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1 ries from 0 through 10 days depending on the research protocol.
2 t-estimate procedure and lithium response by research protocol.
3 appreciation of the information concerning a research protocol.
4 aluate individuals' capacity to consent to a research protocol.
5 tion-approved biopsy system and not within a research protocol.
6 ent according to an institutionally approved research protocol.
7  for CDKN2A should be done only as part of a research protocol.
8 splants are currently permitted only under a research protocol.
9 rolled in a prospective, strict weight loss, research protocol.
10 ts answered a questionnaire relating to each research protocol.
11 als (HIV+), provided it is performed under a research protocol.
12 res can be used under a compassionate-use or research protocol.
13 l trials, only a fraction will enroll onto a research protocol.
14 eoadjuvant therapy may benefit from LT under research protocols.
15 mon to include SPECT imaging in clinical and research protocols.
16 from initial submission to final approval of research protocols.
17 ms, rather then having them being limited to research protocols.
18 or inclusion of critically ill patients into research protocols.
19 capacity to consent to clinical treatment or research protocols.
20  judges of the burdens and risks of specific research protocols.
21 first-line platinum-based chemotherapy or in research protocols.
22 may benefit from liver transplantation under research protocols.
23 ic Criteria for TMD (DC-TMD) examination and research protocols.
24 HIV to recipients with HIV (HIV D+/R+) under research protocols.
25 mandatory single-time review for multicenter research protocols, additional financial support for IRB
26 ndees at community meetings for an emergency research protocol and determine whether these meetings a
27 andard of care, compassionate care, or local research protocols and 11 (26%), 25 (60%), 9 (21%), and
28 objective measurement tools with transparent research protocols and data reduction strategies would a
29           These global data might help guide research protocols and prioritisation efforts and focus
30 posure areas, these results might help guide research protocols and prioritisation efforts and focus
31 CReDO protocols, and 73% had initiated other research protocols and published papers.
32 , risk from nontherapeutic components of the research protocol, and the psychological impact of parti
33 on-making to determine study direction, plan research protocols, and conduct project activities.
34  fine-grained reporting of methodologies and research protocols, and the importance of independent st
35           All studies were conducted under a research protocol approved by the National Institutes of
36     Special scrutiny recognizes that not all research protocols are equally ethically challenging and
37      Standardized phytosanitary measures and research protocols are needed to improve the flow of inf
38  from 104 patients prospectively enrolled in research protocols at our institution were retrospective
39 757 volunteers who were participating in our research protocols at the Mayo Clinic between 1995 and 2
40 , relapsed, and refractory SAA in 3 separate research protocols at the National Institutes of Health.
41 esonance images from men who participated in research protocols at the Veterans Affairs Palo Alto Hea
42               Differences in interlaboratory research protocols contribute to the conflicting data in
43 cting violations like p-hacking in fictional research protocols, correcting 88.6% of blatantly presen
44 ided whenever possible within the context of research protocols designed to evaluate clinical outcome
45 recent literature and our large personal and research protocol experience of bone marrow failure in t
46  informed, 66% reported participating in the research protocol for personal reasons, and 34% reported
47 ent, (v) clinical provision of UTx, and (vi) research protocols for further studies of UTx.
48           The detailed know-how to implement research protocols frequently remains restricted to the
49 ese hospital setting.Trial registration: The research protocol had obtained the favorable opinion of
50 ymptom assessed during administration of the research protocol, had used alcohol and/or other drugs w
51 information on organization, governance, and research protocols; half address institutional review bo
52 ls, it might be successfully done outside of research protocols if attention is paid to selection, ed
53 ingly utilized in clinical management and in research protocols in the approach to DME.
54                                         In a research protocol involving autozygome mapping and exome
55  comorbidity in both clinical assessment and research protocols involving children with ADHD.
56 diction tool envisioned to be most useful in research protocols involving the psychosis prodrome.
57 ation for early stage intrahepatic CCA under research protocols is emerging as a viable therapeutic o
58 noma should, whenever possible, occur within research protocols, it might be successfully done outsid
59 acity strengthening can allow AYAs to review research protocols, join ethical review committees, and
60                                     Although research protocols may take as long as 60-90 min, much m
61                                          Our research protocol measured blood pressure noninvasively
62                 All participants underwent a research protocol MRI, and 41% were classified as having
63  propose a hierarchical incremental learning research protocol named HiDiscover to systematically exp
64         To advance the state of the science, research protocols need to provide more explicit rationa
65 lingness to participate in four hypothetical research protocols of varying risk/benefit profiles were
66 e are as a group able to distinguish between research protocols of varying risk/benefit profiles.
67 hosocial factors, which can aid in tailoring research protocols, optimizing patient randomization in
68 under the minimal risk threshold; and 5) the research protocol provides sufficient latitude for treat
69 ence exists that patients who participate in research protocols (PRP) significantly differ from nonpa
70 rd investigators who fully disseminate their research protocols, reports, and participant-level datas
71 herapy, cardiogenic shock, and enrollment in research protocols requiring 4 weeks of ticlopidine were
72 ontext of standard clinical practice and the research protocol, risks must be minimized, potential be
73 ther than the ovary, and future clinical and research protocols should employ thorough examination of
74 th the participant consent agreement and the research protocol submitted to the IRB.
75  tumors and were subsequently entered into a research protocol that consisted of accelerated radiatio
76 ed using the Penn Medicine BioBank (PMBB), a research protocol that recruits adult participants durin
77 ly studied as part of a pre-existing ongoing research protocol to evaluate the effects of maternal ma
78  for cancer susceptibility in two structured research protocols to accurately anticipate emotional re
79 specially as these therapies transition from research protocols to standard care.
80                                   The animal research protocol was approved by the Institutional Anim
81                                         This research protocol was approved by the institutional revi
82                                              Research protocol was HIPAA compliant and approved by in
83                                          The research protocol was registered in PROSPERO.
84                            Four hypothetical research protocols were rated.
85 V-positive transplantations will occur under research protocols with safeguards and criteria mandated
86 can be incorporated into survey and pedigree research protocols without hindering projects with exten