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...

Centering Patients' Voices in Artificial Intelligence‒Based Telemedicine

American journal of public health (1971), 2023-05, Vol.113 (5), p.470-471

Kraft, Stephanie A

2023

Volltextzugriff (PDF)

The evolving landscape of expanded carrier screening: challenges and opportunities

Genetics in medicine, 2019-04, Vol.21 (4), p.790-797

2019

Volltextzugriff (PDF)

Mold, Mycotoxins and a Dysregulated Immune System: A Combination of Concern?

International journal of molecular sciences, 2021-11, Vol.22 (22), p.12269

2021

Volltextzugriff (PDF)

Beyond Consent: Building Trusting Relationships With Diverse Populations in Precision Medicine Research

American journal of bioethics, 2018-04, Vol.18 (4), p.3-20

2018

Volltextzugriff (PDF)

Engaging populations underrepresented in research through novel approaches to consent

American journal of medical genetics. Part C, Seminars in medical genetics, 2018-03, Vol.178 (1), p.75-80

2018

Volltextzugriff (PDF)

Better recognition for research participants: what society should learn from covid-19

BMJ (Online), 2023-01, Vol.380, p.e071178

2023

Volltextzugriff (PDF)

Respect and Trustworthiness in the Patient-Provider-Machine Relationship: Applying a Relational Lens to Machine Learning Healthcare Applications

American journal of bioethics, 2020-11, Vol.20 (11), p.51-53

Kraft, Stephanie A.

2020

Volltextzugriff (PDF)

Respecting Donor-Recipient Relationships in Research Decision-Making Commentary on: When Living Donor and Kidney Transplant Recipient Are Both Research Subjects

American journal of bioethics, 2021-04, Vol.21 (4), p.112-114

Kraft, Stephanie A.

2021

Volltextzugriff (PDF)

Patient priorities for fulfilling the principle of respect in research: findings from a modified Delphi study

BMC medical ethics, 2023-09, Vol.24 (1), p.73-73, Article 73

2023

Volltextzugriff (PDF)

Patient perspectives on how to demonstrate respect: Implications for clinicians and healthcare organizations

PloS one, 2021-04, Vol.16 (4), p.e0250999-e0250999

2021

Volltextzugriff (PDF)

“I don’t want to be Henrietta Lacks”: diverse patient perspectives on donating biospecimens for precision medicine research

Genetics in medicine, 2019-01, Vol.21 (1), p.107-113

2019

Volltextzugriff (PDF)

Can a Parent Refuse the Brain Death Examination?

Pediatrics (Evanston), 2020-04, Vol.145 (4), p.e20192340

2020

Volltextzugriff (PDF)

Development of the Better Research Interactions for Every Family (BRIEF) intervention to support recruitment for neonatal clinical trials: an intervention mapping guided approach

Trials, 2024-09, Vol.25 (1), p.610-14, Article 610

2024

Volltextzugriff (PDF)

Untersuchung des Erlebens von Pflegefachkräften hinsichtlich Gewalt gegenüber Patienten in der stationären Akutpflege – eine qualitative Analyse

HeilberufeSCIENCE, 2022-05, Vol.13 (1-2), p.69-80

Kraft, Stephanie

2022

Volltextzugriff (PDF)

What Does the Word "Treatable" Mean? Implications for Communication and Decision-Making in Critical Illness

Critical care medicine, 2019-03, Vol.47 (3), p.369-376

2019

Volltextzugriff (PDF)

Begünstigt der Fachkräftemangel Gewalt?

Pflege Zeitschrift, 2021-10, Vol.74 (10), p.67-69

Kraft, Stephanie

2021

Volltextzugriff (PDF)

Pediatric Death by Neurologic Criteria: The Ever-Changing Landscape and the Expanding Role of Palliative Care Professionals

Journal of pain and symptom management, 2021-11, Vol.62 (5), p.1079-1085

2021

Volltextzugriff (PDF)

“I'm completely off base here on what this child is capable of”: A qualitative analysis of how medical ableism manifests in PICU clinicians' care of children with severe neurological impairment

Disability and health journal, 2024-08, p.101691, Article 101691

2024

Volltextzugriff (PDF)

Fostering Relationships in Pediatric Oncology Research: A Relational Ethics Approach to Clinically Integrated Research

American journal of bioethics, 2021-04, Vol.21 (4), p.85-88

2021

Volltextzugriff (PDF)

Modern Pregnancies and (Im)Perfect Babies

American journal of bioethics, 2017-01, Vol.17 (1), p.1-2

Kraft, Stephanie A.

