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1                                              PET amyloid data were obtained with 18F-flutemetamol (Vi
2                                              PET findings were compared between the 2 radiotracers an
3                                              PET images showed focal myocardial (18)F-FOL uptake colo
4                                              PET images were reconstructed with 4-mm voxels and 2-mm
5                                              PET imaging identified significantly higher left ventric
6                                              PET using O-(2-(18)F-fluoroethyl)-l-tyrosine ((18)F-FET)
7                                              PET was associated with a 10% lower absolute rate of CMV
8                                              PET-2 was classified according to both 5-PS and percenta
9                                              PET/MR (18)F-FAC images showed a 12% increase in tumor (
10 s: All (18)F-fluciclovine and (68)Ga-PSMA-11 PET studies performed at the University of California Sa
11 body (from vertex to toes) in (68)Ga-PSMA-11 PET/CT imaging revealed additional bone lesions in 6% of
12 , patients with corresponding (68)Ga-PSMA-11 PET/CT scans were matched.
13 s and bone metastases in 5 on (68)Ga-PSMA-11 PET/MRI.
14  vivo tau pathology (measured by 18F-AV-1451 PET), neuroinflammation (measured by 11C-PK11195 PET) an
15 nce and reduced energy expenditure and 18FDG-PET uptake in brown adipose tissue.
16 sistence), 4 of 16 had new lesions only (25% PET recurrence), and 2 had no disease on post-SLND PET.
17 lly, for 5 patients who completed at least 3 PET/CT scans after administration of (124)I-MIBG, we est
18 thy male volunteers received [(11)C]CIMBI-36 PET scans before and 3 h after an oral dose of d-ampheta
19 one lesion already detected at baseline (63% PET persistence), 4 of 16 had new lesions only (25% PET
20 o investigate the efficacy of (18)F-rhPSMA-7 PET for primary N-staging of patients with prostate canc
21  specificity, and accuracy of (18)F-rhPSMA-7 PET were 53.8%, 96.9%, and 90.9%, respectively, and thos
22                   Conclusion: (18)F-rhPSMA-7 PET/CT offers high PPV in BCR after RP.
23 oethyl)-L-tryptophan (1-L-[(18)F]FETrp) as a PET imaging probe for this common malignant pediatric br
24 labeled pH-targeted peptide can be used as a PET imaging tool to assess therapy response within PDAC
25 ns, showed excellent kinetic properties as a PET radioligand.
26 binds to K(V)1 channels and can be used as a PET tracer for the detection of demyelinated lesions in
27 tential use of (89)Zr-HDL nanoparticles as a PET tracer to quickly monitor the response to CSF1R inhi
28                           Here, we present a PET biodistribution and radiation dosimetry study of (68
29 ied as AD dementia but having negative Abeta PET scans show little increase but plasma p-tau181 is in
30 significant correlation between AIs of Abeta PET and TSPO PET in 4 investigated Abeta mouse models (A
31 CSF Abeta has already changed prior to Abeta PET changes.
32 simultaneous fluorodihydroxyphenyl-l-alanine PET (18F-DOPA-PET) and resting state functional MRI (rs-
33                                   First, all PET-positive lesions were noted.
34                                      Amyloid PET, (18)F-FDG PET, and CSF test combinations may add ac
35 nger age (P = 0.02), higher baseline amyloid PET (P = 0.05), APOE epsilon4 (P = 0.05), and better cog
36  information equivalent to that from amyloid PET.
37  reached by combining (18)F-FDG PET, amyloid PET, and nonimaging variables.
38 bility to typical clinical settings, amyloid PET, (18)F-FDG PET, and MRI were highly sensitive for ne
39 stinct biomarker sequences, in which amyloid-PET and (18)F-FDG-PET are placed at different positions
40 high diagnostic performance when both CT and PET images are used.
41 om a retrospective analysis using PET/CT and PET/MRI examinations to investigate the efficacy of (18)
42              The concordance between CT- and PET-based criteria and the capability of each method to
43  the beneficial effect bioactive factors and PET incorporation have on ACL regeneration and signal a
44 rbon-11-labelled complex pharmaceuticals and PET radioligands, including a one-step radiosynthesis of
45 1 of 10 and 7 of 10 cases for PET/static and PET/matched, respectively.
