British Journal of Haematology · 2007 · 101 citations · 12 references
MedicineGeneticsHematologyGenetic EpidemiologyHemostasisMedical GeneticsCoagulation DisordersCoagulation Factor DeficienciesCoagulation PhysiologyHemostatic DisordersThrombosisThrombotic DisordersComparative Disease SeverityEndothelial Protein C PathwayFactor V Leiden ThrombophiliaNatural Anticoagulant DeficiencyNatural Anticoagulant ProteinsPlasminogen ActivatorsThrombosis MechanismsTissue Factor Pathway Inhibitor Deficiency
The role of natural anticoagulants, fibrinolytic cascade factors and common prothrombotic gene polymorphisms in modulating disease severity were studied in 35 'clinically mild' and 37 'clinically severe' haemophilia patients with severe factor VIII or IX deficiency (<0.01 IU/ml). Strong association of deficiencies of proteins C and S, antithrombin III, tissue factor pathway inhibitor and tissue plasminogen activator, together with factor V Leiden and endothelial protein C receptor 23 bp insertion polymorphisms were observed in the 'clinically milder' group as compared with the 'clinically severe' group. These results indicate a synergistic modulation of bleeding tendency in haemophilia patients by factors in the anticoagulant and fibrinolytic systems.
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Moderation of hemophilia A phenotype by the factor V R506Q mutation
WC Nichols, Kagehiro Amano, PM Cacheris et al. · Blood · 1996 · 144 citations · Full text
Medicine, Genetics, Hematology +14
An In Vitro Analysis of the Combination of Hemophilia A and Factor VLEIDEN
Cornelis van ′t Veer, Neal J. Golden, Michael Kalafatis et al. · Blood · 1997 · 89 citations · Full text