ライフサイエンスコーパス: perfusion

1 umor spheroids instead of single cells under perfusion.

2 and facilitating greater intramuscular blood perfusion.

3 qual to 65 mm Hg and signs of altered tissue perfusion.

4 ative substrate consumption, efficiency, and perfusion.

5 -time visualization of tumor vasculature and perfusion.

6 a subsequent 3 hours of normothermic machine perfusion.

7 quire multi-organ systems linked by vascular perfusion.

8 ing basal vascular tone and impairing tissue perfusion.

9 data acquisition precludes quantification of perfusion.

10 he sweat gland resulting in a lack of tissue perfusion.

11 espectively) indicated significantly reduced perfusion.

12 supplied by a vasculature-like microfluidic perfusion.

13 intracranial pressure and decreased cerebral perfusion.

14 of high metabolic activity and insufficient perfusion.

15 ers as a result of cold ischemia and machine perfusion.

16 f neighboring host vessels with microchannel perfusion.

17 ging of function and fibrosis in addition to perfusion.

18 ure and heart rate induced by falls in brain perfusion.

19 ad an initial rhythm of bradycardia and poor perfusion.

20 or renal venous pressures to increase renal perfusion.

21 s have not exceeded three days of continuous perfusion.

22 of warm ischemia, before hypothermic machine perfusion.

23 armacokinetics for different combinations of perfusion (0.001-0.1 mL/g/min) and receptor density (1-1

24 However, even better results (perfusion, 0.018 +/- 0.009 mL/g/min; receptor density, 1

25 Perfusion, a measure of microvascular blood flow, provid

26 h multiple microhemorrhages (11.3%), 22 with perfusion abnormalities (47.7%), and three with restrict

27 indicate the onset of subclinical pulmonary perfusion abnormalities that could herald the developmen

28 Correlations between individual perfusion, age and cognitive scores (COGNITO battery) we

29 Understanding early preclinical perfusion alterations may improve understanding of AD pa

30 f spastic hypertonia and intramuscular blood perfusion among individuals with chronic stroke.

31 tion, and Cept1Lp/LpCre (+) mice had reduced perfusion and angiogenesis in ischemic hind limbs.

32 Cortical perfusion and CA impairment were heterogeneously distrib

33 a symptom complex caused by impaired digital perfusion and can occur as a primary phenomenon or secon

34 luorouracil for five days through continuous perfusion and cell viability was analysed on-chip at dif

35 Manifesting in abnormal cerebral perfusion and cerebrospinal fluid convection, present ob

36 the association between a decrease in tumor perfusion and clinical benefit warrants further investig

37 function depends on adequate cerebrovascular perfusion and control.

38 l vasculature in tumors leads to poor tissue perfusion and cytostatic drug delivery.

39 osis, associated findings, adenopathies, and perfusion and diffusion parameters.

40 ngiography, and CTP with Rapid Processing of Perfusion and Diffusion software mismatch determination)

41 nor selection, pancreas processing, pancreas perfusion and digestion, islet counting and culture, isl

42 igher perfusion, ECV, and MBV at stress, and perfusion and ECV at rest (p < 0.01 for all).

43 Sex is an independent contributor to perfusion and ECV, beyond other physiological factors th

44 The connected chambers allowed for perfusion and enabled replication of pressure/volume rel

45 cement (i.e. central hypovolaemia), cerebral perfusion and g-tolerance, and their inter-relationships

46 AHC) upon cardiovascular responses, cerebral perfusion and g-tolerance.

47 Tumor perfusion and hypoxia are two important features; howeve

48 neys, ascertaining the impact of the drug on perfusion and IRI-related parameters.

49 for detection of CAD by assessing myocardial perfusion and late gadolinium enhancement (LGE) imaging.

50 transdermal delivery of DFO improves tissue perfusion and mitigates chronic radiation-induced skin f

51 une signaling and contributes to recovery of perfusion and preservation of ischemic tissue.

