Associated Papers
Congenital Inferior Vena Cava Atresia Unmasked by Pyrexia and Extensive Bilateral Deep Vein Thrombosis in a Young Adult With MTHFR Mutation.
Mani Jacob D et al.
Cureus, 2025
Cerebrovascular Thrombosis in Pediatric Ulcerative Colitis: A Case Report.
Sansotta N et al.
Reports (mdpi), 2025
The Roles of NOTCH3 p.R544C and Thrombophilia Genes in Vietnamese Patients With Ischemic Stroke: Study Involving a Hierarchical Cluster Analysis.
Bui HTT et al.
Jmir Bioinformatics and Biotechnology, 2024
Genetics of spontaneous cervical and coronary artery dissections.
Rada I et al.
Frontiers in Global Women's Health, 2023
Analytical validation of GenoPharm a clinical genotyping open array panel of 46 pharmacogenes inclusive of variants unique to people of African ancestry.
Kanji CR et al.
Plos One, 2023
Maternal Inherited Thrombophilia in Monochorionic Twin Pregnancy with Twin-Twin Transfusion Syndrome.
Giannubilo SR et al.
Journal of Clinical Medicine, 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
Thrombophilia and hormonal therapy in transgender persons: A literature review and case series.
Kerrebrouck M et al.
International Journal of Transgender Health, 2022
Thrombophilic alterations, migraine, and vascular disease: results from a case-control study.
Cavestro C et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2021
PlA2 Polymorphism of Platelet Glycoprotein IIb/IIIa and C677T Polymorphism of Methylenetetrahydrofolate Reductase (MTHFR), but Not Factor V Leiden and Prothrombin G20210A Polymorphisms, Are Associated with More Severe Forms of Legg-Calvé-Perthes Disease.
García-Alfaro MD et al.
Children (basel, Switzerland), 2021
Papillophlebitis Associated With Coexisting Heterozygous Mutations of Factor V Leiden and Methylenetetrahydrofolate Reductase Enzyme-(C677T).
Ntora E et al.
Cureus, 2021
Direct-to-consumer genetic testing for factor V Leiden and prothrombin 20210G>A: the consumer experience.
Elson SL et al.
Molecular Genetics & Genomic Medicine, 2020
Inherited Thrombophilia in a Lebanese Family of Four Generations: A Case Report of Recurrent Miscarriage.
Khalife S et al.
Vascular Health and Risk Management, 2020
A Novel Heterozygous Variant in F2 Gene in a Chinese Patient With Coronary Thrombosis and Acute Myocardial Infarction Leads to Antithrombin Resistance.
Tang Y et al.
Frontiers in Genetics, 2020
Factor V Leiden 1691G > A mutation and the risk of recurrent pregnancy loss (RPL): systematic review and meta-analysis.
Eslami MM et al.
Thrombosis Journal, 2020
Intravascular Lymphomatosis Presenting with Spinal Cord Infarction and Recurrent Ischemic Strokes.
Lyden S et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association, 2019
Genetic abnormalities and pregnancy loss.
Blue NR et al.
Seminars in Perinatology, 2019
Placenta-mediated pregnancy complications are not associated with fetal or paternal factor V Leiden mutation.
Nevalainen J et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology, 2018
Screening and functional exploration of prothrombin Arg596 related mutations in Chinese venous thromboembolism patients.
Wu X et al.
Journal of Clinical Pathology, 2018
Clinical outcomes and a high prevalence of abnormalities on comprehensive arterial and venous thrombophilia screening in TIA or ischaemic stroke patients with a patent foramen ovale, an inter-atrial septal aneurysm or both.
Lim ST et al.
Journal of the Neurological Sciences, 2017
Contribution of inherited thrombophilia to recurrent miscarriage in the Polish population.
Wolski H et al.
Ginekologia Polska, 2017
Review article: the aetiology of primary Budd-Chiari syndrome - differences between the West and China.
Qi X et al.
Alimentary Pharmacology & Therapeutics, 2016
Association between the V Leiden G1691A mutation and sudden sensorineural hearing loss in Italian population: a meta-analysis.
Shu J et al.
European Archives of Oto-rhino-laryngology : Official Journal of the European Federation of Oto-rhino-laryngological Societies (eufos) : Affiliated With the German Society for Oto-rhino-laryngology - Head and Neck Surgery, 2016
Association of C677T MTHFR and G20210A FII prothrombin polymorphisms with susceptibility to myocardial infarction.
Hmimech W et al.
