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Informed approval for participation in the study was collected from decision-capable individuals that chose to participate in the study.
Informed approval for participation in the study was collected from decision-capable individuals choosing to participate in the study.
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All participants gave written informed consent, and approval for the study was obtained from the University of Milan Departmental Institutional Review Board.
All of the patients provided written informed consent, and approval for the study was received from the Ethics Committee of China Medical University.
All the human samples were obtained with informed consent and approval for usage was received from the ethics committee of Zhongshan Hospital and Xinhua Hospital.
For use of human brain tissue in this study, patients provided written informed consent and approval for the consent procedure and experiments were obtained from the NHS National Research Ethics Committee of the UK (Approval No. 02/N093).
Such difficulties are more apparent if the cases are to be created from real life records (mainly patient informed consent issues and hospital approval for retrieving information from clinical records).
All participants gave written informed consent, and ethical approval for the study was granted by the Regional Ethics Committee for Copenhagen and Frederiksberg Communes in Denmark (references: KF 01 272 753, KF 11 297 287).
Study participants in the MACS provided written informed consent and IRB approval for this study was obtained from the University of Washington and the MACS parent institutions.
Participants provided written informed consent, and ethics approval for the study was given by the Norwich District Ethics Committee.
All participants provided informed consent and ethical approval for this study was obtained through the University of British Columbia's Behavioural Ethics Committee.
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