| V |
| Vaanaanen H. |
- |
P-Selectin deficiency results in impaired thrombus formation and frequent embolization in mouse model of carotid artery thrombosis |
| Vaccarino A. |
- |
Prolonged APTT children undergoing elective tonsillectomy |
| |
- |
Anti-protein S antibodies in patients with venous and/or arterial thrombosis |
| Vadasz Z. |
- |
Warfarin and overanticoagulation |
| Vaidyula V. R. |
- |
Anti-platelet agents clopidogrel and aspirin inhibit expression of tissue factor procoagulant activity in patients with peripheral artery disease |
| Vaigot P. |
- |
A study of gene expression profiles during megakaryocytopoiesis |
| Vainchenker W. |
- |
Cross-talk between alpha2beta1 integrin and GPVI receptors regulates actin polymerization through Rho GTPase and MAP kinase Erk1/2 signaling pathways in human megakaryocytes |
| Vaitkus P. T. |
- |
A randomized placebo controlled trial of dalteparin for the prevention of venous thromboembolism in 3706 acutely Ill medical patients: the PREVENT medical thromboprophylaxis study |
| Vajda S. |
- |
Thrombin receptors on the cells of the bloodbrain barrier |
| Valarani B. |
- |
A clinical outcome-based prospective study on venous thromboembolism in cancer surgery: the @RISTOS project |
| Valdre L. |
- |
Thrombophilia and residual vein thrombosis are independent risk factors for recurrent venous thromboembolism |
| |
- |
D-dimer and residual vein thrombosis assessed at 3 months after anti-coagulation withdrawal are independent risk factors for recurrent venous thromboembolism |
| Valdrè L. |
- |
The risk of recurrence after a first episode of venous thromboembolism in cancer patients |
| Valdre L. |
- |
Venous thromboembolic complications in patients with multiple myeloma treated with thalidomide:prophylatic effect of fixed dose Wafarin L |
| Valenti G. |
- |
Diagnosis of deep vein thrombosis in hospitalized elderly patients: poor discriminant value of clinical pretest probability unless integrated by d-dimer assay |
| Valentini G. |
- |
Increased intima-media thickness to show relationship between atherosclerosis and inflammation in a human model: patients affected by rheumatoid arthritis and absence of common markers of atherosclerosis |
| Valentino L. A. |
- |
Type 2 M von Willebrand disease due to linked P1266Q and V1279I substitutions in the von Willebrand factor A1 domain |
| Valentino L. |
- |
Low-molecular-weight heparin dose requirements are age-related through childhood |
| Valention L. A. |
- |
Enhancing hemophilia care and patient adherence using Advoy.com |
| Vallés J. |
- |
Plateleterythrocyte interactions enhance GPIIbIIIa receptor activation and P-selectin expression during platelet recruitment. These effects are amplified in type I diabetic patients |
| Vallés J. |
- |
Insufficient thromboxane A2 inhibition in patients with vascular disease chronically treated with aspirin: implications for platelet function |
| Vallez M. O. |
- |
Evolution of a nonocclusive deep vein thrombosis in the rabbit vena cava |
| Vallez M. O. |
- |
Anti-thrombotic and anticoagulant effects of S35898 an orally active thrombin inhibitor |
| Valliere J. |
- |
Asymptomatic venous thrombosis is a frequent event in protein C deficiency: a systematic ultrasound assessment of 208 family members with the 3363-C insertion mutation (IPCI: International Protein C Investigation) |
| Vallve C. |
- |
The 46C®T polymorphism in the F12 gene as a risk factor for venous thrombosis: association after linkage analysis |
| |
- |
Complexity of the genetic contribution to Factor VII deficiency in two Spanish families: clinical and biological implications |
| |
- |
Genetic dissection of thrombin-activatable fibrinolysis inhibitor (TAFI) |
| |
- |
The 46C®T polymorphism in F12 gene is a risk factor for coronary artery disease |
| |
- |
The 46C®T polymorphism in the F12 gene is a risk factor for ischemic stroke |
| Valsecchi C. |
- |
Standardization of activated protein C resistance testing: effect of residual platelets in frozen plasmas assessed with commercial and home made methods |
| Van Aarle F. G. B. |
- |
Two sensitive chromogenic assays of fondaparinux sodium (Arixtra®), a new synthetic and selective inhibitor of factor Xa, in plasma |
| Van Aken B. E. |
- |
Symptomatic plaques of type 2 diabetic patients show more plaque complications but similar expression patterns of markers for coagulation and inflammation compared to nondiabetic controls |
| Van Aken H. |
- |
Thrombospondin-1 promotes transendothelial migration of monocytes associated with platelets |
| Van Aken B. |
- |
Recombinant factor VIIa reverses the anticoagulant effect of the long-acting pentasaccharide idraparinux in healthy volunteers |
| Van Amsterdam R. G. M. |
- |
Potential reversal agents for the long-acting pentasaccharide idraparinux |
| Van Assche K. W. A. |
- |
Endogenous factor V synthesis in megakaryocytes contributes negligibly to the platelet factor V pool |
| Van Beek E. J. R. |
- |
Long-term follow-up of patients with suspected deep vein thrombosis of the upper extremities: survival, risk factors and postthrombotis syndrome |
| Van Belle E. |
- |
Tissue factor predicts long-term outcome after percutaneous coronary revascularization |
| |
- |
Tissue factor pathway in carotid atherosclerotic plaques: relationships with clinical patterns and risk factors |
| |
- |
Effect of in vivo thrombin inhibition on bFGF-induced angiogenesis in a murine angiogenic model |
| Van Cott E.* |
- |
The effect of drotrecogin alfa (Xigris) on the biphasic PTT waveform in patients with sepsis |
| Van Cott E. M. |
- |
Biphasic PTT waveform and adverse events in nonintensive care unit patients |
| Van De Poel M. |
- |
Risk assessment of venous thromboembolism in pregnant women with factor V Leiden, prothrombin 20210 A mutation, elevated factor VIII levels or mild hyperhomocystinaemia |
| Van De Ree M. A. |
- |
Atorvastatin strongly reduces C-reactive protein, but shows less marked effect on other prognostic inflammatory markers |
| |
- |
Decrease of thrombophilia variables by aggressive vs. conventional atorvastatin treatment in patients with type 2 diabetes mellitus |
| Van De Water N. |
- |
Protein Z-dependent protease inhibitor (ZPI) deficiency: a new thrombotic risk factor? |
| Van De Werf F. |
- |
Combination therapy with low-molecular weight heparin and glycoprotein IIb/IIIa inhibitors in acute coronary syndromes: insights from the Global Registry of Acute Coronary Events (GRACE) |
| |
- |
Combination therapy with low-molecular-weight heparin and glycoprotein IIb/IIIa inhibitors in acute coronary syndromes: insights from the Global Registry of Acute Coronary Events (GRACE) |
| Van De Wouwer M. |
- |
Establishing links between coagulation and inflammation: The lectin-like domain of thrombomodulin confers protection in a murine model of rheumatoid arthritis |
| Van Den Berg H. M. |
- |
The relation between clinical phenotype and genotype of severe hemophilia A |
| Van Den Berg E. |
- |
Duplex screening for quality assurance of postoperative thromboembolism prophylaxis in neurosurgery Krefeld Study Thrombo 2000 |
| Van Den Berg H. M. |
- |
Effects of bleeds on health-related quality of life in patients with hemophilia |
| Van Den Berk N. |
- |
a4 integrins and P-selectin mediate rolling and initial attachment of platelet-monocyte complexes to activated endothelium under flow conditions |
| Van Den Berkmortel F. W. P. J. |
- |
Homocysteine concentrations are associated with increased t-PA and PAI concentrations in smokers |
| Van Den Besselaar A. M. H. P. |
- |
European action on anti-coagulation cost effectiveness of computer assisted anti-coagulant dosage |
| |
- |
European concerted action on anti-coagulation (ECAA). Correction of displayed INR on two point-of-care test (POCT) whole blood prothrombin time monitors (CoaguChek Mini and TAS PT-NC) by independent International Sensitivity Index (ISI) calibration |
| |
- |
European concerted action on anti-coagulation (ECAA). reliability of International Normalized Ratios (INR) from CoaguChek mini and TAS PT-NC whole blood point-of-care test monitor systems |
| Van Den Blink B. |
- |
Coagulation factor profiles respond strongly during human endotoxemia |
| Van Den Ende A. E. |
- |
Alterations in lipoprotein homeostasis during experimental and clinical sepsis in primates |
| Van Den Heuvel M. W. |
- |
Two sensitive chromogenic assays of fondaparinux sodium (Arixtra®), a new synthetic and selective inhibitor of factor Xa, in plasma |
| Van Der A. D. |
- |
Coronary risk prediction and the role of C-reactive protein |
| Van Der Berg M. |
- |
Outcome measures in hemophilia: a physician's perspective |
| Van Der Bom J. G. |
- |
The relation between clinical phenotype and genotype of severe hemophilia A |
| Van Der Bom J. G. |
- |
Coronary risk prediction and the role of C-reactive protein |
| Van Der Bom J. G. |
