Abstract
In the article «Genetic factors of fibrinolysis violation and the role of inhibitor plasminogen activator genes polymorphism in the development of secondary thrombus bleeding complications in patients with brain injury», briefly summarized the impact of molecular-genetic mechanisms peculiarities on the system of hemostasis, the results of investigations were provide in case of thrombohemorrhagic complications appearance while PAI-1 plasma levels and computed tomographic manifestations changes in 200 patients with TBI, -675 gene polymorphism and PAI-1.
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