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1 iant study was approved by the institutional review board.
2 tive study was approved by the institutional review board.
3 consent under approval of the institutional review board.
4 tive study was approved by the institutional review board.
5 trol study was approved by the institutional review board.
6 tive study was approved by the institutional review board.
7 with HIPAA and approved by the institutional review board.
8 iant study was approved by the institutional review board.
9 mpliant study was exempted from the internal review board.
10 compliant and approved by the institutional review board.
11 a-analysis was approved by the institutional review board.
12 tive study was approved by the institutional review board.
13 This study was approved by the institutional review board.
14 The study was approved by the institutional review board.
15 tudy was approved by the local institutional review board.
16 tive study was approved by the institutional review board.
17 was approved by the university institutional review board.
18 with HIPAA and approved by the institutional review board.
19 hods Approval was obtained from the regional review board.
20 nth period and approved by the institutional review board.
21 iant study was approved by the institutional review board.
22 tive study was approved by the institutional review board.
23 care and use committee and the institutional review board.
24 This study was approved by the institutional review board.
25 l animal studies committee and institutional review board.
26 iant study was approved by the institutional review board.
27 iant study was approved by the institutional review board.
29 This study was approved by the institutional review board and all participants gave informed consent.
30 This study was approved by the institutional review board and by national government authorities.
31 This study was approved by the institutional review board and compliant with HIPAA and included BCSC
40 ementation were overseen by an institutional review board and conformed to HIPAA guidelines on patien
42 tional Military Medical Center institutional review board and is compliant with HIPAA guidelines.
43 tional Military Medical Center institutional review board and is compliant with HIPAA guidelines.
46 s compliant with HIPAA and the institutional review board and required written consent from the parti
47 stem cells was approved by the institutional review board and the stem cell research oversight commit
49 spective study approved by the institutional review board and was HIPAA compliant with waiver of info
50 The study was approved by the institutional review board and written informed consent with HIPAA aut
52 ablishing common protocols for institutional review boards and data sharing, creating protocols for r
54 The study was approved by the institutional review board, and all participants gave informed consent
55 This study was approved by the institutional review board, and all participants gave written informed
56 This study was approved by the institutional review board, and all subjects gave signed informed cons
57 tudy was approved by the local institutional review board, and informed consent was obtained from all
60 tive study was approved by the institutional review board, and the requirement for informed consent w
61 tive study was approved by the institutional review board, and the requirement for informed consent w
62 tive study was approved by the institutional review board, and the requirement to obtain informed con
63 tive study was approved by the institutional review board, and the requirement to obtain informed con
64 etrospective study was approved by an ethics review board, and the requirement to obtain informed wri
65 This study was approved by the institutional review board, and written informed consent was obtained
66 tive study was approved by the institutional review board, and written informed consent was obtained.
67 onal study was approved by the institutional review boards, and all participants gave informed consen
68 tive study was approved by the institutional review boards, and written informed consent was obtained
69 terials and Methods This is an institutional review board- and U.S. Food and Drug Administration-appr
71 and Methods The study received institutional review board approval and all patients gave written info
72 his prospective study received institutional review board approval and fully complied with HIPAA regu
73 Materials and Methods With institutional review board approval and Health Insurance Portability a
76 aterials and Methods Following institutional review board approval and informed consent, 26 subjects
87 ctal liver metastases, whereas institutional review board approval is required before glass microsphe
88 Methods In accordance with the institutional review board approval obtained at the two participating
117 in U.S. Materials and Methods Institutional review board approval was waived, as the study used publ
118 HISTORY: Materials and Methods Institutional review board approval was waived, as the study used publ
121 nter HIPAA-compliant study had institutional review board approval, and all participants gave written
122 als and Methods This study had institutional review board approval, and informed consent was obtained
123 This HIPAA-compliant study had institutional review board approval, and informed consent was obtained
124 nd Methods This study received institutional review board approval, and patients gave informed consen
125 and Methods The study received institutional review board approval, and patients in the CLQ cohort pr
126 This HIPAA-compliant study had institutional review board approval, and the need for informed consent
127 s This retrospective study had institutional review board approval, and the need to obtain informed p
128 taining antemortem consent and institutional review board approval, the authors compared postmortem n
131 s retrospective study received institutional review board approval, with a waiver of the HIPAA requir
132 aterials and Methods Following institutional review board approval, with waiver of consent and with H
139 s This retrospective study had institutional review board approval; written informed consent was obta
142 This retrospective study was institutional review board approved and HIPAA compliant; informed cons
148 aterials and Methods The local institutional review board approved this HIPAA-compliant retrospective