- |
Effects of bleeds on health-related quality of life in patients with hemophilia |
| Van Der Graaf Y. |
- |
Procoagulant factors and the risk of myocardial infraction in young women |
| Van Der Heide Y. T. |
- |
A two-stage thrombophilia screening protocol: more efficient use of laboratory tests |
| Van Der Heijden J. F. |
- |
CYP2C9 polymorphisms have differential effects on acenocoumarol metabolism, but do not increase bleeding risk |
| van der Heijden J. |
- |
PT20210 and Factor V Leiden mutations are not protective against bleeding during treatment with vitamin K antagonists |
| Van Der Heijden J. |
- |
CYP2C9 polymorphisms have differential effects on the quality of acenocoumarol treatment |
| Van Der Heul C. |
- |
Diagnostic performances of two new d-dimer assays in the diagnostic work-up of patients with suspected pulmonary emboli |
| Van Der Horst-Bruinsma I. E. |
- |
Thromboprophylaxis in orthopedic surgery: Clinical practice in the Netherlands |
| Van Der Kuip D. A. M. |
- |
Association between genetic variability of von Willebrand factor and peripheral atherosclerosis: the Rotterdam Study |
| |
- |
Genetic variability of von Willebrand factor and coronary heart disease: the Rotterdam Study |
| Van Der Linden M. |
- |
A novel method to accurately measure collagen/serotonin-induced platelet aggregation by whole blood impedance aggregometry in humans |
| Van Der Linden I. |
- |
Preconceptional, gestational and puerperal low anti-annexin A5 antibody levels in women who develop pre-eclampsia |
| Van Der Meer J. |
- |
Venous and arterial thromboembolic risk in first degree family members of patients with elevated plasma levels of clotting factor VIII:c |
| |
- |
Absolute risk of venous and arterial thromboembolism associated with mild hyperhomocysteinemia. Preliminary results of a family cohort study |
| |
- |
High-dose interferon-alpha induction treatment combined with ribavirin for chronic hepatitis C in congenital coagulation disorders. A randomized, double-blind, placebo-controlled clinical trial |
| Van Der Meer F. J. M. |
- |
European action on anti-coagulation cost effectiveness of computer assisted anti-coagulant dosage |
| Van Der Meer J. |
- |
Individual variations of the level of oral anticoagulation in patients with venous thromboembolism (VTE) as predictor of clinical outcome |
| |
- |
Arterial thromboembolism (ATE) in patients with systemic lupus erythematosus (SLE): the contribution of inherited thrombophilic risk factors |
| |
- |
The risk of pregnancy complications in women from families with thrombophilic defects |
| Van Der Meer I. M. |
- |
Association between genetic variability of von Willebrand factor and peripheral atherosclerosis: the Rotterdam Study |
| Van Der Meer F. J. M. |
- |
Common genetic abnormalities in blood coagulation (Factor V Leiden, prothrombin G20210A) increase the incidence of central vein catheter related thrombosis |
| Van Der Meer J. |
- |
The contribution of inherited thrombophilic risk factors to venous thromboembolism (VTE) in patients with systemic lupus erythematosus (SLE) |
| |
- |
Increased risk for venous thromboembolism and myocardial infarction in family members of patients with prothrombin 20210 A mutation |
| Van Der Meer I. M. |
- |
Genetic variability of von Willebrand factor and coronary heart disease: the Rotterdam Study |
| Van Der Meer J. |
- |
Risk assessment of venous thromboembolism in pregnant women with factor V Leiden, prothrombin 20210 A mutation, elevated factor VIII levels or mild hyperhomocystinaemia |
| |
- |
Absolute risk of venous thromboembolism (VTE) associated with a single or combined thrombophilic disorder. Preliminary results of a family cohort study |
| Van Der Meer F. J. M. |
- |
Incidence of venous thrombosis in carriers of familial thrombophilia with a personal history of venous thrombosis |
| Van Der Neut Kolfschoten M. |
- |
Activated factor V is inactivated by activated protein C in the absence of APC cleavage sites at Arg306, Arg506 and Arg679 |
| |
- |
Characterization of an immunologic polymorphism in the heavy chain of human factor V, due to a dimorphism of residue 79 |
| Van Der Poll T. |
- |
Inhibition of plasmin activity by tranexamic acid does not influence inflammatory pathways during human endotoxemia |
| |
- |
Coagulation factor profiles respond strongly during human endotoxemia |
| |
- |
Plasminogen activator inhibitor type I-deficient (PAI–/–) mice show an improved early host defense in E. coli peritonitis by a neutrophil-dependent mechanism |
| Van Der Schouw Y. T. |
- |
Coronary risk prediction and the role of C-reactive protein |
| Van Der Spoel J. I. |
- |
Lepirudin anti-coagulation in critically ill patients with (suspected) heparin-induced thrombocytopenia and thrombosis |
| Van Der Straaten H. M. |
- |
Elevated levels of d-dimer and fragment 1 + 2 upon central venous catheter insertion and factor V Leiden predict subclavian vein thrombosis |
| Van Der Ven-Jongekrijg J. |
- |
IL-6 concentration in the acute phase of deep-vein thrombosis is a strong predictor of elevated venous outflow resistance as a proxy of post-trombotic syndrome |
| Van Der Vorst M. M. J. |
- |
Evaluation of a bed-side device to assess the APTT for heparin monitoring in infants |
| Van Der Wal A. C. |
- |
Symptomatic plaques of type 2 diabetic patients show more plaque complications but similar expression patterns of markers for coagulation and inflammation compared to nondiabetic controls |
| Van Der Zee M. |
- |
Recombinant truncated tissue factor triggers coagulation in normal human plasma via the extrinsic pathway |
| Van Der Zwaan C. |
- |
Exposure of a binding site for the low-density lipoprotein receptor-related protein (LRP) upon activation of factor V |
| Van Deventer S. J. |
- |
Alterations in lipoprotein homeostasis during experimental and clinical sepsis in primates |
| Van Dijk K. |
- |
The relation between clinical phenotype and genotype of severe hemophilia A |
| Van Dijk K. |
- |
Effects of bleeds on health-related quality of life in patients with hemophilia |
| Van Dinther T. G. |
- |
Two sensitive chromogenic assays of fondaparinux sodium (Arixtra®), a new synthetic and selective inhibitor of factor Xa, in plasma |
| Van Dongen C. J. J. |
- |
The optimal duration of treatment with vitamin K antagonists in patients with a first episode of venous thromboembolism: a decision analytic approach |
| Van Dreden P. |
- |
The role of tissue factor on the inhibition of prothrombin activation and thrombin generation by the synthetic pentasaccharide (fondaparinux) |
| |
- |
Normal values of total and free TFPI levels in the newborn and in children |
| |
- |
Measurement of synthetic pentasaccharide fondaparinux (arixtra) anti-Xa activity |
| |
- |
The role of tissue factor on the inhibition of prothrombin activation and thrombin generation by the synthetic pentasaccharide (fondaparinux) |
| |
- |
Genetic analysis of hereditary factor X deficiency in a French patient of Sri Lanka ancestry: in vitro expression study identified Gly366Ser substitution as the molecular basis of the dysfunctional factor X |
| Van Eck A. T. C. J. |
- |
Duplex screening for quality assurance of postoperative thromboembolism prophylaxis in neurosurgery Krefeld Study Thrombo 2000 |
| Van Geest-Daalderop J. H. H. |
- |
Age and first INR after standard initiation of oral anti-coagulant therapy with acenocoumarol predict the maintenance dosage |
| |
- |
Relation between compliance and quality of treatment with vitamin K antagonists |
| Van Geet C. |
- |
The Gs agonist PACAP(138) is a physiological inhibitor of platelet aggregation and megakaryocyte maturation |
| |
- |
Functional polymorphisms in the paternally expressed XLas and its cofactor ALEX decrease their mutual interaction and enhance receptor-mediated cAMP formation resulting in platelet Gs hyperfunction |
| Van Gestel M. A. |
- |
In vivo involvement of ADP in thromboembolism through its receptors P2Y1 and P2Y12 |
| Van Gorp E. C. M. |
- |
Coagulation abnormalities in dengue virus infections: more common than currently perceived? |
| Van Gorp C. |
- |
Pharmacodynamic profile of Intimatan as an antithrombotic agent for venous thrombosis |
| |
- |
Intimatan ameliorates the activation of human platelets by heparin/heparin antibody from patients with heparin-induced thrombocytopenia |
| Van Gorp E. C. M. |
- |
Endothelial cell and monocyte-derived microparticles in severe dengue virus infections |
| Van Gulik T. M. |
- |
Factor VIII expression in liver disease |
| Van Heerde W. L. |
- |
Screening for annexin A5 gene mutations and the risk of the C-1T mutation in venous thrombosis and myocardial infarction |
| Van Heerde W. |
- |
Preconceptional, gestational and puerperal low anti-annexin A5 antibody levels in women who develop pre-eclampsia |
| |
- |
