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4. Consent to cancer registration--an unnecessary burden. Paterson IC BMJ; 2001 May; 322(7294):1130. PubMed ID: 11337454 [No Abstract] [Full Text] [Related]
5. The duty to register phase I trials. Saunders PT Am J Bioeth; 2009 Aug; 9(8):41-2. PubMed ID: 19998160 [No Abstract] [Full Text] [Related]
6. Need for moral audit in evaluating quality in health care. Doyal L Qual Health Care; 1992 Sep; 1(3):178-83. PubMed ID: 10136860 [No Abstract] [Full Text] [Related]
7. Informed consent for cancer registration. Chantler C Lancet Oncol; 2001 Jan; 2(1):8. PubMed ID: 11905627 [No Abstract] [Full Text] [Related]
8. Confidence matters: the rise and fall of informational autonomy in medical law. Case P Med Law Rev; 2003; 11(2):208-36. PubMed ID: 15085818 [No Abstract] [Full Text] [Related]
9. Data protection and patients' consent. Informed consent should be sought before data are used by registries. Morrow JI BMJ; 2001 Mar; 322(7285):549-50. PubMed ID: 11230085 [No Abstract] [Full Text] [Related]
10. The ethics of medicine: an annotated bibliography of recent literature. Jonsen AR; Cassel C; Lo B; Perkins HS Ann Intern Med; 1980 Jan; 92(1):136. PubMed ID: 6985781 [No Abstract] [Full Text] [Related]
11. Legal and ethical myths about informed consent. Meisel A; Kuczewski M Arch Intern Med; 1996 Dec 9-23; 156(22):2521-6. PubMed ID: 8951294 [TBL] [Abstract][Full Text] [Related]
12. Handbook on medical ethics: medical ethics and the practitioner. Issues Med Ethics; 1996; 4(2):54-8. PubMed ID: 15011679 [No Abstract] [Full Text] [Related]
13. Scientific and ethical issues of computer-linked records. Elwood JM Int J Cancer; 1996 Aug; 67(4):586-7. PubMed ID: 8759620 [No Abstract] [Full Text] [Related]
14. To tell or not to tell. Carlisle D Nurs Times; 1991 Apr 17-23; 87(16):46-7. PubMed ID: 2020599 [No Abstract] [Full Text] [Related]