Research and Practice in Thrombosis and Haemostasis

Papers
(The median citation count of Research and Practice in Thrombosis and Haemostasis is 0. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-04-01 to 2025-04-01.)
ArticleCitations
Editorial Board72
von Willebrand factor, ADAMTS-13, and thrombospondin 1 in relation to clinical outcomes in elderly patients with a recent myocardial infarction66
Uncertainties on the prognostic value of admission D‐dimer on venous thromboembolism occurrence in patients with COVID‐1961
Issue Information52
Letter in response to Colpani et al “A comparative study in type 2 von Willebrand disease patients using four different platelet-dependent von Willebrand factor assays”44
How We Write a Manuscript Discussion42
Factor V Leiden interferes with protein S activity assay42
Editorial Board41
Reply to “Comment on: A comparative study in type 2 von Willebrand disease patients using four different platelet-dependent von Willebrand factor assays”39
Thrombotic potential during pediatric acute lymphoblastic leukemia induction: Role of cell‐free DNA37
Characterization of the procoagulant phenotype of amniotic fluid across gestation in rhesus macaques and humans36
Impact of antiplatelet therapy on hemostatic plug formation in the setting of thrombocytopenia34
Andexanet alfa: trials just leave us with more questions34
Beyond platelet activation: dysregulated lipid metabolism in defining risk and pathophysiology of VITT32
Plasma microRNA-145-5p as a diagnostic biomarker for acute deep vein thrombosis30
Real-world andexanet alfa utilization and the association between delay in administration due to hospital transfer and all-cause inpatient mortality30
Risk assessment and prevention of cancer-associated venous thromboembolism in ambulatory patients with solid malignancies27
Fibrinogen levels and bleeding risk in adult extracorporeal cardiopulmonary resuscitation: multicenter observational study subanalysis25
Reassessment of dextran sulfate in anti-Xa assay for unfractionated heparin laboratory monitoring25
Outcomes of direct oral anticoagulants with aspirin vs warfarin with aspirin: a registry-based cohort study24
Recombinant porcine factor VIII: Lessons from the past and place in the management of hemophilia A with inhibitors in 202124
How to use and report data on D‐dimer testing in the COVID‐19 era?23
Transmembrane thiol isomerase TMX1 counterbalances the effect of ERp46 to inhibit platelet activation and integrin αIIbβ3 function23
Measuring the impact of hemophilia on families: Development of the Hemophilia Family Impact Tool (H‐FIT)22
Risk of venous thromboembolism in pediatric hospitalized patients undergoing noncardiac surgery: A report from the Children's Hospital‐Acquired Thrombosis consortium22
Issue Information22
Properdin (factor P) as a new target cleaved by factor XIa: Intrinsic coagulation at the crossroads with inflammation21
Comparison of novel thrombin generation methods with established techniques is mandatory20
Issue Information19
Antithrombotic treatment switching in elderly patients with atrial fibrillation and the risk of thromboembolism, bleeding, and cardiac death19
Thrombo‐inflammatory biomarkers and D‐dimer in a biracial cohort study19
Impact of oral anticoagulant choice for the secondary prevention of venous thromboembolism on the risk of inpatient bleeding19
18
Current practices in pediatric hospital‐acquired thromboembolism: Survey of the Children's Hospital Acquired Thrombosis (CHAT) Consortium18
Hormonal therapies and venous thrombosis: Considerations for prevention and management18
Loss of endogenous Nox2-NADPH oxidase does not prevent age-induced platelet activation and arterial thrombosis in mice18
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Inhibitor development upon switching from plasma-derived to recombinant factor VIII in previously untreated patients with severe hemophilia A: the PUP-SWITCH study17
