| V |
| V Chantarangkul |
- |
The Detection of Lupus Anticoagulants in Hemophiliacs: The Need for Different Assay Systems |
| V Mathews |
- |
Thirty Novel Mutations in the Factor VIII Gene of Indian Patients with Haemophilia A |
| v. Mackensen S |
- |
Quality of Life in Patients with Haemophilia An European Comparison Study (ESCHQoL) |
| v. Mackensen S |
- |
Health-related Quality of Life in Adult Patients with Haemophilia Assessment with a New Disease-specific Questionnaire (Haem-A-QoL) |
| v. Mackensen S |
- |
Quality of Life in Hemophilic Patients without Inhibitors: The Coche Study |
| v. Mackensen S |
- |
Assessment of Treatment Satisfaction in Patients with Haemophilia Development and Validation of the First Disease-Specific Questionnaire (Hemo-SatA) |
| Vadas MA |
- |
Expression Profiling Reveals Functionally Important Genes and Coordinately Regulated Signalling Pathway Genes During in vitro Angiogenesis |
| Vaidyula VR |
- |
Circulating Tissue Factor Activity Is Increased by Hyperglycemia and Hyperinsulinemia in Normal Human Subjects |
| Vainchenker W |
- |
A Novel Case of Familial Thrombocytopenia with Evidence for a Critical Role of Proteins Involved in Ca2+ Signaling in Megakaryocytopoiesis |
| |
- |
Apaf-1 and Caspase 9 Regulate Early and Late Stages of Megakaryocyte Differentiation |
| Vale AAL |
- |
Increased Plasma Levels of Lipoprotein(a) Correlate with Severity of Angiographically Defined Coronary Artery Disease |
| Valente S |
- |
Antiaggreganting Agents Do Not Influence the Sonoclot Profile |
| |
- |
High Rate of Non Responders to Aspirin and/or Clopidogrel Treatment in the First Days Following Percutaneous Coronary Interventions: An Ex Vivo Study |
| |
- |
Platelet Function Predicts Myocardial Damage in Patients with Acute Coronary Syndromes Treated with Multiple Antiplatelet Agents |
| |
- |
Protein Z Decreases During Follow-up of Patients with Acute Coronary Syndromes |
| Valentin N |
- |
Modulating Murine Platelet Function by Expressing Integrin aIIbb3 Locked-In Its High Affinity State |
| Valentino L |
- |
Efficacy and Safety of FEIBA VH Prophylaxis in a Patient with Hemophilia B and a High-Titer Inhibitor |
| Valentino L |
- |
Synovitis in a Murine Model of Human Factor VIII Deficiency: Pathology and the Molecular Basis of Disease |
| Valentino LA |
- |
Prophylaxis with Factor Eight Inhibitor Bypassing Activity, Vapor Heated (FEIBA VH) Decreases Bleeding Frequency and Maintains or Improves Joint Status |
| Vallez MO |
- |
Evaluation of PAI-1 Inhibitors in the Microcirculation of the Hamster Cheek Pouch |
| Vallvé C |
- |
The ABO Blood Group Genotype and Factor VIII Levels as Independent Risk Factors for Venous Thromboembolism |
| Van Aken H |
- |
Prothrombotic Tendency upon Inflammatory Conditions Alpha Defensins (HNP-1/2/3) Are Strong Platelet Agonists |
| |
- |
New Function for Protease Inhibitors Alpha1 Antitrypsin and Antithrombin III Inhibit the Activation of Platelets by Alpha Defensins from Neutrophils |
| Van Bavel E |
- |
Microparticle-associated P-selectin Is a Marker of Platelet Activation in Preeclampsia |
| |
- |
Microparticles From Preeclamptic Patients Do Not Affect Transcription of Inflammation-related Genes in Endothelial Cells |
| Van Belle E |
- |
Plasma Levels of Tissue Factor and von Willebrand Factor Predict Long Term Clinical Outcome after Percutaneous Coronary Revascularization |
| van Berkel ThJC |
- |
Platelet Activation by Oxidized Low-Density Lipoprotein Is Mediated by CD36 and Scavenger Receptor-A |
| van Beurden-Lourenssen GJACM |
- |
Administration of Recombinant Activated Factor VII Causes Activation of Integrin aIIbb3 on Blood Platelets both in vivo and in vitro, Lowering the Threshold for Activation by Thrombin |
| Van Cott EM |
- |
Massive Sinus Thrombosis in a Six-Year-Old Girl: Acute Management and Identification of a Possible New Hypercoagulable State |
| Van Cott E |
- |
Use of the D-Dimer for Exclusion of VTE: Difficulties Revealed through the Proficiency Testing Program of the College of American Pathologists (CAP) |
| van de Kar NCAJ |
- |
Predictive Value of the Platelet Function Analyser (PFA-100®) for Post Biopsy Bleedings in Patients Undergoing Renal Biopsy |
| Van de Poel MHW |
- |
Absolute Risk of Venous and Arterial Thromboembolism Associated with Mild Hyperhomocysteinemia. Results from a Retrospective Family Cohort Study |
| Van de Poel MH |
- |
A Prospective Cohort Study of Asymptomatic Individuals with Elevated Factor VIII : c to Determine the Absolute Incidence of Venous and Arterial Thromboembolism |
| Van de Poel MHW |
- |
The Contribution of Cosegregation to the Absolute Risk of Venous Thromboembolism (VTE) in Relatives with Either the Prothrombin G20210A Mutation, High Factor VIII : C Levels or Mild Hyperhomocysteinemia |
| van de Velde A |
- |
Characterisation and Classification of Von Willebrand Diseases |
| van de Ven AJAM |
- |
Malaria Infection Induced Thrombocytopenia Is not Related to Systemic Platelet Activation |
| Van de Walle G |
- |
Functional Evidence for Three I-domain Activation States for Platelet a2b1 Integrin |
| Van de Walle G |
- |
Different Active Conformations Are Induced in the Collagen Receptor Integrin a2b1 by Outside Manipulation and Inside-out Signalling |
| Van de Walle G |
- |
Crosstalk Between Integrins a2b1 and aIIbb3 during Platelet Activation |
| Van de Water NS |
- |
ZPI Gene Mutations and Myocardial Infarction |
| Van de Werf F |
- |
Bleeding Events with Lytics and Thienopyridines in Patients with ST-Segment Elevation Myocardial Infarction. The Global Registry of Acute Coronary Events |
| van Delden OM |
- |
Alternative Clinical Diagnoses with Spiral CT in Patients with Suspected Pulmonary Embolism |
| Van den Berg HM |
- |
Influence of Type of Factor VIII Gene Mutation on Inhibitor Development in a Single Centre Cohort of Severe Haemophilia a Patients |
| van den Berg E |
- |
Early Anticoagulation for Prevention and Therapy of Deep Venous Thrombosis In Patients Undergoing Craniotomy For Brain Tumor Risk of Postoperative Intra-cranial Hemorrhage in a Prospective Long-term Study |
| van den Berg HM |
- |
Factor VIII Inhibitors in Hemophilia A during Immune Tolerance Induction |
| Van den Berg HM |
- |
Late Prophylaxis for Severe Hemophilia: Effects of Prophylaxis Started in Adulthood |
| Van den Berg E |
- |
Perioperative Prophylaxis Against Thromboembolism in Patients Undergoing Craniotomy for Brain Tumor: Analysis of Efficacy of Early Low Molecular Weight Heparin |
| Van den Berg HM |
- |
Increased Fibrinolytic Activity in Patients with a More Severe Clinical Phenotype of Severe Hemophilia A |
| Van den Besselaar AMHP |
- |
Preanalytical Variables and Off-Site Blood Collection: Influences on the Results of the Prothrombin Time/International Normalized Ratio Test and Implications for Monitoring of Oral Anticoagulant Therapy |
| van den Besselaar AMHP |
- |
INR Results of the CoaguChek® PT Test Compare Well with INR Results of International Reference Thromboplastins |
| |
- |
Results of the Master Lot Calibration of a New Coagulation Monitoring System for Patient Self Testing |
| van den Biggelaar M |
- |
Intracellular Assembly of Factor VIII and von Willebrand Factor |
| Van den Brink R |
- |
Thromboembolic and Bleeding Complications during Non-cardiac Surgery in Patients with Mechanical Heart Valves |
| Van der Bom JG |
- |
Increased Fibrinolytic Activity in Patients with a More Severe Clinical Phenotype of Severe Hemophilia A |
| van der Bom JG |
- |
Hemorrhagic risk in Female Carriers of Hemophilia |
| Van der Bom JG |
- |
Influence of Type of Factor VIII Gene Mutation on Inhibitor Development in a Single Centre Cohort of Severe Haemophilia a Patients |
| Van der Elst L |
- |
Antigen Binding Site Glycosylation Determines the Anticoagulant Activity of a Type II Factor VIII Antibody without Modifying Affinity or Epitope Specificity |
| van der Heide Y |
- |
Soluble Tissue Factor: A Marker of Microvascular Disease in Patients with Type 2 Diabetes |
| Van der Heijde D |
- |
Rofecoxib (Vioxx) Increases Thrombin Generation in Platelet Rich Plasma |
| Van der Linden S |
- |
Rofecoxib (Vioxx) Increases Thrombin Generation in Platelet Rich Plasma |
| Van der Meer J |
- |
A Prospective Cohort Study of Asymptomatic Individuals with Elevated Factor VIII : c to Determine the Absolute Incidence of Venous and Arterial Thromboembolism |
| |
- |
Absolute Risk of Venous Thromboembolism (VTE) Associated with Nephrotic Syndrome. Results from the Coltrane Study |
| |
- |
A Prospective Study to Assess the Absolute Incidence of Venous Thromboembolism (VTE) Associated with Hereditary Deficiencies of Protein C, Protein S and Antithrombin and the Contribution of Cosegregation of Other Thrombophilic Defects |
| van der Meer J |
- |
Clinical Implications of Individual Time Within Target Range (ITTR) in Patients with Atrial Fibrillation (AF) treated with Vitamin K Antagonists |
| |
- |
Fetal Loss in Hereditary Antithrombin, Protein C and Protein S Deficiencies |
| |
- |
The Contribution of Cosegregation to the Absolute Risk of Venous Thromboembolism (VTE) in Relatives with Either the Prothrombin G20210A Mutation, High Factor VIII : C Levels or Mild Hyperhomocysteinemia |
| van der Meer RW |
- |
Right Ventricular Dysfunction and the Pulmonary Obstruction Index Assessed with Helical CT Predict Clinical Outcome During Three-month Follow-up in Patients with Acute Pulmonary Embolism |
| van der Meer FJM |
- |
Risk of Arterial Thrombosis in Carriers of a Familial Thrombophilic Defect |
| Van der Meer J |
- |
Protein C/S Ratio to Identify Protein S Type I Non-Deficient Relatives at High Risk of Venous Thromboembolism (VTE). Results from a Family Cohort Study (DESCARTES) |
| |
- |
Effects of Highly Active Antiretroviral Therapy on the Risk of Venous and Arterial Thromboembolism in Male and Female HIV Positive Patients |
| |
- |
High Risk of Venous Thromboembolism (VTE) Associated with Oral Contraceptives in Women with Hereditary Deficiencies of Protein S, Protein C or Antithrombin Is Due to Acceleration Rather Than Overall Increased Risk. A Retrospective Family Cohort Study (DESCARTES) |
| van der Meer J |
- |
Individual Time within Target Range (ITTR), an Accurate Predictor of Clinical Outcome in Patients with Acute Myocardial Infarction (AMI) Treated with Vitamin K Antagonists |
| Van der Meer J |
- |
Absolute Risk of Venous Thromboembolism (VTE) Associated with Hereditary Deficiencies of Protein C, Protein S or Antithrombin Strongly Depends on Cosegregation of other Thrombophilic Disorders. A Retrospective Family Cohort Study (DESCARTES) |
| |
- |
Incidence of Venous and Arterial Thromboembolism in Asymptomatic Carriers of the Prothrombin 20210A Mutation A Prospective Cohort Study |