Biomedical Reports, 2016
The Evaluation of Serum Copeptin Levels and Some Commonly Seen Thrombophilic Mutation Prevalence in Acute Pulmonary Embolism.
Ozturk N et al.
Biochemical Genetics, 2016
Evaluation of cases with cerebral thrombosis in children.
Ünver O et al.
Turk Pediatri Arsivi, 2016
Factor V Leiden, Prothrombin and MTHFR Mutation in Patients with Preeclamsia, Intrauterine Growth Restriction and Placental Abruption.
Livrinova V et al.
Open Access Macedonian Journal of Medical Sciences, 2015
Prothrombin G20210A and methylenetetrahydrofolate reductase C677T polymorphisms in peripheral capillary nonperfusion: a case report.
Wathek C et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis, 2015
[Discovery and prospects of a novel thrombophilia: antithrombin resistance].
Takagi Y et al.
Nihon Rinsho. Japanese Journal of Clinical Medicine, 2014
Evaluation of chromosomal abnormalities and common trombophilic mutations in cases with recurrent miscarriage.
Karatas A et al.
African Health Sciences, 2014
Impact of inherited thrombophilia on the risk of recurrent venous thromboembolism onset in Georgian population.
Pirtskhelani N et al.
Georgian Medical News, 2014
The role of point mutations in the genes, predisposing inherited thrombophilia in the pathogeneses of proximal and distal deep vein thrombosis in Georgian population.
Pirtskhelani N et al.
Georgian Medical News, 2014
Risk of prostate cancer and thrombosis-related factor polymorphisms.
Ghasemi S et al.
Biomedical Reports, 2014
A deep vein thrombosis caused by 20209C>T mutation in homozygosis of the prothrombin gene in a Caucasian patient.
Alvarez SI et al.
Biochemia Medica, 2014
The association between inherited thrombophilia and recurrent pregnancy loss in Turkish women.
Isaoglu U et al.
Clinical and Experimental Obstetrics & Gynecology, 2014
"20209C-T" a variant mutation of prothrombin gene mutation in a patient with recurrent pregnancy loss.
Prat M et al.
Annals of Clinical and Laboratory Science, 2014
Maternal factor V Leiden and prothrombin mutations do not seem to contribute to the occurrence of two or more than two consecutive miscarriages in Caucasian patients.
Baumann K et al.
American Journal of Reproductive Immunology (new York, N.y. : 1989), 2013
Who are at risk for thromboembolism after arthroplasty? A systematic review and meta-analysis.
Zhou X et al.
Thrombosis Research, 2013
The distribution of Factor V Leiden mutation.
Eroğlu A
Journal of Thrombosis and Thrombolysis, 2013
A novel prothrombin mutation in two families with prominent thrombophilia--the first cases of antithrombin resistance in a Caucasian population.
Djordjevic V et al.
Journal of Thrombosis and Haemostasis : Jth, 2013
Effect of thrombosis-related gene polymorphisms upon oral cancer: a regression analysis.
Vylliotis A et al.
Anticancer Research, 2013
Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controls.
Simone B et al.
European Journal of Epidemiology, 2013
PLA2 polymorphism of platelet glycoprotein IIb/IIIa but not Factor V Leiden and prothrombin G20210A polymorphisms is associated with venous thromboembolism and more recurrent events in central Iran.
Pourgheysari B et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis, 2013
Prothrombotic polymorphisms in patients with Raynaud's phenomenon and migraine.
Takáts AT et al.
Acta Physiologica Hungarica, 2012
High prevalence of three prothrombotic polymorphisms among Palestinians: factor V G1691A, factor II G20210A and methylenetetrahydrofolate reductase C677T.
Hussein AS
Journal of Thrombosis and Thrombolysis, 2012
Thrombophilias and adverse pregnancy outcomes: results from the Danish National Birth Cohort.
Lykke JA et al.
Journal of Thrombosis and Haemostasis : Jth, 2012
[Molecular diagnostic tests for thrombophilia in patients referred to genetic counseling clinic because due to recurrent pregnancy failure. One center's experience].
Pasińska M et al.
Ginekologia Polska, 2012
Prevalence of H1299R polymorphism in the Factor V gene among the Taif-Saudi Arabia population using polymerase chain reaction-reverse hybridization technique.
Awad NS et al.
Molecular Biology Reports, 2012
Posterior ocular involvement in Behçet's disease and thrombophilic mutations.
Vayá A et al.
Clinical Hemorheology and Microcirculation, 2012
Lack of Association between Recurrent Pregnancy Loss and Inherited Thrombophilia in a Group of Colombian Patients.
Cardona H et al.
Thrombosis, 2012