46 city, and time between initial treatment and PET imaging was evaluated.
47                                 Small-animal PET imaging demonstrated high tumor uptake within 20 min
48 wn in preclinical evaluation by small-animal PET studies, organ distribution, and a patient applicati
49 rolled trial that compared valganciclovir as PET or prophylaxis for 100 days in 205 D+R- liver transp
50 a acquired from patient volunteers to assess PET quantitative bias in vivo.
51 inary study is a first step toward automated PET/CT assessment for lymphoma.(C) RSNA, 2020.
52  in Wistar rats by in vitro autoradiography, PET imaging, ex vivo biodistribution, metabolite experim
53  amyloid-beta positivity using (18)F-AZD4694 PET.
54 mpaired (n = 65)] who underwent amyloid-beta PET with (18)F-AZD4694, lumbar puncture, structural MRI,
55 imilar analysis on longitudinal amyloid-beta-PET (in ADNI subjects only, n = 639), we found significa
56 tudy was to examine the relationship between PET-CT derived tumour glucose uptake as measured by maxi
57  bio-based poly(ethylene terephthalate) (Bio-PET) substrates for the development of flexible electroc
58    During each imaging session, 9 whole-body PET scans were obtained at 5, 10, 20, 30, 40, 50, 60, 12
59 ell cancer, or leukemia underwent whole-body PET/CT imaging 90 min after injection of (18)F-SKI (mean
60 e data acquired on a conventional whole-body PET/CT system with a typical clinical protocol differed
61 le for a first response assessment with both PET- and CT-based criteria.
62  case suggests that (18)F-alpha(v)beta(6)-BP PET/CT is a promising noninvasive approach to identify t
63 stimates in tracer kinetic modeling in brain PET studies.
64 d dosimetry of (68)Ga-Tuna-2 was assessed by PET/CT in 13 individuals with type 2 diabetes as part of
65                The results were confirmed by PET, histology and ICPMS.
66 encing experiments such as ChIP-seq and ChIA-PET that generate coverage files for transcription facto
67 DNase-seq/ATAC-seq, P300, POLR2A, CAGE, ChIA-PET, GRO-seq, STARR-seq and MPRA).
68 E recovers a higher number of published ChIA-PET and HiChIP loops as well as loops linking promoters
69 t high-resolution 3D genome mapping via ChIA-PET to capture RNAPII-associated chromatin interactions
70                    Conclusion: (11)C-choline PET/CT can detect PCa recurrence even among patients wit
71        The correlation between (11)C-choline PET/CT positivity and initial treatment, Gleason score,
72 he 2 readers deemed 66% of the (11)C-choline PET/CT scans as positive.
73 of suspicion for recurrence on (11)C-choline PET/CT was scored (0, negative; 1, equivocal; 2, positiv
74 on correction processing to emulate clinical PET/MRI.
75 ngitudinal PET-only studies, and comparative PET and autopsy studies are included.
76                                  Conclusion: PET with pulmonary administered (11)C-BMP can measure AB
77 ly with regional amyloid burden in congruent PET images.
78                      Deep learning-corrected PET (PET(DL)) images were quantitatively evaluated by us
79           In line with its preclinical data, PET imaging resulted in clear visualization of the cance
80                        Results: (18)F-DCFPyL PET/CT had an overall positivity rate of 85%, which incr
81 aluating the positivity rate of (18)F-DCFPyL PET/CT in patients with biochemical recurrence (BCR) of
82  Patients received 2 whole-body (18)F-DCFPyL PET/CT scans (median dose, 317 MBq; uptake time, 120 min
83 te the lesion detection rate of (18)F-DCFPyL PET/CT, a prostate-specific membrane antigen (PSMA)-targ
84                             By study design, PET/CT scans were performed at baseline and before start
85 from the 4 institutions relying on different PET/CT scanners.
86 ality of lesion delineation in the different PET reconstructions was independently evaluated by 3 exp
87 l or negative or as oligometastatic disease (PET-1).