Long-term in vivo platelet presensitization may explain the mechanism of factor VIIa prophylaxis in factor VII-deficient patients |
| Van Heerde W. L. |
- |
The Nijmegen low-titer factor VIII inhibitor assay: a highly sensitive assay for the detection of low-titer factor VIII inhibitors |
| Van Heerde W. |
- |
The presence of antiphospholipid antibodies is not related to increased levels of annexin A5 in plasma |
| |
- |
Evaluation of the surface-enhanced laser desorption/ionization time-of-flight mass spectrometry proteomic approach to determine Glanzmann Thrombasthenia in blood platelet lysates |
| Van Helden P. M. W. |
- |
A mouse model for inhibitor development in mild hemophilia A |
| Van Hulsteijn L. H. |
- |
A prospective implementation study of out-patient treatment with subcutaneous low-molecular-weight heparin and oral anti-coagulants in patients with deep venous thrombosis in routine clinical practice |
| Van Hylckama Vlieg A. |
- |
The thrombotic risk of different types of oral contraceptives and interaction with factor V Leiden and the prothrombin 20210 A mutation: results of the MEGA study |
| Van Hylckama Vlieg A. |
- |
Estrogens, progestogens and thrombosis |
| Van Kampen R. |
- |
Effects of platelet agonists and antiplatelet agents on thrombin formation in human plasma |
| Van Korlaar I. |
- |
Lower degree of protein C activation in protein C deficient individuals of a large kindred with type I PC deficiency, as measured by the level of APC-PCI complex |
| Van Korlaar I. M. |
- |
Questioning the questionnaire: a sensitivity analysis for data collection on venous thrombosis |
| Van Korlaar I. |
- |
Asymptomatic venous thrombosis is a frequent event in protein C deficiency: a systematic ultrasound assessment of 208 family members with the 3363-C insertion mutation (IPCI: International Protein C Investigation) |
| Van Korlaar I. |
- |
Quality of life and risk perception in a large family with heritable protein C deficiency (IPCI: International Protein C Investigation) |
| Van Kraaij M. G. J. |
- |
Higher reticulated platelet counts and enhanced expression of P-selectin in patients with immune thrombocytopenic purpura compared to patients with myelodysplastic syndromes |
| Van Landeghem A. A. J. |
- |
Effects of genes and environmental factors on homocysteine level |
| Van Lier R. A. W. |
- |
A mouse model for inhibitor development in mild hemophilia A |
| Van Lier M. |
- |
Cholesterol-microdomains in platelet adhesion and aggregation |
| Van Lith-Zanders H. |
- |
Effect of the methionine synthase reductase A66G polymorphism on total homocysteine levels and venous thrombosis risk |
| Van Loon H. |
- |
The quality of care in the management of oral anti-coagulation therapy by the Belgian general practitioner |
| Van Lummel M. |
- |
Binding of b2-glycoprotein I and dimeric b2-glycoprotein I to members of the low-density lipoprotein receptor superfamily: implications for the anti-phospholipid syndrome |
| Van Marion V. |
- |
Co-segregation of Von Willebrands disease type 1 phenotype and Von Willebrand factor gene haplotypes: first results from the multicenter study molecular and clinical markers for the diagnosis and management of type 1 Von Willebrands disease |
| Van Marwijk Kooy M. R. |
- |
Observer variability in the assessment of clinical probability in patients with suspected pulmonary embolism |
| Van Meeteren M. |
- |
Thromboprophylaxis in orthopedic surgery: Clinical practice in the Netherlands |
| Van Mierlo P. J. W. B. |
- |
Effectiveness of excluding pulmonary embolism in the elderly by using a clinical decision rule and d-dimer |
| |
- |
Thrombophilia strikes at all ages |
| Van Montfoort A. P. A. |
- |
Role of PI 3-kinase in glycoprotein VI-dependent calcium signaling in human platelets |
| Van Mourik J. A. |
- |
A mouse model for inhibitor development in mild hemophilia A |
| |
- |
Factor VIII expression in liver disease |
| Van Mourik J. |
- |
Real-time imaging of the dynamics and secretary behavior of WeibelPalade bodies |
| Van Mourik J. |
- |
The small GTP-binding protein Ral is involved in cAMP-mediated release of VWF from endothelial cells |
| Van Nguyen P. |
- |
Influence of thrombophilia on efficacy of warfarin for prevention of recurrent venous thromboembolism: results from a randomized trial |
| |
- |
Influence of warfarin use on symptoms of fatigue: a randomized cross-over trial |
| Van Oerle R. |
- |
Local changes in coagulation and fibrinolysis in patients with a previous deep venous thrombosis |
| Van Ommen C. H. |
- |
Incidence and risk factors for factor VIII antibodies in mild hemophilia A |
| Van Ommen C. H. |
- |
The clinical outcome of pediatric venous thrombo-embolic disease in one tertiary centre |
| Van Oostayen J. A. |
- |
Common genetic abnormalities in blood coagulation (Factor V Leiden, prothrombin G20210A) increase the incidence of central vein catheter related thrombosis |
| Van Os E. |
- |
Thrombopoietin increases platelet adhesion and decreases rolling to von Willebrand factor |
| Van Pampus E. C. M. |
- |
Absolute risk of venous and arterial thromboembolism associated with mild hyperhomocysteinemia. Preliminary results of a family cohort study |
| |
- |
Venous and arterial thromboembolic risk in first degree family members of patients with elevated plasma levels of clotting factor VIII:c |
| |
- |
Storage of apheresis platelets leads to reduced adhesiveness and thrombogenic activity in flowing whole blood ex vivo |
| |
- |
The risk of pregnancy complications in women from families with thrombophilic defects |
| |
- |
Risk assessment of venous thromboembolism in pregnant women with factor V Leiden, prothrombin 20210 A mutation, elevated factor VIII levels or mild hyperhomocystinaemia |
| |
- |
Absolute risk of venous thromboembolism (VTE) associated with a single or combined thrombophilic disorder. Preliminary results of a family cohort study |
| |
- |
Increased risk for venous thromboembolism and myocardial infarction in family members of patients with prothrombin 20210 A mutation |
| Van Rhenen K. |
- |
Exposure of a binding site for the low-density lipoprotein receptor-related protein (LRP) upon activation of factor V |
| Van Rijn H. J. M. |
- |
The effect of oxidized low-density lipoprotein on the activation of platelets |
| |
- |
PECAM-1 inhibits LDL-signaling in platelets |
| |
- |
Platelet sensitization is mediated by Apolipoprotein E Receptor 2 |
| Van Rooden C. J. |
- |
Prescribing anticoagulant prophylaxis in patients with hematological or solid tumor malignancies and central vein catheters: a nationwide survey |
| |
- |
Common genetic abnormalities in blood coagulation (Factor V Leiden, prothrombin G20210A) increase the incidence of central vein catheter related thrombosis |
| Van Rooijen N. |
- |
Gene therapy for hemophilia A with high-capacity adenoviral vectors: preclinical evaluation in hemophilic mice and dogs |
| Van Rooijen M. |
- |
A relationship between SHBG and APCr during OC treatment |
| Van Scherpenzeel M. |
- |
Binding of b2-glycoprotein I and dimeric b2-glycoprotein I to members of the low-density lipoprotein receptor superfamily: implications for the anti-phospholipid syndrome |
| Van Stempvoort G. |
- |
Factor VIII factor IX interactions probed by chimeric factor VIII/V variants: complex assembly and cofactor function involve different residues within the A3 domain region 18031818 |
| |
- |
Molecular events involved in factor IXa stimulation by the factor VIII A2 domain |
| |
- |
Cleavage of factor VIII heavy chain by thrombin increases the affinity for low-density lipoprotein receptor-related protein (LRP) |
| Van Strijen M. J. L. |
- |
The role of spiral CT in alternative diagnosis in patients with clinical suspicion of pulmonary embolism |
| Van Tilburg N. H. |
- |
A comparison of assay methods for thrombin activatable fibrinolysis inhibitor (TAFI) |
| Van Tol A. |
- |
Alterations in lipoprotein homeostasis during experimental and clinical sepsis in primates |
| Van Trotsenburg M. |
- |
Recurrent pregnancy loss between the 8th and 15th week of gestation is not associated with an increased frequency of protein Z deficiency |
| Van Vliet H. H. D. M. |
- |
Use of double virus-inactivated factor VIII concentrate (Immunate®) as treatment of von Willebrand disease |
| Van Wijk R. |
- |
Characterization of an immunologic polymorphism in the heavy chain of human factor V, due to a dimorphism of residue 79 |
| Van Willigen G. |
- |
Thrombopoietin increases platelet adhesion and decreases rolling to von Willebrand factor |
| Van Zanten A. P. |
- |
A two-stage thrombophilia screening protocol: more efficient use of laboratory tests |
| Vandenbroucke J. P. |
- |
Risk factors for recurrent venous thrombosis: a prospective follow-up of the Leiden thrombophilia study (LETS) |
| Vandendriessche T. |
- |
Gene therapy for haemophilias |
| |
- |