52 f this work was to determine a minimal tumor perfusion and receptor density for (177)Lu-DOTATATE ther

53 ells had the strongest effect on the minimal perfusion and receptor density for standard and optimize

54 17beta-Estradiol improved microcirculatory perfusion and reduced intestinal edema and hemorrhage af

55 radiol was effective in improving mesenteric perfusion and reducing intestinal edema and hemorrhage a

56 ICA provides easy-to-implement, in vivo-like perfusion and stable oxygenation culture conditions in v

57 technique to simultaneously quantify muscle perfusion and T(2)* at 7T with improved temporal resolut

58 te successful simultaneous quantification of perfusion and T(2)* in skeletal muscle using the develop

59 The time constants for 50% perfusion and T(2)* recovery were 54.1 +/- 10 s and 68.5

60 poxic conditions by improving uteroplacental perfusion and thereby justify further investigation into

61 unclear, and the effects of HIV on pulmonary perfusion and ventilation are unknown.

62 myocardial oxygen consumption, impair tissue perfusion, and are frequently ineffective.

63 elium-mediated vasorelaxation, microvascular perfusion, and blood pressure during acid-base disturban

64 t role during blood vessel formation, tissue perfusion, and oxygen restoration.

65 irect role of IgE in angiotensin-II (Ang-II) perfusion- and peri-aortic CaCl(2) injury-induced AAA in

66 Abdominal normothermic regional perfusion (aNRP) for donation after circulatory death is

67 w areas associated with focal capillary hypo perfusion areas.

68 nd (2) highlight the potential role of using perfusion as a biosignature of MDD.

69 onary artery disease referred clinically for perfusion assessment.

70 ized liver scaffolds that can maintain blood perfusion at physiological pressures might eventually he

71 EADs and focal activity during isoproterenol perfusion (at 30 nmol/L, n=7/12 and 100 nmol/L n=8/12 he

72 y interrupt the permanent cessation of brain perfusion because, theoretically, collateral circulation

73 PulseCam can detect subtle changes in blood perfusion below the skin with at least two times better

74 ase conditions modify artery tone and tissue perfusion but the involved vascular-sensing mechanisms a

75 In situ kidney perfusion can be performed at either 4 degrees C (in sit

76 Lack of blood perfusion can cause irreversible cell damage.

77 cations, patient outcomes, and use of distal perfusion cannula, were extracted from selected articles

78 was assessed by quantitative 3-Tesla stress perfusion cardiac magnetic resonance imaging and dichoto

79 nce of the benefits of both adenosine stress perfusion cardiac MRI and coronary CT angiography-derive

80 normalized against noninfarcted tissue and 6 perfusion categories from 0% to >100% were defined.

81 determine if arterial spin labeled (ASL) MRI perfusion changes are associated with tumor response and

82 t this system enabled the detection of acute perfusion changes as well as the recording of temporal r

83 ing to detect disease-associated bone marrow perfusion changes.

84 Vasodilator stress and rest myocardial perfusion CMR and LGE imaging had high diagnostic accura

85 atients with early glaucoma had more loss of perfusion compared with conventional structural loss in

86 or complete response are detected by volume perfusion computer tomography (VPCT).

87 time of onset with perfusion-diffusion MRI, perfusion CT, or MRI with diffusion weighted imaging-flu

88 val-time-sensitive (ATS) computed tomography perfusion (CTP) algorithms in Philips IntelliSpace Porta

89 noncontrast computed tomography (CT) and CT perfusion (CTP).

90 how scalable strategies for the fabrication, perfusion culture and volumetric analysis of large tissu

91 nterior segments of human eyes maintained in perfusion culture.

92 creted factor profile during several days of perfusion culture.

93 ates proliferation of endogenous TM cells in perfusion cultured human eyes from aged donors.

94 rences in the total spatial heterogeneity of perfusion (CV(2) (Qtotal)) and its components (CV(2) (Qt

95 lization resulted in significantly decreased perfusion (DCE MRI arterial flow, P = .002; IVIM pseudod

96 erfused blood volume (PBV) maps recorded: i) perfusion defect 'pattern' (wedge-shaped, mottled or amo

97 on, risk area (before treatment), myocardial perfusion defect over time (infarct size), and global lo

98 In patients without regional perfusion defects on clinical read and no known macrovas

99 Perfusion defects on DECT (assessable in 18/20 [90%]) we

100 n=21), mottled (n=4), and wedge-shaped (n=2) perfusion defects were observed (M=20; mean age=56 +/-8.

