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1 y)benzyl)-N-(4-phenoxypyridin-3-yl)acetamide PET scan.
2 dose of (18)F-FDG followed by a dual-imaging PET scan.
3 hologic (astrocytosis) aspects from a single PET scan.
4 dication of a clinically justified (18)F-FDG PET scan.
5 received a 90-min dynamic (S)-(18)F-THK5117 PET scan.
6 83 and micro-CT scan, but not with (18)F-FDG PET scan.
7 and additionally an experimental (11)C-PE2I PET scan.
8 ximab vedotin treatment, patients received a PET scan.
9 ity and underwent a second [(18)F]fallypride PET scan.
10 -FDG was injected, followed by a 3-h dynamic PET scan.
11 intravenously, followed by a 60-min dynamic PET scan.
12 er of visible and measurable lesions on each PET scan.
13 e time interval between baseline and the tau PET scan.
14 with unprecedented precision using data from PET scans.
15 h each undergoing three 90-min (11)C-HOMADAM PET scans.
16 iple organs on the CT scan and copied to the PET scans.
17 tching healthy controls received (11)C-PBR28 PET scans.
18 and therefore diagnostic accuracy of cardiac PET scans.
19 )Tc-based hepatobiliary scans, and (18)F-FDG PET scans.
20 ria or (for MP) by changes in (123)I-MIBG or PET scans.
21 ions can be identified on planar, SPECT, and PET scans.
22 s with negative results on bone or (18)F-NaF PET scans.
23 h, and FTD patients also underwent (18)F-FDG PET scans.
24 icobasal degeneration patients who underwent PET scans.
25 ons that were visible and measurable on both PET scans.
26 sessed by CT and perfusion by (13)N ((13)NN) PET scans.
27 and might be applied to clinical, whole-body PET scans.
28 seline amyloid positron emission tomography (PET) scan.
29 tion using tau positron emission tomography (PET) scans.
30 oxyglucose positron emission tomography (FDG-PET) scans.
31 oxyglucose positron emission tomography (FDG-PET) scans.
32 A subjects showed beta-amyloid deposition on PET scanning.
33 ived three cycles of ABVD and then underwent PET scanning.
34 ) were recruited, and 571 patients underwent PET scanning.
35 abeling an anti-ICOS antibody and performing PET scanning.
36 )C]carfentanil positron emission tomography (PET) scanning.
37 were collected, resulting in a total of 128 PET scans (1-7 d after injection from 36 patients: (89)Z
42 11 of 18 positive baseline (11)C-methionine PET scans (61%) showing less than 25% (11)C-methionine-a
47 abolic RSN expression in cerebral blood flow PET scans acquired at rest and during task performance.
49 f 27 cases (41%), results from the (18)F-FET PET scans added relevant clinical information, including
50 of each other (501 participants had a second PET scan after 2 years, including 150 participants with
51 subset of participants underwent a second MR-PET scan after a median interscan interval of 3.6 months
53 and wild-type control rats underwent dynamic PET scans after administration of (11)C-BMP intravenousl
54 hereafter referred to as simply florbetapir)-PET scan and at least 1 CSF beta-amyloid 1-42 (Abeta1-42
55 younger, more likely to have a positive PiB-PET scan and carry at least one apolipoprotein E varepsi
60 antification is achieved by a 60-min dynamic PET scan and the use of either cerebellum or midbrain as
62 urgh compound B (PIB) and (18)F-flortaucipir PET scans and a magnetization-prepared rapid gradient ec
63 ke value ratios (SUVRs) were calculated from PET scans and a mean global cortical SUVR was calculated
67 ts with cocaine-use disorder (CUD) underwent PET scans and performed two types of cocaine self-admini
69 n 3 cohorts; all underwent dynamic (18)F-FDG PET scans and serial pharmacokinetic sampling at baselin
72 r, we utilized positron emission tomography (PET) scanning and the tracer (18)F-fluorodeoxyglucose (F
75 were perfused and sacrificed after the final PET scan, and radioactivity in dissected tissues was mea