Gene therapy for hemophilia A with high-capacity adenoviral vectors: preclinical evaluation in hemophilic mice and dogs |
| Vander Elst L. |
- |
An anti-idiotypic mouse monoclonal antibody towards idiotopes of human anti-C2 inhibitors mimics C2 the 3D conformation of C2 and restores Factor VIII activity in vivo |
| Vanderschoot J. P. M. |
- |
A new computer algorithm for better dosage of oral anti-coagulants |
| Vandervoort P. |
- |
Characterization of a lupus anticoagulant positive monoclonal antibody against human prothrombin |
| Vanhaeverbeek M. |
- |
A new Global Plasma Fibrinolytic Assay for the rapid analysis of hyper-/hypo-Fibrinolysis: relationship with blood lipids and inflammatory markers |
| Vanholder R. |
- |
The uremic retention solutes p-cresol and indoxyl sulfate inhibit endothelial proliferation and wound repair in vitro |
| Vanhoorelbeke K. |
- |
Identification of a novel inhibitory monoclonal antibody against the integrin a2b1 |
| Vanhoorelbeke K. |
- |
Desaggregation of ristocetin-induced platelet aggregates by an inhibiting anti-GPIb MoAb |
| Vanhoorelbeke K. |
- |
The functional self association of von Willebrand factor is modulated by a multiple domain interaction |
| |
- |
Binding of minute amounts of thrombin to GPIbalpha accelerates early platelet reactions, but not the platelet procoagulant response |
| Vanhoorelbeke K. |
- |
A new Von Willebrand ristocetin cofactor activity assay based on plasma glycocalicin |
| Vanhoorelbeke K. |
- |
A new platelet activation marker specific for activated integrin alpha2beta1: monoclonal antibody IAC-1 |
| |
- |
The platelet glycoprotein Ibalpha HPA-2 polymorphism affects VWF binding, but not thrombin interaction |
| |
- |
Glycoprotein IX Asn45Ser: an ancestral mutation causing BernardSoulier syndrome in Europeans? |
| Vannier J. P. |
- |
Inhibition of angiogenesis by statins: a possible contribution for the protection of the vascular risk in atherosclerotic patients |
| |
- |
Hypercoagulability in sickle cell disease: increased monocyte tissue factor expression and increased erythrocyte microparticles expressing phosphatidyl serine |
| |
- |
Human endothelial cells synthesize Protein Z |
| Vannucchi H. |
- |
A transcobalamin gene polymorphism and the risk of deep venous thrombosis |
| Vanrusselt M. |
- |
Characterization of a lupus anticoagulant positive monoclonal antibody against human prothrombin |
| Vanschoonbeek K. |
- |
Effects of dietary fish oil on coagulation and platelets |
| |
- |
Effects of platelet agonists and antiplatelet agents on thrombin formation in human plasma |
| Vanuzzo D. |
- |
NAD(P)H oxidase C242T gene variations and cardiovascular protection |
| Varadi K. |
- |
Monitoring the pharmacokinetic of inhibitor-bypassing agents with a new thrombin generation assay |
| |
- |
Changes in ADAMTS13 (vWF cleaving protease) activity after induced acute release of von Willebrand factor |
| |
- |
Analytical comparison of recombinant and plasma-derived activated protein C (APC) |
| Varfolomeyev S. D. |
- |
Fibronolytic properties of two-chain urokinase-type plasminogen activator attached to fibrinogen |
| |
- |
Fibrin specificity of synergistic combined action of staphylokinase and single-chain urokinase-type plasminogen activator on in vitro clot lysis |
| Vargas R. N. |
- |
Venous thromboembolism (VTE) in children: a series of cases from a pediatric Brazilian cohort |
| Varghese R. |
- |
Plasma 13-HODE: A novel and powerful predictor of cardiovascular disease (CVD) risk and severity |
| Varlet M. N. |
- |
Venous thromboembolism during pregnancy and postpartum: results from a prospective cohort of women treated according to a risk score |
| Varma S. |
- |
Prevalence of factor V Leiden and FV HR2 haplotypes as risk factors for deep vein thrombosis: a study from north India |
| Varon D. |
- |
Cone and plate(let) analyzer as a diagnostic tool in various types of thrombotic thrombocytopenic purpura and haemolytic uremic syndrome |
| |
- |
Cys61stop is the first identified nonsense mutation in the factor X gene causing severe factor X deficiency in 3 unrelated homozygotes of Arab origin |
| |
- |
Efficacy and safety of two doses of enoxaparin in pregnant women with thrombophilia and recurrent pregnancy loss: the LIVE-ENOX study |
| |
- |
Platelet-leukocyte aggregation under shear stress: Differential involvement of selectins and integrins |
| |
- |
Monitoring the combined effect of integrilin, clopidogrel and aspirin in patients with myocardial infarction by Cone and Plate(let) Analyzer |
| Varsat B. |
- |
There is no north/south gradient distribution of the plasma fibrinogen level and of the C-148T Fg genotype in a French native population (The Fitenat Study) |
| |
- |
Lack of correlation between HPA1 polymorphism and ADP induced platelet activation: study of a large cohort of normal subjects |
| Vartholomatos G. |
- |
Is the G455A polymorphism of the fibrinogen beta gene associated with osteonecrosis? A preliminary report |
| |
- |
Mutations of the methylenetetrahydrofolate reductase (MTHFR) gene and osteonecrosis. A preliminary report |
| Varughese K. I. |
- |
Modulation of von Willebrand factor A1 domain binding to glycoprotein Iba by a-thrombin |
| |
- |
Crystal structure of the amino terminal domain of glycoprotein Iba in complex with a-thrombin |
| Varvarikis C. |
- |
Plasma fibrinolytic capacity and 4G/5G polymorphism of PAI-1 gene in heart and kidney transplant recipients with or without steroid immunosuppression |
| Varvenne M. |
- |
The development of inhibitors directed against factor VIII after continuous infusion of factor VIII concentrates in patients with hemophilia A |
| |
- |
New mutations in the fibrinogen genes of patients with dys, hypo- or fibrinogenemia |
| Vasiljev S. A. |
- |
Dynamics of changes of parameters of a hemostasis in patients with sepsis |
| Vasiloglou G. |
- |
Early therapeutic splenectomy may reduce morbidity and management costs in selected resistant or relapsing cases of TTP/HUS |
| Vasilyev S. A. |
- |
Laboratory (on base coagulological tests) it is latent proceeding hematogenous thrombophilias |
| |
- |
Dynamics of changes of parameters of a hemostasis in patients with sepsis |
| Vasse M. |
- |
Hypercoagulability in sickle cell disease: increased monocyte tissue factor expression and increased erythrocyte microparticles expressing phosphatidyl serine |
| |
- |
Human endothelial cells synthesize Protein Z |
| Vassy J. |
- |
Platelet aggregates modulate the adhesion of breast adenocarcinoma cells (MDA-MB-231) to endothelial cells and their matrix in whole blood and under flow conditions |
| Vaughan D. |
- |
PAI-1, arteriosclerosis and coronary thrombosis: insights from genetically modified mice |
| Vaughan D. E. |
- |
Chronic paclitaxel exposure increases human endothelial expression of plasminogen activator inhibitor-1, tissue-type plasminogen activator and tissue inhibitor of metalloproteinase-1 |
| |
- |
Differences in protease activated receptor-1 stimulation between vWF and P-selectin release in endothelial cells-implications of distinct signaling of WeibelPalade release |
| Vaulin N. A. |
- |
Changes of hemostatic parameters in patients with non-ST elevation acute coronary syndrome treated with atorvastatin or pravastatin (randomized comparative study) |
| Vauterin S. |
- |
Identification of a novel inhibitory monoclonal antibody against the integrin a2b1 |
| |
- |
The functional self association of von Willebrand factor is modulated by a multiple domain interaction |
| |
- |
The platelet glycoprotein Ibalpha HPA-2 polymorphism affects VWF binding, but not thrombin interaction |
| Vaux D. J. |
- |
A novel pathway of phospholipase Cg2 activation downstream of the platelet integrin aIIbb3 |
| Vayá A. |
- |
The 4678G/C polymorphism in the endothelial protein C receptor (EPCR) gene reduces the risk of venous thromboembolism in carriers of the factor V Leiden mutation |
| |
- |
Circulating activated protein C in Behcet's disease and risk of thrombosis |
| |
- |
The 4678G/C polymorphism in the endothelial protein C receptor (EPCR) gene is associated with levels of soluble plasma EPCR |
| Vázquez C. |
- |
Quantitative real-time gene expression analysis for several components of fibrinolytic and matrix metalloproteinase systems in primary breast cancer |
| Vázquez R. |
- |
Gene transfer of naked plasmid DNA encoding VEGF121 leads to revascularization of ischemic tissue in animal models of vascular diseases |
| Vazquez R. |
- |
Gene transfer of naked plasmid DNA encoding VEGF121 leads to revascularization of ischemic tissue in animal models of vascular diseases |
| Vdovin V. V. |
- |
Cases of development of an idiopathic thrombocytopenic purpura at children associated with introduction of a tuberculin |
| |
- |
Plasma glycocalicin level in diagnosis of the idiopathic thrombocytopenic purpura (ITP) in children |
| |
- |
Results of clinical use of NovoSeven in Russia |
