| Genome editing and assisted reproduction: curing embryos, society or prospective parents? |
11 |
| How to distinguish medicalization from over-medicalization? |
9 |
| E-health beyond technology: analyzing the paradigm shift that lies beneath |
8 |
| Practical wisdom in complex medical practices: a critical proposal |
8 |
| Consumer-driven and commercialised practice in dentistry: an ethical and professional problem? |
8 |
| Lost in Culturation': medical informed consent in China (from a Western perspective) |
7 |
| The moral obligation to be vaccinated: utilitarianism, contractualism, and collective easy rescue |
6 |
| Public trust and 'ethics review' as a commodity: the case of Genomics England Limited and the UK's 000 genomes project |
6 |
| Dualism and its place in a philosophical structure for psychiatry |
5 |
| The spectrum of end of life care: an argument for access to medical assistance in dying for vulnerable populations |
5 |
| Professional ethics: the case of neonatology |
4 |
| Reflection in medical education: intellectual humility, discovery, and know-how |
4 |
| I would rather have it done by a doctorlaypeople's perceptions of direct-to-consumer genetic testing (DTC GT) and its ethical implications |
4 |
| The Care Dialog: the ethics of care approach and its importance for clinical ethics consultation |
4 |
| Towards precision medicine; a new biomedical cosmology |
4 |
| Relational autonomy in the care of the vulnerable: health care professionals' reasoning in Moral Case Deliberation (MCD) |
4 |
| That is why I have trust: unpacking what 'trust' means to participants in international genetic research in Pakistan and Denmark |
4 |
| The evolution of public health ethics frameworks: systematic review of moral values and norms in public health policy |
4 |
| Between quality of life and hope. Attitudes and beliefs of Muslim women toward withholding and withdrawing life-sustaining treatments |
3 |
| Responsibility for scientific misconduct in collaborative papers |
3 |
| Rethinking moral distress: conceptual demands for a troubling phenomenon affecting health care professionals |
3 |
| Mobile health ethics and the expanding role of autonomy |
3 |
| The particularity of dignity: relational engagement in care at the end of life |
3 |
| Assumptions and moral understanding of the wish to hasten death: a philosophical review of qualitative studies |
3 |
| Phenomenology of pregnancy and the ethics of abortion |
3 |
| Spirituality in medical education: a concept analysis |
3 |
| The psychological slippery slope from physician-assisted death to active euthanasia: a paragon of fallacious reasoning |
3 |
| Just choice: a Danielsian analysis of the aims and scope of prenatal screening for fetal abnormalities |
2 |
| A non-ideal authenticity-based conceptualization of personal autonomy |
2 |
| Learning from deep brain stimulation: the fallacy of techno-solutionism and the need for 'regimes of care' |
2 |
| Narrative methods for assessing quality of life in hand transplantation: five case studies with bioethical commentary |
2 |
| Valuing biomarker diagnostics for dementia care: enhancing the reflection of patients, their care-givers and members of the wider public |
2 |
| Getting what you desire: the normative significance of genetic relatedness in parent-child relationships |
2 |
| Sharing lives, sharing bodies: partners negotiating breast cancer experiences |
2 |
| The logic of the interaction between beneficence and respect for autonomy |
2 |
| Engagement and practical wisdom in clinical practice: a phenomenological study |
2 |
| Appeal to the Rule of Rescue in health care: discriminating and not benevolent? |
2 |
| What deserves our respect? Reexamination of respect for autonomy in the context of the management of chronic conditions |
2 |
| Trauma and intersubjectivity: the phenomenology of empathy in PTSD |
2 |
| Relational autonomy in informed consent (RAIC) as an ethics of care approach to the concept of informed consent |
2 |
| The history of autonomy in medicine from antiquity to principlism |
2 |
| Human dignity as a basis for providing post-trial access to healthcare for research participants: a South African perspective |
2 |
| Medical oath: use and relevance of the Declaration of Geneva. A survey of member organizations of the World Medical Association (WMA) |
2 |
| Dementia, identity and the role of friends |
2 |
| Incentivized goodness |
2 |
| The gene-editing of super-ego |
2 |
| How to respond to resistiveness towards assistive technologies among persons with dementia |
2 |
| Relieving one's relatives from the burdens of care |
1 |
| Towards living within my body and accepting the past: a case study of embodied narrative identity |
1 |
| Let us talk about eggs! Professional resistance to elective egg vitrification and gendered medical paternalism |
1 |
