ライフサイエンスコーパス: arterial blood

1 of 25-um microspheres recovered in systemic arterial blood.

2 .72), or partial carbon-dioxide pressure in arterial blood (-0.3 mm Hg; 95% CI, -0.8 to 0.2 mm Hg; P

3 ICH was induced by injecting autologous arterial blood (30mul) into a mouse brain.

4 s that die after successful reperfusion with arterial blood actually are killed by changes initiated

5 , blood gases, and plasma-free hemoglobin in arterial blood, as well as blood entering and exiting th

6 Arterial blood CO2 tension when increased by 25 mm Hg ca

7 heral venous Abeta concentration compared to arterial blood concentration.

8 whose activities are regulated by changes in arterial blood content, including oxygen.

9 retina at PO(2)s more than ten-fold that of arterial blood (Damsgaard et al., 2019).

10 stimulate breathing when oxygenation of the arterial blood decreases; and pulmonary arterial smooth

11 Clinically, human arterial blood directly sampled from the ischemic cerebr

12 by the level of impaired O2 extraction from arterial blood during peak exercise.

13 No correlation was seen between pulmonary arterial blood flow and BPD outcomes.

14 trated by observations of faster recovery of arterial blood flow and large numbers of newly formed ar

15 serelaxin for 120 min increased total renal arterial blood flow by 65% (95% CI 40%, 95%; p < 0.001)

16 ge-field capacitor technology, for measuring arterial blood flow in both contact and non-contact mode

17 There was no significant difference in arterial blood flow measured with Bayesian multipoint ve

18 The arterial blood flow that underlies the stigmata rarely i

19 In IUGR baboons there was increased carotid arterial blood flow velocity during late systole and dia

20 -aorta (PA/AO) diameter ratio, and pulmonary arterial blood flow were determined.

21 , deep-tissue and ultrafast imaging of mouse arterial blood flow with an unprecedented frame rate of

22 tional microvascular density, independent of arterial blood flow, while disturbance of the microcircu

23 nce of vascular WNT signaling in maintaining arterial blood flow.

24 During multidisciplinary rounds, all arterial blood gas (ABG) results, ventilator settings an

25 nd-tidal alveolar dead space fraction (first arterial blood gas after intubation) (per 0.1 unit incre

26 The results of arterial blood gas analyses at t = 4 minutes and t = 13

27 In total, 295,079 arterial blood gas analyses, including the PaO2, between

28 Arterial blood gas and CE are required in LT candidates

29 Secondary outcomes included changes in arterial blood gas and respiratory parameters, weaning d

30 limited incremental cycle exercise test with arterial blood gas collection.

31 exercise maintained alveolar ventilation and arterial blood gas homeostasis but at the expense of ear

32 echanically ventilated patients may not have arterial blood gas measurements available at relevant ti

33 ventilation), comorbidities, chest imaging, arterial blood gas measurements, and pulse oximetry.

34 Arterial blood gas parameters, clinical symptoms, health

35 Severity criteria often depend on arterial blood gas results.

36 In one cohort, the maternal arterial blood gas status, the value at which 50% of the

37 The arterial blood gas test showed partially compensated pul

38 Arterial blood gas testing, chest radiographs, and RBC t

39 een blood eosinophil count on admission with arterial blood gas values, duration of mechanical ventil

40 O2 and VCO2), heart rate, cardiac output and arterial blood gas variables at peak exercise on a cycle

41 ompared with the baseline period, unadjusted arterial blood gas, chest radiograph, and RBC utilizatio

42 ased provider financial incentives targeting arterial blood gas, chest radiograph, and RBC utilizatio

43 ventilation, for each protocol, we recorded arterial blood gas, respiratory mechanics, alveolar recr

44 ygen saturation by pulse oximetry (SpO(2) ), arterial blood gas, spirometry, and contrast-enhanced ec

45 ome was change in PFR from baseline to final arterial blood gas.

46 tion were recorded at the time of a clinical arterial blood gas.

47 dead space marker, was calculated with each arterial blood gas.

