Empirical examination of the ability of children to consent to clinical research.
Ondrusek, N., Abramovitch, R., Pencharz, P., & Koren, G. (1998). Empirical examination of the ability of children to consent to clinical research. Journal of Medical Ethics, 24(3). pp. 158-165.
Methodological and ethical issues in conducting qualitative research with children and young people: A literature review.
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Child and parent reactions to participation in clinical research.
Kassam-Adams, N., & Newman, E. (2005). Child and parent reactions to participation in clinical research. General Hospital Psychiatry, 27(1). pp. 29-35.
Incidental findings on brain magnetic resonance imaging of children with sickle cell disease.
Jordan, L. C., McKinstry, R. C., Kraut, M. A., Ball, W. S., Vendt, B. A., Casella, J. F., DeBaun, M. R., for the Silent Infarct Transfusion Trial Investigators, & Strouse, J. J. (2010). Incidental findings on brain magnetic resonance imaging of children with sickle cell disease. Pediatrics, 126(1). pp. 53-61.
Informed consent for enrolling minors in genetic susceptibility research: A qualitative study of at-risk children’s and parents’ views about children’s role in decision-making.
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Informed consent in children and adolescents: Age, maturation and psychological state.
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Researching chronic childhood illness: The example of childhood cancer.
Dixon-Woods, M., Young, B., & Ross, E. (2006). Researching chronic childhood illness: The example of childhood cancer. Chronic Illness, 2(3). pp. 165-177.
The legal ethics of pediatric research.
Coleman, D. L. (2007). The legal ethics of pediatric research. Duke Law Journal, 57. pp. 517-624.
The influence of relationships on children’s and adolescents’ participation in research.
Broome, M. E., & Richards, D. J. (2003). The influence of relationships on children's and adolescents' participation in research. Nursing Research, 52(3). pp. 191-197.