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Thalassemia Reports, Volume 16, Issue 4

2026 December - 3 articles

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Articles (3)

  • Article
  • Open Access
279 Views
13 Pages

Allogeneic Hematopoietic Cell Transplantation for Pediatric Unstable Hemoglobinopathies: An Aggregated Cohort with Long-Term Follow-Up from a Brazilian Center

  • Annie Karoline Feijó Costa,
  • Joana Teresa Bisinella de Faria,
  • Gabriela Ventura de Almeida Silva,
  • Renata Fittipaldi da Costa Guimarães and ,
  • Carlos Eduardo Setanni Grecco,
  • Thalita Cristina de Mello Costa,
  • Fabíola Traina,
  • Belinda Pinto Simões and
  • Luiz Guilherme Darrigo
  • + 4 authors+ 0 author

Background/Objectives: Severe unstable hemoglobinopathies may cause transfusion dependence from early childhood, and allogeneic hematopoietic cell transplantation (allo-HCT) is the only established curative option. Pediatric experience with allo-HCT...

(This article belongs to the Topic New Drugs and Combinations in the Management of Hematological Malignancies and Rare Diseases)
  • Article
  • Open Access
214 Views
15 Pages

Background/Objectives: Beta-thalassemia and sickle cell disorders are among the most common inherited hemoglobin disorders affecting tribal populations in India, with marked ethnic and geographic heterogeneity. Although exploratory multivariate appro...

  • Review
  • Open Access
369 Views
19 Pages

Background: Sickle cell disease (SCD) and β-thalassemia are chronic thromboinflammatory disorders associated with venous, arterial, and microvascular thrombotic complications. However, evidence regarding disease-specific risk stratification and...

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Thalass. Rep. - ISSN 2039-4365