77 d positive Tau positron emission tomography (PET) scans (area under the curve (AUC) = 0.87-0.91 for d
78 ts from group 2, who underwent a second PSMA PET scan as a follow-up, were evaluated to determine the
79 uoride positron emission tomography (18F-NaF PET) scans as target-to-background ratios (TBRs), a prom
80 ocols using (18)F-DCFPyL (n = 62, 269.8 MBq, PET scan at 120 min after injection) or (68)Ga-PSMA-HBED
81 ocols using (18)F-DCFPyL (n = 62, 269.8 MBq, PET scan at 120 min after injection) or (68)Ga-PSMA-HBED
82 nt at magnetic resonance imaging, a positive PET scan at baseline, or lack of improvement at repeat P
83 - 82 MBq of (18)F-FGln, followed by 2 static PET scans at 97 +/- 14 and 190 +/- 12 min after injectio
86 -tau217 discriminated abnormal vs normal tau-PET scans (AUC, 0.93 [95% CI, 0.91-0.96]) with significa
88 thy male volunteers received [(11)C]CIMBI-36 PET scans before and 3 h after an oral dose of d-ampheta
89 anced solid tumors underwent (11)C-erlotinib PET scans before and after a 1,000-mg dose of elacridar.
92 [(11)C]FLB457 positron emission tomography (PET) scans before and 3-hours after amphetamine administ
93 nteers (HV) underwent two [(11)C]carfentanil PET scans, before and after an oral administration of 0.
100 ved a negative positron emission tomography (PET) scan (Deauville score of 1-3) received 30 Gy ISRT.
102 n a series of pregnant women who underwent a PET scan during a clinical workup for malignancies.
103 tative stability assessment for simultaneous PET scanning during functional MRI studies was performed
105 onsidered for quantitative (18)F-florbetaben PET scans, especially in assessing patients with brain a
107 all, 15 of 549 (2.7%) patients with baseline PET scans experienced biopsy-confirmed HT (median follow
108 Patients achieving complete response (CR) on PET scan following cycle 2 of ABVD (PET2) continued 4 ad
111 ere quantified in 60 clinical (68)Ga-PSMA-11 PET scans for recurrent disease as well as the 9 primary
112 tinely used in positron emission tomography (PET) scans for cancer diagnosis, staging, and monitoring
113 w SPECT/CT scans, and whole-body (124)I-MIBG PET scans found 25, 32, and 87 total lesions, respective
114 cer patients who underwent staging (18)F-FDG PET scans from 2002 to 2013 at the Peter MacCallum Cance
115 follow-up ( approximately 24 mo) florbetapir PET scans from 332 Abeta+ and Abeta- subjects participat
118 with a shorter OS than a negative (18)F-FDG PET scan (hazard ratio: 3.8; 95% CI: 2.4-5.9; P < 0.001)
119 enty patients (77.8%) showed a positive PSMA-PET scan, identifying a total of 287 lesions: 37 prostat
121 lations were based on a whole-body (18)F-FDG PET scan in which differently sized spheres were placed
124 ale subjects each had two 120-min [11C]PBR28 PET scans in 1 d, before and after an LPS challenge.
125 ined baseline 6-[(18)F]fluoro-L-DOPA (FDOPA)-PET scans in 15 nonsmokers and 30 nicotine-dependent smo
132 C]-carfentanil positron emission tomography (PET) scans in 19 schizophrenia patients and 20 age-match
136 C-RO6931643, and (11)C-RO6924963 to baboons, PET scans indicated good brain entry, rapid washout, and
137 diation burden of a diagnostic (18)F-FAPI-74 PET scan is even lower than that of PET scans with (18)F
139 fication of subjects on the basis of amyloid PET scans is increasingly being used in research studies
141 (89)Zr-bevacizumab accumulation assessed by PET scanning may help in the selection of patients with
142 ed prostate-specific membrane antigen (PSMA) PET scans may be used to monitor treatment response in p
144 valuation with positron emission tomography (PET) scan may improve selection of patients who need red
145 as remote from the tumor on the preoperative PET scan (n = 6) (2.92 +/- 1.24 vs. 1.62 +/- 0.75; P < 0
148 thy tissues were estimated on (68)Ga-DOTATOC PET scans of 11 meningioma patients and 12 HGG patients.