Blocking domain 6 of high molecular weight kininogen to understand intrinsic clotting mechanisms17
Stability of specimens for use in the Centers for Disease Control and Prevention assays for factor VIII and IX inhibitors17
17
Risk factors for neurologic sequelae in children and adolescents with hemophilia after intracranial hemorrhage16
Revisiting important issues in cancer and atrial fibrillation16
Hormonal therapies in females with blood disorders: thrombophilia, thrombosis, hemoglobinopathies, and anemias16
RPTH year 6 article collection16
Use of rotational thromboelastometry to predict hemostatic complications in pediatric patients undergoing extracorporeal membrane oxygenation: A retrospective cohort study16
Thromboelastography and thrombin generation assessments for pediatric severe hemophilia A patients are highly variable and not predictive of clinical phenotypes16
Primary thromboprophylaxis in ambulatory symptomatic patients with COVID-19: a systematic review and meta-analysis of randomized controlled trials16
Factor eight inhibitor bypassing activity for refractory bleeding in coronary artery bypass grafting: A propensity‐matched analysis16
A systematic review of biomarkers among hospitalized patients with COVID‐19 predictive of venous thromboembolism: A communication from the Predictive and Diagnostic Variables Scientific and Standardiz16
Thrombus composition and thrombolysis resistance in stroke15
Untreated bleeds in people with hemophilia A in a noninterventional study and intrapatient comparison after initiating emicizumab in HAVEN 1–315
Thiol isomerase ERp18 enhances platelet activation and arterial thrombosis15
PB0965 Delphi Survey of Canadian Physicians to Determine Optimal Anticoagulant Treatment Approaches for Patients with Cancer and Splanchnic Venous Thrombosis14
PB0182 Development of a Non-Viral Gene Therapy Approach for Severe Bleeding Disorders14
PB0170 Evaluation of the Extended-Half Life FVIII Products' Measurement Accuracy and Precision With Five Different Types of Laboratory Assays14
PB0178 Factor X Enhances the Coagulant Potentials of Emicizumab14
Pseudohomozygous dysfibrinogenemia14
PB0165 Gene Correction of Human Hemophilia B Mutation by PAM-Flexible Cas9-Mediated Base-Editing Approach14
PB0197 Efficacy of Adjusted Weight-Based Dosing of DDAVP in Type 1 von Willebrand Disease13
PB0193 Financial Impact of Switching to Emicizumab from Conventional Haemostatic Agents in Acquired Haemophilia A13
PB0186 Results from BeneGene-1 Study: Prospective Collection of Bleeding Rate in Hemophilia B Patients Prior to Phase 3 Study (BeneGene-2) of Fidanacogene Elaparvovec13
PB0189 Knowledge and Attitudes of Haemophilic Patients Toward Gene Therapy13
PB0192 Novel Patient-Directed Learning in the Era of Novel Therapies13
PB0184 Ultrasound Mediated Delivery of CRISPR/Cas9 Plasmid in Hemophilia A Mice Shows Therapeutic levels of FVIII Following NHEJ Gene Editing13
PB0993 Thromboelastometry (ROTEM) in Detection of Hypercoagulability in Patients Referred for Thrombophilia Screening13
PB0201 Efanesoctocog Alfa Versus Extended Half-Life Factor VIII Therapies for Prophylaxis in Adolescents and Adults with Severe Hemophilia A: A Matching-Adjusted Indirect Comparison and Meta-Analysis13
PB0191 myGTR: A Patient Engagement Tool from the World Federation of Hemophilia Gene Therapy Registry13
PB1021 Using an Age and Fibrinogen Levels Adjusted D-Dimer Cutoff Significantly Improves the Specificity of D-Dimer Testing for Excluding Pulmonary Embolism12
PB0209 Clinical Manifestations of Patients with Congenital Dysfibrinogenemia with the Most Common Hotspot Mutation in FGA Gene p.Arg35His12
PB1015 Venous Thromboembolism in Patients with Newly Diagnosed Lymphoma and Its Association with ThroLy and Khorana Risk Scores12
