A New Edition of Hastings Center Report is Now Available

September 21, 2015

Hastings Center Report (vol. 45, no. 4, 2015) is available online by subscription only.

Articles include:

  • “When Should Genome Researchers Disclose Misattributed Parentage?” by Amulya Mandava, Joseph Millum, and Benjamin E. Berkman
  • “Fevered Decisions: Race, Ethics, and Clinical Vulnerability in the Malarial Treatment of Neurosyphillis, 1922-1953” by Matthew Gambino
  • “Drifting Away from Informed Consent in the Era of Personalized Medicine” by Erik Parens
  • “Training in Research Ethics and Standards for Community Health Workers and Promotores Engaged in Latino Health Research” by Camille Nebeker, et al.

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Posted in Clinical / Medical, Genetic Ethics, Global Bioethics, Informed Consent, Journal Articles, Public Health, Research Ethics

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