Hemoglobin and End-Organ Damage in Individuals with Sickle Cell Disease

BACKGROUND: Sickle cell disease (SCD) is an inherited, chronic, multifaceted blood disorder. Patients with SCD develop anemia, which has been associated with end-organ damage (EOD). OBJECTIVES: This retrospective, observational, repeated-measures study systematically characterizes the relationship b...

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Detalles Bibliográficos
Autores principales: Ershler, William B., De Castro, Laura M., Pakbaz, Zahra, Moynahan, Aaron, Weycker, Derek, Delea, Thomas E., Agodoa, Irene, Cong, Ze
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025127/
https://www.ncbi.nlm.nih.gov/pubmed/36950457
http://dx.doi.org/10.1016/j.curtheres.2023.100696

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