Associated Papers
Assessment of Genetic Variants Linked to Susceptibility to Mechanical Prosthetic Valve Thrombosis.
Kalkan S et al.
The American Journal of Cardiology, 2025
Clinical characteristics and thrombophilia associated gene variants in Egyptians with unprovoked venous thromboembolism: three centers experience.
Efat A et al.
Molecular Biology Reports, 2024
The Impact of Cardiovascular Disease Gene Polymorphism and Interaction with Homocysteine on Deep Vein Thrombosis.
Niu LL et al.
Acs Omega, 2024
Genetic landscape of thrombophilia in recurrent miscarriages.
Athar A et al.
Obstetrics & Gynecology Science, 2024
The relevance of prothrombotic genetic variants in women who experienced pregnancy loss or embryo implantation failure: A retrospective analysis of 1922 cases.
Cernera G et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics, 2024
Risk Factors of Thrombophilia-Related Mutations for Early and Late Pregnancy Loss.
Borsi E et al.
Medicina (kaunas, Lithuania), 2024
Association of inherited thrombophilia mutations and their combinations among palestinian women with unexplained recurrent miscarriage.
Najjar AA et al.
Thrombosis Journal, 2024
Inherited Thrombophilia Associated With Ischemic Pediatric Stroke in Parent-Child Pairs.
Krleza JL et al.
Pediatric Neurology, 2023
Thrombophilic gene polymorphisms and recurrent pregnancy loss: a systematic review and meta-analysis.
Wen Y et al.
Journal of Assisted Reproduction and Genetics, 2023
Maternal Thrombophilic and Hypofibrinolytic Genetic Variants in Idiopathic Recurrent Pregnancy Loss: a Continuing Mystery.
Younis M et al.
Reproductive Sciences (thousand Oaks, Calif.), 2023
Genetic Markers for Thrombophilia and Cardiovascular Disease Associated with Multiple Sclerosis.
Hadjiagapiou MS et al.
Biomedicines, 2022
Association of polymorphisms in genes encoding prothrombotic and cardiovascular risk factors with disease severity in COVID-19 patients: A pilot study.
Lapić I et al.
Journal of Medical Virology, 2022
Molecular Analysis of Prothrombotic Gene Variants in Patients with Acute Ischemic Stroke and with Transient Ischemic Attack.
Cernera G et al.
Medicina (kaunas, Lithuania), 2021
Genetic polymorphisms in early-onset myocardial infarction in a sample of Iraqi patients: a pilot study.
Mohammad AM et al.
Bmc Research Notes, 2020
Prothrombotic gene variants in acute myocardial infarction at a young age (yAMI). Rationale for tailored prevention strategies in specific risk-group subjects for acute coronary disease?
Cernera G et al.
Nutrition, Metabolism, and Cardiovascular Diseases : Nmcd, 2020
The effects of genetic polymorphisms and diabetes mellitus on the development of peripheral artery disease.
Yalım Z et al.
Turk Kardiyoloji Dernegi Arsivi : Turk Kardiyoloji Derneginin Yayin Organidir, 2020
Analysis of thrombophilic gene mutations in coronary artery ectasia.
Yalım Z et al.
Turk Kardiyoloji Dernegi Arsivi : Turk Kardiyoloji Derneginin Yayin Organidir, 2020
Molecular Analysis of Prothrombotic Gene Variants in Venous Thrombosis: A Potential Role for Sex and Thrombotic Localization.
Cernera G et al.
Journal of Clinical Medicine, 2020
[Hemostatic Gene Polymorphisms in Acute Coronary Syndrome with Nonobstructive Coronary Atherosclerosis].
Fedorova SB et al.
Kardiologiia, 2019
Association of Polymorphisms in Coagulation Factor Genes and Enzymes of Homocysteine Metabolism With Arterial Ischemic Stroke in Children.
Coen Herak D et al.
Clinical and Applied Thrombosis/hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/hemostasis, 2017
[Effect of Bisoprolol on Heart Rate Variability in Patients With Coronary Atherosclerosis: Dependence on Polymorphisms of -1 Adrenergic Receptor Gene].
Bunova SS et al.
Kardiologiia, 2017
Atherosclerotic and thrombotic genetic and environmental determinants in Egyptian coronary artery disease patients: a pilot study.
Fawzy MS et al.
Bmc Cardiovascular Disorders, 2017
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
Association of Hemostatic Gene Polymorphisms With Early-Onset Ischemic Heart Disease in Egyptian Patients.
