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1 r 133Xe SPECT, subjects received 22 +/- 4mCi 99mTc-HMPAO, and images were acquired 15 min after injec
4 ning began on average 11.5 +/- 2.8 min after 99mTc-HMPAO injection and 41.8 +/- 10.1 min after 99mTc-
5 rinogen (0.18 +/- 0.02% ID/g) (p < 0.05) and 99mTc-HMPAO-platelets (0.14 +/- 0.02% ID/g, p < 0.05).
9 ith symmetric cerebral perfusion measured by 99mTc-HMPAO SPECT may still have a high long-term compli
11 min/100 g, 133Xe) or regional count density (99mTc-HMPAO) were extracted from 24 ROI located 6 cm abo
14 esearch aimed to compare cerebral images for 99mTc-HMPAO and 99mTc-ECD in discriminating patients wit
15 n the BNT correlated with low frontotemporal 99mTc-HMPAO (Spearman r = 0.97, P = 0.004) in the 5 pati
18 aged up to 3 hours after injection of 10-mCi 99mTc-HMPAO-labeled autologous leukocytes (Tc-WBC), and
22 , 99mTc-D,L-hexamethylpropylene amine oxide (99mTc-HMPAO, or exametazime) or 99mTc-ethylene-dicystein
26 nvestigated the relationship between reduced 99mTc-HMPAO uptake and the severity of dysnomia in PPA.
27 chnetium-99m-ECD shows greater contrast than 99mTc-HMPAO between affected and unaffected brain struct
30 133Xe SPECT, although our data suggest that 99mTc-HMPAO mildly underestimates rCBF above 80 ml/min/1
31 pus and small areas of the cerebellum in the 99mTc-HMPAO group as compared to the 99mTc-ECD group.
36 bjective of this study was to assess whether 99mTc-HMPAO brain SPECT imaging can identify patients at
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