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1 on (infection and decreased mental status or perfusion).
2 ent rates in patients with normal myocardial perfusion.
3 with the extent of abnormality of myocardial perfusion.
4 re and a large penumbra on their baseline CT perfusion.
5 ely after HIFD showed improved microvascular perfusion.
6 train), coronary artery flow, and myocardial perfusion.
7 ustment, which affects the quantification of perfusion.
8 pression of blood vessels and improved tumor perfusion.
9  based on wider areas of visible retinal non-perfusion.
10 effect on systemic blood pressure or hepatic perfusion.
11 tochemical images of HA, collagen and vessel perfusion.
12  after 24 hours of near-normothermic ex situ perfusion.
13 a direct effect on tumor vascularization and perfusion.
14 lical loading and simulated body fluid (SBF) perfusion.
15 ature, affecting cell distribution and blood perfusion.
16 reservation techniques, such as normothermic perfusion.
17 r blood vessels, resulting in improved tumor perfusion.
18 tion or injury concomitant with increased Ab perfusion.
19 applied to screening drugs that modify tumor perfusion.
20 levating interstitial pressure and impairing perfusion.
21 ncy of interictal bursts increased after CBZ perfusion.
22  in total tissue pressure and increased drug perfusion.
23 onsecutive examination rounds in relation to perfusion.
24 ocess effacement following protamine sulfate perfusion.
25 n limbs maintained for 24 hours with ex situ perfusion.
26 nal excretion of sodium were measured during perfusion.
27 elet aggregation, and improved microvascular perfusion.
28                Nalmefene did not alter brain perfusion.
29 ies is the prerequisite of normal myocardial perfusion.
30 lated negatively with baseline microvascular perfusion.
31 enal resistance decreased over the course of perfusion (0 hour, 1.6 +/- 0.51 mm per minute vs 7 hours
32                            RAMT(+) increased perfusion 1.5-fold in stroke-affected gastrocnemius as c
33 e constants K1, K1/k2, and k3-surrogates for perfusion, (18)F-FMISO distribution volume, and hypoxia-
34 ich is considered a biomarker of poor tissue perfusion, a key element in the management of severe sep
35                         We found that ROX SE perfusion achieves excellent delineation of the cerebral
36 rated improved postamputation stump healing, perfusion, adductor muscle neovascularization, and decre
37 odel, PUT induced a 68.5% reduction in blood perfusion after 7 days (p < 0.001) without damaging the
38                  The change in microvascular perfusion after transfusion correlated negatively with b
39                                     Improved perfusion alleviates hypoxia, which reprograms the immun
40     Here, we combined arterial spin labeling perfusion and blood oxygen level-dependent functional ma
41 reatment, pFUS + MSC significantly increased perfusion and CD31 expression, while reducing fibrosis c
42 retest precision in same subject, (3) stress perfusion and CFR after adenosine compared with dipyrida
43 ntified (1) the protocol with maximum stress perfusion and CFR, (2) test-retest precision in same sub
44 y of coronary flow capacity combining stress perfusion and CFR, and (5) potential relevance for patie
45 stemically validated for absolute myocardial perfusion and coronary flow reserve (CFR) by positron em
46        Quantitative assessment in myocardial perfusion and determination of absolute myocardial blood
47 ining can be implemented to improve coronary perfusion and diastolic function in the elderly.
48      Sildenafil treatment protects placental perfusion and fetal growth, but whether the effects of s
49 nce shows that sildenafil protects placental perfusion and fetal growth.
50                      Amputation stump tissue perfusion and healing were evaluated in C57BL/6J adult m
51 D18 inhibitor mAb107, improves microvascular perfusion and histopathology, reduces intrarenal pro-inf
52             Multiparametric imaging of tumor perfusion and hypoxia with dynamic (18)F-fluoromisonidaz
53 hibited tumor angiogenesis and reduced tumor perfusion and inflammation in vivo, while standard gemci
54 del allowed adequate decoupling of (18)F-FET perfusion and internalization by cells in the different
55 and (13)C-urea to investigate differences in perfusion and metabolism between low- and high-grade tum
56 f the high-grade TRAMP tumors, a mismatch in perfusion and metabolism measurements was observed, with
57                 MR imaging measures of brain perfusion and metabolism were compared among eight patie
58 increase in insulin-stimulated microvascular perfusion and molecular signaling at the level of TBC1D4
59  duration and termination of SD caused by K+ perfusion and oxygen-glucose deprivation.
