| scholarly article | Q13442814 |
| P50 | author | Christopher McKevitt | Q56433296 |
| P2093 | author name string | Mary Adams | |
| P2860 | cites work | Clinical trials and medical care: defining the therapeutic misconception | Q21144663 |
| The meaning of translational research and why it matters | Q28264016 | ||
| Storylines of research in diffusion of innovation: a meta-narrative approach to systematic review | Q33341163 | ||
| Methods for the synthesis of qualitative research: a critical review | Q33492573 | ||
| False hopes and best data: consent to research and the therapeutic misconception | Q34172812 | ||
| What influences recruitment to randomised controlled trials? A review of trials funded by two UK funding agencies | Q34511939 | ||
| "Ready-to-Recruit" or "Ready-to-Consent" Populations?: Informed Consent and the Limits of Subject Autonomy | Q34602091 | ||
| The therapeutic misconception at 25: treatment, research, and confusion | Q34733687 | ||
| 'Transport to Where?': Reflections on the problem of value and time à propos an awkward practice in medical research | Q37059524 | ||
| Close to the bench as well as at the bedside: involving service users in all phases of translational research. | Q37332859 | ||
| A critique of clinical equipoise. Therapeutic misconception in the ethics of clinical trials | Q39220096 | ||
| Accounting for EBM: notions of evidence in medicine | Q40360866 | ||
| Biobanks, bioethics and concepts of donated blood in the UK. | Q45951412 | ||
| The rise of 'recruitmentology': clinical research, racial knowledge, and the politics of inclusion and difference | Q46066716 | ||
| Empty ethics: the problem with informed consent | Q47413950 | ||
| Solidarity in contemporary bioethics--towards a new approach | Q47566253 | ||
| Informed consent for clinical trials: in search of the "best" method | Q47624289 | ||
| Gift relationships in genetics research | Q48133090 | ||
| Enterprising or altruistic selves? Making up research subjects in genetics research | Q48141123 | ||
| Turning a practice into a science: reconceptualizing postwar medical practice. | Q53639979 | ||
| Distinguishing research from clinical care in cancer genetics: theoretical justifications and practical strategies | Q56782061 | ||
| Doctor–patient interaction in a randomised controlled trial of decision-support tools | Q59055262 | ||
| Scaling crowdsourced health studies: the emergence of a new form of contract research organization | Q73183922 | ||
| The construction of lay expertise: AIDS activism and the forging of credibility in the reform of clinical trials | Q74787577 | ||
| P433 | issue | 2 | |
| P304 | page(s) | 138-148 | |
| P577 | publication date | 2015-03-13 | |
| P1433 | published in | Anthropology and Medicine | Q15763369 |
| P1476 | title | Configuring the patient as clinical research subject in the UK national health service | |
| P478 | volume | 22 |
Search more.