48 A total of 409 patients with arterial blood gases analyzed at least once and with a c

49 in Sherpa compared to lowlanders we measured arterial blood gases and global cerebral blood flow (dup

50 he respiratory center's output to changes in arterial blood gases and pH, is one of the most importan

51 rcised at approximately 85% of maximum while arterial blood gases and work of breathing were assessed

52 very (CDO(2) ), oesophageal temperature, and arterial blood gases during exposure to three commonly e

53 We studied 1,034 arterial blood gases from 703 patients; 650 arterial blo

54 r OHS is not very high (<20%) but to measure arterial blood gases in patients strongly suspected of h

55 arterial blood gases from 703 patients; 650 arterial blood gases were associated with SpO2 less than

56 Cardiorespiratory and arterial blood gases were collected throughout both exer

57 Arterial blood gases were within the normal range and ef

58 dmissions of ventilated TBI patients who had arterial blood gases within 24 h of admission to the ICU

59 e intervention was associated with 128 fewer arterial blood gases, 73 fewer chest radiographs, and 16

60 imate diaphragm energy expenditure (effort), arterial blood gases, airway pressure, tidal volume and

61 ntaris muscles while monitoring respiration, arterial blood gases, and blood glucose in mice exposed

62 genation macrocirculation, echocardiography, arterial blood gases, and microcirculation parameters di

63 the last minutes of each phase, we measured arterial blood gases, changes in end-expiratory lung vol

64 t program designed to decrease the avoidable arterial blood gases, chest radiographs, and RBC utiliza

65 primary outcome was the number of orders for arterial blood gases, chest radiographs, and RBCs per pa

66 Arterial blood gases, dyspnea, and comfort were recorded

67 3 +/- 2 kg m(-2) ), FMD (Duplex ultrasound), arterial blood gases, Hct and [Hb], blood viscosity, and

68 Toward the end of each phase, we measured arterial blood gases, inspiratory effort, and work of br

69 e end-expiratory pressure level, we assessed arterial blood gases, respiratory mechanics, ventilation

70 Arterial blood gases, respiratory rate, and patient comf

71 Mechanical ventilator settings, arterial blood gases, vital signs, and use of vasopresso

72 Acid-base physiology was measured with arterial blood gases.

73 Although it is well established that arterial blood generally has higher concentrations of gl

74 rinsulinemic (4x basal) hyperglycemic clamp (arterial blood glucose 146 +/- 2 mg/dL) with portal GLC

75 od leaving the CNS capillary bed compared to arterial blood, indicating efflux from the CNS into the

76 brain arterio-venous malformations, shunting arterial blood into the brain's deep venous system throu

77 fter percutaneous coronary intervention, and arterial blood lactate at admission >5 mmol/l.

78 We suggest that the rapid rise pattern of arterial blood nicotine concentration stimulates and the

79 arotid body is a sensory organ for detecting arterial blood O2 levels and reflexly mediates systemic

80 sensing method for measuring pulse rate and arterial blood oxygenation.

81 Arterial blood PaO2 and PaCO2 during the first 24 hours

82 Hypercapnia is clinically defined as an arterial blood partial pressure of CO2 of above 40 mmHg

83 ts (44.8%) had lactic acidosis defined as an arterial blood pH less than 7.35 and a lactate concentra

84 control rate (defined as achievement of mean arterial blood pressure >=65 mm Hg, with urine flow >=0.

85 etting by low systolic (</=90 mm Hg) or mean arterial blood pressure (</=65 mm Hg) accompanied by sig

86 increases sympathetic nerve activity (SNA), arterial blood pressure (ABP) and breathing.

87 er 9th, 2014), with continuous monitoring of arterial blood pressure (ABP) and intracranial pressure

88 arotid sinus nerve denervation (CSD) reduces arterial blood pressure (ABP) in SHR.

89 Real arterial blood pressure (ABP) measurements from 34 traum

90 pertonic NaCl produces a greater increase in arterial blood pressure (ABP) than equi-osmotic mannitol

91 The arterial blood pressure (ABP) was gradually reduced unti

92 lin is a ubiquitous peptide that can elevate arterial blood pressure (ABP) yet understanding of the m

93 n of central chemoreceptors by CO2 increases arterial blood pressure (ABP), sympathetic nerve activit

94 red whether the methods identify the optimal arterial blood pressure (ABPopt) and lower limit of auto

95 calculated by transfer function analysis of arterial blood pressure (BP) and cerebral blood flow vel

96 al mechanisms responsible for maintenance of arterial blood pressure (BP) during haemorrhage in human

97 The kidney is an important organ for arterial blood pressure (BP) maintenance.

98 can predict the limb BCG in responses to the arterial blood pressure (BP) waves in the aorta was deve

99 minute ventilation (VI), heart rate (HR) and arterial blood pressure (BP).