PB1010 Exercise Could Reveal Pulmonary Vascular Abnormalities in Patients with Chronic Thromboembolic Pulmonary Disease - A Hemodynamic Study12
PB0998 Clinical Performance Evaluation of New Stago Systems for Protein S Levels Determination: sthemO PS Clot and sthemO PS Free on sthemO 301 Analyzer12
PB1003 The Factor V HR2 Haplotype and the Risk of Venous Thromboembolism (VTE): A Single Center Study12
PB1020 Simultaneous Generation of Thrombin and Plasmin in Patients with Deep Vein Thrombosis and High Levels of Lipoprotein (a)12
PB0206 Isolated Prolongation of APTT with Abnormal Bleeding Phenotype due to Intrinsic Tenase Defect - A Case Series12
PB0208 Spleen Rupture in Afibrinogenemia: Hemorrhagic or Thrombotic12
PB0238 Prospective, Phase III Study of the Efficacy, Safety, and Pharmacokinetics of a Human Antithrombin III Concentrate in Congenital Antithrombin Deficiency during Surgery or Childbirth11
PB0260 Immune Complex-Mediated Acquired von Willebrand Syndrome in a 5-year-old Boy after Allogeneic Hematopoietic Stem Cell Transplantation11
PB0249 Some Coagulation Profiles (PT, APTT, TT, FIB), Red Cell, Total White Cell, Platelet Counts and Their Indices Activity Levels in Persons Exposed to Wood Smoke (Firewood) in Calabar, Nigeria11
PB1077 A Novel C238G, PROC Mutation in Patients with Thromboembolism, Causes Intracellular Protein Retention11
PB1090 Modelling the Effects of 4-Factor Prothrombin Complex Concentrate for the Management of Factor Xa Inhibitor-Associated Bleeding11
PB1071 A Single-Domain Antibody Enhancing Protein S Activity Reduces Vaso-Occlusion in a Murine Model of Sickle Cell Disease11
PB0235 Phase 3 Study of the Efficacy, Pharmacokinetics, Immunogenicity and Safety of von Willebrand Factor/Factor VIII Concentrate in Patients with Severe von Willebrand Disease under 6 Years of Age11
PB1053 Protective Role of the SerpinE2 PN-1 in Renal Disease11
PB1060 Thrombin Generation and Fibrin Clot Structure in Nephrotic Patients with Primary Glomerular Disorders11
PB0269 Health-Related Quality of Life of, and Burden of Caring for, Thai Patients with Hemophilia Using the Canadian Hemophilia Outcomes-Kids' Life Assessment Tool v3.0 and Hemophilia Family Impact To11
PB0286 Population Pharmacokinetics and Pharmacodynamics of Bivalirudin in Children on Ventricular Assist Device Support11
PB1033 Delphi Consensus Recommendations for Neuraxial Anesthesia in Adults with Platelet Disorders and Coagulation Defects11
PB1047 A Patient with Severe, Refractory ITP and GI Bleeding is kept Hemodynamically Stable over Days with a Combination Therapy of Tranexamic Acid, Recombinant FVIIa, F XIII and Red Blood Cell Concen11
PB1078 Severe Thromboembolic Events in A Patient with Protein C and Protein S Heterozygous Deficiencies11
PB1081 Identification of Related Molecular Biological Effects on Two Novel Point Mutations in Inherited Antithrombin Deficiency11
PB0289 Association of Elevated Coagulation Factors VIII, IX and XI with Recurrent Thrombotic Events in Children with Non-Central Venous Line Deep Vein Thrombosis11
PB0300 Diagnosis of Thromboembolism in Children with Cancer: Validation of Diagnostic Algorithms Using Real-World Data10
PB0308 Anticoagulation Monitoring of UFH (Unfractioned Heparin) in a Pediatric Patient during Long Term ECMO (Extracorporeal Membrane Oxygenation)10
PB1117 Congenital Thrombotic Thrombocytopenic Purpura: Identification of Two Heterozygous Mutations in Splice Sites through NGS Sequencing10
PB0856 Time Course of Thrombocytopenia during DDAVP Test in a Boy with a De Novo c.4121G>A ( p.Arg1374His) Variant of the VWF Gene10
PB0299 Surface Modification of Lung Assist Device for Neonates by Dual-Modification with Antithrombin-Heparin (ATH) and Tissue Plasminogen Activator (t-PA)10
PB1103 Clinical Performance Evaluation of the New Stago Systems for APTT Determination: sthemO PTTA and sthemO CK Prest on sthemO 301 Analyzer10