88 ased analysis, the sensitivity of (18)F-DOPA PET/CT in detecting soft-tissue and bone or bone-marrow
89 %, 75% and 54%, respectively, for (18)F-DOPA PET/CT.
90 ssessed as K(i)(cer) value using [(18)F]DOPA PET before and 6 weeks after antipsychotic discontinuati
91 thermore, they also underwent an [(18)F]DOPA PET scan to quantify striatal dopamine synthesis capacit
92 luorodihydroxyphenyl-l-alanine PET (18F-DOPA-PET) and resting state functional MRI (rs-fMRI).
93 ents were evaluated with gallium 68 DOTATATE PET/CT, and in cases of high-grade tumors, they were als
94                  Conclusion: (64)Cu-DOTATATE PET/CT is a safe imaging technique that provides high-qu
95 rwent PET/CT scanning with a 120-min dynamic PET scan centered on the pancreas.
96                              In vivo dynamic PET studies were performed on mice bearing U87 (CXCR4 lo
97 ility of [(18)F]FGlc-FAPI may allow extended PET studies of FAP-related diseases, such as cancer, but
98 edicated DDG approaches for axially extended PET, compared with DDG for conventional step-and-shoot s
99        We have installed a custom-fabricated PET insert into our small-animal MRI instrument and used
100 -treated EAE mice were imaged with (18)F-FAC PET to assess if this approach can monitor the effect of
101                      Addition of (18)F-FACBC PET derived parameters (V(T), SUV) to DWI and RAFF deriv
102     Results: Compared with ceCT, (68)Ga-FAPI PET/CT results led to changes in TNM staging in 10 of 19
103  to assess the performance of full-dose (FD) PET image synthesis in both image and sinogram space fro
104 cation of glucose metabolic rates with 2-FDG PET, a method that permits the noninvasive assessment of
105 greements between whole-body DW MRI- and FDG PET/MRI-based response classifications with Krippendorff
106 o were untreated showed no change in any FDG PET or cardiac MRI parameter.
107          Patients underwent CT and (18)F-FDG PET at baseline and after 4 cycles (the first evaluation
108 ach was established and tested for (18)F-FDG PET brain imaging.
109                                    (18)F-FDG PET imaging shows these changes are accompanied by alter
110 o changed management compared with (18)F-FDG PET in 1 patient (1%; 95% CI, 0%-5%).
111 what higher sensitivity than CT or (18)F-FDG PET in lymph nodes (92.4% vs. 69.7% and 89.4%, respectiv
112  demonstrates lower conspicuity on (18)F-FDG PET than the more common invasive ductal carcinoma.
113  accuracy was reached by combining (18)F-FDG PET, amyloid PET, and nonimaging variables.
114                       Amyloid PET, (18)F-FDG PET, and CSF test combinations may add accuracy to clini
115 al clinical settings, amyloid PET, (18)F-FDG PET, and MRI were highly sensitive for neuropathologic A
116 -weighted early-phase acquisition ((18)F-FDG PET-equivalent), a single scan potentially contains comp
117                                    (18)F-FDG PET/CT detected previously unidentified metastases in 8
118             End-of-treatment (EOT) (18)F-FDG PET/CT findings are variable among patients with negativ
119 FES PET/CT compared favorably with (18)F-FDG PET/CT for detection of metastases in patients with meta
120 uate the diagnostic performance of (18)F-FDG PET/CT for the detection of posttransplantation lymphopr
121                        Conclusions (18)F-FDG PET/CT had high specificity for all IE subtypes; however
122 sify uptake patterns of whole-body (18)F-FDG PET/CT images in patients with lung cancer and lymphoma.
123 Results: Twenty-seven patients had (18)F-FDG PET/CT imaging at baseline and after at least 4 cycles p
124 for uniformity in conjunction with (18)F-FDG PET/CT imaging of mini image-quality phantoms designed t
125 ncer underwent baseline and repeat (18)F-FDG PET/CT imaging within 7 d.
