|
Nr. |
Eintrag |
|
1 |
Ikuenobe, Polycarp:
African communal basis for autonomy and life choices
In: Developing World Bioethics, 2018, Vol. 18 (3), 212-221 |
|
2 |
Metz, Thaddeus:
A bioethic of communion : beyond care and the four principles with regard to reproduction
In: The ethics of reproductive genetics : between utility, principles, and virtues / Marta Soniewicka, ed, 2018, 128, 49-66 |
|
3 |
Wilson, Geoff A.:
Community resilience and social memory
In: Environmental Values, 2015, Vol. 24 (2), 227-257 |
|
4 |
Hughes, Robert C.:
Justifying community benefit requirements in international research
In: Bioethics, 2014, Vol. 28 (8), 397-404 |
|
5 |
Friele, Minou Bernadette:
Die Deklaration von Helsinki und die Regelung des Informed consent : zur Berücksichtigung interkultureller Aspekte nach der Revision von 2008
In: Die Deklaration von Helsinki : Revisionen und Kontroversen ; mit der Dokumentation der 28. Jahresversammlung des Arbeitskreises Medizinischer Ethik-Kommissionen in der Bundesrepublik Deutschland am 26. und 27. November 2010 in München / H.-J. Ehni ; U. Wiesing (Hrsg.). Mit Beitr. von E.R.M. Cohen, H.-J. Ehni, E.J. Emanuel, M. Friele ... - Köln : Deutscher Ärzte-Verlag, (2012). - 95-102 |
|
6 |
Friele, Minou Bernadette:
Sowohl als auch? Zur Koppelung des Informed Consent und des Community Consent Prinzips in kulturuebergreifenden klinischen Forschungsvorhaben.
In: Ethik in der Medizin, 2012, Vol. 24 (4), 313-322 |
|
7 |
Blohm, María Cristina:
Zugang zu humangenetischen Ressourcen indigener Völker Lateinamerikas : eine Stakeholderanalyse
2010 |
|
8 |
Burgess, Michael M.; Tansey, James:
Cultural authority of informed consent : indigenous participation in biobanking and salmon genomic focus groups
In: The limits of consent : a socio-ethical approach to human subject research in medicine / ed. by Oonagh Corrigan ; John McMillan ; Kathleen Liddell ... - Oxford [u.a.] : Oxford Univ. Press, (2009). - 199-211 |
|
9 |
Burhansstipanov, Linda; Bemis, Lynne Taylor; Petereit, Daniel G.:
Native American communities: perspectives on healthcare genetics
In: Monsen, Rita Black, ed. Genetics and Ethics in Health Care: New Questions in the Age of Genomic Health. Silver Spring, MD: American Nurses Association, 2009: 179-199 |
|
10 |
Geransar, Rose:
Banking on trust: issues of informed consent in pharmacogenetic research
In: Einsiedel, Edna F., ed. Emerging Technologies: From Hindsight to Foresight. Vancouver: UBC Press, 2009: 185-202 |
|
11 |
Kajlich, Helena:
Indigenous peoples and genetic population research: reflections on a culturally appropriate model of indigenous participant consent
In: Hocking, Barbara Ann, ed. The Nexus of Law and Biology: New Ethical Challenges. Farnham, England; Burlington, VT: Ashgate Pub., 2009: 45-56 |
|
12 |
Osrin, David et al.:
Ethical challenges in cluster randomized controlled trials: experiences from public health interventions in Africa and Asia
In: Bulletin of the World Health Organization , 2009, Vol. 87 (10), 772-779 Accessed: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2755306/pdf/08 [2011 February 3] |
|
13 |
Patra, Prasanna Kumar; Sleeboom-Faulkner, Margaret:
The Indian genomic biobank initiative and emerging bioethical issues: a community-based perspective
In: Sleeboom-Faulkner, Margaret, ed. Human Genetic Biobanks in Asia: Politics of Trust and Scientific Advancement. London; New York: Routledge, 2009: 151-167 |
|
14 |
Árnason, Vilhjálmur; Hjörleifsson, Stefán:
Population databanks and democracy in light of the Icelandic experience
In: Launis, Veikko; Räikkä, Juha, eds. Genetic Democracy: Philosophical Perspectives. New York: Springer, 2008: 93-104 |
|
15 |
Artizzu, Federica:
The informed consent aftermath of the genetic revolution. An Italian example of implementation
In: Medicine, Health Care and Philosophy, 2008, Vol. 11 (2), 181-190 |
|
16 |
Elger, Bernice S.:
Consent and use of samples
In: Ethical issues in governing biobanks : global perspectives / ed. by Bernice Elger ; Nikola Biller-Andorno ; Alexandre Mauron ... - Aldershot [u.a.] : Ashgate, (2008). - 57-88 |
|
17 |
Fan, Chien-Te; Lin, Jui-Chu; Lee, Chung-His:
Taiwan Biobank: a project aiming to aid Taiwan's transition into a biomedical island.
In: Pharmacogenomics, 2008, Vol. 9 (2), 235-246 |
|
18 |
Ganguli-Mitra, Agomoni:
Collective consent
In: Ethical issues in governing biobanks : global perspectives / ed. by Bernice Elger ; Nikola Biller-Andorno ; Alexandre Mauron ... - Aldershot [u.a.] : Ashgate, (2008). - 121-130 |
|
19 |
Haga, Susanne B.; Beskow, Laura M.:
Ethical, legal, and social implications of biobanks for genetics research.
In: Advances in Genetics, 2008, 60, 505-544 |
|
20 |
Hellenic National Bioethics Commission:
Report on the collection and use of genetic data
In: Dracopoulou, Marianna, ed. Reflections on Contemporary Issues: Opinions and Reports, 2000-2008. Athens, Greece: National Bioethics Commission, 2008: 73-100 |
