Associations of oxytocin receptor gene (OXTR) variants and autism spectrum disorders
(ASD) have been reported in earlier studies; in one of the studies associations with IQ and …

To investigate the relationship between clinical phenotype, clotting activity (FVIIc) and FVII
genotype, a multi-center study of factor VII (FVII) congenital deficiency with centralized …

The congenital FVII deficiency (FVIID) is a rare haemorrhagic disorder with an autosomal
recessive pattern of inheritance. Data on phenotype and the genotype from 717 subjects in …

Inherited factor X deficiency (FXD) is a rare (1: 1 000 000) recessive bleeding disorder. The
clinical and laboratory phenotypes of FXD are poorly correlated and few regional studies on …

Thrombosis in congenital factor (F) VII deficiency was investigated through extensive
phenotypic and molecular-genetic studies. Patients with a history of thrombosis among 514 …

OBJECTIVE:: Hyperhomocysteinemia is associated with atherosclerotic risk. Although
vitamins can lower homocysteine (Hcy), information about effects on atherosclerosis is …

The filament winding technique has evolved in recent decades moving from classical lathe-
type towards winding with an increased number of degrees of freedom using more complex …

Resistance to activated protein C (APC) is the most common inherited risk factor for venous
thrombosis. Most cases of APC resistance are caused by the point mutation nt 1691 G–A in …

Factor VII is a vitamin K‐dependent coagulation protease essential for the initiation phase of
normal hemostasis. The human factor VII gene (FVII, also known as F7) spans 13 kb and is …

Ischemic stroke in young adults is a well-known disease, but despite extensive clinical and
laboratory investigations, its etiology remains unclear in approximately half of the cases. We …