-
1
-
-
84856005737
-
Cameron promotes new partnership between research, industry, and the NHS
-
Cameron promotes new partnership between research, industry, and the NHS. Hawkes N, BMJ 2011 343 1179
-
(2011)
BMJ
, vol.343
, pp. 1179
-
-
Hawkes, N.1
-
2
-
-
77953478638
-
Understanding confidentiality and the law on access to medical records
-
10.1016/j.ogrm.2010.02.005
-
Understanding confidentiality and the law on access to medical records. Nicholas N, Nicholas S, Obstet Gynaecol Reprod Med 2010 20 161 163 10.1016/j.ogrm.2010.02.005
-
(2010)
Obstet Gynaecol Reprod Med
, vol.20
, pp. 161-163
-
-
Nicholas, N.1
Nicholas, S.2
-
3
-
-
38049075409
-
Low risk research using routinely collected identifiable health information without informed consent: Encounters with the Patient Information Advisory Group
-
10.1136/jme.2006.019661 18156520
-
Low risk research using routinely collected identifiable health information without informed consent: encounters with the Patient Information Advisory Group. Metcalfe C, Martin RM, Noble S, Lane JA, Hamdy FC, Neal DE, Donovan JL, J Med Ethics 2008 34 37 40 10.1136/jme.2006.019661 18156520
-
(2008)
J Med Ethics
, vol.34
, pp. 37-40
-
-
Metcalfe, C.1
Martin, R.M.2
Noble, S.3
Lane, J.A.4
Hamdy, F.C.5
Neal, D.E.6
Donovan, J.L.7
-
4
-
-
31344458742
-
Consent, confidentiality, and the Data Protection Act
-
10.1136/bmj.332.7534.165 16424496
-
Consent, confidentiality, and the Data Protection Act. Iversen A, Liddell K, Fear N, Hotopf M, Wessely S, BMJ 2006 332 165 169 10.1136/bmj.332.7534.165 16424496
-
(2006)
BMJ
, vol.332
, pp. 165-169
-
-
Iversen, A.1
Liddell, K.2
Fear, N.3
Hotopf, M.4
Wessely, S.5
-
5
-
-
77953945407
-
Need for a wider view of autonomy in epidemiological research
-
10.1136/bmj.c1172
-
Need for a wider view of autonomy in epidemiological research. Hansson MG, BMJ 2010 340 1172 1174 10.1136/bmj.c1172
-
(2010)
BMJ
, vol.340
, pp. 1172-1174
-
-
Hansson, M.G.1
-
6
-
-
66749176708
-
Written informed consent and selection bias in observational studies using medical records: Systematic review
-
10.1136/bmj.b866 19282440
-
Written informed consent and selection bias in observational studies using medical records: systematic review. Kho ME, Duffett M, Willison DJ, Cook DJ, Brouwers MC, BMJ 2009 338 866 10.1136/bmj.b866 19282440
-
(2009)
BMJ
, vol.338
, pp. 2866
-
-
Kho, M.E.1
Duffett, M.2
Willison, D.J.3
Cook, D.J.4
Brouwers, M.C.5
-
7
-
-
43449106497
-
The impact of consent on observational research: A comparison of outcomes from consenters and non consenters to an observational study
-
10.1186/1471-2288-8-15 18387187
-
The impact of consent on observational research: a comparison of outcomes from consenters and non consenters to an observational study. Macleod U, Watt G, BMC Med Res Methodol 2008 8 15 10.1186/1471-2288-8-15 18387187
-
(2008)
BMC Med Res Methodol
, vol.8
, pp. 15
-
-
Macleod, U.1
Watt, G.2
-
8
-
-
27144485387
-
Bias from requiring explicit consent from all participants in observational research: Prospective, population based study
-
The Scottish Intracranial Vascular Malformation Study (sivms) Steering Committee F. 10.1136/bmj.38624.397569.68 16223793
-
Bias from requiring explicit consent from all participants in observational research: prospective, population based study. Al-Shahi R, Vousden C, Warlow C, for the Scottish Intracranial Vascular Malformation Study (SIVMS) Steering Committee, BMJ 2005 331 942 944 10.1136/bmj.38624.397569.68 16223793
-
(2005)
BMJ
, vol.331
, pp. 942-944
-
-
Al-Shahi, R.1
Vousden, C.2
Warlow, C.3
-
9
-
-
77950513444
-
Measuring morbidity: Self-report or health care records?
