| systematic review | Q1504425 |
| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | Martin H Prins | |
| Paolo Prandoni | |||
| Antonio Marchiori | |||
| Laura Mosena | |||
| P433 | issue | 8 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Factor V Leiden | Q185986 |
| systematic review | Q1504425 | ||
| Prothrombin G20210A | Q2113626 | ||
| heterozygosity | Q124059385 | ||
| venous thromboembolism | Q9397786 | ||
| P304 | page(s) | 1107-14 | |
| P577 | publication date | 2007-08-01 | |
| P1433 | published in | Haematologica | Q5638209 |
| P1476 | title | The risk of recurrent venous thromboembolism among heterozygous carriers of factor V Leiden or prothrombin G20210A mutation. A systematic review of prospective studies | |
| P478 | volume | 92 |
| Q47440459 | Are Prothrombotic Mutations a Time-to-Event Risk Factor? |
| Q26796430 | Assessing the risk of recurrent venous thromboembolism--a practical approach |
| Q37207947 | Cerebropulmonary dysgenetic syndrome |
| Q45877007 | Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders. |
| Q90452318 | Coagulation, Microenvironment and Liver Fibrosis |
| Q43577809 | Contribution of recurrent venous thrombosis and inherited thrombophilia to the pathogenesis of postthrombotic syndrome |
| Q57643254 | Diagnosis of uterine vein thrombosis on transvaginal ultrasound |
| Q46542845 | Diffuse cerebral infarct associated with factor V Leiden and prothrombin 20210A mutations in a patient with tetralogy of Fallot |
| Q35112558 | Effect of Platelet Glycoprotein IIb/IIIa PLA2 Polymorphism on Severity of Pulmonary Thromboembolism |
| Q38385253 | Efficacy of dabigatran versus warfarin in patients with acute venous thromboembolism in the presence of thrombophilia: Findings from RE-COVER®, RE-COVER™ II, and RE-MEDY™. |
| Q38881922 | Electronic health record interventions at the point of care improve documentation of care processes and decrease orders for genetic tests commonly ordered by nongeneticists. |
| Q38986410 | Environmental and Genetic Risk Factors Associated with Venous Thromboembolism |
| Q45941946 | Evaluation of the Nanosphere Verigene System and the Verigene F5/F2/MTHFR Nucleic Acid Tests. |
| Q37641282 | Factor V Leiden and activated protein C resistance |
| Q34152374 | Factor V Leiden thrombophilia |
| Q36045799 | Factor V-Leiden Mutation: A Common Risk Factor for Venous Thrombosis among Lebanese Patients |
| Q40307133 | Gender-related differences in the outcome of patients with venous thromboembolism and thrombophilia |
| Q37396981 | Genetics and the general physician: insights, applications and future challenges |
| Q89002092 | Hypercoagulable States and Thrombophilias: Risks Relating to Recurrent Venous Thromboembolism |
| Q43233746 | Inactivation of thrombomodulin by ionizing radiation in a cell-free system: possible implications for radiation responses in vascular endothelium |
| Q33904210 | Influence of acquired and genetic risk factors on the prevention, management, and treatment of thromboembolic disease |
| Q38178063 | Inherited risk factors for venous thromboembolism |
| Q41124495 | Isolated thrombosis of right spermatic vein with underlying Factor V Leiden mutation |
| Q48297715 | Kallmann syndrome patient with gender dysphoria, multiple sclerosis, and thrombophilia |
| Q46490008 | MTHFR C677TT, PAI1 4G-4G, V Leiden Q506, and prothrombin G20210A in hepatocellular carcinoma with and without portal vein thrombosis |
| Q36718482 | Management of patients with unprovoked venous thromboembolism: an evidence-based and practical approach |
| Q58689588 | Pathophysiology of Post-Thrombotic Syndrome: The Effect of Recurrent Venous Thrombosis and Inherited Thrombophilia |
| Q51047838 | PlA2 Polymorphism in Glycoprotein IIb/IIIa Modulates the Morphology and Nanomechanics of Platelets. |
| Q46047297 | Prothrombotic gene mutations in patients with sudden sensorineural hearing loss and cardiovascular thrombotic disease |
| Q38283515 | Recurrent venous thromboembolism in a patient with heterozygous factor v leiden mutation |
| Q30244631 | Review article: the aetiology of primary Budd-Chiari syndrome - differences between the West and China |
| Q34153343 | Risk assessment for recurrent venous thrombosis |
| Q40135109 | Rs5918ITGB3 Polymorphism, Smoking, and BMI as Risk Factors for Early Onset and Recurrence of DVT in Young Women |
| Q38250865 | The real value of thrombophilia markers in identifying patients at high risk of venous thromboembolism |
| Q44247861 | Thrombophilia differences in splanchnic vein thrombosis and lower extremity deep venous thrombosis in North America |
| Q37892665 | Using the laboratory to predict recurrent venous thrombosis |
| Q33573008 | Variants of a Thermus aquaticus DNA polymerase with increased selectivity for applications in allele- and methylation-specific amplification. |
| Q41496563 | Variants of sequence family B Thermococcus kodakaraensis DNA polymerase with increased mismatch extension selectivity |
| Q38117733 | Venous thrombosis: understanding the paradoxes of recurrence |
| Q82993880 | [Follow-up of pulmonary thromboembolism] |
Search more.