| Vdovin V. V. |
- |
The experience of treatment of children with hemostasis system pathology treatment with recombinant factor VII NovoSeven |
| |
- |
Using NovoSeven (NS) recombinant factor VIIa to control the bleedings in Bernard-Soulier (BSS) girl. Case report |
| Vdovin V. V. |
- |
Idiopathic thrombocytopenic purpura at children, associated with a virus of rubella |
| |
- |
The principles of therapy of hemorrhagic vasculitis at children |
| Vecchioli M. |
- |
Oral anti-coagulant therapy with POC device and remote computer monitoring in the setting of the Italian National Health System (INHS) |
| Vecchione G. |
- |
Endothelial nitric oxide synthase gene variation and hypertension in pregnancy |
| |
- |
Prevalence of haemostatic abnormalities in women with 3 or more implantation failures after in vitro fertilization |
| Veeger N. J. G. M. |
- |
Individual variations of the level of oral anticoagulation in patients with venous thromboembolism (VTE) as predictor of clinical outcome |
| Veeger N. J. G. M. |
- |
High-dose interferon-alpha induction treatment combined with ribavirin for chronic hepatitis C in congenital coagulation disorders. A randomized, double-blind, placebo-controlled clinical trial |
| Veenstra D. |
- |
Clinical outcomes and medical resource utilization in patients with and without malignancy treated with warfarin |
| Vega-Ostertag M. |
- |
Intracellular events in antiphospholipid-mediated platelet activation |
| Vegh P. |
- |
A pharmacokinetic study of tinzaparin in pediatric patients |
| |
- |
Poor correlation between aPTT, anti-Xa levels and heparin dose in children receiving therapeutic doses of unfractionated heparin |
| |
- |
A dose-finding study of Tinzaparin in pediatric patients |
| |
- |
Ex vivo thrombin generation capacity in pediatric patients receiving Tinzaparin |
| Velan T. |
- |
Active thrombin concentrations and the rate of thrombin inhibition during cardiopulmonary bypass |
| Velasco F. |
- |
Increased tissue factor expression in monocytes from patients with anti-phospholipid syndrome depends on NFkB activation |
| |
- |
A promising therapeutic strategy in acute promyelocytic leukemia (APL): disruption of MEK/ERK, arsenic and retinoids |
| Veldman A. |
- |
Protein C activation and possible use in different disease states - Neonatal sepsis |
| Vele O. |
- |
Induction of fractalkine by endothelial cells under shear stress |
| Vemulapalli S. |
- |
Antithrombotic effects of selective P2Y1 and P2Y12 antagonists in anesthetized rats |
| Venco A. |
- |
Determinants of delayed thrombus regression after deep vein thrombosis of the lower limbs: a prospective cohort study |
| |
- |
Weight changes after acute deep venous throbosis: a prospective observational study |
| |
- |
Early developments of the post-thrombotic syndrome in overweight and obese patients |
| Vene N. |
- |
Safety of the transfer of patients on anticoagulant therapy from hospital anticoagulant clinics to general practitioners using a computer-decision support |
| Ventura J. S. |
- |
Platelet responses mediated by venom snake metalloproteases (MP1 and MP3) |
| Verbeuren T. J. |
- |
Anti-thrombotic and anticoagulant effects of S35898 an orally active thrombin inhibitor |
| |
- |
Specific phosphatidylserine exposure and microparticules shedding induced by a synthetic peptide |
| |
- |
Evolution of a nonocclusive deep vein thrombosis in the rabbit vena cava |
| |
- |
Role of NADPH oxidase on mechanisms implicated in anoxia/reoxygenation-induced leukocyte adhesion to HUVECs |
| |
- |
Influence of selective nonpeptide PAR-1 and PAR-4 antagonists on thrombin-induced aggregation of human platelets |
| Verbruggen H. |
- |
Long-term in vivo platelet presensitization may explain the mechanism of factor VIIa prophylaxis in factor VII-deficient patients |
| Verbruggen B. |
- |
The Nijmegen low-titer factor VIII inhibitor assay: a highly sensitive assay for the detection of low-titer factor VIII inhibitors |
| Verbruggen H. |
- |
Evaluation of the surface-enhanced laser desorption/ionization time-of-flight mass spectrometry proteomic approach to determine Glanzmann Thrombasthenia in blood platelet lysates |
| Verbruggen H. W. |
- |
Higher reticulated platelet counts and enhanced expression of P-selectin in patients with immune thrombocytopenic purpura compared to patients with myelodysplastic syndromes |
| Vercamer C. |
- |
Effect of in vivo thrombin inhibition on bFGF-induced angiogenesis in a murine angiogenic model |
| Verdi H. |
- |
Role of genetic factors in vascular access thrombosis |
| |
- |
Factor XIII Val34Leu polymorphism in Turkish population |
| |
- |
Alpha-fibrinogen Thr 312 Ala polymorphism in Turkish population |
| |
- |
Thrombotic risk factors in stroke patients |
| Verdy E. |
- |
Inherited thrombophilia is not associated with an increased risk of intrauterine fetal death |
| Verelst K. |
- |
Use of double virus-inactivated factor VIII concentrate (Immunate®) as treatment of von Willebrand disease |
| Vereycken-Holler V. |
- |
Platelet translocation on von Willebrand factor is inhibited by RGDS peptide at high shear rate |
| |
- |
Irradiated endothelial cells promote platelet aggregates at high wall shear rate |
| Vergis J. |
- |
Video Grand Rounds: an assessment of internet based grand rounds to increase collaboration between comprehensive hemophilia treatment centers |
| Vergona R. |
- |
Development of small molecule compounds that inhibit PAI-1 activity in vitro and in vivo |
| Vergura P. |
- |
Women with common prothrombotic mutations are not at higher risk of recurrent intrauterine fetal deaths |
| Verhamme I. |
- |
Mechanisms of conformational activation of prothrombin by staphylocoagulase and fibrinogen substrate recognition |
| Verheijen J. H. |
- |
Tissue-type plasminogen activator (t-PA) gene deletion in apoE3-Leiden mice delays progression of cholesterol-induced atherosclerotic lesion |
| Verheyen C. C. P. M. |
- |
Day-care or short-stay surgery and venous thromboemolism: an overview |
| Verlato F. |
- |
Correlation between internal carotid artery stenosis and hematological risk factors for thrombosis (CAST study): final results |
| |
- |
Different thromboprophylaxis approaches in patients undergoing knee arthroscopy (KANT study): interim report of prospective randomized study |
| Verlato F. |
- |
Management of hospitalized patients with suspected deep vein thrombosis |
| Vermeer C. |
- |
Mutations in genes of the gamma-glutamyl carboxylase and the vitamin K epoxidase reductase complex are responsible for the phenotype of hereditary combined deficiency of vitamin K-dependent clotting factors |
| Vermes E. |
- |
Aspirine resistance: a particularly high prevalence in patients after ventricular assist device implantation |
| Vermylen J. |
- |
The Gs agonist PACAP(138) is a physiological inhibitor of platelet aggregation and megakaryocyte maturation |
| |
- |
P2X1-induced activation of Ca2+ calmodulin leads to myosin light chain and ERK2 phosphorylation in human platelets |
| |
- |
Diesel exhaust particles deposited in the lung enhance thrombus formation in peripheral vessels in an in vivo model of vascular thrombosis |
| |
- |
Characterization of a lupus anticoagulant positive monoclonal antibody against human prothrombin |
| |
- |
Functional polymorphisms in the paternally expressed XLas and its cofactor ALEX decrease their mutual interaction and enhance receptor-mediated cAMP formation resulting in platelet Gs hyperfunction |
| |
- |
Role of pulmonary inflammation on the peripheral thrombotic risk following intratracheal instillation of diesel exhaust particles |
| |
- |
Deletion of residue Ala2201 in the factor VIII C2 domain impairs FVIII interactions with phospholipids and vWF and results in mild hemophilia A |
| |
- |
Overexpression of the platelet P2X1 ion channel in transgenic mice generates a novel prothrombotic phenotype |
| |
- |
The quality of care in the management of oral anti-coagulation therapy by the Belgian general practitioner |
| |
- |
Platelet recruitment in vivo to injured blood vessels is not prevented by GPIIb/IIIa antagonism |
| |
- |
Response to DDAVP in mild/moderate hemophilia A patients according to the underlying factor VIII genotype |
| Vernersson E. |
- |
Global hemostatic tests, protein C and anti-thrombin in the intensive care unit setting; correlations and ability to predict outcome |
| Verpillat P. |
- |
The Asp299Gly polymorphism of Toll-like receptor 4 as a genetic risk factor for acute coronary events |
| Verschuur M. |
- |
The -148C/T variation in the human fibrinogen b promoter influences basal and IL-6 induced transcription and affects binding of nuclear proteins |
| Versluys D. |
- |
Anti-thrombotic and anticoagulant effects of S35898 an orally active thrombin inhibitor |
| Verso M. |
- |
