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1 tic plaques can be visualized by noninvasive positron emission and computed tomographic imaging with
4 y fluorine 18-labeled AV-1451 ([18F]AV-1451) positron emission tomographic (PET) imaging are linked w
10 s underwent fludeoxyglucose F 18 ([18F]-FDG) positron emission tomographic scanning for assessment of
11 computed tomography, and fluorodeoxyglucose positron emission tomographic scans revealed strikingly
14 ed in tumor xenografts by using small-animal positron emission tomographic/computed tomographic imagi
16 d potentially have changed 332 of 1732 (19%) positron emission tomographies at low-risk physiological
20 ion delivered to the liver utilizing an oral positron emission tomography (18) F-isotopologue validat
21 using fluorine-18-labeled fluorodeoxyglucose positron emission tomography ([(18)F]FDG PET), [(18)F]FD
24 l that used early interim fluorodeoxyglucose positron emission tomography (FDG-PET) imaging to determ
25 t and high-resolution (18)fluorodeoxyglucose positron emission tomography (FDG-PET) imaging to unders
27 pir F 18 (previously known as AV 1451, T807) positron emission tomography (FTP-PET) imaging for tau a
31 single-photon emission tomography (SPECT) or positron emission tomography (PET) and coronary computed
32 hcare, Shanghai, China) followed by combined positron emission tomography (PET) and CT (hereafter, PE
34 y menstruating, asymptomatic women completed positron emission tomography (PET) and functional magnet
35 fluorine 18 ((18)F) fluorodeoxyglucose (FDG) positron emission tomography (PET) and hyperpolarized ca
36 18 ((18)F) fluorodeoxyglucose (FDG) combined positron emission tomography (PET) and magnetic resonanc
37 h-resolution neuroimaging data consisting of positron emission tomography (PET) and magnetic resonanc
39 vity at fluorine 18 fluorodeoxyglucose (FDG) positron emission tomography (PET) and survival in patie
40 22 healthy recreationally active males using positron emission tomography (PET) and the MOR-selective
41 is to synthesise current evidence on amyloid-positron emission tomography (PET) burden and presumed p
42 racy of fluorine 18 fluorodeoxyglucose (FDG) positron emission tomography (PET) combined with diagnos
43 d mass spectrometric detection to quantify a positron emission tomography (PET) detection tracer for
44 fluorine 18 ((18)F) fluorodeoxyglucose (FDG) positron emission tomography (PET) has added value over
49 ing (FL) and photodynamic therapy (PDT) with positron emission tomography (PET) imaging and internal
51 exploited the potential targeting of TF for positron emission tomography (PET) imaging of pancreatic
55 ized male nonhuman primates (n = 3), we used positron emission tomography (PET) imaging with the radi
56 employed in the realm of nanoparticle-based positron emission tomography (PET) imaging, whereas its
58 ased attenuation correction (ATAC) for brain positron emission tomography (PET) in an integrated time
60 surgery on the human brain immune system by positron emission tomography (PET) in relation to blood
65 tem (CNS) disorders, we sought to identify a positron emission tomography (PET) ligand to enable targ
66 ed that fluorine 18 fluorodeoxyglucose (FDG) positron emission tomography (PET) may detect the inflam
67 tional magnetic resonance imaging (fMRI) and positron emission tomography (PET) multimodal imaging wi
68 DPGM) is developed for MR/photoacoustic (PA)/positron emission tomography (PET) multimodal imaging-gu
69 Here we report a non-invasive quantitative positron emission tomography (PET) nanoreporter technolo
73 by analyzing motor defects and binding of a positron emission tomography (PET) radioligand to the ve
74 ation is possible with the recent advance in positron emission tomography (PET) radioligands that bin
75 ch toward the radiosynthesis of heterocyclic positron emission tomography (PET) radioligands using th
77 (CCR2)-binding peptide adapted for use as a positron emission tomography (PET) radiotracer for nonin
82 nonsmokers participated in two [(11)C]ABP688 positron emission tomography (PET) scans on the same day
84 ur objective was to determine the pattern of positron emission tomography (PET) tau tracer AV-1451 up
85 racer [(11)C]DAA1106 (a ligand for TSPO) and positron emission tomography (PET) to determine the effe
86 a radioligand that binds to the mGluR5, and positron emission tomography (PET) to quantify in vivo m