2017

Volltextzugriff (PDF)

Promoting Disclosure and Understanding in Informed Consent: Optimizing the Impact of the Common Rule "Key Information" Requirement

American journal of bioethics, 2021-05, Vol.21 (5), p.70-72

2021

Volltextzugriff (PDF)

Patient Perspectives on the Learning Health System: The Importance of Trust and Shared Decision Making

American journal of bioethics, 2015-09, Vol.15 (9), p.4-17

2015

Volltextzugriff (PDF)

Toward Meeting the Obligation of Respect for Persons in Pragmatic Clinical Trials

The Hastings Center report, 2022-05, Vol.52 (3), p.9-17

2022

Volltextzugriff (PDF)

Equity Concerns Across Pediatric Research Recruitment: An Analysis of Research Staff Interviews

Academic pediatrics, 2024-03, Vol.24 (2), p.318-329

2024

Volltextzugriff (PDF)

Bridging the Researcher-Participant Gap: A Research Agenda to Build Effective Research Relationships

American journal of bioethics, 2020-05, Vol.20 (5), p.31-33

2020

Volltextzugriff (PDF)

1 – 25 von 388

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(342)
Mit Volltextzugriff
(318)

Publikationsform

4 weitere anzeigen...

Weniger anzeigen...

Sprache

Englisch
(378)
Deutsch
(9)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(3)
... seit 90 Tagen
(7)

Menü

Weitere Dienste

Einstellungen

Centering Patients' Voices in Artificial Intelligence‒Based Telemedicine

The evolving landscape of expanded carrier screening: challenges and opportunities

Mold, Mycotoxins and a Dysregulated Immune System: A Combination of Concern?

Beyond Consent: Building Trusting Relationships With Diverse Populations in Precision Medicine Research

Engaging populations underrepresented in research through novel approaches to consent

Better recognition for research participants: what society should learn from covid-19

Respect and Trustworthiness in the Patient-Provider-Machine Relationship: Applying a Relational Lens to Machine Learning Healthcare Applications

Respecting Donor-Recipient Relationships in Research Decision-Making Commentary on: When Living Donor and Kidney Transplant Recipient Are Both Research Subjects

Patient priorities for fulfilling the principle of respect in research: findings from a modified Delphi study

Patient perspectives on how to demonstrate respect: Implications for clinicians and healthcare organizations

“I don’t want to be Henrietta Lacks”: diverse patient perspectives on donating biospecimens for precision medicine research

Can a Parent Refuse the Brain Death Examination?

Development of the Better Research Interactions for Every Family (BRIEF) intervention to support recruitment for neonatal clinical trials: an intervention mapping guided approach

Untersuchung des Erlebens von Pflegefachkräften hinsichtlich Gewalt gegenüber Patienten in der stationären Akutpflege – eine qualitative Analyse

What Does the Word "Treatable" Mean? Implications for Communication and Decision-Making in Critical Illness

Begünstigt der Fachkräftemangel Gewalt?

Pediatric Death by Neurologic Criteria: The Ever-Changing Landscape and the Expanding Role of Palliative Care Professionals

“I'm completely off base here on what this child is capable of”: A qualitative analysis of how medical ableism manifests in PICU clinicians' care of children with severe neurological impairment

Fostering Relationships in Pediatric Oncology Research: A Relational Ethics Approach to Clinically Integrated Research

Modern Pregnancies and (Im)Perfect Babies

Promoting Disclosure and Understanding in Informed Consent: Optimizing the Impact of the Common Rule "Key Information" Requirement

Patient Perspectives on the Learning Health System: The Importance of Trust and Shared Decision Making

Toward Meeting the Obligation of Respect for Persons in Pragmatic Clinical Trials

Equity Concerns Across Pediatric Research Recruitment: An Analysis of Research Staff Interviews

Bridging the Researcher-Participant Gap: A Research Agenda to Build Effective Research Relationships

Suchergebnisse filtern