Factor V Leiden (FVL) mutation is the most common genetic defect that predisposes to thrombosis. The reconstruction of hepatic artery with arterial graft is a documented risk factor for HAT. However, the relationship among \\{FVL\\} mutation, arterial graft, and \\{HAT\\} remains to be ...
The factor V Leiden mutation is not a common cause of recurrent miscarriage Some investigators suggest that placental thrombosis and infarction can cause recurrent miscarriage. We have shown that the common missense mutation in the... DS Dizon-Townson,S Kinney,DW Branch,... - 《Journal of Repro...
机译:因子V莱顿突变-少见中风案例” 3. A rare case of arterial thrombosis in a 37-year-old male with Factor V Leiden mutation [J] . S. O’Gorman, R. Osman, M. Smith, Irish Journal of Medical Science . 2009,第3期 机译:一名37岁的男性,患有因子V Leiden突变的动脉血栓形成的罕见病...
Case Report: Factor v Leiden mutation is the most common hereditary disorder in patients with venous thromboembolism. Other genetic disorders seen more common are prothrombin G20210A mutation, protein C deficiency, protein S deficiency, antithrombin III deficiency and hiperhomosistinemia. The patients ...
Factor V Leiden (factor V Arg506Gln), the genetic defect underlying resistance to activated protein C, is the most common risk factor for venous thrombosis... FR Rosendaal - 《Blood》 被引量: 897发表: 1997年 High prevalence of a mutation in the factor V gene within the U.K. population...
AIMS: To investigate if the presence of factor V Leiden has an influence on the prognosis in central retinal vein occlusion (CRVO). METHODS: 166 patients with CRVO were studied retrospectively. They were tested for factor V Leiden using DNA analysis. The presence of the mutation was studied ...
In addition to the genetic variants currently used in clinical assessment of hereditary thrombophilia (e.g., Factor V Leiden, prothrombin mutation) there are other more recently discovered common gene variants that contribute to VTE risk15,16,17. However, even when these are also incorporated into...
Is recurrent venous thromboembolism more frequent in homozygous patients for the factor V Leiden mutation than in heterozygous patients? 来自 Semantic Scholar 喜欢 0 阅读量: 25 作者: None 摘要: Whether the factor V Leiden mutation increases the risk of recurrent venous thromboembolism (VTE) ...
The sentinel SNP of the third identified locus (rs1736891, MAF = 0.38) was associated with the expression of several nearby genes annotated as zinc fingers (Supplementary Data8), but most strongly with downregulation of the expression of the nearby transcription factor35ZSCAN9gene located on...
C677T MTHFR Mutation and Factor V Leiden Mutation in Patients with TIA/Minor Stroke: A Case-Control Study A common C677T mutation in the gene for the enzyme 5,10-methylenetetrahydrofolate reductase (5,10-MTHFR) has been linked to elevated levels of homocysteine... Wolfgang,Lalouschek,and,...