SURVIVING WITH THALASSEMIA MAJOR: The Italian Experience
Author:
Publisher
Informa UK Limited
Subject
Oncology,Hematology,Pediatrics, Perinatology, and Child Health
Link
http://www.tandfonline.com/doi/pdf/10.1080/08880010601001461
Reference15 articles.
1. Hematopoietic Cell Transplantation for Benign Hematological Disorders and Solid Tumors
2. Unrelated Bone Marrow Transplantation for β-Thalassemia Patients: The Experience of the Italian Bone Marrow Transplant Group
3. Cardiac morbidity and mortality in deferoxamine- or deferiprone-treated patients with thalassemia major
4. Subcellular distribution of desferrioxamine and hydroxypyridin-4-one chelators in K562 cells affects chelation of intracellular iron pools
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1. Thalassemia patients in transfussion dependent period and after hematopoietic stem cell transplantation: how are the psychiatric status and life quality of these patients?;Pediatric Hematology and Oncology;2023-07-30
2. HEALTH-RELATED QUALITY OF LIFE IN CHILDREN WITH HEMOGLOBIN E-Β-THALASSEMIA WITH SPECIAL REFERENCE TO IRON OVERLOAD;Indian Journal of Child Health;2019-12-25
3. Arrhythmias and Sudden Cardiac Death in Beta-Thalassemia Major Patients: Noninvasive Diagnostic Tools and Early Markers;Cardiology Research and Practice;2019-11-30
4. National registry of hemoglobinopathies in Greece: updated demographics, current trends in affected births, and causes of mortality;Annals of Hematology;2018-09-08
5. Long-term survival of beta thalassemia major patients treated with hematopoietic stem cell transplantation compared with survival with conventional treatment;American Journal of Hematology;2017-09-25
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