Associated Papers
-455A Allele May Be a Protective Locus for Aseptic Lower Extremity Superficial Thrombophlebitis.
Luo R et al.
Genetic Testing and Molecular Biomarkers, 2025
Genetic landscape of thrombophilia in recurrent miscarriages.
Athar A et al.
Obstetrics & Gynecology Science, 2024
Fibrinogen B β promoter polymorphism may not be associated with pulmonary embolism.
Chen W et al.
Phlebology, 2024
Risk Factors of Thrombophilia-Related Mutations for Early and Late Pregnancy Loss.
Borsi E et al.
Medicina (kaunas, Lithuania), 2024
A Prothrombotic Score Based on Genetic Polymorphisms of the Hemostatic System Differs in Patients with Ischemic Stroke, Myocardial Infarction, or Peripheral Arterial Occlusive Disease.
Herm J et al.
Frontiers in Cardiovascular Medicine, 2017
High Incidence of ACE/PAI-1 in Association to a Spectrum of Other Polymorphic Cardiovascular Genes Involving PBMCs Proinflammatory Cytokines in Hypertensive Hypercholesterolemic Patients: Reversibility with a Combination of ACE Inhibitor and Statin.
AlBacha Jd et al.
Plos One, 2015
Study of associated genetic variants in Indian subjects reveals the basis of ethnicity related differences in susceptibility to venous thromboembolism.
Kumari B et al.
Thrombosis, 2014
Combined effects of fibrinogen genetic variability on atherosclerosis in patients with or without stable angina pectoris: focus on the coagulation cascade and endothelial function.
Papageorgiou N et al.
International Journal of Cardiology, 2013
Genetic polymorphisms associated with retinal vein occlusion: a Greek case-control study and meta-analysis.
Yioti GG et al.
Ophthalmic Genetics, 2013
Genetic polymorphisms and the risk of myocardial infarction in patients under 45 years of age.
Sakowicz A et al.
Biochemical Genetics, 2013
Impact of hemostatic gene single point mutations in patients with non-diabetic coronary artery disease.
Var A et al.
Molecular Biology Reports, 2009
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis.
Martinelli N et al.
Plos One, 2008
Impact of thrombophilic gene mutations and graft-versus-host disease on thromboembolic complications after allogeneic hematopoietic stem-cell transplantation.
Pihusch M et al.
Transplantation, 2004
The Ischemic Stroke Genetics Study (ISGS) Protocol.
Meschia JF et al.
Bmc Neurology, 2003
Thrombophilic gene mutations and recurrent spontaneous abortion: prothrombin mutation increases the risk in the first trimester.
Pihusch R et al.
American Journal of Reproductive Immunology (new York, N.y. : 1989), 2001
The Correlation Between FGB Promoter Polymorphism and Clotting Function in Patients With Idiopathic Lower Extremity Deep Venous Thrombosis.
Han S et al.
Clinical and Applied Thrombosis/hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/hemostasis, 0