Works matching AU Santoro, Cristina
Results: 79
The psychosocial impact of haemophilia from patients' and caregivers' point of view: The results of an Italian survey.
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- Haemophilia, 2024, v. 30, n. 2, p. 449, doi. 10.1111/hae.14926
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Laying the foundations for gene therapy in Italy for patients with haemophilia A: A Delphi consensus study.
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- Haemophilia, 2023, v. 29, n. 2, p. 435, doi. 10.1111/hae.14709
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- Article
IDEAL study: A real‐world assessment of pattern of use and clinical outcomes with recombinant coagulation factor IX albumin fusion protein (rIX‐FP) in patients with haemophilia B in Italy.
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- Haemophilia, 2023, v. 29, n. 1, p. 135, doi. 10.1111/hae.14689
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Haemophilia management and treatment: An Italian survey on patients', caregivers' and clinicians' point of view.
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- Haemophilia, 2022, v. 28, n. 2, p. 254, doi. 10.1111/hae.14504
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Predictors of inhibitor eradication by primary immune tolerance induction in severe haemophilia A with high responding inhibitors.
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- Haemophilia, 2022, v. 28, n. 1, p. 55, doi. 10.1111/hae.14431
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Single centre experience on Acquired Haemophilia A patients: Diagnosis, clinical management and analysis of factors predictive of response and outcome.
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- Haemophilia, 2021, v. 27, n. 6, p. e667, doi. 10.1111/hae.14395
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Comparison of quality of life, and emotional and functional profiles in older people with and without severe haemophilia.
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- Haemophilia, 2021, v. 27, n. 4, p. e525, doi. 10.1111/hae.14268
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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.
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- Haemophilia, 2020, v. 26, n. 6, p. 937, doi. 10.1111/hae.14172
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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.
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- Haemophilia, 2019, v. 25, n. 6, p. 1003, doi. 10.1111/hae.13859
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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.
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- Haemophilia, 2019, v. 25, n. 4, p. e288, doi. 10.1111/hae.13757
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The burden of bleeds and other clinical determinants on caregivers of children with haemophilia (the BBC Study).
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- Haemophilia, 2019, v. 25, n. 3, p. 416, doi. 10.1111/hae.13736
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The impact of psychosocial determinants on caregivers' burden of children with haemophilia (results of the BBC study).
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- Haemophilia, 2019, v. 25, n. 3, p. 424, doi. 10.1111/hae.13684
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Rate and appropriateness of polypharmacy in older patients with hemophilia compared with age‐matched controls.
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- Haemophilia, 2018, v. 24, n. 5, p. 726, doi. 10.1111/hae.13595
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Clinical and Prognostic Features of Essential Thrombocythemia: Comparison of 2001 WHO Versus 2008/2016 WHO Criteria in a Large Single-center Cohort.
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- 2021
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- journal article
Bioequivalence of recombinant factor VIII products: a position paper from the Italian Association of Hemophilia Centers.
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- Blood Transfusion (17232007), 2023, v. 21, n. 5, p. 441, doi. 10.2450/2023.0235-22
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Acquired haemophilia A: Italian Consensus Recommendations on diagnosis, general management and treatment of bleeding.
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- Blood Transfusion (17232007), 2022, v. 20, n. 3, p. 245, doi. 10.2450/2022.0238-21
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Pain assessment and management in Italian Haemophilia Centres.
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- Blood Transfusion (17232007), 2021, v. 19, n. 4, p. 335, doi. 10.2450/2020.0085-20
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Emergency management in patients with haemophilia A and inhibitors on prophylaxis with emicizumab: AICE practical guidance in collaboration with SIBioC, SIMEU, SIMEUP, SIPMeL and SISET.
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- Blood Transfusion (17232007), 2020, v. 18, n. 2, p. 143, doi. 10.2450/2019.0186-19
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- Article
Maternal Thrombophilia and Adverse Pregnancy Outcome: A Case-Control Study.
