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Comment
. 2022 Aug;69(8):e29805.
doi: 10.1002/pbc.29805. Epub 2022 Jun 10.

New therapeutics for children with sickle cell disease: A time for celebration, caution, or both?

Charles T Quinn  1   2 , Russell E Ware  1   2   3
Affiliations
Comment

New therapeutics for children with sickle cell disease: A time for celebration, caution, or both?

Charles T Quinn et al. Pediatr Blood Cancer. 2022 Aug.
No abstract available

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References

REFERENCES

    1. Therrell BL Jr, Lloyd-Puryear MA, Eckman JR, Mann MY. Semin Perinatol. 2015;39:238-251. https://doi.org/10.1053/j.semperi.2015.03.008
    1. Estepp JH, Kalpatthi R, Woods G, et al. Safety and efficacy of voxelotor in pediatric patients with sickle cell disease, age 4 to 11 years. Pediatr Blood Cancer. 2022;21:e29716. https://doi.org/10.1002/pbc.29716
    1. Hebbel RP, Hedlund BE. Sickle hemoglobin oxygen affinity-shifting strategies have unequal cerebrovascular risks. Am J Hematol. 2018;93:321-325. https://doi.org/10.1002/ajh.24975
    1. Henry ER, Metaferia B, Li Q, et al. Treatment of sickle cell disease by increasing oxygen affinity of hemoglobin. Blood. 2021;138:1172-1181. https://doi.org/10.1182/blood.2021012070
    1. Quinn CT, Ware RE. Increased oxygen affinity: to have and to hold. Blood. 2021;138:1094-1095. https://doi.org/10.1182/blood.2021013242

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