1
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Who should receive life support during a public health emergency? Using ethical principles to improve allocation decisions.
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Ann Intern Med
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2009
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5.35
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2
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Expanding the paradigm of the physician's role in surrogate decision-making: an empirically derived framework.
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Crit Care Med
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2010
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3.54
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3
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The impact of health information on the Internet on health care and the physician-patient relationship: national U.S. survey among 1.050 U.S. physicians.
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J Med Internet Res
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2003
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3.48
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4
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The impact of health information on the internet on the physician-patient relationship: patient perceptions.
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Arch Intern Med
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2003
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3.35
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5
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Bioethics consultation in the private sector.
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Hastings Cent Rep
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2002
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3.01
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6
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Prognostication during physician-family discussions about limiting life support in intensive care units.
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Crit Care Med
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2007
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2.96
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7
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An Official ATS/AACN/ACCP/ESICM/SCCM Policy Statement: Responding to Requests for Potentially Inappropriate Treatments in Intensive Care Units.
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Am J Respir Crit Care Med
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2015
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2.86
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8
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New ISSCR guidelines underscore major principles for responsible translational stem cell research.
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Cell Stem Cell
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2008
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2.61
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9
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Decisions to limit life-sustaining treatment for critically ill patients who lack both decision-making capacity and surrogate decision-makers.
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Crit Care Med
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2006
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2.61
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10
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Are physicians' recommendations to limit life support beneficial or burdensome? Bringing empirical data to the debate.
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Am J Respir Crit Care Med
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2009
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2.46
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11
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Surrogate decision-makers' perspectives on discussing prognosis in the face of uncertainty.
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Am J Respir Crit Care Med
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2008
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2.40
|
12
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"It's not just what the doctor tells me:" factors that influence surrogate decision-makers' perceptions of prognosis.
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Crit Care Med
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2010
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2.25
|
13
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Last-resort options for palliative sedation.
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Ann Intern Med
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2009
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2.19
|
14
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The roles and experiences of nonaffiliated and non-scientist members of institutional review boards.
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Acad Med
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2003
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1.94
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15
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Strategies for culturally effective end-of-life care.
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Ann Intern Med
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2002
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1.77
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16
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Clinical decision-making: Patients' preferences and experiences.
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Patient Educ Couns
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2006
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1.67
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17
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Patient-centered communication: do patients really prefer it?
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J Gen Intern Med
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2004
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1.63
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18
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Discussing overall prognosis with the very elderly.
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N Engl J Med
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2011
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1.60
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19
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Obtaining consent for future research with induced pluripotent cells: opportunities and challenges.
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PLoS Biol
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2009
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1.58
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20
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Hope, truth, and preparing for death: perspectives of surrogate decision makers.
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Ann Intern Med
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2008
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1.54
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21
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A multicenter study of key stakeholders' perspectives on communicating with surrogates about prognosis in intensive care units.
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Ann Am Thorac Soc
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2015
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1.46
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22
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Direct-to-consumer advertising: physicians' views of its effects on quality of care and the doctor-patient relationship.
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J Am Board Fam Pract
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2004
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1.45
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23
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Human subjects issues and IRB review in practice-based research.
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Ann Fam Med
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2005
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1.44
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24
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Navigating language barriers under difficult circumstances.
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Ann Intern Med
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2008
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1.32
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25
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The language of prognostication in intensive care units.
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Med Decis Making
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2008
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1.29
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26
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The challenges of IRB review and human subjects protections in practice-based research.
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Med Care
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2002
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1.29
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27
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Life support for patients without a surrogate decision maker: who decides?
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Ann Intern Med
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2007
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1.27
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28
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Survey of u.s. Human research protection organizations: workload and membership.
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J Empir Res Hum Res Ethics
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2008
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1.26
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29
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Untapped potential: IRB guidance for the ethical research use of stored biological materials.
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IRB
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2004
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1.24
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30
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Answers and questions about ethics consultations.
