Background Inherited thrombophilias are well‐established predisposing factors for venous
thromboembolism, but their role in arterial thrombosis, such as arterial ischemic stroke …

There are many genetic and acquired risk factors that are known to cause venous
thromboembolic disorders (VTE). One of these is the Prothrombin G20210A mutation, which …

Ischemic strokes are one of the leading causes of death worldwide. The aim of this meta-
analysis is to elaborate on the role of inherited predisposition to thrombophilia in the etiology …

Ischemic stroke is an acute episode of neurological dysfunction resulting from the focal brain
and spinal cord infarction. Many etiologies have been reported and vary significantly with …

Aim To investigate the prevalence of common genetic variants that can serve as markers of
thrombophilia and warfarin pharmacogenetics in Bosnia and Herzegovina. Methods The …

Objective: Abnormalities in the coagulation pathway are often included in the diagnostic
work-up of stroke patients, especially in young adults with cryptogenic stroke. Methods …

Abstract The 1691G> A FV variant has been described as a common genetic risk factor in
venous thromboembolism. The purpose of this study was to provide a further frequency …

Warfarin-induced skin necrosis (WISN) is a rare complication of anticoagulant therapy
associated with a high incidence of morbidity and mortality requiring immediate drug …

Summary Introduction: Factor V Leiden (FVL) and prothrombin G20210A mutation (PTM) are
the two most common genetic polymorphisms known to predispose to a first episode of …

Prothrombin gene mutation (prothrombin thrombophilia) is an inherited disorder that
increases the risk of venous thrombosis. However, limited data exist on the risk of arterial …