Child’s objection to non-beneficial research: capacity and distress based models-Reference-Cited by-同舟云学术

Child’s objection to non-beneficial research: capacity and distress based models

Published:2015-04-28 Issue:1 Volume:19 Page:65-70
ISSN:1386-7423
Container-title:Medicine, Health Care and Philosophy
language:en
Short-container-title:Med Health Care and Philos

Author:

Waligora Marcin^ORCID,Różyńska Joanna,Piasecki Jan

Funder

Narodowe Centrum Nauki

Publisher

Springer Science and Business Media LLC

Subject

Health Policy,Education,Health (social science)

Link

http://link.springer.com/content/pdf/10.1007/s11019-015-9643-8.pdf

Reference36 articles.

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2. Alderson, P. 2007. Competent children? Minors’ consent to health care treatment and research. Social Science and Medicine 65(11): 2272–2283. doi: 10.1016/j.socscimed.2007.08.005 .

3. Alderson, P., K. Sutcliffe, and K. Curtis. 2006. Children as partners with adults in their medical care. Archives of Disease in Childhood 91(4): 300–303. doi: 10.1136/adc.2005.079442 .

4. Berger, J.T. 2011. Is best interests a relevant decision making standard for enrolling non-capacitated subjects into clinical research? Journal of Medical Ethics 37(1): 45–49. doi: 10.1136/jme.2010.037515 .

5. Brassington, I. 2011. Defending the duty to research? Bioethics 25(1): 21–26. doi: 10.1111/j.1467-8519.2009.01745.x .

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