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1 first 5 minutes, without changes in cerebral oxygen extraction fraction.
2 d flow, blood volume, oxygen metabolism, and oxygen extraction fraction.
3 lood flow, cerebral blood volume, CMRO2, and oxygen extraction fraction.
4 7% vs. 11+/-15%, p<.05, and increased global oxygen extraction fraction.
5 ue oxygen and significantly reduced regional oxygen extraction fraction.
6 ed as the product of cerebral blood flow and oxygen extraction fraction.
7 tween OxFlow and PET-only measurements of WB oxygen extraction fraction (0.30 0.09 and 0.31 0.09) and
9 erebral blood flow = 46.2-56.8 ml/100 g/min; oxygen extraction fraction = 0.39-0.50) relative to cont
10 /min, p < .05) and a significant decrease in oxygen extraction fraction (33.4 +/- 5.9 vs. 30.3 +/- 4.
11 [range, 34-88] mumol/100 mL/min) but a lower oxygen extraction fraction (38% [range, 29%-50%] vs 89%
12 n tomography for the measurement of cerebral oxygen extraction fraction and (b) computed tomographic
16 d flow (p<.001) and resulted in increases in oxygen extraction fraction and ischemic brain volume (17
17 ese 'discordant' voxels differed in baseline oxygen extraction fraction and regulated oxygen demand v
18 measured cerebral blood flow, blood volume, oxygen extraction fraction, and 18F-FDG transport into t
19 (15)O-CO scans were used to derive RV flow, oxygen extraction fraction, and blood volume, respective
20 volume, cerebral oxygen metabolism (CMRO2), oxygen extraction fraction, and brain tissue oximetry we
21 found in seven of 36 patients with increased oxygen extraction fraction, and in two of 39 with normal
22 ned by (15) O-PET cerebral blood flow (CBF), oxygen extraction fraction, and oxygen metabolism was us
23 f regional cerebral blood flow, the regional oxygen extraction fraction, and the regional metabolic r
24 cranial pressure spikes suggesting increased oxygen extraction fraction, and therefore, worsening sup
25 evaluate physiological relationships between oxygen extraction fraction, cerebral blood flow, and cli
26 hout sickle cell trait to assess whole-brain oxygen extraction fraction, cerebral blood flow, degree
27 ion fraction and regulated oxygen demand via oxygen extraction fraction changes, whereas 'concordant'
28 to evaluate whether cerebral blood flow and oxygen extraction fraction could together predict the pr
29 , we studied whether cerebral blood flow and oxygen extraction fraction differed among patients with
31 only in symptomatic patients with increased oxygen extraction fraction (eight of 36 patients; P =.00
34 o quickly and non-invasively detect elevated oxygen extraction fraction in individuals with sickle ce
35 traction fraction of 40% (the mean value for oxygen extraction fraction in normal controls) was 14 mm
36 r baseline values of cerebral blood flow and oxygen extraction fraction in the white matter were both
37 We compared baseline cerebral blood flow and oxygen extraction fraction in the whole white matter, no
40 en metabolism (P < 0.001, both comparisons); oxygen extraction fraction increases consistent with isc
41 oxygen delivery associated with reduction in oxygen extraction fraction, independent of Hgb level (p
42 m around layer IV, while the depth-dependent oxygen extraction fraction is increased in layer IV, whe
43 mages were acquired; cerebral blood flow and oxygen extraction fraction maps were obtained from which
44 goal is to determine to what extent elevated oxygen extraction fraction may be uniquely present in pa
46 Longitudinal analyses revealed that adding oxygen extraction fraction measurements to cerebral bloo
47 sonance imaging-based assessment of elevated oxygen extraction fraction might be a viable screening t
48 te the influence of APOE4 on global cerebral oxygen extraction fraction (OEF) and possible mediation
49 ood flow (CBF), cerebral blood volume (CBV), oxygen extraction fraction (OEF) and the cerebral rate f
51 consumption (MMRO2, mL.min-1 x 100 g-1) and oxygen extraction fraction (OEF) by use of positron emis
53 STLCOS) demonstrated that increased cerebral oxygen extraction fraction (OEF) detected by PET scannin
55 t inhalation of (15)O-O(2) provides regional oxygen extraction fraction (OEF) in a shorter acquisitio
56 ase (SCD) on hydroxyurea have lower cerebral oxygen extraction fraction (OEF) than similar patients n
59 Whole-brain cerebral blood flow (CBF) and oxygen extraction fraction (OEF) were measured by magnet
60 ional resting cerebral blood flow (CBF), (2) oxygen extraction fraction (OEF), and (3) cerebral metab
61 y were used to noninvasively assess regional oxygen extraction fraction (OEF), cerebral blood volume,
63 ng a multiple-variable sensor, and images of oxygen extraction fraction (OEF), derived from positron
64 delivery (DO(2)), oxygen metabolism (MO(2)), oxygen extraction fraction (OEF), or thickness after the
65 cular oxygen tension (PO2) and inner retinal oxygen extraction fraction (OEF), whereas outer retinal
66 bral metabolic stress, reflected by elevated oxygen extraction fraction (OEF), which likely drives st
68 type indicator [MTI]) and oxygen metabolism (oxygen extraction fraction [OEF] and cerebral metabolic
69 brain tissue oxygen value associated with an oxygen extraction fraction of 40% (the mean value for ox
72 ction fraction, and in two of 39 with normal oxygen extraction fraction (P =.08, difference not signi
73 relationship between brain tissue oxygen and oxygen extraction fraction (r = .21, p < .05); the brain
74 a prevents the CMRO(2)-surge by constraining oxygen extraction fraction, reduces mitochondrial oxidat
75 olic rate of oxygen consumption (rMMRO2) and oxygen extraction fraction (rOEF) quantitatively and non
76 issue oxygen than the percentage decrease in oxygen extraction fraction; this suggests that the oxyge
84 very, cerebral metabolic rate of oxygen, and oxygen extraction fraction) were measured every 30 minut
85 test metabolic stress, indicated by elevated oxygen extraction fraction, would have the lowest connec