PB0333 Therapeutic Plasma Exchange-Related Complications in Patients with Immune-Mediated Thrombotic Thrombocytopenic Purpura10
PB1132 Comparison of Thrombophilia Assay Results for the ISTH/SSC Plasma Standard from Different EQA Providers – Data from the EQATH Group10
PB1116 Applications of DOAC Removal in the Laboratory10
PB1106 A 2-min 30 sec at 4500g Centrifugation or a 11-min at 2500g are Comparable on 13 Coagulation Assays10
PB0295 Off-Label Use of Rivaroxaban in the Management of Three Cases of Pediatric Arterial Ischemic Stroke10
PB0301 Ocular Vein Occlusion in Pediatrics: Should Thrombophilia Investigation and Anticoagulant Treatment be Initiated?10
PB1125 Qualitative and Quantitative Assessment of Direct Oral Anticoagulants (DOACs) in Routine Clinical Practice10
PB0330 Relevance of ADAMTS13 Antigenic Levels in the Characterization of Pathological Mechanisms Associated with Immune-Mediated Thrombotic Thrombocytopenic Purpura (iTTP)10
PB0287 Thromboembolic and Hemorrhagic Events in Pediatric Patients Assisted with Mechanical Circulatory Support and Bivalirudin Anticoagulation: A Retrospective Observational Study10
PB0902 The Effect of Hypercortisolism on Platelet Function in Dogs with Cushing's Syndrome9
PB0867 Alpha-2-Macroglobulin Precludes Platelet Aggregation in Response to the Brain-Derived Neurotrophic Factor (BDNF)9
PB1220 DNase-1 Overcomes Thrombolytic rT-PA Resistance of Platelet-Rich Ischemic Stroke Thrombi9
PB1218 Aptamer Inhibitor of Von Willebrand Factor Induces Thrombolysis and Improves Vascular Patency Upon Immediate and Delayed Treatment in a Microfluidic Model of Stroke9
PB0527 Assessment of the Rats Model of Hemophilic Arthritis by Micro CT Scanning9
PB0480 Tinzaparin Safety in Patients with Severe Renal Impairment9
PB0478 Safety and Efficacy of Rivaroxaban as Extended-Phase Anticoagulation in Patients with Cancer and Venous Thromboembolism: A Preliminary Data Analysis from the MAC Project9
PB1245 Efficacy, Safety and Dosing of Pasteurized Plasma-Derived von Willebrand Factor/Factor VIII Concentrate for the Treatment of von Willebrand Disease: A Systematic Review9
PB0455 Bilateral Asynchronous Adrenal Infarction in JAK2-Positive Essential Thrombocythemia9
PB0896 Time-and Distance-Resolved Robotic Imaging of Fluid Flow in Vertical Microfluidic Strips: A New Technique for Quantitative, Multiparameter Global Measure of Haemostasis9
PB0883 Defining the Role of Hepcidin and Ferroportin Interactions in Regulating Platelet Function9
PB0866 Glycoprotein VI: An Interesting Target to Prevent Early Stent Thrombosis?9
PB1226 Acquired Haemophilia A in Finland: A Nationwide Study of Incidence, Treatment and Outcomes9
PB1273 Inhibitor Recurrence on Emicizumab Prophylaxis in Tolerized Patients with Severe Hemophilia A9
PB1249 Prospective, Observational Study of the Clinical Characteristics of Adults and Adolescents with Severe Hemophilia A9
PB0477 Safety and Efficacy of Direct Oral Anticoagulants in Patients with Chronic Thromboembolic Pulmonary Hypertension9
PB0900 Developing Standards to Support Platelets and Platelet Components9
PB0886 Novel Small-Molecule Inhibitors of Clot Retraction and Thrombin- Induced Platelet Aggregation, That Do Not Inhibit PAR-1-Induced Platelet Aggregation9
PB0858 Evaluation of Automated Chemiluminescent von Willebrand Factor Assays in the Diagnosis of von Willebrand Disease9
PB0884 Development of a Platform to Study Thrombogenicity of Clinically- Used Stents9
PB0464 Smaller Nadroparin Dose Reductions Required for Patients with Renal Impairment: A Multicenter Study9
PB1254 A New Tool to Assist in Treatment Selection - The World Federation of Hemophilia (WFH) Shared Decision-Making (SDM) Tool9
PB1275 Multicenter and Cross-Sectional Study of Joint Damage of Patients with Non-Severe Hemophilia: A “Mediterranean Group” Study9