150 ase dementia patients, received flortaucipir PET scans of 20 min in duration beginning 80 min after i
152 thods: We analyzed 523 cross-sectional Abeta PET scans of 5 different Abeta mouse models (APP/PS1, PS
157 meters were estimated from dynamic (18)F-FDG PET scans of breast cancer patients and used to simulate
158 e evaluated pre- and postoperative (18)F-FET PET scans of glioma patients with particular emphasis on
165 al Status (BSMSS), an MRI and an [(11)C]EKAP PET scan on the High Resolution Research Tomograph.
167 tobacco smokers had one set of [(11)C]FLB457 PET scans on the same day, one before and one at 2.5-3 h
168 [(11)C]ABP688 positron emission tomography (PET) scans on the same day-before and during intravenous
169 cipants who underwent two [(11)C]carfentanil PET scans, one before and one 3 h following a 0.5 mg/kg
170 be SUVAUC derived from 2 consecutive static PET scans, one centered on a large blood-pool structure
171 70 d underwent (11)C-metoclopramide baseline PET scans or scans after intraperitoneal treatment with
172 days underwent (11)C-metoclopramide baseline PET scans or scans after intraperitoneal treatment with
175 itative) and DeltaSUV(max) scales to interim PET scans performed after 2 cycles of chemotherapy.
176 er radiomic features extracted from baseline PET scans predicted relapsed or refractory disease statu
178 Results: For 3,774 sequential rest-stress PET scans, regional, artery-specific, severely reduced c
185 eek prior to a positron emission tomography (PET) scan session, during which the subject's head was s
186 ied as AD dementia but having negative Abeta PET scans show little increase but plasma p-tau181 is in
187 of the CSF Abeta1-42 samples and florbetapir-PET scans showed a nonlinear association (R2 = 0.48-0.66
188 f levels; and different pipelines to process PET scans showed correlated but not identical results.
189 resulting full width at half maximum of the PET scans showed the spatial resolution improved by up t
192 , 20 drug-free patients) underwent a dynamic PET scan to measure [(11)C] MePPEP distribution volume (
193 thermore, they also underwent an [(18)F]DOPA PET scan to quantify striatal dopamine synthesis capacit
194 n the satiated state) and blood draws during PET scanning to determine TSPO affinity genotype and pla
195 disorder were followed up for 12 weeks after PET scanning to document relapse and relate it to V(T).
