151 results on '"Frith, Lucy"'
Search Results
2. Evidence-Based Health, Patient Consent and Consumerism
3. Using symbiotic empirical ethics to explore the significance of relationships to clinical ethics: findings from the Reset Ethics research project
4. The long term safety of assisted reproductive technologies
5. Medical ethics, equity and social justice
6. Delivering compassionate NHS healthcare: A qualitative study exploring the ethical implications of resetting NHS maternity and paediatric services following the acute phase of the COVID-19 pandemic
7. Direct-to-consumer genetic testing and the changing landscape of gamete donor conception: key issues for practitioners and stakeholders
8. Developing translational bioethics—Suggestions for ways forward
9. Public involvement and engagement in big data research: A scoping review
10. Guidance to inform research recruitment processes for studies involving critically ill patients
11. Developing a combined framework for priority setting in integrated health and social care systems
12. Donor-Conceived People’s Views and Experiences of Their Genetic Origins: A Critical Analysis of the Research Evidence
13. Democratic Justifications for Patient Public Involvement and Engagement in Health Research: An Exploration of the Theoretical Debates and Practical Challenges
14. Bringing context into ethical discussion: what, when and who?
15. Broadening the debate: the future of JME feature articles
16. The United Kingdom and the Netherlands maternity care responses to COVID-19: A comparative study
17. ‘To me, it's ones and zeros, but in reality that one is death’: A qualitative study exploring researchers' experience of involving and engaging seldom‐heard communities in big data research
18. Extending the data collection from a clinical trial: The Extended Salford Lung Study research cohort
19. Facial kinship verification and searching for genetic origins in gamete/embryo donor conception—an overview of potential legal and ethical issues
20. The disposable and protected fetus: contradictions in fetal status
21. Organisational ethics
22. Medical ethics and the climate change emergency
23. Use of the Hashtag #DataSavesLives on Twitter: Exploratory and Thematic Analysis
24. Public contributors' preferences for the organization of remote public involvement meetings in health and social care: A discrete choice experiment study
25. Remote working in public involvement: findings from a mixed methods study
26. Artificial intelligence and health inequities in primary care: a systematic scoping review and framework
27. Learning from stakeholders to inform good practice guidance on consent to research in intensive care units: a mixed-methods study
28. Involvement and engagement of seldom-heard communities in big data research.
29. Relationships, Rights, and Responsibilities: (Re)viewing the NHS Constitution for the post-pandemic ‘new normal’
30. Public involvement in big data projects: an ethnographically-informed study.
31. P02 Artificial Intelligence and Health Inequities in Primary Care: A Scoping Review and Framework
32. Qualitative study exploring lessons from Liberia and the UK for building a people-centred resilient health systems response to COVID-19
33. Editorial – The ethical implications of treating a pregnant woman to benefit the fetus
34. Publishing Research in Empirical Bioethics: Quality, Disciplines and Expertise
35. 120:oral Developing and implementing a framework for priority setting in health and social care in Scotland
36. Mortality after admission with pneumonia is higher than after admission with an exacerbation of COPD
37. Effects of switching from a metered dose inhaler to a dry powder inhaler on climate emissions and asthma control: post-hoc analysis
38. The concise argument – choice, choices and the choice agenda
39. Access to genetic and biographical history in donor conception: An analysis of recent trends and future possibilities
40. Change from MDI to DPI in asthma: effects on climate emissions and disease control
41. Strategies to enhance recruitment and consent to intensive care studies: a qualitative study with researchers and patient–public involvement contributors
42. Community engagement in genomic research: Proposing a strategic model for effective participation of indigenous communities
43. Public involvement and engagement in big data research: protocol for a scoping review and a systematic review of delivery and effectiveness of strategies for involvement and engagement
44. Neither ‘Crisis Light’ nor ‘Business as Usual’: Considering the Distinctive Ethical Issues Raised by the Contingency and Reset Phases of a Pandemic
45. Relatedness in clinical practice
46. Reproductive Technologies: Ethical Debates
47. FEV1 Minimum Important Difference versus Minimal Detectable Difference? In Search of the Unicorn
48. Which ethical values underpin England’s National Health Service reset of paediatric and maternity services following COVID-19: a rapid review
49. Safety data in randomised real-world evidence studies: Salford Lung Study learnings
50. Corrigendum to: The ethics of preconception expanded carrier screening in patients seeking assisted reproduction
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