126  overview of the current status of (18)F-FDG PET/CT in the monitoring of tumoral and systemic immune
127 ggest adding (18)F-FLT PET/CT when (18)F-FDG PET/CT is inconclusive or positive within the previously
128     The specificity of both CT and (18)F-FDG PET/CT is low because of radiation-induced changes.
129                           Although (18)F-FDG PET/CT is widely available and is increasingly being use
130 ethods: One hundred forty baseline (18)F-FDG PET/CT scans were selected from U.K. and Dutch studies o
131           Our objective was to use (18)F-FDG PET/CT to identify a high-risk subgroup requiring therap
132 on tomography/computed tomography ((18)F-FDG PET/CT) has recently emerged as another IE imaging modal
133 Of 21 patients with UrC-ADC before (18)F-FDG PET/CT, Mayo staging was I/II in 8, III in 3, and IV in
134 41 patients, of whom 216 underwent (18)F-FDG PET/CT-guided biopsy and 125 underwent CT-guided biopsy.
135 d STS of the extremities underwent (18)F-FDG PET/MRI before and after ILP with melphalan and tumor ne
136  provide a rationale and overview of the FDG PET/CT Profile claims as well as its context, and to out
137                                      (18)FDG-PET/CT can visualize both inflammation and malignancy an
138                               Use of 18F-FDG-PET/CT at the initial presentation of patients with susp
139 de of TRL-positive patients misleads 18F-FDG-PET/CT for detecting nodal metastasis.
140 sion tomography-computed tomography (18F-FDG-PET/CT) can be influenced by the increased glycolytic ac
141 equences, in which amyloid-PET and (18)F-FDG-PET are placed at different positions in the order of di
142 cose positron emission tomography ((18)F-FDG-PET).
143                Herein, we report a (18)F-FDG-PET/CT-based deep learning model, which demonstrates hig
144              Recent studies suggest that FDG-PET/CT could help discriminate between active and residu
145         These findings indicate [(18)F]FDOPA PET dopamine imaging has potential as biomarker to guide
146                        Conclusion: (18)F-FES PET/CT compared favorably with (18)F-FDG PET/CT for dete
147 ; range, 6-44 d) and postoperative (18)F-FET PET (time after surgery: median, 14 d; range, 5-28 d) we
148 tabolic responders to ICI or TT on (18)F-FET PET had a significantly longer stable follow-up (thresho
149                Threshold values of (18)F-FET PET parameters to predict outcome were established by re
150 In all lesions, static and dynamic (18)F-FET PET parameters were obtained (i.e., mean tumor-to-brain
151 )F-fluorofuranylnorprogesterone ((18)F-FFNP) PET/CT imaging of tumor glucose metabolism and progester
152 ght stencil-printed electrodes on a flexible PET (polyethylene terephthalate) substrate is proposed f
153 ne and 1-year follow-up MRI and flortaucipir PET.
154                           (18)F-flortaucipir PET alone may convey additional information equivalent t
155 mission tomography (PET), (18)F-flortaucipir PET, and adjusted hippocampal volume (aHCV).
156           The diagnostic impact of (18)F-FLT PET/CT was highest after cRT.
157                  We suggest adding (18)F-FLT PET/CT when (18)F-FDG PET/CT is inconclusive or positive
158 d to define the role of (18)F-flubrobenguane PET, particularly in comparison to standard diagnostic p
159 st-processing methods for (18)F-Fluciclovine PET and multisequence multiparametric MRI in the predict
160  (Fig 2), and fluorine 18 fluorodeoxyglucose PET/CT (Fig 3) were performed.
161 valuated with fluorine 18 fluorodeoxyglucose PET/CT, with imaging findings reviewed as part of the sy
162 greement with fluorine 18 fluorodeoxyglucose PET/MRI for treatment response assessment in children an
163 sification of fluorine 18-fluorodeoxyglucose PET uptake patterns in foci suspicious and nonsuspicious
164                     (18)F-fluorodeoxyglucose PET and CSF p-tau changes occurred later in the fourth d
165                                  Flurpiridaz PET was safe and well tolerated.
166 nil positron emission tomography ([(18)F]FMZ-PET) and GABA concentrations by using proton magnetic re
167 s increased in 1 of 10 and 7 of 10 cases for PET/static and PET/matched, respectively.
168 he clinical PCWG3 subtype was determined for PET versus CI by 3 masked readers.
