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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.
28          After approval by the institutional review board, 1,022 LNs in the PET/CT examinations of 14
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
32 tive study was approved by the institutional review board and compliant with HIPAA.
33 tive study was approved by the institutional review board and compliant with HIPAA.
34 tive study was approved by the institutional review board and compliant with HIPAA.
35 tive study was approved by the institutional review board and compliant with HIPAA.
36 This study was approved by the institutional review board and compliant with HIPAA.
37 This study was approved by the institutional review board and compliant with HIPAA.
38 onal study was approved by the institutional review board and compliant with HIPAA.
39 This study was approved by the institutional review board and complied with HIPAA.
40 ementation were overseen by an institutional review board and conformed to HIPAA guidelines on patien
41          Materials and Methods Institutional review board and informed consent were waived for this s
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.
44          Materials and Methods Institutional review board and local ethics committee approval and wri
45  The study was approved by the institutional review board and local ethics committee.
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
48 hort study was approved by the institutional review board and was compliant with HIPAA.
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
51 tive study was approved by the institutional review boards and compliant with HIPAA.
52 ablishing common protocols for institutional review boards and data sharing, creating protocols for r
53 y protocol was approved by the institutional review boards and was HIPAA compliant.
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
58 prospective study was approved by the ethics review board, and informed consent was obtained.
59 tive study was approved by the institutional review board, and informed consent was waived.
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
70 esignation and is exempt from Human Subjects Review Board approval (11-DRDS-NR03).
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
74          Materials and Methods Institutional review board approval and informed consent were obtained
75          Materials and Methods Institutional review board approval and informed consent were obtained
76 aterials and Methods Following institutional review board approval and informed consent, 26 subjects
77                          After institutional review board approval and informed consent, consecutive
78 als and Methods This study had institutional review board approval and was HIPAA compliant.
79          Materials and Methods Institutional review board approval and written informed consent from
80                                Institutional review board approval and written informed consent from
81          Materials and Methods Institutional review board approval and written informed consent were
82          Materials and Methods Institutional review board approval and written informed consent were
83                                Institutional review board approval and written informed consent were
84          Materials and Methods Institutional review board approval and written informed consent were
85 tudy was HIPAA compliant, with institutional review board approval and written informed consent.
86          Materials and Methods Institutional review board approval and written informed patient conse
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
89 tional new drug submission and institutional review board approval standards.
90          Materials and Methods Institutional review board approval was given and patient consent was
91 ation was accessed; therefore, institutional review board approval was not sought.
92                                Institutional review board approval was obtained and informed consent
93          Materials and Methods Institutional review board approval was obtained and informed consent
94          Materials and Methods Institutional review board approval was obtained and the requirement f
95          Materials and Methods Institutional review board approval was obtained for active or passive
96          Materials and Methods Institutional review board approval was obtained for this HIPAA-compli
97          Materials and Methods Institutional review board approval was obtained for this HIPAA-compli
98          Materials and Methods Institutional review board approval was obtained for this HIPAA-compli
99          Materials and Methods Institutional review board approval was obtained for this HIPAA-compli
100          Materials and Methods Institutional review board approval was obtained for this prospective
101          Materials and Methods Institutional review board approval was obtained for this retrospectiv
102          Materials and Methods Institutional review board approval was obtained for this study; all p
103          Materials and Methods Institutional review board approval was obtained from Leipzig Universi
104          Materials and Methods Institutional review board approval was obtained with waiver of consen
105          Materials and Methods Institutional review board approval was obtained, and informed consent
106                                Institutional review board approval was obtained, and informed consent
107          Materials and Methods Institutional review board approval was obtained, and informed consent
108          Materials and Methods Institutional review board approval was obtained, and patient consent
109          Materials and Methods Institutional review board approval was obtained, and the requirement
110                        Materials and Methods Review board approval was obtained, with waiver of infor
111          Materials and Methods Institutional review board approval was obtained, with waiver of infor
112                                Institutional review board approval was obtained, with waiver of the n
113 iver of informed consent after institutional review board approval was obtained.
114          Materials and Methods Institutional review board approval was obtained.
115          Materials and Methods Institutional review board approval was obtained.
116                                Institutional review board approval was obtained.
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
119                          After institutional review board approval with a waiver of informed consent
120 nd Methods This study received institutional review board approval with waiver of consent.
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
129                           With institutional review board approval, we searched our prospectively acq
130          Materials and Methods Institutional review board approval, with a waiver of informed consent
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
133 e database were evaluated with institutional review board approval.
134 tive study was completed after institutional review board approval.
135 eers with informed consent and institutional review board approval.
136 and is, therefore, exempt from institutional review board approval.
137 nce with HIPAA regulations and institutional review board approval.
138 ectional study was exempt from institutional review board approval.
139 s This retrospective study had institutional review board approval; written informed consent was obta
140 als and Methods This study was institutional review board approved and HIPAA compliant.
