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1 ve cohort study were included, which was approved by the local ethics board and written informed consent was obtained from all participants.
2 Written informed consent was obtained from all participants.
3 This prospective study was approved by the local ethics committee, and written informed consent was obtained from all participants.
4 Written informed consent was obtained from all participants.
5 U.S. Food and Drug Administration and institutional review board approval, and written informed consent was obtained from all participants.
6 Written informed consent was obtained from all participants.
7 The study was approved by the institutional review board, and written informed consent was obtained from all participants.
8 This prospective study was approved by the local ethics committee, and written informed consent was obtained from all participants.
9 Ethical approval was obtained from the Dutch Health Council, and written informed consent was obtained from all participants.
10 This study was approved by the local committee on ethics, and written informed consent was obtained from all participants.
11 The protocol was approved by the institutional review board, and written informed consent was obtained from all participants.
12 s approved by the institutional review boards of all participating centers, and written informed consent was obtained from all participants.
13 udies were approved by the institutional review board and were HIPAA compliant; written informed consent was obtained from all participants.
14 s approved by the institutional review boards of all participating centers, and written informed consent was obtained from all participants.
15 The local research ethics committee approved the study, and written informed consent was obtained from all participants.
16 Research ethics committee approval was obtained for this study, and written informed consent was obtained from all participants.
17 thy volunteers (5 women, 5 men; age +/- SD, 34.3 +/- 6.5 y) were recruited, and written informed consent was obtained from all participants.
18 Written informed consent was obtained from all participants.
19 Written informed consent was obtained from all participants.
20 SHIP was approved by the institutional review board, and written informed consent was obtained from all participants.
21 s approved by the institutional review boards of all participating centers, and written informed consent was obtained from all participants.
22 The local ethics committee approved this prospective study, and written informed consent was obtained from all participants.
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