A New Edition of Journal of Medical Ethics Is Now Available

July 12, 2018

Journal of Medical Ethics (vol. 44, no. 6, 2018) is available online by subscription only.

Articles include:

  • “Face Transplantation for the Blind: More Than Being Blind in a Sighted World” by Joseph Lee
  • “From Whom Do Physicians Obtain Consent for Surgery?” by Zahra Jarayedi and Fariba Asghari
  • “Chronic Disease as Risk Multiplier for Disadvantage” by Francisca Stutzin Donoso
  • “Resuscitation Decisions at the End of Life: Medical Views and the Juridification of Practice” by Fiona MA MacCormick, Charlotte Emmett, Paul Paes, and Julian C Hughes
  • “Montgomery, Informed Consent and Causation of Harm: Lessons from Australia or a Uniquely English Approach to Patient Autonomy?” by Malcolm K Smith and Tracey Carver
  • “Content Analysis of Requests for Religious Exemptions from a Mandatory Influenza Vaccination Program for Healthcare Personnel” by Armand H Antommaria and Cynthia A Prows
  • “Consent and the Ethical Duty to Participate in Health Data Research” by Angela Ballantyne and G Owen Schaefer
  • “Towards a National Genomics Medicine Service: The Challenges Facing Clinical-Research Hybrid Practices and the Case of the 100 000 Genomes Project” by Sandi Dheensa, Gabrielle Samuel, Anneke M Lucassen, and Bobbie Farsides
  • “Artificial Gametes, the Unnatural and the Artefactual” by Anna Smajdor, Daniela Cutas, and Tuija Takala

 

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Posted in Disability Ethics, End of Life, Genetic Ethics, Informed Consent, Journal Articles, Organ Donation / Transplantation, Public Health, Public Policy, Research Ethics, Synthetic Biology

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