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Nr. |
Eintrag |
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1 |
Sleurs, Elke; Kalokairinou, Louiza; Howard, Heidi Carmen:
Promotion and sales of self-tests on the internet
In: Routledge handbook of medical law and ethics / ed. by Yann Joly and Bartha Maria Knoppers. - London [u.a.] : Routledge, (2015). - 286-300 |
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2 |
Meier-Abt, Peter; Salath , Michelle:
Stellungnahme der SAMW zu den Verordnungen zum Bundesgesetz ueber die Forschung am Menschen.
In: |
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3 |
Arning, Marian et al.:
Datenschutz: Forschung mit genetischen Daten.
In: Deutsches Aerzteblatt, 2011, Vol. 108 (10), A-518-519 |
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4 |
Aultman, Julie M; Borges, Nicole J:
The ethics of HIV testing and disclosure for healthcare professionals: what do our future doctors think?
In: Medical teacher, 2011, Vol. 33 (1), e50-6 |
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5 |
Markovitz, Amanda R et al.:
Primary antiretroviral drug resistance in newly human immunodeficiency virus-diagnosed individuals testing anonymously and confidentially.
In: Microbial drug resistance (Larchmont, N.Y.), 2011, Vol. 17 (2), 283-9 |
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6 |
Braun, Stefan:
Das neue Gendiagnostikgesetz. Sanktionierung "heimlicher Vaterschaftstests".
In: Humboldt-Forum Recht, 2010, Vol. 16 (11), 148-158 |
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7 |
Loukides, Grigorios; Gkoulalas-Divanis, Aris; Malin, Bradley:
Anonymization of electronic medical records for validating genome-wide association studies.
In: Proceedings of the National Academy of Sciences of the United States of America 2010 Apr 27; 107(17): 7898-903 |
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8 |
Brett, Sanora et al.:
Can we improve recruitment of oocyte donors with loss of donor anonymity? A hospital-based survey.
In: Human Fertility, 2008, Vol. 11 (2), 101-107 |
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9 |
Cavu o lu, A Celebiler et al.:
A pilot study for human tumor/DNA banking: returned more questions than answers
In: Medical Oncology; 2008; 25(4): 471-473 |
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10 |
Coors, Marilyn et al.:
Directives for retained DNA: preferences of adolescent patients with substance and conduct problems and their siblings.
In: American Journal of Bioethics, 2008, Vol. 8 (10), 77-79; reply by Sara Chandros Hull, et al. W7-W8 |
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11 |
Crawshaw, Marilyn:
Prospective parents' intentions regarding disclosure following the removal of donor anonymity.
In: Human Fertility, 2008, Vol. 11 (2), 95-100 |
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12 |
Edginton, Mary E.; Selgelid, Michael J.:
Ethics and research: the case of informed consent [editorial]
In: International Journal of Tuberculosis and Lung Disease, 2008, Vol. 12 (5), 465-466 |
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13 |
Greenbaum, Dov; Du, Jiang; Gerstein, Mark:
Genomic anonymity: have we already lost it?
In: American Journal of Bioethics, 2008, Vol. 8 (10), 71-74; reply by Sara Chandros Hull, et al. W7-W8 |
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14 |
Harmon, Amy:
Fear of insurance trouble leads many to shun or hide DNA tests
In: New York Times, 2008 (2008-02-24), A1, A25 |
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15 |
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 |
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16 |
Hull, Sara Chandros et al.:
Patients' views on identifiability of samples and informed consent for genetic research.
In: American Journal of Bioethics, 2008, Vol. 8 (10), 62-70 |
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17 |
Hull, Sara Chandros; Wilfond, Benjamin S.:
What does it mean to be identifiable?
In: American Journal of Bioethics, 2008, Vol. 8 (10), W7-W8 |
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18 |
Lipworth, Wendy; Morrell, Bronwen; Kerridge, Ian:
Ethics as an act of listening.
In: American Journal of Bioethics, 2008, Vol. 8 (10), 80-81; reply by Sara Chandros Hull, et al. W7-W8 |
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19 |
McGuire, Amy L.:
Identifiability of DNA data: the need for consistent federal policy.
In: American Journal of Bioethics, 2008, Vol. 8 (10), 75-76; reply by Sara Chandros Hull, et al. W7-W8 |
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20 |
Greely, Henry T.:
The uneasy ethical and legal underpinnings of large-scale genomic biobanks.
In: Annual Review of Genomics and Human Genetics, 2007, 8, 343-364 |
