CureSCi Metadata Catalog-Finding and harmonizing studies for secondary analysis of hydroxyurea discontinuation in sickle cell disease.

<h4>Objectives</h4>Sickle cell disease (SCD) is a rare group of inherited red blood cell disorders that affect hemoglobin, resulting in serious multi-system complications. The limited number of patients available to participate in research studies can inhibit investigating sophisticated...

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Bibliographic Details
Main Authors: Xin Wu, Jeran Stratford, Karen Kesler, Cataia Ives, Tabitha Hendershot, Barbara Kroner, Ying Qin, Huaqin Pan
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2025-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0309572
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