60        Three months after infusion, cortical perfusion and RBF rose in the STK (151.8-185.5 ml/min, P
61           Stenotic kidney cortical/medullary perfusion and RBF were measured using contrast-enhanced
62 shment of AKI rapidly restores microvascular perfusion and small molecule accessibility, with improve
63 cy, preimplantation biopsy, dual KT, machine perfusion and special immunosuppressive protocols.
64 itical hypoperfusion between the baseline CT perfusion and the 36-hour follow-up magnetic resonance i
65 revent the impairment of renal microvascular perfusion and the heightened inflammatory response that
66 spective case series assesses gingival blood perfusion and tissue molecular responses in relation to
67 s critical for optimization of microvascular perfusion and to define which patients can benefit from
68 sed to distinguish between tumors of varying perfusion and to screen the efficacy of blood flow-modif
69                          pFUS + MSC improved perfusion and vascular density in this clinically-releva
70 ironments by identifying areas with variable perfusion and vascular permeability, since individual tu
71 es in white matter integrity, cerebral blood perfusion, and brain metabolism in the infarcted tissue.
72 dial edema, myocardial siderosis, myocardial perfusion, and diffuse myocardial fibrosis.
73 steonecrosis, bone loss, reduction in vessel perfusion, and excessive osteoclastogenesis in the femor
74 ually displayed contraction until the end of perfusion, and histology showed no myocyte injury.
75 fe and feasible method to assess anastomotic perfusion, and its use might affect the incidence of ana
76 growth, angiogenesis, osteogenesis, coronary perfusion, and oxygen delivery.
77 o generate parametric maps of tumor hypoxia, perfusion, and radiotracer distribution volume.
78  We measured cortical and medullary volumes, perfusion, and RBF using multidetector computed tomograp
79                            Tumor hypoxia and perfusion are independent prognostic indicators of patie
80 vascular dysfunction and inadequate coronary perfusion are likely mechanisms of diastolic dysfunction
81  effects of RBC transfusion on microvascular perfusion are not well documented.
82 nd hydralazine were used to manipulate tumor perfusion before 2-(18)F-FEtOH quantification.
83 tabolism measurements was observed, with low perfusion being associated with increased kPL This perfu
84                   In addition, renal volume, perfusion, blood flow, and oxygenation were assessed.
85 anied by a progressive loss in renal volume, perfusion, blood flow, and oxygenation.
86 ted increase in frontal cortical grey matter perfusion but unexpected perfusion decreases in regions
87 eutic ultrasound cavitation increased muscle perfusion by 7-fold in normal mice, reversed tissue isch
88                     These tumors show normal perfusion by clinical imaging and lack histological evid
89                       Augmentation in muscle perfusion by ultrasound cavitation was assessed in a pro
90 clerotic-arterial occlusions decrease tissue perfusion causing ischemia to lower limbs in patients wi
91 t, positive significant correlations between perfusion changes and evoked responses could be seen, su
92 im of this study was to verify whether ictal perfusion changes, both hyper- and hypoperfusion, corres
93 othelial cells (HUVEC) grown on laminar-flow perfusion channels were stimulated with 1 mug/mL lipopol
94                               Therefore, ASL perfusion CMR may be an alternative method for quantifyi
95                                Capillary non-perfusion (CNP) lesions are central to the pathogenesis
96 mb-tissue necrosis and increased limb tissue perfusion compared with Met81- (n=25) or green fluoresce
97 th diffusion-weighted and dynamic sequences, perfusion computed tomography, cone beam computed tomogr
98 nd SPECT, per-patient diagnostic accuracy of perfusion CT and perfusion MR imaging was 63% (58 of 92)
99 my had the same baseline computed tomography perfusion (CTP) ischemic core threshold to predict infar
100  a high concentration (>20 million cells/mL) perfusion culture of an IgG1-producing Chinese hamster o
101 tention device based on inertial sorting for perfusion culture of suspended mammalian cells.