Alkhiary W et al.
Clinical and Applied Thrombosis/hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/hemostasis, 2016
Multiple thrombophilic single nucleotide polymorphisms lack a significant effect on outcomes in fresh IVF cycles: an analysis of 1717 patients.
Patounakis G et al.
Journal of Assisted Reproduction and Genetics, 2016
Genetic association between FXIII and β-fibrinogen genes and women with recurrent spontaneous abortion: a meta- analysis.
Li J et al.
Journal of Assisted Reproduction and Genetics, 2015
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
A novel polymorphism in the PAI-1 gene promoter enhances gene expression. A novel pro-thrombotic risk factor?
Liguori R et al.
Thrombosis Research, 2014
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
The association between thrombophilic gene mutations and recurrent pregnancy loss.
Poursadegh Zonouzi A et al.
Journal of Assisted Reproduction and Genetics, 2013
Lack of association between polymorphisms of thrombogenic genes and disease susceptibility in rheumatoid arthritis.
Dimitroulas T et al.
Rheumatology International, 2013
Genetic polymorphisms associated with retinal vein occlusion: a Greek case-control study and meta-analysis.
Yioti GG et al.
Ophthalmic Genetics, 2013
Prevalence of myocardial infarction polymorphisms in Afyonkarahisar, Western Turkey.
Onrat ST et al.
Molecular Biology Reports, 2012
Recurrent pregnancy loss and its relation to combined parental thrombophilic gene mutations.
Ozdemir O et al.
Genetic Testing and Molecular Biomarkers, 2012
Combination of thrombophilic gene polymorphisms as a cause of increased the risk of recurrent pregnancy loss.
Torabi R et al.
Journal of Reproduction & Infertility, 2012
Analysis of plasminogen activator inhibitor-1, integrin beta3, beta fibrinogen, and methylenetetrahydrofolate reductase polymorphisms in Iranian women with recurrent pregnancy loss.
Jeddi-Tehrani M et al.
American Journal of Reproductive Immunology (new York, N.y. : 1989), 2011
Prevalence of the fibrinogen beta-chain, angiotensin-converting enzyme and plasminogen activator inhibitor-1 polymorphisms in Costa Rican young adults with thrombotic disease.
Hidalgo A et al.
Cell Biochemistry and Function, 2010
The effect of four hemostatic gene polymorphisms on the outcome of septic critically ill patients.
Tsantes AE et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis, 2010
A prospective case-control study analyzes 12 thrombophilic gene mutations in Turkish couples with recurrent pregnancy loss.
Yenicesu GI et al.
American Journal of Reproductive Immunology (new York, N.y. : 1989), 2010
Impact of hemostatic gene single point mutations in patients with non-diabetic coronary artery disease.
Var A et al.
Molecular Biology Reports, 2009
Early pregnancy loss in celiac women: The role of genetic markers of thrombophilia.
Ciacci C et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver, 2009
A patient with ascending aortic dilatation, similar to phenotypes of connective tissue disorders.
Onrat ST et al.
Genetics and Molecular Research : Gmr, 2009
Comparison of thrombophilic gene mutations among patients experiencing recurrent miscarriage and deep vein thrombosis.
Coulam CB et al.
American Journal of Reproductive Immunology (new York, N.y. : 1989), 2008
Mutational spectrum of F8 gene and prothrombotic gene variants in haemophilia A patients from Southern Italy.
Sanna V et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2008
Fibrinogen Aalpha Thr312Ala polymorphism is associated with chronic thromboembolic pulmonary hypertension.
Suntharalingam J et al.
The European Respiratory Journal, 2008
Epistatic effect of plasminogen activator inhibitor 1 and beta-fibrinogen genes on risk of glomerular microthrombosis in lupus nephritis: interaction with environmental/clinical factors.
Gong R et al.
Arthritis and Rheumatism, 2007
Which thrombophilic gene mutations are risk factors for recurrent pregnancy loss?
Goodman CS et al.
American Journal of Reproductive Immunology (new York, N.y. : 1989), 2006
Multiple thrombophilic gene mutations rather than specific gene mutations are risk factors for recurrent miscarriage.
Coulam CB et al.
American Journal of Reproductive Immunology (new York, N.y. : 1989), 2006
Genetic influence on thrombotic risk markers in the elderly--a Danish twin study.
Bladbjerg EM et al.
Journal of Thrombosis and Haemostasis : Jth, 2006