PB1228 Inhibitor Detection in Acquired Hemophilia A: A Comparison between the Nijmegen Modified Bethesda Assay and an Anti-FVIII ELISA9
PB1344 Impact of Spleen Tyrosine Kinase Inhibition on Vaccine-Induced Thrombotic Thrombocytopenia Antibody-Induced Procoagulant Platelet and Thrombus Formation8
PB0551 A Comparison of USP Potency Adjusted and Mass Adjusted Heparins of Bovine, Ovine, and Porcine Origin in Various Assays8
PB1290 Successful Very Low Dose Immune Tolerance Induction with Albutrepenonacog Alfa in a Severe Hemophilia B Child with Anaphylactic Reaction to Factor IX8
PB0533 New Low Molecular Weight Heparin Antidote Based on an Antithrombin Mutant8
PB0532 The Factor XIa Antibody Osocimab Combined with Enoxaparin Strongly Inhibits Clotting in Extracorporeal Circuits in vitro8
PB1317 Assessment of the Combined Effects of Emicizumab and Fitusiran with In Vitro Spiking of Emicizumab and Simulated Fitusiran into Factor VIII Deficient Plasma Using Thrombin Generation Assay8
PB0566 Prediction and Validation of the Effects of Targeting either Coagulation FXI Activation or Activity on Thrombin Generation8
PB1348 Thrombopoietin Receptor Agonist and Rituximab Combination Therapy in Patients with Refractory Primary Immune Thrombocytopenia. A Single-Center Study8
PB1300 Intramural Hematoma of Gastrointestinal Tract in People With Hemophilia: A Pooled Study8
PB0534 Rapid Measurement of DOAC Concentration and Platelet Function Using Whole Blood in a Disposable Microfluidic Device8
PB1314 Risk Assessing Medical Inpatients for Bleeding Events: The Medical Inpatients Thrombosis and Hemostasis (MITH) Study8
PB0562 Effects of High-Fat and High-Carbohydrate Meals on Coagulation and Anticoagulation Factors and Lipid Profile8
PB1332 Heightened Thrombosis in Immune Thrombocytopenia: Insights into the Risk Factors and Clinical Outcomes from an Australian Hospital Cohort8
PB1352 A Survey on Anticoagulation in Patient with ITP8
PB1301 Low-Titer Inhibitor and Decreased FVIII Activity to 1.1% with Increased Bleeding in a 4 Year Old Patient with Congenital Mild Hemophilia A8
PB0542 Investigating Thrombin-Loaded Fibrin in Whole Blood Clot Microfluidic Assay via Fluorogenic Peptide8
PB1315 Weight-Band Dosing with Mim8: Using Modelling to Support a Streamlined Approach to Haemophilia A Treatment8
PB1329 Retrospective Study of the Effectiveness and Safety of the Use of rIX- FP in Patients with Haemophilia B. Experience of Four Centres in the Region of Castilla y León8
PB0586 Protein S Deficiency is Associated with an Increased Risk of Deep Vein Thrombosis in Pregnant Women Using Oral Contraceptive7
PB1390 Gray Platelet Syndrome- Novel NBEAL2 Pathogenic Variants and Hemostasis Evaluation by Global Coagulation Assays7
PB0634 A Phase 3, Single-Arm, Multicenter, Open-Label, One-Way Crossover Study to Evaluate the Efficacy and Safety of Fitusiran Prophylaxis in People with Severe Hemophilia A or B, with or without Inh7
PB0352 Non-Pathogenic Anti-PF4 Antibodies after SARS-CoV-2 Vaccines: Long Term Follow-Up7
PB1143 Analytical Performance Evaluation of a New Stago System SthemO 2017
PB1381 Value of Next-Generation Sequencing in the Diagnosis of Platelet Function Disorders7
PB1411 Study of Endothelial Dysfunction in Patients with Unprovoked Venous Thromboembolism through Endothelial Colony-Forming Cell In Vitro Characterization7
PB1385 Developing a Stem Cell-Based Model for Glanzmann Thrombasthenia to Explore VWF-GPIb Axis during Megakaryopoeisis7
PB1359 Fc Modified KKO Blocks Thrombosis in Heparin-Induced Thrombocytopenia (HIT), But not in Vaccine-Induced Immune Thrombotic Thrombocytopenia (VITT)7
PB1357 Addition of Platelet Factor 4 in the Heparin-Induced Platelet Activation (HIPA) Test for the Diagnosis of Heparin Induced Thrombocytopenia (HIT): Results from a Restrospective Monocentric Study7
