Commentary on Special Issue on Informed Consent With Families of Ill Children (February 2001): Understanding Devastation and Difference in Informed Permission and Assent
Restricted accessOtherFirst published online May, 2001
Commentary on Special Issue on Informed Consent With Families of Ill Children (February 2001): Understanding Devastation and Difference in Informed Permission and Assent
Broome, M. E.
, Richards, D. J., & Hall, J. (2001). Children in research: The experience of ill children and adolescents. Journal of Family Nursing, 7, 32-49.
2.
Hall, J. M.
, Stevens, P. E., & Pletsch, P. K. (2001). Team research using qualitative methods: Investigating children’s involvement in clinical research. Journal of Family Nursing, 7, 7-31.
3.
Liaschenko, J.
, & Underwood, S. M. (2001). Children in research: Fathers in cancer research—Meanings and reasons for participation. Journal of Family Nursing, 7, 71-91.
4.
National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research
. (1979). The Belmont report: Ethical principles and guidelines for the protection of human subjects of research (RN Doc 79-12065). Washington, DC: Government Printing Office.
5.
Pletsch, P. K.
, & Stevens, P. E. (2001). Children in research: Informed consent and critical factors affecting mothers. Journal of Family Nursing, 7, 50-70.
6.
Snethen, J.
, & Broome, M. E. (2001). Children in research: The experiences of siblings in research as a family affair. Journal of Family Nursing, 7, 92-110.