Search Results Search Sort by RelevanceMost Recent Case and Commentary Jul 2017 Should Dementia Be Accepted as a Disability to Help Restore Hope during Cognitive Decline? Nathaniel M. Robbins, MD and James L. Bernat, MD Patients with dementia need social supports and opportunities and acceptance of their disability in order to feel hopeful despite their functional decline. AMA J Ethics. 2017;19(7):649-655. doi: 10.1001/journalofethics.2017.19.7.ecas2-1707. In the Literature Jul 2017 When Does Therapeutic Misconception Affect Surrogates’ or Subjects’ Decision Making about Whether to Participate in Dementia Research? Laura B. Dunn, MD and Barton W. Palmer, PhD Research is needed on surrogates’ susceptibility to believing that clinical trials provide individual therapeutic benefit. AMA J Ethics. 2017;19(7):678-685. doi: 10.1001/journalofethics.2017.19.7.nlit1-1707. State of the Art and Science Jul 2012 Do Patient-Accessible Electronic Medical Records Help Or Complicate Shared Decision Making? Steven D. Freedman, MD, PhD and Camilia R. Martin, MD, MS Merely giving patients access to electronic health records made for use by clinicians will not help patients make use of the information they contain. Virtual Mentor. 2012;14(7):560-562. doi: 10.1001/virtualmentor.2012.14.7.stas1-1207. Case and Commentary Mar 2017 Why It’s Unjust to Expect Location-Specific, Language-Specific, or Population-Specific Service from Students with Underrepresented Minority or Low-Income Backgrounds Barret Michalec, PhD, Maria Athina Martimianakis, PhD, Jon C. Tilburt, MD, MPH, and Frederic W. Hafferty, PhD Expectations implicit in medical school funding and professional socialization lead underrepresented minorities to work with underserved populations. AMA J Ethics. 2017;19(3):238-244. doi: 10.1001/journalofethics.2017.19.3.ecas1-1703. Pagination First page « First Previous page ‹ Previous Page 1 Page 2 Page 3 Page 4 Page 5 Page 6 Page 7 Current page 8
Case and Commentary Jul 2017 Should Dementia Be Accepted as a Disability to Help Restore Hope during Cognitive Decline? Nathaniel M. Robbins, MD and James L. Bernat, MD Patients with dementia need social supports and opportunities and acceptance of their disability in order to feel hopeful despite their functional decline. AMA J Ethics. 2017;19(7):649-655. doi: 10.1001/journalofethics.2017.19.7.ecas2-1707.
In the Literature Jul 2017 When Does Therapeutic Misconception Affect Surrogates’ or Subjects’ Decision Making about Whether to Participate in Dementia Research? Laura B. Dunn, MD and Barton W. Palmer, PhD Research is needed on surrogates’ susceptibility to believing that clinical trials provide individual therapeutic benefit. AMA J Ethics. 2017;19(7):678-685. doi: 10.1001/journalofethics.2017.19.7.nlit1-1707.
State of the Art and Science Jul 2012 Do Patient-Accessible Electronic Medical Records Help Or Complicate Shared Decision Making? Steven D. Freedman, MD, PhD and Camilia R. Martin, MD, MS Merely giving patients access to electronic health records made for use by clinicians will not help patients make use of the information they contain. Virtual Mentor. 2012;14(7):560-562. doi: 10.1001/virtualmentor.2012.14.7.stas1-1207.
Case and Commentary Mar 2017 Why It’s Unjust to Expect Location-Specific, Language-Specific, or Population-Specific Service from Students with Underrepresented Minority or Low-Income Backgrounds Barret Michalec, PhD, Maria Athina Martimianakis, PhD, Jon C. Tilburt, MD, MPH, and Frederic W. Hafferty, PhD Expectations implicit in medical school funding and professional socialization lead underrepresented minorities to work with underserved populations. AMA J Ethics. 2017;19(3):238-244. doi: 10.1001/journalofethics.2017.19.3.ecas1-1703.