Associated Papers
Investigation of Prothrombin G20210A and Factor V Leiden G1691A Variants in Patients with Acute Coronary Syndrome Presenting to the Emergency Department with Chest Pain.
Yukcu F et al.
Genes, 2025
Screening of Factor V Leiden mutation and activated protein C resistance in Sudanese children with sickle cell disease and stroke: A descriptive cross-sectional study.
Ahmed AA et al.
Medicine, 2025
Genes predisposing to acute cerebral circulatory failure in severe pre-eclampsia in the Kazakh population.
Svyatova G et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics, 2025
Complex Venous Thromboembolism in a Young Woman With Multisystem Manifestations: A Case Report.
Alswij MA et al.
Cureus, 2025
Venous thromboembolism laboratory testing (factor V Leiden and factor II c.∗97G>A), 2025 revision: A technical standard of the American College of Medical Genetics and Genomics (ACMG).
Kang BE et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2025
Lipoprotein(a) and prothrombotic effects: Evidence from a genetic association study.
Olmastroni E et al.
European Journal of Internal Medicine, 2025
Cerebrovascular Thrombosis in Pediatric Ulcerative Colitis: A Case Report.
Sansotta N et al.
Reports (mdpi), 2025
Assessment of Genetic Variants Linked to Susceptibility to Mechanical Prosthetic Valve Thrombosis.
Kalkan S et al.
The American Journal of Cardiology, 2025
Indications of the SERPINE 1 variant rs1799768's role in anti-VEGF therapy resistance in neovascular age-related macular degeneration.
Çevik MÖ et al.
Plos One, 2025
Hereditary thrombophilia parameters in children with autism spectrum disorder and their mothers.
Ray PC et al.
Frontiers in Pediatrics, 2025
Recurrent Early Pregnancy Loss and Congenital Thrombophilia: A Prospective Study.
Basha A et al.
Journal of Clinical Medicine, 2024
The effect of hereditary thrombophilia on recurrent pregnancy loss: a retrospective cohort study.
Sayal HB et al.
Bmc Pregnancy and Childbirth, 2024
F2c.*C20209T mutation in patients with a history of thrombosis: A case report, retrospective 2 site-results and review of the literature.
Jambou D et al.
International Journal of Laboratory Hematology, 2024
Venous thromboembolism risk in adults with hereditary thrombophilia: a systematic review and meta-analysis.
Alnor AB et al.
Annals of Hematology, 2024
Extensive Deep Vein Thrombosis and Pulmonary Embolism in a Young Patient With Heterozygous Factor V Leiden Mutation and Antiphospholipid Syndrome.
Sava EA et al.
Cureus, 2024
ATR1 A1166C (rs5186), FII G20210A (rs1799963), FV G1691A (rs6025), FXIII 97G > T (rs11466016) and MTHFR A1298C (rs1801131) polymorphisms and the risk of ST-elevation myocardial infarction in young Mexican individuals.
Isordia-Salas I et al.
Molecular Biology Reports, 2024
Systematic review and meta-analysis of the genetics of peripheral arterial disease.
Ochoa Chaar CI et al.
Jvs-vascular Science, 2024
Inherited Thrombophilia and Risk of Thrombosis in Children with Cancer: a Single-center Experience.
Đordević A et al.
Acta Medica Academica, 2023
Maternal inherited thrombophilia and recurrent pregnancy loss: a Tunisian study and review of literature.
Frikha R et al.
African Health Sciences, 2023
Long-term haematological response and maintained immunological function after laparoscopic subtotal splenectomy in patients with hereditary spherocytosis.
Münch AL et al.
European Journal of Haematology, 2023
High Prevalence of Plasminogen Activator Inhibitor-1 4G/5G Polymorphism among Patients with Venous Thromboembolism in Kerala, India.
Tony AM et al.
Hamostaseologie, 2023
The Impact of Thrombophilic Factors on Disease Progression in Children with Biliary Atresia-A Single-Centre Cohort Study.
Ohlendorf J et al.
Journal of Clinical Medicine, 2023
Role of Genetic Thrombophilia Markers in Thrombosis Events in Elderly Patients with COVID-19.
Fevraleva I et al.
Genes, 2023
Impact of pharmacogenetics on aspirin resistance: a systematic review.
Silva GFD et al.
Arquivos De Neuro-psiquiatria, 2023
The Progress of Research on Genetic Factors of Recurrent Pregnancy Loss.
