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1 DMSA scans were obtained by both pinhole and SPECT techn
2 etallic ligand-protected cluster, Ag(4)Ni(2)(DMSA)(4) (DMSA = meso-2,3-dimercaptosuccinic acid) was s
3 gand-protected cluster, Ag(4)Ni(2)(DMSA)(4) (DMSA = meso-2,3-dimercaptosuccinic acid) was synthesized
4 nization (ESI) mass spectrometry to be Ag(7)(DMSA)(4), where DMSA represents meso-2,3-dimercaptosucci
7 njection of a cortical fixation agent, 99mTc-DMSA or 99mTc-GH, and requires effective immobilization
9 enal length measurements determined by 99mTc-DMSA SPECT is similar to that reported previously using
10 ior image quality in the evaluation of 99mTc-DMSA renal SPECT data, with the potential for markedly r
12 Fifty sequential pediatric patient 99mTc-DMSA SPECT studies of 98 kidneys were retrospectively an
13 d a literature review, we suggest that 99mTc-DMSA scintigraphy be performed early when evaluating gir
14 1-16 y; mean age, 5.4 y) who underwent 99mTc-DMSA SPECT were measured independently by 2 observers.
15 case, such a kidney was detected with 99mTc-DMSA scintigraphy but not by intravenous pyelography.
17 lutions of meso-2,3-dimercaptosuccinic acid (DMSA) at increasing concentration (0.025, 0.050, and 0.1
18 (DMPS) or meso-2,3-dimercaptosuccinic acid (DMSA) caused a significant reduction (P < 0.0001) in the
19 imaging with 99mTc-dimercaptosuccinic acid (DMSA) has become the imaging test of choice for the diag
20 ter delivery, and a dimercaptosuccinic acid (DMSA) radioisotope scan at 3 months was done on those wi
21 renograms, (99m)Tc-dimercaptosuccinic acid (DMSA) renal cortical scans, (99m)Tc-based hepatobiliary
22 Quantitative 99mTc-dimercaptosuccinic acid (DMSA) renal uptake was studied in unilateral reflux-rela
24 had early and late dimercaptosuccinic acid (DMSA) scans to detect acquired focal defects, and their
25 phy, technetium 99m-dimercaptosuccinic acid (DMSA) scintigraphy, contrast material-enhanced computed
27 ad, tibia lead, and dimercaptosuccinic acid (DMSA)-chelatable lead and measures of neurobehavioral an
31 ramme data, we describe change in VBLL after DMSA treatment courses in a cohort of 1,156 children </=
34 footprinting and DNA mobility shift assays (DMSA) using rat liver nuclear extracts identify a number
35 In most patients with fixed defects on both DMSA and MAG3-F(0), follow-up studies showed no resoluti
36 ient decrease in C/EBP alpha, as measured by DMSA, and an increase in beta 2 AR mRNA levels and rate
43 al uptake persisted, but the elevated global DMSA accumulation seen for group C (with irreversible im
45 heir mutual interdependence for detection in DMSA, and 4) inhibition of expression of HMG proteins by
46 differential uptake resulted from increased DMSA accumulation (absolute % dose uptake) by the nondis
50 so raises questions about the sensitivity of DMSA, considering that only a small percentage of patien
53 eurobehavioral performance than was tibia or DMSA-chelatable lead, mainly in the domains of executive
56 elonephritis is slightly better than pinhole DMSA scan, the overall accuracy of these two imaging tec
62 ta for 537 children, with a positive (99m)Tc-DMSA scan prevalence of 59% overall, and seven studies w
63 n UTI who had undergone both MCU and (99m)Tc-DMSA scintigraphy, and which also reported both positive
64 eficient mice an increased amount of (99m)Tc-DMSA was excreted in an approximately 27-kDa form, which
67 )Tc-labeled dimercaptosuccinic acid ((99m)Tc-DMSA) accumulates in the kidney cortex and is widely use
68 99m-labeled dimercaptosuccinic acid ((99m)Tc-DMSA) renal scintigraphy in 2 cases of preemptive LKT de
78 nous blood lead level (VBLL) associated with DMSA treatment in the largest cohort of children </= 5 y
80 ower specificity for MAG3-F(0) compared with DMSA (86%); this finding needs further study, because it
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