| |
- |
Absolute Risk of Venous Thromboembolism (VTE) Associated with Oral Contraceptives in Women with Hereditary Deficiencies Of Protein S, Protein C or Antithrombin Strongly Depends on Cosegregation of Thrombophilic Disorders. A Retrospective Family Cohort Study (DESCARTES) |
| |
- |
Hereditary Deficiencies of Protein C, Protein S And Antithrombin Protect Against Bleeding During Anticoagulant Treatment. Results from a Family Cohort Study (DESCARTES) |
| van der Meer J |
- |
Reduction of Fetal Loss Rate by Anticoagulant Treatment during Pregnancy in Women with Hereditary Deficiency of Antithrombin, Protein C or Protein S Type I. A Prospective Study |
| |
- |
Absolute Risk of Venous and Arterial Thromboembolism Associated with Mild Hyperhomocysteinemia. Results from a Retrospective Family Cohort Study |
| van der Meer FJM |
- |
Subtherapeutic Oral Anticoagulant Therapy Frequency and Risk Factors |
| Van der Meer J |
- |
Low CD4/CD8 Ratios In HIV Negative Haemophilia Patients Cause High HCV Viraemia |
| van der Meer J |
- |
Risk of Thromboembolic Events and Major Bleeding in Patients Treated with Vitamin K Antagonists after Heart Valve Replacement (HVR); Individual Time within Target Range (ITTR) an Accurate Predictor |
| Van Der Meer FJM |
- |
Comparison between Two Computer Algorithms in Oral Anticoagulant Dosage A Doubleblind Randomised Controlled Trial |
| |
- |
A Randomised Controlled Trial Comparing Warfarin and Phenprocoumon on Quality of Oral Anticoagulant Treatment |
| Van der Meer J |
- |
Protein C/S Ratio Improves Accuracy to Identify Hereditary Protein S Deficiency Type I. Results from a Family Cohort Study (DESCARTES) |
| |
- |
Absolute Risk of Arterial Thromboembolism (ATE) Associated with Nephrotic Syndrome. Results from the Coltrane Study |
| van der Meer J |
- |
The Incidence of Venographically Detected Deep Vein Thrombosis after Knee Arthroscopy without Thromboprophylaxis |
| Van der Meer J |
- |
Absolute Incidence of Recurrent Venous Thromboembolism in Patients with Elevated Levels of Factor VIII : c |
| |
- |
Risk of Recurrent Venous Thromboembolism (VTE) Associated with Hereditary Deficiencies of Protein C, Protein S and Antithrombin Depends on Cosegregation with Other Thrombophilic Disorders: A Prospective Family Cohort Study |
| |
- |
Hereditary Deficiencies of Protein C, Protein S or Antithrombin Are No Risk Factors for Arterial Thromboembolism (ATE). Results from a Large Family-Cohort Study (DESCARTES) |
| Van der Meijden PEJ |
- |
P2Y12 Receptor Stimulation Prolongs Thrombin-Induced Calcium Responses and Procoagulant Activity Via Novel Signaling Pathways; Variable Effect of Clopidogrel Treatment |
| van der Meijden PEJ |
- |
Disclosure of Microdomain Structure and Function in Arterial Thrombi of Heterogeneous Composition |
| Van der Meulen PA |
- |
Effects of Highly Active Antiretroviral Therapy on the Risk of Venous and Arterial Thromboembolism in Male and Female HIV Positive Patients |
| van der Planken M |
- |
Pretreatment with Aspirin and Loading Dose Clopidogrel Obviates the Need for Glycoprotein Iib/Iiia Antagonists During Elective Coronary Stenting |
| |
- |
Characterisation and Classification of Von Willebrand Diseases |
| Van der Poel MHW |
- |
Absolute Incidence of Recurrent Venous Thromboembolism in Patients with Elevated Levels of Factor VIII : c |
| |
- |
Incidence of Venous and Arterial Thromboembolism in Asymptomatic Carriers of the Prothrombin 20210A Mutation A Prospective Cohort Study |
| van der Poll T |
- |
Endogenous Tissue-Type Plasminogen Activator Is Essential for an Adequate Host Defense During  Induced Abdominal Sepsis |
| |
- |
Local Attenuation of the Protein C Pathway in Patients Developing Pneumonia |
| |
- |
The Role of PAI-1 Deficiency and a Reduced Capacity to Generate Activated Protein C on Coagulation Activation and Fibrin Formation during Murine Influenza Pneumonia |
| |
- |
Lung-Protective Mechanical Ventilation Attenuates Fibrin Generation in Healthy Lungs |
| |
- |
Endotoxemia Induces Factor VIII-mediated Resistance to Activated Protein C in Healthy Humans |
| |
- |
Thrombin-Activatable Fibrinolysis Inhibitor Deficiency Influences the Inflammatory But Not the Procoagulant/Fibrinolytic Response to Escherichia coli-Induced Abdominal Sepsis in Mice |
| van der Putten HHAGM |
- |
The Prothrombin G19911A Is a Functional Non-coding Polymorphism |
| Van der Schaaf W |
- |
Absolute Risk of Venous Thromboembolism (VTE) Associated with Hereditary Deficiencies of Protein C, Protein S or Antithrombin Strongly Depends on Cosegregation of other Thrombophilic Disorders. A Retrospective Family Cohort Study (DESCARTES) |
| |
- |
Hereditary Deficiencies of Protein C, Protein S And Antithrombin Protect Against Bleeding During Anticoagulant Treatment. Results from a Family Cohort Study (DESCARTES) |
| |
- |
A Prospective Study to Assess the Absolute Incidence of Venous Thromboembolism (VTE) Associated with Hereditary Deficiencies of Protein C, Protein S and Antithrombin and the Contribution of Cosegregation of Other Thrombophilic Defects |
| |
- |
Risk of Recurrent Venous Thromboembolism (VTE) Associated with Hereditary Deficiencies of Protein C, Protein S and Antithrombin Depends on Cosegregation with Other Thrombophilic Disorders: A Prospective Family Cohort Study |
| |
- |
Hereditary Deficiencies of Protein C, Protein S or Antithrombin Are No Risk Factors for Arterial Thromboembolism (ATE). Results from a Large Family-Cohort Study (DESCARTES) |
| Van Der Schueren B |
- |
Angiographic Documentation of the Efficacy of Recombinant Activated Factor VII (Novo Seven) to Control Diffuse Bleeding in Major Trauma |
| van der Sluijs KF |
- |
The Role of PAI-1 Deficiency and a Reduced Capacity to Generate Activated Protein C on Coagulation Activation and Fibrin Formation during Murine Influenza Pneumonia |
| van der Spoel JI |
- |
The Diagnosis and the Estimated Incidence of Heparin-Induced Thrombocytopenia in the Critically Ill According to ISTH SSC Criteria |
| Van der Velde EF |
- |
Reliability and Interobserver Variability of the Simplify® D-Dimer Assay for Detecting D-Dimers in Capillary Blood |
| van der Vleuten GM |
- |
A Genome-Wide Linkage Scan for Homocysteine Levels Identifies Three Regions of Interest |
| van der Voort D |
- |
Changes in Fibrinolysis Activity after Angiotensin II Receptor Blockade in Patients Undergoing Renal Artery Angiography |
| |
- |
ASIS Blocks Tissue Factor Activity in the Heart after Ischemia/Reperfusion Injury in Mice |
| |
- |
Plasminogen Activator Inhibitor-1 Plasma Levels Increase after Myocardial Ischemia/Reperfusion Injury in Mice |
| van der Wal AC |
- |
Impaired Thrombus Formation after Sterile Inflammation Induced by Endotoxin in a Murine Carotid Artery Thrombosis Model |
| van der Zee PM |
- |
P-selectin- and CD63-Exposing Platelet Microparticles Reflect Platelet Activation in Peripheral Arterial Disease and Myocardial Infarction |
| van der Zwaan C |
- |
Clusters of Ligand-Binding Domains of Low-density Lipoprotein Receptor-related Protein Bind both Heavy and Light Chain of Activated Factor V and Inhibit Cofactor Function |
| |
- |
Functional Duplication of Ligand-Binding Domains within Low-Density Lipoprotein Receptor-Related Protein for Interaction with Alpha2-Macroglobulin, Factor IXa and Factor VIII |
| |
- |
An Antibody Fragment Against Factor VIII That inhibits Factor VIII assembly with von Willebrand Factor and LDL Receptor Family Members |
| van Diemen-Homan JEM |
- |
Hemorrhagic risk in Female Carriers of Hemophilia |
| Van Dijk K |
- |
Influence of Type of Factor VIII Gene Mutation on Inhibitor Development in a Single Centre Cohort of Severe Haemophilia a Patients |
| |
- |
Late Prophylaxis for Severe Hemophilia: Effects of Prophylaxis Started in Adulthood |
| |
- |
Increased Fibrinolytic Activity in Patients with a More Severe Clinical Phenotype of Severe Hemophilia A |
| Van Dongen CJ |
- |
Thromboembolic and Bleeding Complications during Non-cardiac Surgery in Patients with Mechanical Heart Valves |
| |
- |
Reliability and Interobserver Variability of the Simplify® D-Dimer Assay for Detecting D-Dimers in Capillary Blood |
| van Dongen CJ |
- |
C-reactive Protein in Combination with Clinical Decision Rule and D-Dimer to Safely Rule out Pulmonary Embolism |
| van Dongen MC |
- |
Genetic and Environmental Regulation of Factor VII Levels: Results from the IMMIDIET Project |
| van Dongen C |
- |
Predictors of Recurrent Venous Thromboembolism. Balancing Benefits and Risks A Decision Approach |
| Van Dongen MC |
- |
Comparison of Global Risk of Fatal Cardiovascular Disease in Three European Populations Using SCORE Equations: Results from the IMMIDIET Project |
| van Dongen CJ |
- |
Clinical Usefulness of Prothrombin Fragment 1+2 in Patients with Suspected Pulmonary Embolism |
| van Doornum GJ |
- |
Naturally Occurring Acute Viral Respiratory Tract Infections in Elderly Patient Results in Increased von Willebrand and Enhanced Fibrinolysis |
| Van Doren S |
- |
Therapeutic Plasma Exchange (TPE) for Thrombotic Thrombocytopenic Purpura (TTP) Using Plasma Prepared With Photochemical Treatment: Clinical Responses, vWF CP Levels and vWF-CP Inhibitor Levels |
| Van Dreden P |
- |
High Concentrations of Procoagulant Microparticles in Patients with Multiple Trauma |
| |
- |
Protein Z and the Protein C System in Normal Pregnancies and Patients with Early Foetal Loss |
| van Eck ATCJ |
- |
Perioperative Prophylaxis Against Thromboembolism in Patients Undergoing Craniotomy for Brain Tumor: Analysis of Efficacy of Early Low Molecular Weight Heparin |
| van Eck M |
- |
Platelet Activation by Oxidized Low-Density Lipoprotein Is Mediated by CD36 and Scavenger Receptor-A |
| van Eck ATCJ |
- |
Early Anticoagulation for Prevention and Therapy of Deep Venous Thrombosis In Patients Undergoing Craniotomy For Brain Tumor Risk of Postoperative Intra-cranial Hemorrhage in a Prospective Long-term Study |
| van Eeden S |
- |
Imaging of Highly Organized Vitronectin-Vimentin Polymeric Complexes that Express on the Surface of Activated Platelets and Platelet Microparticles using Atomic Force Microscopy |
| van Erpecum KJ |
- |
Childhood Acquired Hepatitis C Infection in Patients with Hemophilia: A Cohort Study |
| Van Geest-Daalderop JHH |
- |
Preanalytical Variables and Off-Site Blood Collection: Influences on the Results of the Prothrombin Time/International Normalized Ratio Test and Implications for Monitoring of Oral Anticoagulant Therapy |
| Van Geet C |
- |
Impaired Platelet Adhesion on Collagen Surfaces and Secretion Defect in Duchenne Muscular Dystrophy Patients |
| |
- |
Loss of Gs Activity in Platelets from Carriers with a Heterozygous Missense Mutation in the Regulator of G-protein Signaling 2 (RGS2) |
