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1 tic plaques can be visualized by noninvasive positron emission and computed tomographic imaging with
2                               Using combined positron emission and computed tomography in 35 asymptom
3                 Visual assessment of amyloid positron emission tomographic (PET) images has been appr
4 y fluorine 18-labeled AV-1451 ([18F]AV-1451) positron emission tomographic (PET) imaging are linked w
5 n 11-labeled Pittsburgh Compound B (11C-PiB) positron emission tomographic (PET) imaging.
6                           (11)C-(R)-rolipram positron emission tomographic (PET) scans were performed
7                           Using [11C]DPA-713 positron emission tomographic data from 12 active or for
8           Investigations in humans have used positron emission tomographic metabolic and myocardial b
9 ere unchanged, and a fluorodeoxyglucose F 18 positron emission tomographic scan was normal.
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
12            This cross-sectional case-control positron emission tomographic study was performed in the
13 mmunology, human translational research, and positron emission tomographic vascular imaging.
14 ed in tumor xenografts by using small-animal positron emission tomographic/computed tomographic imagi
15         Eight patients with asthma completed positron emission tomographic/computed tomographic lung
16 d potentially have changed 332 of 1732 (19%) positron emission tomographies at low-risk physiological
17 s of 1344 pixel range of perfusion in paired positron emission tomographies.
18 n was assessed by MRI and fludeoxyglucose-18 positron emission tomography ((18)FDG-PET).
19                   Combined oxygen 15-labeled positron emission tomography (15O PET) and brain tissue
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
22            Whole-body (18)F-fluodeoxyglucose positron emission tomography ([(18)F]FDG-PET) imaging ha
23                     (18)F-Fluorodeoxyglucose-positron emission tomography (FDG-PET) has become a cent
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
26 ce imaging (MRI) and (18)F-fluordeoxyglucose positron emission tomography (FDG-PET).
27 pir F 18 (previously known as AV 1451, T807) positron emission tomography (FTP-PET) imaging for tau a
28                          We show that immuno-positron emission tomography (immuno-PET) can visualize
29                                              Positron emission tomography (PET) -computed tomography
30                                     Combined positron emission tomography (PET) and computed tomograp
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
33               (18)F-Fluorodeoxyglucose (FDG)-positron emission tomography (PET) and diffusion-weighte
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
38                  Nevertheless, studies using positron emission tomography (PET) and radioligands for
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
45                                      Dynamic positron emission tomography (PET) images were acquired
46                       BACKGROUND AND Amyloid-positron emission tomography (PET) imaging (API) detects
47                                              Positron emission tomography (PET) imaging agents that d
48                                              Positron Emission Tomography (PET) imaging allows the es
49 ing (FL) and photodynamic therapy (PDT) with positron emission tomography (PET) imaging and internal
50                                      Amyloid positron emission tomography (PET) imaging is a valuable
51  exploited the potential targeting of TF for positron emission tomography (PET) imaging of pancreatic
52                         Over the past years, positron emission tomography (PET) imaging studies have
53                             Here we describe positron emission tomography (PET) imaging with (18)F-Ma
54                                              Positron emission tomography (PET) imaging with radiotra
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
57 g, or synthetic organic molecule for in vivo positron emission tomography (PET) imaging.
58 ased attenuation correction (ATAC) for brain positron emission tomography (PET) in an integrated time
59                            Use of [(18)F]FDG-positron emission tomography (PET) in clinical breast ca
60  surgery on the human brain immune system by positron emission tomography (PET) in relation to blood
61                                              Positron emission tomography (PET) is a powerful analyti
62                           Here, we show that positron emission tomography (PET) is advantageous for d
63                                              Positron emission tomography (PET) is an important drive
64                        18-Fluorodeoxyglucose positron emission tomography (PET) is commonly utilized
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
70                              The method uses positron emission tomography (PET) of [(11)C]yohimbine b
71                                              Positron emission tomography (PET) offers superior contr
72                      Here, we characterize a positron emission tomography (PET) probe for imaging DIP
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
76                Radiolabeling with long-lived positron emission tomography (PET) radionuclides, such a
77  (CCR2)-binding peptide adapted for use as a positron emission tomography (PET) radiotracer for nonin
78          While the benefits of MRI are many, positron emission tomography (PET) radiotracers are stil
79                                            A positron emission tomography (PET) scan confirmed the lu
80               Early response evaluation with positron emission tomography (PET) scan may improve sele
81                Ten subjects also completed a positron emission tomography (PET) scan to quantify DRN
82 nonsmokers participated in two [(11)C]ABP688 positron emission tomography (PET) scans on the same day
83                                     Previous positron emission tomography (PET) studies targeting the
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
88               Recent studies have shown that positron emission tomography (PET) tracer AV-1451 exhibi
89  individuals: (1) Tau, detected with a novel positron emission tomography (PET) tracer known as (18)F
90                                Consequently, positron emission tomography (PET) tracers addressing tr
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
94                                              Positron emission tomography (PET) using radiolabeled li
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
97                  Purpose To demonstrate that positron emission tomography (PET) with fluorine 18 ((18
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
101          Radiocaine, an F-18 radiotracer for positron emission tomography (PET), is the first SCN5A i
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
105                      In our phase 2 study of positron emission tomography (PET)-adapted salvage thera
106 stine, prednisone (R-CHOP14) induction and a positron emission tomography (PET)-driven ASCT or standa
107 yloid deposition, measured using florbetapir positron emission tomography (PET).
