155 results on '"van Delden, Johannes JM"'
Search Results
2. Continuous deep sedation at the end of life: a qualitative interview-study among health care providers on an evolving practice
3. Stimulating solidarity to improve knowledge on medications used during pregnancy: A contribution from the ConcePTION project
4. Requests for euthanasia or assisted suicide of people without (severe) illness
5. An ethics framework for the transition to an operational learning healthcare system.
6. Getting to Know Your Patient: Content Analysis of Patients’ Answers to a Questionnaire for Promoting Person-Centered Care
7. Commitments for Ethically Responsible Sourcing, Use, and Reuse of Patient Data in the Digital Age: Cocreation Process
8. Getting to Know Your Patient: Content Analysis of Patients’ Answers to a Questionnaire for Promoting Person-Centered Care (Preprint)
9. Dynamic consent, communication and return of results in large-scale health data reuse: Survey of public preferences
10. Healthcare use and healthcare costs for patients with advanced cancer; the international ACTION cluster-randomised trial on advance care planning
11. Symptom evolution in the dying
12. Commitments for Ethically Responsible Sourcing, Use, and Reuse of Patient Data in the Digital Age: Co-creation Process (Preprint)
13. Learning accountable governance: Challenges and perspectives for data-intensive health research networks
14. Parental experiences with a paediatric palliative care team: A qualitative study
15. Vulnerability of pregnant women in clinical research
16. Healthcare use and healthcare costs for patients with advanced cancer; the international ACTION cluster-randomised trial on advance care planning.
17. The utility of the surprise question: A useful tool for identifying patients nearing the last phase of life? A systematic review and meta-analysis
18. sj-pdf-2-pmj-10.1177_02692163221142950 – Supplemental material for Healthcare use and healthcare costs for patients with advanced cancer; the international ACTION cluster-randomised trial on advance care planning
19. sj-pdf-1-pmj-10.1177_02692163221142950 – Supplemental material for Healthcare use and healthcare costs for patients with advanced cancer; the international ACTION cluster-randomised trial on advance care planning
20. sj-pdf-4-pmj-10.1177_02692163221142950 – Supplemental material for Healthcare use and healthcare costs for patients with advanced cancer; the international ACTION cluster-randomised trial on advance care planning
21. sj-pdf-5-pmj-10.1177_02692163221142950 – Supplemental material for Healthcare use and healthcare costs for patients with advanced cancer; the international ACTION cluster-randomised trial on advance care planning
22. sj-pdf-3-pmj-10.1177_02692163221142950 – Supplemental material for Healthcare use and healthcare costs for patients with advanced cancer; the international ACTION cluster-randomised trial on advance care planning
23. sj-pdf-6-pmj-10.1177_02692163221142950 – Supplemental material for Healthcare use and healthcare costs for patients with advanced cancer; the international ACTION cluster-randomised trial on advance care planning
24. A systematic review of reasons for gatekeeping in palliative care research
25. Symptom evolution in the dying
26. Societal impacts of regenerative medicine: reflections on the views of orthopedic professionals
27. The inherent ethical challenge of first-in-human pluripotent stem cell trials
28. CLARIFYING APPEALS TO DIGNITY IN MEDICAL ETHICS FROM AN HISTORICAL PERSPECTIVE
29. Opinions of health care professionals and the public after eight years of euthanasia legislation in the Netherlands: A mixed methods approach
30. Regenerative medicine interventions for orthopedic disorders: ethical issues in the translation into patients
31. Artificial nutrition and hydration for patients with advanced dementia: perspectives from medical practitioners in the Netherlands and Australia
32. Ethical and research governance approval across Europe: Experiences from three European palliative care studies
33. Real-Time Access to Electronic Health Record via a Patient Portal: Is it Harmful? A Retrospective Observational Study
34. Being there: parenting the child with acute lymphoblastic leukaemia
35. IDEALS REGARDING A GOOD LIFE FOR NURSING HOME RESIDENTS WITH DEMENTIA: VIEWS OF PROFESSIONAL CAREGIVERS
36. THE PRINCIPLE OF RESPECT FOR AUTONOMY IN THE CARE OF NURSING HOME RESIDENTS
37. Real-Time Access to Electronic Health Record via a Patient Portal in a Tertiary Hospital: Is it Harmful? A Retrospective Mixed Methods Observational Study (Preprint)
38. Use and the Users of a Patient Portal: Cross-Sectional Study
39. Palliative sedation: The end of heated debate?
40. Use and the Users of a Patient Portal: Cross-Sectional Study (Preprint)
41. Modified informed consent procedure: consent to postponed information. (Education and debate)
42. It Takes Two Teams to Save Integrity
43. One Size Fits All?: Ethical Considerations for Examining Efficacy in First-in-Human Pluripotent Stem Cell Studies
44. Doctor-assisted dying: what difference does legalisation make?
45. Erratum: Big Data in medical research and EU data protection law: challenges to the consent or anonymise approach
46. Studying the lay of the land: views and experiences of professionals in the translational pluripotent stem cell field
47. Respiratory syncytial virus trials and beyond
48. A systematic review of reasons for gatekeeping in palliative care research
49. Opinions about euthanasia and advanced dementia: a qualitative study among Dutch physicians and members of the general public
50. Consent procedures in pediatric biobanks
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