PB1370 Thrombocytosis and Acquired Bleeding Disorders in Patients with Myeloproliferative Neoplasms7
PB1402 NBEAL2 and the Intragranular Proteoglycan, Serglycin, Both Contribute to the Initiation and Progression of Aortic Aneurysms7
PB0358 Hereditary Bleeding Disorders Web-Based Registry of Patients with Inherited Platelet Disorders7
PB0347 Argatroban or Bivalirudin for Suspected or Confirmed Heparin Induced Thrombocytopenia at a Large Academic Medical Center7
PB1140 Laboratory Features and Genotype of a Family with Heritable Dysfibrinogenaemia (HD)7
PB0625 Emicizumab Prophylaxis in People with Hemophilia A Aged >50 Years withComorbidities:ExperienceFromtheATHN7Hemophilia Natural History Study7
PB1405 Development of a Method for the Detection of the JAK2V617F Mutation in Human Circulating Endothelial Cells7
PB1378 Complex Phenotypic Expression of an ADP Receptor (P2Y12) Defect in Greater Swiss Mountain Dogs7
PB1376 Periprocedural Hemostatic Outcomes in Bleeding of Unknown Cause7
PB0589 Human Transthyretin (hTTR) Amyloid Fibrils Induce Plasma Clotting by Activating the Intrinsic Pathway of Blood Coagulation: Implications in the Pathogenesis of hTTR Intracardiac Thrombosis7
PB0590 The Control of Protein Binding on Bio-Interface by a Novel Coating to Prevent Contact Activation on Biomaterials7
PB0627 Management of Invasive Procedures in Patients with Hemophilia A Receiving Emicizumab Prophylaxis: Real-World Data from a National Hemophilia Treatment Center7
PB0369 New Insights into the Formation of Platelets (Thrombopoiesis) from Infused Megakaryocytes (Mks) into Mice7
PB0349 Anti-PF4-Antibodies in Patients Suspected of Vaccine-Induced Immune Thrombotic Thrombocytopenia After SARS-CoV-2 Vaccination7
PB1160 Detection of Drug-Induced Platelet Inhibition with Sonic Estimation of Elasticity via Resonance Using the QuantraTM: An Observational invitro Study with Healthy Volunteers7
PB0664 Treatment Adherence in Young People with Hemophilia: Perceptions of UK Healthcare Professionals7
PB0622 A Report of the Measurement of Steady State Emicizumab Levels in an Irish Cohort of Persons with Severe Haemophilia A7
PB1142 A Rapid Centrifugation 4000 g, 4 min Does not Impact Routine Coagulation Assays7
PB0612 COVID-19: Predictive Value of Methemoglobinemia7
PB0594 Factor XI Localization in Human Deep Venous Thrombus and Function of Activated Factor XI on Mural Thrombus Formation Under Low-Shear Condition7
PB1429 NETs Promote Gasdermin-D-Dependent Pulmonary Thrombosis in Mice Exposed to Cigarette Smoke and Flu6
PB1465 Venous Thromboembolism in Hospitals Belonging to APHP: A Retrospective Cross-Sectional Study Using the Hospital Discharge Database (PMSI) from Clinical Data Warehouse6
PB1471 Age- and Sex Specific Risks of Major Cardiovascular Complications and Death following Elective Hip and Knee Arthroplasty in the Netherlands: A Dutch Hospital Data Registry Study6
PB1447 Factor V Leiden: An Independent, Gender-Dependent Risk Factor for Venous Thromboembolism6
PB1189 Concentrations of Direct Oral Anticoagulants Acting as FXa Inhibitors Could not be Accurately Determined in Patients Treated with Therapeutic Doses of Low Molecular Heparin as Bridging Therapy6
PB0386 Increased Platelet Expression of the Transcriptional Suppressor ETV6 Can Be Detected by Immunofluorescence on the Blood Smear and Associates with ETV6-Related Thrombocytopenia6
PB0376 Vacuolar-Type ATPase Dependent Acidification of Megakaryocyte and Platelet α-Granules Maintains Packaging of VWF6
PB1208 Thrombin Activatable Fibrinolysis Inhibitor Dependent Effects on Whole Blood Clot Formation and Lysis Dynamics Across the Peripartum Period6
PB1431 Effect of Allele-Selective Silencing of von Willebrand Factor in Mice on Experimental Bleeding and Thrombosis Models6
PB0698 Determinants of Desmopressin Response in Bleeding Disorders: a Systematic Review and Meta-Analysis6