169 imaging tools such as (89)Zr-Df-IAB22M2C for PET imaging is of prime importance to identify patients
170 8) F radionuclide incorporation required for PET imaging.
171                   The cellular substrate for PET signal was identified using brain section immunostai
172 ored PET scans (n = 103), the 5-year TTP for PET-negative cases by Deauville criteria (D1-D3, DX) was
173 vasive clinical absolute quantification from PET/MR to PET/CT by allowing the accurate determination
174                         Median DeltaSUV on i-PET was 86.2%.
175                                       Immuno-PET had a somewhat higher sensitivity than CT or (18)F-F
176 nstrate successful CD38-targeted immunologic PET imaging of multiple myeloma in a murine model and in
177 0.4%) in the CT group and 5 of 216 (2.3%) in PET group (P = 0.001).
178 l networks were trained to segment organs in PET/CT acquisitions (training CTs: 8,632, validation CTs
179      The distance between tumor positions in PET and CT were characterized in visual interpretation b
180 information associated with fully integrated PET/MRI.
181 d to assess agreement between intraprostatic PET/CT findings and histopathologic findings.
182  image and sinogram space from low-dose (LD) PET images and sinograms without sacrificing diagnostic
183 gy studies, cross-sectional and longitudinal PET-only studies, and comparative PET and autopsy studie
184  modalities, including radiography, CT, MRI, PET/CT, and US.
185 2 patients, the coregistration of multimodal PET/MRI tumor data was improved by using the reverse pha
186 tablished coronary artery disease, (18)F-NaF PET provides powerful independent prediction of fatal or
187                           Results: (18)F-NaF PET/CT scans from 219 patients with PCa were included, o
188                           Methods: (18)F-NaF PET/CT scans were retrieved from all patients who partic
189 ver agreement in (18)F-sodium fluoride (NaF) PET/CT for the detection of bone metastases in patients
190                 (18)F-flurpiridaz is a novel PET MPI agent with superior image and defect resolution.
191 in tumor perfusion measured with (15)O-H(2)O PET after only 14 d of therapy showed an association wit
192 xtensive simulation studies, the analyses of PET-imaging outcomes from the Alzheimer's Disease Neuroi
193 be proposed as the standardized criterion of PET complete metabolic response, confirming the value of
194              Finally, the reproducibility of PET measurements from test and retest scans was assessed
195 n of many cooperative groups in the study of PET-guided therapy.
196 nt lesions were missed in 1.2% (12/1,003) on PET/MRI, leading to a change in TNM staging in 0.5% (5/1
197 lated in the tumor lesions, as also shown on PET/CT imaging using (68)Ga-FAPI-46.
198 nowpit from the Austrian Alps; however, only PET was detected in the nanometer range for both snowpit
199  Finally, visual inspection of (18)F-PM-PBB3-PET images was indicated to facilitate individually base
200  PERCIST and immunotherapy-modified PERCIST, PET-based response maintained prognostic significance in
201 abeling an anti-ICOS antibody and performing PET scanning.
202 argeted imaging with zirconium 89-pertuzumab PET/CT was successful in detecting HER2-positive metasta
203                 Deep learning-corrected PET (PET(DL)) images were quantitatively evaluated by using t
204 , neuroinflammation (measured by 11C-PK11195 PET) and brain atrophy (derived from structural MRI) pre
205 en combined with 5-PS assessment, a positive PET-2 result was highly predictive of treatment failure.
206          Therefore, [(11)C]13 is a potential PET imaging ligand for mGluR2 in different central nervo
207 pivotal role, standardization of preclinical PET/CT protocols, including CT absorbed dose guidelines,
208                 The quality of the predicted PET images was assessed by 2 nuclear medicine specialist
209                             Because previous PET studies in HCC have been hampered by high background
210 -to-1 Prism-PET module, and one 9-to-1 Prism-PET module) to introduce intercrystal light sharing, whi
211  uniform glass light-guide, one 4-to-1 Prism-PET module, and one 9-to-1 Prism-PET module) to introduc
212      By comparison, the 4-to-1 coupled Prism-PET module achieved a DOI resolution of 2.5 mm FWHM and
213 dition to the standard imaging in Ga-68 PSMA PET/CT, particularly in patients presenting for restagin
214                        Management after PSMA PET was recorded but not mandated.
215       The combined use of SN biopsy and PSMA PET/CT identified all pN1 patients (100% sensitivity; 95
216                             Conclusion: PSMA PET results are highly predictive of FFP at 3 y in men u
217  29% of patients, all lesions on (68)Ga-PSMA PET resolved in response to treatment.