102                                    Lab-scale perfusion cultures (350 mL) were used to demonstrate the
103 e endothelial glycocalyx using neuraminidase perfusion decreased endothelial glycocalyx depth and inc
104                                   Myocardial perfusion decreased significantly during HD and HDF.
105 ortical grey matter perfusion but unexpected perfusion decreases in regions of the brain normally ass
106                                         Mean perfusion defect volumes measured with adenosine and hyp
107                            To detect macular perfusion defects in glaucoma using projection-resolved
108 llowing: chest/abdominal/back pain, syncope, perfusion deficit, and if AAS was in the differential di
109  [5.2] versus -0.73 [1.9], P=0.65; and total perfusion deficit: -1.33 [3.3] versus -2.19 [6.6], P=0.6
110  2.60 [2.6] versus 3.63 [3.6], P=0.52; total perfusion deficit: 3.60 [3.6] versus 5.01 [4.3], P=0.32;
111                         Patients with normal perfusion demonstrated low annual event rates (primary o
112 cular zone (FAZ) area, vessel densities, and perfusion densities of the superficial capillary plexus
113  a novel, oxygenated and hypothermic machine perfusion device (HMP Airdrive system) improves the qual
114 T1 and 67NR tumors was consistent with known perfusion differences within and between these tumors.
115 graphy (CTA) confirmed persistent aneurysmal perfusion due to the incomplete neck coverage.
116 ible for shear-dependent increases in muscle perfusion during therapeutic cavitation.
117          Consistent with poor feto-placental perfusion, Egfl7 knockout resulted in reduced placental
118                   Normothermic ex situ liver perfusion enabled assessment and transplantation of 12 l
119 hemic times, before and during ex vivo heart perfusion (EVHP), to identify features associated with a
120 iomarkers during ex vivo normothermic kidney perfusion (EVKP) may aid in the assessment of a kidney p
121 nor blood circulating within an ex vivo lung perfusion (EVLP) system.
122                           Using ex vivo lung perfusion (EVLP) to investigate the pathophysiology of i
123 al hypometabolism, predates changes in brain perfusion, exacerbates and works synergistically with am
124 an scattering (CARS) microscopy and isotopic perfusion experiments.
125 k human livers were perfused with HBOC-based perfusion fluid and matched to 5 RBC-perfused livers.
126 a-reperfusion [I/R] injury) were measured in perfusion fluid at regular intervals.
127  oxygen carrier to packed red cells in NMP-L perfusion fluid.
128 and facilitated the recovery of blood vessel perfusion function in a murine hindlimb ischemia model.
129 nors, had a higher frequency of poor ex vivo perfusion, had longer cold ischemic times, and were tran
130                   Normothermic ex situ liver perfusion has the potential to increase liver utilizatio
131 ighted proton (hydrogen 1 [(1)H]) images and perfusion images by using arterial spin labeling were ob
132  conventional T1-weighted (1)H images and to perfusion images from arterial spin labeling.
133 n of the left ventricle for SPECT myocardial perfusion imaging (MPI) quantification often requires ma
134           The prognostic value of myocardial perfusion imaging (MPI) with the cadmium-zinc-telluride
135 of stress myocardial magnetic resonance (MR) perfusion imaging in the detection of coronary artery di
136 r the first time non-invasive whole-placenta perfusion imaging in utero.
137 rdial dynamic computed tomography myocardial perfusion imaging lacks standardization.
138 is of dynamic computed tomography myocardial perfusion imaging may permit robust discrimination betwe
139                                    Real-time perfusion imaging revealed markedly improved microvascul
140                                    Placental perfusion imaging was performed using velocity-selective
141 tress dynamic computed tomography myocardial perfusion imaging with a second-generation dual-source s
142 e (CAD) is ambiguous, but nuclear myocardial perfusion imaging with single-photon emission tomography
143 c susceptibility contrast magnetic resonance perfusion imaging, we demonstrate that lack of ABCD1 fun
144 s evaluated by low-power contrast ultrasound perfusion imaging.
145 ic NPs similarly increased the GFR and renal perfusion in both genotypes.
146 insulin-stimulated increase in microvascular perfusion in both legs and abrogated the greater glucose
147 (RXFP1) and has been shown to increase renal perfusion in healthy human volunteers.
148         There was a significant reduction in perfusion in high-grade tumors that associated with incr
149 rmalities, mucus plugging, and abnormal lung perfusion in infants and toddlers (P < 0.05 to P < 0.001
150 g endothelial cells that could restore blood perfusion in nutrient-deprived regions where angiogenic
151 alysis for histograms of 1344 pixel range of perfusion in paired positron emission tomographies.