| |
- |
The b1-Tubulin Q43p Functional Polymorphism Reduces the Risk of Cardiovascular Disease by Modulating Platelet Function and Structure |
| van Genderen H |
- |
Annexin A5 Regulates the Engulfment Protein Repertoire on the Membrane of PS Expressing Apoptotic Cells |
| Van Genderen H |
- |
Apoptosis of Monocytes Reduces Their Interaction with P-Selectin Expressing Platelets Under Flow Conditions by Disruption of the Interaction of PSGL-1 with the Actin Cytoskeleton |
| van Goor MPJ |
- |
Pathogenesis of Increased VWF Levels and the Association with the Risk of Ischemic Stroke: Proteolysis, Inflammation or Genetic Variation? |
| van Gorp E |
- |
Plasma Levels of PAI-1 and Risk of Death from Dengue: No Association with the 4G/5G Promoter Polymorphism |
| van Gorp ECM |
- |
Naturally Occurring Acute Viral Respiratory Tract Infections in Elderly Patient Results in Increased von Willebrand and Enhanced Fibrinolysis |
| |
- |
The Role of PAI-1 Deficiency and a Reduced Capacity to Generate Activated Protein C on Coagulation Activation and Fibrin Formation during Murine Influenza Pneumonia |
| van Haeften T |
- |
Impaired Insulin Signaling in Platelets from Patients with Diabetes Mellitus Type 2 |
| |
- |
Inhibition of Collagen-Induced Thrombus Formation by Insulin Is Absent in Diabetes Mellitus Type 2 |
| van Haeften TW |
- |
Acute Hyperglycemia Perturbs Endothelial Glycocalyx and Induces a Prothrombotic State in Healthy Volunteers |
| van Haren BJT |
- |
von Willebrand Factor in Platelets |
| van Haren B |
- |
DDAVP Treatment Is Not Recommended in Patients with von Willebrand Disease Type 2N |
| van Heerde WL |
- |
Relevance of Very Low Titres of Factor VIII Inhibitors in Nijmegen-Bethesda Assay-Negative Patients |
| |
- |
DDAVP Treatment Is Not Recommended in Patients with von Willebrand Disease Type 2N |
| |
- |
13 Novel Mutations in the Factor VIII Gene in the Nijmegen Hemophilia A Patient Population |
| van Heerde WL |
- |
The Nijmegen Hemostasis Assay Is a Useful Tool to Screen Thrombophilia |
| van Heerde WL |
- |
The Nijmegen Haemostasis Assay to Study the Interplay between Coagulation and Fibrinolysis |
| van Heerde WL |
- |
The Importance of the Low-Density Lipoprotein Receptor-Related Protein (LRP) and Megalin Receptor in the Clearance of Factor VIII in Humans |
| |
- |
Administration of Recombinant Activated Factor VII Causes Activation of Integrin aIIbb3 on Blood Platelets both in vivo and in vitro, Lowering the Threshold for Activation by Thrombin |
| |
- |
Discrepancy between FVIII Activity Peak Levels and Thrombin and Plasmin Generation in Severe Hemophilia A Patients Treated with FVIII |
| van Heerde WL |
- |
Malaria Infection Induced Thrombocytopenia Is not Related to Systemic Platelet Activation |
| van Heerde WL |
- |
Low Amounts Of rVIIa Are Sufficient to Trigger Initiation of Thrombin Generation in Factor VII Deficient Patients |
| |
- |
von Willebrand Factor in Platelets |
| van Heerde WL |
- |
The Effect of Statin Therapy on Coagulation and Fibrinolysis in Patients with Heterozygous Familial Hypercholesterolemia |
| |
- |
The Role of Annexin A5 and Anti-Annexin A5 Antibodies in the Antiphospholipid Syndrome |
| |
- |
Determination of Platelet Activation Biomarkers Using the Surface Enhanced Laser Desorption/Ionisation Time of Flight (SELDI-TOF) Proteomic Approach |
| van Heerde WL |
- |
Screening Fibrinolytic Disorders with the Nijmegen Haemostasis Assay |
| |
- |
Laboratory Identification of Severe Haemophilia Is APTT-Reagent Dependent |
| Van Hees L |
- |
The b1-Tubulin Q43p Functional Polymorphism Reduces the Risk of Cardiovascular Disease by Modulating Platelet Function and Structure |
| van Hees T |
- |
Naturally Occurring Acute Viral Respiratory Tract Infections in Elderly Patient Results in Increased von Willebrand and Enhanced Fibrinolysis |
| van Helden PMW |
- |
Factor VIII Inhibitors in Hemophilia A during Immune Tolerance Induction |
| van Hinsbergh VWM |
- |
Effect of Thrombin Activatable Fibrinolysis Inhibitor (TAFI) and Pancreatic Carboxypeptidase B (CPB) on the Capillary Tube Formation in an in vitro Angiogenesis System |
| van Hoogen PCM |
- |
The Importance of the Low-Density Lipoprotein Receptor-Related Protein (LRP) and Megalin Receptor in the Clearance of Factor VIII in Humans |
| Van kerckhoven S |
- |
P-selectin Antagonist Gallic Acid is Antithrombotic Via Inhibition of Circulating Tissue Factor Deposition in Developing Murine Arterial Thrombi |
| van Korlaar IM |
- |
Attitudes about Genetic Testing for Thrombophilia in a Large Family with Heritable Protein C Deficiency |
| van Kraaij mgJ |
- |
The Nijmegen Hemostasis Assay Is a Useful Tool to Screen Thrombophilia |
| van Kraaij MGJ |
- |
13 Novel Mutations in the Factor VIII Gene in the Nijmegen Hemophilia A Patient Population |
| |
- |
Relevance of Very Low Titres of Factor VIII Inhibitors in Nijmegen-Bethesda Assay-Negative Patients |
| van Kraaij M |
- |
DDAVP Treatment Is Not Recommended in Patients with von Willebrand Disease Type 2N |
| van Kraaij MGJ |
- |
The Importance of the Low-Density Lipoprotein Receptor-Related Protein (LRP) and Megalin Receptor in the Clearance of Factor VIII in Humans |
| |
- |
Administration of Recombinant Activated Factor VII Causes Activation of Integrin aIIbb3 on Blood Platelets both in vivo and in vitro, Lowering the Threshold for Activation by Thrombin |
| van Kraaij M |
- |
The Nijmegen Haemostasis Assay to Study the Interplay between Coagulation and Fibrinolysis |
| van Kraaij MGJ |
- |
Discrepancy between FVIII Activity Peak Levels and Thrombin and Plasmin Generation in Severe Hemophilia A Patients Treated with FVIII |
| van Kraaij mgJ |
- |
Low Amounts Of rVIIa Are Sufficient to Trigger Initiation of Thrombin Generation in Factor VII Deficient Patients |
| van Kraaij MGJ |
- |
Screening Fibrinolytic Disorders with the Nijmegen Haemostasis Assay |
| |
- |
von Willebrand Factor in Platelets |
| Van Leeuwen Y |
- |
Comparison between Two Computer Algorithms in Oral Anticoagulant Dosage A Doubleblind Randomised Controlled Trial |
| |
- |
A Randomised Controlled Trial Comparing Warfarin and Phenprocoumon on Quality of Oral Anticoagulant Treatment |
| van Lier M |
- |
Adhesive Surface Determines Raft Composition in Platelets Adhering Under Flow |
| van Lieshout MHP |
- |
Acute Hyperglycemia Perturbs Endothelial Glycocalyx and Induces a Prothrombotic State in Healthy Volunteers |
| Van Lummel M |
- |
Interaction of Beta2-Glycoprotein I with Members of the Low-density Lipoprotein Receptor (LDLR) Super Family |
| van Lummel M |
- |
Platelet Adhesion to Dimeric Beta2-Glycoprotein-I Under Conditions of Flow Is Mediated by Glycoprotein Iba |
| Van Lummel M |
- |
C-Terminal Domain of Beta2-Glycoprotein I Is Involved in Binding to Apoer2' |
| Van Marion V |
- |
Linkage Analysis of von Willebrand Disease Type 1 Phenotype, von Willebrand Factor Levels and Bleeding Symptoms with Von Willebrand Factor Gene Locus in the European Multicenter MCMDM-1VWD Study |
| van MierloBüller PJWBHR |
- |
Diagnostic Strategy Using a Modified Clinical Decision Rule and D-Dimer Test to Rule Out Pulmonary Embolism in Elderly in- and Outpatients |
| van Minkelen R |
- |
The Marburg I Polymorphism of Factor Seven-Activating Protease Is Not Associated with Venous Thrombosis |
| |
- |
Interleukin 1 Haplotypes and the Risk of Venous Thrombosis |
| van Mourik JA |
- |
Protein Kinase A-dependent Clustering of Weibel-Palade Bodies in Endothelial Cells |
| |
- |
Von Willebrand Factor-mediated Sorting of Endothelial Secretory Proteins |
| Van Noorden CR |
- |
Effect of Modified Normothrombotic Heparin on Cancer Progression and Metastasis |
| van Oerle R |
- |
ASIS Blocks Tissue Factor Activity in the Heart after Ischemia/Reperfusion Injury in Mice |
| |
- |
Changes in Fibrinolysis Activity after Angiotensin II Receptor Blockade in Patients Undergoing Renal Artery Angiography |
| |
- |
Soluble Tissue Factor: A Marker of Microvascular Disease in Patients with Type 2 Diabetes |
| |
- |
Analysis of Blood Coagulation in Mice: Pre-analytical Conditions and Comparison of a Home-made Assay for Thrombin-antithrombin Complexes with Two Commercial Assays |
| Van Oerle R |
- |
Activity and Localization of Tissue Factor and Factor VII in Organs of Normal and Endotoxemic Mice |
| van Oerle R |
- |
Laboratory Markers of Cardiovascular Disease in Systemic Lupus Erythematosus: Evidence of a Latent Hypercoagulable State |
| |
- |
A Hypercoagulable State in Myeloperoxidase Deficient Mice |
| Van Oerle R |
- |
Platelet Derived Microparticles in Blood Bank Products Do Not Expose Functionally Active Tissue Factor But Are Highly Procoagulant |
| van Oerle R |
- |
Plasminogen Activator Inhibitor-1 Plasma Levels Increase after Myocardial Ischemia/Reperfusion Injury in Mice |
| van Ommen CH |
- |
Clinical Experience with Nadroparin in Pediatric Patients with Venous Thrombosis |
| van Pampus ECM |
- |
Integrins Mediate Shedding of Procoagulant Microparticles at Minimal Platelet Activation |
| |
- |
Plasma Ecto-NTPDase Prevents Platelet P2X1 and P2Y12 Receptor Desensitization During Storage |
| Van Raak EPM |
- |
P2Y12 Receptor Stimulation Prolongs Thrombin-Induced Calcium Responses and Procoagulant Activity Via Novel Signaling Pathways; Variable Effect of Clopidogrel Treatment |
| van Rijn JC |
- |
Alternative Clinical Diagnoses with Spiral CT in Patients with Suspected Pulmonary Embolism |
| Van Stempvoort G |
- |
The Contribution of Somatic Mutations in an Antibody against Factor VIII to the Kinetics of Factor VIII Binding and Inhibition of Factor VIII Activity |
| Van Stralen KJ |
- |
Upper Extremity Venous Thrombosis; Risk estimations for Surgery, Plaster Cast, Unusual Activities and Exercise |
| |
- |
Effect of Regular Sports Activities on the Risk of Venous Thrombosis: Results from the MEGA Study |
| van Strijen MJL |
- |
Right Ventricular Dysfunction and the Pulmonary Obstruction Index Assessed with Helical CT Predict Clinical Outcome During Three-month Follow-up in Patients with Acute Pulmonary Embolism |
| van t Veer C |
- |
Thrombin-Activatable Fibrinolysis Inhibitor Deficiency Influences the Inflammatory But Not the Procoagulant/Fibrinolytic Response to Escherichia coli-Induced Abdominal Sepsis in Mice |
| van Tilburg NH |
- |
The Effect of ABO Blood Group Genotypes on the Loading of von Willebrand Factor with A and B Antigens |
| van Tits LJ |
- |
The Effect of Statin Therapy on Coagulation and Fibrinolysis in Patients with Heterozygous Familial Hypercholesterolemia |
| van Veen JJ |
- |
Reproducibility of the Endogenous Thrombin Potential by Calibrated Automated Thrombogram Assay |
| |
- |
Clinical Use of Protamine for the Emergency Reversal of Anticoagulation with Low Molecular Weight Heparin (LMWH) |