A double-blind placebo-controlled randomized study on the efficacy and safety of enoxaparin for the prevention of upper limb deep vein thrombosis in cancer patients with central vein catheter |
| Versteeg H. |
- |
Tissue factor/factor Vlla interaction induces activation of the pro-inflammatory JAK/STAT pathway |
| Verstuyft C. |
- |
Variations of INR and Factor VII Level are linked to Cytochrome P450 2C9 genotype |
| Vesela P. |
- |
Resveratrol and trolox scavenge hydroxyl radicals produced in platelets activated by collagen |
| |
- |
Resveratrol and trolox scavenge hydroxyl radicals produced in platelets activated by collagen |
| Vesely S. |
- |
Long-term outcomes following recovery from thrombotic thrombocytopenic purpura hemolytic uremic syndrome (TTP-HUS) measured by health-related quality-of-life (QOL) assessments |
| |
- |
Complications of plasma exchange in thrombotic thrombocytopenic purpurahemolytic uremic syndrome (TTP-HUS): A study of 149 consecutive patients 19962002 |
| |
- |
Analysis of ADAMTS13 activity in consecutive patients with clinically diagnosed thrombotic thrombocytopenic purpura hemolytic uremic syndrome (TTP-HUS) |
| Veyradier A. |
- |
Identification of seven new candidate mutations of ADAMTS13 gene in four French families related to congenital thrombotic thrombocytopenic purpura |
| Vial C. |
- |
A key role of the fast ATP-gated P2X1 cation channel in the thrombosis of small arteries in vivo |
| |
- |
A key role of the fast ATP-gated P2 X 1 cation channel in the thrombosis of small arteries in vivo |
| Vianello F. |
- |
Factor VII deficiency associated with severe hemophilia A |
| Vianello M. |
- |
Heterogeneous molecular pattern of Factor VII deficiency associated to cerebral hemorrhage |
| Vicari F. |
- |
Hemostasis and inflammation in advanced heart failure and after successful heart transplantation |
| Vicente V. |
- |
Mutations in the shutter region of anti-thrombin result in severe episodic thrombosis and unlike other serpins in formation of disulfide-linked dimers |
| |
- |
Genetic variations of the extra-large stimulatory G protein a-subunit and risk of thrombotic and hemorrhagic disorders |
| |
- |
Conformational basis of homozygous heparin cofactor II deficiency confirms critical role of P17 glutamate in serpins |
| |
- |
Pharmacogenetics in the thrombolytic treatment of myocardial infarction: role of the FXIII V34L polymorphism |
| |
- |
Detection of conformational transformation of antithrombin in blood by crossed immunoelectrophoresis: new application for a classical method. Effect of temperature in plasmatic antithrombin; role in senescence of antithrombin and thrombosis |
| |
- |
Analysis of the HPS-1 gene in patients with single platelet dense-granule deficiency and mild bleeding diathesis |
| Vicini P. |
- |
Pharmacokinetics of recombinant human FXIII in cynomolgus monkeys |
| Vickers M. A. |
- |
Procoagulant changes in human macrophages induced by environmental microparticles [PM10]: a possible pathogenetic mechanism in cardiovascular disease |
| Vidal C. |
- |
Human platelet microparticles shedding is independent of the Cdc42/Rac1/PAK Pathway |
| Viegas E. |
- |
Evaluating the interaction of allopurinol with the oral anticoagulants |
| Vieira J. G. H. |
- |
Use of a decision-making system based on the Fuzzy sets theory applied to the routine of results' release in the haemostasis laboratory: how to do it better and quicker |
| Vieira L. M. |
- |
Hemostatic parameters in Brazilian asymptomatic carriers of Factor V Leiden, prothrombin (G20210A) and methylenetetrahydrofolate reductase (C677T) mutations |
| |
- |
Markers of hypercoagulability in Brazilian patients with DVT undergoing oral anti-coagulation therapy |
| Viel K. |
- |
Functional resequencing of the factor IX (f-IX) gene: identifying quantitative trait nucleotides (QTNs) underlying the variation in plasma f-IX activity levels in the GAIT project |
| |
- |
Functional re-sequencing of the factor VIII (f-VIII) gene: identifying quantitative trait nucleotides (QTNs) underlying the variation in plasma f-VIII activity levels in the Gait Project |
| Vigh I. |
- |
Association between factor XIII Val34Leu polymorphism and risk of ischemic stroke in young patients |
| Vigh TH. |
- |
Important Role of FV G1691A and FII G20210A in women with pregnancy loss without apparent causes |
| Vigh T. |
- |
Clinical manifestations of the antiphospholipid syndrome in patients with highly elevated anticardiolipin antibodies |
| Vigilante M. |
- |
Occurrence of myocardial infarction and PAI-1 4G/5G and ACE I/D gene polymorphisms in patients on chronic dialysis |
| Vignoli A. |
- |
Role of polymorphonuclear (PMN) leukocyte activation in the formation of PMN-platelet aggregates in Essential Thrombocythemia (ET) and Polycythemia Vera (PV) |
| |
- |
Effect of the LMWHs dalteparin and enoxaparin on tissue factor and thrombomodulin expression by endothelial cells |
| |
- |
Low-molecular weight heparin (LMWH) enoxaparin counteracts the expression of endothelial cell tissue factor elicited by malignant cells |
| Vignolo A. |
- |
Low-molecular weight heparins (LMWH) modulate the functional adhesion of tumor cells to the vascular endothelium |
| Vigorito E. |
- |
Involvement of the p110d catalytic subunit of phosphatidylinositol 3-kinase in platelet spreading on fibrinogen |
| Vijgen J. |
- |
The quality of care in the management of oral anti-coagulation therapy by the Belgian general practitioner |
| Vila V. |
- |
Endothelial and angiogenesis activity in terminal heart failure and heart-transplant patients: a prospective study |
| Vila V. |
- |
Inflammation and thrombogenic activity in terminal heart failure patients and heart transplantation: a prospective study |
| Vila V. |
- |
Inflammation and thrombogenic activity in terminal heart failure patients and heart transplantation: a prospective study |
| Vilahur G. |
- |
Local blockade of the collagen binding domain to vWF-A3 with Saratin decreases thrombotic risk in human atherosclerotic lesions |
| |
- |
Local blockade of vWF binding epitopes on damaged vessel wall exposed collagen with Saratin inhibits thrombotic risk at different hemodynamic conditions |
| Vilaire G. |
- |
Activation of the platelet integrin aIIbb3 by thermodynamic modulation of transmembrane helix associations |
| Villa G. |
- |
Factor VII polymorphisms and the risk of myocardial infarction in coronary atherosclerosis |
| Villa P. |
- |
The 4678G/C polymorphism in the endothelial protein C receptor (EPCR) gene reduces the risk of venous thromboembolism in carriers of the factor V Leiden mutation |
| |
- |
Inflammation and thrombogenic activity in terminal heart failure patients and heart transplantation: a prospective study |
| |
- |
Circulating activated protein C in Behcet's disease and risk of thrombosis |
| Villa V. |
- |
Endothelial and angiogenesis activity in terminal heart failure and heart-transplant patients: a prospective study |
| Villa P. |
- |
The 4678G/C polymorphism in the endothelial protein C receptor (EPCR) gene is associated with levels of soluble plasma EPCR |
| Villaça P. R. |
- |
Inherited prothrombotic risk factors in a Brazilian cohort with CVT |
| Villaça P. R. |
- |
Factor VII deficiency and stroke: case report |
| Villaça P. R. |
- |
Successful use of Arixtra® in a patient with PNH, BuddChiari syndrome and HIT |
| |
- |
Acquired prothrombotic-associated factors in cerebral venous thrombosis (CVT) |
| Villalta S. |
- |
Subcutaneous adjusted-dose unfractionated heparin vs. fixed-dose low-molecular-weight heparin in the initial treatment of venous thromboembolism |
| |
- |
Risk factors for venous thromboembolism in chronically bedridden patients admitted to the Hospice Unit |
| Villar A. |
- |
A retrospective evaluation of the use of B-domain deleted recombinant Factor VIII (ReFacto®) administered by continuous infusion during surgical procedures |
| Villard S. |
- |
Peptide decoys selected by phage display block in vitro and in vivo activity of a human anti-FVIII inhibitor |
| Villard S. |
- |
Studies of anti-idiotypic polyclonal antibodies developed against antihuman Factor VIII monoclonal antibodies |
| Villegas-Mendez A. |
- |
Impaired interaction of protein C Gla domain variants with the endothelial cell protein C receptor (EPCR) |
| Villela M. S. H. |
- |
Comparative analysis of methods for detection of Activated Protein C resistance: an analysis of 755 consecutive patients |
| Villela M. S. H. |
- |
Effects of isolated and combined use of ticlopidine, clopidogrel and aspirin on platelet function as evaluated by platelet aggregometry |
| Villela M. S. H. |
- |
Use of a decision-making system based on the Fuzzy sets theory applied to the routine of results' release in the haemostasis laboratory: how to do it better and quicker |
| Villemson A. L. |
- |
Development of novel delivery systems of aprotinin |
| Villeval J. L. |
- |
Platelet activation causes a metalloprotease-mediated down-regulation of GlycoproteinVI |
