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1 ay) and in vivo (biodistribution studies and gamma-camera imaging).
2 -99m labelled autologous red blood cells and gamma camera imaging.
3 , 7, and 14 days) for in vivo pinhole planar gamma camera imaging.
4 rgeting was evaluated by biodistribution and gamma camera imaging.
5 ls and subjected to blood pool analysis with gamma camera imaging.
6 91 could detect regional ischemia in vivo by gamma camera imaging.
7 y assessed blood activity concentrations and gamma-camera imaging.
8 tained by that method with those obtained by gamma-camera imaging.
9 2-expressing tumors was easily visualized by gamma camera imaging 3 h after injection.
10                 To estimate human dosimetry, gamma camera imaging and pharmacokinetic analysis was pe
11                                       Serial gamma-camera imaging and blood sampling over 24 h were p
12 185-370 MBq) followed by serial quantitative gamma-camera imaging and estimation of absorbed doses of
13 abelled polymer conjugate was assessed using gamma-camera imaging and single-photon emission computed
14             PET has greater sensitivity than gamma-camera imaging and therefore would have an advanta
15    A combination of methods was used: planar gamma-camera imaging as part of the clinical dosimetry p
16 ositron emission tomography) than for (131)I gamma camera imaging but can be limited for small and lo
17          ERPF was measured concurrently with gamma-camera imaging by previously published single-inje
18  assess lesion detectability by (111)In-J591 gamma-camera imaging compared with standard imaging meth
19                                 Quantitative gamma-camera imaging is difficult and requires scatter s
20                                       Planar gamma-camera imaging is still widely used clinically.
21 ection was monitored noninvasively by serial gamma camera imaging of (123)I-iodide biodistribution.
22                                              gamma-camera imaging of AB001 was feasible, even at a mi
23 SSTR2) has been used as a reporter probe for gamma-camera imaging of gene transfer in animal models.
24 NIS was noninvasively demonstrated by serial gamma-camera imaging of iodine-123 (123I) uptake both in
25 pers and radioactivity was quantitated using gamma-camera imaging on multiple days after (131)I-Lym-1
26 proved indium 111 octreotide was followed by gamma camera imaging (planar imaging and single photon e
27                                              Gamma camera imaging revealed accumulation in spleen and
28 99m)Tc(VII) tracer at <10(-10) mol L(-1) and gamma camera imaging showed full retention of (99m)Tc in
29                                              gamma camera imaging studies using purified eosinophils
30                   Results were recorded on a gamma camera imaging system.
31 9mTc-radiolabeled annexin V and radionuclide gamma camera imaging to serially study the sites, extent
32  objective was to explore the feasibility of gamma-camera imaging to assess biodistribution and uptak
33 an and tissue activities over time by serial gamma-camera imaging to calculate radiation-absorbed dos
34                                              Gamma camera imaging was performed during the first 4 hr
35                                              Gamma camera imaging was used to noninvasively quantify
36                                       Planar gamma-camera imaging was performed after 30 min, followe
37                                      Ex vivo gamma-camera imaging was performed.
38 termined by biodistribution measurements and gamma camera imaging with an 111In-labeled rat IgG2b mon
39 nd regional blood volumes were determined by gamma camera imaging with technetium-99m labelled erythr
40 3 additional rats, serial in vivo whole-body gamma-camera imaging with each tracer was performed.