Horn, Ruth ca. 20. / 21. Jh.
Horn, Ruth
Ruth Horn researcher
VIAF ID: 9138150033015111180000 ( Personal )
Permalink: http://viaf.org/viaf/9138150033015111180000
Preferred Forms
- 200 _ | ‡a Horn ‡b Ruth
- 100 1 _ ‡a Horn, Ruth ‡d ca. 20. / 21. Jh.
- 100 0 _ ‡a Ruth Horn ‡c researcher
4xx's: Alternate Name Forms (1)
Works
Title | Sources |
---|---|
Advance directives in English and French law: different concepts, different values, different societies | |
Can there be wrongful life at the end of life? German courts revisit an old problem in a new context | |
concept of dignity and its use in end-of-life debates in England and France | |
Democratic research: setting up a research commons for a qualitative, comparative, longitudinal interview study during the COVID-19 pandemic | |
“I don’t need my patients’ opinion to withdraw treatment”: patient preferences at the end-of-life and physician attitudes towards advance directives in England and France | |
droit de mourir: choisir sa fin de vie, en France et en Allemagne | |
Empathy in healthcare: the limits and scope of empathy in public and private systems | |
ethical landscape(s) of non-invasive prenatal testing in England, France and Germany: findings from a comparative literature review | |
ethics of genomic medicine: redefining values and norms in the UK and France | |
France et la Grande-Bretagne à l’ère de la médecine génomique: nouveaux défis éthiques en médecine de la reproduction | |
‘French exception’: the right to continuous deep sedation at the end of life | |
Health professionals and scientists’ views on genome-wide NIPT in the French public health system: critical analysis of the ethical issues raised by prenatal genomics | |
Making space for empathy: supporting doctors in the emotional labour of clinical care | |
Managing expectations, rights, and duties in large-scale genomics initiatives: a European comparison | |
Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocol | |
NIPT and the concerns regarding 'routinisation' | |
Normative positions towards COVID-19 contact-tracing apps: findings from a large-scale qualitative study in nine European countries | |
Not putting the cart before the horse: the complex social and ethical terrain of prenatal exome sequencing | |
Opening Pandora's box? Ethical issues in prenatal whole genome and exome sequencing | |
Preserving women’s reproductive autonomy while promoting the rights of people with disabilities? The case of Heidi Crowter and Maire Lea-Wilson in the light of NIPT debates in England, France and Germany | |
right to a self-determined death as expression of the right to freedom of personal development: the German Constitutional Court takes a clear stand on assisted suicide | |
Solidarity and autonomy: two conflicting values in English and French health care and bioethics debates? | |
Solidarity during the COVID-19 pandemic: evidence from a nine-country interview study in Europe | |
Überblick über den Verlauf der Sterbehilfe-Debatte in Frankreich | |
"Uninformed consent" in clinical trials with cancer patients: a qualitative analysis of patients' and support persons' communication experiences and needs | |
use of advance directives in the context of limited resources for healthcare | |
Welche Art von Selbstbestimmung für sterbenskranke Patienten? Eine vergleichende Studie in Frankreich und Deutschland | |
“Why should I question a patient’s wish?”: a comparative study on physicians’ perspectives on their duties to respect advance directives |