Abstract. Resistance to activated protein C determined by factor V Leiden (FVL) is the most frequent inherited risk factor of venous thrombosis. The purpose of our work was to reveal the frequency of FVL in Slovak patients with venous thromboses, to characterise the nature of venous thromboses in this inherited thrombophilia, and to consider the screening approach to investigation of FVL in patients with venous thromboses. 350 patients with a diagnosis of venous thromboembolic disease from various regions of Slovakia were investigated. FVL, detected by polymerase chain reaction, was found in 128/350 (37%) patients with venous thromboses. 118/128 (92%) patients were heterozygous and 10/128 (8%) were homozygous carriers. In 108/128 (84%) pati...
The aim of this study was to examine the occurrence of venous thromboembolism (VTE) in relation to f...
Inherited resistance to activated protein C caused by the factor V Leiden (FVL) mutation is the most...
Background. Polymorphisms of factor V (Leiden) (G1691A) and the gene for prothrombin (G20210A) are t...
Factor V Leiden is the most common genetic defect associated with venous thromboembolism. Its clinic...
Factor V Leiden is the most common genetic defect associated with venous thromboembolism. Its clinic...
Factor V Leiden is the most common genetic defect associated with venous thromboembolism. Its clinic...
Factor V Leiden is the most common genetic defect associated with venous thromboembolism. Its clinic...
The subject of this thesis is Leiden mutation, its signification and methods of examination. This wo...
International audienceThe factor V Leiden (FVL) mutation, a genetic abnormality with an autosomal mo...
Aim: To determine the prevalence of factor V Leiden mutation in patients with different presentation...
Background. A tendency to venous thromboembolism is otherwise called hypercoagulability or thrombop...
Abstract Background Activated protein C resistance (APCR) due to factor V Leiden (FVL) mutation (R50...
Aim: To determine the prevalence of factor V Leiden mutation in patients with different presentation...
ABSTRACT This study determined the prevalence of inherited factor V Leiden mutation in a group of 12...
Several inherited polymorphisms are associated with risk of venous thrombosis, including Mutation at...
The aim of this study was to examine the occurrence of venous thromboembolism (VTE) in relation to f...
Inherited resistance to activated protein C caused by the factor V Leiden (FVL) mutation is the most...
Background. Polymorphisms of factor V (Leiden) (G1691A) and the gene for prothrombin (G20210A) are t...
Factor V Leiden is the most common genetic defect associated with venous thromboembolism. Its clinic...
Factor V Leiden is the most common genetic defect associated with venous thromboembolism. Its clinic...
Factor V Leiden is the most common genetic defect associated with venous thromboembolism. Its clinic...
Factor V Leiden is the most common genetic defect associated with venous thromboembolism. Its clinic...
The subject of this thesis is Leiden mutation, its signification and methods of examination. This wo...
International audienceThe factor V Leiden (FVL) mutation, a genetic abnormality with an autosomal mo...
Aim: To determine the prevalence of factor V Leiden mutation in patients with different presentation...
Background. A tendency to venous thromboembolism is otherwise called hypercoagulability or thrombop...
Abstract Background Activated protein C resistance (APCR) due to factor V Leiden (FVL) mutation (R50...
Aim: To determine the prevalence of factor V Leiden mutation in patients with different presentation...
ABSTRACT This study determined the prevalence of inherited factor V Leiden mutation in a group of 12...
Several inherited polymorphisms are associated with risk of venous thrombosis, including Mutation at...
The aim of this study was to examine the occurrence of venous thromboembolism (VTE) in relation to f...
Inherited resistance to activated protein C caused by the factor V Leiden (FVL) mutation is the most...
Background. Polymorphisms of factor V (Leiden) (G1691A) and the gene for prothrombin (G20210A) are t...