1 7 (17.1%) were diagnosed as having dementia, and 634 (9.
3%)
provided written informed consent to participate.
2 rmed about the investigational nature of the procedures
and provided written informed consent.
3 hemical failure after radiation therapy for prostate
cancer provided written informed consent and were enrolled in a pros
4 l institutional review boards approved the study and
donors provided written informed consent before death.
5 L-12-02/1/2/3/4) and all the patients and the control
group provided written informed consent.
6 med a retrospective data review of stem cell donors who
had provided written informed consent for stem cell donation and
7 in the HERA trial, three patients had no evidence of
having provided written informed consent to participate.
8 nt in the dyad spoke English, and all participating
parents provided written informed consent.
9 l was approved by local ethical committee; each
participant provided written informed consent.
10 Participants provided written informed consent to a protocol that was appr
11 Participants provided written informed consent.
12 tional review board approved the study and all
participants provided written informed consent.
13 All
participants provided written informed consent.
14 All
participants provided written informed consent.
15 dy approval by the local ethics committee, all
participants provided written informed consent.
16 d institutional review board approval, and all
participants provided written informed consent.
17 ved by the institutional review board, and all
participants provided written informed consent.
18 al was obtained at each clinical site, and all
participants provided written informed consent.
19 This study received ethics approval, and all
participants provided written informed consent.
20 onal board approved multicenter study, and all
participants provided written informed consent.
21 All ethics were approved, and
participants provided written informed consent.
22 institutional review board of each center and
participants provided written informed consent.
23 al of the institutional review boards, and all
participants provided written, informed consent.
24 Patients provided written informed consent, or, at select sites, there
25 All
patients provided written informed consent before the study; the need
26 All
patients provided written informed consent for study participation, th
27 principles of the Declaration of Helsinki, and all
patients provided written informed consent prior to enrollment.
28 All
patients provided written informed consent prior to undergoing any stu
29 All
patients provided written informed consent.
30 All
patients provided written informed consent.
31 pproved by the institutional review board, and all
patients provided written informed consent.
32 local review board approved the protocol, and all
patients provided written informed consent.
33 tional review board approval was obtained, and all
patients provided written informed consent.
34 All
patients provided written informed consent.
35 All
patients provided written informed consent.
36 eview board of all four participating centers, and
patients provided written informed consent.
37 ltiple sclerosis ( SPMS secondary progressive MS )
patients provided written informed consent and underwent 3-T MR imagin
38 All
subjects provided written informed consent, and the local institutiona
39 osture, and muscle tone, Materials and Methods All
subjects provided written informed consent, and the protocol was appro
40 view board-approved prospective study in which all
subjects provided written informed consent, six patients with relapsin
41 All
subjects provided written informed consent.
42 All
subjects provided written informed consent.
43 tional review board approval was obtained, and all
subjects provided written informed consent.
44 All
subjects provided written informed consent.
45 All
subjects provided written informed consent; the study protocol was app
46 etween 2011 and 2013 were included in this study after
they provided written informed consent.
47 r this institutional review board-approved study after
they provided written informed consent.
48 pitalization were monitored over 5 years in 91 subjects
who provided written informed consent.
49 lation (all participants randomly assigned to treatment
who provided written informed consent).
50 Between Jan 14, 2008, and July 31, 2012, 4512
women provided written informed consent of whom 3977 (88%) were eli