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Genetics in Medicine, ISSN 1098-3600, 06/2017, Volume 19, Issue 6, p. 609
  β-Thalassemia is caused by reduced (β+ ) or absent (β0 ) synthesis of the β-globin chains of hemoglobin. Three clinical and hematological conditions of... 
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2010, Volume 5, Issue 1, pp. 11 - 11
Journal Article
Thalassemia Reports, ISSN 2039-4357, 12/2014, Volume 4, Issue 3
The availability of oral iron chelators and new non-invasive methods for early detection and treatment of iron overload, have significantly improved the life... 
deferiprone | iron chelation | therapies | deferoxamine | thalassemia
Journal Article
MEDITERRANEAN JOURNAL OF HEMATOLOGY AND INFECTIOUS DISEASES, ISSN 2035-3006, 03/2019, Volume 11, Issue 1, pp. e2019019 - e2019019
Journal Article
British Journal of Haematology, ISSN 0007-1048, 08/2019, Volume 186, Issue 4, pp. 625 - 636
Journal Article
Pediatric endocrinology reviews : PER, ISSN 1565-4753, 03/2011, Volume 8, pp. 263 - 270
In beta thalassemia, unbalanced alpha globin chain synthesis results in severely rheologically compromised erythrocytes with premature destruction in the... 
Anemia - physiopathology | Cardiovascular Diseases - physiopathology | Gallstones - physiopathology | Humans | beta-Thalassemia - physiopathology | Bone Diseases - physiopathology | Child | Iron Overload - physiopathology
Journal Article
Journal Article
Haematologica, ISSN 0390-6078, 05/2007, Volume 92, Issue 5, pp. 583 - 588
Journal Article
Journal Article
Health and quality of life outcomes, ISSN 1477-7525, 11/2018, Volume 16, Issue 1, pp. 216 - 12
Journal Article
American Journal of Hematology, ISSN 0361-8609, 12/2017, Volume 92, Issue 12, pp. 1349 - 1355
Journal Article