-
10.1093/fampra/cmp098 20019091
-
Measuring morbidity: self-report or health care records? Barber J, Muller S, Whitehurst T, Hay E, Fam Pract 2010 27 25 30 10.1093/fampra/cmp098 20019091
-
(2010)
Fam Pract
, vol.27
, pp. 25-30
-
-
Barber, J.1
Muller, S.2
Whitehurst, T.3
Hay, E.4
-
10
-
-
3142748608
-
Patterns of Consent in Epidemiologic Research: Evidence from over 25,000 Responders
-
10.1093/aje/kwh141 15155293
-
Patterns of Consent in Epidemiologic Research: Evidence from Over 25,000 Responders. Dunn KM, Jordan K, Lacey RJ, Shapley M, Jinks C, Am J Epidemiol 2004 159 1087 1094 10.1093/aje/kwh141 15155293
-
(2004)
Am J Epidemiol
, vol.159
, pp. 1087-1094
-
-
Dunn, K.M.1
Jordan, K.2
Lacey, R.J.3
Shapley, M.4
Jinks, C.5
-
11
-
-
0033859590
-
What proportion of patients refuse consent to data collection from their records for research purposes
-
11042920
-
What proportion of patients refuse consent to data collection from their records for research purposes. Baker R, Shiels C, Stevenson K, Fraser R, Stone M, Br J Gen Pract 2000 50 655 656 11042920
-
(2000)
Br J Gen Pract
, vol.50
, pp. 655-656
-
-
Baker, R.1
Shiels, C.2
Stevenson, K.3
Fraser, R.4
Stone, M.5
-
12
-
-
2342455758
-
Data protection, informed consent, and research
-
10.1136/bmj.328.7447.1029 15117769
-
Data protection, informed consent, and research. Peto J, Fletcher O, Gilham C, BMJ 2004 328 1029 1030 10.1136/bmj.328.7447.1029 15117769
-
(2004)
BMJ
, vol.328
, pp. 1029-1030
-
-
Peto, J.1
Fletcher, O.2
Gilham, C.3
-
13
-
-
0036790701
-
Why we should not seek individual informed consent for participation in health services research
-
10.1136/jme.28.5.313 12356960
-
Why we should not seek individual informed consent for participation in health services research. Cassell J, Young A, J Med Ethics 2002 28 313 317 10.1136/jme.28.5.313 12356960
-
(2002)
J Med Ethics
, vol.28
, pp. 313-317
-
-
Cassell, J.1
Young, A.2
-
14
-
-
0034727367
-
Using patient-identifiable data for observational research and audit
-
10.1136/bmj.321.7268.1031 11053151
-
Using patient-identifiable data for observational research and audit. Al-Shahi R, Warlow C, BMJ 2000 321 1031 1032 10.1136/bmj.321.7268.1031 11053151
-
(2000)
BMJ
, vol.321
, pp. 1031-1032
-
-
Al-Shahi, R.1
Warlow, C.2
-
15
-
-
37749048008
-
Extracting information from hospital records: What patients think about consent
-
10.1136/qshc.2006.020313 18055882
