Cargando…
Barriers in transition from pediatrics to adult medicine in sickle cell anemia
Transition of care from pediatric to adult providers is an essential step in the care of young adults with sickle cell anemia. Transition programs should be developed by individual institutions to systematically enhance the transition process for their patients. Prior to transfer, patients must be e...
Autores principales: | Lebensburger, Jeffrey D, Bemrich-Stolz, Christina J, Howard, Thomas H |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3460672/ https://www.ncbi.nlm.nih.gov/pubmed/23055784 http://dx.doi.org/10.2147/JBM.S32588 |
Ejemplares similares
-
Hydroxyurea decreases hospitalizations in pediatric patients with Hb SC and Hb SB+ thalassemia
por: Lebensburger, Jeffrey D, et al.
Publicado: (2015) -
Natural history and variability in albuminuria in pediatric and murine sickle cell anemia
por: Kasztan, Malgorzata, et al.
Publicado: (2023) -
High bias and low precision for estimated versus measured glomerular filtration rate in pediatric sickle cell anemia
por: Lebensburger, Jeffrey D., et al.
Publicado: (2020) -
End Stage Kidney Disease Outcomes in Children and Young Adults with Sickle Cell Disease in the United States Renal Data System
por: Zahr, Rima S., et al.
Publicado: (2023) -
Magnetic resonance imaging in pediatric sickle cell anemia
por: Zhang, Xinxian, et al.
Publicado: (2016)