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