-
Extracting information from hospital records: what patients think about consent. Campbell B, Thomson H, Slater J, Coward C, Wyatt K, Sweeney K, Qual Saf Health Care 2007 16 404 408 10.1136/qshc.2006.020313 18055882
-
(2007)
Qual Saf Health Care
, vol.16
, pp. 404-408
-
-
Campbell, B.1
Thomson, H.2
Slater, J.3
Coward, C.4
Wyatt, K.5
Sweeney, K.6
-
17
-
-
50249149723
-
Research on Medical Records Without Informed Consent
-
10.1111/j.1748-720X.2008.304.x 18840249
-
Research on Medical Records Without Informed Consent. Miller FG, J Law Med Ethics 2008 36 560 566 10.1111/j.1748-720X.2008.304.x 18840249
-
(2008)
J Law Med Ethics
, vol.36
, pp. 560-566
-
-
Miller, F.G.1
-
18
-
-
65349172379
-
Feasibility and cost of obtaining informed consent for essential review of medical records in large-scale health services research
-
10.1258/jhsrp.2008.008085 19299260
-
Feasibility and cost of obtaining informed consent for essential review of medical records in large-scale health services research. Noble S, Donovan J, Turner E, Metcalfe C, Lane A, Rowlands MA, Neal D, Hamdy F, Ben-Shlomo Y, Martin R, J Health Serv Res Policy 2009 14 77 81 10.1258/jhsrp.2008.008085 19299260
-
(2009)
J Health Serv Res Policy
, vol.14
, pp. 77-81
-
-
Noble, S.1
Donovan, J.2
Turner, E.3
Metcalfe, C.4
Lane, A.5
Rowlands, M.A.6
Neal, D.7
Hamdy, F.8
Ben-Shlomo, Y.9
Martin, R.10
-
19
-
-
4043071277
-
Obstacles to conducting epidemiological research in the UK general population
-
10.1136/bmj.329.7460.277 15284154
-
Obstacles to conducting epidemiological research in the UK general population. Ward HJT, Cousens SN, Smith-Bathgate B, Leitch M, Everington D, Will RG, Smith PG, BMJ 2004 329 277 279 10.1136/bmj.329.7460.277 15284154
-
(2004)
BMJ
, vol.329
, pp. 277-279
-
-
Ward, H.J.T.1
Cousens, S.N.2
Smith-Bathgate, B.3
Leitch, M.4
Everington, D.5
Will, R.G.6
Smith, P.G.7
-
20
-
-
33747175973
-
Consent for the use of personal medical data in research
-
10.1136/bmj.333.7561.255 16873867
-
Consent for the use of personal medical data in research. Singleton P, Wadsworth M, BMJ 2006 333 255 258 10.1136/bmj.333.7561.255 16873867
-
(2006)
BMJ
, vol.333
, pp. 255-258
-
-
Singleton, P.1
Wadsworth, M.2
-
21
-
-
69049109909
-
Consent for use of personal information for health research: Do people with potentially stigmatizing health conditions and the general public differ in their opinions?
