OBJECTIVES: To assess the clinical and biochemical factors associated with inter-individual variation in susceptibility to coronary artery disease (CAD) in treated heterozygous familial hypercholesterolaemia. DESIGN: A cross sectional study was conducted of 410 patients recruited from six lipid clinics in the UK. RESULTS: CAD was documented in 104 of the 211 men and in 55 of the 199 women with mean ages of onset of 43.1 and 46.5 years, respectively. CAD was significantly more common in men (49% v 28%, p < 0.001) and in patients who had smoked cigarettes versus patients who had never smoked (51% v 28%, p < 0.001). After adjusting for age, sex, and current smoking status, there were no significant differences between patients with or without ...
AIMS: The first aim was to critically evaluate the extent to which familial hypercholesterolaemia (F...
Author: Gintarė Valterytė Title: Identification of Patients with Familial Hypercholesterolemia (FH) ...
AIMS: The first aim was to critically evaluate the extent to which familial hypercholesterolaemia (F...
BACKGROUND: Heterozygous familial hypercholesterolemia (hFH) and familial combined hyperlipidemia (F...
OBJECTIVE: To assess the relationship of levels of inflammatory risk markers to presence of clinical...
Patients with familial hypercholesterolemia (FH) have high levels of LDL-C, owing to defective uptak...
Familial hypercholesterolemia (FH) is an autosomal dominant disorder in which the primary defect is ...
Background: Heterozygous Familial hypercholesterolemia (FH) is a common autosomal d...
Background: Familial hypercholesterolemia (FH) is a common autosomal dominant disorder caused by mu...
OBJECTIVE: Early coronary artery disease (CAD) is associated with risk factors (RF). Offspring of pa...
Background and aims: Familial hypercholesterolaemia (FH) is the commonest monogenic disorder that ac...
textabstractFamilial hypercholesterolemia (FH) (OMIM #143890) is an autosomal dominant disorder pres...
BACKGROUND: The prognosis from coronary heart disease (CHD) for patients with heterozygous familial ...
International audienceBackgroundThe identification of high-risk patients with Heterozygous Familial ...
BACKGROUND: Hypertension, hypercholesterolemia, obesity and smoking are highly prevalent among patie...
AIMS: The first aim was to critically evaluate the extent to which familial hypercholesterolaemia (F...
Author: Gintarė Valterytė Title: Identification of Patients with Familial Hypercholesterolemia (FH) ...
AIMS: The first aim was to critically evaluate the extent to which familial hypercholesterolaemia (F...
BACKGROUND: Heterozygous familial hypercholesterolemia (hFH) and familial combined hyperlipidemia (F...
OBJECTIVE: To assess the relationship of levels of inflammatory risk markers to presence of clinical...
Patients with familial hypercholesterolemia (FH) have high levels of LDL-C, owing to defective uptak...
Familial hypercholesterolemia (FH) is an autosomal dominant disorder in which the primary defect is ...
Background: Heterozygous Familial hypercholesterolemia (FH) is a common autosomal d...
Background: Familial hypercholesterolemia (FH) is a common autosomal dominant disorder caused by mu...
OBJECTIVE: Early coronary artery disease (CAD) is associated with risk factors (RF). Offspring of pa...
Background and aims: Familial hypercholesterolaemia (FH) is the commonest monogenic disorder that ac...
textabstractFamilial hypercholesterolemia (FH) (OMIM #143890) is an autosomal dominant disorder pres...
BACKGROUND: The prognosis from coronary heart disease (CHD) for patients with heterozygous familial ...
International audienceBackgroundThe identification of high-risk patients with Heterozygous Familial ...
BACKGROUND: Hypertension, hypercholesterolemia, obesity and smoking are highly prevalent among patie...
AIMS: The first aim was to critically evaluate the extent to which familial hypercholesterolaemia (F...
Author: Gintarė Valterytė Title: Identification of Patients with Familial Hypercholesterolemia (FH) ...
AIMS: The first aim was to critically evaluate the extent to which familial hypercholesterolaemia (F...