101 Geometric perfusion deficits, an OCTA biomarker based on oxygen di

102 , parafoveal vessel length density (VD), and perfusion density (PD) were corrected for magnification

103 Vessel length density (VLD), perfusion density (PD), and foveal avascular zone (FAZ)

104 Perfusion density and vessel length density (VD) were ex

105 Perfusion did not correlate with cognitive test scores.

106 Likewise, raising pH or apical perfusion did not improve clearance of mucus strands fro

107 atment, whereas post-cardiac arrest cerebral perfusion differences were diminished.

108 with stroke with unknown time of onset with perfusion-diffusion MRI, perfusion CT, or MRI with diffu

109 Area of trans-catheter perfusion dynamically quantified on representative slice

110 ermined by quantitative real-time myocardial perfusion echocardiography and speckle tracking echocard

111 nfarct size obtained by real-time myocardial perfusion echocardiography and their value in preventing

112 Compared to males, females had higher perfusion, ECV, and MBV at stress, and perfusion and ECV

113 To test this, we combined fast perfusion electrophysiology, molecular dynamics simulati

114 ubstrate plus inhibitor using electroosmotic perfusion (EOP).

115 lgorithm that helps us reduce error in blood perfusion estimate below 10% in different motion scenari

116 The role of ex vivo normothermic perfusion (EVNP) in both organ viability assessment and

117 Renal perfusion/flow improved with CD47 blockade, with a corre

118 anced first-pass vasodilator stress and rest perfusion followed by LGE imaging.

119 evidence for ASL in detecting differences in perfusion for multiple brain regions thought to be impor

120 f death, or the use of normothermic regional perfusion for the in situ preservation of organs.

121 Perfusion fraction (f) was significantly higher for tumo

122 Radionuclide imaging of myocardial perfusion, function, and viability has been established

123 the impact of hyperoxia upon global cerebral perfusion (gCBF), cognitive performance and cortical ele

124 Hyperoxia reduces global cerebral perfusion (gCBF), increases reactive oxygen species with

125 that is not explained by differences in mean perfusion, gravitational gradients, or large vessel anat

126 at is not explainable by differences in mean perfusion, gravitational gradients, or large vessel anat

127 e perfusate throughout the perfusion in both perfusion groups.

128 rkload in beating and nonbeating Langendorff perfusions had no effect on the calculated HBP flux at ~

129 sion (NEVKP) with hypothermic anoxic machine perfusion (HAMP) and static cold storage (SCS) in a porc

130 Micropush-pull perfusion has been used to determine which nitric oxide

131 d patients with PAH have increased pulmonary perfusion heterogeneity that is not explainable by diffe

132 physiology and PAH have increased pulmonary perfusion heterogeneity that is not explained by differe

133 high pressures, but remodelling may increase perfusion heterogeneity.

134 pplemental oxygen during hypothermic machine perfusion (HMP) could improve the outcome of kidneys don

135 nation during continuous hypothermic machine perfusion (HMP).

136 ted blocks to oxygenated hypothermic machine perfusion (HMPO(2)), the other to HMP without oxygenatio

137 ith and without hypothermic oxygenated liver perfusion (HOPE) before transplantation.

138 ed a limit of hypothermic oxygenated machine perfusion (HOPE).

139 tu NMP, and the ongoing development of organ perfusion hubs.

140 cle by processing an incoming time series of perfusion images.

141 The performance of SPECT myocardial perfusion imaging (MPI) may deteriorate in smaller heart

142 exclude haemorrhage, but the addition of CT perfusion imaging and angiography allows a positive diag

143 (Stress CMR Perfusion Imaging in the United States [SPINS]; NCT03192

144 In the multicenter SPINS (Stress CMR Perfusion Imaging in the United States) study, 2,349 con

145 as a non-invasive and non-contrast enhanced perfusion imaging method, is an attractive approach for

146 Existing camera-only blood perfusion imaging modality suffers from two core challen

147 d, motion-robust, and highly sensitive blood perfusion imaging modality with 1 mm spatial resolution

148 of patients in an extended time window using perfusion imaging.

149 tiffening was also related to lower cerebral perfusion in 18.4% of GM, with associations surviving Bo

150 ly increased in the perfusate throughout the perfusion in both perfusion groups.

151 genation, mitochondrial function, and tissue perfusion in EAE.

152 We evaluated regional pulmonary perfusion in Fontan patients (n = 5), healthy young cont

153 nd fMRI analysis revealed improved allograft perfusion in LP versus NA mice.

154 nalysis revealed significantly improved skin perfusion in mice receiving prophylactic DFO.

