The factor V Leiden variant, responsible for the phenomenon of activated protein C resistance, was found to be less frequent among British (0.06) and Swedish/Danish (0.15) protein C deficiency patients than previously reported in a Dutch study (0.19). In the Swedish population, a significantly increased frequency of the factor V Leiden allele was apparent in protein C deficiency patients as compared to healthy controls. However, this was not found in the British population. Coinheritance of the factor V Leiden variant is therefore unlikely to be the sole determinant of whether a person with protein C deficiency will come to clinical attention. Nevertheless, when patient data were analysed by type of protein C deficiency, it was noted that t...
Four hundred and ninety-three consecutive patients referred for arterial or venous thrombosis were s...
Factor V gene polymorphisms were investigated to detect components that may contribute to the activa...
Two patients from two unrelated families with a history of thrombosis showed severe plasma activated...
The factor V Leiden variant, responsible for the phenomenon of activated protein C resistance, was f...
Reported prevalence rates for protein C (PC) deficiency in the population at large have varied widel...
Our study grew from an attempt to solve a controversy. In 1987 protein C antigen level was assessed ...
A difference in the prevalence of venous thromboembolism (TE) in major human groups has been describ...
We have previously identified a group of blood donors with inherited deficiencies of either antithro...
Activated protein C resistance (APC-R) due to the single-nucleotide polymorphism factor V Leiden (FV...
A CGA→TGA transition in the protein C gene, resulting in an Arg306→Term substitution, was detected i...
A point mutation (FV:R506Q) in the human coagulation factor V gene is associated with resistance to ...
Summary: Blood samples from 104 patients with clinically suspected thrombophilia were analyzed for c...
The clinical severity of haemophilia is usually related to residual clotting factor activity. Report...
AbstractOne of the most frequent hereditary causes of thrombophilia is, without a doubt, resistance ...
Inherited resistance to activated protein C caused by the factor V Leiden (FVL) mutation is the most...
Four hundred and ninety-three consecutive patients referred for arterial or venous thrombosis were s...
Factor V gene polymorphisms were investigated to detect components that may contribute to the activa...
Two patients from two unrelated families with a history of thrombosis showed severe plasma activated...
The factor V Leiden variant, responsible for the phenomenon of activated protein C resistance, was f...
Reported prevalence rates for protein C (PC) deficiency in the population at large have varied widel...
Our study grew from an attempt to solve a controversy. In 1987 protein C antigen level was assessed ...
A difference in the prevalence of venous thromboembolism (TE) in major human groups has been describ...
We have previously identified a group of blood donors with inherited deficiencies of either antithro...
Activated protein C resistance (APC-R) due to the single-nucleotide polymorphism factor V Leiden (FV...
A CGA→TGA transition in the protein C gene, resulting in an Arg306→Term substitution, was detected i...
A point mutation (FV:R506Q) in the human coagulation factor V gene is associated with resistance to ...
Summary: Blood samples from 104 patients with clinically suspected thrombophilia were analyzed for c...
The clinical severity of haemophilia is usually related to residual clotting factor activity. Report...
AbstractOne of the most frequent hereditary causes of thrombophilia is, without a doubt, resistance ...
Inherited resistance to activated protein C caused by the factor V Leiden (FVL) mutation is the most...
Four hundred and ninety-three consecutive patients referred for arterial or venous thrombosis were s...
Factor V gene polymorphisms were investigated to detect components that may contribute to the activa...
Two patients from two unrelated families with a history of thrombosis showed severe plasma activated...