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...

What About Us? Experiences of Relatives Regarding Physician-Assisted Death for Patients Suffering from Mental Illness: A Qualitative Study

Culture, medicine and psychiatry, 2023-03, Vol.47 (1), p.237-251

2023

Volltextzugriff (PDF)

The perspectives of professional caregivers on quality of life of persons with profound intellectual and multiple disabilities: a qualitative study

International journal of developmental disabilities, 2022, Vol.68 (2), p.190-197

2022

Volltextzugriff (PDF)

Dignity of informal caregivers of migrant patients in the last phase of life: a qualitative study

BMC palliative care, 2021-02, Vol.20 (1), p.26-26, Article 26

2021

Volltextzugriff (PDF)

The role of research in improving responsiveness of palliative care to migrants and other underserved populations in the Netherlands: a qualitative interview study

BMC palliative care, 2021-01, Vol.20 (1), p.5-5, Article 5

2021

Volltextzugriff (PDF)

Experiences and views of Dutch general practitioners regarding physician-assisted death for patients suffering from severe mental illness: a mixed methods approach

Scandinavian journal of primary health care, 2021-06, Vol.39 (2), p.166-173

2021

Volltextzugriff (PDF)

How to help researchers in palliative care improve responsiveness to migrants and other underrepresented populations: developing and testing a self-assessment instrument

BMC palliative care, 2019-10, Vol.18 (1), p.83-83, Article 83

2019

Volltextzugriff (PDF)

A dignified last phase of life for patients with a migration background: A qualitative study

Palliative medicine, 2020-12, Vol.34 (10), p.1385-1392

2020

Volltextzugriff (PDF)

Where is the citizen? Comparing civic spaces in long-term mental healthcare

Health & place, 2013-07, Vol.22, p.11-18

2013

Volltextzugriff (PDF)

Parent perspectives on the assessment of quality of life of their children with profound intellectual and multiple disabilities in the Netherlands

Research in developmental disabilities, 2023-08, Vol.139, p.104536-104536, Article 104536

2023

Volltextzugriff (PDF)

Euthanasia, Physician-Assisted Suicide, and Other Medical Practices Involving the End of Life in the Netherlands, 1990–1995

The New England journal of medicine, 1996-11, Vol.335 (22), p.1699-1705

1996

Volltextzugriff (PDF)

Challenges in the implementation and evaluation of a transmural palliative care pathway for acutely hospitalized older adults; lessons from the PalliSupport program: A qualitative process evaluation study

Archives of gerontology and geriatrics, 2022-11, Vol.103, p.104782-104782, Article 104782

2022

Volltextzugriff (PDF)

How parents and physicians experience end-of-life decision-making for children with profound intellectual and multiple disabilities

Research in developmental disabilities, 2016-12, Vol.59, p.283-293

2016

Volltextzugriff (PDF)

Parenting by persons with intellectual disability: an explorative study in the Netherlands

Journal of intellectual disability research, 2007-07, Vol.51 (7), p.537-544

2007

Volltextzugriff (PDF)

Thoughts of patients with advanced heart failure on dying

Palliative medicine, 2004-09, Vol.18 (6), p.564-572

2004

Volltextzugriff (PDF)

Ethical issues of genetic susceptibility testing for occupational diseases: opinions of trainees in a high-risk job

International archives of occupational and environmental health, 2013-10, Vol.86 (7), p.827-836

2013

Volltextzugriff (PDF)

Clinical Problems with the Performance of Euthanasia and Physician-Assisted Suicide in the Netherlands

The New England journal of medicine, 2000-02, Vol.342 (8), p.551-556

2000

Volltextzugriff (PDF)

Context-Relative Norms Determine the Appropriate Type of Consent in Clinical Biobanks: Towards a Potential Solution for the Discrepancy between the General Data Protection Regulation and the European Data Protection Board on Requirements for Consent

Science and engineering ethics, 2020-12, Vol.26 (6), p.3271-3284

2020

Volltextzugriff (PDF)

Considering quality of life in end-of-life decisions for severely disabled children

Research in developmental disabilities, 2018-02, Vol.73, p.67-75

2018

Volltextzugriff (PDF)

The end of life: informal care for dying older people and its relationship to place of death

