In order to investigate the influence of genetic factors in childhood stroke, we compared the distributions of mutations/polymorphisms affecting hemostasis and/or endothelial function (factor V [FV] Leiden, factor II [FII] G20210A, methylenetetrahydrofolate reductase [MTHFR] C677T, angiotensin-converting enzyme [ACE] insertion/deletion [1D], and endothelial nitric oxide synthase [eNOS] G894T) among children with stroke and controls. A total number of 26 children with arterial ischemic stroke and a control group of 50 healthy children were included in the study. No statistically significant differences in allelic and genotypic distribution were detected in comparisons between groups. However, when combined genotypes were analyzed, statistica...
<div><p>Endothelial nitric oxide synthase (<i>eNOS</i>) is localized in caveole and has important ef...
Aim. To study the frequency of polymorphic gene variants encoding proteins of renin-angiotensin syst...
Homozygosity for the methylenetetrahydrofolate reductase (MTHFR) 677C>T mutation (MTHFR TT) has b...
Introduction The association between ischemic stroke and genetic polymorphisms of methylenetetrahydr...
Introduction The association between ischemic stroke and genetic polymorphisms of methylenetetrahydr...
Abstract The 677C[T polymorphism within methyle-netetrahydrofolate reductase (MTHFR) gene is related...
Background and Objective: Evidence indicates that genetic factors may be involved in the risk of isc...
<b>Introduction</b>\ud \ud The association between ischemic stroke and genetic polymorphisms of meth...
The endothelial nitric oxide synthase (eNOS) rs1799983 polymorphism is known to increase the risk to...
Endothelial nitric oxide synthase (eNOS) is localized in caveole and has important effects on caveol...
Background The purpose of this study was threefold. First, it was to determine the relationship betw...
Understanding the genetic risk factors for stroke is an essential step to decipher the underlying me...
The etiology of arterial ischemic stroke (AIS) in children is complex, and different from that in...
The association between polymorphism 4b/a, T-786C and G894T in endothelial NO synthase gene (eNOS) a...
Ischemic stroke is a significant health condition, whose frequency in childhood is increasing day by...
<div><p>Endothelial nitric oxide synthase (<i>eNOS</i>) is localized in caveole and has important ef...
Aim. To study the frequency of polymorphic gene variants encoding proteins of renin-angiotensin syst...
Homozygosity for the methylenetetrahydrofolate reductase (MTHFR) 677C>T mutation (MTHFR TT) has b...
Introduction The association between ischemic stroke and genetic polymorphisms of methylenetetrahydr...
Introduction The association between ischemic stroke and genetic polymorphisms of methylenetetrahydr...
Abstract The 677C[T polymorphism within methyle-netetrahydrofolate reductase (MTHFR) gene is related...
Background and Objective: Evidence indicates that genetic factors may be involved in the risk of isc...
<b>Introduction</b>\ud \ud The association between ischemic stroke and genetic polymorphisms of meth...
The endothelial nitric oxide synthase (eNOS) rs1799983 polymorphism is known to increase the risk to...
Endothelial nitric oxide synthase (eNOS) is localized in caveole and has important effects on caveol...
Background The purpose of this study was threefold. First, it was to determine the relationship betw...
Understanding the genetic risk factors for stroke is an essential step to decipher the underlying me...
The etiology of arterial ischemic stroke (AIS) in children is complex, and different from that in...
The association between polymorphism 4b/a, T-786C and G894T in endothelial NO synthase gene (eNOS) a...
Ischemic stroke is a significant health condition, whose frequency in childhood is increasing day by...
<div><p>Endothelial nitric oxide synthase (<i>eNOS</i>) is localized in caveole and has important ef...
Aim. To study the frequency of polymorphic gene variants encoding proteins of renin-angiotensin syst...
Homozygosity for the methylenetetrahydrofolate reductase (MTHFR) 677C>T mutation (MTHFR TT) has b...