Deutsches Referenzzentrum für Ethik in den Biowissenschaften (DRZE)

Recherche in BELIT – Bioethik-Literaturdatenbank

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Zahl der Einträge: 303
Seite: 1 von 16

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Nr. Eintrag
1 Bombard, Yvonne et al.:
Eliciting ethical and social values in health technology assessment: A participatory approach.
In: Social science & medicine (1982), 2011, Vol. 73 (1), 135-44
2 Chen, Ruth P:
Student participation in health professions education research: in pursuit of the Aristotelian mean.
In: Advances in health sciences education : theory and practice, 2011, Vol. 16 (2), 277-86
3 Chiovitti, Rosalina F:
Theory of protective empowering for balancing patient safety and choices.
In: Nursing ethics, 2011, Vol. 18 (1), 88-101
4 Collier, Roger:
Ontario introduces "hospital secrecy clause".
In: CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne, 2011, Vol. 183 (9), E552
5 Habal, Marlena V et al.:
How aware of advanced care directives are heart failure patients, and are they using them?
In: The Canadian journal of cardiology, 2011, Vol. 27 (3), 376-81
6 Kekewich, Michael A et al.:
Mind the gap: the lack of common language in healthcare ethics.
In: The Journal of clinical ethics, 2011, Vol. 22 (3), 261-6
7 Norman, Geoff:
Issues in (inter)professionalism.
In: Advances in health sciences education : theory and practice, 2011, Vol. 16 (1), 1-3
8 Pope, Thaddeus Mason:
Legal briefing: futile or non-beneficial treatment.
In: The Journal of clinical ethics, 2011, Vol. 22 (3), 277-96
9 Singer, Peter:
How not to save a life.
In: Bioethics, 2011, Vol. 25 (5), ii-iii
10 Vogel, Lauren:
Legal ambiguities surround authority to make end-of-life decisions.
In: CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne, 2011, Vol. 183 (10), E617-8
11 Watine, Joseph:
What sort of bioethical values are the evidence-based medicine and the GRADE approaches willing to deal with?
In: Journal of medical ethics, 2011, Vol. 37 (3), 184-6
12 Chapman, Blake A:
Limiting donation after cardiac death: questions on consent.
In: Health law journal, 2010, 18, 159-86
13 Cheung, Winson Y et al.:
The contents and readability of informed consent forms for oncology clinical trials.
In: American journal of clinical oncology, 2010, Vol. 33 (4), 387-92
14 Choong, Karen et al.:
A framework for resolving disagreement during end of life care in the critical care unit.
In: Clinical and investigative medicine. Médecine clinique et experimentale, 2010, Vol. 33 (4), E240-53
15 Cleaver, S; Ouellette-Kuntz, H; Sakar, A:
Participation in intellectual disability research: a review of 20 years of studies.
In: Journal of intellectual disability research : JIDR 2010 Mar ; 54(3): 187-93
16 Downar, James; Seccareccia, Dori:
Palliating a pandemic: "all patients must be cared for".
In: Journal of Pain and Symptom Management, 2010, Vol. 39 (2), 291-295
17 Etchegary, Holly et al.:
Attitude and knowledge about genetics and genetic testing.
In: Public Health Genomics, 2010, Vol. 13 (2), 80-88
18 Geist, Rose; Opler, Susan E:
A guide for health care practitioners in the assessment of young people's capacity to consent to treatment.
In: Clinical pediatrics, 2010, Vol. 49 (9), 834-9
19 Hansen, Deborah:
Dying under a cloud.
In: Journal of palliative care, 2010, Vol. 26 (4), 303-4
20 Hizo-Abes, Patricia et al.:
Attitudes to sharing personal health information in living kidney donation.
In: Clinical journal of the American Society of Nephrology : CJASN, 2010, Vol. 5 (4), 717-22

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