Associated Papers
Plasminogen activator inhibitor-1 promoter sequence variations in idiopathic osteonecrosis of head of femur.
Raman S et al.
The Indian Journal of Medical Research, 2021
Association Between Plasminogen Activator Inhibitor-1 Genetic Polymorphisms and Stroke Susceptibility.
Hu X et al.
Molecular Neurobiology, 2017
Complex history of the discovery and characterization of congenital factor X deficiency.
Girolami A et al.
Seminars in Thrombosis and Hemostasis, 2015
Significant associations of PAI-1 genetic polymorphisms with osteonecrosis of the femoral head.
Kim H et al.
Bmc Musculoskeletal Disorders, 2011
Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene.
Herrmann FH et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2006
Factor X Stockton: a mild bleeding diathesis associated with an active site mutation in factor X.
Messier TL et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis, 1996
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