-
10.1186/1472-6939-10-10 19630941
-
Consent for use of personal information for health research: Do people with potentially stigmatizing health conditions and the general public differ in their opinions? Willison D, Steeves V, Charles C, Schwartz L, Ranford J, Agarwal G, Cheng J, Thabane L, BMC Med Ethics 2009 10 10 10.1186/1472-6939-10-10 19630941
-
(2009)
BMC Med Ethics
, vol.10
, pp. 10
-
-
Willison, D.1
Steeves, V.2
Charles, C.3
Schwartz, L.4
Ranford, J.5
Agarwal, G.6
Cheng, J.7
Thabane, L.8
-
24
-
-
33751209201
-
Patients' opinions on privacy, consent and the disclosure of health information for medical research
-
16867240
-
Patients' opinions on privacy, consent and the disclosure of health information for medical research. Page S, Mitchell I, Chronic Dis Can 2006 27 60 67 16867240
-
(2006)
Chronic Dis Can
, vol.27
, pp. 60-67
-
-
Page, S.1
Mitchell, I.2
-
25
-
-
57649130687
-
Alternatives to project-specific consent for access to personal information for health research: Insights from a public dialogue
-
10.1186/1472-6939-9-18 19019239
-
Alternatives to project-specific consent for access to personal information for health research: Insights from a public dialogue. Willison D, Swinton M, Schwartz L, Abelson J, Charles C, Northrup D, Cheng J, Thabane L, BMC Med Ethics 2008 9 18 10.1186/1472-6939-9-18 19019239
-
(2008)
BMC Med Ethics
, vol.9
, pp. 18
-
-
Willison, D.1
Swinton, M.2
Schwartz, L.3
Abelson, J.4
Charles, C.5
Northrup, D.6
Cheng, J.7
Thabane, L.8
-
26
-
-
0842305807
-
Patients' consent preferences regarding the use of their health information for research purposes: A qualitative study
-
10.1258/135581904322716076 15006236
-
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 9 22 27 10.1258/135581904322716076 15006236
-
(2004)
J Health Serv Res Policy
, vol.9
, pp. 22-27
-
-
Nair, K.1
Willison, D.2
Holbrook, A.3
Keshavjee, K.4
-
27
-
-
0037442380
-
Patients' consent preferences for research uses of information in electronic medical records: Interview and survey data
-
10.1136/bmj.326.7385.373 12586673
-
Patients' consent preferences for research uses of information in electronic medical records: interview and survey data. Willison DJ, Keshavjee K, Nair K, Goldsmith C, Holbrook AM, BMJ 2003 326 373 10.1136/bmj.326.7385.373 12586673
-
(2003)
BMJ
, vol.326
, pp. 373
-
-
Willison, D.J.1
Keshavjee, K.2
Nair, K.3
Goldsmith, C.4
Holbrook, A.M.5
-
28
-
-
0642307855
-
The Use of Medical Records in Research: What Do Patients Want
-
10.1111/j.1748-720X.2003.tb00105.x 14626550
-
The Use of Medical Records in Research: What Do Patients Want. Kass NE, Natowicz MR, Hull SC, Faden RR, Plantinga L, Gostin LO, Slutsman J, J Law Med Ethics 2003 31 429 433 10.1111/j.1748-720X.2003.tb00105.x 14626550
-
(2003)
J Law Med Ethics
, vol.31
, pp. 429-433
-
-
Kass, N.E.1
Natowicz, M.R.2
Hull, S.C.3
Faden, R.R.4
Plantinga, L.5
Gostin, L.O.6
Slutsman, J.7
-
29
-
-
39049148089
-
-
London: The Wellcome Trust
-
Armstrong V, Barnett J, Cooper H, Monkman M, Moran-Ellis J, Shepherd R, Public perspectives on the governance of biomedical research: a qualitative study in a deliberatve context London: The Wellcome Trust 2007
-
(2007)
Public Perspectives on the Governance of Biomedical Research: A Qualitative Study in A Deliberatve Context
-
-
Armstrong, V.1
Barnett, J.2
Cooper, H.3
Monkman, M.4
Moran-Ellis, J.5
Shepherd, R.6
-
31
-
-
78049462739
-
