Impaired Physicians: What Should Patients Know?
Cambridge Quarterly of Healthcare Ethics 2 (03):331- (1993)
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M. Lavin (1988). What Doctors Should Call Their Patients. Journal of Medical Ethics 14 (3):129-131.
Erich H. Loewy (1988). Oh Death, Where is Thy Sting? Reflections on Dealing with Dying Patients. Journal of Medical Humanities and Bioethics 9 (2):135-142.
Rajendra D. Badgaiyan (2009). Theory of Mind and Schizophrenia☆. Consciousness and Cognition 18 (1):320-322.
Derek R. Bell (2003). Rawls and Research on Cognitively Impaired Patients: A Reply to Maio. Theoretical Medicine and Bioethics 24 (5):381-393.
Amy M. Bovi (2003). Ethical Guidelines for Use of Electronic Mail Between Patients and Physicians. American Journal of Bioethics 3 (3):43-47.
Laurent Jeanpierre & François Charpillet (2004). Automated Medical Diagnosis with Fuzzy Stochastic Models: Monitoring Chronic Diseases. Acta Biotheoretica 52 (4).
Jerome Lowenstein (2005). The Midnight Meal and Other Essays About Doctors, Patients, and Medicine. University of Michigan Press.
Winston Chiong (2006). The Real Problem with Equipoise. American Journal of Bioethics 6 (4):37 – 47.
Aaron D. Levine & Leslie E. Wolf (2012). The Roles and Responsibilities of Physicians in Patients' Decisions About Unproven Stem Cell Therapies. Journal of Law, Medicine and Ethics 40 (1):122-134.
Lee Black & Emily Anderson (2007). Physicians, Patients and Confidentiality: The Role of Physicians in Electronic Health Records. American Journal of Bioethics 7 (3):50-51.
PD Dr Giovanni Maio (2002). The Relevance of Rawls' Principle of Justice for Research on Cognitively Impaired Patients. Theoretical Medicine and Bioethics 23 (1).
Eugene J. Stein (1980). Doctors and Patients: Partners or Adversaries? Bioethics Quarterly 2 (2):118-122.
Malcolm Parker (2006). Patients as Rational Traders: Response to Stewart and DeMarco. Journal of Bioethical Inquiry 3 (3).
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