| van Vliet H |
- |
Characterisation and Classification of Von Willebrand Diseases |
| van Vliet HHDM |
- |
Pathogenesis of Increased VWF Levels and the Association with the Risk of Ischemic Stroke: Proteolysis, Inflammation or Genetic Variation? |
| van Vlijmen BJM |
- |
Clearance of Plasminogen Activator Inhibitor-1 in Low-Density Lipoprotein Receptor-Related Protein Deficient Mice |
| Van Vlijmen EFW |
- |
High Risk of Venous Thromboembolism (VTE) Associated with Oral Contraceptives in Women with Hereditary Deficiencies of Protein S, Protein C or Antithrombin Is Due to Acceleration Rather Than Overall Increased Risk. A Retrospective Family Cohort Study (DESCARTES) |
| |
- |
Absolute Risk of Venous Thromboembolism (VTE) Associated with Oral Contraceptives in Women with Hereditary Deficiencies Of Protein S, Protein C or Antithrombin Strongly Depends on Cosegregation of Thrombophilic Disorders. A Retrospective Family Cohort Study (DESCARTES) |
| Van Weert HC |
- |
Reliability and Interobserver Variability of the Simplify® D-Dimer Assay for Detecting D-Dimers in Capillary Blood |
| van Zandvoort MAMJ |
- |
Crucial Role of Glycoprotein VI in Thrombus Formation and Coagulation during Venous and Arterial Thrombosis |
| |
- |
Disclosure of Microdomain Structure and Function in Arterial Thrombi of Heterogeneous Composition |
| van Zanten AP |
- |
Soluble Tissue Factor: A Marker of Microvascular Disease in Patients with Type 2 Diabetes |
| Vana L |
- |
Development of Non-Anticoagulant Derivatives of K5-Derived Sulfaminoheparosans and Investigation of Their Non-Anticoagulant Effects |
| Vandekerckhove J |
- |
Protein Profiling of Human Blood Platelets from Young and Aged Individuals |
| Vandendries ER |
- |
Maximal Platelet Accumulation, But Not Fibrin Deposition, Is Dependent on Protease-Activated Receptor 4 in a Mouse Model of Thrombosis |
| VanderPost J |
- |
Microparticle-associated P-selectin Is a Marker of Platelet Activation in Preeclampsia |
| |
- |
Microparticles From Preeclamptic Patients Do Not Affect Transcription of Inflammation-related Genes in Endothelial Cells |
| Vandervoort PAH |
- |
Domain A1 in Unfolded von Willebrand Factor Can Recruit Flowing Platelets to Collagen Surfaces Independently of Domain A3 |
| Vandhuick O |
- |
Premature Atherosclerosis in HIV Positive Patients and Cumulated Time of Exposure to Antiretroviral Therapy (SHIVA Study) |
| Vanhaeverbeek M |
- |
Circulating Platelet-Monocyte Complexes Are Inversely Correlated with Serum Apo-A Levels |
| Vanhoorelbeke K |
- |
A Gain of Function Mutation in aIIbb3 Results in a Glanzmann Thrombasthenia Phenotype |
| Vanhoorelbeke K |
- |
A Common Ancestral Glycoprotein (GP) IX Gene Mutation (Asn45Ser) Causes Bernard-Soulier Syndrome (BSS) in European Families from Northern Europe and Australia |
| |
- |
Cloning Strategy and Humanization of the Potent Antithrombotic Agent 6B4, an Anti-Glycoprotein Ib Monoclonal Antibody |
| |
- |
Determination of Interacting Residues within the VWF A3-Domain and the Antithrombotic Antibody 82D6A3 by Docking, Cocrystallisation and Mutagenesis |
| |
- |
Different Active Conformations Are Induced in the Collagen Receptor Integrin a2b1 by Outside Manipulation and Inside-out Signalling |
| |
- |
Non-helical Peptide Sequence SRHPRVGVYHVFDSA Binds Specifically to Human Integrin a2b1 |
| |
- |
Humanisation of an Antithrombotic Anti-von Willebrand Factor (VWF) Monoclonal Antibody, 82D6A3, by Variable Domain Resurfacing |
| |
- |
Shielding of the A1-Domain by the Amino-Terminal Domain (AA7641035) of von Willebrand Factor Modulates Its Interaction with Platelet Glycoprotein Ib-IX-V |
| |
- |
Production of Anti-ADAMTS-13 Monoclonal Antibodies by DNA Immunization |
| |
- |
False Positives Account For Low Conversion Frequency In Chimeraplasty For Von Willebrand Disease |
| |
- |
Combination of Loss of Function of Recombinant R1334A-VWF and Gain of Function of R1336A-VWF Results in a Loss of Function of RKR1334-1335-1336A-VWF |
| |
- |
Crosstalk Between Integrins a2b1 and aIIbb3 during Platelet Activation |
| Vanier M-C |
- |
Optimizing Thromboembolic and Stroke Prevention: Interim Analysis of a Randomized Controlled Trial of Pharmacist-Managed Oral Anticoagulotherapy (PHARMA Trial) |
| Vannier JP |
- |
The Stable Prostacyclin Analog Iloprost Induces The Production of the Angiogenic Factor Oncostatin M by Monocytes in a p38K-dependent Pathway |
| |
- |
S6-Kinase as a Possible Target for the Angiogenic Activity of Interleukin-4 |
| van't Hof AWJ |
- |
Role of Platelet Aggregation Testing in Acute Stent Thrombosis |
| van't Veer C |
- |
Low Molecular Weight Heparin Attenuates Multiorgan Failure in DIC |
| |
- |
Endogenous Tissue-Type Plasminogen Activator Is Essential for an Adequate Host Defense During  Induced Abdominal Sepsis |
| Vanyusheva OV |
- |
Study of the Methylenetetrahydrofolate Reductase Gene Promoter in Patients With Heterozygous C677T MTHFR Gene Polymorphism and Hyperhomocysteinemia |
| Vanzan A |
- |
The G20210A Prothrombin Variant (PT-G20210A) and the Risk of Thromboembolism and Foetal Loss in Pregnant Women: A Retrospective Cohort Study |
| Váradi B |
- |
Modulation of Fibrinolysis by Some Components Present in Arterial Thrombus |
| Varadi K |
- |
The Effects of Supra-Normal Protein C Levels on Markers of Coagulation, Fibrinolysis and Inflammation in a Human Model of Endotoxemia |
| Váradi K |
- |
TECHNOTHROMBIN® TGA a Novel Thrombin Generation Assay Suitable for the New Routine Coagulation Analyzer Ceveron® Alpha |
| |
- |
Protective Effect of Human Plasma-Derived Protein C in Septic Neonatal Mice |
| Varakin Ya |
- |
Platelet Function in Patients with Cerebrovascular Pathology in Changes of Geomagnetic Field of Earth |
| Varcoe R |
- |
The Circulating Progenitor in Intimal Hyperplasia: Could It Be the Fibrocyte? |
| Vardimon H |
- |
A New Approach for Pre Analytical Screening of Hospitalized Patients Receiving Anticoagulant Therapy |
| Varfolomeyev SD |
- |
Fibrin-Monomer Prepared Using Thrombin-Like Enzyme from Snake Venom Agkistrodon Halys as Stimulator of Plasminogen Activation By t-PA |
| |
- |
Inhibition Kinetics of Plasmin-staphylokinase (Pm-STA) and Plasmin-Streptokinase (Pm-SK) Complexes with Different Protein Inhibitors |
| |
- |
Activation Kinetics of Glycoform of GLU-Plasminogen and Lys-Plasminogen by Plasmin-Staphylokinase Complex |
| Vargová K |
- |
Statins Do Not Interfere with the Antiplatelet Effect of Loading Dose Clopidogrel in Patients with Ischemic Heart Disease |
| Varlack S |
- |
Glucose Uptake Via GLUT3 in Human Platelets Is Regulated Via PKB |
| Varma S |
- |
Prevalence of Risk Factors for Venous Thromboembolism: A Study from North India |
| Varon D |
- |
Platelet-Derived Microparticles Induce Angiogenesis and Stimulate Post-Ischemic Revascularization |
| |
- |
Statins Confer a Direct Anti-Platelet Effect in Patients with Acute Myocardial Infarction Treated with Aspirin and Clopidrogel: Ex-vivo and in-vitro Study Results |
| |
- |
Platelet Mediated Clot Formation in Whole Blood under Flow: A New Screening Method for Coagulation Disorders and for Drug Monitoring |
| |
- |
Aspirin Resistance in Acute Brain Ischemia: Association with Stroke Severity and Outcome |
| Varon D |
- |
Dynamic Responsiveness to Aspirin in Patients Undergoing PCI |
| Varon D |
- |
High Rate of Unresponsiveness to Clopidogrel in Patients with Acute Coronary Syndrome (ACS) As Determined by the Impact-R [Cone And Plate(let) Analyzer] |
| |
- |
Low rate of Responsiveness to Aspirin in Acute Brain Ischemia: Association with Stroke Severity and Clinical Outcome |
| |
- |
CRP Induces Platelet-Endothelial Adhesion Under Flow |
| Vartholomatos G |
- |
Factor V Leiden and R2 Mutations, Prothrombin G20210A Mutation and Osteonecrosis |
| |
- |
Assessing Acquired and Inherited Factors in Cases of Idiopathic and Secondary Pulmonary Embolism |
| Vartholomatos G |
- |
Is Screening for Thrombophilia Mutations Necessary Prior to Free Functional Muscle Transfer? |
| Varughese KI |
- |
Modulation of Von Willebrand Factor A1 Domain-Mediated Platelet Aggregation by a-Thrombin |
| Varvenne M |
- |
Detection and Expression of Three Missense Mutations in the Bb Fibrinogen Gene Resulting in A- and/or Hypofibrinogenaemia |
| Vasilchuk G |
- |
The Role of Mild Forms of Coagulopathias and Pathology of Platelets in the Development of Menorrhagia and Metrorrhagia |
| |
- |
The Role of Mild Forms of Coagulopathias and Pathology of Platelets in the Development of Menorrhagia and Metrorrhagia |
| Vasiliadis N |
- |
An Inquiry into Death Causes Based on Autopsy Findings |
| Vasiljevic Z |
- |
Homocysteine Levels and MTHFR C677T Genotypes in Patients with Myocardial Infarction under Age 45 years |
| Vasovic V |
- |
RNA Interference Targeting Tissue Factor in a Murine Melanoma Metastasis Model |
| Vasquez J |
- |
Investigation of Performance and Sample Interferences for a New Automated Protein S Functional Activity Assay (HemosIL ProS) |
| Vasse M |
- |
S6-Kinase as a Possible Target for the Angiogenic Activity of Interleukin-4 |
| |
- |
The Stable Prostacyclin Analog Iloprost Induces The Production of the Angiogenic Factor Oncostatin M by Monocytes in a p38K-dependent Pathway |
| Vassiliou M |
- |
Assessing Acquired and Inherited Factors in Cases of Idiopathic and Secondary Pulmonary Embolism |
| Vaughan DE |
- |
PAI-1 and Atherothrombosis |
| Vauterin S |
- |
Humanisation of an Antithrombotic Anti-von Willebrand Factor (VWF) Monoclonal Antibody, 82D6A3, by Variable Domain Resurfacing |
| |
- |
Determination of Interacting Residues within the VWF A3-Domain and the Antithrombotic Antibody 82D6A3 by Docking, Cocrystallisation and Mutagenesis |
| |
- |
Non-helical Peptide Sequence SRHPRVGVYHVFDSA Binds Specifically to Human Integrin a2b1 |
| |
- |
Production of Anti-ADAMTS-13 Monoclonal Antibodies by DNA Immunization |
| Vavilova T |
- |
The New Single Nucleotide Polymorphisms of Adp Receptor P2y12 Gene Affected Platelet Aggregation and Myocardial Infarction Development Were Found in Russia |
| Vavilova T |
- |
Inherited Thrombophilias in the Patients with Prosthetic Heart Valves |
| |
- |
Pharmacogenetics of WarfarinCytochrome Cyp2c9 and Vitamin K Epoxide Reductase Gene Polymorphisms in Russian Population |
| Vayá A |
- |
Protein CValencia: Symptomatic Type II Protein C Deficiency Associated with a Mutation in the Gla Domain (Glu16 to Lys) |
| |
- |
Influence of Polymorphisms in the Endothelial Protein C Receptor Gene on the Risk of Venous Thromboembolism in Carriers of the Factor V Leiden Mutation |
| Vayro S |
- |
Tissue Factor Synthesis and Expression by Human Proximal Tubular Cells: the Source of Increased Urinary Tissue Factor Secretion in Disease? |
| Vaz FAC |
- |