Palliative medicine, 2004-07, Vol.18 (5), p.468-477

2004

Volltextzugriff (PDF)

The perspectives of in-hospital healthcare professionals on the timing and collaboration in advance care planning: A survey study

Heliyon, 2023-04, Vol.9 (4), p.e14772-e14772, Article e14772

2023

Volltextzugriff (PDF)

End-of-life decision-making for children with severe developmental disabilities: The parental perspective

Research in developmental disabilities, 2016-02, Vol.49-50, p.235-246

2016

Volltextzugriff (PDF)

Proxy reporting in after-death interviews: the use of proxy respondents in retrospective assessment of chronic diseases and symptom burden in the terminal phase of life

Palliative medicine, 2003-03, Vol.17 (2), p.191-201

2003

Volltextzugriff (PDF)

Individual responsibility, solidarity and differentiation in healthcare

Journal of medical ethics, 2014-11, Vol.40 (11), p.770-773

2014

Volltextzugriff (PDF)

Evaluation of the Notification Procedure for Physician-Assisted Death in the Netherlands

The New England journal of medicine, 1996-11, Vol.335 (22), p.1706-1712

1996

Volltextzugriff (PDF)

Value judgements that matter to patients remain implicit in oncology guidelines : an observational study

Netherlands journal of medicine, 2009-02, Vol.67 (2), p.62-68

2009

Volltextzugriff (PDF)

1 – 25 von 1.915

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(1.501)
Mit Volltextzugriff
(1.535)

Publikationsform

6 weitere anzeigen...

Weniger anzeigen...

Sprache

2 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(3)
... seit 90 Tagen
(8)

Menü

Weitere Dienste

Einstellungen

What About Us? Experiences of Relatives Regarding Physician-Assisted Death for Patients Suffering from Mental Illness: A Qualitative Study

The perspectives of professional caregivers on quality of life of persons with profound intellectual and multiple disabilities: a qualitative study

Dignity of informal caregivers of migrant patients in the last phase of life: a qualitative study

The role of research in improving responsiveness of palliative care to migrants and other underserved populations in the Netherlands: a qualitative interview study

Experiences and views of Dutch general practitioners regarding physician-assisted death for patients suffering from severe mental illness: a mixed methods approach

How to help researchers in palliative care improve responsiveness to migrants and other underrepresented populations: developing and testing a self-assessment instrument

A dignified last phase of life for patients with a migration background: A qualitative study

Where is the citizen? Comparing civic spaces in long-term mental healthcare

Parent perspectives on the assessment of quality of life of their children with profound intellectual and multiple disabilities in the Netherlands

Euthanasia, Physician-Assisted Suicide, and Other Medical Practices Involving the End of Life in the Netherlands, 1990–1995

Challenges in the implementation and evaluation of a transmural palliative care pathway for acutely hospitalized older adults; lessons from the PalliSupport program: A qualitative process evaluation study

How parents and physicians experience end-of-life decision-making for children with profound intellectual and multiple disabilities

Parenting by persons with intellectual disability: an explorative study in the Netherlands

Thoughts of patients with advanced heart failure on dying

Ethical issues of genetic susceptibility testing for occupational diseases: opinions of trainees in a high-risk job

Clinical Problems with the Performance of Euthanasia and Physician-Assisted Suicide in the Netherlands

Context-Relative Norms Determine the Appropriate Type of Consent in Clinical Biobanks: Towards a Potential Solution for the Discrepancy between the General Data Protection Regulation and the European Data Protection Board on Requirements for Consent

Considering quality of life in end-of-life decisions for severely disabled children

The end of life: informal care for dying older people and its relationship to place of death

The perspectives of in-hospital healthcare professionals on the timing and collaboration in advance care planning: A survey study

End-of-life decision-making for children with severe developmental disabilities: The parental perspective

Proxy reporting in after-death interviews: the use of proxy respondents in retrospective assessment of chronic diseases and symptom burden in the terminal phase of life

Individual responsibility, solidarity and differentiation in healthcare

Evaluation of the Notification Procedure for Physician-Assisted Death in the Netherlands

Value judgements that matter to patients remain implicit in oncology guidelines : an observational study

Suchergebnisse filtern