to cardiovascular care. In this review, we conducted a literature search in databases Pubmed/Medline and ScienceDirect. We included a comprehensive analysis of findings from articles in English related and summarized the effects of the pandemic on cardiovascular care through dir...
Heterozygous familial hypercholesterolemia (HeFH) patients are the prime example of subjects who are...
In recent studies, the reported prevalence of heterozygous familial hypercholesterolemia (FH) has be...
Familial hypercholesterolaemia remains largely unrecognised and undertreated in Australian primary c...
Familial hypercholesterolemia (FH) is a hereditary condition caused by mutations in the lipid pathwa...
Patients with familial hypercholesterolemia (FH) are likely at increased risk for COVID-19 complicat...
A recent meta-analysis of over 20,000 individuals showed that hospitalized COVID-19 patients with ac...
Familial hypercholesterolemia (FH) is a common genetic cause of premature cardiovascular disease (CV...
Background and aims: Familial hypercholesterolaemia (FH) is a known major cause of premature heart d...
Familial hypercholesterolemia (FH) is a common genetic cause of elevated low-density lipoprotein cho...
Familial hypercholesterolemia (FH) is a common heritable condition in which mutations of genes gover...
Familial hypercholesterolemia (FH) is caused by a major genetic defect in the low-density lipoprotei...
AbstractPurposeThe goal of this study was to determine cardiovascular disease (CVD) risk associated ...
Publisher Copyright: © 2021 The AuthorsSARS-CoV-2 infection continues to cause increased morbidity a...
This editorial refers to ‘Prediction of cardiovascular risk in patients with familial hypercholeste...
Background: The potential for global collaborations to better inform public health policy regarding ...
Heterozygous familial hypercholesterolemia (HeFH) patients are the prime example of subjects who are...
In recent studies, the reported prevalence of heterozygous familial hypercholesterolemia (FH) has be...
Familial hypercholesterolaemia remains largely unrecognised and undertreated in Australian primary c...
Familial hypercholesterolemia (FH) is a hereditary condition caused by mutations in the lipid pathwa...
Patients with familial hypercholesterolemia (FH) are likely at increased risk for COVID-19 complicat...
A recent meta-analysis of over 20,000 individuals showed that hospitalized COVID-19 patients with ac...
Familial hypercholesterolemia (FH) is a common genetic cause of premature cardiovascular disease (CV...
Background and aims: Familial hypercholesterolaemia (FH) is a known major cause of premature heart d...
Familial hypercholesterolemia (FH) is a common genetic cause of elevated low-density lipoprotein cho...
Familial hypercholesterolemia (FH) is a common heritable condition in which mutations of genes gover...
Familial hypercholesterolemia (FH) is caused by a major genetic defect in the low-density lipoprotei...
AbstractPurposeThe goal of this study was to determine cardiovascular disease (CVD) risk associated ...
Publisher Copyright: © 2021 The AuthorsSARS-CoV-2 infection continues to cause increased morbidity a...
This editorial refers to ‘Prediction of cardiovascular risk in patients with familial hypercholeste...
Background: The potential for global collaborations to better inform public health policy regarding ...
Heterozygous familial hypercholesterolemia (HeFH) patients are the prime example of subjects who are...
In recent studies, the reported prevalence of heterozygous familial hypercholesterolemia (FH) has be...
Familial hypercholesterolaemia remains largely unrecognised and undertreated in Australian primary c...