218 5477), 69 mPC patients underwent (68)Ga-PSMA PET/CT before bone biopsy.
219 nd accuracy for LNM detection on (68)Ga-PSMA PET/CT in the PLND cohort were 30.6%, 96.5%, 68.8%, 84.5
220                      Multiphasic (68)Ga-PSMA PET/CT led to a better determination of equivocal findin
221                            Also, (68)Ga-PSMA PET/CT positivity was correlated with clinical parameter
222                However, whether and how PSMA PET/CT affects the management of patients undergoing sca
223 W2 criteria but adds value by including PSMA PET criteria.
224 irty-two percent of men with a negative PSMA PET result did not receive treatment.
225        In particular, men with negative PSMA PET results or disease identified as still confined to t
226 ing SN biopsy in patients with negative PSMA PET/CT results increased the combined sensitivity to 100
227 ifferent criteria for interpretation of PSMA PET were published: the European Association of Nuclear
228                Yet, the implications of PSMA PET-derived whole-body tumor volume for overall survival
229  DR was calculated as the proportion of PSMA PET-positive patients to all patients independent of the
230 y or correlative imaging within 3 mo of PSMA PET.
231 ents without suspected LN metastases on PSMA PET/CT were considered candidates for SN biopsy with ind
232 tients who had at least 1 true-positive PSMA PET lesion localized that corresponded with the referenc
233   Conclusion: PSMA(TV50) is a promising PSMA PET biomarker that is reproducible and easily quantified
234 the Roach formula and compared with the PSMA PET/CT results.
235 ly prostate-specific membrane antigen (PSMA) PET findings, are not considered.
236 )F prostate-specific membrane antigen (PSMA) PET/CT, a newer examination, is unclear.
237  reproducibility in evaluating (68)Ga-PSMA11 PET, there are some factors causing interreader disagree
238 n radiation doses were extrapolated from rat PET data.
239          Methods: Tumors extracted from real PET/CT scans of patients with non-small cell lung cancer
240                     Methods: High-resolution PET detector modules were fabricated with single-ended r
241 ucted to explore the potential of (68)Ga-RGD PET/CT imaging for guiding current treatment decisions a
242          For those with Deauville (D)-scored PET scans (n = 103), the 5-year TTP for PET-negative cas
243                        In pre- and post-SLND PET comparison, 10 of 16 had at least one lesion already
244 currence), and 2 had no disease on post-SLND PET.
245        Conclusion: Microdose (11)C-sorafenib PET did not predict intratumoral sorafenib concentration
246 11)C-(S)-NR2B-SMe has adequate NR2B-specific PET signal in rat brain to warrant further evaluation in
247 nsfer fluorescence correlation spectroscopy (PET-FCS) to show how a small alpha-helical domain, the N
248                           These data suggest PET at 2 h after oral (18)F-FDG administration should yi
249 rmine whether imaging with the HER2-targeted PET tracer zirconium 89 ((89)Zr)-pertuzumab can depict H
250 te-specific membrane antigen (PSMA)-targeted PET agent, in patients with biochemically relapsed prost
251 e-specific membrane antigen (PSMA)-targeting PET imaging is becoming the reference standard for prost
252 sy), EUS, CT or MRI, and/or (68)Ga-DOTA-TATE PET/CT.