100 NMES on muscle mass, insulin sensitivity and arterial blood pressure (BP).

101 (CBF) recovery following a sudden change in arterial blood pressure (BP).

102 P=0.007), but with only modest falls in mean arterial blood pressure (by 4 mm Hg; P=0.004).

103 from t = 0-70 min plus hemorrhage to a mean arterial blood pressure (MAP) of 30 mmHg from t = 40-70

104 ntraoperative laser speckle imaging and mean arterial blood pressure (MAP) recording.

105 heart rate (HR) and digital heart-level mean arterial blood pressure (MAP) were continuously recorded

106 gulation (CA) is often expressed by the mean arterial blood pressure (MAP)-cerebral blood flow (CBF)

107 ow (CBF) response to a sudden change in mean arterial blood pressure (MAP).

108 transient tachycardia and a biphasic caudal arterial blood pressure (PCA) response that are in direc

109 vessels to appropriately react to changes in arterial blood pressure (pressure reactivity) is impaire

110 ion coefficient = -0.29; p = 0.015) and mean arterial blood pressure (repeated-measures correlation c

111 dichotomized subjects into two groups: mean arterial blood pressure 70-90 and greater than 90 mm Hg.

112 er than 90 mm Hg (42%) as compared with mean arterial blood pressure 70-90 mm Hg (15%) (absolute risk

113 No cases of sustained resumption of arterial blood pressure activity were recorded, and no i

114 We calculated the mean arterial blood pressure and a priori dichotomized subjec

115 an important role in homeostatic control of arterial blood pressure and brain blood flow.

116 Fetuses were first instrumented to measure arterial blood pressure and carotid artery blood flow an

117 if cardiopulmonary resuscitation-targeted to arterial blood pressure and coronary perfusion pressure

118 n system (RAS) is a principal determinant of arterial blood pressure and fluid and electrolyte balanc

119 er hemodilution, treated animals show higher arterial blood pressure and have a stable body temperatu

120 thetic control circuits to increase systemic arterial blood pressure and heart rate with the purpose

121 [OH]D) concentration is associated with high arterial blood pressure and hypertension risk, but wheth

122 gical or biochemical measure, including mean arterial blood pressure and inotrope use during the 48 h

123 on of AIP into the PVN significantly reduced arterial blood pressure and lumbar sympathetic nerve dis

124 he association of systolic and mean invasive arterial blood pressure and noninvasive blood pressure w

125 difference between clinically observed mean arterial blood pressure and optimal mean arterial blood

126 difference between clinically observed mean arterial blood pressure and optimal mean arterial blood

127 difference between clinically observed mean arterial blood pressure and optimal mean arterial blood

128 erve activity (SNA) and fluctuations in mean arterial blood pressure and R-R interval.

129 tor-PKC activity in the hypothalamus reduces arterial blood pressure and sympathetic nerve discharges

130 arterial blood pressure outside optimal mean arterial blood pressure and the absolute difference betw

131 Arterial blood pressure and ventilation rate (breaths/mi

132 lood volume and subsequent titration of mean arterial blood pressure approximately 40 mm Hg).

133 perfusion pressure (CPP), calculated as mean arterial blood pressure at midbrain level minus ICP, was

134 Metaboreceptor function, defined as mean arterial blood pressure at the end of postexercise circu

135 diopulmonary bypass did not differ, the mean arterial blood pressure at the limit of autoregulation a

136 rial blood pressure was defined as that mean arterial blood pressure at the lowest cerebral oximetry

137 The longest period of cessation of arterial blood pressure before resumption was 89 seconds

138 terial blood pressure closer to optimal mean arterial blood pressure calculated by bedside multimodal

139 ure have worse outcomes than those with mean arterial blood pressure closer to optimal mean arterial

140 Optimal mean arterial blood pressure could be calculated in 89 patien

141 Mean arterial blood pressure decreased and heart rate increas

142 Mean velocity index based on arterial blood pressure did not reach statistical signif

143 Although the average mean arterial blood pressure during cardiopulmonary bypass di

144 spital cardiopulmonary resuscitation with 1) arterial blood pressure during cardiopulmonary resuscita

145 01 to 0.37 +/- 0.01 mm (P < 0.001), and mean arterial blood pressure from 83 +/- 1 to 78 +/- 2 mmHg (

146 ean arterial blood pressure and optimal mean arterial blood pressure greater than 10 mm Hg and durati

147 bility of good neurologic outcome, with mean arterial blood pressure greater than 110 mm Hg having th

148 n 10 mm Hg and duration outside optimal mean arterial blood pressure greater than 80% had increased m

149 significantly higher in patients with a mean arterial blood pressure greater than 90 mm Hg (42%) as c

150 el adjusting for potential confounders, mean arterial blood pressure greater than 90 mm Hg was associ

151 269 patients included, 159 (59%) had a mean arterial blood pressure greater than 90 mm Hg.

