308 results on '"Van Delden, Johannes J.M."'
Search Results
2. Ethical implications of defining longstanding anorexia nervosa
3. Physicians' Opinion and Practice With the Continuous Use of Sedatives in the Last Days of Life
4. Experiences and perceptions of continuous deep sedation:An interview study among Dutch patients and relatives
5. Experiences and perceptions of continuous deep sedation: An interview study among Dutch patients and relatives
6. Changing Practices in the Use of Continuous Sedation at the End of Life: A Systematic Review of the Literature
7. The Rising Frequency of Continuous Deep Sedation in the Netherlands, a Repeated Cross-Sectional Survey in 2005, 2010, and 2015
8. Regulatory sanctions for ethically relevant GCP violations
9. The Stability of Treatment Preferences Among Patients With Advanced Cancer
10. Selecting and evaluating decision-making strategies in the intensive care unit: A systematic review
11. Interventions Guiding Advance Care Planning Conversations: A Systematic Review
12. Overcoming ethical and legal obstacles to data linkage in health research: stakeholder perspectives
13. From Privacy to Data Protection in the EU : Implications for Big Data Health Research
14. Advance Care Planning in a Multicultural Family Centric Community: A Qualitative Study of Health Care Professionals', Patients', and Caregivers' Perspectives
15. Mini-guts in a dish: Perspectives of adult Cystic Fibrosis (CF) patients and parents of young CF patients on organoid technology
16. Is It Our Duty To Hunt for Pathogenic Mutations?
17. Series: Pragmatic trials and real world evidence: Paper 4. Informed consent
18. Ethics of Informed Consent for Pragmatic Trials with New Interventions
19. The unique status of first-in-human studies: strengthening the social value requirement
20. Experiences and perceptions of continuous deep sedation: An interview study among Dutch patients and relatives
21. Self-efficacy of advanced cancer patients for participation in treatment-related decision-making in six European countries:the ACTION study
22. Impacts of an advance care planning intervention on close relationships
23. Symptom evolution in the dying
24. Healthcare use and healthcare costs for patients with advanced cancer; the international ACTION cluster-randomised trial on advance care planning
25. Overcoming ethical and legal obstacles to data linkage in health research: stakeholder perspectives
26. Dynamic consent, communication and return of results in large-scale health data reuse: Survey of public preferences
27. Healthcare use and healthcare costs for patients with advanced cancer; the international ACTION cluster-randomised trial on advance care planning
28. Symptom evolution in the dying
29. Drug regulators and ethics: which GCP issues are also ethical issues?
30. Comorbidity and favorable neurologic outcome after out-of-hospital cardiac arrest in patients of 70 years and older
31. Pragmatic randomized trials in drug development pose new ethical questions: a systematic review
32. Postmortem disclosure of genetic information to family members: active or passive?
33. Justification of exclusion criteria was underreported in a review of cardiovascular trials
34. Ethical implications of regenerative medicine in orthopedics: an empirical study with surgeons and scientists in the field
35. Reflective Equilibrium as a Normative Empirical Model: The Case of Ashley X
36. Learning accountable governance: Challenges and perspectives for data-intensive health research networks
37. Learning accountable governance: Challenges and perspectives for data-intensive health research networks
38. The utility of the surprise question: A useful tool for identifying patients nearing the last phase of life? A systematic review and meta-analysis
39. Asking the right questions: towards a person-centered conception of shared decision-making regarding treatment of advanced chronic kidney disease in older patients
40. Decision theory and the evaluation of risks and benefits of clinical trials
41. Determinants of successful implementation of population-based cancer screening programmes
42. Is informed consent necessary for randomized Phase IV ‘observational’ drug studies?
43. Autonomy in an ascribed relationship: The case of adult children and elderly parents
44. Advance care planning met patiënten met gevorderde kanker
45. Reconsidering the ethics of sham interventions in an era of emerging technologies
46. Accuracy of the Wells Clinical Prediction Rule for Pulmonary Embolism in Older Ambulatory Adults
47. Classification of end-of-life decisions by dutch physicians:Findings from a cross-sectional survey
48. Advance care planning met patiënten met gevorderde kanker: Een cluster-gerandomiseerde studie in 6 Europese landen
49. How should the 'privilege' in therapeutic privilege be conceived when considering the decision-making process for patients with borderline capacity?
50. The implications of today's family structures for support giving to older parents
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