| Villoutreix B. O. |
- |
Anti-thrombin F229L: a new homozygous variant leading to spontaneous anti-thrombin polymerization in vivo and severe childhood thrombosis |
| |
- |
Factor V New Brunswick: Ala221Val associated with FV deficiency reproduced in vitro and functionally characterized |
| |
- |
Functional properties of recombinant factor Va mutated in a potential calcium-binding site |
| |
- |
Changed inactivation pathway of factor Va by activated protein C in the presence of heparin |
| |
- |
Molecular recognition in the protein C anticoagulant pathway |
| Villoutreix B. O. |
- |
Theoretical and experimental investigation of the D2194G subsitution in the C2 domain of coagulation factor V |
| Vincent L. |
- |
Inhibition of angiogenesis by statins: a possible contribution for the protection of the vascular risk in atherosclerotic patients |
| Vincent M. |
- |
Ischemia induces early and enhanced expression of a new transcription factor (6A3-5) in human and rat kidney vascular smooth muscle cells |
| Vincent D. |
- |
The platelet ADP receptor P2Y12 is a critical player on the pathway of aIIbb3 activation by multiple agonists |
| |
- |
Anticoagulants (thrombin inhibitors) and aspirin synergize with P2Y12 receptor antagonism in thrombosis |
| |
- |
P2Y12 regulates platelet adhesion/activation, thrombus growth and thrombus stability in injured arteries |
| Vincentelli A. |
- |
Tissue factor pathway in carotid atherosclerotic plaques: relationships with clinical patterns and risk factors |
| Vinciguerra C. |
- |
Three abnormal patterns for inversion breaking intron 1 of the FVIII gene |
| Vinciguerra C. |
- |
Clinical manifestation of severe hemophilia B ameliorated by Prothrombin 20210A |
| Vink R. |
- |
Recombinant factor VIIa reverses the anticoagulant effect of the long-acting pentasaccharide idraparinux in healthy volunteers |
| Vink R. |
- |
Optimal intensity of oral anti-coagulant therapy in patients with mechanical heart valves |
| Vink R. |
- |
The optimal duration of treatment with vitamin K antagonists in patients with a first episode of venous thromboembolism: a decision analytic approach |
| Violi F. |
- |
Enhanced TNF-a and oxidative stress in patients with heart failure: effect of TNF-a on platelet O2 production |
| |
- |
Aggregometric evidence of a progressive reduction of platelet sensitivity to aspirin |
| |
- |
A polyphenol mixture inhibits collagen induced platelet aggregation |
| |
- |
Increased platelet superoxide anion production in patients with hypertension: role of AT1 receptors |
| |
- |
Antioxidant effect of wine in human: role of polyphenols |
| |
- |
Fibrinogen as predictor of ischemic stroke in patients with nonvalvular atrial fibrillation |
| Virtanen K. S. |
- |
Inhibition of P2Y12-receptor in vivo and in vitro in patients undergoing elective percutaneous coronary intervention (PCI) |
| Visconte C. |
- |
Thrombolysis induced by streptokinase or recombinant plasminogen activator (rt-PA) is improved by SSR182289A, a direct orally active thrombin inhibitor, in rabbit models of thrombosis |
| Visich J. E. |
- |
Pharmacokinetics of recombinant human FXIII in cynomolgus monkeys |
| Vispo N. S. |
- |
Gene transfer of naked plasmid DNA encoding VEGF121 leads to revascularization of ischemic tissue in animal models of vascular diseases |
| |
- |
Gene transfer of naked plasmid DNA encoding VEGF121 leads to revascularization of ischemic tissue in animal models of vascular diseases |
| Vissac A.-M. |
- |
A new Global Plasma Fibrinolytic Assay for the rapid analysis of hyper-/hypo-Fibrinolysis: relationship with blood lipids and inflammatory markers |
| Vissac A. M. |
- |
The clinical relevance of anti-b2-GP1 antibodies assays in the presence of antiphospholipid antibodies and/or lupus anticoagulant |
| |
- |
Inflammation and endothelial dysfunction in patients with carotid stenosis |
| Visvikis S. |
- |
Phenotypic sensitivity to activated protein C in healthy families: importance of genetic components and environmental factors in the Stanislas Cohort |
| Viswabandya A. |
- |
Administration of gentamicin does not increase factor levels in severe hemophilia-B due to premature termination codons |
| Vitale S. |
- |
Transdermal hormone replacement therapy does not affect hemostasis and inflammation |
| Vitali M. S. |
- |
Development, scale up and characterization of the first regional high purity Factor VIII: the Argentinean experience |
| |
- |
Preparation of prothrombin complex concentrate (PCC) at intermediate scale: first experience in Argentina |
| Vitkovsky Y. |
- |
Nitric oxide, cytokine and hemostasis in stroke |
| Vitkovsky YU. |
- |
Influence of peloidotherapy on hemostasis, cytokines productions and lymphocyte-platelet adhesion |
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Disseminated intravascular coagulation in surgary |
| Vitsenya M. |
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The influence of exercise and stress on markers of activation of coagulation and fibrinolysis in young postinfarction patients |
| Vizcarra E. |
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Hypercoagulability in cerebrovascular disease (CD): factor V Leiden, prothrombin G20210A and MTHFR C677T mutations and polymorphism in the annexin V kozac sequence |
| Vizintin T. |
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Safety of the transfer of patients on anticoagulant therapy from hospital anticoagulant clinics to general practitioners using a computer-decision support |
| Vlasin M. |
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Paradoxical effect of unfractionated heparin in combination with streptokinase on arterial recanalization |
| Vo H. C. |
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Molecular basis of the bleeding disorder caused by Prothrombin-Vancouver |
| Voest E. E. |
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Tissue-type plasminogen activator is a multiligand cross-b structure receptor |
| Vogel G. M. T. |
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Human cell-derived microparticles promote thrombus formation in vivo in a tissue factor-dependent manner |
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Potential reversal agents for the long-acting pentasaccharide idraparinux |
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Soluble tissue factor released by cultured human umbilical vein endothelial cells is microparticle-associated and triggers thrombus formation in vivo |
| Voinea M. |
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Effects of enoxaparin on high glucose induced activation of human endothelial cells |
| Volgmann T. |
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Expression and function of platelet glycoproteins in newborns and adults |
| Völkl D. |
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Towards the development of a recombinant von Willebrand factor-cleaving protease (ADAMTS-13) |
| Volkova M. V. |
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Molecular risk factors are important causes for the thrombosis in childhood |
| Volpe S. |
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Enhanced TNF-a and oxidative stress in patients with heart failure: effect of TNF-a on platelet O2 production |
| Volpe E. |
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The strong incidence of acquired and inherited thrombophilia in recurrent first trimester fetal loss |
| Volpone J. |
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Agreement between FXIII activity assays and calibrator plasma pools: the need for a FXIII reference standard with regulatory recognition |
| Volteas S. |
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Thromboprophylaxis in laparoscopic cholecystectomy: identification of a high-risk group of patients |
| Von Auer C. |
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The development of inhibitors directed against factor VIII after continuous infusion of factor VIII concentrates in patients with hemophilia A |
| Von Auer C. |
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Mild ADAMTS-13 deficiency in patients with ischemic stroke |
| Von Dem Borne P. A. KR. |
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Complex formation of Thrombin-Activatable Fibrinolysis Inhibitor (TAFI) with fibrin(ogen) |
| Von Depka M. |
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New mutations in the fibrinogen genes of patients with dys, hypo- or fibrinogenemia |
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Expression of Plasminogen activator inhibitor-1 (PAI-1) mRNA in human ciliary processes and determination of PAI-1 in human aqueous humor |
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A mutation leading to a stop codon in the FVIII gene is the cause of severe canine Hemophilia A |
| Von Depka- Prodzinski M. |
