UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

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

PloS one, 2022-09, Vol.17 (9), p.e0273259

2022

Volltextzugriff (PDF)

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

Journal of medical ethics, 2024-09, p.jme-2024-110046

2024

Volltextzugriff (PDF)

Dynamic consent: a royal road to research consent?

Journal of medical ethics, 2024-07, p.jme-2024-110153

2024

Volltextzugriff (PDF)

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

Journal of medical ethics, 2023-08, Vol.50 (6), p.398-406

2023

Volltextzugriff (PDF)

Finanzielle Auswirkung von Krebserkrankungen und sozialethische Implikationen

Der Onkologe, 2020-05, Vol.26 (5), p.425-430

2020

Volltextzugriff (PDF)

Vorausschauende Behandlungsplanung und Therapiebegrenzung: Überlegungen aus medizinethischer und psychoonkologischer Sicht

Deutsche Zeitschrift für Onkologie (Heidelberg, Germany : 2001), 2018-06, Vol.50 (2), p.60-65

2018

Volltextzugriff (PDF)

When do we need to care about the caregiver? Supportive care needs, anxiety, and depression among informal caregivers of patients with cancer and cancer survivors

Cancer, 2015-05, Vol.121 (9), p.1513-1519

2015

Volltextzugriff (PDF)

“Often Relatives are the Key […]” –Family Involvement in Treatment Decision Making in Patients with Advanced Cancer Near the End of Life

The oncologist (Dayton, Ohio), 2021-05, Vol.26 (5), p.e831-e837

2021

Volltextzugriff (PDF)

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

PloS one, 2024-02, Vol.19 (2), p.e0274032-e0274032

2024

Volltextzugriff (PDF)

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

Journal of medical Internet research, 2022-08, Vol.24 (8), p.e37665-e37665

2022

Volltextzugriff (PDF)

Vorausschauende Behandlungsplanung und Therapiebegrenzung

Deutsche medizinische Wochenschrift, 2016-03, Vol.141 (6), p.394-398

2016

Volltextzugriff (PDF)

Anaerobic Fe(II)-Oxidizing Bacteria Show As Resistance and Immobilize As during Fe(III) Mineral Precipitation

Environmental science & technology, 2010-01, Vol.44 (1), p.94-101

2010

Volltextzugriff (PDF)

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

Journal of medical Internet research, 2021-06, Vol.23 (6), p.e26631-e26631

2021

Volltextzugriff (PDF)

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

Journal of medical ethics, 2022-12, p.jme-2022-108539

2022

Volltextzugriff (PDF)

Is Dupras and Bunnik's Framework for Assessing Privacy Risks in Multi-Omic Research and Databases Still Too Exceptionalist?

American journal of bioethics, 2021-12, Vol.21 (12), p.80-82

2021

Volltextzugriff (PDF)

Patient data for commercial companies? An ethical framework for sharing patients’ data with for-profit companies for research

Journal of medical ethics, 2023-05, p.jme-2022-108781

2023

Volltextzugriff (PDF)

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

The Journal of law, medicine & ethics, 2024-01, Vol.52 (1), p.101-117

2024

Volltextzugriff (PDF)

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

Cancer discovery, 2024-01, Vol.14 (1), p.30-35

2024

Volltextzugriff (PDF)

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

BMC cancer, 2020-06, Vol.20 (1), p.529-529, Article 529

2020

Volltextzugriff (PDF)

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

BMC medical ethics, 2020-01, Vol.21 (1), p.7-12, Article 7

2020

Volltextzugriff (PDF)

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

Psycho-oncology (Chichester, England), 2018-12, Vol.27 (12), p.2733-2739

2018

Volltextzugriff (PDF)

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

Cancers, 2021-10, Vol.13 (19), p.5015

2021

Volltextzugriff (PDF)

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

Journal of medical Internet research, 2020-01, Vol.22 (1), p.e15102

2020

Volltextzugriff (PDF)

Patients' Preferences in Non-Curable Cancer Disease

Oncology research and treatment, 2019-01, Vol.42 (1-2), p.31-34

2019

Volltextzugriff (PDF)

“Rather one more chemo than one less…”: Oncologists and Oncology Nurses’ Reasons for Aggressive Treatment of Young Adults with Advanced Cancer

The oncologist (Dayton, Ohio), 2018-02, Vol.23 (2), p.256-262

2018

Volltextzugriff (PDF)

1 – 25 von 495

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(364)
Mit Volltextzugriff
(392)

Publikationsform

4 weitere anzeigen...

Weniger anzeigen...

Sprache

Englisch
(368)
Deutsch
(123)
Ungarisch
(4)
Slowakisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(246)
Life Sciences & Biomedicine
(205)
Humans
(131)
Female
(61)
Oncology
(59)
Male
(52)
Medicine
(43)
Adult
(41)
Middle Aged
(41)
Patients
(39)
Medicine & Public Health
(38)
Ethics
(33)
Aged
(32)
Social Sciences
(30)
Medical Ethics
(26)
Technology
(26)
Cancer
(25)
Physical Sciences
(25)
Science & Technology - Other Topics
(24)
Animals
(19)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(4)
... seit 90 Tagen
(10)

Menü

Weitere Dienste

Einstellungen

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

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

Dynamic consent: a royal road to research consent?

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

Finanzielle Auswirkung von Krebserkrankungen und sozialethische Implikationen

Vorausschauende Behandlungsplanung und Therapiebegrenzung: Überlegungen aus medizinethischer und psychoonkologischer Sicht

When do we need to care about the caregiver? Supportive care needs, anxiety, and depression among informal caregivers of patients with cancer and cancer survivors

“Often Relatives are the Key […]” –Family Involvement in Treatment Decision Making in Patients with Advanced Cancer Near the End of Life

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

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

Vorausschauende Behandlungsplanung und Therapiebegrenzung

Anaerobic Fe(II)-Oxidizing Bacteria Show As Resistance and Immobilize As during Fe(III) Mineral Precipitation

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

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

Is Dupras and Bunnik's Framework for Assessing Privacy Risks in Multi-Omic Research and Databases Still Too Exceptionalist?

Patient data for commercial companies? An ethical framework for sharing patients’ data with for-profit companies for research

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

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

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

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

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

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

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

Patients' Preferences in Non-Curable Cancer Disease

“Rather one more chemo than one less…”: Oncologists and Oncology Nurses’ Reasons for Aggressive Treatment of Young Adults with Advanced Cancer

Suchergebnisse filtern