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1 (64)Cu-FBP8 administration to estimate human radiation dosimetry.
2 th (18)F-FPEB, we performed studies of human radiation dosimetry.
3 alternative with improved image quality and radiation dosimetry.
4 easure their comparative biodistribution and radiation dosimetry.
5 on, tissue iNOS levels, and calculated human radiation dosimetry.
6 al assessments of pharmacokinetics and organ radiation dosimetry.
7 1 provided good imaging of NHL and favorable radiation dosimetry.
8 fter infusion to assess pharmacokinetics and radiation dosimetry.
9 a is a general approach for medical internal radiation dosimetry.
10 entation; 2) 10 days of personal ultraviolet radiation dosimetry; 3) a sun exposure and physical acti
11 re conducted to evaluate biodistribution and radiation dosimetry after intravenous injection of (18)F
12 ated in 2 studies: in the first study, human radiation dosimetry and biodistribution of (11)C-metform
13 erformed over 48 h for calculation of tissue radiation dosimetry and for evaluation of clinical safet
15 uorodeoxyglucose (FDG), to contribute to its radiation dosimetry and to define a suitable proxy for a
16 mical parameters before and after treatment, radiation dosimetry, and complications were recorded.
20 tives of this phase I study were to evaluate radiation dosimetry, biodistribution, human safety, tole
21 human experience with (18)F-FEOBV, including radiation dosimetry, biodistribution, tolerability and s
24 The 188Re(Sn)HEDP has biodistribution and radiation dosimetry characteristics that are similar to
26 F-FETrp tumoral uptake, biodistribution, and radiation dosimetry data provide strong preclinical evid
35 The (18)F-PEG(6)-IPQA pharmacokinetic and radiation dosimetry estimates were determined using volu
37 conventional formulations, and the predicted radiation dosimetry estimations for some organs varied s
42 aim of this study was to derive PET/CT-based radiation dosimetry for (89)Zr-cetuximab, with special e
43 macokinetic data and 90Y physical constants, radiation dosimetry for 90Y-21T-BAD-Lym-1 was determined
45 dy was to determine the pharmacokinetics and radiation dosimetry for the initial 131I-Lym-1 therapy d
55 y was to assess safety, biodistribution, and radiation dosimetry in humans for the highly selective s
57 onuclides and the need for greater accuracy, radiation dosimetry in nuclear medicine is evolving from
58 rt the safety, biodistribution, and internal radiation dosimetry, in humans with thyroid cancer, of (
60 s and assessed the feasibility of generating radiation dosimetry maps in liver regions with high and
62 e calculational ease of the Medical Internal Radiation Dosimetry (MIRD) system with the additional in
63 ole-body PET/CT was used to characterize the radiation dosimetry of (11)C-DPA-713, a specific PET lig
64 , we measured the whole-body biokinetics and radiation dosimetry of (123)I-IMPY in AD patients and co
65 describe the initial clinical experience and radiation dosimetry of (18)F-DCFBC in men with metastati
68 cokinetics, biodistribution, metabolism, and radiation dosimetry of (18)F-PEG(6)-IPQA in nonhuman pri
69 evaluate the biodistribution, kinetics, and radiation dosimetry of (64)CuCl2 in humans and to assess
71 measure the biodistribution and estimate the radiation dosimetry of (68)Ga-ABY-025 for 2 different pe
72 lism, pharmacokinetics, biodistribution, and radiation dosimetry of (68)Ga-bombesin antagonist (68)Ga
76 etics for 67Cu and 64Cu was assumed, and the radiation dosimetry of 64Cu was assessed using quantitat
77 ding 131I-labeled monoclonal antibodies, the radiation dosimetry of 90Y-2-iminothiolane-2-[p-(bromoac
83 man safety, whole-organ biodistribution, and radiation dosimetry of LMI1195 were evaluated in a phase
91 uptake reflects PARP expression and that its radiation dosimetry profile is compatible with those of
92 rt the safety, biodistribution, and internal radiation dosimetry profiles of (18)F-D4-FCH in 8 health
93 rt the safety, biodistribution, and internal radiation dosimetry profiles of (18)F-ICMT-11 in 8 healt
94 sed in conjunction with the Medical Internal Radiation Dosimetry schema to: estimate absorbed doses i
95 indicated that both disposition kinetics and radiation dosimetry support its clinical use for imaging
110 the dosimetry group, the biodistribution and radiation dosimetry were calculated using whole-body PET
112 based biodistribution, pharmacokinetics, and radiation dosimetry were performed on nonhuman primates.
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