von Willebrand Diseases Concept

subject area of

• A comparison of the quantitative ristocetin von willebrand factor assay by using fresh and fixed platelets  Academic Article
• A phase III study comparing secondary long-term prophylaxis versus on-demand treatment with vWF/FVIII concentrates in severe inherited von Willebrand disease.  Academic Article
• ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease  Academic Article
• ASH ISTH NHF WFH 2021 guidelines on the management of von Willebrand disease  Academic Article
• An international survey to inform priorities for new guidelines on von Willebrand disease  Academic Article
• Anemia-Induced Bleeding in Patients with Platelet Disorders  Academic Article
• Aortic stenosis and bleeding gastrointestinal angiodysplasia: is acquired von Willebrand's disease the link?  Academic Article
• Approaches to investigating common bleeding disorders: An evaluation of North American coagulation laboratory practices  Academic Article
• Assessment of von Willebrand disease as a risk factor for primary postpartum haemorrhage  Academic Article
• Bleeding assessment tools in the diagnosis of VWD in adults and children: a systematic review and meta-analysis of test accuracy  Academic Article
• Bleeding disorders, menorrhagia and iron deficiency: impacts on health-related quality of life  Academic Article
• Blood Disorders in Patients Undergoing Transcatheter Aortic Valve Replacement  Academic Article
• Challenges in defining type 2M von Willebrand disease: results from a Canadian cohort study  Academic Article
• Child with Wilms' tumor and von Willebrand disease at diagnosis and apparent complete response to chemotherapy after multiple relapses  Academic Article
• DDAVP—The Multipotent Drug in Patients With Coagulopathies  Academic Article
• Does an enzyme other than thrombin contribute to unexpected changes in the levels of the different forms of thrombin activatable fibrinolysis inhibitor in patients with hemophilia A, hemophilia B and von Willebrand disease?  Academic Article
• Efficacy and Safety of the Factor VIII/von Willebrand Factor Concentrate, Haemate-P/Humate-P: Ristocetin Cofactor Unit Dosing in Patients with von Willebrand Disease  Academic Article
• Efficacy of parenteral formulations of desmopressin in the treatment of bleeding disorders: A systematic review  Academic Article
• Evaluation of an automated method for measuring von Willebrand factor activity in clinical samples without ristocetin  Academic Article
• Evidence about HUI and hemophilia in response to Young et al. “How well does the Canadian hemophilia outcomes‐kids' life assessment tool (CHO‐KLAT) measure the quality of life of boys with hemophilia?”  Academic Article
• Frequent association of factor VII defects with other clotting disorders  Academic Article
• Gastrointestinal Angiodysplasia and Aortic Stenosis  Academic Article
• Gastrointestinal bleeding, angiodysplasia, cardiovascular disease, and acquired von Willebrand syndrome  Academic Article
• Gynecologic and obstetric management of women with von Willebrand disease: summary of 3 systematic reviews of the literature  Academic Article
• HIV Infection in a Defined Population of Swedish Haemophiliacs  Academic Article
• HIV-serology and lymphocyte subsets in relation to therapy and clinical development in haemophiliacs  Academic Article
• Haemostatic and replacement therapy in von Willebrand disease  Academic Article
• Health status and health-related quality of life associated with von Willebrand disease  Academic Article
• Helicobacter pylori causes gastrointestinal hemorrhage in patients with congenital bleeding disorders  Academic Article
• Hemophilia and von Willebrand's disease: 1. Diagnosis, comprehensive care and assessment. Association of Hemophilia Clinic Directors of Canada.  Academic Article
• Hemophilia and von Willebrand's disease: 2. Management. Association of Hemophilia Clinic Directors of Canada.  Academic Article
• Hepatitis, Epidemiology and Liver Function in Hemophiliacs in Sweden  Academic Article
• ISTH/SSC bleeding assessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders  Academic Article
• Immunoglobulin levels in haemophiliacs at HIV seroconversion and during follow up  Academic Article
• Laboratory assays of VWF activity and use of desmopressin trials in the diagnosis of VWD: a systematic review and meta-analysis  Academic Article
• Management of Inheritedvon Willebrand Disease in Italy: Results from the Retrospective Study on 1234 Patients  Academic Article
• Modification of von Willebrand Disease after Liver Transplantation  Academic Article
• Monocyte-macrophage (M-M) functions in asymptomatic hemophiliacs and supertransfused thalassemics.  Academic Article
• ON THE BLEEDER: A CASE OF VON WILLEBRAND'S DISEASE AND ITS TREATMENT WITH HUMAN ANTI-HAEMOPHILIC FACTOR.  Academic Article
• ON THE BLEEDER: A CASE OF VON WILLEBRAND'S DISEASE AND ITS TREATMENT WITH HUMAN ANTI‐HÆMOPHILIC FACTOR  Academic Article
• Outcomes of long‐term von Willebrand factor prophylaxis use in von Willebrand disease: A systematic literature review  Academic Article
• Platelet adhesion to multimerin 1 in vitro: influences of platelet membrane receptors, von Willebrand factor and shear  Academic Article
• Prevalence of hepatitis C virus infection among patients with inherited bleeding disorders in Newfoundland.  Academic Article
• Prophylactic efficacy and pharmacokinetically guided dosing of a von Willebrand factor/factor VIII concentrate in adults and children with von Willebrand's disease undergoing elective surgery: a pooled and comparative analysis of data from USA and European Union clinical trials.  Academic Article
• Reported prevalence of von Willebrand disease worldwide in relation to income classification  Academic Article
• Response to “The 2021 von Willebrand disease guidelines: Clarity and controversy”  Academic Article
• Safety and Efficacy of Continuous Infusion of a Combined Factor VIII – von Willebrand Factor (vWF) Concentrate (Haemate-P™) in Patients with von Willebrand Disease  Academic Article
• Studies of multimerin in patients with von Willebrand disease and platelet von Willebrand factor deficiency  Academic Article
• Surgical management of patients with von Willebrand disease: summary of 2 systematic reviews of the literature  Academic Article
• Technological advances in diagnostic testing for von Willebrand disease: new approaches and challenges  Academic Article
• The ISTH bleeding assessment tool as predictor of bleeding events in inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology  Academic Article
• The World Federation of Hemophilia Annual Global Survey 1999‐2018  Academic Article
• Treatment and prevention of acute bleedings in von Willebrand disease - efficacy and safety of Wilate^®, a new generation von Willebrand factor/factor VIII concentrate  Academic Article
• Unraveling von Willebrand factor deficiency  Academic Article
• Utilization of a surgical database to provide care and assess perioperative treatment and outcomes in patients with bleeding disorders  Academic Article
• VON WILLEBRAND'S DISEASE  Academic Article
• Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC  Academic Article
• Von Willebrand Disease: Gaining a global perspective  Academic Article
• Von Willebrand's Syndrome Presenting as an Acquired Bleeding Disorder in Association With a Monoclonal Gammopathy  Academic Article
• [Desmopressin--an effective agent in many hemorrhagic disorders].  Academic Article
• von Willebrand Disease Associated with Superficial Temporal Artery Pseudoaneurysm  Academic Article
• von Willebrand disease: an update in the Åland islandsSummary of a Nordic Symposium on von Willebrand disease, 24-25 September 1998, Mariehamn, Åland  Academic Article
• von Willebrand disease: proposing definitions for future research.  Academic Article
• von Willebrand factor levels in the diagnosis of von Willebrand disease: a systematic review and meta-analysis  Academic Article
• von Willebrand factor propeptide variants lead to impaired storage and ER retention in patient‐derived endothelial colony‐forming cells  Academic Article