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Use of Deferasirox Film-Coated Tablets in Pediatric Patients with Transfusion Dependent Thalassemia: A Single Center Experience

SIMPLE SUMMARY: Thalassemia is a hereditary anemia characterized by defect in hemoglobin synthesis. Patients with severe forms of the disease require regular blood transfusions, as well as iron chelation. Available chelators have demonstrated long-term efficacy and safety, but present various limita...

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Detalles Bibliográficos
Autores principales:	Adramerina, Alkistis, Printza, Nikoleta, Hatzipantelis, Emmanouel, Symeonidis, Symeon, Tarazi, Labib, Teli, Aikaterini, Economou, Marina
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8869542/ https://www.ncbi.nlm.nih.gov/pubmed/35205113 http://dx.doi.org/10.3390/biology11020247

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