732 results on '"Federici, A. B."'
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2. Von Willebrand factor propeptide and pathophysiological mechanisms in European and Iranian patients with type 3 von Willebrand disease enrolled in the 3WINTERS‐IPS study
3. Genotypes of European and Iranian patients with type 3 von Willebrand disease enrolled in 3WINTERS-IPS
4. Bleeding symptoms in patients diagnosed as type 3 von Willebrand disease: Results from 3WINTERS‐IPS, an international and collaborative cross‐sectional study
5. Von Willebrand disease: Gaining a global perspective
6. A need to increase von Willebrand disease awareness: vwdtest.com – A global initiative to help address this gap
7. SARS-CoV-2 infection in patients with chronic lymphocytic leukemia: The Italian Hematology Alliance on COVID-19 cohort
8. Supportive transfusion therapy in cancer patients with acquired defects of hemostasis
9. Sixth Åland Island Conference on von Willebrand disease
10. Treatment of acquired von Willebrand syndrome in childhood
11. PL-11 Transfusion issues in cancer patients
12. Use of the von Willebrand factor concentrate with low factor VIII content to manage patients with inherited von Willebrand disease requiring surgical or secondary long‐term prophylaxis: an expert opinion paper from an Italian panel
13. How I treat the acquired von Willebrand syndrome
14. Evaluation and management of acute menorrhagia in women with and without underlying bleeding disorders: consensus from an international expert panel
15. Antibodies to von Willebrand factor in von Willebrand disease
16. Abnormal VWF modifies megakaryocytopoiesis: studies of platelets and megakaryocyte cultures from patients with von Willebrand disease type 2B
17. Principles in the Treatment of Bleeding
18. Efficacy and safety evaluation of Fanhdi ® , a plasma‐derived factor VIII/ von Willebrand factor concentrate, in Von Willebrand's disease patients undergoing surgery or invasive procedures: A prospective clinical study
19. Prophylaxis in patients with von Willebrand disease: who, when, how?
20. Activated prothrombin complex concentrate in acquired hemophilia A: an Italian registry-THE F.A.I.R. study: OR027
21. The natural history of occult or angiodysplastic gastrointestinal bleeding in von Willebrand disease
22. Clinical and molecular predictors of thrombocytopenia and risk of bleeding in patients with von Willebrand disease type 2B: a cohort study of 67 patients
23. Classification of inherited von Willebrand disease and implications in clinical practice
24. Von Willebrand Factor Promotes Endothelial Cell Adhesion via an Arg-Gly-Asp-Dependent Mechanism
25. Von Willebrand Factor Synthesized by Endothelial Cells from a Patient with Type IIB Von Willebrand Disease Supports Platelet Adhesion Normally but Has an Increased Affinity for Platelets
26. Classification and Clinical Aspects of von Willebrand Disease
27. Identification of type 1 von Willebrand disease patients with reduced von Willebrand factor survival by assay of the VWF propeptide in the European study: Molecular and Clinical Markers for the Diagnosis and Management of Type 1 VWD (MCMDM-1VWD)
28. Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): results from the European Study MCMDM-1VWD
29. Evaluation and management of postpartum hemorrhage: consensus from an international expert panel
30. Secondary prophylaxis in von Willebrand disease with highly purified VWF/FVIII concentrates: interim results of the PRO.WILL study: VWF25
31. New insights into type 3 von Willebrand disease: the 3Winters-Ips project update: VWF22
32. Von Willebrand disease and other bleeding disorders in women:: consensus on diagnosis and management from an international expert panel
33. Clinical characteristics and risk factors associated with COVID-19 severity in patients with haematological malignancies in Italy: a retrospective, multicentre, cohort study
34. Pregnancy complications and obstetric care in women with inherited bleeding disorders
35. Caution during use of desmopressin in IPSS
36. von Willebrand disease patients with associated risk factor(s) of venous thromboembolism: efficacy and safety of a von Willebrand factor product with a low factor VIII content: PB 1.43–1
37. Previously missed mutations in the MCMDM-1VWD type 1 von Willebrand disease study: PA 3.09–4
38. Re-evaluation of sequence variation in type 1 von Willebrand disease in the MCMDM-1VWD cohort: PA 3.09–1
39. Clinical efficacy and safety of DDAVP with or without tranexamic acid in inherited VWD: final results of the prospective and international study on 229 patients: PA 2.08–1
40. Macrothrombocytopenias with abnormalities of the VWF/GPIb-IX/filamin A/myosin 2A axis correspond to defects in megakaryocyte membrane formation and abnormal granule repartition.: OC 45.4
41. Distribution of the von Willebrand disease Types In 337 patients followed by a single hemophilia center since 2002: a comparison of von Willebrand disease patients classification after 10 years: OC 13.5
42. Third Åland islands conference on von Willebrand disease, 26–28 September 2012: meeting report
43. Current Diagnostic and Therapeutic Approaches to Patients with Acquired von Willebrand Syndrome: A 2013 Update
44. Prophylaxis in severe forms of von Willebrandʼs disease: results from the von Willebrand Disease Prophylaxis Network (VWD PN)
45. Efficacy and safety during formulation switch of a pasteurized VWF/FVIII concentrate: results from an Italian prospective observational study in patients with von Willebrand disease
46. On the Use of Desmopressin in von Willebrand Disease
47. Clinical, Laboratory, and Molecular Markers of Type 3 von Willebrand Disease
48. Classification and Clinical Aspects of Von Willebrand Disease
49. von Willebrandʼs disease: a report from a meeting in the Åland islands
50. Molecular characterization, recombinant protein expression, and mRNA analysis of type 3 von Willebrand disease: Studies of an Italian cohort of 10 patients
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