Thromboembolic Complications of Acute Lymphoblastic Leukemia in Children, Adolescents and Young Adults: Effects of the Disease and the Therapy on the Hemostatic System |
| Vaz MLS |
- |
Anticardiolipin Antibodies (ACL), Factor V Leiden (FVL) and G20210A Prothrombin Mutation (G20210AII) Do Not Predispose Renal Transplant Recipients to Thrombotic Complications or Graft Loss |
| Vázquez-González G |
- |
Oral Anticoagulant Treatment (OAT) with Portable PT Monitor in Primary Health Care Centres with Immediate Dose Adjustment by the Hospital OAT Unit |
| Vdovin VV |
- |
Ulcerous Colitis in Children with Hemophilia A |
| Vdovin V |
- |
The State of Fibrinolytic and Coagulation Systems in Hemophiliacs |
| |
- |
The Occasions of Factor XII Deficiency in Children |
| Veber B |
- |
Heparin-PF4 Elisa Antibodies Detection Is Not Relevant to Diagnose HIT During Sepsis |
| Vecchioli M |
- |
Absence of Interaction Between Influenza Vaccination and Oral Anticoagulant Therapy: A Randomized Blinded Clinical Trial |
| Vecchione G |
- |
Successful Diagnosis in Pregnant Obligate Carriers of Hemophilia a of Fetal Sex Using Conventional Pcr Analysis of Maternal Plasma |
| Vedovati MC |
- |
High Incidence of Bilateral Deep Vein Thrombosis in Cancer Patients |
| Veeger NJGM |
- |
Risk of Recurrent Venous Thromboembolism (VTE) Associated with Hereditary Deficiencies of Protein C, Protein S and Antithrombin Depends on Cosegregation with Other Thrombophilic Disorders: A Prospective Family Cohort Study |
| |
- |
Hereditary Deficiencies of Protein C, Protein S or Antithrombin Are No Risk Factors for Arterial Thromboembolism (ATE). Results from a Large Family-Cohort Study (DESCARTES) |
| Veeger NJ |
- |
Absolute Incidence of Recurrent Venous Thromboembolism in Patients with Elevated Levels of Factor VIII : c |
| Veeger NJGM |
- |
Absolute Risk of Venous and Arterial Thromboembolism Associated with Mild Hyperhomocysteinemia. Results from a Retrospective Family Cohort Study |
| |
- |
Reduction of Fetal Loss Rate by Anticoagulant Treatment during Pregnancy in Women with Hereditary Deficiency of Antithrombin, Protein C or Protein S Type I. A Prospective Study |
| |
- |
Protein C/S Ratio Improves Accuracy to Identify Hereditary Protein S Deficiency Type I. Results from a Family Cohort Study (DESCARTES) |
| Veeger NJGM |
- |
Risk of Thromboembolic Events and Major Bleeding in Patients Treated with Vitamin K Antagonists after Heart Valve Replacement (HVR); Individual Time within Target Range (ITTR) an Accurate Predictor |
| Veeger NJGM |
- |
The Contribution of Cosegregation to the Absolute Risk of Venous Thromboembolism (VTE) in Relatives with Either the Prothrombin G20210A Mutation, High Factor VIII : C Levels or Mild Hyperhomocysteinemia |
| Veeger NJGM |
- |
Clinical Implications of Individual Time Within Target Range (ITTR) in Patients with Atrial Fibrillation (AF) treated with Vitamin K Antagonists |
| Veeger NJGM |
- |
Fetal Loss in Hereditary Antithrombin, Protein C and Protein S Deficiencies |
| |
- |
A Prospective Study to Assess the Absolute Incidence of Venous Thromboembolism (VTE) Associated with Hereditary Deficiencies of Protein C, Protein S and Antithrombin and the Contribution of Cosegregation of Other Thrombophilic Defects |
| |
- |
Protein C/S Ratio to Identify Protein S Type I Non-Deficient Relatives at High Risk of Venous Thromboembolism (VTE). Results from a Family Cohort Study (DESCARTES) |
| |
- |
High Risk of Venous Thromboembolism (VTE) Associated with Oral Contraceptives in Women with Hereditary Deficiencies of Protein S, Protein C or Antithrombin Is Due to Acceleration Rather Than Overall Increased Risk. A Retrospective Family Cohort Study (DESCARTES) |
| Veeger NJGM |
- |
Individual Time within Target Range (ITTR), an Accurate Predictor of Clinical Outcome in Patients with Acute Myocardial Infarction (AMI) Treated with Vitamin K Antagonists |
| Veeger NJGM |
- |
Absolute Risk of Venous Thromboembolism (VTE) Associated with Oral Contraceptives in Women with Hereditary Deficiencies Of Protein S, Protein C or Antithrombin Strongly Depends on Cosegregation of Thrombophilic Disorders. A Retrospective Family Cohort Study (DESCARTES) |
| Veeger NJ |
- |
Incidence of Venous and Arterial Thromboembolism in Asymptomatic Carriers of the Prothrombin 20210A Mutation A Prospective Cohort Study |
| Veeger NJGM |
- |
Hereditary Deficiencies of Protein C, Protein S And Antithrombin Protect Against Bleeding During Anticoagulant Treatment. Results from a Family Cohort Study (DESCARTES) |
| |
- |
Absolute Risk of Venous Thromboembolism (VTE) Associated with Hereditary Deficiencies of Protein C, Protein S or Antithrombin Strongly Depends on Cosegregation of other Thrombophilic Disorders. A Retrospective Family Cohort Study (DESCARTES) |
| VeegerBüller NHR |
- |
The Incidence of Venographically Detected Deep Vein Thrombosis after Knee Arthroscopy without Thromboprophylaxis |
| Vega-Ostertag ME |
- |
Induction of Tolerance to b2Glycoprotein I in Mice |
| |
- |
A Monoclonal Anti-C5 Antibody Reverses Antiphospholipid Antibody-mediated Thrombosis |
| Vega-Ostertag ME |
- |
A Peptide Derived from Cytomegalovirus Reverses Antiphospholipid-Mediated Thrombosis by Displacing Binding of b2glycoprotein I to Endothelial Cells in Mice |
| Vega-Ostertag ME |
- |
Toll Like Receptor 4 Is Involved in Antiphospholipid-mediated Thrombosis: In vivo Studies |
| |
- |
Antiphospholipid Antibodies Impair the Clearance of Apoptotic Platelets |
| Vegh P |
- |
Comparison of the Anticoagulant Effects of Melagatran and LMWH in an Acquired Antithrombin Deficiency in Children with ALL Treated with L-Asparaginase: An Ex Vivo Study |
| |
- |
No Difference in Incidences of Thrombosis between Heparin Bonded Catheters and Non Heparin Bonded Catheters in Infants in the Critical Care Unit Following Surgery for Congenital Heart Disease: A Randomised Controlled Triple Blind Study |
| Veglia F |
- |
Platelet Associated Tissue Factor Expression in Patients with Antiphospholipid Syndrome |
| Vekaria R |
- |
Prothrombin Binding to Phospholipid Membranes A Proposed Mechanism |
| Vekris M |
- |
Is Screening for Thrombophilia Mutations Necessary Prior to Free Functional Muscle Transfer? |
| Velásquez H |
- |
Endothelial Microparticle Binding to Neutrophils Is an Important Determinant of Neutrophil Activation In Vivo in Different Clinical Conditions |
| Veldman A |
- |
Effect of Protein C and Activated Protein C on Alveolar Fibrin Deposition and Turnover in a Piglet Model of Septic Shock |
| Veljkovic D |
- |
Pediatric Thrombosis |
| Venco A |
- |
The Risk of Venous and Arterial Thrombosis in Patients with HIV Infection |
| |
- |
D-Dimer and the Risk of Venous Thromboembolism in Medical Patients |
| |
- |
Incidence of Deep Vein Thrombosis Following Gynecologic Laparoscopy: A Prospective Cohort Study |
| |
- |
D-Dimer Measurement after Acute Ischemic Stroke Does Not Predict Long Term Outcome Events |
| |
- |
Prevalence of the Metabolic Syndrome in Patients with Provoked or Unprovoked Deep Vein Thrombosis and in Controls |
| Venge P |
- |
Nitric Oxide Enhances Eosinophil and Basophil Degranulation without Affecting Contact and Complement Activation |
| Vengust R |
- |
Methyl-Methacrylate Bone Cement Surface Does Not Promote Platelet Aggregation or Plasma Coagulation in vitro |
| Ventura C |
- |
The Spectrum of Mutations and Molecular Pathogenesis of Haemophilia A in 163 Portuguese Patients |
| Venz S |
- |
Proteomics as a Tool for Assessment of Therapeutics in Transfusion Medicine: Evaluation of Prothrombin Complex Concentrates |
| Vera E |
- |
Determination of ADAMTS-13 Activity in 13 Patients with Ischemic Stroke |
| |
- |
Genetic Study of von Willebrand Factor in Twenty-two Members of an Argentinian Family |
| |
- |
Partial Purification of ADAMTS-13 |
| Vera E |
- |
Von Willebrand Factor and ADAMTS-13 in 23 Doberman Pinschers Dogs |
| Verbeek K |
- |
13 Novel Mutations in the Factor VIII Gene in the Nijmegen Hemophilia A Patient Population |
| Verbeuren TJ |
- |
Silencing of Plasminogen Activator Inhibitor-1 by Small Interfering RNA Increases the Expression of Tissue Plasminogen Activator |
| |
- |
Evaluation of PAI-1 Inhibitors in the Microcirculation of the Hamster Cheek Pouch |
| Verbruggen H |
- |
Platelet Function Analyser Is a Good Alternative for Classical Bleeding Time to Detect von Willebrand Disease and Thrombocytopathy |
| |
- |
Determination of Platelet Activation Biomarkers Using the Surface Enhanced Laser Desorption/Ionisation Time of Flight (SELDI-TOF) Proteomic Approach |
| |
- |
von Willebrand Factor in Platelets |
| Verbruggen HW |
- |
Laboratory Identification of Severe Haemophilia Is APTT-Reagent Dependent |
| Verbruggen H |
- |
Screening Fibrinolytic Disorders with the Nijmegen Haemostasis Assay |
| Verbruggen HW |
- |
13 Novel Mutations in the Factor VIII Gene in the Nijmegen Hemophilia A Patient Population |
| Verbruggen HW |
- |
Relevance of Very Low Titres of Factor VIII Inhibitors in Nijmegen-Bethesda Assay-Negative Patients |
| Verbruggen H |
- |
DDAVP Treatment Is Not Recommended in Patients with von Willebrand Disease Type 2N |
| |
- |
The Nijmegen Hemostasis Assay Is a Useful Tool to Screen Thrombophilia |
| Verbruggen HW |
- |
Discrepancy between FVIII Activity Peak Levels and Thrombin and Plasmin Generation in Severe Hemophilia A Patients Treated with FVIII |
| Verbruggen H |
- |
The Nijmegen Haemostasis Assay to Study the Interplay between Coagulation and Fibrinolysis |
| Verbruggen HW |
- |
Predictive Value of the Platelet Function Analyser (PFA-100®) for Post Biopsy Bleedings in Patients Undergoing Renal Biopsy |
| Verbruggen HW |
- |
The Importance of the Low-Density Lipoprotein Receptor-Related Protein (LRP) and Megalin Receptor in the Clearance of Factor VIII in Humans |
| |
- |
Administration of Recombinant Activated Factor VII Causes Activation of Integrin aIIbb3 on Blood Platelets both in vivo and in vitro, Lowering the Threshold for Activation by Thrombin |
| |
- |
Low Amounts Of rVIIa Are Sufficient to Trigger Initiation of Thrombin Generation in Factor VII Deficient Patients |
| Verdier M |
- |
Polymorphism A36G of the Tumor Necrosis Factor Receptor 1 Gene Is Associated with HDL Cholesterol, TNFR1 and PAI-1 Levels in Obese Women |
| |
- |
Lipopolysaccharide-Induced Endotoxemia in the Mouse is Aggravated by PAI-1 Overexpression |
| Vereb G |
- |
Comparison of Platelet Deposition on Collagen in Cone-And-Plate and Parallel Plate Flow Chambers |
| |
- |
Time Dependent Increase in Thrombus Size Formed under Flow Conditions upon Exposure to Collagen Correlates Inversely with Surface Expressed VWF |
| |
- |
A Novel Homozygous Mutation (1619delC) in GPIIb Gene Associated with Glanzmann Thrombasthenia, the Decay of GPIIb-mRNA and the Synthesis of a Truncated GPIIb Unable to Form Complex with GPIIIa |