152 mean arterial pressure outside optimal mean arterial blood pressure have worse outcomes than those w

153 The apelin-apelin receptor system affects arterial blood pressure homeostasis; however, the centra

154 (100 mg/kg i.p.) significantly lowered mean arterial blood pressure in normotensive and hypertensive

155 mortality (p < 0.001) than systolic invasive arterial blood pressure in the same range (</=70 mm Hg).

156 Mean arterial blood pressure increased significantly over tim

157 n sympathetic nerve activity, heart rate and arterial blood pressure induced by reductions in cerebra

158 Arterial blood pressure is a major determinant of region

159 othesis that elevated postresuscitation mean arterial blood pressure is associated with neurologic ou

160 When mean arterial blood pressure is below the lower limit of auto

161 Arterial blood pressure is controlled by vasodilatory fa

162 py-based bedside calculation of optimal mean arterial blood pressure is feasible and might be a promi

163 EY POINTS: Dysfunctions in CNS regulation of arterial blood pressure lead to an increase in sympathet

164 Orthostatic intraocular pressure and mean arterial blood pressure may be a helpful early screening

165 st compressions for >/=1 minute and invasive arterial blood pressure monitoring before and during CPR

166 ant association between ventilation rate and arterial blood pressure occurred in children 1 year old

167 Several studies document high mean arterial blood pressure of giraffes of about 200 mm Hg.

168 zard analysis, duration outside optimal mean arterial blood pressure of greater than 80% of monitorin

169 ean arterial blood pressure and optimal mean arterial blood pressure of more than 10 mm Hg (adjusted

170 increase cardiac output but reduce systemic arterial blood pressure only modestly.

171 s with no significant changes in either mean arterial blood pressure or heart rate, consistent with t

172 Neither losartan nor divalinal affected arterial blood pressure or significantly altered the amy

173 s associated with a shorter duration of mean arterial blood pressure outside optimal mean arterial bl

174 in rats by withdrawing blood until the mean arterial blood pressure reached 27 +/- 1 mm Hg for the f

175 bilateral wrist) and, when available, intra-arterial blood pressure readings (IABP) were included.

176 In four subjects, arterial blood pressure resumed following cessation of a

177 de a novel method for precisely guiding mean arterial blood pressure targets during cardiopulmonary b

178 t rest led to significantly higher values of arterial blood pressure than without muscle loading, and

179 patients (97%), and the median optimal mean arterial blood pressure was 89.7 mm Hg (84.6-100 mm Hg).

180 s of an ICU admission, the minimum diastolic arterial blood pressure was a hemodynamic variable that

181 on and the duration and degree to which mean arterial blood pressure was below the autoregulation thr

182 Optimal mean arterial blood pressure was defined as that mean arteria

183 Mean arterial blood pressure was measured noninvasively after

184 Mean arterial blood pressure was normal in the NA group; seve

185 Mean arterial blood pressure was reduced during the early rep

186 Surface ECG and peripheral arterial blood pressure waveform via arterial line were

187 ased analysis of cerebral blood velocity and arterial blood pressure waveforms in 11 astronauts befor

188 Absence of slow arterial blood pressure waves (odds ratio, 2.7; p < 0.00

189 Heart rate (HR) and mean arterial blood pressure were monitored continuously.

190 tput, systemic vascular resistance, and mean arterial blood pressure were unchanged.

191 vity, adrenal sympathetic nerve activity and arterial blood pressure whereas equi-osmotic mannitol/so

192 ed vasoactive drugs to achieve a target mean arterial blood pressure with 82 centers (68.9%) employin

193 d to determine if targeting an elevated mean arterial blood pressure would improve neurologic outcome

194 by peak exercise cardiac power output (mean arterial blood pressure x cardiac output) and functional

195 ls as inputs (intracranial pressure and mean arterial blood pressure) is an additional asset.

