These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
164 related articles for article (PubMed ID: 16867240)
1. Patients' opinions on privacy, consent and the disclosure of health information for medical research. Page SA; Mitchell I Chronic Dis Can; 2006; 27(2):60-7. PubMed ID: 16867240 [TBL] [Abstract][Full Text] [Related]
2. Perspectives of Australian adults about protecting the privacy of their health information in statistical databases. King T; Brankovic L; Gillard P Int J Med Inform; 2012 Apr; 81(4):279-89. PubMed ID: 22306206 [TBL] [Abstract][Full Text] [Related]
3. Access to medical records for research purposes: varying perceptions across research ethics boards. Willison DJ; Emerson C; Szala-Meneok KV; Gibson E; Schwartz L; Weisbaum KM; Fournier F; Brazil K; Coughlin MD J Med Ethics; 2008 Apr; 34(4):308-14. PubMed ID: 18375687 [TBL] [Abstract][Full Text] [Related]
4. Patients' consent preferences regarding the use of their health information for research purposes: a qualitative study. Nair K; Willison D; Holbrook A; Keshavjee K J Health Serv Res Policy; 2004 Jan; 9(1):22-7. PubMed ID: 15006236 [TBL] [Abstract][Full Text] [Related]
5. Confidentiality and access to sexual health services. Ryder N; McNulty AM Sex Health; 2009 Jun; 6(2):153-5. PubMed ID: 19457295 [TBL] [Abstract][Full Text] [Related]
7. Holding personal information in a disease-specific register: the perspectives of people with multiple sclerosis and professionals on consent and access. Baird W; Jackson R; Ford H; Evangelou N; Busby M; Bull P; Zajicek J J Med Ethics; 2009 Feb; 35(2):92-6. PubMed ID: 19181880 [TBL] [Abstract][Full Text] [Related]
8. Opt-out plus, the patients' choice: preferences of cancer patients concerning information and consent regimen for future research with biological samples archived in the context of treatment. Vermeulen E; Schmidt MK; Aaronson NK; Kuenen M; van der Valk P; Sietses C; van den Tol P; van Leeuwen FE J Clin Pathol; 2009 Mar; 62(3):275-8. PubMed ID: 19017681 [TBL] [Abstract][Full Text] [Related]
9. Patients' attitudes towards sharing their health information. Whiddett R; Hunter I; Engelbrecht J; Handy J Int J Med Inform; 2006 Jul; 75(7):530-41. PubMed ID: 16198142 [TBL] [Abstract][Full Text] [Related]
10. The CMA's Health Information Privacy Code: does it go too far? Hoey J CMAJ; 1998 Oct; 159(8):953-4. PubMed ID: 9834721 [No Abstract] [Full Text] [Related]
11. Public attitudes to the use in research of personal health information from general practitioners' records: a survey of the Irish general public. Buckley BS; Murphy AW; MacFarlane AE J Med Ethics; 2011 Jan; 37(1):50-5. PubMed ID: 21071570 [TBL] [Abstract][Full Text] [Related]
12. Public good, personal privacy: a citizens' deliberation about using medical information for pharmacoepidemiological research. Parkin L; Paul C J Epidemiol Community Health; 2011 Feb; 65(2):150-6. PubMed ID: 19948532 [TBL] [Abstract][Full Text] [Related]
13. Patients, privacy and trust: patients' willingness to allow researchers to access their medical records. Damschroder LJ; Pritts JL; Neblo MA; Kalarickal RJ; Creswell JW; Hayward RA Soc Sci Med; 2007 Jan; 64(1):223-35. PubMed ID: 17045717 [TBL] [Abstract][Full Text] [Related]
14. Confidentiality versus disclosure of a patient's infectious status. Nicol TE Gen Dent; 1997; 45(1):78-80. PubMed ID: 9171485 [TBL] [Abstract][Full Text] [Related]
15. Patients' perceptions of information received about medication prescribed for bipolar disorder: implications for informed choice. Bowskill R; Clatworthy J; Parham R; Rank T; Horne R J Affect Disord; 2007 Jun; 100(1-3):253-7. PubMed ID: 17174406 [TBL] [Abstract][Full Text] [Related]
16. Trends in collection, use and disclosure of personal information in contemporary health research: challenges for research governance. Willison DJ Health Law Rev; 2005; 13(2-3):107-13. PubMed ID: 16459423 [No Abstract] [Full Text] [Related]
17. Income and employment of people living with combined HIV/AIDS, chronic mental illness, and substance abuse disorders. Conover CJ; Arno P; Weaver M; Ang A; Ettner SL J Ment Health Policy Econ; 2006 Jun; 9(2):71-86. PubMed ID: 17007485 [TBL] [Abstract][Full Text] [Related]
18. Joint replacement recipients' post-surgery views about health information privacy and registry participation. Terry AL; Chesworth BM; Stolee P; Bourne RB; Speechley M Health Policy; 2008 Mar; 85(3):293-304. PubMed ID: 17904684 [TBL] [Abstract][Full Text] [Related]
19. Personal health care of residents: preferences for care outside of the training institution. Dunn LB; Moutier C; Green Hammond KA; Lehrmann J; Roberts LW Acad Psychiatry; 2008; 32(1):20-30. PubMed ID: 18270277 [TBL] [Abstract][Full Text] [Related]
20. A patient registry for cognitive rehabilitation research: a strategy for balancing patients' privacy rights with researchers' need for access. Schwartz MF; Brecher AR; Whyte J; Klein MG Arch Phys Med Rehabil; 2005 Sep; 86(9):1807-14. PubMed ID: 16181947 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]