152 nges that occur in BBB function and cerebral perfusion in patients with MS and highlight genetic and
153 eripheral artery disease, and doubled muscle perfusion in patients with sickle cell disease.
154 ing revealed markedly improved microvascular perfusion in response to the blockade of NET-induced coa
155 psychopathology was associated with elevated perfusion in several regions including the right dorsal
156 uction in left ventricular mass and superior perfusion in the infarct zone.
157   Psychosis symptoms were related to reduced perfusion in the left frontal operculum and insula, wher
158                   The observation of reduced perfusion in the posterior cingulate and cuneal cortex,
159 reas fear symptoms were associated with less perfusion in the right occipital/fusiform gyrus and left
160  of PR-OCTA, glaucoma preferentially affects perfusion in the SVC in the macula more than the deeper
161                                              Perfusion-independent regulation of epithelial pattern f
162 responses were significantly different under perfusion, indicating a distinct biological response of
163 l design may be informed by new anatomic and perfusion insights.
164                                  Solid tumor perfusion is a proven variable of interest for predictin
165                            Here we show that perfusion is a vital factor for engineered human tissues
166               Evaluation of microcirculation perfusion is critical for optimization of microvascular
167 dic system with computer controlled compound perfusion is presented that offers a novel methodology f
168                                       ROX SE perfusion is therefore a novel and highly useful techniq
169  surrogate biomarkers of tumor hypoxia (k3), perfusion (K1), and (18)F-FMISO distribution volume.
170 at can distinguish between tumors of varying perfusion levels and can be applied to screening drugs t
171 hole-body PBPK model consisting of seventeen perfusion-limited compartments.
172 irrhotic livers, a significantly lower total perfusion, lower fractional volume of the vascular space
173 e effects are capable of increasing cerebral perfusion, making trigeminal nerve stimulation (TNS) a p
174 l density (P < 0.01) and lower uptake of the perfusion marker Hoechst 33342 (P < 0.05).
175                Avoidance of hyperoxia during perfusion may prevent postreperfusion syndrome and vasop
176 ze-specific dose estimate per two-volume FPA perfusion measurement were 10.8 and 17.8 mGy, respective
177 ze-specific dose estimate per two-volume FPA perfusion measurement were also determined.
178 cans were used for maximum slope model (MSM) perfusion measurement, but only two volume scans were us
179  but only two volume scans were used for FPA perfusion measurement.
180 ries combined were compared with microsphere perfusion measurements by using regression, root-mean-sq
181                                              Perfusion measurements in the LAD, left circumflex arter
182 ion being associated with increased kPL This perfusion-metabolism mismatch was also associated with m
183                  Normothermic ex vivo kidney perfusion might help to decrease posttransplant delayed
184    We determined the association of cerebral perfusion (mL/100mL/min) with risk of dementia (until 20
185  applying a dual-input two-compartment liver perfusion model to patients with different pathologies.
186 C-iodoantipyrine perfusion reporter, and the perfusion-modifying drugs nicotinamide, pentoxifylline,
187 (14)C-iodoantipyrine and reflected the tumor perfusion-modifying effects of each drug.
188 as a coupling device between heart and brain perfusion, modulating the amount of pressure and flow pu
189 ient diagnostic accuracy of perfusion CT and perfusion MR imaging was 63% (58 of 92) and 75% (69 of 9
190           SWI can be used as an accessory to perfusion MR technique in preoperative tumor grading.
191                  CONSLUSIONS: In conclusion, perfusion MRI and SWI using 3T MR and 32-channel head co
192  voxelwise basis using arterial spin labeled perfusion MRI at 3T.
193 azole ((18)F-FMISO) PET and conventional and perfusion MRI before surgery.
194                                Diffusion and perfusion MRI, and transcranial magnetic stimulation wer
195      A program of normothermic ex situ liver perfusion (NESLiP) was developed to facilitate better as
196 ssure-controlled normothermic ex vivo kidney perfusion (NEVKP) with static cold storage (SCS) in a po
197 mes of a first clinical normothermic machine perfusion (NMP) liver trial in the United Kingdom demons
198 ence of intraoperative lidocaine intravenous perfusion (odds ratio: 0.182, 95% CI 0.042-0.788; P = 0.
199                                     In vivo, perfusion of a nonhuman primate kidney TLN-supplemented
200 resistance, which greatly increases vascular perfusion of BAT.
