Deutsches Referenzzentrum für Ethik in den Biowissenschaften (DRZE)

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Your request: (keywords:("consentement %E9clair%E9") OR keywords:(("Informierte Zustimmung" "Einwilligungsformular" "Consent forms" "consent forms" "written consent" "Consent Forms (D032962)" "consentement écrit" "formulaire de consentement" "Informed consent" "informed consent" "Informed Consent (D007258)" "consentement éclairé")) OR keywords:(("informed consent" "consent forms" "Consent forms" "consent forms" "written consent" "Consent Forms (D032962)" "consentement écrit" "formulaire de consentement" "Informed consent" "informed consent" "Informed Consent (D007258)" "consentement éclairé")) )

 

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Nr. Eintrag
1 Hirschberg, Irene; Kahrass, Hannes; Strech, Daniel:
Variation bei Einwilligungsdokumenten in der Biobankforschung : eine Untersuchung von deutschen Biobanken
In: Vom Konflikt zur Lösung : ethische Entscheidungswege in der Biomedizin / Oliver Rauprich ; Ralf J. Jox ; Georg Marckmann [Hrsg.]. - Münster : mentis, (2016). - 327-345
2 Allen, Clarissa; Foulkes, William D:
Qualitative thematic analysis of consent forms used in cancer genome sequencing.
In: BMC medical ethics, 2011, 12, 14
3 Beauchamp, Tom L:
Informed consent: its history, meaning, and present challenges.
In: Cambridge quarterly of healthcare ethics : CQ : the international journal of healthcare ethics committees, 2011, Vol. 20 (4), 515-23
4 Bernabe, Rosemarie D C et al.:
Informed consent and phase IV non-interventional drug research.
In: Current medical research and opinion, 2011, Vol. 27 (3), 513-8
5 Boddington, Paula et al.:
Consent forms in genomics: the difference between law and practice.
In: European journal of health law, 2011, Vol. 18 (5), 491-519
6 Boga, Mwanamvua et al.:
Strengthening the informed consent process in international health research through community engagement: The KEMRI-Wellcome Trust Research Programme Experience.
In: PLoS medicine, 2011, Vol. 8 (9), e1001089
7 Desch, Karl et al.:
Analysis of informed consent document utilization in a minimal-risk genetic study.
In: Annals of internal medicine, 2011, Vol. 155 (5), 316-22
8 Jerrold, Laurance:
Litigation and legislation: what do patients actually consent to?
In: American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics, 2011, Vol. 139 (1), 133-5
9 Knapp, Peter et al.:
Can user testing of a clinical trial patient information sheet make it fit-for-purpose?--a randomized controlled trial.
In: BMC medicine, 2011, 9, 89
10 Lee, Robin et al.:
Subjects agree to participate in environmental health studies without fully comprehending the associated risk.
In: International journal of environmental research and public health, 2011, Vol. 8 (3), 830-41
11 Mak, Donna B et al.:
Resending a consent form and information package to non-responders increases school-based consent return rate.
In: Australian and New Zealand journal of public health, 2011, Vol. 35 (1), 89-90
12 Palmour, Nicole et al.:
Informed consent for MRI and fMRI research: analysis of a sample of Canadian consent documents.
In: BMC medical ethics, 2011, 12, 1
13 Solsona Durán, J F et al.:
[Informed consent in a university hospital: evaluation of 291 consents and the opinion of the physicians and patients]. = El consentimiento informado en un hospital universitario: evaluación de 291 consentimientos y de la opinión de médicos y pacientes.
In: Revista clínica española, 2011, Vol. 211 (3), 167-8
14 Albala, Ilene; Doyle, Margaret; Appelbaum, Paul S:
The evolution of consent forms for research: a quarter century of changes.
In: IRB, 2010, Vol. 32 (3), 7-11
15 Barritt, Andrew W. et al.:
Assessing the adequacy of procedure-specific consent forms in orthopaedic surgery against current methods of operative consent.
In: Annals of the Royal College of Surgeons of England, 2010, Vol. 92 (3), 246-249; quiz 2p following 249
16 Beskow, Laura M et al.:
Simplifying informed consent for biorepositories: stakeholder perspectives.
In: Genetics in medicine : official journal of the American College of Medical Genetics, 2010, Vol. 12 (9), 567-72
17 Cheung, Winson Y et al.:
The contents and readability of informed consent forms for oncology clinical trials.
In: American journal of clinical oncology, 2010, Vol. 33 (4), 387-92
18 Cortés, Dharma E et al.:
How to achieve informed consent for research from Spanish-speaking individuals with low literacy: a qualitative report.
In: Journal of health communication 2010; 15 Suppl 2: 172-82
19 Fovargue, Sara; Miola, José:
How much information is 'enough'?
In: Clinical Ethics, 2010, Vol. 5 (1), 13-15
20 Jeyaseelan, Luckshmana et al.:
Quality of consent form completion in orthopaedics: are we just going through the motions?
In: Journal of medical ethics, 2010, Vol. 36 (7), 407-8

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