| |
- |
Three Novel Heterozygous Mutations in a Patient with Type II Glanzmann Thrombasthenia |
| Vergnes C |
- |
Fibrinogen Variants of the Gamma Chain Coiled-Coil Portion Detected by Reverse Phase HPLC in Patients with Venous Thrombosis |
| |
- |
Influence of 10 Polymorphisms Located in Genes Coding for Factors Involved in Coagulation and Fibrinolysis on the Risk of Venous Thrombosis in Factor V Leiden Homozygotes: Study of 233 Subjects |
| Vergura P |
- |
Successful Diagnosis in Pregnant Obligate Carriers of Hemophilia a of Fetal Sex Using Conventional Pcr Analysis of Maternal Plasma |
| |
- |
The COX-2 G/C-765 Polymorphism Modulates the Occurrence of Cerebrovascular Ischemia |
| Verheyen K |
- |
Extended Thromboprophylaxis with Fondaparinux (Arixtra®) after Major Orthopedic Lower Limb Surgery: The EXPERT Study |
| Verheyen CCPM |
- |
Incidence of Deep Vein Thrombosis after Knee Arthroscopy without Thromboprophylaxis |
| Verheyen K |
- |
Use of Neuraxial Catheter for Anesthesia/Analgesia in Major Orthopedic Lower Limb Surgery Patients Treated With Prophylactic Doses of Fondaparinux (Arixtra®) in Routine Practice: The EXPERT Study |
| Verhoef S |
- |
Adhesive Surface Determines Raft Composition in Platelets Adhering Under Flow |
| Verkerk R |
- |
A Novel Coupled Enzymatic Assay for the Fast Kinetic Characterization of Synthetic and Physiological CPU (TAFIa) Substrates |
| Verlato F |
- |
Is There a Role of Thrombophilia in the Progression of Carotid Plaques and/or in the Onset of Cerebrovascular Ischemic Events in Asymptomatic Patients? Results of a Prospective Study (CAST Study) |
| |
- |
Different Thromboprophylaxis Approaches in Patients Undergoing Knee Arthroscopy (KANT Study): A Prospective Randomized Study |
| |
- |
Utility Of D-Dimer in the Diagnosis of Deep Venous Thrombosis in Hospitalized Patients at High Risk of Venous Thromboembolism |
| Vermeulen HHM |
- |
A Genome-Wide Linkage Scan for Homocysteine Levels Identifies Three Regions of Interest |
| Vermylen J |
- |
Macrophage-neutrophil Cross Talk During Pulmonary Exposure to Silica Particles Triggers Peripheral Platelet Activation Via Elastase |
| |
- |
The b1-Tubulin Q43p Functional Polymorphism Reduces the Risk of Cardiovascular Disease by Modulating Platelet Function and Structure |
| |
- |
Domain A1 in Unfolded von Willebrand Factor Can Recruit Flowing Platelets to Collagen Surfaces Independently of Domain A3 |
| |
- |
Thrombospondin-1 Secures Thrombus Adherence in vivo by Protecting (Sub)Endothelial VWF from Leavage by ADAMTS13 |
| |
- |
Loss of Gs Activity in Platelets from Carriers with a Heterozygous Missense Mutation in the Regulator of G-protein Signaling 2 (RGS2) |
| Verschuren F |
- |
Inappropriateness of Diagnostic Management in Patients with Suspected Pulmonary Embolism: Frequency, Predictors and Association with Outcome |
| |
- |
Angiographic Documentation of the Efficacy of Recombinant Activated Factor VII (Novo Seven) to Control Diffuse Bleeding in Major Trauma |
| Versiero M |
- |
Association Between -675 4G/5G Polymorphism of the PAI-1 Gene and Obesity in Men: Longitudinal Findings of the Olivetti Heart Study |
| Verso M |
- |
Risk Factors for CVC-Associated Thrombosis in Cancer Patients: Analysis of the ETHIC Study |
| |
- |
A Prospective Registry on the Long-Term Clinical Outcome of Venous Thromboembolism (Multicenter Advanced Study for a ThromboEmbolism Registry MASTER): Description of the study cohort |
| Verspyck E |
- |
Protein Z Polymorphisms, Protein Z Plasma Concentration and Severe Pre Eclampsia |
| Versteeg HH |
- |
Antithrombotics Inhibit Tumor Metastasis |
| |
- |
Signal Transduction by Tissue Factor An Unusual Cytokine Receptor |
| |
- |
Coagulation Factors VIIa and Xa Promote Apoptosis in Human Tumor Cells in Association with CREB Activation |
| Versteeg HH |
- |
TF:FVIIa-Induced CREB Activation Occurs Via a Mechanism That Is Distinct from That Involved in TF:FVIIa-Induced STAT5 Activation |
| Vertrees J |
- |
Independent Qa Exercise to Validate Poc Coagulometer Reliability in Support of the Thinrs Trial and to Allay Perceptions of Possible Coagulometer Dysfunction |
| |
- |
Independent QA Exercise to Validate INR Test Strip Performance and Evaluate Perceptions of Excess Test Strip Error Messages in Support of the THINRS Trial |
| |
- |
Utility and Multi-site Acceptance of Patient Self-Reporting of INR Self-Test Results to a Central Database Utilizing a Computerized Interactive Voice Response System in the THINRS Study |
| Veszpremi A |
- |
Lack of P-selectin Glycoprotein Ligand-1 Protects Mice from Thrombosis after Thrombotic Challenges |
| Vetr H |
- |
Diagnosis of Acute Idiopathic Thrombotic Thrombocytopenic Purpura by Rapid Detection of ADAMTS 13 IgG Antibodies |
| Vetr H |
- |
TECHNOZYM® ADAMTS 13 Assays for Analyzing the vWF Cleaving Protease ADAMTS 13 |
| Vettore S |
- |
High Prevalence of Cardiac Abnormalities in Patients with Congenital FV Deficiency |
| |
- |
Mutations in Homozygotes and Compound Heterozygotes with FXII Deficiency |
| |
- |
Non-Catheter Induced Venous Thrombosis in Haemophellia A E B Patients |
| Vey M |
- |
Efficient Reduction of Prions by the Manufacturing Process of Plasma-Derived Products |
| Vicaretti M |
- |
The Opposing Roles of Monocytes in Atherosclerosis |
| |
- |
The Circulating Progenitor in Intimal Hyperplasia: Could It Be the Fibrocyte? |
| Vicente MA |
- |
Failure of the Outpatient Bleeding Risk Index to Predict Major Bleeding in Older Patients Receiving Coumarin for Atrial Fibrillation |
| Vicente V |
- |
Conformational and Functional Changes in Antithrombin by Oxidation |
| |
- |
Pharmacogenetic Effect of Factor VII -323 Del/Ins Polymorphism on Diurnal Variation of Factor VII Coagulant Activity and INR in Steady Anticoagulated Patients with Atrial Fibrillation |
| |
- |
Protective Role of the Platelet GP IIIa Polymorphism HPA-1 (PlA) in Subarachnoid Hemorrhage |
| |
- |
Clearance of Latent and Polymeric Antithrombin. Are These Conformational Variants Prothrombotic? |
| |
- |
Synergistic Association between Hypercholesterolemia and C46T Factor XII Polymorphism in the Development of Premature Myocardial Infarction |
| |
- |
Inflammation and Coagulation in Two Models of Endotoxemia in Resistant and Sensitive Mice: Low Relevance of Activation of Coagulation in the Outcome |
| |
- |
Acquired Antithrombin Deficiency in Acute Lymphoblastic Leukaemia (ALL) Induced by L-Asparaginase (ASNase): A Conformational Mechanism Modulated by Dexamethasone |
| Vicente MA |
- |
Validation of a Clinical Score (CS) Plus D-Dimer (DDi) Combination As a Diagnostic Strategy to Exclude Pulmonary Embolism (PE) |
| Vicente V |
- |
Interaction of Selected Septin Proteins with Platelet Microtubules: Role in the Regulation of Platelet Exocytosis |
| |
- |
Non-enzymatic Glycation of Antithrombin: Implications in Diabetes Mellitus |
| |
- |
Platelet Dysfunction Associated with Reduced Gai Expression in a family with Inherited Bleeding Disorder |
| |
- |
Factor XIII Val34Leu Polymorphism Showed an Adverse Pharmacogenetic Effect on the Thrombolytic Therapy for Acute Myocardial Infarction |
| |
- |
Deleterious Effect of the Common FXIII Val34Leu Polymorphism in Patients with Ischemic Stroke Treated with Fibrinolytic Therapy |
| |
- |
Ciclooxygenase-1 C50T Polymorphism Modulates the Thromboxane A2 Level and might Affect the Efficacy of Aspirin |
| |
- |
Synergism between Functional Hemostatic Polymorphisms and Risk of Premature Myocardial Infarction |
| |
- |
Antagonism of TxA2 Receptor Plays a Major Role in the Inhibitory Effect of Flavonoids in Platelet Function |
| Vickers C |
- |
Diagnostic Dilemma of a Patient with Strong Lupus Anticoagulant and Intramuscular Haemorrhage, Requiring Treatment with Recombinant FVIIa |
| Vickers MA |
- |
ABO and Secretor Genotypes and the Risk of Pre-Eclampsia |
| Vidler V |
- |
Early FVIII Exposure and Subsequent Inhibitor Development in Children with Severe Haemophilia A |
| |
- |
A UK Survey of Prophylaxis in Paediatric Patients with Haemophilia |
| Vieira LM |
- |
Factor V Leiden: An Important Risk Factor for Venous and Arterial Thrombosis in Brazilian Patients |
| |
- |
Type 2 Diabetes: Endothelium Lesion and Fibrinolytic System Markers Assessment |
| |
- |
Natural Anticoagulation Evaluation in Type 2 Diabetes |
| |
- |
Methylenetetrahydrofolate Reductase (MTHFR) Gene Polymorphism and Plasma Levels of Homocysteine in Patients with Type 2 Diabetes |
| Vieira LM |
- |
Monocytes and Plasma Tissue Factor Levels in Normal Individuals and Patients with Lower-Limbs Deep Venous Thrombosis: Potential Diagnostic Tools? |
| Vieira LM |
- |
Impact of the First Trimester of Hormone Replacement Therapy on the Levels of Hypercoagulability Markers |
| Viel KR |
- |
The Pharmacogenetics and Inhibitor Risk (PIR) Study: Do the Multiple Forms of Wildtype Factor (F)VIII Contribute to the Development of Anti-FVIII Antibodies in Hemophilia a Patients during Coagulation Factor Replacement Therapy? |
| Vielle B |
- |
Inappropriateness of Diagnostic Management in Patients with Suspected Pulmonary Embolism: Frequency, Predictors and Association with Outcome |
| Vielpeau C |
- |
Symptomatic Venous Thromboembolism and Mortality after Hip Fracture Surgery: The ESCORTE Study |
| Viera M |
- |
Anticoagulation Therapy in the Osteonecrosis |
| Viganò MG |
- |
The G1691A Factor V and G20210A Prothrombin Gene Mutations Are Not Associated to an Increased Risk of Venous Thromboembolism (VTE) in Patients with Gastrointestinal (GI) Carcinoma |
| Vigano' D'Angelo S |
- |
LMWH-Induced Thrombocytopenia (Type II) Successfully Treated with Fondaparinux (Arixtra®) |
| Vigh T |
- |
Extensive Venous Malformation Associated with Coagulation Abnormality: Treatment with Peginterferon Alfa 2a |
| Vigiani S |
- |
Protein Z Plasma Levels in Different Phases of Activity of Coronary Atherosclerosis |
| |
- |
Protein Z Decreases During Follow-up of Patients with Acute Coronary Syndromes |
| Vigneau C |
- |
Thrombin Induced Upregulation of Plasminogen Activator Inhibitor 1 (PAI-1) is Mediated by a Pathway Including S100 A9 Ca++ Binding Protein |
| Vignoli A |
- |
ADAMTS-13 Activity Profile in Thrombotic Thrombocytopenic Purpura (TTP) Patients Prospectively Followed At A Single Centre |
| |
- |
Parallel Changes in Procoagulant Activity and Proangiogenic Capacity of Breast Cancer and Leukaemia Cells Exposed to All Trans Retinoic Acid (ATRA) |
| Vigorito E |
- |
Vav Family Proteins Are Required for Optimal Platelet Spreading on Fibrinogen |
| Vik A |
- |
Heparin Induces Release of Osteoprotegerin (OPG) |
| |
- |
Serum Osteoprotegerin in Young Survivors of Myocardial Infarction |
| Vilarrasa N |
- |