150 Materials and Methods The institutional review board approved this prospective hypotheses-genera
152 Materials and Methods The institutional review board approved this prospective, HIPAA-compliant,
154 Materials and Methods The institutional review board approved this retrospective cohort study, w
155 Materials and Methods The institutional review board approved this retrospective HIPAA-compliant
156 Materials and Methods The institutional review board approved this retrospective study and infor
158 Materials and Methods The institutional review board approved this retrospective study of 31 pat
161 Materials and Methods The institutional review board approved this retrospective study, with wai
165 This retrospective study was Institutional Review Board approved, and informed consent was waived.
166 Materials and Methods This institutional review board approved, HIPAA-compliant retrospective rev
171 als and Methods The respective institutional review boards approved this HIPAA-compliant study and wa
172 rials and Methods The relevant institutional review boards approved this HIPAA-compliant study, with
176 Materials and Methods In this institutional review board-approved and HIPAA-compliant protocol, 408
177 erials and Methods This was an institutional review board-approved and HIPAA-compliant retrospective
178 aterials and Methods This was an intuitional review board-approved and HIPAA-compliant retrospective
179 e enrolled in this prospective institutional review board-approved and HIPAA-compliant study between
180 Materials and Methods This institutional review board-approved and HIPAA-compliant study was a 6-
182 multicenter, HIPAA-compliant, institutional review board-approved clinical trial was performed by ex
183 node resection (MLNR) under an Institutional Review Board-approved common protocol from 1992 to 2014.
184 uly 2012 to October 2013, this institutional review board-approved HIPAA-compliant prospective study
185 Materials and Methods In this institutional review board-approved HIPAA-compliant retrospective anal
186 Materials and Methods For this institutional review board-approved HIPAA-compliant retrospective stud
187 Materials and Methods This institutional review board-approved HIPAA-compliant retrospective stud
188 Materials and Methods In this institutional review board-approved HIPAA-compliant retrospective stud
189 Materials and Methods In this institutional review board-approved HIPAA-compliant retrospective stud
190 Materials and Methods For this institutional review board-approved HIPAA-compliant retrospective stud
193 = 19) and NHL (n = 2) onto the Institutional Review Board-approved investigation of (11)C-MET PET/CT.
194 = 19) and NHL (n = 2) onto the Institutional Review Board-approved investigation of (11)C-MET PET/CT.
