Cristina Santoro
0000-0002-7181-447X
23 papers found
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Immune thrombocytopenia management during COVID‐19 pandemic: An Italian monocentric experience
Predictors of inhibitor eradication by primary immune tolerance induction in severe haemophilia A with high responding inhibitors
Comparison of quality of life, and emotional and functional profiles in older people with and without severe haemophilia
Clinical phenotype, fibrinogen supplementation and health-related quality of life in patients with afibrinogenemia
Management of patients with severe haemophilia a without inhibitors on prophylaxis with emicizumab: AICE recommendations with focus on emergency in collaboration with SIBioC, SIMEU, SIMEUP, SIPMeL and SISET
A multicenter real‐life study on anticoagulant treatment with direct oral anticoagulants in patients with P h‐negative myeloproliferative neoplasms
Effect of low or high doses of low‐molecular‐weight heparin on thrombin generation and other haemostasis parameters in critically ill patients with COVID‐19
Anagrelide in Essential Thrombocythemia (ET): Results from 150 patients over 25 years by the ‘Ph1‐negative Myeloproliferative Neoplasms Latium Group’
Right elbow arthropathy in a patient with severe haemophilia A
BAY 81‐8973 prophylaxis and pharmacokinetics in haemophilia A: Interim results from the TAURUS study
Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC
Dental invasive procedures in von Willebrand disease outpatients treated with high purity FVIII/VWF complex concentrate (Fanhdi®): experience of a single center
Identification of the Profile of the Patients with Hemophilia B Eligible for Treatment with Nonacog Alfa Once-Weekly
Immune tolerance induction with moroctocog‐alpha (Refacto/Refacto AF) in a population of Italian haemophilia A patients with high‐titre inhibitors: Data from REF.IT Registry
Thrombopoietin receptor agonists to control immune thrombocytopenia in patients with active lymphoma
The role of an accurate diagnosis of inherited thrombocytopenia as the basis for an effective treatment. A case of MYH9 syndrome treated with a TPO‐RA
The impact of psychosocial determinants on caregivers’ burden of children with haemophilia (results of the BBC study)
The burden of bleeds and other clinical determinants on caregivers of children with haemophilia (the BBC Study)
Clinical practice of personalized prophylaxis in hemophilia: Illustrations of experiences and benefits from two continents
Rate and appropriateness of polypharmacy in older patients with hemophilia compared with age-matched controls
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