155 usion of the descending aorta prevents brain perfusion in most cases.

156 peutic strategy for restoring uteroplacental perfusion in pregnancy disorders.

157 ects of subnormothermic (22 degrees C) blood perfusion in the preservation of porcine donation after

158 Perfusion increased from cycle 4 to disease progression

159 entify using existing modalities such as the perfusion index measured using a pulse oximeter.

160 n survivors than in nonsurvivors; peripheral perfusion index was similar in the two groups.

161 Impaired microvascular perfusion is central to the development of coma and lact

162 However, quantification of perfusion is challenging due to the non-linearity betwee

163 -dependent (BOLD) cardiac MRI for myocardial perfusion is limited by inadequate spatial coverage, ima

164 lowing the Fontan procedure, where pulmonary perfusion is passive, and heterogeneity may be increased

165 Hypothermic machine perfusion is systematically used.

166 ular degeneration (AMD), the role of retinal perfusion is unclear.

167 ical biopsy tool for use during in vivo lung perfusion (IVLP) procedures within a hospital setting.

168 eumonia but also markedly impaired pulmonary perfusion likely caused by pulmonary angiopathy and thro

169 crostructural integrity and reduced cerebral perfusion, likely due to increased transmission of pulsa

170 XY movement, peristaltic pumps equipped with perfusion lines for chemical transport, and mirrors for

171 ng: D-dimer, CTPA, scintillation ventilation perfusion lung scanning or formal pulmonary angiography.

172 The low-perfusion map and LPA and FPL parameters are able to ass

173 The described CNN was capable of cardiac perfusion mapping and integrated an automated inline imp

174 we developed computational tools to generate perfusion maps in 3D of tumor blood flow, and identified

175 r than curve fitting, obtaining whole volume perfusion maps in just over 10 s.

176 e lung function, oxygenation and ventilation/perfusion matching, without impairment of hemodynamics o

177 itative thresholds and analysis based on DSA perfusion may assist with real-time dosage estimation an

178 Background Tumor perfusion may inform therapeutic response and resistance

179 Increased perfusion may reflect a functional 'compensation' mechan

180 Interestingly, a decrease in tumor perfusion measured with (15)O-H(2)O PET after only 14 d

181 useful biomarkers include the NIHSS and the perfusion measurements MTT and Tmax.

182 stent and saturated oxygen distribution from perfusion media (i.e., blood, or cell culture media) to

183 Using a constant pressure perfusion method, outflow facility was measured in paire

184 ical vasospasm and quantified the changes in perfusion metrics between pre- and post- verapamil admin

185 The electroosmotic perfusion-microdialysis probe and associated method were

186 The ventilation-perfusion mismatch was elevated (median, 34% [32-45%] of

187 th unknown time of onset with a DWI-FLAIR or perfusion mismatch, intravenous alteplase resulted in be

188 mbination of pulmonary embolism, ventilation-perfusion mismatching in the noninjured lung, and normal

189 Quantitative MBV [%] and perfusion [ml/min/g] maps were acquired during adenosine

190 function declines during ESHP regardless of perfusion mode.

191 The benefits of cold pulsatile machine perfusion (MP) for the storage and transportation of kid

192 Machine perfusion (MP) is at the forefront of innovation in mode

193 e short time interval (<30 days) between DCE perfusion MRI and biopsy, DCE perfusion MRI performed be

194 rospective study, patients who underwent DCE perfusion MRI and lesion biopsy between May 2015 and May

195 Diffusion and perfusion MRI can be used to evaluate the response of HC

196 most promising clinical application for IVIM perfusion MRI is oncology.

197 ground Dynamic contrast agent-enhanced (DCE) perfusion MRI may help differentiate between nonneoplast

198 DCE perfusion MRI parameter V(p) was calculated by using the

199 dicated that dynamic contrast agent-enhanced perfusion MRI parameter, fractional plasma volume, was a

200 rfusion MRI performed before biopsy, and DCE perfusion MRI performed at the same spine level as biops

201 s) between DCE perfusion MRI and biopsy, DCE perfusion MRI performed before biopsy, and DCE perfusion

202 treatment on vertebrae of interest, poor DCE perfusion MRI quality, nondiagnostic biopsy, and extensi

203 ported by two prior state-of-the-art cardiac perfusion MRI studies.

