327 related articles for article (PubMed ID: 10732878)
21. Obligation and consent.
Lesser H
J Med Ethics; 1989 Dec; 15(4):195-6. PubMed ID: 2614789
[TBL] [Abstract][Full Text] [Related]
22. The tension between self governance and absolute inner worth in Kant's moral philosophy.
Häyry M
J Med Ethics; 2005 Nov; 31(11):645-7. PubMed ID: 16269562
[TBL] [Abstract][Full Text] [Related]
23. Information waivers: reply to Strasser.
Ost DE
J Med Philos; 1986 Aug; 11(3):279-84. PubMed ID: 11643941
[TBL] [Abstract][Full Text] [Related]
24. Obstetric ethics and the abortion controversy.
Chervenak FA; McCullough LB
Am J Ethics Med; 1994; 3(1):3-6. PubMed ID: 11652828
[No Abstract] [Full Text] [Related]
25. To know or not to know? Genetic ignorance, autonomy and paternalism.
Wilson J
Bioethics; 2005 Oct; 19(5-6):492-504. PubMed ID: 16425486
[TBL] [Abstract][Full Text] [Related]
26. Conflicting duties and restitution of the trusting relationship.
Eriksen A
J Med Ethics; 2018 Nov; 44(11):768-773. PubMed ID: 29907578
[TBL] [Abstract][Full Text] [Related]
27. Bioethics and the liberal state: Just Doctoring: Medical Ethics in the Liberal State, by Troyen A. Brennan.
Douard J
J Clin Ethics; 1993; 4(1):92-5. PubMed ID: 11643116
[No Abstract] [Full Text] [Related]
28. Response to Erich Loewy: commentary.
Thomasma DC
J Clin Ethics; 1991; 2(2):90-1. PubMed ID: 11642928
[TBL] [Abstract][Full Text] [Related]
29. Bioethics: private choice and common good.
Callahan D
Hastings Cent Rep; 1994; 24(3):28-31. PubMed ID: 8089005
[No Abstract] [Full Text] [Related]
30. Genetic knowledge and third-party interests.
Boetzkes E
Camb Q Healthc Ethics; 1999; 8(3):386-92. PubMed ID: 10388938
[No Abstract] [Full Text] [Related]
31. The right to genetic information: some reflections on Dutch developments.
Van Leeuwen E; Hertogh C
J Med Philos; 1992 Aug; 17(4):381-93. PubMed ID: 1431657
[TBL] [Abstract][Full Text] [Related]
32. Self-identification and the morality of abortion.
Lusby K
Univ Toledo Law Rev; 1992; 24(1):121-58. PubMed ID: 11656258
[No Abstract] [Full Text] [Related]
33. Assessing the social impact of human genome research: a status report.
Juengst ET
Kans Med; 1995; 96(2):50-1, 57. PubMed ID: 7500593
[No Abstract] [Full Text] [Related]
34. Physicians, friendship, and moral strangers: an examination of a relationship.
Loewy EH
Camb Q Healthc Ethics; 1994; 3(1):52-9. PubMed ID: 8032519
[No Abstract] [Full Text] [Related]
35. Whose genes are these anyway?: familial conflicts over access to genetic information.
Suter SM
Mich Law Rev; 1993 Jun; 91(7):1854-908. PubMed ID: 10129309
[No Abstract] [Full Text] [Related]
36. A Genealogy of Autonomy: Freedom, Paternalism, and the Future of the Doctor-Patient Relationship.
Genuis QIT
J Med Philos; 2021 Jun; 46(3):330-349. PubMed ID: 33948633
[TBL] [Abstract][Full Text] [Related]
37. Ethical problems in genetic counselling.
Murray RF
Ghana Med J; 1973 Sep; 12(3):304-9. PubMed ID: 11662058
[No Abstract] [Full Text] [Related]
38. The right not to know--worthy of preservation any longer? An ethical perspective.
Austad T
Clin Genet; 1996 Aug; 50(2):85-8. PubMed ID: 8937766
[TBL] [Abstract][Full Text] [Related]
39. Genetic ignorance and reasonable paternalism.
Takala T
Theor Med Bioeth; 2001 Sep; 22(5):485-91. PubMed ID: 11808682
[TBL] [Abstract][Full Text] [Related]
40. Children's competence and children's rights.
Schoeman F
IRB; 1982; 4(6):1-6. PubMed ID: 11649186
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
