1 in Scotland), were diagnosed with paracetamol overdose,
and gave written informed consent.
2 thy men (mean age, 36.6 years +/- 7.7 [standard
deviation])
gave written informed consent to participate in this prospect
3 board approval, nine asthmatic and four healthy
individuals gave written informed consent.
4 Eight healthy volunteers (mean age 31, five were
male)
gave written informed consent and both of their IONs were ima
5 e local Ethics Committee, and all patients or their
parents gave written informed consent.
6 Participants (or
parents)
gave written informed consent.
7 Participants gave written informed consent and the study was approved by t
8 Participants gave written informed consent, and the Norwegian committee fo
9 Participants gave written informed consent.
10 Materials and Methods All
participants gave written informed consent to undergo brain magnetic reson
11 d institutional review board approval, and all
participants gave written informed consent.
12 e overseen by the national government, and all
participants gave written informed consent.
13 y the local research ethics committee, and all
participants gave written informed consent.
14 was approved by the ethics committee, and all
participants gave written informed consent.
15 e overseen by the national government, and all
participants gave written informed consent.
16 trial had ethical committee approval, and all
participants gave written informed consent.
17 ved by the institutional review board, and all
participants gave written informed consent.
18 ocal ethics committees approved the study; all
participants gave written informed consent.
19 dy was institutional review board-approved and
participants gave written informed consent.
20 s approved by a research ethics committee, and
participants gave written informed consent.
21 All study
participants gave written informed consent, and the study was approved by
22 oard approval for this study was obtained, and each
patient gave written informed consent.
23 Patients gave written informed consent for study enrollment, including
24 Patients gave written informed consent.
25 Materials and Methods All
patients gave written informed consent prior to inclusion in this inst
26 All
patients gave written informed consent prior to their examination.
27 All
patients gave written informed consent.
28 ltiparametric MR imaging of the breast at 7 T, all
patients gave written informed consent.
29 approved the protocol (number 1225/2012), and all
patients gave written informed consent.
30 All
patients gave written informed consent.
31 pproved by the institutional review board, and all
patients gave written informed consent.
32 was approved by the regional ethics committee; all
patients gave written informed consent.
33 local ethics committee approved the study and all
patients gave written informed consent.
34 All
patients gave written informed consent.
35 ceived institutional review board approval and all
patients gave written informed consent.
36 ew board approval was obtained for this study; all
patients gave written informed consent.
37 dy was approved by the local ethics committee, and
patients gave written informed consent prior to their inclusion in the
38 All subjects and their legal
representatives gave written informed consent prior to data collection.
39 Each
subject gave written informed consent to participate in this institut
40 as approved by the local ethics committee, and all
subjects gave written informed consent.
41 as approved by the local ethics committee, and all
subjects gave written informed consent.
42 d by the local institutional review board, and all
subjects gave written informed consent.
43 institutional review board approved the study; all
subjects gave written informed consent.
44 s approved by the medical ethics committee and all
subjects gave written informed consent.
45 institutional review board approved the study; all
subjects gave written informed consent.
46 women; mean age, 59 years) with malignant liver lesions
who gave written informed consent underwent preoperative gadoxeti
47 Patients scheduled for PD
who gave written informed consent were included and randomized du
48 The study received ethics committee approval, and all
women gave written informed consent.
49 Participating
women gave written informed consent.
50 ers (mean age, 30.9 years; 78% [29] men, 22% [eight]
women)
gave written informed consent and completed a questionnaire t