ライフサイエンスコーパス: written informed consent was obtained from

1 The institutional review board approved this study, and written informed consent was obtained from 25 symptomatic pat

2 Written informed consent was obtained from 67 consecutive pat

3 as approved by the National Research Ethical Committee, and written informed consent was obtained from all individuals.

4 Written informed consent was obtained from all participants b

5 Written informed consent was obtained from all participants f

6 Written informed consent was obtained from all participants,

7 included, which was approved by the local ethics board and written informed consent was obtained from all participants.

8 men, 5 men; age +/- SD, 34.3 +/- 6.5 y) were recruited, and written informed consent was obtained from all participants.

9 Written informed consent was obtained from all participants.

10 Written informed consent was obtained from all participants.

11 Written informed consent was obtained from all participants.

12 SHIP was approved by the institutional review board, and written informed consent was obtained from all participants.

13 stitutional review boards of all participating centers, and written informed consent was obtained from all participants.

14 local ethics committee approved this prospective study, and written informed consent was obtained from all participants.

15 Written informed consent was obtained from all patients and l

16 liant study was approved by the local ethics committee, and written informed consent was obtained from all patients for u

17 Materials and Methods Written informed consent was obtained from all patients in th

18 Materials and Methods Written informed consent was obtained from all patients, and

19 Written informed consent was obtained from all patients, and

20 Written informed consent was obtained from all patients, and

21 approved by the National Research Ethics Service Committee; written informed consent was obtained from all patients.

22 etrospective study had institutional review board approval; written informed consent was obtained from all patients.

23 prospective study was approved by our ethics committee, and written informed consent was obtained from all patients.

24 The study was approved by the local ethics committee, and written informed consent was obtained from all patients.

25 Written informed consent was obtained from all patients.

26 s study was approved by the institutional review board, and written informed consent was obtained from all patients.

27 Written informed consent was obtained from all patients.

28 Written informed consent was obtained from all patients.

29 Written informed consent was obtained from all patients.

30 s study was approved by the institutional review board, and written informed consent was obtained from all study particip

31 roved by the local ethical committees on human studies, and written informed consent was obtained from all subjects befor

32 This study was approved by the local ethical committee, and written informed consent was obtained from all subjects befor

33 tive study was approved by the local ethics committees, and written informed consent was obtained from all subjects prior

34 Written informed consent was obtained from all subjects.

35 ty Medical Center and Leiden University Medical Center, and written informed consent was obtained from all subjects.

36 Written informed consent was obtained from all subjects.

37 Written informed consent was obtained from all subjects.

38 This study was approved by the local ethical committee, and written informed consent was obtained from all subjects.

39 this prospective multi-institutional HIPAA-compliant study; written informed consent was obtained from all subjects.

40 inations were performed with ethical review board approval; written informed consent was obtained from all volunteers.

41 fibrillation) from the John Radcliffe Hospital, Oxford, UK; written informed consent was obtained from each participant.

42 This study was approved by the local ethics committee, and written informed consent was obtained from each participant.

43 vivo study was approved by the local ethics committee, and written informed consent was obtained from each patient.

44 Written informed consent was obtained from each patient.

45 Written informed consent was obtained from each subject.

46 Written informed consent was obtained from each subject.

47 ctive study was approved by the institutional board review; written informed consent was obtained from healthy subjects a

48 Written informed consent was obtained from patients or their

49 e study was approved by the institutional review board, and written informed consent was obtained from patients.

50 t study was approved by the institutional review board, and written informed consent was obtained from the patient's pare