Search Results Search Sort by RelevanceMost Recent Health Law Nov 2003 Grimes v. Kennedy Krieger Institute: Nontherapeutic Research with Children Richard Morse, MA Ethical and legal questions arise when public health research that provides a benefit to society at large can potentially cause harm to the subjects. Virtual Mentor. 2003;5(11):503-507. doi: 10.1001/virtualmentor.2003.5.11.hlaw1-0311. Personal Narrative Jan 2013 The Median Isn’t the Message Stephen Jay Gould, PhD Reprint of Stephen Jay Gould's essay “The Median Isn't the Message.” Virtual Mentor. 2013;15(1):77-81. doi: 10.1001/virtualmentor.2013.15.1.mnar1-1301. AMA Code Says Jan 2002 The Use of DNA Databanks in Genomic Research Faith Lagay, PhD The AMA's Code of Medical Ethics' opinion on the use of databanks in genomic research requires informed consent by groups and individuals who are subjects of research. Virtual Mentor. 2002;4(1):15-18. doi: 10.1001/virtualmentor.2002.4.1.code1-0201. Personal Narrative Jul 2002 Through the Patient's Eyes: Paying Interest on Borrowed Time Stephen Foster, MD A patient reflects on his past medical care and his desire to give back to society by volunteering in a clinical research study. Virtual Mentor. 2002;4(7):214-215. doi: 10.1001/virtualmentor.2002.4.7.prsp1-0207. Pagination First page « First Previous page ‹ Previous … Page 10 Page 11 Page 12 Page 13 Page 14 Page 15 Page 16 Page 17 Current page 18
Health Law Nov 2003 Grimes v. Kennedy Krieger Institute: Nontherapeutic Research with Children Richard Morse, MA Ethical and legal questions arise when public health research that provides a benefit to society at large can potentially cause harm to the subjects. Virtual Mentor. 2003;5(11):503-507. doi: 10.1001/virtualmentor.2003.5.11.hlaw1-0311.
Personal Narrative Jan 2013 The Median Isn’t the Message Stephen Jay Gould, PhD Reprint of Stephen Jay Gould's essay “The Median Isn't the Message.” Virtual Mentor. 2013;15(1):77-81. doi: 10.1001/virtualmentor.2013.15.1.mnar1-1301.
AMA Code Says Jan 2002 The Use of DNA Databanks in Genomic Research Faith Lagay, PhD The AMA's Code of Medical Ethics' opinion on the use of databanks in genomic research requires informed consent by groups and individuals who are subjects of research. Virtual Mentor. 2002;4(1):15-18. doi: 10.1001/virtualmentor.2002.4.1.code1-0201.
Personal Narrative Jul 2002 Through the Patient's Eyes: Paying Interest on Borrowed Time Stephen Foster, MD A patient reflects on his past medical care and his desire to give back to society by volunteering in a clinical research study. Virtual Mentor. 2002;4(7):214-215. doi: 10.1001/virtualmentor.2002.4.7.prsp1-0207.