Li Q et al.
Genetics Research, 2023
Genetics of spontaneous cervical and coronary artery dissections.
Rada I et al.
Frontiers in Global Women's Health, 2023
Genetic Architecture of Pregnancy Loss: Co-inheritance of Risk Factors in Bosnian Women.
Adler G et al.
Folia Biologica, 2023
Methylenetetrahydrofolate Reductase 677T Allele Is a Risk Factor for Arterial Thrombosis in Chinese Han Patients with Antiphospholipid Syndrome.
Tang Z et al.
Biomedicines, 2022
Maternal Inherited Thrombophilia in Monochorionic Twin Pregnancy with Twin-Twin Transfusion Syndrome.
Giannubilo SR et al.
Journal of Clinical Medicine, 2022
Association of Inherited Thrombophilia with Recurrent Pregnancy Loss in A Population of Lebanese Women: A Case Control Study.
Khalife S et al.
International Journal of Fertility & Sterility, 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
Thrombophilia screening in women with recurrent first trimester miscarriage: is it time to stop testing? - a cohort study and systematic review of the literature.
Shehata H et al.
Bmj Open, 2022
Large-scale screening for factor V Leiden (G1691A), prothrombin (G20210A), and MTHFR (C677T) mutations in Greek population.
Raptopoulou A et al.
Health Science Reports, 2022
Multiple sclerosis and genetic polymorphisms in fibrinogen-mediated hemostatic pathways: a case-control study.
Abbadessa G et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2022
A rare case of catastrophic antiphospholipid syndrome triggered by estrogen-containing oral contraceptives in a patient with double heterozygous factor V Leiden and prothrombin G20210A mutations.
McRae HL et al.
American Journal of Hematology, 2022
Current Knowledge on Factor V Leiden Mutation as a Risk Factor for Recurrent Venous Thromboembolism: A Systematic Review and Meta-Analysis.
Eppenberger D et al.
Frontiers in Cardiovascular Medicine, 2022
Association of venous thromboembolism and myocardial infarction with Factor V Leiden and Factor II gene mutations among Libyan patients.
Msalati A et al.
The Libyan Journal of Medicine, 2021
Risk Factors of Venous Thromboembolism in Sudanese Pregnant Women.
Abdalhabib EK et al.
Balkan Journal of Medical Genetics : Bjmg, 2021
Livedoid vasculopathy and its association with genetic variants: A systematic review.
Gao Y et al.
International Wound Journal, 2021
Polymorphisms of F2 (G20210A), F5 (G1691A), F 7 (G10976A), F 13(G13T), FGB, ITGA2, ITGB3, PAI-I genes and its association with thrombotic complications in patients suffering from Takayasu aortoarteritis of Urals population.
Borodina I et al.
Turk Kardiyoloji Dernegi Arsivi : Turk Kardiyoloji Derneginin Yayin Organidir, 2021
VARIANTS OF IL1 (C3954T, RS1143634), PON1 (C108T, RS705379) GENES AS PROGNOSTIC MARKERS OF OSTEOMYELITIS RISK AND ITS COMPLICATIONS.
Kolov G et al.
Georgian Medical News, 2021
Factor V Leiden G1691A and Prothrombin Gene G20210A Mutations on Pregnancy Outcome.
Padda J et al.
Cureus, 2021
Association of Factor V Leiden G1691A and Prothrombin gene G20210A mutations with adverse pregnancy outcomes.
Ali SA et al.
Jpma. the Journal of the Pakistan Medical Association, 2021
Hereditary thrombophilia and recurrent pregnancy loss: a systematic review and meta-analysis.
Liu X et al.
Human Reproduction (oxford, England), 2021
Recurrent miscarriage is not associated with a higher prevalence of inherited and acquired thrombophilia.
Vomstein K et al.
American Journal of Reproductive Immunology (new York, N.y. : 1989), 2021
Prevalence of Factor V Leiden G1691A and Prothrombin G20210A Gene Mutation Among Pregnant Women: Experience from a Multi-Center Study in Nigeria.
John-Olabode SO et al.
Journal of Blood Medicine, 2021
Prevalence and Multiplicity of Thrombophilia Genetic Polymorphisms of F V, MTHFR, F II, and PAI -I: A Cross-Sectional Study on a Healthy Jordanian Population.
Al-Zoubi N et al.
International Journal of General Medicine, 2021