87 calisation and magnitude of the presumed tau Positron Emission Tomography (PET) tracer [(18)F]Flortau
89 individuals: (1) Tau, detected with a novel positron emission tomography (PET) tracer known as (18)F
91 )-3 ([(11)C]-(R)-IPMICF16), a first-in-class positron emission tomography (PET) TrkB/C-targeting radi
92 They came to an academic research center for positron emission tomography (PET) using [(18)F]fallypri
93 duced D2R internalization can be imaged with positron emission tomography (PET) using D2R radiotracer
95 ents of the New York metropolitan area using Positron Emission Tomography (PET) with [(11)C]racloprid
96 n of dopamine to value-based attention using positron emission tomography (PET) with [(11)C]racloprid
98 d tumor cytopenia on repeat (68)Ga-DOTA-TATE positron emission tomography (PET) within 6 months, sugg
99 d included magnetic resonance imaging (MRI), positron emission tomography (PET), and single-photon em
100 sease (PD) with 18F-fluorodeoxyglucose (FDG) positron emission tomography (PET), and their associatio
102 nitive continuum aged >60 years with amyloid positron emission tomography (PET), tau PET, and magneti
103 g a combination of functional MRI (fMRI) and positron emission tomography (PET), we investigated whet
104 ANCE STATEMENT: We present a high-resolution positron emission tomography (PET)- and magnetic resonan
106 stine, prednisone (R-CHOP14) induction and a positron emission tomography (PET)-driven ASCT or standa
117 Purpose To assess the accuracy of staging positron emission tomography (PET)/computed tomography (
118 time using a combination of autoradiography, positron emission tomography (PET)/computed tomography (
119 eath hold (DIBH) in fluorodeoxyglucose (FDG) positron emission tomography (PET)/computed tomography (
122 e of flourine 18 ((18)F) fluorocholine (FCH) positron emission tomography (PET)/magnetic resonance (M
125 arbon 11-labeled Pittsburgh Compound B (PiB) positron emission tomography after long-term prospective
126 3) or elevated (n = 202) brain amyloid using positron emission tomography amyloid imaging or a cerebr
128 inical evaluation and imaging at enrollment (positron emission tomography and 2-dimensional echo).
129 ers, and 18 nonsmokers who were scanned with positron emission tomography and [(11)C]raclopride, afte
130 14 healthy individuals using [(11)C]-acetate positron emission tomography and cardiovascular magnetic
131 disease, thanks to advances in MRI, amyloid positron emission tomography and cerebrospinal fluid bio
132 nt for pathogenesis and treatment.IMPORTANCE Positron emission tomography and computed tomography (PE
133 luorodeoxyglucose [FDG] avidity) measured by positron emission tomography and computed tomography at
135 essment in patients with lymphoma, including positron emission tomography and computed tomography sca
136 stic accuracy of Fluor-18-fluorodeoxyglucose positron emission tomography and computed tomography, la
137 d 77 years underwent 11C-(R)PK11195, 11C-PIB positron emission tomography and magnetic resonance imag
138 d the activity of the PSMA-PI3K axis through positron emission tomography and magnetic resonance imag
139 tients underwent (11)C-Pittsburgh compound B positron emission tomography and magnetic resonance imag
140 MENT We here show that combined simultaneous positron emission tomography and magnetic resonance imag
144 ects and 23 healthy controls participated in positron emission tomography and structural magnetic res
145 agnetic resonance imaging, amyloid (11C-PiB) positron emission tomography and tau (18F-AV-1451) posit
146 he results of their florbetapir F-18 (Abeta) positron emission tomography and their Alzheimer disease
147 ndication of neuroinflammation in vivo using positron emission tomography and TSPO-specific radioliga
149 ter stress testing with myocardial perfusion positron emission tomography and with left ventricular e
151 ned by fluorodeoxyglucose F 18 [FDG]-labeled positron emission tomography and/or hippocampal volume [
152 beta-cells in pigs and nonhuman primates by positron emission tomography as well as in immunodeficie
153 amyloid-beta plaques measured as florbetapir positron emission tomography binding antecedent to 18F-A
154 dementia) and 12 healthy controls underwent positron emission tomography brain imaging with [(18)F]A
155 tomography, magnetic resonance imaging, and positron emission tomography can be used to assess pulmo
157 rticipants underwent 18-F Fluorodeoxyglucose Positron Emission Tomography Computed Tomography (18-FDG
