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1 These data support routine use of pulsatile perfusion.
2 d electrolytes were measured serially during pulsatile perfusion.
3 ic kidneys have led to the infrequent use of pulsatile perfusion.
4 entilation and one for the reconstruction of pulsatile perfusion.
5 ioning, 34 on preservation fluids, and 21 on pulsatile perfusion.
8 ere identified in which one kidney underwent pulsatile perfusion and transplantation at our center, w
9 lity to image changes due to ventilation and pulsatile perfusion, as well as regional inhomogeneity.
11 donated human kidneys undergoing hypothermic pulsatile perfusion deemed unsuitable for transplantatio
12 System (OCS; TransMedics) uses normothermic pulsatile perfusion during organ transport for heart tra
13 rafts were maintained on hypothermic ex vivo pulsatile perfusion for delayed implantation (mean cold
15 r donor kidney before transplant, could make pulsatile perfusion for the expanded donor financially a
16 nt outcome when organs are preserved through pulsatile perfusion; however, the underlying mechanisms
17 susceptivity images of both ventilation and pulsatile perfusion in real time using the ACT 5 EIT sys
18 hat these channels are activated by enhanced pulsatile perfusion in vivo and contribute substantially
21 tive pressure mechanical ventilation or from pulsatile perfusion of lungs held motionless by continuo
22 d retrospectively to determine the impact of pulsatile perfusion on initial function and 1-year graft
28 Conflicting literature on the benefit of pulsatile perfusion (PP) over cold storage (CS) warrants
30 a novel servopump system to control mean and pulsatile perfusion pressure within the isolated vascula
31 e baseline flow 66 % markedly amplified this pulsatile perfusion response (+82.6 +/- 14.3 % increase
32 n preservation solutions in conjunction with pulsatile perfusion shows promise in improving early out
35 an adaptation of the BrainEx extracorporeal pulsatile-perfusion system and cytoprotective perfusate
37 eys were preserved by continuous hypothermic pulsatile perfusion using Belzer-MPS or Belzer II soluti
38 phasic coronary flow responses to increasing pulsatile perfusion were assessed in anaesthetized dogs,
39 tion and subjected to static cold storage or pulsatile perfusion with an RM3 pump at 22 degrees C for
40 and susceptivity imaging of ventilation and pulsatile perfusion, with the potential to aid in the ev