141                 This study was institutional review board approved and HIPAA compliant.
142   This retrospective study was institutional review board approved and HIPAA compliant; informed cons
143                           Each institutional review board approved the prospective study protocol, an
144                            The institutional review board approved the study and all participants pro
145                      The local institutional review board approved the study, and all participants ga
146      Materials and Methods The institutional review board approved the study.
147      Materials and Methods The institutional review board approved this cross-sectional study.
148 aterials and Methods The local institutional review board approved this HIPAA-compliant retrospective
149      Materials and Methods The institutional review board approved this prospective Health Insurance
150      Materials and Methods The institutional review board approved this prospective hypotheses-genera
151                            The institutional review board approved this prospective study.
152      Materials and Methods The institutional review board approved this prospective, HIPAA-compliant,
153                            The institutional review board approved this retrospective chart review st
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
157       Materials and Methods An institutional review board approved this retrospective study and waive
158      Materials and Methods The institutional review board approved this retrospective study of 31 pat
159                            The institutional review board approved this retrospective study of 403 pa
160          Materials and Methods Institutional review board approved this retrospective study, with wai
161      Materials and Methods The institutional review board approved this retrospective study, with wai
162                            The institutional review board approved this study and waived the need for
163      Materials and Methods The institutional review board approved this study.
164  This study was retrospective, institutional review board approved, and HIPAA compliant.
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
167 ompliant prospective study was institutional review board approved.
168   This retrospective study was institutional review board approved.
169 is study was HIPAA compliant and institution review board approved.
170                 This study was institutional review board approved; the need for signed informed cons
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
173                 The applicable institutional review boards approved this study, and all participants
174 ods This prospective study was institutional review board- approved and HIPAA compliant.
175                        In this institutional review board-approved and Health Insurance Portability a
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-
181 erials and Methods This was an institutional review board-approved and HIPAA-compliant study.
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
191                           This institutional review board-approved HIPAA-compliant retrospective stud
192 thods This was a retrospective institutional review board-approved HIPAA-compliant study.
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
196 metastases were enrolled in an institutional review board-approved prospective clinical trial.
197 metastases were enrolled in an Institutional Review Board-approved prospective clinical trial.
198       Materials and Methods An institutional review board-approved prospective database of 257 patien
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
202 oma (MP) were treated using an institutional review board-approved protocol.
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
206       Materials and Methods An institutional review board-approved retrospective review was performed
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
211                        In this institutional review board-approved retrospective study, subjects were
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
217                           This institutional review board-approved study from June 2007 to December 2
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
237 vided informed consent in this institutional review board-approved study.
238 vided informed consent in this institutional review board-approved study.
239 nd maintained in a prospective institutional review board-approved study.
240 nstitution HIPAA-compliant and institutional review board-approved study.
241 ncluded in this retrospective, institutional review board-approved study.
242 itant CT were enrolled in this institutional review board-approved study.
243 ent prior to inclusion in this institutional review board-approved study.
244 pared in this HIPAA-compliant, institutional review board-approved study.
245                 This study was institutional review board-approved with waivers of informed consent.
246 nd Methods In this binational, institutional review board-approved, HIPAA-compliant prospective study
247                           This institutional review board-approved, HIPAA-compliant prospective study
248 er 2011 to September 2012 with institutional review board-approved, HIPAA-compliant protocols.
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
254                        In this institutional review board-approved, HIPAA-compliant study, a silicon
255 Materials and Methods For this institutional review board-approved, HIPAA-compliant study, thoracic e
256 hods This was a retrospective, institutional review board-approved, HIPAA-compliant study.
257                          In an institutional review board-approved, HIPAA-compliant, prospective stud
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
260                        In this institutional review board-approved, informed consent-waived, HIPAA-co
261 erials and Methods This was an institutional review board-approved, prospectively conducted (written
262                     This is an Institutional Review Board-approved, retrospective study.
263 ials and Methods SIESTA was an institutional review board-approved, single-center, prospective, rando
264 tive HIPAA-compliant study was institutional review board-approved.
265                            The institutional review board at each site approved the trial.
266      Materials and Methods The institutional review board exempted this HIPAA-compliant retrospective
267                             An institutional review board exemption and a waiver for informed consent
268                                Institutional review board exemptions were granted prior to the collec
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
271 s research was approved by the institutional review board (IRB) and was HIPAA compliant.
272  protocol design, choice of an institutional review board (IRB), and trial outcomes.
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
275  Methods The study was approved by the local review board (NL42888.029.13).
276                            The institutional review board of Beth Israel Deaconess Medical Center app
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
281 tive study was approved by the institutional review board of three institutions.
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
285 t protocol was approved by the institutional review boards of the participating centers.
286 om-based study was exempt from institutional review board oversight.
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,
289 iew by the Columbia University Institutional Review Board, Protocol ID# AAAO3003.
290                            The institutional review board provided a waiver of informed consent.
291  was compliant with the HIPAA (Institutional Review Board Reg. #00000940).
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
294                            The institutional review board waived the need for consent.
295                            The institutional review board waived the requirement for 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
298 iant study was approved by our institutional review board with a waiver of informed consent.
299 tive study was approved by the institutional review board with patient informed consent.
300 ticenter study was approved by institutional review boards with written informed consent.

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