201 d the bradycardic response to intralaryngeal perfusion of capsaicin, which was associated with up-reg
202                                              Perfusion of cochlea with fixative greatly improved pres
203  also allows analysis of the effect of local perfusion of compounds within the same area being sample
204 roangiography and 3D imaging revealed patchy perfusion of Egfl7(-/-) placentas marked by impeded bloo
205  human blood, suggesting that pre-transplant perfusion of genetically modified porcine organs with CH
206 evaluate the feasibility of directly imaging perfusion of human brain tissue by using magnetic resona
207                                              Perfusion of the microengineered vessel with human RBCs
208 prolonged decrease of coronary microvascular perfusion often occurs even after flow is restored in an
209                 No differences in myocardial perfusion or adverse events were observed between the co
210 alone reduced fibrosis, but did not increase perfusion or CD31.
211 lder, have altered mobility, experience poor perfusion, or who are receiving a vasopressor infusion.
212 y end point was change in resting myocardial perfusion over 6 months.
213 serelaxin in the rat models increased kidney perfusion, oxygenation, and function through reduction i
214 Levels of KIM-1 were not associated with the perfusion parameters (P = 0.649) or renal function in th
215 entage area of blood vessels, while other US perfusion parameters did not.
216 simultaneous quantification of metabolic and perfusion parameters in tumors.
217                                  Endocardial perfusion parameters obtained by semiautomatic analysis
218                                   Initially, perfusion parameters were extracted according to standar
219                                 Quantitative perfusion parameters, such as blood flow, were calculate
220        Purpose To prospectively evaluate the perfusion patterns at quantitative dynamic contrast mate
221 ted tomography can demonstrate complex ictal perfusion patterns.
222 % women) referred for rest/stress myocardial perfusion positron emission tomography scans from Januar
223 th unfavorable outcome (odds ratio %cerebral perfusion pressure < lower limit of reactivity, 1.04; 95
224 -fitting method that determined the cerebral perfusion pressure (CPP) at which the pressure reactivit
225 nce of Kir6.1 did not elevate basal coronary perfusion pressure in eKO mice.
226 l pressure, percentage of time with cerebral perfusion pressure less than lower limit of reactivity w
227 tomatically the "lower" and "upper" cerebral perfusion pressure limits of reactivity, respectively.
228 ndividualized autoregulation-guided cerebral perfusion pressure management may be a plausible alterna
229 min for 2.0 Hz and increased global cerebral perfusion pressure of 91 mm Hg for 0 Hz, 100.5 mm Hg for
230 stant level despite fluctuations of cerebral perfusion pressure or arterial blood pressure.
231 be a plausible alternative to fixed cerebral perfusion pressure threshold management in severe trauma
232                                 The cerebral perfusion pressure values at which this "U-shaped curve"
233 erived mean velocity index based on cerebral perfusion pressure, and autoregulation reactivity index
234                    METHODS AND MAIN Cerebral perfusion pressure-pressure reactivity index curves were
235 tween pressure reactivity index and cerebral perfusion pressure.
236 ell retention device is thus ideal for rapid perfusion process development in a biomanufacturing work
237 y information is needed along with pulmonary perfusion quantification; and in (d) renal function imag
238                                          The perfusion range between these thresholds was termed the
239 to enhance angiogenesis, arteriogenesis, and perfusion recovery in experimental PAD.
240 VEGF165a and hence inhibits angiogenesis and perfusion recovery in PAD muscle.
241 arization, angiogenesis, arteriogenesis, and perfusion recovery.
242 To determine the role of HPV in the regional perfusion redistribution in bronchoconstricted patients
243 s not the only mechanism that contributes to perfusion redistribution in bronchoconstricted patients
244 terial spin labelling that measures cerebral perfusion related to ongoing neural activity.
245 he diffusion-related coefficient (D) and the perfusion-related parameter (f) can be obtained simultan
246 tus, and to further elucidate the effects of perfusion-related variables.
247 ng microbubble cavitation to increase muscle perfusion relies on shear-dependent increases in ATP, wh
248 s 2-(18)F-fluoroethanol (2-(18)F-FEtOH) as a perfusion reporter that can distinguish between tumors o
249 ectly compared with the (14)C-iodoantipyrine perfusion reporter, and the perfusion-modifying drugs ni
250 oach to coupling MPS with distinct media and perfusion requirements.