PB0679 Clinical Characteristics and Disease Outcomes in Previously Treated Patients with Haemophilia: Results from a Real-World Study in Europe and United States6
PB0669 Final Analysis of Long-Term Clinical Outcomes of Recombinant Factor IX Fc Fusion Protein Prophylaxis in Adults ≥50 Years with Severe Hemophilia B6
PB1203 The Influence of Human Immunodeficiency Virus Infection and Antiretroviral Therapy on Plasma Clot Properties in a Group of Black South African Women6
PB0429 Potential Difference in Platelet Aggregation between Clinical Dexmedetomidine and Experimental Medetomidine Due to Dose Differences6
PB0403 A Common Variant in GRK5 Reveals a PAR1-Specific Regulation in Platelets6
PB1204 Synergistic Role in Accelerating Clot Formation and Fibrin Polymerisation of Cancer Cells and Platelets: a Thromboelastometric Study6
PB0387 Characterising the Molecular Pathways Controlled by ETV6 during Megakaryopoiesis6
PB0715 H3 Alters the Behavior of Endothelial Cells In Vitro6
PB0694 A Chemiluminescent-Based Multiparameter Platform for Simultaneous Measurement of Factor VIII Activity and Thrombin Generation6
PB1441 The Risk of Recurrent Venous Thromboembolism of Patients with Homozygous or Double Heterozygous Factor V Leiden and/or Prothrombin G20210A Mutation: A Prospective Cohort Study6
PB1453 Clinical Course and Long-Term Outcomes of Cerebral Venous Sinus Thrombosis in Asians6
PB0444 Residual Pulmonary Vascular Obstruction is Associated with Prothrombotic Fibrin Clot Phenotype in Patients Following Pulmonary Embolism6
PB0412 Simulating the Impact of Thrombin on Platelet Function Requires Simultaneous Activation of Both PAR-1 and PAR-46
PB1166 The True Effect of Haemolysis Interference on Routine Coagulation Tests Using Paired Matched Samples Performed on the Sysmex CN-Series Coagulation Analyser6
PB0397 Differential Requirement for Ligand Valency in the Activation of CLEC-2 in Human and Humanised Mouse Platelets6
PB1526 Impact of Maternal Cannabis Use on Fetal Vascularized Tissue Development5
OC 20.4 The Impact of Gene Therapy on the Musculoskeletal Health of Patients with Severe Hemophilia A5
OC 18.1 The Role of Mitochondrial Calcium Uniporter in Platelet Function5
Editorial Board5
OC 20.5 The WFH Gene Therapy Registry: A Collaborative Approach Towards a Global Resource for the Long-Term Follow-up of People with Hemophilia Treated with Gene Therapy5
HTRS2023.P2.20 Common documentation errors in the electronic health records of persons with hemophilia B5
OC 06.4 Therapeutic Efficacy of aNovel Humanized anti-ADAMTS13 Antibody to Treat Left Ventricular Assist Device-Induced Acquired Von Willebrand Syndrome5
HTRS2023.O6B.2 Allosteric regulation of coagulation factor IXa5
OC 02.3 OC 02.3 Risk Factors for Severe Postpartum Hemorrhage after Assisted Reproductive Technology: Data from the French HEMOTHEPP Cohort Study5
PB0727 The Role of Thrombin and Thrombin Signaling in Chronic LCMV Infection5
OC 03.2 Characterization of Peripheral Monocyte Subsets in a Prospective Cohort of Patients with Acute Stroke Suspicion: Results of BOOST Study5
PB1486 Quality of Anticoagulation Management in Patients Receiving Warfarin at Private Cardiac Centers in Addis Ababa, Ethiopia5
PB1463 Clinical Predictors of In-Hospital Mortality in Patients with Acute Pulmonary Embolism: 15-Years Experience in a Single Center in Argentina5
PB1505 C-Reactive Protein Across the Menstrual Cycle in Females with Sickle Cell Disease5
LB 02.3 Targeted Thromboprophylaxis in Patients with Lower Limb Trauma Requiring Immobilization : Stepped Wedge Randomized Trial5
OC 24.5 A Phase 1 Study to Evaluate the Pharmacokinetics and Safety of a PEGylated-Recombinant Human Coagulation Factor VIII-Fc Fusion Protein in Patients with Severe Hemophilia A5
