subject area of
- Antithrombin alfa in hereditary antithrombin deficient patients: A phase 3 study of prophylactic intravenous administration in high risk situations Academic Article
- Genomic approaches to bleeding disorders Conference Paper
- Haemophilia clinical care and research needs: Assessing priorities Academic Article
- Haemophilia: provision of factors and novel therapies: World Federation of Hemophilia goals and achievements Academic Article
- Home therapy for inherited bleeding disorders in South Africa: Results of a modified Delphi consensus process Academic Article
- Hypercoagulable States Academic Article
- Inherited Thrombophilia and the Risk of Arterial Ischemic Stroke: A Systematic Review and Meta‐Analysis Academic Article
- Inherited platelet disorders Academic Article
- Italian Registry of Haemophilia and Allied Disorders. Objectives, methodology and data analysis Academic Article
- Joint WFH-ISTH session: issues in clinical trial design Academic Article
- Life-Threatening Thrombosis in Mice With Targeted Arg48-to-Cys Mutation of the Heparin-Binding Domain of Antithrombin Academic Article
- Prothrombotic conditions in an unselected cohort of children with venous thromboembolic disease Academic Article
- Test-retest properties of the Patient Reported Outcomes, Burdens and Experiences (PROBE) questionnaire and its constituent domains Academic Article
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The 1st
WFH Gene Therapy Round Table: Understanding the landscape and challenges of gene therapy for haemophilia around the world Academic Article - Treatment for all: a vision for the future Academic Article
- Vaccination against COVID‐19: Rationale, modalities and precautions for patients with haemophilia and other inherited bleeding disorders Academic Article
- Variability of clinical manifestation of factor VII-deficiency in homozygous and heterozygous subjects of the European F7 gene mutation A294V Academic Article