253                                          Tau PET was a significant mediator CBF/sPDGFRbeta-MoCA relat
254 hort where the correlation with 18F-GTP1 tau PET was evaluated (Alzheimer's disease = 38, control = 1
255 imer's disease are different for MRI and tau-PET and may differ across phenotypes, particularly for M
256 ification of six polyethylene terephthalate (PET) and four polybutylene terephthalate (PBT) oligomers
257                  Polyethylene terephthalate (PET) is selectively depolymerized by a carbon-supported
258 f microplastics (polyethylene terephthalate (PET), polyvinyl chloride, and polypropylene carbonate),
259                                          The PET radioligand (68)Ga-DO3A-VS-Tuna-2 ((68)Ga-Tuna-2) wa
260                                          The PET radiotracer (18)F-(2S,4R)4-fluoroglutamine ((18)F-Gl
261                        CD8-IHC confirmed the PET imaging results.
262 ate determination of motion vectors from the PET data itself.
263 Weekly blood samples through 100 days in the PET group were tested for HHV-6 viremia using a real-tim
264 : Of 609 DLBCL patients participating in the PET-Guided Therapy of Aggressive Non-Hodgkin Lymphomas t
265 aluate the correlation between uptake of the PET ligand (68)Ga-NOTA-AE105, targeting the urokinase-ty
266 gents were evaluated for their impact on the PET brain imaging data.
267 nge in TNM staging in 2.9% (29/1,003) due to PET/MRI.
268 nical absolute quantification from PET/MR to PET/CT by allowing the accurate determination of motion
269  (FDG) and simultaneous time-of-flight (TOF) PET/MRI with hippocampal subfield analysis of AD, mild c
270 portant cancer positron emission tomography (PET) agent [(18)F]5-fluorouracil ([(18)F]FU).
271 1)C]-LY2795050 positron emission tomography (PET) as a predictor of response to naltrexone.
272 ards this end, positron emission tomography (PET) imaging has emerged as one of the most informative
273 maceutical for positron emission tomography (PET) imaging that is used to image Parkinson's disease,
274 ve MOR agonist positron emission tomography (PET) radioligand, to investigate endogenous opioid tone
275 ects underwent positron emission tomography (PET) scans with two different radiotracers at baseline p
276 F-florbetaben) positron emission tomography (PET), (18)F-flortaucipir PET, and adjusted hippocampal v
277          Using positron emission tomography (PET), we identified the dorsal striatum as the brain are
278 ing results of positron emission tomography (PET)-directed treatment approaches, we designed a Nation
279 py (NIRS), and positron-emission tomography (PET).
280 yglucose (FDG) positron emission tomography (PET)/computed tomography (CT) is currently the standard
281 myloid and tau positron emission tomography [PET]) structural magnetic resonance imaging (MRI), and r
282 orrelation between AIs of Abeta PET and TSPO PET in 4 investigated Abeta mouse models (APP/PS1: R = 0
283 here was a significant increase in the tumor PET signal in PEGPH20-treated PDX animals, and this sign
284                         Of 150, 97 underwent PET; 22 of the 97 (mean age, 71 years +/- 6; 13 women) w
285                        Individuals underwent PET/CT scanning with a 120-min dynamic PET scan centered
286 nto our small-animal MRI instrument and used PET/MRI hybrid imaging to define regions of amyloid vuln
287                                      We used PET in vivo with (i) 11C-PK-11195, a marker of activated
288                                Next, we used PET/MRI to define uptake in six brain regions.
289 ent data from a retrospective analysis using PET/CT and PET/MRI examinations to investigate the effic
290 , NCNs have been successfully captured using PET with (18)F-FDG.
291                    The first Biograph Vision PET/CT system (Siemens Healthineers) was installed at th
292             In May 2018, the Biograph Vision PET/CT system was installed at the University Medical Ce
293 64)Cu-LLP2A uptake, as quantified by in vivo PET (R = 0.69, P < 0.01).
294 : Among 668 patients, we selected 27 in whom PET/CT results obtained with (68)Ga-PSMA-11, (18)F-DCFPy
295 xcellently reproduced (166 with CT; 164 with PET; and 164 with MRI).
296 net cost-savings per patient associated with PET was $8,707 compared to prophylaxis.
297 that multicancer blood testing combined with PET-CT can be safely incorporated into routine clinical
298                    In visual comparison with PET/ex, the rate of good alignment was increased in 1 of
299 -Deoxy-2-(18)F-fluoro-d-glucose (2-FDG) with PET is undeniably useful in the clinic, being able, amon
300 ty of alpha7-nAChR in the brain in vivo with PET.

 
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