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JAMA
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2003
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1.21
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31
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Direct-to-consumer advertising: public perceptions of its effects on health behaviors, health care, and the doctor-patient relationship.
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J Am Board Fam Pract
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2004
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1.19
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32
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IRB Chairs' Perspectives on Genomics Research Involving Stored Biological Materials: Ethical Concerns and Proposed Solutions.
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J Empir Res Hum Res Ethics
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2008
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1.14
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33
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HPV vaccine and adolescents' sexual activity.
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BMJ
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2006
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1.05
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34
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Clinical decision-making: physicians' preferences and experiences.
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BMC Fam Pract
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2007
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1.05
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35
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Choices physicians would make if they were the parents of a child with hypoplastic left heart syndrome.
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Am J Cardiol
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2003
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1.04
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36
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Survey of U.S. Boards that Review Mental Health-related Research.
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J Empir Res Hum Res Ethics
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2008
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1.04
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37
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IRBs and ethically challenging protocols: views of IRB chairs about useful resources.
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IRB
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2010
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1.00
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38
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'She gave it her best shot right away': patient experiences of biomedical and patient-centered communication.
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Patient Educ Couns
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2005
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1.00
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39
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Responsible oversight of human stem cell research: the California Institute for Regenerative Medicine's medical and ethical standards.
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PLoS Med
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2007
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0.97
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40
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Medical students' experiences with medical errors: an analysis of medical student essays.
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Med Educ
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2008
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0.95
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41
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The certificate of confidentiality application: a view from the NIH Institutes.
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IRB
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2004
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0.95
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42
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Research Participants' Perceptions of the Certificate of Confidentiality's Assurances and Limitations.
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J Empir Res Hum Res Ethics
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2007
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0.94
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43
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Lessons from an HIV transmission pair.
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J Infect Dis
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2007
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0.94
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44
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When previously expressed wishes conflict with best interests.
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JAMA Intern Med
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2013
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0.92
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45
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Legal barriers to implementing recommendations for universal, routine prenatal HIV testing.
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J Law Med Ethics
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2004
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0.91
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46
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Strengthening community consultation in critical care and emergency research.
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Crit Care Med
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2006
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0.90
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47
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Clinical trial design issues raised during recombinant DNA advisory committee review of gene transfer protocols.
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Hum Gene Ther
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2006
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0.89
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48
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Perceptions of conflict of interest disclosures among peer reviewers.
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PLoS One
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2011
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0.88
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49
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How do patients view the role of the primary care physician in inpatient care?
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Dis Mon
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0.87
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50
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Key clinical, ethical, and policy issues in the evaluation of the safety and effectiveness of solid organ transplantation in HIV-infected patients.
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Arch Intern Med
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2003
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0.87
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51
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Informed consent for innovative surgery: a survey of patients and surgeons.
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0.85
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52
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How pediatricians counsel parents when no "best-choice" management exists: lessons to be learned from hypoplastic left heart syndrome.
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Arch Pediatr Adolesc Med
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53
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Acquisition, Analysis, and Sharing of Data in 2015 and Beyond: A Survey of the Landscape: A Conference Report From the American Heart Association Data Summit 2015.
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J Am Heart Assoc
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0.84
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54
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Pilot study demonstrating effectiveness of targeted education to improve informed consent understanding in AIDS clinical trials.
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AIDS Care
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0.82
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55
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An educational intervention to improve resident comfort with communication at the end of life.
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J Palliat Med
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0.82
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56
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The end of therapeutic privilege?
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57
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Avoiding family feuds: responding to surrogate demands for life-sustaining interventions.
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58
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BMJ
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AIDS Behav
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60
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Medical journals and conflicts of interest.
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J Law Med Ethics
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61
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62
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64
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Responding to incidental findings on research imaging studies: now what?
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65
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Establishing procedures for institutional oversight of stem cell research.
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Retainer medicine: why not for all?
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Consent: criteria should be drawn up for tissue donors.
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68
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70
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71
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Role of academic medical centers in cell-based therapeutic clinical trials.
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78
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79
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Updating research oversight for the 21st century.
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