Latest results from the UK trials evaluating prostate cancer screening and treatment: The CAP and ProtecT studies
-
10.1016/j.ejca.2010.09.016 21047592
-
Latest results from the UK trials evaluating prostate cancer screening and treatment: The CAP and ProtecT studies. Lane JA, Hamdy FC, Martin RM, Turner EL, Neal DE, Donovan JL, Eur J Cancer 2010 46 3095 3101 10.1016/j.ejca.2010.09. 016 21047592
-
(2010)
Eur J Cancer
, vol.46
, pp. 3095-3101
-
-
Lane, J.A.1
Hamdy, F.C.2
Martin, R.M.3
Turner, E.L.4
Neal, D.E.5
Donovan, J.L.6
-
32
-
-
84971585775
-
Qualitative Research: Introducing focus groups
-
10.1136/bmj.311.7000.299 7633241
-
Qualitative Research: Introducing focus groups. Kitzinger J, BMJ 1995 311 299 302 10.1136/bmj.311.7000.299 7633241
-
(1995)
BMJ
, vol.311
, pp. 299-302
-
-
Kitzinger, J.1
-
34
-
-
0030096228
-
A 12-item short-form health survey - Construction of scales and preliminary tests of reliability and validity
-
10.1097/00005650-199603000-00003 8628042
-
A 12-item short-form health survey-Construction of scales and preliminary tests of reliability and validity. Ware JE, Kosinski M, Keller SD, Medical Care 1996 34 220 233 10.1097/00005650-199603000-00003 8628042
-
(1996)
Medical Care
, vol.34
, pp. 220-233
-
-
Ware, J.E.1
Kosinski, M.2
Keller, S.D.3
-
35
-
-
81855225276
-
What do people affected by cancer think about electronic health information exchange? Results from the 2010 LIVESTRONG Electronic Health Information Exchange Survey and the 2008 Health Information National Trends Survey
-
10.1200/JOP.2011.000324 22043188
-
What do people affected by cancer think about electronic health information exchange? Results from the 2010 LIVESTRONG Electronic Health Information Exchange Survey and the 2008 Health Information National Trends Survey. Beckjord EBR, J Oncol Pract 2011 7 237 241 10.1200/JOP.2011.000324 22043188
-
(2011)
J Oncol Pract
, vol.7
, pp. 237-241
-
-
Beckjord, E.B.R.1
-
36
-
-
33847158024
-
Do characteristics of HIPAA consent forms affect the response rate
-
10.1097/01.mlr.0000241062.79855.35 17279027
-
Do characteristics of HIPAA consent forms affect the response rate. Bolcic-Jankovic D, Clarridge BR, Fowler FJ Jr, Weissman JS, Med Care 2007 45 100 103 10.1097/01.mlr.0000241062.79855.35 17279027
-
(2007)
Med Care
, vol.45
, pp. 100-103
-
-
Bolcic-Jankovic, D.1
Clarridge, B.R.2
Fowler Jr., F.J.3
Weissman, J.S.4
-
37
-
-
0032962011
-
Potential effect of authorization bias on medical record research
-
10.4065/74.4.330 10221460
-
Potential effect of authorization bias on medical record research. Jacobsen SJ, Xia Z, Campion ME, Darby CH, Plevak MF, Seltman KD, Melton LJ, Mayo Clin Proc 1999 74 330 338 10.4065/74.4.330 10221460
-
(1999)
Mayo Clin Proc
, vol.74
, pp. 330-338
-
-
Jacobsen, S.J.1
Xia, Z.2
Campion, M.E.3
Darby, C.H.4
Plevak, M.F.5
Seltman, K.D.6
Melton, L.J.7
-
38
-
-
0033368991
-
Patient consent for release of sensitive information from their medical records: An exploratory study
-
10.1002/(SICI)1099-0798(199910/12)17:4<445: AID-BSL359>3.0.CO;2-P 10653993
-
Patient consent for release of sensitive information from their medical records: an exploratory study. Merz JF, Spina BJ, Sankar P, Behav Sci Law 1999 17 445 454 10.1002/(SICI)1099-0798(199910/12)17:4<445::AID-BSL359>3.0. CO;2-P 10653993
-
(1999)
Behav Sci Law
, vol.17
, pp. 445-454
-
-
Merz, J.F.1
Spina, B.J.2
Sankar, P.3
-
40
-
-
0034538696
