Patients' refusal to consent to storage and use of samples in Swedish biobanks: cross sectional study.
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The Swedish personal identity number: possibilities and pitfalls in healthcare and medical researchRare disease research: Breaking the privacy barrierImproving the informed consent process in international collaborative rare disease research: effective consent for effective research.Respecting Autonomy Over Time: Policy and Empirical Evidence on Re-Consent in Longitudinal Biomedical ResearchEvaluating the consent preferences of UK research volunteers for genetic and clinical studiesFormative research on perceptions of biobanking: what community members thinkPublic perspectives regarding data-sharing practices in genomics researchHypothetical and factual willingness to participate in biobank research"It's for a good cause, isn't it?" - Exploring views of South African TB research participants on sample storage and re-useInclusion of residual tissue in biobanks: opt-in or opt-out?Biobanking research on oncological residual material: a framework between the rights of the individual and the interest of society.Ethical aspects of human biobanks: a systematic review.Thematic analysis of cardiac care patients' explanations for declining contribution to a genomic research-based biobankCommunity-based partnership to identify keys to biospecimen research participation.Pilot intervention outcomes of an educational program for biospecimen research participation.Ethics of clear health communication: applying the CLEAN Look approach to communicate biobanking information for cancer researchEthical and practical challenges to studying patients who opt out of large-scale biorepository research.A trial of consent procedures for future research with clinically derived biological samples."It's my blood": ethical complexities in the use, storage and export of biological samples: perspectives from South African research participants.Incorporating exclusion clauses into informed consent for biobanking.Where should we draw the line between quality of care and other ethical concerns related to medical registries and biobanks?Consent to DNA collection in epidemiological studies: findings from the Whitehall II cohort and the English Longitudinal Study of Ageing.Four themes in recent Swedish bioethics debates.Planning Today for Tomorrow's Research: Analysis of Factors Influencing Participation in a Pediatric Cancer Research Biorepository.
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Patients' refusal to consent to storage and use of samples in Swedish biobanks: cross sectional study.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 10 July 2008
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Patients' refusal to consent t ...... obanks: cross sectional study.
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Patients' refusal to consent t ...... obanks: cross sectional study.
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type
label
Patients' refusal to consent t ...... obanks: cross sectional study.
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Patients' refusal to consent t ...... obanks: cross sectional study.
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Patients' refusal to consent t ...... obanks: cross sectional study.
@en
Patients' refusal to consent t ...... obanks: cross sectional study.
@nl
P2860
P921
P356
P1433
P1476
Patients' refusal to consent t ...... obanks: cross sectional study.
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P2093
Linus Johnsson
Mats G Hansson
P2860
P356
10.1136/BMJ.A345
P407
P577
2008-07-10T00:00:00Z