204 volume (V(p)), a parameter derived from DCE perfusion MRI, and histopathologic diagnosis for spinal

205 P either at the start (n = 6), or end of the perfusion (n = 5) and outcomes were compared to standard

206 pared continuous normothermic ex vivo kidney perfusion (NEVKP) with hypothermic anoxic machine perfus

207 Normothermic machine perfusion (NMP) bears the potential for significant prol

208 Normothermic machine perfusion (NMP) enables optimized ex-vivo preservation o

209 Normothermic machine perfusion (NMP) is an emerging modality for kidney prese

210 Normothermic machine perfusion (NMP) technologies are emerging as an importan

211 mothermically perfused (normothermic machine perfusion, NMP) human kidneys with urine recirculation (

212 In situ normothermic regional perfusion (NRP) or restarting the heart in the donor's b

213 ]) or 33-36 degrees C (normothermic regional perfusion [NRP]).

214 vasoconstriction and compromise brain tissue perfusion.Objectives: To determine if the magnitude of P

215 tion with response, with a decrease in tumor perfusion of 56% +/- 23% (mean +/- SD) versus 18% +/- 32

216 ed Controlled Trials for hypothermic machine perfusion of kidneys.

217 Normothermic perfusion of liver grafts before transplantation effecti

218 Perfusion of TEBVs at a physiological shear stress with

219 ssessment was performed using NMP via double perfusion of the hepatic artery and portal vein.

220 smatching in the noninjured lung, and normal perfusion of the relatively small fraction of injured lu

221 yocardium, and compares the effect of acute (perfusion only) versus prolonged (2 weeks pre-treatment

222 ges of small metastases, tumor inflammation, perfusion, oxygenation, and acidity.

223 ements in superficial capillaries with known perfusion pathways, and determined sO(2) responses to hy

224 ch as vessel enlargement and regional mosaic perfusion patterns are common in COVID-19 pneumonia.

225 ents using cardiovascular magnetic resonance perfusion permit automated measurement clinically.

226 sessed the time-weighted average of the mean perfusion pressure (MPP) deficit (i.e., the percentage d

227 on-brain oxygen tension gradient to cerebral perfusion pressure (p = 0.004) when comparing normoxia t

228 itor intraspinal pressure (ISP), spinal cord perfusion pressure (SCPP), tissue metabolism and inflamm

229 e acutely sensitive to decreases in cerebral perfusion pressure and may function as intracranial baro

230 is appears necessary to establish a cerebral perfusion pressure on the order of 100 mm Hg at the cran

231 lar venous bulb oxygen tension, and cerebral perfusion pressure were 29 mm Hg (SD, 9), 45 mm Hg (SD,

232 nges occurred in the presence of reduced leg perfusion pressure, indicating that these augmentations

233 gen tension, intracranial pressure, cerebral perfusion pressure, mean arterial pressure, and jugular

234 Perfusion pressure, temperature, and circuit flow were m

235 ions is essential for effective tailoring of perfusion pressure-based treatment strategies.

236 lity and relaxation while restoring coronary perfusion pressure.

237 uld close a slit and prevent leakage at high perfusion pressure.

238 Measurements were made at perfusion pressures of 10 mmHg, 20 mmHg, 30 mmHg, and 40

239 Perfusion properties can be estimated from pharmacokinet

240 ng models to capture subtle multi-parametric perfusion properties, including heterogeneity.

241 However, there is no clear consensus on perfusion protocols.

242 state connectivity was correlated with tumor perfusion (R = 0.74, P < .01).

243 Blood perfusion rate decreased immediately postoperatively (P

244 Constrained by empirical blood perfusion rates, metabolic heat generation rates reached

245 Buccal flap blood perfusion recovery and changes in bone thickness were re

246 Exogenous RvD1 enhances perfusion recovery during ischemia, and mice deficient i

247 e determined whether such extreme degrees of perfusion redistribution are physiologically plausible,

248 Myocardial perfusion reflects the macro- and microvascular coronary

249 Perfusion relative dispersion was greater in both Fontan

250 A myocardial perfusion reserve index (MPRI) (stress/rest slope) was c

251 ls in the tumor vasculature lead to impaired perfusion, resulting in reduced accessibility to immune

252 canner took less than 1 second for a typical perfusion scan of three slices.