196 ody mass index, waist-height ratio, and mean arterial blood pressure).

197 orrelated with diastolic, systolic, and mean arterial blood pressure, a surrogate marker for arterial

198 e ionotropy, angiogenesis, reduction of mean arterial blood pressure, and apoptosis.

199 No differences were found in temperature, arterial blood pressure, and oxygenation between alpha-s

200 Cerebral blood flow (CBF) is controlled by arterial blood pressure, arterial CO2, arterial O2, and

201 Waveforms of intracranial pressure and arterial blood pressure, baseline Glasgow Coma Scale and

202 mean occlusive divided by mean nonocclusive arterial blood pressure, both subtracted by central veno

203 ct brain perfusion in the face of changes in arterial blood pressure, but little is known about indiv

204 Arterial blood pressure, cardiac output, tissue oxygen t

205 art rate variability, intracranial pressure, arterial blood pressure, cerebral perfusion pressure, an

206 hAT expression in CD4(+) cells have elevated arterial blood pressure, compared to littermate controls

207 Invasive arterial blood pressure, electrocardiogram, and oxygen s

208 ide (ETCO2), oxygen saturation (SaO2), intra-arterial blood pressure, electrocardiography (EKG), and

209 vasodilation, SIL unexpectedly elevated mean arterial blood pressure, failed to inhibit MFS aortic ro

210 observed in controls; normalization of mean arterial blood pressure, heart rate, and increased survi

211 Mean arterial blood pressure, heart rate, and survival were m

212 Mean arterial blood pressure, heart rate, intracranial pressu

213 All patients had continuous monitoring of arterial blood pressure, intracranial pressure, and cere

214 For every period, mean values (+/- SDs) of arterial blood pressure, intracranial pressure, pressure

215 concomitant measurement of continuous intra-arterial blood pressure, the gold standard for shock mon

216 Over ascending ranges of mean arterial blood pressure, there was a dose-response incre

217 uctuations of cerebral perfusion pressure or arterial blood pressure.

218 ges in femoral vascular conductance and mean arterial blood pressure.

219 tion as a promising novel mechanism to lower arterial blood pressure.

220 anglion (SNA), left cardiac vagus (VNA), and arterial blood pressure.

221 ttenuated high-fat diet-induced elevation in arterial blood pressure.

222 usly with continuous recording of peripheral arterial blood pressure.

223 ctivity continued after the disappearance of arterial blood pressure.

224 late regional sympathetic nerve activity and arterial blood pressure.

225 ean arterial blood pressure and optimal mean arterial blood pressure.

226 o compare survival outcomes and intra-arrest arterial blood pressures between children receiving card

227 ered (strain B) or decreased (strain C) mean arterial blood pressures compared to their corresponding

228 nalysis of exosomes purified from fetal cord arterial blood revealed a total of 328 proteins, among w

229 t model together with a metabolite-corrected arterial blood sampler input function (BSIF).

230 ty-shear rate relationship was obtained from arterial blood samples analyzed using a standard viscosi

231 Subjects were imaged for 3.5 h, with arterial blood samples obtained throughout.

232 Collection of nine arterial blood samples over 24 hours for iohexol plasma

233 Arterial blood samples were collected as a reference sta

234 Arterial blood samples were collected as the reference s

235 Arterial blood samples were collected to calculate the m

236 Arterial blood samples were drawn for arterial input fun

237 Discrete arterial blood samples were taken during (11)C-HED scans

238 Manual arterial blood samples were used for calibration and cor

239 Arterial blood samples, collected at 7 time points, were

240 pted microcatheter aspiration of 3 different arterial blood samples: (1) within the core of the occlu

241 In addition, arterial blood sampling and dynamic (15)O-H(2)O scans we

242 Full tracer kinetic models require arterial blood sampling and dynamic image acquisition.

243 n rhesus macaques were acquired for 2 h with arterial blood sampling and metabolite analysis to measu

244 A 90-min dynamic PET scan with arterial blood sampling and metabolite analysis was acqu

245 Methods: A 90-min dynamic PET scan with arterial blood sampling and metabolite analysis was acqu

246 Arterial blood sampling and metabolite analysis were con

247 Arterial blood sampling and metabolite analysis were con

248 ders) underwent (18)F-DPA-714 PET scans with arterial blood sampling and metabolite analysis.

