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

• Κύριοι συγγραφείς: William B. Ershler, MD (Συγγραφέας), Laura M. De Castro, MD, MHSc (Συγγραφέας), Zahra Pakbaz, MD (Συγγραφέας), Aaron Moynahan, MA (Συγγραφέας), Derek Weycker, PhD (Συγγραφέας), Thomas E. Delea, MSIA (Συγγραφέας), Irene Agodoa, MD (Συγγραφέας), Ze Cong, PhD (Συγγραφέας)
• Μορφή: Βιβλίο
• Έκδοση: Elsevier, 2023-01-01T00:00:00Z.
• Θέματα: article
• Διαθέσιμο Online: Connect to this object online.

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 rela...