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DNA databanks and consent: A suggested policy option involving an authorization model

BMC Medical Ethics, 01 January 2003, Vol.4(1), p.1 [Peer Reviewed Journal]

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The unique ethical challenges of conducting research in the rehabilitation medicine population

BMC Medical Ethics, 01 June 2003, Vol.4(1), p.2 [Peer Reviewed Journal]

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Clinical Ethics Consultation: Examining how American and Japanese experts analyze an Alzheimer's case

BMC Medical Ethics, 01 January 2008, Vol.9(1), p.2 [Peer Reviewed Journal]

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Understanding and retention of the informed consent process among parents in rural northern Ghana

BMC Medical Ethics, 01 June 2008, Vol.9(1), p.12 [Peer Reviewed Journal]

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Identifying structures, processes, resources and needs of research ethics committees in Egypt

BMC Medical Ethics, 01 June 2010, Vol.11(1), p.12 [Peer Reviewed Journal]

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How informed is consent in vulnerable populations? Experience using a continuous consent process during the MDP301 vaginal microbicide trial in Mwanza, Tanzania

BMC Medical Ethics, 01 June 2010, Vol.11(1), p.10 [Peer Reviewed Journal]

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Informed consent for MRI and fMRI research: Analysis of a sample of Canadian consent documents

BMC Medical Ethics, 2011, Vol.12, p.1 [Peer Reviewed Journal]

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Access and use of human tissues from the developing world: ethical challenges and a way forward using a tissue trust

BMC Medical Ethics, 01 January 2011, Vol.12(1), p.2 [Peer Reviewed Journal]

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Ethical issues of unrelated hematopoietic stem cell transplantation in adult thalassemia patients

BMC Medical Ethics, 2011, Vol.12, p.4 [Peer Reviewed Journal]

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Be known, be available, be mutual: a qualitative ethical analysis of social values in rural palliative care

BMC Medical Ethics, 01 September 2011, Vol.12(1), p.19 [Peer Reviewed Journal]

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by this Author/Contributor:

  1. Pedersen, Reidar
  2. Parker, Michael
  3. Moodley, Keymanthri
  4. de Vries, Jantina
  5. Førde, Reidun

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