Switch to: Citations

Add references

You must login to add references.
  1. The silent world of doctor and patient.Jay Katz - 1984 - Baltimore: Johns Hopkins University Press.
    In this eye-opening look at the doctor-patient decision-making process, physician and law professor Jay Katz examines the time-honored belief in the virtue of silent care and patient compliance. Historically, the doctor-patient relationship has been based on a one-way trust -- despite recent judicial attempts to give patients a greater voice through the doctrine of informed consent. Katz criticizes doctors for encouraging patients to relinquish their autonomy, and demonstrates the detrimental effect their silence has on good patient care. Seeing a growing (...)
    Download  
     
    Export citation  
     
    Bookmark   152 citations  
  • Foreword.Ellen Wright Clayton - 2001 - Journal of Law, Medicine and Ethics 29 (s2):1-2.
    Download  
     
    Export citation  
     
    Bookmark   1 citation  
  • Involving Study Populations in the Review of Genetic Research.Richard R. Sharp & Morris W. Foster - 2000 - Journal of Law, Medicine and Ethics 28 (1):41-51.
    Research on human genetic variation can present collective risks to all members of a socially identifiable group. Research that associates race or ethnicity with a genetic disposition to disease, for example, presents risks of group discrimination and stigmatization. To better protect against these risks, some have proposed supplemental community-based reviews of research on genetic differences between populations. The assumption behind these appeals is that involving members of study populations in the review process can help to identify and minimize collective risks (...)
    Download  
     
    Export citation  
     
    Bookmark   30 citations  
  • Involving Study Populations in the Review of Genetic Research.Richard R. Sharp & Morris W. Foster - 2000 - Journal of Law, Medicine and Ethics 28 (1):41-51.
    Research on human genetic variation can present collective risks to all members of a socially identifiable group. Research that associates race or ethnicity with a genetic disposition to disease, for example, presents risks of group discrimination and stigmatization. To better protect against these risks, some have proposed supplemental community-based reviews of research on genetic differences between populations. The assumption behind these appeals is that involving members of study populations in the review process can help to identify and minimize collective risks (...)
    Download  
     
    Export citation  
     
    Bookmark   28 citations  
  • The Silent World of Doctor and Patient.Daniel Callahan & Jay Katz - 1984 - Hastings Center Report 14 (6):47.
    Download  
     
    Export citation  
     
    Bookmark   102 citations