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2. 7. Water
3. 4. Disease
4. 3. Health
5. 5. Drugs
6. 8. Global Bioethics in Practice
7. Index
8. 6. Food
9. 2. Biodiversity
10. 1. Global Bioethics and the Environment
11. Contents
12. Title, Copyright, Dedication
13. Preface
14. Word Formation as a Naming Device
15. TWENTY-ONE: Drugs and Dementia: Pharmacotherapy and Decision Making by Primary Caregivers
16. Index
17. Appendix A. The Declaration of Berg en Dal on Ethical Principles Guiding Palliative Care of Persons with Alzheimer’s Disease
18. Appendix B. Framework for an Educational Module for Health Professionals
19. TWENTY: Conducting Research in the Alzheimer Disease Population: Balancing Individual, Group, Family, and Societal Interests
20. NINETEEN: Biomedical Research in Alzheimer Disease
21. Part VI: Research Underpinnings for an Ethical Model of Palliative Care
22. Commentary on Part V: A Clinician’s Commentary from a Post-Soviet Society on Organizational Issues of Care for Alzheimer Disease
23. SEVENTEEN: Changing Patterns of Protection and Care for Incapacitated Adults: Perspectives from a European Society in Transition
24. EIGHTEEN: Social Marginalization of Persons with Disability: Justice Considerations for Alzheimer Disease
25. FIFTEEN: The Role of Nurses and Nursing Education in the Palliative Care of Patients and Their Families
26. SIXTEEN: Ethical Dimensions of Alzheimer Disease Decision Making: The Need for Early Patient and Family Education
27. Part V: Organizational Ethics Issues: Educational Initiatives, Laws, and Allocation Decisions
28. TWELVE: Saying No to Patients with Alzheimer Disease: Rethinking Relations among Personhood, Autonomy, and World
29. FOURTEEN: Alzheimer Disease and Euthanasia
30. THIRTEEN: The Ethical Challenge of Treating Pain in Alzheimer Disease: A Dental Case
31. ELEVEN: Advance Directives and End-of-Life Decision Making in Alzheimer Disease: Practical Challenges
32. Part III: Philosophical and Theological Explorations
33. EIGHT: The Moral Self as Patient
34. Part IV: Clinical Ethics Issues: Focus on Patients and Caregivers
35. TEN: The Tendency of Contemporary Decision-making Strategies to Deny the Condition of Alzheimer Disease
36. SEVEN: Autonomy and the Lived Body in Cases of Severe Dementia
37. FOUR: Expanding the Scope of Palliative Care
38. FIVE: Hospital-based Palliative Care and Dementia, or What Do We Treat Patients For and How Do We Do It?
39. NINE: The Practice of Palliative Care and the Theory of Medical Ethics: Alzheimer Disease as an Example
40. SIX: Elderly Persons with Advanced Dementia: An Opportunity for a Palliative Culture in Medicine
41. THREE: The Clinical Challenge of Uncertain Diagnosis and Prognosis in Patients with Dementia
42. Part II: European Voices on U.S. and European Models of Palliative Care
43. TWO: Neuropathology and Symptomatology in Alzheimer Disease: Implications for Caregiving and Competence
44. Introduction: Historical Overview of a Current Global Challenge
45. List of Contributors
46. ONE: Darkness Cometh: Personal, Social, and Economic Burdens of Alzheimer Disease
47. Part I: The Health Care Challenge of Alzheimer Disease: Basic Societal, Pathological, and Clinical Issues
48. Preface
49. Acknowledgments
50. Contents
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