335 results on '"Casale, Maddalena"'
Search Results
2. Absence of blood donors’ anti-SARS-CoV-2 antibodies in pre-storage leukoreduced red blood cell units indicates no role of passive immunity for blood recipients
3. Transient erythroblastopenia of childhood after Covid-19 infection: a case report
4. Beta thalassemia major, hypogonadism and cardiovascular risk
5. Mortality in β-thalassemia patients with confirmed pulmonary arterial hypertension on right heart catheterization
6. Limited access to transcranial Doppler screening and stroke prevention for children with sickle cell disease in Europe: Results of a multinational EuroBloodNet survey.
7. Recommendations for the management of acute immune thrombocytopenia in children. A Consensus Conference from the Italian Association of Pediatric Hematology and Oncology.
8. Headache in beta-thalassemia: An Italian multicenter clinical, conventional MRI and MR-angiography case-control study
9. Disease burden and quality of life in children with sickle cell disease in Italy: time to be considered a priority
10. Manual erythroexchange in sickle cell disease: multicenter validation of a protocol predictive of volume to exchange and hemoglobin values
11. No increased cerebrovascular involvement in adult beta-thalassemia by advanced MRI analyses
12. Absence of blood donors’ anti-SARS-CoV-2 antibodies in pre-storage leukoreduced red blood cell units indicates no role of passive immunity for blood recipients
13. P1461: INFLAMMATORY AND SENESCENCE-ASSOCIATED MEDIATORS AFFECT THE PERSISTENCE OF HUMORAL RESPONSE TO COVID-19 MRNA VACCINATION IN TRANSFUSION-DEPENDENT BETA-THALASSEMIC PATIENTS
14. Early splenectomy in sickle cell disease: another piece of the puzzle
15. Juvenile erythrocytosis in children after liver transplantation: prevalence, risk factors and outcome
16. Asymptomatic intracranial aneurysms in beta-thalassemia: a three-year follow-up report
17. Inflammatory and senescence‐associated mediators affect the persistence of humoral response to COVID ‐19 mRNA vaccination in transfusion‐dependent beta‐thalassemic patients
18. Reply to “Hepatocellular carcinoma in thalassemia and other hemoglobinopathies”
19. Current challenges in the management of patients with sickle cell disease – A report of the Italian experience
20. The Areal Project: How Virtual Reality Application Could Enhance Patient's Quality Time during Transfusion Therapy in Adult Patients with Thalassemia and Sickle Cell Disease
21. Incidence of cancer and related deaths in hemoglobinopathies: A follow‐up of 4631 patients between 1970 and 2021
22. Premature aging of the immune system affects the response to SARS-CoV-2 mRNA vaccine in β-thalassemia: role of an additional dose
23. Hereditary hypochromic microcytic anemia associated with loss‐of‐function DMT1 gene mutations and absence of liver iron overload
24. Introductory Chapter: Introduction to the History, Pathology and Clinical Management of Sickle Cell Disease
25. Long-term treatment with deferiprone enhances left ventricular ejection function when compared to deferoxamine in patients with thalassemia major
26. Premature aging of the immune system affects the response to SARS-CoV-2 mRNA vaccine in β-Thalassemia: additional dose role
27. Incidence of cancer and related deaths in hemoglobinopathies: A follow‐up of 4631 patients between 1970 and 2021.
28. Thalassaemia is paradoxically associated with a reduced risk of in‐hospital complications and mortality in COVID‐19: Data from an international registry
29. Good Clinical Practice of the Italian Society of Thalassemia and Haemoglobinopathies (SITE) for the Management of Endocrine Complications in Patients with Haemoglobinopathies
30. Transfusional Approach in Multi-Ethnic Sickle Cell Patients: Real-World Practice Data From a Multicenter Survey in Italy
31. Tricuspid-valve regurgitant jet velocity as a risk factor for death in β-thalassemia
32. Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families
33. Italian patients with hemoglobinopathies exhibit a 5‐fold increase in age‐standardized lethality due to SARS‐CoV‐2 infection
34. Limited Access to Transcranial Doppler Screening and Stroke Prevention for Children with Sickle Cell Disease in Europe: Results of a Multinational Eurobloodnet Survey
35. Hemoglobinopathies and Cancer: Preliminary Results of an Italian Multicenter Experience
36. Endocrine function and bone disease during long-term chelation therapy with deferasirox in patients with β-thalassemia major
37. Subarachnoid haemorrhage and cerebral vasculopathy in a child with sickle cell anaemia
38. Response to Measles, Mumps and Rubella (MMR) Vaccine in Transfusion-Dependent Patients
39. Association of Immune Thrombocytopenia and Coeliac Disease in Children (Retrospective Case Control Study)
40. Will the changing therapeutic landscape meet the needs of patients with sickle cell disease?
41. Selecting β-thalassemia Patients for Gene Therapy: A Decision-making Algorithm
42. Nephrolithiasis in patients exposed to deferasirox and desferioxamine: probably an age-linked event with different effects on some renal parameters
43. Red blood cell alloimmunisation in transfusion-dependent thalassaemia: A systematic review
44. Risk factors for endocrine complications in transfusion-dependent thalassemia patients on chelation therapy with deferasirox: a risk assessment study from a multi-center nation-wide cohort
45. Quando la carenza di ferro diventa rara…
46. Thalassemia Is Paradoxically Associated with a Reduced Risk of In-Hospital Complications and Mortality in COVID-19: Data from an International Registry
47. Vaccinazione Antinfluenzale in soggetti con Asplenia: warning in tempo di Coronavirus
48. MOESM1 of Asymptomatic intracranial aneurysms in beta-thalassemia: a three-year follow-up report
49. Influenza Vaccination in Asplenia: Improving Quality of Care in Time of Coronavirus
50. Effect of splenectomy on iron balance in patients with β-thalassemia major: a long-term follow-up
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