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- Acta Haematologica, 2015, v. 133, n. 2, p. 242, doi. 10.1159/000363048
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- Article
Rituximab in Previously Treated Primary Immune Thrombocytopenia Patients: Evaluation of Short- and Long-Term Efficacy and Safety.
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- Acta Haematologica, 2014, v. 132, n. 1, p. 24, doi. 10.1159/000355650
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- Article
Secondary prophylaxis of venous thromboembolism (VTE) with low dose apixaban or rivaroxaban in major-thrombophilia carriers.
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- Annals of Hematology, 2024, v. 103, n. 11, p. 4731, doi. 10.1007/s00277-024-06021-2
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- Article
Increased risk of recurrent thrombosis in patients with essential thrombocythemia carrying the homozygous JAK2 V617F mutation.
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- Annals of Hematology, 2010, v. 89, n. 2, p. 141, doi. 10.1007/s00277-009-0788-5
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- Article
Perceived well-being and mental health in haemophilia.
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- Psychology, Health & Medicine, 2020, v. 25, n. 9, p. 1062, doi. 10.1080/13548506.2020.1717556
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- Article
Direct oral anticoagulants for the treatment of atrial fibrillation in patients with hematologic malignancies.
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- Journal of Thrombosis & Thrombolysis, 2022, v. 54, n. 4, p. 625, doi. 10.1007/s11239-022-02702-9
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- Article
Italian experience with rVIII-single chain: a survey of patients with haemophilia A and their physicians.
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- Journal of Thrombosis & Thrombolysis, 2022, v. 53, n. 4, p. 934, doi. 10.1007/s11239-021-02599-w
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- Article
Von Willebrand factor with increased binding capacity is associated with reduced platelet aggregation but enhanced agglutination in COVID-19 patients: another COVID-19 paradox?
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- Journal of Thrombosis & Thrombolysis, 2021, v. 52, n. 1, p. 105, doi. 10.1007/s11239-020-02339-6
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PICC-related upper deep venous thrombosis in patients with hematological malignancies. Management of anticoagulant therapy according to the platelet count.
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- Journal of Thrombosis & Thrombolysis, 2020, v. 49, n. 3, p. 426, doi. 10.1007/s11239-020-02040-8
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- Article
Pharmacokinetics of Efmoroctocog alfa by Two-Compartment Model Highlights Hemophilia A Patients with Biphasic Decay, Long Mean Residence Time, and Beta Half-Life.
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- Journal of Clinical Medicine, 2024, v. 13, n. 17, p. 4986, doi. 10.3390/jcm13174986
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- Article
Intracranial Haemorrhage in Haemophilia Patients Is Still an Open Issue: The Final Results of the Italian EMO.REC Registry.
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- Journal of Clinical Medicine, 2022, v. 11, n. 7, p. 1969, doi. 10.3390/jcm11071969
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Current Choices and Management of Treatment in Persons with Severe Hemophilia A without Inhibitors: A Mini-Delphi Consensus.
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- Journal of Clinical Medicine, 2022, v. 11, n. 3, p. 801, doi. 10.3390/jcm11030801
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- Article
(Auto)Antibody Responses Shape Memory NK Cell Pool Size and Composition.
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- Biomedicines, 2022, v. 10, n. 3, p. 625, doi. 10.3390/biomedicines10030625
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Use of edoxaban for the treatment of venous thromboembolism in HIV‐infected patients.
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- HIV Medicine, 2020, v. 21, n. 3, p. e7, doi. 10.1111/hiv.12803
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- Article
Secondary prophylaxis of venous thromboembolism with direct oral anticoagulants: comparison between patients with major congenital thrombophilia versus non-thrombophilic patients.
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- Internal & Emergency Medicine, 2022, v. 17, n. 4, p. 1081, doi. 10.1007/s11739-021-02917-3
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A Comparative Study of Fine Needle Aspiration and Fine Needle Non-Aspiration Biopsy on Suspected Thyroid Nodules.
