Iron incorporation in red blood cells of pediatric sickle cell anemia: a stable isotope pilot investigation
Author:
Funder
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro
Publisher
Springer Science and Business Media LLC
Link
https://www.nature.com/articles/s41430-024-01465-1.pdf
Reference40 articles.
1. Inusa BPD, Hsu LL, Kohli N, Patel A, Ominu-Evbota K, Anie KA, et al. Sickle cell disease – genetics, pathophysiology, clinical presentation and treatment. Int J Neonatal Screen. 2019;5:20 https://doi.org/10.3390/ijns5020020.
2. Rees DC, Williams TN, Gladwin MT. Sickle-cell disease. Lancet. 2010;376:2018–31. https://doi.org/10.1016/S0140-6736(10)61029-X.
3. Nascimento MI, Przibilski ALF, Coelho CSG, Leite KFA, Makenze M, Jesus SB. Mortality attributed to sickle cell disease in children and adolescents in Brazil, 2000-2019. Rev Saude Publica. 2022;56:65 https://doi.org/10.11606/s1518-8787.2022056003681.
4. Lobo CLC, Nascimento EMD, Jesus LJC, Freitas TG, Lugon JR, Ballas SK. Mortality in children, adolescents and adults with sickle cell anemia in Rio de Janeiro, Brazil. Rev Bras Hematol Hemoter. 2018;40:37–42. https://doi.org/10.1016/j.bjhh.2017.09.006.
5. Inati A, Khoriaty E, Mussalam KM. Iron sickle-cell disease: what have we learned over the years? Pediatr Blood Cancer. 2011;56:182–90. https://doi.org/10.1002/pbc.22721.
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