-
Selection Bias from Requiring Patients to Give Consent to Examine Data for Health Services Research
-
10.1001/archfami.9.10.1111 11115216
-
Selection Bias From Requiring Patients to Give Consent to Examine Data for Health Services Research. Woolf SH, Rothemich SF, Johnson RE, Marsland DW, Arch Fam Med 2000 9 1111 1118 10.1001/archfami.9.10.1111 11115216
-
(2000)
Arch Fam Med
, vol.9
, pp. 1111-1118
-
-
Woolf, S.H.1
Rothemich, S.F.2
Johnson, R.E.3
Marsland, D.W.4
-
41
-
-
0031796369
-
The impact of requiring patient authorization for use of data in medical records research
-
9834771
-
The impact of requiring patient authorization for use of data in medical records research. Yawn BP, Yawn RA, Geier GR, Xia Z, Jacobsen SJ, J Fam Pract 1998 47 361 365 9834771
-
(1998)
J Fam Pract
, vol.47
, pp. 361-365
-
-
Yawn, B.P.1
Yawn, R.A.2
Geier, G.R.3
Xia, Z.4
Jacobsen, S.J.5
-
42
-
-
33751003263
-
Patients, privacy and trust: Patients' willingness to allow researchers to access their medical records
-
10.1016/j.socscimed.2006.08.045 17045717
-
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 64 223 235 10.1016/j.socscimed. 2006.08.045 17045717
-
(2007)
Soc Sci Med
, vol.64
, pp. 223-235
-
-
Damschroder, L.J.1
Pritts, J.L.2
Neblo, M.A.3
Kalarickal, R.J.4
Creswell, J.W.5
Hayward, R.A.6
-
43
-
-
80054018958
-
The effect of seeking consent on the representativeness of patient cohorts: Iron-deficiency anaemia and colorectal cancer
-
10.1111/j.1463-1318.2011.02724.x 21831101
-
The effect of seeking consent on the representativeness of patient cohorts: iron-deficiency anaemia and colorectal cancer. Damery S, Ryan R, McManus RJ, Warmington S, Draper H, Wilson S, Colorectal Dis 2011 13 366 e373 10.1111/j.1463-1318.2011.02724.x 21831101
-
(2011)
Colorectal Dis
, vol.13
-
-
Damery, S.1
Ryan, R.2
McManus, R.J.3
Warmington, S.4
Draper, H.5
Wilson, S.6
-
44
-
-
1342266572
-
Public attitudes towards the use of primary care patient record data in medical research without consent: A qualitative study
-
10.1136/jme.2003.005157 14872086
-
Public attitudes towards the use of primary care patient record data in medical research without consent: a qualitative study. Robling MR, Hood K, Houston H, Pill R, Fay J, Evans HM, J Med Ethics 2004 30 104 109 10.1136/jme.2003.005157 14872086
-
(2004)
J Med Ethics
, vol.30
, pp. 104-109
-
-
Robling, M.R.1
Hood, K.2
Houston, H.3
Pill, R.4
Fay, J.5
Evans, H.M.6
-
45
-
-
33644786831
-
-
Sheffield: School of Health and Related Research, University of Sheffield
-
Shickle D, Carlisle J, Wallace S, Patient Electronic Record, Information and Consent (PERIC)-Public Attitudes to Protection and Use of Personal Health Information Sheffield: School of Health and Related Research, University of Sheffield 2002
-
(2002)
Patient Electronic Record, Information and Consent (PERIC)-Public Attitudes to Protection and Use of Personal Health Information
-
-
Shickle, D.1
Carlisle, J.2
Wallace, S.3
-
46
-
-
78650307648
-
Public attitudes to the use in research of personal health information from general practitioners' records: A survey of the Irish general public
-
10.1136/jme.2010.037903 21071570
-
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 37 50 55 10.1136/jme.2010.037903 21071570
-
(2011)
J Med Ethics
, vol.37
, pp. 50-55
-
-
Buckley, B.S.1
Murphy, A.W.2
Macfarlane, A.E.3
-
47
-
-
34548058860
-
-
Ottawa, ON: Canadian Policy Research Networks 23713556
