This study was a I-year clinical study on 16 (7 males and 9 females) pediatric patients with heterozygous familial hypercholesterolemia treated with hypocholesterolemic diet only or with diet plus drug (simvastatin 10 mg/day). According to the study protocol, the children were submitted to a 3-month washout (free diet). Then they were given a diet (American Heart Association, step 2) for 6 months. After 6 months they were divided into two groups matched for sex, age and body mass index (BMI). Diet only was given to group A (n=8); simvastatin (10 mg/daily) was given to group B, for 1 year. All patients were examined at baseline, and monitored for safety during the study by pediatricians. All patients were submitted to noninvasive cardiovascu...
In the heterozygous form of familial hypercholesterolemia (FH), blood concentrations of low-density ...
Abstract Background: Children with familial hypercholesterolemia may develop early endothelial dama...
Familial hypercholesterolemia (FH) is a common, genetic, autosomal dominant condition, resulting in ...
Background-A multicenter, randomized, double-blind, placebo-controlled study was conducted to evalua...
Familial hypercholesterolemia is one of the most common inherited metabolic diseases and is an autos...
Atherosclerosis represents a disease that begins in childhood and in which LDL cholesterol plays a p...
The effect of diet on plasma lipids and lipoproteins was examined in 19 patients with familial hyper...
AIMS: To assess efficacy and safety of HMG-CoA reductase inhibitor (statin) treatment in children an...
ObjectivesThis study was undertaken to evaluate the efficacy and safety of rosuvastatin therapy for ...
Background and aims: Familial Hypercholesterolaemia (FH) is characterised by a genetic alteration in...
Aim: According to Italian Guidelines, statin therapy is recommended for children aged 10 or more who...
ObjectivesThe study evaluated the efficacy and safety of long-term coadministration of ezetimibe and...
This review covers the current knowledge about plant stanol esters as a dietary treatment option for...
Familial hypercholesterolaemia is a disorder of low-density lipoprotein (LDL) cholesterol metabolism...
Familial hypercholesterolemia Is the most common genetic disease in the world. It is characterized b...
In the heterozygous form of familial hypercholesterolemia (FH), blood concentrations of low-density ...
Abstract Background: Children with familial hypercholesterolemia may develop early endothelial dama...
Familial hypercholesterolemia (FH) is a common, genetic, autosomal dominant condition, resulting in ...
Background-A multicenter, randomized, double-blind, placebo-controlled study was conducted to evalua...
Familial hypercholesterolemia is one of the most common inherited metabolic diseases and is an autos...
Atherosclerosis represents a disease that begins in childhood and in which LDL cholesterol plays a p...
The effect of diet on plasma lipids and lipoproteins was examined in 19 patients with familial hyper...
AIMS: To assess efficacy and safety of HMG-CoA reductase inhibitor (statin) treatment in children an...
ObjectivesThis study was undertaken to evaluate the efficacy and safety of rosuvastatin therapy for ...
Background and aims: Familial Hypercholesterolaemia (FH) is characterised by a genetic alteration in...
Aim: According to Italian Guidelines, statin therapy is recommended for children aged 10 or more who...
ObjectivesThe study evaluated the efficacy and safety of long-term coadministration of ezetimibe and...
This review covers the current knowledge about plant stanol esters as a dietary treatment option for...
Familial hypercholesterolaemia is a disorder of low-density lipoprotein (LDL) cholesterol metabolism...
Familial hypercholesterolemia Is the most common genetic disease in the world. It is characterized b...
In the heterozygous form of familial hypercholesterolemia (FH), blood concentrations of low-density ...
Abstract Background: Children with familial hypercholesterolemia may develop early endothelial dama...
Familial hypercholesterolemia (FH) is a common, genetic, autosomal dominant condition, resulting in ...