249 and time activity curve were assessed using arterial blood sampling and served as measures for recep

250 netic analysis of a 90-min dynamic scan with arterial blood sampling is recommended for the quantific

251 standardized uptake values, suggesting that arterial blood sampling may not be necessary for modelin

252 Continuous arterial blood sampling over the first 15 min was follow

253 Continuous and manual arterial blood sampling provided calibrated plasma trace

254 dynamic (18)F-JNJ-64413739 PET/MRI scan with arterial blood sampling to determine the appropriate kin

255 inyl)acetamide) PET scans were acquired with arterial blood sampling to estimate the metabolite-corre

256 culation, a dynamic (18)F-FHNP PET scan with arterial blood sampling was acquired from rats treated w

257 1)C-PBR28 or (R)-(11)C-PK11195 PET scan with arterial blood sampling was obtained.

258 Dynamic PET imaging with arterial blood sampling was performed in 3 baboons, with

259 Arterial blood sampling was performed with chromatograph

260 ing of dynamic tumor uptake data with online arterial blood sampling was performed.

261 Small-animal PET scans with arterial blood sampling were obtained for 4 groups of is

262 Input functions were obtained through arterial blood sampling with metabolite analysis.

263 a input functions were obtained using online arterial blood sampling with metabolite corrections deri

264 The need for arterial blood sampling, however, limits clinical applic

265 PET quantification of tau deposits, avoiding arterial blood sampling.

266 PET quantification of tau deposits avoiding arterial blood sampling.

267 min after bolus injection of (18)F-T807 with arterial blood sampling.

268 underwent 180-min PET with (18)F-AV-1451 and arterial blood sampling.

269 underwent 180-min PET with (18)F-AV-1451 and arterial blood sampling.

270 min after bolus injection of (18)F-T807 with arterial blood sampling.

271 subjects underwent two PET measurements with arterial blood sampling.

272 n dynamic (11)C-HED PET/CT scans with online arterial blood sampling.

273 a method to eliminate the need for invasive arterial blood sampling.

274 th static whole-body PET scans not requiring arterial blood sampling.

275 d Yorkshire x Landrace pigs, concurrent with arterial blood sampling.

276 ) underwent 150-min dynamic SPECT scans with arterial blood sampling.

277 put functions were obtained using continuous arterial blood-sampling as well as using image-derived m

278 citabine directly into the pancreas, via its arterial blood supply, has a superior therapeutic effect

279 onally accumulated in watershed areas of low arterial blood supply.

280 ncer classification because of its exclusive arterial blood supply.

281 The human circulatory system consists of arterial blood that delivers nutrients to tissues, and v

282 ke ( VO2 ) at which La(-) accumulates in the arterial blood (the lactate threshold; LT).

283 ted hypoxemia (partial pressure of oxygen in arterial blood to fraction of inspired oxygen ratio [PFR

284 ohimbine with 90-min dynamic PET and sampled arterial blood to measure intact (11)C-yohimbine in plas

285 MRI to quantify rates of water delivery from arterial blood to ventricular cerebrospinal fluid.

286 Global CBF, intra-cranial arterial blood velocities, extra-cranial blood flows, an

287 hamber) RV volume (RV(EV)), distal pulmonary arterial blood vessel volume (arterial BV5: vessels <5 m

288 nature and span a wide range of scales, from arterial blood vessels and bronchial mucus transport in

289 ociated with increased mineralization of the arterial blood vessels and cardiac valves.

290 inal ganglion cell layer and in the edges of arterial blood vessels in the transgenic mice.

291 Less permeable arterial blood vessels maintain haematopoietic stem cell

292 Sufficient blood flow to tissues relies on arterial blood vessels, but the mechanisms regulating th

293 ic mineralization in the skin, eyes, and the arterial blood vessels.

294 ctopic tissue mineralization in the skin and arterial blood vessels.

295 he bolus at the infusion rate = 60 min), and arterial blood was collected for data quantification.

296 Arterial blood was collected for invasive kinetic modeli

297 For 3 of the brain SPECT studies, arterial blood was collected for invasive modeling.

298 iably reduce CBF or CDO(2) Oxygen content in arterial blood was fully restored with acclimatisation t

299 During all PET scans, arterial blood was monitored continuously.

300 Arterial blood was sampled for measurement of blood radi