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1 This case-control study was approved by the local research ethics committee.
2 on of prospectively acquired data was approved by the local ethics committee.
3 d Methods The animal experiments were approved by the local ethics committee.
4 s retrospective analysis was approved by the local research ethics committee.
5 Each treatment was approved by the clinical ethics committee.
6 This retrospective study was approved by the institutional ethics committee.
7 dy was approved by the institutional review board and local ethics committee.
8 ls and Methods The study protocol was approved by the local ethics committee.
9 Materials and Methods The study was approved by the local ethics committee.
10 ods This HIPAA-compliant study was approved by the regional ethics committee.
11 Materials and Methods Approval was obtained from the local ethics committee.
12 Retrospective evaluation of data was approved by the local ethics committee and informed consent was waived.
13 is prospective case-control study was approved by the local ethics committee and the research department of Nottingham Un
14 nd Methods This study was approved by the national research ethics committee and was performed with informed consent.
15 ted with the approval of the Newcastle and North Tyneside 2 ethics committee and written consent.
16 edefined and serious adverse events (SAEs) were reported to ethics committees and a central safety monitor.
17 ls and Methods The study was approved by the local research ethics committee, and all participants gave written informed
19 Materials and Methods The study was approved by the local ethics committee, and all subjects gave written informed cons
20 This retrospective study was approved by the institutional ethics committee, and informed consent was waived.
21 Materials and Methods The study was approved by a research ethics committee, and participants gave written informed cons
22 ods Retrospective data evaluation was approved by the local ethics committee, and the requirement to obtain informed cons
23 terials and Methods This two-part study was approved by the ethics committee, and written consent was obtained from all p
24 ls and Methods This in vivo study was approved by the local ethics committee, and written informed consent was obtained f
25 ials and Methods This prospective study was approved by our ethics committee, and written informed consent was obtained f
26 The study was approved by the local ethics committee, and written informed consent was obtained f
27 The study was approved by the national research ethics committee, and written patient consent was obtained.
29 nd Methods This prospective study was approved by the local ethics committees, and written informed consent was obtained
30 Materials and Methods Institutional ethics committee approval and informed consent were obtained.
31 unteer study, performed between 2006 and 2016 with research ethics committee approval and written informed consent from e
32 Materials and Methods Institutional review board and local ethics committee approval and written informed consent were o
36 ials and Methods Written informed consent and institutional ethics committee approval were obtained.
40 Materials and Methods The institutional ethics committee approved the study and waived the requiremen
44 Materials and Methods This study was approved by the local ethics committee at all participating sites.
45 (RCTs) based on archived protocols approved by six research ethics committees between 13 January 2000 and 25 November 200
47 ials and Methods This prospective study was approved by the ethics committee of the University Hospital of Munster (AZ 20
48 Retrospective data evaluation was approved by the local ethics committee of the University of Heidelberg (ethics appr
49 hods This prospective study was approved by the independent ethics committees of Kanton Bern and Kanton Zurich, and signe
50 ive population-based cohort study was approved by a medical ethics committee overseen by the national government, and all
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