108 (sr39tk) reporter gene for cell detection by positron emission tomography (PET).
109 entual application in molecular imaging with positron emission tomography (PET).
110 , a dopamine D2/D3 receptor radiotracer, and positron emission tomography (PET).
111 ton emission computed tomography (SPECT) and positron emission tomography (PET).
112 lthy comparison subjects using [(11)C]IMA107 positron emission tomography (PET).
113 -L1 VHH) to track PD-L1 expression by immuno-positron emission tomography (PET).
114 tion and whole-body dosimetry assessments by positron emission tomography (PET).
115                                            A positron emission tomography (PET)/ computed tomography
116         Purpose [(18)F]Sodium fluoride (NaF) positron emission tomography (PET)/computed tomography (
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 (
120          In this report, a case of fire in a positron emission tomography (PET)/magnetic resonance (M
121          Materials and Methods An integrated positron emission tomography (PET)/magnetic resonance (M
122 e of flourine 18 ((18)F) fluorocholine (FCH) positron emission tomography (PET)/magnetic resonance (M
123                         Purpose To develop a positron emission tomography (PET)/magnetic resonance (M
124  correction (AC) (termed deep MRAC) in brain positron emission tomography (PET)/MR imaging.
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
127 ents received a second Pittsburgh compound B positron emission tomography analysis.
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
134                                              Positron emission tomography and computed tomography ima
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
141                                       Hybrid positron emission tomography and magnetic resonance in t
142 20 min, and 50 min with (15)O-water by using positron emission tomography and MRI.
143                       A meta-analysis of 142 positron emission tomography and single photon emission
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
148                     (18)F-fluorodeoxyglucose-positron emission tomography and ultrasmall superparamag
149 ter stress testing with myocardial perfusion positron emission tomography and with left ventricular e
150                                 Staging used positron emission tomography and/or computed tomography.
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
156                                              Positron emission tomography can be useful to identify a
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
159                 Systemic venous sampling and positron emission tomography confirm uptake of glucose a
160 s an insufficient explanation of 18F-AV-1451 positron emission tomography data in vivo, at least in t
161                                   Fluorodopa positron emission tomography demonstrated significant in
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
165 healthy control subjects had 11C-(R)-PK11195 positron emission tomography for comparison.
166                         New radioligands for positron emission tomography have generated considerable
167                                              Positron emission tomography image analysis was complete
168 aphy with iron oxide particles, and targeted positron emission tomography imaging are currently under
169                      New recommendations for positron emission tomography imaging for the evaluation
170 nflammation, were measured with [(11)C]PBR28 positron emission tomography imaging in 15 healthy contr
171                                              Positron emission tomography imaging of mice bearing PC3
172                                              Positron emission tomography imaging reveals neuroinflam
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
178 sessments, seizures, corticosteroid use, and positron emission tomography imaging.
179 onic uptake of [(18)F]-fluorodeoxyglucose by positron emission tomography in Hdc(-/-) mice.
