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Paul J Ford

Biographic Data

ID181306
NAMEPaul J Ford
GIVEN NAMESPaul J
FAMILY NAMEFord
SIGNATUREFORD P J
AFFILIATIONSCleveland Clinic
ORCID0000-0002-5423-8845
VERIFIEDYes
TOTAL WORKS6
TOTAL CITATIONS0
WORKS AS AUTHOR6
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2001
LATEST PUBLICATION YEAR2023
H-INDEX0
  • Overcoming barriers to informed consent in neurological research

    Open Access•Lauren R Sankary, Megan E Zelinsky et al.•ARTICLE•Research Ethics•2023

    The ethical recruitment of participants with neurological disorders in clinical research requires obtaining initial and ongoing informed consent. The purpose of this study is to characterize barriers faced by research personnel in obtaining informed consent from research participants with neurological disorders and to identify strategies applied by researchers to overcome those barriers. This study was designed as a web-based survey of US researc…

  • Incorporating Stakeholder Perspectives on Scarce Resource Allocation

    Open Access•Bethany Bruno, Heather Mckee Hurwitz et al.•ARTICLE•Cambridge Quarterly of Healthcare…•2021

    The coronavirus disease (COVID-19) crisis provoked an organizational ethics dilemma: how to develop ethical pandemic policy while upholding our organizational mission to deliver relationship- and patient-centered care. Tasked with producing a recommendation about whether healthcare workers and essential personnel should receive priority access to limited medical resources during the pandemic, the bioethics department and survey and interview meth…

  • Applying Guidelines to Individual Patients

    Open Access•Bryn S Esplin, André G Machado et al.•ARTICLE•The AMA Journal of Ethic•2015

    When deciding whether to offer deep brain stimulation earlier than usual for Parkinson disease, it is important to consider not only the patient's autonomy but also the validity of the evidence and concepts of harm that are being used to form practice policies

  • Bioethics in Social Context

    Open Access•Paul J Ford•ARTICLE•Medical Anthropology Quarterly•2002

    Bioethics in Social Context. Barry Hoffmaster. ed. Philadelphia: Temple University Press, 2001.vii. 234 pp

  • Paralysis Lost

    Paul J Ford•ARTICLE•Social Theory and Practice•2001

  • Prenatal Testing and Disability Rights

    Open Access•Paul J Ford•ARTICLE•Medical Anthropology Quarterly•2001

    Prenatal Testing and Disability Rights. Erik Parens and Adrienne Asch. eds. Washington, DC: Georgetown University Press, 2000.xvi. 371pp

No prominent works on this page.

  • Paralysis Lost

    Paul J Ford•ARTICLE•Social Theory and Practice•2001

  • Prenatal Testing and Disability Rights

    Open Access•Paul J Ford•ARTICLE•Medical Anthropology Quarterly•2001

    Prenatal Testing and Disability Rights. Erik Parens and Adrienne Asch. eds. Washington, DC: Georgetown University Press, 2000.xvi. 371pp

  • Bioethics in Social Context

    Open Access•Paul J Ford•ARTICLE•Medical Anthropology Quarterly•2002

    Bioethics in Social Context. Barry Hoffmaster. ed. Philadelphia: Temple University Press, 2001.vii. 234 pp

  • Applying Guidelines to Individual Patients

    Open Access•Bryn S Esplin, André G Machado et al.•ARTICLE•The AMA Journal of Ethic•2015

    When deciding whether to offer deep brain stimulation earlier than usual for Parkinson disease, it is important to consider not only the patient's autonomy but also the validity of the evidence and concepts of harm that are being used to form practice policies

  • Incorporating Stakeholder Perspectives on Scarce Resource Allocation

    Open Access•Bethany Bruno, Heather Mckee Hurwitz et al.•ARTICLE•Cambridge Quarterly of Healthcare…•2021

    The coronavirus disease (COVID-19) crisis provoked an organizational ethics dilemma: how to develop ethical pandemic policy while upholding our organizational mission to deliver relationship- and patient-centered care. Tasked with producing a recommendation about whether healthcare workers and essential personnel should receive priority access to limited medical resources during the pandemic, the bioethics department and survey and interview meth…

  • Overcoming barriers to informed consent in neurological research

    Open Access•Lauren R Sankary, Megan E Zelinsky et al.•ARTICLE•Research Ethics•2023

    The ethical recruitment of participants with neurological disorders in clinical research requires obtaining initial and ongoing informed consent. The purpose of this study is to characterize barriers faced by research personnel in obtaining informed consent from research participants with neurological disorders and to identify strategies applied by researchers to overcome those barriers. This study was designed as a web-based survey of US researc…

Medicine (5 works) · Political science (3 works) · Psychology (3 works) · Bioethics (2 works) · Disease (2 works) · Ethics in medical practice (2 works) · Law (2 works) · Psychiatry (2 works) · Sociology (2 works) · Alternative medicine (1 work)

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