1,233 results on '"Rodeghiero, F"'
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2. Thrombotic risk in patients with primary immune thrombocytopenia is only mildly increased and explained by personal and treatment‐related risk factors
3. Bleeders, bleeding rates, and bleeding score
4. Salvage Therapy for Resistant or Relapsing Acute Lymphoblastic Leukemia (ALL) after Idarubicin-Based Induction
5. Hematologic malignancies and thrombosis
6. Association of Platelet Thromboxane Inhibition by Low-Dose Aspirin With Platelet Count and Cytoreductive Therapy in Essential Thrombocythemia
7. Deep intronic variations may cause mild hemophilia A
8. Prospective evaluation of the clinical utility of quantitative bleeding severity assessment in patients referred for hemostatic evaluation
9. Alterations of mRNA processing and stability as a pathogenic mechanism in von Willebrand factor quantitative deficiencies
10. ISTH/SSC bleeding assessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders
11. Homozygous type 2N R854W von Willebrand factor is poorly secreted and causes a severe von Willebrand disease phenotype
12. von Willebrand factor variant p.Arg924Gln marks an allele associated with reduced von Willebrand factor and factor VIII levels
13. Validation of a rapid test (VWF-LIA) for the quantitative determination of von Willebrand factor antigen in type 1 von Willebrand disease diagnosis within the European multicenter study MCMDM-1VWD
14. Bleeding complications of antiangiogenic therapy: pathogenetic mechanisms and clinical impact
15. Molecular and phenotypic determinants of the response to desmopressin in adult patients with mild hemophilia A
16. Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM-1VWD study
17. Reduced von Willebrand factor survival in von Willebrand disease: pathophysiologic and clinical relevance
18. Incidence and risk factors for bleeding in 1104 patients with essential thrombocythemia or prefibrotic myelofibrosis diagnosed according to the 2008 WHO criteria
19. Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM‐1VWD)
20. Diagnosing type 1 von Willebrand disease: good for patientʼs health or for doctorʼs prestige?: reply
21. Addressing and proposing solutions for unmet clinical needs in the management of myeloproliferative neoplasm-associated thrombosis: A consensus-based position paper
22. Identification and functional characterization of a cytoplasmic nucleophosmin leukaemic mutant generated by a novel exon-11 NPM1 mutation
23. The dilution of vanadyl pyrophosphate, catalyst for n-butane oxidation to maleic anhydride, with aluminum phosphate: unexpected reactivity due to the contribution of the diluting agent
24. How to estimate bleeding risk in mild bleeding disorders
25. Impact of plasma von Willebrand factor levels in the diagnosis of type 1 von Willebrand disease: results from a multicenter European study (MCMDM‐1VWD)
26. ABO-incompatible bone marrow transplantation: a GITMO survey of current practice in Italy and comparison with the literature
27. THE CYTOTOXICITY OF CYTOKINE INDUCED KILLER CELLS IS FULLY RETAINED BY THE SORTED CD56+ CELL FRACTION AND SEEMS TO BE INDEPENDENT BY LYTIC DEGRANULATION: PH-P067
28. ABSENCE OF MICRONUCLEUS FORMATION IN CHO-K1 CELLS CULTIVATED IN PLATELET LYSATE ENRICHED MEDIUM PRODUCED BY PLATELET RICH PLASMA SONICATION: PH-P063
29. FAST PRODUCTION OF HUMAN PLATELET LYSATE BY USE OF ULTRASOUND FOR THE EX-VIVO EXPANSION OF BONE MARROW-DERIVED MESENCHYMAL STROMAL CELLS: PH-P062
30. Treatment of elderly patients (≥60 years) with newly diagnosed acute promyelocytic leukemia. Results of the Italian multicenter group GIMEMA with ATRA and idarubicin (AIDA) protocols
31. Survival and prognosis among 1545 patients with contemporary polycythemia vera: an international study
32. Four novel von Willebrand factor mutations in mild von Willebrand disease: PB 4.43–2
33. Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor
34. Hemorrhagic symptoms and bleeding risk in obligatory carriers of type 3 von Willebrand disease: an international, multicenter study
35. Distinctive natural history in hepatitis C virus positive diffuse large B-cell lymphoma: analysis of 156 patients from northern Italy
36. DCEP (dexamethasone, cyclophosphamide, etoposide, and cisplatin) is an effective regimen for peripheral blood stem cell collection in multiple myeloma
37. A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM‐1 VWD)
38. Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD
39. Factor VIII and von Willebrand factor changes after desmopressin and during pregnancy in type 2M von Willebrand disease Vicenza: a prospective study comparing patients with single (R1205H) and double (R1205H‐M740I) defect
40. Non-steady catalytic performance as a tool for the identification of the active surface in VPO, catalyst for n-butane oxidation to maleic anhydride
41. Reduced von Willebrand factor secretion is associated with loss of Weibel–Palade body formation
42. Different bleeding risk in type 2A and 2M von Willebrand disease: a 2-year prospective study in 107 patients
43. Further evidence of heterogeneity of gene defects in Italian families with factor XIII deficiency
44. Effect of the VWF promoter (GT)n repeat and single-nucleotide polymorphism c.-2527G>A on circulating von Willebrand factor levels under normal conditions
45. A comparison between two semi-quantitative bleeding scales for the diagnosis and assessment of bleeding severity in type 1 von Willebrand disease
46. Alternate use of thrombopoietin receptor agonists in adult primary immune thrombocytopenia patients: A retrospective collaborative survey from Italian hematology centers
47. Blood group significantly influences von Willebrand factor increase and half-life after desmopressin in von Willebrand disease Vicenza
48. F8 mRNA studies in haemophilia A patients with different splice site mutations
49. The discriminant power of bleeding history for the diagnosis of type 1 von Willebrand disease: an international, multicenter study
50. Homozygous R854W von willebrand factor is poorly secreted and causes a severe von willebrand disease phenotype: OC-WE-136
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