Effect of Cigarrette Smoking on Fibrinogen and Von Willebrand Factor and Their Association with Risk Factors for Microangiopathy |
| Villa M |
- |
Conjoint Analysis to Elicit Preferences on Anticoagulant Treatment in Patients Receiving Vitamin K Antagonists (VKA) |
| |
- |
Differences between Patients, Physicians and Pharmacists Preferences for Treatment Products in Hemophilia. A Discrete Choice Experiment |
| Villa G |
- |
Effect of TGN 255, a Novel Intravenous Direct Thrombin Inhibitor, on the Prolongation of ACT in Patients Undergoing Haemodialysis |
| |
- |
Polymorphisms in the Hemostatic Pathway Genes and the Risk of Myocardial infarction in Patients with Advanced Coronary Artery Disease. Results from the Verona Heart Project |
| Villa P |
- |
Influence of Polymorphisms in the Endothelial Protein C Receptor Gene on the Risk of Venous Thromboembolism in Carriers of the Factor V Leiden Mutation |
| |
- |
Protein CValencia: Symptomatic Type II Protein C Deficiency Associated with a Mutation in the Gla Domain (Glu16 to Lys) |
| Villaça P |
- |
Sticky Platelet Syndrome Is a Cause of Cerebral Venous Thrombosis |
| Villaça PR |
- |
Treatment of Extensive Venous Malformation-Associated Localized Intravascular Coagulation with Interferon-Alpha: Case Report |
| Villamil F |
- |
Impact of Different Thromboplastins on the International Normalized Ratio and MELD Score in Patients with Cirrhosis Listed for Liver Transplantation |
| Villar A |
- |
Optimal Oral Anticoagulation Therapy and Major Bleeding in Patients with Heart Diseases in a Peruvian Heart Institute |
| |
- |
Immunotolerance Induction (ITI) with High Purity FVIII/VWF Concentrates in Inhibitors Patients with a High Risk of a Poor Response to ITI: A Prospective Surveillance |
| |
- |
Surgery in Haemophilic Patients with Inhibitor |
| |
- |
Polipectomia in a Patient with a Moderate Congenital Deficiency of Factor V |
| Villard S |
- |
A Spot Peptide Approach to Identify Binding Regions Between the TF-FVIIa Complex and its Macromolecular Substrates FIX and FX |
| |
- |
Fine Epitope Mapping of Human Monoclonal Antibodies Directed Against the B Domain of Factor VIII |
| Villegas-Mendez A |
- |
EPCR Cleavage and inactivation by Neutrophil Proteinase 3 |
| Villela MSH |
- |
Frequency of Anticardiolipin (aCL) Antibodies in Patients with Lupus Anticoagulant (LA) Detected by Different Methods: An Analysis of 4265 Cases |
| Villoutreix BO |
- |
Functional Analysis of the Factor Ix Egf-Like Domain Mutation Ile66thr Associated with Mild Hemophilia B |
| Vincelette J |
- |
Tissue Factor-Neutralizing Antibody Fused to Thrombomodulin (Ab(TF)-TM) Has Amplified Anticoagulant Efficacy in a Rat Model of Thromboembolism |
| Vincent J |
- |
Is the Maternal anti HPA-1a Antibody Concentration a Useful Parameter for Antenatal Management of High-risk Pregnancies? |
| Vincenzi D |
- |
Inherited Bleeding Disorders: The Emilia-Romagna Region Register, 2004 Update |
| Vinciguerra C |
- |
Genetic Study of 16 Women with Decreased FVIII Level and Assessment of Haemophilia a Carrier Status |
| Vinciguerra C |
- |
Combined Type 1 and Type 2N von Willebrand Disease: Contribution of Real Time PCR in Genotype Study |
| Viney E |
- |
Molecular Dissection of Platelet Production Via Random Mutagenesis |
| Vink H |
- |
Acute Hyperglycemia Perturbs Endothelial Glycocalyx and Induces a Prothrombotic State in Healthy Volunteers |
| Vink R |
- |
Thromboembolic and Bleeding Complications during Non-cardiac Surgery in Patients with Mechanical Heart Valves |
| Vinnikov I |
- |
Hyperglycemia Induces Loss of the Protective Endothelial Thrombomodulin Protein C System |
| Violi F |
- |
Thrombus Growth Is Mediated by Gp91phox |
| |
- |
Aspirin Does Not Equally Inhibit ThromboxaneA2 Formation in Long-Term Treated Patients |
| Virdis A |
- |
Adrenergic and Cholinergic Regulation of Local t-PA Release in Human Vasculature |
| Virtanen KS |
- |
Limited Antiplatelet Effect of Clopidogrel In Aspirin-treated Patients with Coronary Artery Disease Associates with Cardiac Endpoints |
| Vishnubhotla P |
- |
Successful Management of Pregnancy in a Patient with Type III Von Willebrand Disease and Platelet Storage Pool Disorder |
| Viskov C |
- |
The New Anticoagulant Octaparin Displays High Antithrombotic Action in Venous Thrombosis in Rabbits and Rats without Impairment of Hemostasis |
| Vissac AM |
- |
A Novel, Specific and Quantitative Assay for Measuring Factor V-Leiden, with a Single Step Clotting Method |
| |
- |
Measurement of Hirudin and Synthetic Thrombin Inhibitors in Plasma with a New Clotting Method, without Interference of Clotting Factor Levels |
| |
- |
Binding of B2GP1 to Various Phospholipid Mixtures Is Calcium Dependent and Is Dramatically Enhanced by Antibodies: Understanding the Anticoagulant Paradox |
| |
- |
Antibodies to Phospholipid Cofactor Proteins Inhibit Their Binding to High Affinity Plps But Strongly Enhance Their Binding to Low Affinity Plps |
| Viswabandya A |
- |
Data From APTT Clot Curves of Automated Photo-Optical Coagulometers Correlates Better with Heterogeneity of Clinical Presentation in Severe Hemophilia A than FVIII: C Levels |
| |
- |
Successful Surgical Haemostasis in Patients with von Willebrand Disease with Koate®DVI |
| |
- |
Molecular Characterization of Haemophilia B: 17 Novel Mutations in Patients of Indian Origin |
| Vitale G |
- |
Assessment of Protein S on Hepatopaths at the Last Stage |
| Vitale J |
- |
Abdominal Obesity and the Risk of Recurrent Deep Vein Thrombosis |
| Vitale G |
- |
Assessment of the Thrombophilic Risk in Women Candidates to Hormone Replacement Therapy |
| |
- |
Idiopathic Acquired Haemophilia: Two Case Reports with Different Severity of Clinical Manifestation, Both in Rapid Disappearing with Non-Aggressive Immunotherapy |
| Vitkovsky Y |
- |
Tissue Factor Expression and Proinflammatory Cytokines in Viral Hepatitis |
| Vitkovsky Y |
- |
Platelets Promote CD4+ Lymphocyte Adhesion to Extracellular Matrix and Fibronectin Under Flow: Role of Integrins, CD40 Ligand and P-Selectin Glycoprotein Ligand-1 |
| |
- |
Influence of Interleukins on CD 4+ T-lymphocyte Adhesion to Extracellular Matrix in Presence of Platelets under Flow Condition |
| Vitkovsky Yu A |
- |
Comparative Analysis of the APC Resistance in East Siberian Residences |
| Vitsenya M |
- |
Homocystein and Hemostatic Variables in Young Postinfarction Patients |
| Viuff D |
- |
Effect of rFVIIa Following Experimental Hemodilution with Two Different Colloids in a Rabbit Cuticle Bleeding Model |
| Viviani L |
- |
D-Dimer Measurement after Acute Ischemic Stroke Does Not Predict Long Term Outcome Events |
| Vlahovic G |
- |
Pediatric Thrombosis |
| Vlodavsky I |
- |
Effect of Heparanase on TF Expression and TFPI Release |
| Voest EE |
- |
Activation of the Fibrinolytic System by Amyloid Cross-b Structure Results In reply to: Cell Detachment AND Processing of Neuroendocrine Factors |
| |
- |
The Interaction of Platelets-tumor Cell Complexes with Vitronectin |
| Vogt L |
- |
Absolute Risk of Arterial Thromboembolism (ATE) Associated with Nephrotic Syndrome. Results from the Coltrane Study |
| Vogt C |
- |
Inhibition of Platelet Activation in Diabetic Rats by Chronic Treatment with the Guanylyl Cyclase Activator HMR1766 |
| Vogt L |
- |
Absolute Risk of Venous Thromboembolism (VTE) Associated with Nephrotic Syndrome. Results from the Coltrane Study |
| Vogt A |
- |
Association between Platelet Function Analyzer 100 (PFA-100) Closure Times (CT), Bleeding Time (BT), Platelet Aggregation (PA), Blood Cell Counts, Fibrinogen, Factor VIII (FVIII) and Von Willebrand Factor (VWF) |
| |
- |
Reliability of Platelet Function Analyzer 100 (PFA-100) Closure Times (CT) Induced by Collagen/Epinephrine (CO/EPI) and by Collagen/ADP (CO/ADP) |
| Voigt MW |
- |
TECHNOTHROMBIN® TGA a Novel Thrombin Generation Assay Suitable for the New Routine Coagulation Analyzer Ceveron® Alpha |
| Voinea M |
- |
VCAM-1 as Target for Immunoliposome-Mediated Drug Delivery to Activated Endothelial Cells |
| Voith B |
- |
Effect of Enoxaparin on the Safety, Tolerability, Pharmacodynamics, and Pharmacokinetics of BAY 59-7939 an Oral, Direct Factor Xa Inhibitor |
| Vojtech I |
- |
Hyperbaric Oxygen Therapy in Chronic Non-Healing Diabetic and Venous Ulcer |
| Volf I |
- |
Albumin Mildly Oxidized by the Myeloperoxidase Product Hypochlorous Acid Strongly Activates Platelets and Monocytes Via CD36 |
| Völker U |
- |
Proteomics as a Tool for Assessment of Therapeutics in Transfusion Medicine: Evaluation of Prothrombin Complex Concentrates |
| Vollot F |
- |
Influence of 10 Polymorphisms Located in Genes Coding for Factors Involved in Coagulation and Fibrinolysis on the Risk of Venous Thrombosis in Factor V Leiden Homozygotes: Study of 233 Subjects |
| Vollset SE |
- |
Low Methionine Concentration as a Risk Factor for Recurrent Venous Thrombosis |
| Volot F |
- |
Management of Glanzmann's Thrombasthenia Surgery: Contribution of Thrombelastogram (ROTEM®) |
| Volot F |
- |
WILFACTIN: Efficacy and Safety Evaluation of WILFACTIN (a Triple Secured Von Willebrand Factor Product with a Low Factor VIII Content) in Women with Severe Von Willebrand Disease during Gynaecological/Obstetrical Events |
| von Arbin M |
- |
Hemostatic and Inflammatory Disturbances are Present in Ischemic Stroke |
| Von Atzinger M |
- |
Effects of Leptospiral Proteins on Human Endothelial Cells |
| von Auer C |
- |
Extensive Venous Malformation Associated with Coagulation Abnormality: Treatment with Peginterferon Alfa 2a |
| Von Auer C |
- |
The Relation of Laboratory and Clinical Features to the Response to Plasma Exchange Therapy in the Treatment of Acquired Thrombotic Thrombocytopenic Purpura (TTP) |
| von Auer C |
- |
Epitope Mapping of Inhibitory Antibodies and Inhibitor Elimination with Rituximab in Patients with Acquired Haemophilia |
| von Auer C |
- |
Inhibitor Development in PTP's: A Retrospective Study in Germany |
| von Auer C |
- |
Evaluation of Thrombotic Events in Haemophiliacs Undergoing Major Orthopaedic Surgery without Thrombosis Prophylaxis |
| von Depka M |
- |
Detection and Expression of Three Missense Mutations in the Bb Fibrinogen Gene Resulting in A- and/or Hypofibrinogenaemia |
| von Elverfeldt D |
- |
Superparamagnetic Iron Oxide Uptake as Imaged By Magnetic Resonance Is Mediated by the Integrin Receptor MAC-1 (CD11b/CD18) Possible Implications on Imaging of Atherosclerotic Plaques |
| von Holt K |
- |
Initial Data on the Effects of Long-term Cigarette Mainstream Smoke Exposure and High Fat Diet in Apolipoprotein E-deficient Mice |
| von Kummer R |
- |
Prophylaxis of Thromboembolic Complications in Acute Ischemic Stroke with the Low Molecular Weight Heparin Certoparin (PROTECT) |
| von Rosen J |
- |
A Baltic Origin of the Common ADAMTS13 Mutation 4143insA |
