Undas, Fibrin clot properties in women het- erozygous for factor V Leiden mutation: effects of oral contraceptives, Thromb. Res. 130 (2012) e216-e221.M. Krzek, M. Ciesla-Dul, M. Zabczyk, and A. Undas, "Fibrin clot properties in women heterozygous for factor v Leiden mutation: ...
Genetic study revealed factor V Leiden mutation and homozygous mutation G20210A in prothrombin gene. CONCLUSIONS: Both mutations found in this case, alone, are not a high risk factors for venous thrombosis but together may increase 5-10 fold risk of venous thrombosis. Venous stroke must be ...
The Mechanisms by Which Both Heterozygous Peroxisome Proliferator-activated Receptor γ (PPARγ) Deficiency and PPARγ Agonist Impro... The risk of recurrent deep venous thrombosis among heterozygous carriers of both factor V Leiden and the G20210A prothrombin mutation...
The risk of recurrent venous thromboembolism in patients with an Arg506Gln mutation in the gene for factor V (factor V Leiden). N Engl J Med. 1997;2399- 403Google ScholarCrossref 9. Simioni PPrandoni PLensing AWA et al. Risk of subsequent venous thromboembolic complications...
This patient, determined to be heterozygous for factor V Leiden, is the first reported case of neonatal stroke associated with this common mutation. 关键词: beta-lactamase sultamicillin sulbactam ampicillin pediatric infections DOI: 10.1016/S0887-8994(97)00166-5 被引量: 39 年份: 1998 ...
Whether the factor V Leiden mutation increases the risk of recurrent venous thromboembolism (VTE) remains controversial, and homozygous carriers have not been extensively evaluated. In the present cohort study, we have assessed the incidence of recurrent VTE in a subset of non-treated patients previou...
Survival advantage associated with heterozygous factor V Leiden mutation in patients with severe sepsis and in mouse endotoxemia Sepsis is associated with systemic inflammation, coagulopathy, and disrupted protein C (PC) pathway function. The effect of prothrombotic polymorphism, fac... B Kerlin - 《...
Identification of a Novel Heterozygous IGF1 Splicing Mutation in a Large Kindred with Familial Short Stature Background/Aims: Insulin-like growth factor (IGF)-I is critical for normal human growth. Extremely rare homozygous mutations of the IGF1 gene severely ... JS Fuqua,M Derr,RG Rosenfeld,...
Finally, there is currently a lack of evidence that risk for recurrent VTE is increased in patients with a first episode of venous thromboembolism and heterozygous factor V Leiden mutation or the G2021OA prothrombin mutation... Huisman,V Menno - 《Current Opinion in Pulmonary Medicine》 被引量:...
Basilar artery thrombosis in a child heterozygous for factor V Leiden mutation. Pediatr Neurol 2001;24:69-71.VERDU, A.; CAZORLA, M. R.; GRANADOS, M. A. Basilar artery thrombosis in a child heterozygous for factor V Leiden mutation. Pediat Neurol , v. 24, n. 1, 2001....