OC 20.3 Improved Joint Health After Gene Therapy with Dirloctocogene Samoparvovec (SPK-8011) in People with Hemophilia A5
OC 14.4 Recombinant ADAMTS13 Prophylaxis in Patients with Congenital Thrombotic Thrombocytopenic Purpura: Interim Analysis from Phase 3B Continuation Study5
HTRS2023.P4.14 Using heparin-calibrated assays to estimate anti-factor Xa activity of factor Xa inhibitors: correlation analysis of published data5
OC 12.1 First Evidence of Improvement of Long-term Joint Outcomes through Ultrasound for Hemophilia; from 3-Years Prospective J-DaUPHIN Study5
HTRS2023.P2.18 Pediatric persons with hemophilia A on EHL-FVIII or emicizumab prophylaxis require iron therapy despite low annualized bleeding rate5
OC 05.2 Impact of Heparin on Disease State Transition in Hospitalized, Non-Critically Ill Patients with COVID-19; Secondary Analysis of an International Multi-Platform RCT5
LB 02.1 Extending Venous Thromboembolism Secondary Prevention with Apixaban in Cancer Patients. The EVE Trial5
OC 02.1 Dose-Dependent Elimination of HPA-1a Platelets by Subcutaneous RLYB212, a Monoclonal Antibody to Prevent Fetal and Neonatal Alloimmune Thrombocytopenia5
PB1503 Significant Effect of Hormonal Contraception on Venous Thromboembolism Risk in Women with Sickle Cell Disease, but is Estrogen the Culprit?5
PB0729 Thrombophilia in Patients with Acute Viral Infections of the Respiratory Tract5
PB0713 Increased Tissue Factor mRNA Expression is Associated with High Plasma Levels of Activated Factor VII-Antithrombin Complex and Predicts Mortality in Primary Liver Cancer5
LB 02.4 Anti-Platelet Factor 4 Induced Immunothrombosis Independent of Heparin or Vaccination5
LB 01.2 Emicizumab Prophylaxis Instead of Immunosuppressive Therapy in Patients with Acquired Hemophilia A (AHA)5
OC 23.2 In Vitro Generated Megakaryocytes for the Detection of HPAAlloantibodies in Clinical Samples5
OC 19.5 Epithelial Neuropilin-1 is Regulated by the Gut Microbiota Promoting Vascularization of Small Intestinal Villus Structures5
PB1511 Systematic Review on Hemostatic Biomarkers Predictive for Postpartum Hemorrhage5
OC 15.4 ADAMTS13 Results for the SSC Plasma Standard from ECAT and UK NEQAS External Quality Assessment Programmes5
HTRS2023.P3.2 Clinical outcomes in patients with acute hepatic porphyria treated with givosiran who stopped hemin prophylaxis at study entry: post hoc analyses from the phase 3 ENVISION study through 5
OC 09.4 C1-Inhibitor Levels and Venous Thromboembolism: Results from a Mendelian Randomization Study5
HTRS2023.P2.1 Will my patient bleed? Management and outcomes for patients with severe FXI deficiency5
OC 05.3 Incidence and Risk Factors for Venous Thromboembolism in Hospitalized Patients Across Three Major COVID-19 Variants in an Asian Cohort5
PB1510 Circulating Extracellular Vesicles and Neutrophil Extracellular Traps Contribute to Endothelial Dysfunction in Pregnant Women with Preeclampsia5
OC 14.2 Pharmacokinetic Characteristics of ADAMTS13 in Patients with Congenital Thrombotic Thrombocytopenic Purpura: Interim Results from a Phase 3 Randomized, Controlled, Open-Label, Crossover Study5
PB1498 Risk of Venous Thromboembolic Disease and Adequacy of Prophylaxis in Hospitalized Cancer Patients in Uruguay5
PB1476 Occurrence of Hospital-Associated Thrombosis Despite Thromboprophylaxis in the Setting of Current Thromboprophylaxis Strategies: An Observational Cross-Sectional Study5
LB 01.3 Factor XIII 24-Hour Trajectory Analysis in Severely Injured Patients: Post-hoc Analysis of the Pragmatic Randomized Optimal Platelet and Plasma Ratios (PROPPR) Study5
PB1500 In-Hospital Vein Thromboembolism Prevention in Patients with Atrial Fibrillation5
PB0037 Thrombotic Cerebrovascular Outcomes in Patients with Fibromuscular Dysplasia Treated with Antiplatelet Agents or Anticoagulants: A Single-Center Experience4
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