251 rome, issues such as aggregate microvascular perfusion resistance, mass transport and exchange within
252                        Selective Aortic Arch Perfusion (SAAP) combines thoracic aortic balloon hemorr
253 t correlations (P < 0.05) were found between perfusion scores and evoked responses in 61% of studies.
254 ting a miniature respiratory and anaesthetic perfusion set-up for live adult zebrafish, allowing for
255 pregnancies with fetal CHD, global placental perfusion significantly decreased and regional variation
256 ecreased and regional variation of placental perfusion significantly increased with advancing gestati
257                      In control experiments, perfusion solution was supplemented with isotonic saline
258                                     Relative perfusion, specific ventilation (sV), and gas fraction (
259 ith standard clinical software (quantitative perfusion SPECT) by 2 experts, adjusting the VP if neede
260 total of 36 subtraction ictal and interictal perfusion studies were analysed in 31 consecutive medica
261 d, 190 patients with an adequate baseline CT perfusion study who underwent angiography were included
262 kg) underwent whole-body cooling via a water perfusion suit at 5 degrees C, on four occasions, to ind
263 , 14 patients (56%) with pulmonary lymphatic perfusion syndrome (PLPS), and 9 patients (36%) with cen
264                                    We used a perfusion system to study the effect of patient plasma (
265 ith gramicidin A were conducted using a fast perfusion system.
266 es and induces microvascular thrombosis in a perfusion system.
267  and is characterized by impairment of organ perfusion, systemic inflammatory response, and multiple
268                                      Machine perfusion techniques have decreased delayed graft functi
269                             Ex vivo isolated perfusion testing confirms transfer of glucose and mediu
270 orrhage control with intra-aortic oxygenated perfusion to achieve return of spontaneous circulation (
271            Animals underwent vessel painting perfusion to label the entire cortex at 1 day post TBI f
272             RATIONALE: Angiogenesis improves perfusion to the ischemic tissue after acute vascular ob
273 ) in right ventricular filling and pulmonary perfusion, ultimately resulting in right ventricular fai
274 ent continuous hypothermic pulsatile machine perfusion until transplant: 69 with simultaneous kidney
275 s at these electrodes were compared to ictal perfusion values noted at these locations.
276                                        Liver perfusion values were measured from both focal liver les
277                            However, relative perfusion was also significantly reduced in sVlow subreg
278 n after on average 5.7 years, lower baseline perfusion was associated with accelerated decline in cog
279                               Lower cerebral perfusion was associated with higher risk of dementia (a
280                                Microvascular perfusion was evaluated by low-power contrast ultrasound
281                                    Acellular perfusion was limited to 6 hours on the OCS system due t
282                                              Perfusion was maintained at an average systolic pressure
283                               Gingival blood perfusion was measured by laser Doppler flowmetry (LDF).
284 rol and treatment groups, although increased perfusion was observed within each group from baseline t
285                   Normothermic ex situ liver perfusion was performed using an erythrocyte-based perfu
286 parison with dynamic susceptibility contrast perfusion weighted imaging (DSC-PWI).
287 le clinical tool, and the "mismatch" between perfusion-weighted and diffusion-weighted abnormalities
288 bility was assessed at 24 hour follow up via perfusion-weighted imaging.
289                                              Perfusion-weighted or diffusion-weighted MRI is a widely
290 tive and negative trends between hypoxia and perfusion were observed in individual lesions.
291 an K1 reflects a reduction in tumor vascular perfusion, whereas the increased k3 reflects a rise in h
292  decreased angiogenesis, arteriogenesis, and perfusion, whereas transfer of wild-type macrophages to
293 iogenesis, arteriogenesis, and the extent of perfusion, which correlated with more M2-like macrophage
294  asthma is spatially associated with reduced perfusion, which is proposed to result from hypoxic pulm
295 multiparametric imaging of tumor hypoxia and perfusion with (18)F-fluoromisonidazole ((18)F-FMISO) dy
296 d female guinea pig brain preparation during perfusion with 4-AP.
297 )F-based radiotracer for investigating tumor perfusion with PET imaging.
298 ing cerebral vasospasm using cerebrovascular perfusion with ROX, SE (5-Carboxy-X-Rhodamine, Succinimi
299 f stress myocardial computed tomography (CT) perfusion with that of stress myocardial magnetic resona
300 ours; our primary analysis at 24H focused on perfusion with WB versus RBC.

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