A New Edition of Journal of Medical Ethics is Now Available

October 16, 2015

Journal of Medical Ethics (vol. 41, no. 10, 2015) is available online by subscription only.

Articles include:

  • “End-of-Life Decisions for Children under 1 Year of Age in the Netherlands: Decreased Frequency of Administration of Drugs to Deliberately Hasten Death” by Katja ten Cate, et al.
  • “Implications of the Concept of Minimal Risk in Research on Informed Choice in Clinical Practice” by Kyoko Wada and Jeff Nisker
  • “Ethical Implications of HIV Self-Testing” by Jonathan Youngs and Carwyn Hooper
  • “Public Participation in Genetic Databases: Crossing the Boundaries between Biobanks and Forensic DNA Databases through the Principle of Solidarity” by Helena Machado and Susana Silva
  • “Putting a Price on Empathy: Against Incentivising Moral Enhancement” by Sarah Carter
  • “Getting the Facts Right: Time for Evidence-Based Ethics” by David MacKintosh
  • “Opt-out and Consent” by Douglas MacKay
  • “The Nature and Ethics of Natural Experiments” by Angus Dawson and Julius Sim
  • “How Medical Students Learn Ethics: An Online Log of Their Learning Experiences” by Carolyn Johnston and Jonathan Mok
  • “Hypoactive Sexual Desire Disorder: Inventing a Disease to Sell Low Libido” by Antonie Meixel, Elena Yanchar, and Adrianne Fugh-Berman

Posted by

Posted in Disability Ethics, Education, Euthanasia / Suicide, Genetic Ethics, Global Bioethics, Human Dignity, Human Enhancement, Informed Consent, Journal Articles, Mental Health, Neuroethics, Pediatric, Pharma, Public Health, Public Policy, Research Ethics

Ad