How and When Does Consent Bias Research? (English)
- New search for: Groenwold, R. H. H.
- New search for: van der Graaf, R.
- New search for: van Delden, J. J. M.
- New search for: Groenwold, R. H. H.
- New search for: van der Graaf, R.
- New search for: van Delden, J. J. M.
In:
The American Journal of Bioethics
;
13
, 4
;
46-48
;
2013
- Article (Journal) / Electronic Resource
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Title:How and When Does Consent Bias Research?
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Contributors:
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Published in:The American Journal of Bioethics ; 13, 4 ; 46-48
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Publisher:
- New search for: Taylor & Francis Group
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Publication date:2013-04-01
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Size:3 pages
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Source:
Table of contents – Volume 13, Issue 4
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 1
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Can Informed Consent Go Too Far? Balancing Consent and Public Benefit in ResearchMilner, Lauren C. / Magnus, David et al. | 2013
- 3
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Sickle Cell Disease and the “Difficult Patient” ConundrumBergman, Edward J. / Diamond, Nicholas J. et al. | 2013
- 11
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De-Escalating Conflict: Mediation and the “Difficult” PatientFiester, Autumn et al. | 2013
- 12
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Disrespectful Care in the Treatment of Sickle Cell Disease Requires More Than Ethics ConsultationHaywood, CarltonJr. et al. | 2013
- 14
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Pain, Chronic Pain, and Sickle Cell Chronic PainAmundson, Ron et al. | 2013
- 16
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Acknowledging Levels of Racism in the Definition of “Difficult”Creary, Melissa / Eisen, Arri et al. | 2013
- 18
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Not Your Typical Frequent Flyer: Overcoming Mythology in Caring for Sickle Cell Disease PatientsBoatright, Dowin H. / Abbott, Jean et al. | 2013
- 20
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The “Difficult Patient” Conundrum in Sickle Cell Disease in Kenya: Complex Sociopolitical Problems Need Wide Multidimensional SolutionsMarsh, Vicki / Mocamah, George / Mabibo, Emmanuel / Kombe, Francis / Williams, Thomas N. et al. | 2013
- 22
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Intractable Difficulties in Caring for People With Sickle Cell DiseaseCrowther, Helen Jane / Kerridge, Ian et al. | 2013
- 24
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Distinguishing Difficult Patients From Difficult MaladiesRich, Ben A. et al. | 2013
- 27
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Does Consent Bias Research?Rothstein, Mark A. / Shoben, Abigail B. et al. | 2013
- 38
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Data Citizenship and Informed ConsentFrancis, Leslie P. / Francis, John G. et al. | 2013
- 40
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Informed Consent, Big Data, and the Oxymoron of Research That Is Not ResearchIoannidis, John P. A. et al. | 2013
- 42
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A Review of Evidence on Consent Bias in ResearchEmam, Khaled El / Jonker, Elizabeth / Moher, Ester / Arbuckle, Luk et al. | 2013
- 44
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A Thick Opt-Out Is Often SufficientGiesbertz, Noor A. A. / Bredenoord, Annelien L. / van Delden, Johannes J. M. et al. | 2013
- 46
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How and When Does Consent Bias Research?Groenwold, R. H. H. / van der Graaf, R. / van Delden, J. J. M. et al. | 2013
- 49
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The Interaction Between Research Consent and Random ErrorTrafimow, David et al. | 2013
- 50
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Electronic Fences Make Good Neighbors: The Importance of Medical Records Managers to Protecting AutonomyFox, Mark D. / Munoz, Ricky T. et al. | 2013
- 53
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Review of Peter Ubel, Critical Decisions: How You and Your Doctor Can Make the Right Medical Choices Together 1Berger, Zackary et al. | 2013
- 54
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Review of Anne-Maree Farrell, The Politics of Blood: Ethics, Innovation and the Regulation of Risk 1Galarneau, Charlene et al. | 2013
- W1
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An Unbiased Response to the Open Peer Commentaries on “Does Consent Bias Research?”Rothstein, Mark A. / Shoben, Abigail B. et al. | 2013