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74 results on '"Winkler EC"'

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1. Complexity of care and strategies of self-management in patients with colorectal cancer

3. When time is of the essence: ethical reconsideration of XAI in time-sensitive environments.

4. Wilson and Jungner Revisited: Are Screening Criteria Fit for the 21st Century?

5. Dynamic consent: a royal road to research consent?

6. Comparative ethical evaluation of epigenome editing and genome editing in medicine: first steps and future directions.

7. Physicians' attitudes towards secondary use of clinical data for biomedical research purposes in Germany. Results of a quantitative survey.

8. UNCAN.eu: Toward a European Federated Cancer Research Data Hub.

9. Prioritization and Resource Allocation in the Context of the COVID-19 Pandemic: Recommendations for Colorectal and Pancreatic Cancer in Germany.

10. Do Physicians Have a Duty to Support Secondary Use of Clinical Data in Biomedical Research? An Inquiry into the Professional Ethics of Physicians.

11. Patient data for commercial companies? An ethical framework for sharing patients' data with for-profit companies for research.

12. Ethics of the fiduciary relationship between patient and physician: the case of informed consent.

13. Neither carrots nor sticks? Challenges surrounding data sharing from the perspective of research funding agencies-A qualitative expert interview study.

14. Ethical challenges of precision cancer medicine.

15. Patients' Willingness to Provide Their Clinical Data for Research Purposes and Acceptance of Different Consent Models: Findings From a Representative Survey of Patients With Cancer.

16. Experience of Time and Subjective Age When Facing a Limited Lifetime: The Case of Older Adults with Advanced Cancer.

17. The COVID-19 Pandemic and Cancer Patients in Germany: Impact on Treatment, Follow-Up Care and Psychological Burden.

18. Sequential Geriatric Assessment in Older Patients with Colorectal Cancer during Chemotherapy: Subgroup Analysis of a Prospective, Multicenter Study EpiReal 75.

20. GA4GH: International policies and standards for data sharing across genomic research and healthcare.

21. Patient-Reported Financial Distress in Cancer: A Systematic Review of Risk Factors in Universal Healthcare Systems.

22. Dealing with Family Conflicts in Decision-making in End-of-Life Care of Advanced Cancer Patients.

23. Secondary Use of Clinical Data in Data-Gathering, Non-Interventional Research or Learning Activities: Definition, Types, and a Framework for Risk Assessment.

24. "Often Relatives are the Key […]" -Family Involvement in Treatment Decision Making in Patients with Advanced Cancer Near the End of Life.

25. [Individual financial burden following a cancer diagnosis from the perspective of social services in Germany].

26. Multicenter Analysis of Treatment Outcomes for Systemic Therapy in Well Differentiated Grade 3 Neuroendocrine Tumors (NET G3).

27. Nipping Diseases in the Bud? Ethical and Social Considerations of the Concept of 'Disease Interception'.

28. Completion rate and impact on physician-patient relationship of video consultations in medical oncology: a randomised controlled open-label trial.

29. Late decisions about treatment limitation in patients with cancer: empirical analysis of end-of-life practices in a haematology and oncology unit at a German university hospital.

30. Caregivers' role in using a personal electronic health record: a qualitative study of cancer patients and caregivers in Germany.

31. The patient-level effect of the cost of Cancer care - financial burden in German Cancer patients.

32. [Ethical frameworks as a corrective in daily clinical practice? : Reflection on the significance of organizational ethics in tackling the challenges of economization in the medical system].

33. Digitalizing Health Services by Implementing a Personal Electronic Health Record in Germany: Qualitative Analysis of Fundamental Prerequisites From the Perspective of Selected Experts.

34. Do patients and research subjects have a right to receive their genomic raw data? An ethical and legal analysis.

35. Do Researchers in Empirical Ethics Studies Have a Duty to Act Upon their Findings? Case Study in End-of-Life Decision Making.

36. Methods for measuring financial toxicity after cancer diagnosis and treatment: a systematic review and its implications.

37. Clinical characteristics, treatment outcomes and potential novel therapeutic options for patients with neuroendocrine carcinoma of the prostate.

38. Cancer Patients' Preferences for either Quality of Life or a Longer Life Determine Their Willingness to Talk about Forgoing Cancer-Specific Treatment.

39. Patients' Preferences in Non-Curable Cancer Disease.

40. High prevalence of moral distress reported by oncologists and oncology nurses in end-of-life decision making.

41. Trust and responsibility in molecular tumour boards.

42. Utilizing a Prototype Patient-Controlled Electronic Health Record in Germany: Qualitative Analysis of User-Reported Perceptions and Perspectives.

43. Development and Evaluation of an Ethical Guideline for Decisions to Limit Life-Prolonging Treatment in Advanced Cancer: Protocol for a Monocentric Mixed-Method Interventional Study.

44. The second patient? Family members of cancer patients and their role in end-of-life decision making.

45. "Rather one more chemo than one less…": Oncologists and Oncology Nurses' Reasons for Aggressive Treatment of Young Adults with Advanced Cancer.

46. Applying systems biology to biomedical research and health care: a précising definition of systems medicine.

47. [Frequency and Timing of Decisions to Limit Intensive Medical Care and Tumor-Specific Therapy in University Hematology and Oncology].

48. [Personal health records on the Internet. A narrative review of attitudes, expectations, utilization and effects on health outcomes].

49. A Personal Electronic Health Record: Study Protocol of a Feasibility Study on Implementation in a Real-World Health Care Setting.

50. Cross-sectoral cancer care: views from patients and health care professionals regarding a personal electronic health record.

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