158 cted by (18)F-fluorodeoxyglucose ((18)F-FDG) positron emission tomography computed tomography (PET/CT
160 s an insufficient explanation of 18F-AV-1451 positron emission tomography data in vivo, at least in t
162 and insulin sensitivity were measured using positron emission tomography during an isoglycemic clamp
163 ose concentrations) with 1-[(11)C]-d-glucose positron emission tomography during hyperinsulinemic glu
164 nts underwent magnetic resonance imaging and positron emission tomography for amyloid-beta ((11) C-Pi
168 aphy with iron oxide particles, and targeted positron emission tomography imaging are currently under
170 nflammation, were measured with [(11)C]PBR28 positron emission tomography imaging in 15 healthy contr
173 We assessed the radiotracer 18F-AV-1451 with positron emission tomography imaging to compare the dist
174 had available plasma total tau levels, Abeta positron emission tomography imaging, and a complete neu
175 l and structural magnetic resonance imaging, positron emission tomography imaging, and behavioral dat
176 structural MRI, [(18)F]flutemetamol amyloid positron emission tomography imaging, apolipoprotein E g
177 d quantitative techniques, including in vivo positron emission tomography imaging, gamma counting, an
180 etic resonance imaging and spectroscopy, and positron emission tomography in these areas and discusse
184 ing fundamentals necessary to understand how positron emission tomography makes robust, quantitative
185 e in PCC fludeoxyglucose F 18 ([(18) F] FDG) positron emission tomography measured in Alzheimer's Dis
186 pleasant, and neutral images), and underwent positron emission tomography measurements of dopamine D2
187 latform for magnetic resonance/photoacoustic/positron emission tomography multimodal imaging and ligh
188 t state-of-the-art hardware and software for positron emission tomography myocardial perfusion imagin
189 lume of denervated myocardium (defect of the positron emission tomography norepinephrine analog (11)C
190 [(11)C]5-hydroxy-tryptophan ([(11)C]5-HTP) positron emission tomography of the pancreas has been sh
194 id (defined by cerebrospinal fluid assays or positron emission tomography regional summaries) can be
195 ated variability; and (iii) this 18F-AV-1451 positron emission tomography retention pattern significa
197 ed with age, and cross-sectional florbetapir positron emission tomography retention, but not with yea
201 dard for reporting the results of an amyloid positron emission tomography scan is to assign a dichoto
202 tently associated with an Abeta+ florbetapir positron emission tomography scan, not all Abeta+ subjec
203 = 306) and (18) fluorodeoxyglucose (n = 305) positron emission tomography scanning to assess amyloid
205 F]fluoro-levo-dihydroxyphenylalanine dynamic positron emission tomography scans and striatal regions
206 resonance imaging and Pittsburgh compound B-positron emission tomography scans enrolled in the Mayo
207 3)I-MIBG scans, or [(18)F]fluorodeoxyglucose-positron emission tomography scans for MIBG-nonavid dise
208 eferred for rest/stress myocardial perfusion positron emission tomography scans from January 2006 to
209 ional resting-state (18)F-fluorodeoxyglucose positron emission tomography scans from VPA-exposed and
210 ne (MIBG) scans or [(18)F]fluorodeoxyglucose-positron emission tomography scans if the tumor is MIBG
211 atients were evaluated by fluorodeoxyglucose-positron emission tomography scans performed at baseline
212 DS AND In 127 volunteers, serial rest-stress positron emission tomography scans using rubidium-82 wit
213 D and 12 healthy controls (HC) completed two positron emission tomography scans with [(11)C]-(+)-PHNO
214 tomography binding antecedent to 18F-AV-1451 positron emission tomography scans, and to what extent t
215 betapir retention, antecedent to 18F-AV-1451 positron emission tomography scans, in the parieto-tempo
217 on between 18 kDa translocator protein brain positron emission tomography signal, which arises largel
218 years), response (PR v CR) after R-CHOP, and positron emission tomography status at assignment (negat
219 usion, this is one of the first longitudinal positron emission tomography studies evaluating longitud
222 study and invited these individuals back for positron emission tomography study with [(18)F]-fluorode
225 ulti-session [(15)O]-water and [(18)F]-FDOPA positron emission tomography to determine striatal blood