253 worsened ventilation defects on ventilation-perfusion scanning (VQ) or increased motion artifacts on

254 onary hypertension (CTEPH), with ventilation-perfusion scanning and echocardiography being the initia

255 omography pulmonary angiography, ventilation/perfusion scanning, pulmonary angiography, a combination

256 study, consecutive adenosine stress and rest perfusion scans were acquired from three hospitals betwe

257 Resting perfusion scans were performed in 10 patients with a CIE

258 ing method (SC) or 2-dimensional planar lung perfusion scintigraphy (PS).

259 Although ventilation/perfusion scintigraphy has been supplanted by computed t

260 vealed that sex and MBV were associated with perfusion (sex beta -0.31, p = 0.03; MBV beta -0.37, p =

261 d, the retinal and choriocapillaris vascular perfusion showed focal defects in every layer.

262 Bone marrow perfusion signal changed with the labeling size, suggest

263 ze, suggesting that the measured bone marrow perfusion signal is flow-associated.

264 The angiogenic response to ischemia restores perfusion so as to preserve tissue.

265 uses on current clinical outcomes with novel perfusion strategies in organ transplantation.

266 SNR, and temporal SNR from the quantitative perfusion study were 38.3 +/- 5.2 mL/100 g/min, 3.31 +/-

267 heart rates at different levels of cerebral perfusion, supporting the hypothesis of connexin hemicha

268 The QV600 perfusion system may service as a viable tool to enhance

269 irkstall QuasiVivo 600 (QV600) multi-chamber perfusion system.

270 he odds that that patients in the peripheral perfusion-targeted resuscitation arm had Sequential Orga

271 (95% CI, 1.02-2.37).Conclusions: Peripheral perfusion-targeted resuscitation may result in lower mor

272 the posterior probability that a peripheral perfusion-targeted resuscitation strategy is superior to

273 on the surface of the organ providing tissue perfusion through an intricate network of penetrating sm

274 ning laser ophthalmoscopy can visualize live perfusion through microcapillaries and structural change

275 icoagulation and strategies to improve brain perfusion through rhythm and rate control approaches.

276 ime is a noninvasive method to assess tissue perfusion to determine shock status.

277 and skin-permeable peroxide by micropipette perfusion to unwounded zebrafish tail fins.

278 ue used to measure cerebral blood flow (CBF; perfusion) to understand brain function and detect diffe

279 versus prolonged (2 weeks pre-treatment plus perfusion) UDCA administration.

280 89%) and less than or equal to 21 arbitrary perfusion unit (sensitivity 84%, specificity 81%), respe

281 values less than or equal to 1.25 arbitrary perfusion unit/ degrees C (sensitivity 88%, specificity

282 T (4.3 [1.7-10.9] vs 0.9 [0.4-2.9] arbitrary perfusion unit/s) were greater in survivors than in nons

283 ood flow (31 [17-113] vs 16 [9-32] arbitrary perfusion units; p = 0.01) and DeltaSBF/DeltaT (4.3 [1.7

284 Perfusion was compared between responders and nonrespond

285 Cerebral perfusion was compared vertex-wise according to APOE eps

286 Immediately after the exercise, perfusion was elevated to 79.3 +/- 9 mL/100 g/min and T(

287 Perfusion was maintained from organ retrieval to implant

288 injections of IL1B and intestinal recycling perfusion was measured; some mice were given dextran sod

289 Cortical perfusion was normalized against noninfarcted tissue and

290 Mean perfusion was similar (Fontan = 2.50 +/- 1.02 ml min(-1)

291 Together with a perfusion-weighted early-phase acquisition ((18)F-FDG PE

292 image noise, vertical and axial gradients in perfusion were calculated.

293 Energy status and kidney perfusion were correlated with kidney injury.

294 essel leak from barrier dysfunction, and non-perfusion were not associated with severe brain swelling

295 factors affect the distribution of pulmonary perfusion, which may be disrupted by cardiopulmonary dis

296 Hypothermic ex situ perfusion with an oxygenated acellular Steen solution ma

297 Perfusion with blood leads to increased monocyte adhesio

298 ters displayed a significant decrease of NIR perfusion with increased distance to the renal pelvis, i

299 litary metastases, with percutaneous hepatic perfusion with melphalan or with tebentafusp.

300 ction responses and progressive decreases in perfusion with repeated thermal stimulation in SCD are i