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

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

ABSTRACT: 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 rel...

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Bibliographic Details
Main Authors: William B. Ershler, MD, Laura M. De Castro, MD, MHSc, Zahra Pakbaz, MD, Aaron Moynahan, MA, Derek Weycker, PhD, Thomas E. Delea, MSIA, Irene Agodoa, MD, Ze Cong, PhD
Format: Article
Language:English
Published: Elsevier 2023-01-01
Series:Current Therapeutic Research
Subjects:
anemia
chronic kidney disease
leg ulcer
pulmonary hypertension
sickle cell disease
stroke
Online Access:http://www.sciencedirect.com/science/article/pii/S0011393X23000061

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http://www.sciencedirect.com/science/article/pii/S0011393X23000061

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