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Hereditary elliptocytosis: A novel mutation in the SPTA1 gene and diagnosis after a stroke in paediatric patients. A two‐case report.
- Published in:
- Pediatric Blood & Cancer, 2023, v. 70, n. 7, p. 1, doi. 10.1002/pbc.30316
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- Publication type:
- Article
Correction to: Spanish registry of hemoglobinopathies and rare anemias (REHem- AR): demographics, complications, and management of patients with β-thalassemia.
- Published in:
- 2024
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- Publication type:
- Correction Notice
Spanish registry of hemoglobinopathies and rare anemias (REHem-AR): demographics, complications, and management of patients with β-thalassemia.
- Published in:
- Annals of Hematology, 2024, v. 103, n. 5, p. 1525, doi. 10.1007/s00277-024-05694-z
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- Publication type:
- Article