Information and consent for newborn screening: practices and attitudes of service providers
Journal of Medical Ethics 34 (9):648-652 (2008)
| Abstract | This article has no associated abstract. (fix it) | |||||||||
| Keywords | No keywords specified (fix it) | |||||||||
| Categories | ||||||||||
| Options |
|
|||||||||
Download options| PhilPapers Archive |
Upload a copy of this paper Check publisher's policy on self-archival Papers currently archived: 5,672 |
| External links |
  Try with proxy. |
| Through your library | Configure |
Similar books and articlesN. Nijsingh (2013). Krabbe Newborn Screening: The Issue of Informed Consent. Public Health Ethics 6 (1):126-128.
S. G. Nicholls (2010). Knowledge or Understanding? Informed Choice in the Context of Newborn Bloodspot Screening. Public Health Ethics 3 (2):128-136.
R. H. Dees & J. M. Kwon (2013). The Ethics of Krabbe Newborn Screening. Public Health Ethics 6 (1):114-128.
Virginia A. Moyer Ned Calonge Steven M. Teutsch Jeffrey R. Botkin (2008). Expanding Newborn Screening: Process, Policy, and Priorities. Hastings Center Report 38 (3):pp. 32-39.
M.-C. Huang (2005). Parental Consent for Newborn Screening in Southern Taiwan. Journal of Medical Ethics 31 (11):621-624.
Ruth Chadwick, Henk ten Have, Jfrgen Husted, Mairi Levitt, Tony McGleenan, Darren Shickle & Urban Wiesing (1998). Genetic Screening and Ethics: European Perspectives. Journal of Medicine and Philosophy 23 (3):255 – 273.
N. J. Kerruish (2005). Newborn Screening: New Developments, New Dilemmas. Journal of Medical Ethics 31 (7):393-398.
Mary Ann Baily Thomas H. Murray (2008). Ethics, Evidence, and Cost in Newborn Screening. Hastings Center Report 38 (3):pp. 23-31.
Lainie Friedman Ross (2010). Mandatory Versus Voluntary Consent for Newborn Screening? Kennedy Institute of Ethics Journal 20 (4):299-328.
Carole Outterson (1993). Newborn Infants with Severe Defects: A Survey of Paediatric Attitudes and Practices in the United Kingdom. Bioethics 7 (5):420-435.
Diane B. Paul (1994). Toward a Realistic Assessment of PKU Screening. PSA: Proceedings of the Biennial Meeting of the Philosophy of Science Association 1994:322 - 328.
Matthew K. Wynia (2006). Routine Screening: Informed Consent, Stigma and the Waning of HIV Exceptionalism. American Journal of Bioethics 6 (4):5 – 8.
Atsushi Asai, Motoki Ohnishi, Etsuyo Nishigaki, Miho Sekimoto, Shunichi Fukuhara & Tsuguya Fukui (2002). Attitudes of the Japanese Public and Doctors Towards Use of Archived Information and Samples Without Informed Consent: Preliminary Findings Based on Focus Group Interviews. BMC Medical Ethics 3 (1):1-10.
Anton Vedder (2001). Accountability of Internet Access and Service Providers – Strict Liability Entering Ethics? Ethics and Information Technology 3 (1):67-74.
Analytics
Monthly downloads
Sorry, there are not enough data points to plot this chart.
|
Added to index2010-08-24Total downloads1 ( #274,652 of 549,069 )Recent downloads (6 months)0How can I increase my downloads? |
My notes
Discussion
