Search Results Search Sort by RelevanceMost Recent Personal Narrative Apr 2016 An Open Letter to Medical Students: Down Syndrome, Paradox, and Medicine George Estreich Physicians must resist judging the quality of life of their patients with Down syndrome and learn to listen and see them as individual personalities. AMA J Ethics. 2016;18(4):438-441. doi: 10.1001/journalofethics.2016.18.4.mnar1-1604. Medicine and Society Oct 2006 Talking with Families about Severely Disabled Children Arthur F. Kohrman, MD Virtual Mentor. 2006;8(10):685-688. doi: 10.1001/virtualmentor.2006.8.10.msoc1-0610. In the Literature Oct 2006 Parental Consent for Pediatric Research Emily E. Anderson, MPH Virtual Mentor. 2006;8(10):667-671. doi: 10.1001/virtualmentor.2006.8.10.jdsc1-0610. Policy Forum Aug 2003 The Ethics of Research with Children Timothy F. Murphy, PhD Virtual Mentor. 2003;5(8):333-335. doi: 10.1001/virtualmentor.2003.5.8.pfor2-0308. Case and Commentary Dec 2015 Enrolling Research Participants in Private Practice: Conflicts of Interest, Consistency, Therapeutic Misconception, and Informed Consent Armand H. Matheny Antommaria, MD, PhD and Kristin Stanley Bramlage, MD Advice for enrolling patients in clinical trials. AMA J Ethics. 2015;17(12):1122-1126. doi: 10.1001/journalofethics.2015.17.12.ecas3-1512. Policy Forum Aug 2008 Role of Independent Advocates for Research Subjects Who Are Child Wards of the State Hafzah Mueenuddin, JD and Eric D. Kodish, MD Specific advocate guidelines are needed for the protection of children in state custody who are potential research subjects in trials that would expose them to greater-than-minimal risk but also hold the prospect of direct benefit. Virtual Mentor. 2008;10(8):524-526. doi: 10.1001/virtualmentor.2008.10.8.pfor1-0808.
Personal Narrative Apr 2016 An Open Letter to Medical Students: Down Syndrome, Paradox, and Medicine George Estreich Physicians must resist judging the quality of life of their patients with Down syndrome and learn to listen and see them as individual personalities. AMA J Ethics. 2016;18(4):438-441. doi: 10.1001/journalofethics.2016.18.4.mnar1-1604.
Medicine and Society Oct 2006 Talking with Families about Severely Disabled Children Arthur F. Kohrman, MD Virtual Mentor. 2006;8(10):685-688. doi: 10.1001/virtualmentor.2006.8.10.msoc1-0610.
In the Literature Oct 2006 Parental Consent for Pediatric Research Emily E. Anderson, MPH Virtual Mentor. 2006;8(10):667-671. doi: 10.1001/virtualmentor.2006.8.10.jdsc1-0610.
Policy Forum Aug 2003 The Ethics of Research with Children Timothy F. Murphy, PhD Virtual Mentor. 2003;5(8):333-335. doi: 10.1001/virtualmentor.2003.5.8.pfor2-0308.
Case and Commentary Dec 2015 Enrolling Research Participants in Private Practice: Conflicts of Interest, Consistency, Therapeutic Misconception, and Informed Consent Armand H. Matheny Antommaria, MD, PhD and Kristin Stanley Bramlage, MD Advice for enrolling patients in clinical trials. AMA J Ethics. 2015;17(12):1122-1126. doi: 10.1001/journalofethics.2015.17.12.ecas3-1512.
Policy Forum Aug 2008 Role of Independent Advocates for Research Subjects Who Are Child Wards of the State Hafzah Mueenuddin, JD and Eric D. Kodish, MD Specific advocate guidelines are needed for the protection of children in state custody who are potential research subjects in trials that would expose them to greater-than-minimal risk but also hold the prospect of direct benefit. Virtual Mentor. 2008;10(8):524-526. doi: 10.1001/virtualmentor.2008.10.8.pfor1-0808.