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The development of inhibitors directed against factor VIII after continuous infusion of factor VIII concentrates in patients with hemophilia A |
| Von Eckardstein A. |
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Sinus venous thrombosis in children a multifactorial etiology |
| Von Heymann C. |
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Management of refractory postoperative cardiac bleeding with recombinant Factor VIIa (rFVIIa): Cases reported to the hemostasis.com registry |
| Von Pape K.-W. |
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Discrepancies in potency assessment of B-domain deleted recombinant factor VIII among different one-stage factor VIII clotting assays |
| Von Sicard N. |
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Triatomine extrinsic pathway inhibitor (TEPI) from the blood sucking insect Dipetalogaster Maxima |
| Voogt P. J. |
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High-dose interferon-alpha induction treatment combined with ribavirin for chronic hepatitis C in congenital coagulation disorders. A randomized, double-blind, placebo-controlled clinical trial |
| Voorberg J. |
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Inhibition of factor VIII binding to phospholipids by single-chain variable domain fragments indicates that F2200 plays a more important role than M2199 in membrane-binding |
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A mouse model for inhibitor development in mild hemophilia A |
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Novel approaches to determine the characteristics of ADAMTS13 inhibitors in patients with acquired TTP |
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Real-time imaging of the dynamics and secretary behavior of WeibelPalade bodies |
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The small GTP-binding protein Ral is involved in cAMP-mediated release of VWF from endothelial cells |
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Cleavage of factor VIII heavy chain by thrombin increases the affinity for low-density lipoprotein receptor-related protein (LRP) |
| Voorbij H. A. M. |
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Coronary risk prediction and the role of C-reactive protein |
| Vorlova Z. |
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The C1 domain substitution His2155Asp severely reduces factor VIII binding to von Willebrand factor |
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Sensitivity and specificity of PFA-100® vs. bleeding time in the diagnosis of type 1 von Willebrand disease (VWD) |
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Molecular and clinical markers for the diagnosis and management of type 1 von Willebrand's disease (VWD): The progress of a European collaboration |
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Significant prevalence of the intron 1 factor VIII gene inversion among patients with severe haemophilia A in the Czech Republic |
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A human factor VIII inhibitor tolerating the endogenous FVIII with a unique A2 domain substitution in CRM + hemophilia A |
| Vorlova Z. |
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Good efficacy of low dosing regimen of a FVIII/vWF concentrate in patients with von Willebrand disease |
| Vorlova Z. |
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Evaluation of a new quantitative, rapid test (VWF-LIA) for the diagnosis of type 1 VWD |
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Co-segregation of Von Willebrands disease type 1 phenotype and Von Willebrand factor gene haplotypes: first results from the multicenter study molecular and clinical markers for the diagnosis and management of type 1 Von Willebrands disease |
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An improved multimeric analysis identifies a subgroup of patients with Type 1 von Willebrand disease characterized by reduced VWF:RCo/Ag ratio |
| Vormittag R. |
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C-reactive protein in patients with venous thromboembolism |
| Vorster H. H. |
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The effect of refined and red palm olein compared to sunflower oil on lipids and homeostatic factors in hyperfibrinogenemic patients |
| Vos H. L. |
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C/EBP |
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Linkage analysis of factor VIII and von Willebrand factor loci as quantitative trait loci |
| Vos P. |
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Plasma markers of hemostatic activation in patients with cancer and deep venous thrombosis |
| Vos H. L. |
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Identification of transcription factor binding sites for HNF1-alpha, FOXA2, HNF4-alpha, Sp1 and Sp3 in the human prothrombin gene enhancer |
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Activated factor V is inactivated by activated protein C in the absence of APC cleavage sites at Arg306, Arg506 and Arg679 |
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The -148C/T variation in the human fibrinogen b promoter influences basal and IL-6 induced transcription and affects binding of nuclear proteins |
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Dimerization and multimerization defects of von Willebrand factor due to mutated cysteine residues |
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Tissue-specific regulation of protein S gene transcription |
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Screening for annexin A5 gene mutations and the risk of the C-1T mutation in venous thrombosis and myocardial infarction |
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Functional analysis of the prothrombin (PT) G20210A variation |
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C-Reactive protein (CRP) is not a strong inducer of tissue factor in human monocytes |
| Vos H. |
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A comparison of assay methods for thrombin activatable fibrinolysis inhibitor (TAFI) |
| Vos H. L. |
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Characterization of an immunologic polymorphism in the heavy chain of human factor V, due to a dimorphism of residue 79 |
| Vossen C. |
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Heritability of clotting factors and the prothrombotic state: results from a large thrombophilic pedigree of French Canadian descent with Type I protein C deficiency |
| Vossen C. Y. |
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Quality of life and risk perception in a large family with heritable protein C deficiency (IPCI: International Protein C Investigation) |
| Vossen C. |
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Lower degree of protein C activation in protein C deficient individuals of a large kindred with type I PC deficiency, as measured by the level of APC-PCI complex |
| Vossen C. Y. |
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Questioning the questionnaire: a sensitivity analysis for data collection on venous thrombosis |
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Incidence of venous thrombosis in carriers of familial thrombophilia with a personal history of venous thrombosis |
| Vossen C. |
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Asymptomatic venous thrombosis is a frequent event in protein C deficiency: a systematic ultrasound assessment of 208 family members with the 3363-C insertion mutation (IPCI: International Protein C Investigation) |
| Vranckx R. |
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Protease-nexin-1 inhibits plasminogen activation-induced apoptosis of adherent cells |
| Vreys I. |
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Overexpression of the platelet P2X1 ion channel in transgenic mice generates a novel prothrombotic phenotype |
| Vu D. |
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Congenital afibrinogenemia: expression and analysis of novel mutations affecting fibrinogen assembly or secretion |
| Vu T. |
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Comparison of inherited and acquired thrombophilia in cerebral venous thrombosis and pulmonary embolism or deep vein thrombosis of the leg |
| Vukovich T. |
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C-reactive protein in patients with venous thromboembolism |
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Is inflammation involved in the development of thrombosis in patients with the lupus anticoagulant? |
| Vystavkin A. |
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Role of protein C system in the advancement of activation zone of coagulation: A two-dimensional mathematical model |