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1 45 days after imaging, and more than 45 days after imaging).
2 e in serum Cr levels and GFRs from before to after imaging.
3 (59.7%) for disease detected up to 12 months after imaging.
4 cases in which the regimen was not completed after imaging.
5 er imaging, 3-5 days after imaging, 6-9 days after imaging, 10-45 days after imaging, and more than 4
6 they were obtained (before imaging, 1-2 days after imaging, 3-5 days after imaging, 6-9 days after im
7 re imaging, 1-2 days after imaging, 3-5 days after imaging, 6-9 days after imaging, 10-45 days after
13 animals of group 2 were euthanized on day 7 after imaging, and Ki-67, TUNEL, ERalpha, and ERbeta sta
15 each group were collected randomly on day 3 after imaging, and terminal deoxyribonucleotidyl transfe
17 ical solution from the mouth, akin to colour after-images appearing on 'white' paper after fixation o
22 residual disease manifesting up to 9 months after imaging but lower (59.7%) for disease detected up
23 GFRs increased in both groups from before to after imaging (CT group, P </= .01; MR imaging group, P
25 ed agent that combines targeted radiotherapy after imaging dosimetry with the potential for single-ag
29 2 hours before imaging and at least one time after imaging (>1 day after administration of contrast m
30 imprecise, with 30-50% of patients recurring after image-guided radiotherapy or radical prostatectomy
39 cies, and by measuring the properties of the after-images, including their duration, size scaling, co
40 30 patients delivered between 18 and 89 days after imaging (mean, 55 days) (late delivery group).
43 of being diagnosed as having an MDD episode after imaging (odds ratio, 0.96; 95% CI, 0.01-0.75; P =
45 ('blindsight') nevertheless reported visible after-images of the stimuli when they were turned off ('
46 ontinued to carry image-specific information after image offset, but most ceased to encode previously
47 row Angle Camera (NAC) temporal ('before and after') image pairs to quantify the contemporary rate of
50 ring the earliest encoding period (0-2000 ms after image presentation) in these trials there was a wi
75 ls recovered by bronchoalveolar lavage (BAL) after imaging were stained immunohistochemically for iNO
77 ed in which a decision not to treat was made after imaging with (111)In-ibritumomab tiuxetan (4.0% of
78 not treated with (90)Y-ibritumomab tiuxetan after imaging with (111)In-ibritumomab tiuxetan, because
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