226 fluorodihydroxyphenyl-l-alanine ([18F]-DOPA) positron emission tomography to examine dopamine synthes
228 hy age-matched control individuals underwent positron emission tomography to measure cerebral metabol
231 labeled with fluorine-18 ((18)F) are used in positron emission tomography to visualize, characterize
232 n tau tangle accumulation (measured with the positron emission tomography tracer 18F-AV-1451) associa
234 evelopment of tools such as radioligands and positron emission tomography tracers that are not curren
236 brain amyloid burden, as detected by amyloid positron emission tomography using 11C-Pittsburgh B comp
237 ith [(11)C]carfentanil and [(18)F]fluorodopa positron emission tomography using a high-resolution sca
238 x-matched control subjects had (18)F-AV-1451 positron emission tomography using a Siemens high-resolu
240 1C-Pittsburgh compound B and 11C-(R)-PK11195 positron emission tomography was used to determine the a
244 dy, flortaucipir tau and florbetapir amyloid positron emission tomography were obtained for 217 subje
246 f functional SGLT2 proteins in rodents using positron emission tomography with 4-[(18)F]fluoro-dapagl
247 iatal D2R binding potential (D2R BPND) using positron emission tomography with a D2R-selective radiol
250 amyloid burden (measured by florbetapir F-18 positron emission tomography) and cognitive performance
251 ng cerebrospinal fluid (CSF) or imaging (tau positron emission tomography) biomarkers for Alzheimer d
252 etic resonance imaging, nuclear imaging, and positron emission tomography) performed on an outpatient
253 onal neuroimaging ([(18)F]fluorodeoxyglucose positron emission tomography) with a fear-regulating ext
255 on emission tomography and tau (18F-AV-1451) positron emission tomography, and episodic and semantic
256 ical assessment, brain 18-fluorodeoxyglucose positron emission tomography, electroneurography, and EL
257 ontribute to disease profiles of 18F-AV-1451 positron emission tomography, especially in primary tauo
258 erebral Abeta on Pittsburgh Compound B (PiB) positron emission tomography, gait speed over 4.57 m (15
261 nonoffenders were included and examined with positron emission tomography, using the radioligand [(11
262 glucose uptake, assessed through noninvasive positron emission tomography, was an effective predictiv
263 perfusion and coronary flow reserve (CFR) by positron emission tomography, where submaximal stress pr
266 Purpose Magnetic resonance imaging (MRI) and positron emission tomography-computed tomography (PET-CT
267 ained from baseline (18)F-fluorodeoxyglucose positron emission tomography-computed tomography (PET-CT
268 l present the analyses of centrally reviewed positron emission tomography-computed tomography (PET-CT
269 TV0 was measured by (18)F-fluorodeoxyglucose-positron emission tomography-computed tomography in 108
270 cation, adenocarcinoma histology, and higher positron emission tomography-computed tomography N stage
271 r extracranial metastatic lesions on choline positron emission tomography-computed tomography, and se
273 the clinical use of RHL30 in the context of positron emission tomography-guided response assessment
282 stenosis underwent (18)F-fluorodeoxyglucose-positron emission tomography/computed tomographic imagin
283 med to determine whether 18F-fludeoxyglucose-positron emission tomography/computed tomography (FDG-PE
284 ng of surveillance [(18)F]fluorodeoxyglucose-positron emission tomography/computed tomography (FDG-PE
286 ings from dual-energy spectral CT(DEsCT) and positron emission tomography/computed tomography (PET/CT
288 ascular inflammation by 18fluorodeoxyglucose positron emission tomography/computed tomography in vivo
289 ned in a single hybrid imaging session using positron emission tomography/computed tomography or sing
290 rom 31 patients and results of early interim positron emission tomography/computed tomography scans i
291 ascular inflammation by 18fluorodeoxyglucose positron emission tomography/computed tomography, with g
294 together to enable simultaneous tetramodal (positron emission tomography/fluorescence/Cerenkov lumin
297 information that could be available from tau positron-emission tomography scans and its use to determ
299 netic melanin nanoparticles is developed for positron-emission tomography/magnetic resonance/photoaco
300 ecombinant cellular systems, and critically, positron-emission-tomography (PET) studies with a specif
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