195 hods For this HIPAA-compliant, institutional review board-approved prospective blinded pilot study, p
199 erials and Methods This was an institutional review board-approved prospective study in 29 patients (
200 ethods In this HIPAA-compliant institutional review board-approved prospective study in which all sub
201 Materials and Methods In this institutional review board-approved prospective study, 27 patients wit
203 thods In this HIPAA-compliant, institutional review board-approved retrospective cohort study, an ins
204 consisted of a HIPAA-compliant institutional review board-approved retrospective review of data in 16
205 Materials and Methods In this institutional review board-approved retrospective review of prospectiv
207 Methods This HIPAA-compliant, institutional review board-approved retrospective study included 108 p
208 d Methods This HIPAA-compliant institutional review board-approved retrospective study included 159 p
209 Methods This HIPAA-compliant, institutional review board-approved retrospective study included 51 pa
210 Materials and Methods This institutional review board-approved retrospective study was performed
212 Materials and Methods This institutional review board-approved retrospective study, with waived i
213 erials and Methods This was an institutional review board-approved retrospective study, with waiver o
214 nd genetic findings as part of institutional review board-approved studies at Children's National Hea
215 2010 to October 2012 for this institutional review board-approved study after they provided written
216 s prospective HIPAA-compliant, institutional review board-approved study between April 2012 and Novem
218 Materials and Methods This institutional review board-approved study included 125 women with inva
219 and Methods This retrospective institutional review board-approved study included 24 patients with pr
220 Methods This HIPAA-compliant, institutional review board-approved study measured the performance of
221 and Methods This retrospective institutional review board-approved study received a waiver of informe
222 retrospective HIPAA-compliant institutional review board-approved study was exempt from informed con
223 itten informed consent in this institutional review board-approved study was obtained from eight heal
224 Methods This HIPAA-compliant, institutional review board-approved study was performed at a tertiary
225 prospective, HIPAA-compliant, institutional review board-approved study was performed by using the s
226 Methods In this retrospective, institutional review board-approved study, 120 patients who underwent
227 etrospective, HIPAA-compliant, institutional review board-approved study, 136 consecutive patients (9
228 ingle-center, HIPAA-compliant, institutional review board-approved study, 157 patients (86 men and 71
229 Materials and Methods In this institutional review board-approved study, 20 patients with chronic th
230 Methods In this retrospective, institutional review board-approved study, 33 patients who underwent a
231 Methods In this retrospective, institutional review board-approved study, 41 pediatric patients (age
232 Materials and Methods In this institutional review board-approved study, a public NSCLC data set tha
233 thods In this HIPAA-compliant, institutional review board-approved study, all patients with ADPKD pro
234 Materials and Methods In this institutional review board-approved study, all unenhanced DE head CT e
235 ods This was a HIPAA-compliant institutional review board-approved study, with informed consent from
236 Materials and Methods In this institutional review board-approved study, with the written informed c
246 nd Methods In this binational, institutional review board-approved, HIPAA-compliant prospective study
249 tireader, multi-institutional, institutional review board-approved, HIPAA-compliant retrospective ana
250 Materials and Methods This institutional review board-approved, HIPAA-compliant retrospective stu
251 and Methods This retrospective institutional review board-approved, HIPAA-compliant review of 7519 wo
252 Materials and Methods This institutional review board-approved, HIPAA-compliant study included 14
253 Materials and Methods In this institutional review board-approved, HIPAA-compliant study, 58 patient
255 Materials and Methods For this institutional review board-approved, HIPAA-compliant study, thoracic e
258 Materials and Methods This institutional review board-approved, HIPAA-compliant, retrospective st
259 Materials and Methods This institutional review board-approved, HIPAA-compliant, retrospective st
261 erials and Methods This was an institutional review board-approved, prospectively conducted (written
263 ials and Methods SIESTA was an institutional review board-approved, single-center, prospective, rando
266 Materials and Methods The institutional review board exempted this HIPAA-compliant retrospective
269 obtained from the centralized institutional review board for this prospective single-arm study, and
270 tive study was approved by the institutional review board; informed consent was obtained from all pat
273 r (TRD) who participated in an Institutional Review Board (IRB)-approved randomised double-blind tria
274 ethical review of research by institutional review boards (IRBs) due to the rush to enter the disast
277 for the study was obtained from the ethical review board of the Netherlands Association for Medical
278 records review approved by the institutional review board of the University Health Network, Toronto.
279 The study was approved by the Institutional Review Board of the University Medical Center Groningen
280 tive study was approved by the institutional review board of the University of Wisconsin School of Me
282 Materials and Methods The institutional review boards of all participating centers approved this
283 Materials and Methods The institutional review boards of each center approved this retrospective
284 Materials and Methods The institutional review boards of the four participating centers approved
287 nography Materials and Methods Institutional review board permission was obtained to use deidentified
288 tients were collected under an institutional review board protocol 2 hours after portal reperfusion,
292 ed research, investigators and Institutional Review Boards should consider a deferred consent process
293 tive study was approved by the institutional review board; the requirement to obtain informed consent
296 re exempted from review by the institutional review board, which consisted of 1007 posteroanterior ch
297 tive study was approved by the institutional review board, which waived the requirement for informed
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