Hypercholesterolemia is an important cardiovascular risk (CV) factor that can be due to environmental or genetic causes. Identification of a young population with high CV risk allows early intervention and prevention, delaying or abolishing occurrence of CHD in adult life. Familial Hypercholesterolemia (FH) is associated with major risk of CV events and usually results from mutations in three different genes involved in lipid metabolism such as LDLR, APOB and PCSK9 genes. The Portuguese FH Study is established in the National Institute of Health, Lisbon, since 1999 where the biochemical characterization and DNA diagnosis have been performed for patients with clinical diagnosis of FH and cascade screening in relatives of the affected inde...
INTRODUCTION : Familial hypercholesterolemia (FH) is a common autosomal dominant disorder of lipid m...
Familial hypercholesterolemia (FH) is a common autosomal dominant disorder of lipid metabolism (1:50...
Familial hypercholesterolemia (FH) is a genetic disorder of cholesterol metabolism caused by mutatio...
Familial hypercholesterolemia (FH) is an inherited disorder of cholesterol metabolism, clinically ch...
Cardiovascular disease (CVD) remains the most common cause of death globally. Dyslipidaemia is one o...
Familial hypercholesterolemia (FH) is an autossomal dominant disorder associated with high levels of...
Familial Hypercholesterolemia (FH) is a genetic disorder characterized by high levels of LDLc in pla...
Familial hypercholesterolemia (FH) is an autosomal dominant genetic disorder caused, in the majority...
Identification of young population with high cardiovascular (CV) risk allows early intervention and ...
Aim: Familial Hypercholesterolemia (FH) is characterized clinically by high LDL plasma concentration...
Familial Hypercholesterolaemia (FH) is a genetic disorder that leads to an increase in levels of tot...
Familial Hypercholesterolaemia (FH) is a genetic disorder that leads to an increase in levels of tot...
Aim: The _ompound_d_otic process begins in childhood and despite the estimated incidence of 1/500 in...
Familial Hypercholesterolaemia is a genetic disorder characterized by an increase in TC and LDLC lea...
Familial hypercholesterolemia (FH) is a genetic disorder of cholesterol metabolism caused by mutatio...
INTRODUCTION : Familial hypercholesterolemia (FH) is a common autosomal dominant disorder of lipid m...
Familial hypercholesterolemia (FH) is a common autosomal dominant disorder of lipid metabolism (1:50...
Familial hypercholesterolemia (FH) is a genetic disorder of cholesterol metabolism caused by mutatio...
Familial hypercholesterolemia (FH) is an inherited disorder of cholesterol metabolism, clinically ch...
Cardiovascular disease (CVD) remains the most common cause of death globally. Dyslipidaemia is one o...
Familial hypercholesterolemia (FH) is an autossomal dominant disorder associated with high levels of...
Familial Hypercholesterolemia (FH) is a genetic disorder characterized by high levels of LDLc in pla...
Familial hypercholesterolemia (FH) is an autosomal dominant genetic disorder caused, in the majority...
Identification of young population with high cardiovascular (CV) risk allows early intervention and ...
Aim: Familial Hypercholesterolemia (FH) is characterized clinically by high LDL plasma concentration...
Familial Hypercholesterolaemia (FH) is a genetic disorder that leads to an increase in levels of tot...
Familial Hypercholesterolaemia (FH) is a genetic disorder that leads to an increase in levels of tot...
Aim: The _ompound_d_otic process begins in childhood and despite the estimated incidence of 1/500 in...
Familial Hypercholesterolaemia is a genetic disorder characterized by an increase in TC and LDLC lea...
Familial hypercholesterolemia (FH) is a genetic disorder of cholesterol metabolism caused by mutatio...
INTRODUCTION : Familial hypercholesterolemia (FH) is a common autosomal dominant disorder of lipid m...
Familial hypercholesterolemia (FH) is a common autosomal dominant disorder of lipid metabolism (1:50...
Familial hypercholesterolemia (FH) is a genetic disorder of cholesterol metabolism caused by mutatio...