143 related articles for article (PubMed ID: 9846770)
1. Permission and confidentiality in publishing pedigrees.
Schrock CR
JAMA; 1998 Dec; 280(21):1826-7. PubMed ID: 9846770
[No Abstract] [Full Text] [Related]
2. Privacy and confidentiality in the publication of pedigrees: a survey of investigators and biomedical journals.
Botkin JR; McMahon WM; Smith KR; Nash JE
JAMA; 1998 Jun; 279(22):1808-12. PubMed ID: 9628712
[TBL] [Abstract][Full Text] [Related]
3. Publication-related risks to privacy: ethical implications of pedigree studies.
Powers M
IRB; 1993; 15(4):7-11. PubMed ID: 11652150
[No Abstract] [Full Text] [Related]
4. Privacy matters.
Nat Genet; 1998 Jul; 19(3):207-8. PubMed ID: 9662383
[No Abstract] [Full Text] [Related]
5. Pedigrees-publish? or perish the thought?
Byers PH; Ashkenas J
Am J Hum Genet; 1998 Sep; 63(3):678-81. PubMed ID: 9718362
[No Abstract] [Full Text] [Related]
6. Commentary: the importance of patients' consent for publication.
Smith R
BMJ; 1996 Jul; 313(7048):16. PubMed ID: 8664761
[No Abstract] [Full Text] [Related]
7. Statements from the International Committee of Medical Journal Editors.
JAMA; 1991 May 22-29; 265(20):2697-8. PubMed ID: 2023351
[No Abstract] [Full Text] [Related]
8. Informed consent for publication.
Fontanarosa PB; Glass RM
JAMA; 1997 Aug; 278(8):682-3. PubMed ID: 9272905
[No Abstract] [Full Text] [Related]
9. Obtain informed consent before publishing information about patients.
Clever LH
JAMA; 1997 Aug; 278(8):628-9. PubMed ID: 9272884
[No Abstract] [Full Text] [Related]
10. Patient consent for publication.
Kirsch M
JAMA; 1997 Dec 24-31; 278(24):2139; author reply 2140-1. PubMed ID: 9416997
[No Abstract] [Full Text] [Related]
11. Privacy in genetics research.
Fuller BP; Kahn MJ; Barr PA; Biesecker L; Crowley E; Garber J; Mansoura MK; Murphy P; Murray J; Phillips J; Rothenberg K; Rothstein M; Stopfer J; Swergold G; Weber B; Collins FK; Hudson KL
Science; 1999 Aug; 285(5432):1359-61. PubMed ID: 10490410
[No Abstract] [Full Text] [Related]
12. Patient consent for publication and the health of the public.
Snider DE
JAMA; 1997 Aug; 278(8):624-6. PubMed ID: 9272883
[No Abstract] [Full Text] [Related]
13. Genotyping in clinical trials: towards a principle of informed request.
Sass HM
J Med Philos; 1998 Jun; 23(3):288-96. PubMed ID: 9736190
[TBL] [Abstract][Full Text] [Related]
14. Protection of patients' rights to privacy.
International Committee of Medical Journal Editors
BMJ; 1995 Nov; 311(7015):1272. PubMed ID: 11644736
[TBL] [Abstract][Full Text] [Related]
15. Participation in pedigree studies and the risk of impeded access to health insurance.
Kass NE
IRB; 1993; 15(5):7-10. PubMed ID: 11659704
[No Abstract] [Full Text] [Related]
16. Patients have a right to privacy and anonymity in medical publication.
Riis P; Nylenna M
JAMA; 1991 May 22-29; 265(20):2720. PubMed ID: 2023355
[No Abstract] [Full Text] [Related]
17. Publishing information about patients.
Smith R
BMJ; 1995 Nov; 311(7015):1240-1. PubMed ID: 7496217
[No Abstract] [Full Text] [Related]
18. Switzerland: legislation -- a) artificial procreation and genetics; b) protection of medical data.
Guillod O
Eur J Health Law; 1994; 1(1):95-7. PubMed ID: 11654552
[No Abstract] [Full Text] [Related]
19. A country unveils its gene pool and debate flares.
Lyall S
N Y Times Web; 1999 Feb; ():F1, F4. PubMed ID: 11647698
[No Abstract] [Full Text] [Related]
20. US privacy laws may curb access to medical data.
Wadman M
Nature; 1997 Apr; 386(6625):533. PubMed ID: 9121564
[No Abstract] [Full Text] [Related]
[Next] [New Search]
