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Journal of Medical Ethics|November 5, 2005
Keep people informed or leave them alone? A suggested tool for identifying research participants who rightly want only limited informationS Eriksson, G HelgessonJournal of Medical Ethics|January 15, 2000
Fraud, misconduct or normal science in medical research--an empirical study of demarcationN Lynöe, L Jacobsson, E LundgrenActa Oncologica (Stockholm, Sweden)|January 1, 1996
Clinical cancer research--some aspects on doctors' attitudes to informing participantsN Lynöe, M Sandlund, L JacobssonScandinavian Journal of Public Health|July 28, 1999
Research ethics committees: a comparative study of assessment of ethical dilemmasN Lynöe, M Sandlund, L JacobssonActa Anaesthesiologica Scandinavica|October 20, 2007
Decision making in a life-threatening cerebral condition: a comparative study of the ethical reasoning of intensive care unit physicians and neurosurgeonsA Rydvall, T Bergenheim, N LynöeInternational Psychogeriatrics|January 30, 1999
When others decide: reasons for allowing patients with Alzheimer's disease to participate in nontherapeutic researchN Lynöe, M Sandlund, L JacobssonSocial Science & Medicine (1982)|March 1, 1993
The attitudes of patients and physicians towards placebo treatment--a comparative studyN Lynöe, B Mattsson, M SandlundJournal of Medical Ethics|March 5, 2008
Views on data use, confidentiality and consent in a predictive screening involving childrenG Helgesson, U SwartlingJournal of Medical Ethics|July 2, 2008
Self-assessed understanding as a tool for evaluating consent: reflections on a longitudinal studyU Swartling, G HelgessonMedicine and Law|January 31, 2002
Informed consent in two Swedish prisons: a study of quality of information and reasons for participating in a clinical trialN Lynöe, M Sandlund, L JacobssonPageof 3