Multi-site study of transition in adolescents with sickle cell disease in the United Kingdom and the United States
Author:
Publisher
Walter de Gruyter GmbH
Subject
Public Health, Environmental and Occupational Health,Pediatrics, Perinatology and Child Health
Link
https://www.degruyter.com/document/doi/10.1515/IJAMH.2005.17.2.169/pdf
Reference8 articles.
1. New Considerations in the Treatment of Sickle Cell Disease
2. Effect of Hydroxyurea on the Frequency of Painful Crises in Sickle Cell Anemia
3. Bone marrow transplantation in sickle cell anemia
4. Factors in the Long Term Adjustment of Children and Adolescents with Sickle Cell Disease:
5. Transfer as a component of the transition of adolescents with sickle cell disease to adult care: Adolescent, adult, and parent perspectives
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1. Social and Structural Drivers of Health and Transition to Adult Care;Pediatrics;2023-12-12
2. Managing the Cerebrovascular Complications of Sickle Cell Disease: Current Perspectives;Journal of Blood Medicine;2023-04
3. Physical Impairment and Function in Children and Adolescents With Sickle Cell Disease: A Systematic Review;Archives of Physical Medicine and Rehabilitation;2021-09
4. Blood Transfusion: Knowledge, Perspectives, and Experience of Individuals With Sickle Cell Disease;Journal of Patient Experience;2020-09-10
5. The influence of perceived racial bias and health-related stigma on quality of life among children with sickle cell disease;Ethnicity & Health;2020-09-08
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