POSTER PRESENTATIONS VWD Connect Foundation Severe Von Willebrand Disease Patient RegistryInternational Society on Thrombosis and Haemostasis Congress 2025 Development Of A Working Definition of Severe Von Willebrand DiseaseAmerican Society of Hematology Conference 2024 VWD Connect Foundation Severe Von Willebrand Disease Patient RegistryThrombosis and Hemostasis Summit of North America 2024 VWD Connect Foundation U.S. Severe Von Willebrand Disease Patient RegistryWorld Federation of Hemophilia World Congress 2022 VWD Connect Foundation Severe Von Willebrand Disease Patient RegistryInternational Society on Thrombosis and Haemostasis Congress 2022 Unmet Needs In Women With Severe Von Willebrand DiseaseNational Hemophilia Foundation Bleeding Disorders Conference 2020 Identification Of Orthopedic And Genetic Needs Reported by Persons With Type 3/Severe Von Willebrand DiseaseNational Hemophilia Foundation Bleeding Disorders Conference 2019 Collection Of Patient Self-Reported Experiences At National Severe Von Willebrand Disease (VWD) ConferenceNational Organization for Rare Disorders Summit 2019 First National USA Type 3 Von Willebrand Disease (VWD) ConferenceWorld Federation of Hemophilia World Congress 2018 Data Collected at USA National Type 3 Von Willebrand Disease ConferenceWorld Federation of Hemophilia World Congress 2018 BACK TO RESEARCH BACK TO RESEARCH