-
MacKinnon MP, Saxena N, Swinton M, Watling J, Willison D, Understanding Canadians' Attitudes and Expectations: Citizens' Dialogue on Privacy and the Use of Personal Information for Health Research in Canada Ottawa, ON: Canadian Policy Research Networks 2006 23713556
-
(2006)
Understanding Canadians' Attitudes and Expectations: Citizens' Dialogue on Privacy and the Use of Personal Information for Health Research in Canada
-
-
Mackinnon, M.P.1
Saxena, N.2
Swinton, M.3
Watling, J.4
Willison, D.5
-
48
-
-
78751706184
-
Views on health information sharing and privacy from primary care practices using electronic medical records
-
10.1016/j.ijmedinf.2010.11.005 21167771
-
Views on health information sharing and privacy from primary care practices using electronic medical records. Perera G, Holbrook A, Thabane L, Foster G, Willison DJ, Int J Med Inform 2011 80 94 101 10.1016/j.ijmedinf.2010. 11.005 21167771
-
(2011)
Int J Med Inform
, vol.80
, pp. 94-101
-
-
Perera, G.1
Holbrook, A.2
Thabane, L.3
Foster, G.4
Willison, D.J.5
-
49
-
-
5444233582
-
Feasibility of a patient decision aid regarding disclosure of personal health information: Qualitative evaluation of the Health Care Information Directive
-
10.1186/1472-6947-4-13 15361257
-
Feasibility of a patient decision aid regarding disclosure of personal health information: qualitative evaluation of the Health Care Information Directive. Tracy CS, Dantas GC, Upshur RE, BMC Med Inform Decis Mak 2004 4 13 10.1186/1472-6947-4-13 15361257
-
(2004)
BMC Med Inform Decis Mak
, vol.4
, pp. 13
-
-
Tracy, C.S.1
Dantas, G.C.2
Upshur, R.E.3
-
50
-
-
33646582652
-
Patients' attitudes towards sharing their health information
-
10.1016/j.ijmedinf.2005.08.009 16198142
-
Patients' attitudes towards sharing their health information. Whiddett R, Hunter I, Engelbrecht J, Handy J, Int J Med Inform 2006 75 530 541 10.1016/j.ijmedinf.2005.08.009 16198142
-
(2006)
Int J Med Inform
, vol.75
, pp. 530-541
-
-
Whiddett, R.1
Hunter, I.2
Engelbrecht, J.3
Handy, J.4
-
51
-
-
0042631503
-
Patient Perspectives of Medical Confidentiality
-
10.1046/j.1525-1497.2003.20823.x 12911650
-
Patient Perspectives of Medical Confidentiality. Sankar P, Mora S, Merz JF, Jones NL, J Gen Intern Med 2003 18 659 669 10.1046/j.1525-1497.2003.20823.x 12911650
-
(2003)
J Gen Intern Med
, vol.18
, pp. 659-669
-
-
Sankar, P.1
Mora, S.2
Merz, J.F.3
Jones, N.L.4
-
52
-
-
33644930832
-
One-time general consent for research on biological samples
-
10.1136/bmj.332.7540.544 16513715
-
One-time general consent for research on biological samples. Wendler D, BMJ 2006 332 544 547 10.1136/bmj.332.7540.544 16513715
-
(2006)
BMJ
, vol.332
, pp. 544-547
-
-
Wendler, D.1
-
53
-
-
84859710797
-
Patients' experiences on donation of their residual biological samples and the impact of these experiences on the type of consent given for the future research use of the tissue: A systematic review
-
10.1111/j.1744-1609.2011.00251.x 22405414
-
Patients' experiences on donation of their residual biological samples and the impact of these experiences on the type of consent given for the future research use of the tissue: a systematic review. Chan TW, Mackey S, Hegney DG, Int J Evid Based Healthc 2012 10 9 26 10.1111/j.1744-1609.2011.00251.x 22405414
-
(2012)
Int J Evid Based Healthc
, vol.10
, pp. 9-26
-
-
Chan, T.W.1
Mackey, S.2
Hegney, D.G.3
|