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- Endocrine Pathology, 2009, v. 20, n. 2, p. 108, doi. 10.1007/s12022-009-9074-2
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Role of treatment on the development of secondary malignancies in patients with essential thrombocythemia.
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- Cancer Medicine, 2017, v. 6, n. 6, p. 1233, doi. 10.1002/cam4.1081
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- Article
Activated prothrombin complex concentrate (FEIBA<sup>®</sup>) in acquired haemophilia A: a large multicentre Italian study – the FAIR Registry.
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- British Journal of Haematology, 2019, v. 184, n. 5, p. 853, doi. 10.1111/bjh.15175
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Analysis of 65 pregnancies in 34 women with five different forms of inherited platelet function disorders.
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- British Journal of Haematology, 2015, v. 170, n. 4, p. 559, doi. 10.1111/bjh.13458
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- Article
Direct oral anticoagulants in patients with hematologic malignancies.
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- Hematological Oncology, 2020, v. 38, n. 4, p. 589, doi. 10.1002/hon.2770
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- Article
The evolving landscape of gene therapy for congenital severe hemophilia: a 2024 state of the art.
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- Bleeding, Thrombosis & Vascular Biology, 2024, v. 3, n. 2, p. 1, doi. 10.4081/btvb.2024.144
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- Article
The evolving landscape of gene therapy for congenital severe hemophilia: a 2024 state of the art.
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- Bleeding, Thrombosis & Vascular Biology, 2024, v. 3, n. 2, p. 1, doi. 10.4081/btvb.2024.144
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Addressing some challenges of congenital fibrinogen disorders in 2023 and beyond.
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- Bleeding, Thrombosis & Vascular Biology, 2023, v. 2, n. 3, p. 13, doi. 10.4081/btvb.2023.75
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- Article
Rituximab in the Treatment of Postpartum Acquired Hemophilia A.
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- Journal of Coagulation Disorders, 2010, v. 2, n. 2, p. 1
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Rituximab in the Treatment of Postpartum Acquired Hemophilia A.
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- Journal of Coagulation Disorders, 2009, v. 1, n. 1, p. 1
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Severe maternal thrombocytopenia and prenatal invasive procedures: still a grey zone.
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- Journal of Perinatal Medicine, 2023, v. 51, n. 7, p. 861, doi. 10.1515/jpm-2022-0491
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- Article
Fostamatinib combined with TPO‐RAs or steroids as a bridge to monotherapy or as time‐limited continuous treatment in relapsed chronic ITP: A single‐centre case series.
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- British Journal of Haematology, 2024, v. 204, n. 5, p. 2129, doi. 10.1111/bjh.19450
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Eltrombopag second‐line therapy in adult patients with primary immune thrombocytopenia in an attempt to achieve sustained remission off‐treatment: results of a phase II, multicentre, prospective study.
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- British Journal of Haematology, 2021, v. 193, n. 2, p. 386, doi. 10.1111/bjh.17334
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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.
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- British Journal of Haematology, 2020, v. 190, n. 4, p. e214, doi. 10.1111/bjh.17003
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Right elbow arthropathy in a patient with severe haemophilia A.
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- British Journal of Haematology, 2020, v. 190, n. 4, p. 484, doi. 10.1111/bjh.16707
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Thrombopoietin receptor agonists to control immune thrombocytopenia in patients with active lymphoma.
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- British Journal of Haematology, 2019, v. 186, n. 6, p. e217, doi. 10.1111/bjh.16114
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Immune thrombocytopenia (ITP) World Impact Survey (iWISh): Patient and physician perceptions of diagnosis, signs and symptoms, and treatment.
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- American Journal of Hematology, 2021, v. 96, n. 2, p. 188, doi. 10.1002/ajh.26045
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