196 and 10 controls also underwent [(11)C]NNC112 PET scans to measure dopamine D1-type receptor availabil
197 two independent cohorts underwent (18)F-DOPA PET scans to measure dopamine synthesis capacity (indexe
199 so completed a positron emission tomography (PET) scan to quantify DRN 5-HT1A availability using [(11
203 ment the region corresponding to BM from the PET scan using algorithms developed in-house, allowing f
208 reward-related questionnaires and underwent PET scans using the D2R-selective and nondisplaceable ra
209 of [(11)C]IMA107 were generated from dynamic PET scans using the simplified reference tissue model wi
210 nce of a larger dynamic range of florbetapir-PET scan values in the higher range compared with the CS
212 risk of hospice claims within 180 d of a NaF PET scan was 2.0-7.5 times higher for patients with evid
214 fter hPBMC inoculation, and a 60-min dynamic PET scan was acquired, followed by ex vivo biodistributi
215 le cohort revealed that a positive (18)F-FDG PET scan was associated with a shorter OS than a negativ
220 G2 patients (n = 140), a positive (18)F-FDG PET scan was the only identifier of high risk for death
223 es without prior local therapy and (18)F-FET PET scanning were retrospectively identified in 2 center
224 es without prior local therapy and (18)F-FET PET scanning were retrospectively identified in 2 center
227 Methods: In 10 patients with lung cancer, PET scans were acquired at 10 min, 1 h, and 3 h after ad
231 was injected via the tail vein, and dynamic PET scans were acquired for 90 min, followed by gamma-co
235 ion of 37 MBq (5 mg) of (89)Zr-fresolimumab, PET scans were acquired on day 2 or day 4 after tracer i
238 )methyl)-N-(6-phenoxy-3-pyridinyl)acetamide) PET scans were acquired with arterial blood sampling to
241 ne imaging, 26 of 38 (68%) bone or (18)F-NaF PET scans were congruent with (18)F-DCFPyL PET, whereas
243 Preoperative MR imaging and (68)Ga-DOTATATE PET scans were fused and used for a spatially precise ne
246 FDOPA and [(11)C]SB217045) and more than 400 PET scans were investigated to assess the applicability
247 During each imaging session, 9 whole-body PET scans were obtained at 5, 10, 20, 30, 40, 50, 60, 12
254 (11)C-DED, (11)C-PiB, and (18)F-FDG dynamic PET scans were obtained in age-matched groups comprising
255 (18)F-fluoroestradiol PET and (18)F-FDG PET scans were performed at baseline, week 2, and week 8
256 -sorafenib and perfusion (15)O-H(2)O dynamic PET scans were performed before and after 2 wk of sorafe
259 ods: (11)C-(R)-rolipram whole-body and brain PET scans were performed on 6 individuals with MAS (3 fo
261 an volunteers (34 +/- 13 years old); the two PET scans were performed on the same day-before (scan 1)
267 ven whole-body positron emission tomography (PET) scans were performed 5, 10, 20, 30, 45, 150, and 24
268 -(R)-rolipram positron emission tomographic (PET) scans were performed in 44 unmedicated patients dur
269 ve microglia in-vivo is often performed with PET scanning whose resolution, cost, and availability pr
271 whom had undergone 3 T MRI scan, 985 amyloid PET scan with 11C-Pittsburgh compound B (PIB) and MRI, a
275 fter tumor inoculation, a dynamic (18)F-FHNP PET scan with arterial blood sampling was acquired from
276 , a dynamic (11)C-PBR28 or (R)-(11)C-PK11195 PET scan with arterial blood sampling was obtained.
278 MRI scan and on a separate visit completed a PET scan with the high affinity D2R tracer [18 F]fallypr
279 underwent 3 T MRI and a 120-min 11C-BU99008 PET scan with volume of distribution (VT) estimated usin
280 complex logistics of combining a whole-body PET scan with whole-body or organ-specific MR imaging.
281 tor protein (TSPO) binding status, underwent PET scanning with TSPO radioligands ((11)C-PBR28 or (18)
282 eless, the results confirm the usefulness of PET scans with (11)C-(R)-rolipram to indirectly measure
283 Methods: Healthy men underwent 2 consecutive PET scans with (11)C-erlotinib: a baseline scan and a se
284 -FAPI-74 PET scan is even lower than that of PET scans with (18)F-FDG and other (18)F tracers; (68)Ga
286 ed-affinity binders) underwent (18)F-DPA-714 PET scans with arterial blood sampling and metabolite an
287 men and 5 women) underwent 2 separate 90-min PET scans with arterial input function and plasma free f
292 g data employed in the study consisted of 26 PET scans with lesions in the lung being created through
295 g (MRI) scans, positron emission tomography (PET) scans with carbon 11-labeled Pittsburgh Compound B
296 eers underwent positron emission tomography (PET) scans with the 5-HT2AR agonist radioligand [(11)C]C
297 ects underwent positron emission tomography (PET) scans with two different radiotracers at baseline p
299 underwent 2 consecutive (11)C-metoclopramide PET scans without and with ABCB1 inhibition using cyclos