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...
Saved in:
| 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 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
CureSCi Metadata Catalog—Finding and harmonizing studies for secondary analysis of hydroxyurea discontinuation in sickle cell disease
by: Xin Wu, et al.
Published: (2025-01-01) -
Optimization of hydroxyurea in sickle cell disease in Brazil
by: Clarisse Lobo, et al.
Published: (2025-04-01) -
The modern use of hydroxyurea for children with sickle cell anemia
by: Charles T. Quinn, et al.
Published: (2025-01-01) -
Influence of hydroxyurea on tubular phosphate handling in sickle cell nephropathy
by: Gabriela Araujo de Abreu, et al.
Published: (2024-11-01) -
Is Hydroxyurea Treatment Changing the Life of Children with Sickle Cell Disease?
by: Mohammed Ali Al Sabbah, et al.
Published: (2023-07-01)