-
1
-
-
33847634546
-
-
Medical Privacy, National Standards to Protect the Privacy of Personal Health Information. Available at:, Accessed September 1, 2006
-
Medical Privacy - National Standards to Protect the Privacy of Personal Health Information. Available at: http://www.hhs.gov/ocr/hipaa. Accessed September 1, 2006.
-
-
-
-
2
-
-
0037430997
-
HIPPA regulations: A new era of medical-record privacy?
-
Annas G. "HIPPA regulations: a new era of medical-record privacy?" N Engl J Med. 2003;348:1486-1490.
-
(2003)
N Engl J Med
, vol.348
, pp. 1486-1490
-
-
Annas, G.1
-
3
-
-
19344377658
-
Potential impact of the HIPPA privacy rule on data collection in a registry of patients with acute coronary syndrome
-
Armstrong D, Kline-Rogers E, Jani SM, et al. Potential impact of the HIPPA privacy rule on data collection in a registry of patients with acute coronary syndrome. Arch Intern Med. 2005;165:1125-1129.
-
(2005)
Arch Intern Med
, vol.165
, pp. 1125-1129
-
-
Armstrong, D.1
Kline-Rogers, E.2
Jani, S.M.3
-
4
-
-
0017953420
-
Informed consent: Consequences for response rate and response quality in social surveys
-
Singer E. Informed consent: consequences for response rate and response quality in social surveys. Am Sociol Rev. 1978;43:144-162.
-
(1978)
Am Sociol Rev
, vol.43
, pp. 144-162
-
-
Singer, E.1
-
5
-
-
21844487520
-
Confidentiality assurances and response: A quantitative review of the experimental literature
-
Singer E, Von Thurn DR, Miller ER. Confidentiality assurances and response: a quantitative review of the experimental literature. Public Opin Q. 1995;59:66-77.
-
(1995)
Public Opin Q
, vol.59
, pp. 66-77
-
-
Singer, E.1
Von Thurn, D.R.2
Miller, E.R.3
-
6
-
-
0036549591
-
Do patient consent procedures affect participation rates in health services research?
-
Nelson K, Garcia E, et al. Do patient consent procedures affect participation rates in health services research? Med Care. 2002;40:283-288.
-
(2002)
Med Care
, vol.40
, pp. 283-288
-
-
Nelson, K.1
Garcia, E.2
-
7
-
-
33644840045
-
Results of the National Initiative for Cancer Care Quality: How can we improve the quality of cancer care in the United States
-
Malin JL, Schneider EC, Epstein AM, et al. Results of the National Initiative for Cancer Care Quality: how can we improve the quality of cancer care in the United States. J Clin Oncol. 2006;24:626-634.
-
(2006)
J Clin Oncol
, vol.24
, pp. 626-634
-
-
Malin, J.L.1
Schneider, E.C.2
Epstein, A.M.3
-
8
-
-
4644281540
-
Interventions to improve research participants' understanding in informed consent for research
-
Flory J, Emanuel E. Interventions to improve research participants' understanding in informed consent for research. JAMA. 2004;292:1593-1601.
-
(2004)
JAMA
, vol.292
, pp. 1593-1601
-
-
Flory, J.1
Emanuel, E.2
-
9
-
-
0034538696
-
Selection bias from requiring patients to give consent to examine data for health services research
-
Woolf SH, Rothemich SF, Johnson RE, et al. Selection bias from requiring patients to give consent to examine data for health services research. Arch Fam Med. 2000;9:1111-1118.
-
(2000)
Arch Fam Med
, vol.9
, pp. 1111-1118
-
-
Woolf, S.H.1
Rothemich, S.F.2
Johnson, R.E.3
-
10
-
-
33847624350
-
Development and testing of informed consent questions to link survey data with administrative records
-
Bates N. Development and testing of informed consent questions to link survey data with administrative records. ASA Proc. 2005;3786-3793.
-
(2005)
ASA Proc
, pp. 3786-3793
-
-
Bates, N.1
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