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1 assessed intersubject (4 donors) as well as intrasubject (3 different blood samples from 1 donor) va
2 ues ranging from 0.3 to 0.8, showed the best intrasubject and intersubject variability and reliabilit
5 was assessed by repeatability coefficients, intrasubject coefficients of variation (CV), and confide
6 pose of this study was to obtain continuous, intrasubject controlled assessment of the relationship b
7 n mean number of defects per section (median intrasubject correlation [r(m)] = 0.01, P = .64) or chan
10 lity assurance and analysis of data improved intrasubject CV from 15.9% to 10.7% for averaged SUV(max
14 ) states and high SI states using a powerful intrasubject design, as well as an intersubject case-cas
16 bility analyses that explicitly accounts for intrasubject fluctuations (e.g., due to measurement nois
18 26 study subjects, 19 showed no evidence of intrasubject K1 sequence variability, but, in 7 subjects
19 n of within-subject standard deviation (Sw), intrasubject precision (1.96xSw), coefficient of variati
28 ly, within each subject, three corresponding intrasubject studies were fitted simultaneously to a sin
29 during filgrastim treatment contained unique intrasubject subclusters that shared a most recent commo
31 ed this approach, examining intersubject and intrasubject variability and the validity of using a sin
32 od to be a consequence of the atypically low intrasubject variability in blood SUV and uptake time an
37 ) when responding to positive stimuli and an intrasubject variable (mood) when responding to negative
39 e classification by comparing the inter- and intrasubject variation of urinary phthalate metabolite l
40 demonstrated high temporal stability (or low intrasubject variation) over the entire study period, th
41 etest reliability was evaluated by comparing intrasubject visual read ratings and SUVrs for 2 PET ima
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