| von Tempelhoff GF |
- |
Prevention of Venous Thromboembolism with Low-Molecular-Weight Heparin in Patients with Metastatic Breast or Lung Cancer Results of the TOPIC Studies |
| von zur Muehlen C |
- |
Superparamagnetic Iron Oxide Uptake as Imaged By Magnetic Resonance Is Mediated by the Integrin Receptor MAC-1 (CD11b/CD18) Possible Implications on Imaging of Atherosclerotic Plaques |
| von, Hertenstein B |
- |
Dose-dependent Platelet Activation and Microparticle Release by Different Clinical Antithymocyte Globulins |
| Voorberg J |
- |
Von Willebrand Factor-mediated Sorting of Endothelial Secretory Proteins |
| |
- |
Protein Kinase A-dependent Clustering of Weibel-Palade Bodies in Endothelial Cells |
| |
- |
Factor VIII Inhibitors in Hemophilia A during Immune Tolerance Induction |
| Vora S |
- |
Prevalence of Thrombophilic Mutations and Polymorphisms in Cases of Recurrent Pregnancy Loss (RPL) |
| Vorlova Z |
- |
Assay of the von Willebrand Factor Propeptide (VWFpp) to Identify Type 1 von Willebrand Disease (VWD) Patients with a Decreased von Willebrand Factor (VWF) Survival Phenotype |
| |
- |
The Incidence and Penetrance of Common VWF Gene Mutations in a Cohort of Type 1 VWD Patients: Results from the EU Funded MCMDM-1VWD Project |
| |
- |
The Factor VIII/von Willebrand Factor Antigen (FVIII/VWF : Ag) Ratio in Determining VWF Defects in Patients with von Willebrand Disease Type 1: Results from the European Multicenter MCMDM-1VWD Study |
| |
- |
In vitro Expression of Ten Missense Mutations in the VWF C-Terminal Domain Identified in Patients Diagnosed with Type 1 VWD: Results from the MCMDM-1VWD Study |
| |
- |
Association of FVIII/Von Willebrand Factor Measurements and PFA-100® with Bleeding Score in Type 1 Von Willebrand Disease (VWD) Families. The MCMDM-1 Study |
| |
- |
Multimer Pattern in Patients Diagnosed with Type 1 von Willebrand Disease in the European Study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 VWD (MCMDM-1VWD) |
| |
- |
Linkage Analysis of von Willebrand Disease Type 1 Phenotype, von Willebrand Factor Levels and Bleeding Symptoms with Von Willebrand Factor Gene Locus in the European Multicenter MCMDM-1VWD Study |
| |
- |
Mutation Profile in Patients Diagnosed with Type 1 von Willebrand Disease in the European Study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 VWD (MCMDM-1VWD) |
| |
- |
Cysteine Mutations in the von Willebrand Factor D3 Domain Correlate with Multimerization Defects in Patients Previously Diagnosed with von Willebrand Disease Type 1 in Patients Entered in the European Multicentre Study MCMDM-1VWD |
| |
- |
Abnormal Multimeric Pattern Is Not Associated with Increased Bleeding Symptoms in Index Cases of Families with Type 1 VWD. Results from the EU MCMDM-1 VWD Study |
| |
- |
Responsiveness to Desmopressin: Influence of Genotype in Patients Diagnosed with Type 1 von Willebrand Disease in the European Study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 VWD |
| |
- |
Analysis of Bleeding Score in Type 1 VWD Families in the MCMDM-1 Study |
| |
- |
Collagen Binding (VWF : CB) Is Less Sensitive Than Ristocetin Cofactor Activity (VWF : RCo) in Suggesting Von Willebrand Factor (VWF) Molecular Defects in Patients with Von Willebrand Disease Type 1: Results From the European Multicenter MCMDM-1VWD Study |
| |
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A Reduced VWF to FVIII Binding Capacity is not Uncommon in Patients With Type 1 Von Willebrand Disease: Results From the MCMDM-1VWD Study |
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Two Novel Type 1 Von Willebrand Disease Causing Mutations (G160W and N166I) in the Von Willebrand Factor Propeptide, Identified in the European Study MCMDM-1VWD, Are Responsible for Multimerization And Secretion Defects |
| Vormittag R |
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High Incidence of Symptomatic Venous Thromboembolism in Patients with Glioblastoma |
| Vormittag R |
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High Levels of Anti-protein Z Immunoglobulin G and M Antibodies, Persistent Lupus Anticoagulant and Thrombosis |
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C-Reactive Protein 3'UTR (+1444) C>T Polymorphism in Patients with Spontaneous Venous Thromboembolism |
| Vormittag R |
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Thrombophilia and Pregnancy Outcomes |
| Vormittag R |
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Favourable Pregnancy Outcome in Women with a History of Venous Thromboembolism and Prophylactic Low Molecular Weight Heparin (LMWH) |
| Voros G |
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Modulation of Angiogenesis during Adipose Tissue Development in Murine Models of Obesity |
| Vos HL |
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The Association of Prothrombin A19911G Polymorphism with Plasma Prothrombin Activity and Venous Thrombosis in a Large Population-Based Case-Control Study; Results of the MEGA Study |
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The Marburg I Polymorphism of Factor Seven-Activating Protease Is Not Associated with Venous Thrombosis |
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MTHFR C677T and the Risk Of Venous Thrombosis Interaction with Factor V Leiden and Prothrombin G20210A Mutations |
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Effects of Arginine Vasopressin 2 Receptor Polymorphisms on von Willebrand Factor and Factor VIII Levels and the Risk for Venous Thrombosis |
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Interleukin 1 Haplotypes and the Risk of Venous Thrombosis |
| Vos HL |
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Alignment of Factor V Sequences in Twelve Mammalian Species Shows Several Strongly Conserved Motifs in the B-Domain |
| Vos HL |
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The Prothrombin G19911A Is a Functional Non-coding Polymorphism |
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Association of Coagulation Factor VIII Haplotypes with Factor VIII Activity and the Risk of Venous and Arterial Thrombosis |
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ABO Blood Group Genotypes and the Risk of Venous Thrombosis: Effect of Factor V Leiden |
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The Effect of ABO Blood Group Genotypes on the Loading of von Willebrand Factor with A and B Antigens |
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Effects of Arginine Vasopressin 2 Receptor Polymorphisms on von Willebrand Factor and Factor VIII Levels and the Risk for Venous Thrombosis |
| Vos HL |
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A Database of Deficiency-Causing Mutations and Polymorphisms in the Factor V Gene |
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Haplotypes of the Fibrinogen Genes, Plasma Fibrinogen Levels and the Risk of Deep Venous Thrombosis |
| Voss H |
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Platelet Activation Markers and Procoagulant Phenotype of Monocytes do Correlate with Markers of Reperfusion Injury Following Reperfusion after Orthotopic Liver Transplantation |
| Vossen CY |
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Risk of Arterial Thrombosis in Carriers of a Familial Thrombophilic Defect |
| Vossen CY |
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Attitudes about Genetic Testing for Thrombophilia in a Large Family with Heritable Protein C Deficiency |
| Vossen CY |
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Linkage Analysis Reveals No Evidence for Loci Other than the Factor VII Gene Influencing Factor VII Levels |
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Evidence for Loci Pleotropically Influencing Inter-Related Clotting Factors |
| Voznyuk V |
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Vascular Complications at Patients with Polycythemia Vera: Interrelation between Endothelial Dysfunction and Haemostasis Disorders |
| Voznyuk V |
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The Role of Mild Forms of Coagulopathias and Pathology of Platelets in the Development of Menorrhagia and Metrorrhagia |
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The Role of Mild Forms of Coagulopathias and Pathology of Platelets in the Development of Menorrhagia and Metrorrhagia |
| Voznyuk V |
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Vascular Complications at Patients with Polycythemia Vera: Interrelation Between Endothelial Dysfunction and Haemostasis Disorders |
| Váradi K |
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Kinetics of in vivo Activation of Protein C In Healthy Animals |
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Thrombin Generation Assay A Sensitive Tool to Follow the Pharmacokinetics of Factor VIII Replacement Therapy in Haemophilia Patients |
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Applications of Thrombin Generation Assay in Characterizing FVIII Bypassing Agents |
| Vrints CJ |
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Pretreatment with Aspirin and Loading Dose Clopidogrel Obviates the Need for Glycoprotein Iib/Iiia Antagonists During Elective Coronary Stenting |
| Vroom M |
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Lung-Protective Mechanical Ventilation Attenuates Fibrin Generation in Healthy Lungs |
| Vu D |
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Investigation of Molecular Mechanisms Regulating Fibrinogen Secretion |
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Heterozygosity for a Novel FGG Trp253Cys Mutation Causes Hypofibrinogenemia by Specifically Impairing Fibrinogen Secretion |
| Vu L |
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Efficacy of the PFA-100® as a Screening Tool for Platelet Dysfunction |
| Vught M |
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Coagulation Disorders in Severe leptospirosis in Indonesia |
| Vukcevic V |
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Homocysteine Levels and MTHFR C677T Genotypes in Patients with Myocardial Infarction under Age 45 years |
| Vukovich T |
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C-Reactive Protein 3'UTR (+1444) C>T Polymorphism in Patients with Spontaneous Venous Thromboembolism |
| Vural O |
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The Prevalence of Von Willebrand's Disease in Trakya Region of Turkey |
| Vyas H |
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Effectiveness of Recombinant Activated FVII (rFVIIa) for the Treatment of Severe Bleeding Episodes in Pediatric Patients |
| Vystavkin AI |
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The Effect of TFPI On Thrombin Generation: a Mathematical Model |