about
The grand leap of the whale up the Niagara Falls: converting philosophical conclusions into policy prescriptions.Scientific dishonesty--a nationwide survey of doctoral students in NorwayMeta Consent - A Flexible Solution to the Problem of Secondary Use of Health Data.Global bioethics -- myth or reality?Large scale surveys for policy formation and research: a study in inconsistency.A rose by any other name... is the research/non-research distinction still important and relevant?Best interest: a philosophical critique.Best interests: what problems in family law should health care law avoid?Pharmacogenetics, race and global injustice.The outcomes and controversies of transplant tourism-Lessons of an 11-year retrospective cohort study from TaiwanClinical genome sequencing and population preferences for information about 'incidental' findings-From medically actionable genes (MAGs) to patient actionable genes (PAGs)Ethical issues in cardiopulmonary resuscitation.New governance arrangements for research ethics committees: is facilitating research achieved at the cost of participants' interestMilgram and Tuskegee--paradigm research projects in bioethics.Stem cell transplantation and ethics: a European overview.The stigmatization dilemma in public health policy--the case of MRSA in Denmark.Direct-to-consumer genetic testing for predicting sports performance and talent identification: Consensus statementWhat should other healthcare professions learn from nursing ethics.Biobanking human embryonic stem cell lines: policy, ethics and efficiency.Obesity interventions and ethics.Attitudes towards clinical research among cancer trial participants and non-participants: an interview study using a Grounded Theory approach.Genetic testing and sports medicine ethics.Commentary: systems, rules and the costs of being ethical--a response to D. Chalmers and to S. Whitney and C. Schneider.Eliciting meta consent for future secondary research use of health data using a smartphone application - a proof of concept study in the Danish population.Investigating the Reliability and Factor Structure of Kalichman's "Survey 2: Research Misconduct" Questionnaire: A Post Hoc Analysis Among Biomedical Doctoral Students in Scandinavia.The job of 'ethics committees' should be ethically informed code consistency review.'New embryos' - new challenges for the ethics of stem cell research.Nicotine conjugate vaccine: is there a right to a smoking future?Ethical aspects of clinical trials: the attitudes of participants in two non-cancer trials.High hopes and automatic escalators: a critique of some new arguments in bioethics.Final responsibility for treatment choice: the proper role of medical doctors?Routinisation of informed consent in online health care systems.Informed consent and registry-based research - the case of the Danish circumcision registry.Can "giving preference to my patients" be explained as a role related duty in public health care systems?Euthanasia: agreeing to disagree?Regulating stem cell research in Europe by the back door.Bioethics down under--medical ethics engages with political philosophy.Why it is not strongly irrational to have children.Commentary on Skene and Parker: the role of a church (or other ideologically based interest group) in developing the law--a plea for ethereal intervention.Self inflicted harm--NICE in ethical self destruct mode?
P50
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P50
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