180 etic resonance imaging and spectroscopy, and positron emission tomography in these areas and discusse
181                  We suggest that 18F-AV-1451 positron emission tomography is a useful biomarker to as
182                          Although, currently positron emission tomography is the most commonly used t
183              Here we compared binding of tau positron emission tomography ligands, PBB3 and AV-1451,
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
191                                  For amyloid positron emission tomography positive (Abeta+) subjects,
192         Here, we report the development of a positron emission tomography probe for live bacterial in
193                                 D2/3 agonist positron emission tomography radiotracer [(11)C]N-propyl
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
196               We found that: (i) 18F-AV-1451 positron emission tomography retention was differentiall
197 ed with age, and cross-sectional florbetapir positron emission tomography retention, but not with yea
198 t increased annualized change in florbetapir positron emission tomography retention.
199                              11C-(R)-PK11195 positron emission tomography reveals increased inflammat
200       Investigations at progression included positron emission tomography scan and biopsy.
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
204                                              Positron emission tomography scanning with the transloca
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
216                       [(18)F]Fludeoxyglucose positron emission tomography showed increased myocardial
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
220                                              Positron emission tomography studies report either no di
221 e disorder (MDD), highlighting insights from positron emission tomography studies.
222 study and invited these individuals back for positron emission tomography study with [(18)F]-fluorode
223 imaging via photoacoustic, fluorescence, and positron emission tomography techniques.
224                   We used [(11)C](R)-PK11195 positron emission tomography to compare TSPO availabilit
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
227                                 Here we used positron emission tomography to investigate whether feed
228 hy age-matched control individuals underwent positron emission tomography to measure cerebral metabol
229              Here, we used [(11)C]NOP-1A and positron emission tomography to measure the in vivo bind
230                              We used in vivo positron emission tomography to test whether feeding tri
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
233                   The advent of tau-targeted positron emission tomography tracers such as flortaucipi
234 evelopment of tools such as radioligands and positron emission tomography tracers that are not curren
235        Using tau-specific and Abeta-specific positron emission tomography tracers, we show that in vi
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
239                                  We acquired positron emission tomography using F18 flortaucipir (tau
240 1C-Pittsburgh compound B and 11C-(R)-PK11195 positron emission tomography was used to determine the a
241                                 [(18)F]CPFPX positron emission tomography was used to quantify A1AR a
242                                              Positron emission tomography was used to visualize neuro
243 on-human primates and in human studies using positron emission tomography were not consistent.
244 dy, flortaucipir tau and florbetapir amyloid positron emission tomography were obtained for 217 subje
245                                              Positron emission tomography with 18F-florbetapir and fl
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
248                         (68)Gallium-DOTATATE positron emission tomography with computed tomography ((
249 t-Enhanced MRI (DCE-MRI) and Fludeoxyglucose Positron Emission Tomography(FDG-PET).
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
254  trial (Prediction of Arrhythmic Events with Positron Emission Tomography).
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
259                                        Using positron emission tomography, magnetic resonance spectro
260        We used [(18)F]AV-1451 and [(11)C]PiB positron emission tomography, structural MRI, and neurop
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
264                  Finally, the authors review positron emission tomography-based imaging techniques to
265                                              Positron emission tomography-based regional measures of
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
272      Vascular inflammation was assessed with positron emission tomography-computed tomography.
273  the clinical use of RHL30 in the context of positron emission tomography-guided response assessment
274 n were measured using 18F-fluorodeoxyglucose positron emission tomography.
275 scular magnetic resonance, and (11)C-acetate positron emission tomography.
276 e to that achieved by expert assessment with positron emission tomography.
277 ostic index, and CFR was quantified by using positron emission tomography.
278  [(18)F]fluorodeoxyglucose ([(18)F]FDG) with positron emission tomography.
279 in the murine brain for up to one week using positron emission tomography.
280  preparation of potential tracers for use in positron emission tomography.
281  new radiotracers for molecular imaging with positron emission tomography.
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
285               (18)F-Fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT
286 ings from dual-energy spectral CT(DEsCT) and positron emission tomography/computed tomography (PET/CT
287             Previously, we demonstrated that 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
292 -to-background ratio by 18fluorodeoxyglucose positron emission tomography/computed tomography.
293 ar inflammation led to the increasing use of positron emission tomography/computed tomography.
294  together to enable simultaneous tetramodal (positron emission tomography/fluorescence/Cerenkov lumin
295                                              Positron emission tomography/magnetic resonance imaging
296                  New radiolabeled probes for positron-emission tomography (PET) are providing an ever
297 information that could be available from tau positron-emission tomography scans and its use to determ
298 metabolic response by 18F-fluorodeoxyglucose positron-emission tomography.
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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