コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 geted at the underlying disease (e.g., acute coronary occlusion).
2 restoration of cardiac function after acute coronary occlusion.
3 extent of myocardial necrosis consequent to coronary occlusion.
4 lead to larger infarcts caused by persistent coronary occlusion.
5 etector computed tomography during the index coronary occlusion.
6 ection of the onset of ischemia during acute coronary occlusion.
7 endent determinant of infarct size following coronary occlusion.
8 pate in the arrhythmogenic response to acute coronary occlusion.
9 ise healthy men even in the absence of acute coronary occlusion.
10 ired with 13N-ammonia at baseline and during coronary occlusion.
11 as was sudden death due to acute thrombotic coronary occlusion.
12 ct ultimate infarct size (IS) at the time of coronary occlusion.
13 cur during reperfusion of a limited-duration coronary occlusion.
14 different stenoses using ATP, adenosine, and coronary occlusion.
15 l axis, as observed with proximal circumflex coronary occlusion.
16 dogs undergoing an AIP 201 injection during coronary occlusion.
17 single left heart injection performed during coronary occlusion.
18 es isolated from hearts subjected to chronic coronary occlusion.
19 perfusion in dogs with chronic single-vessel coronary occlusion.
20 0 micrograms/kg) 10 minutes before the first coronary occlusion.
21 ersibly injured myocardium after 24 hours of coronary occlusion.
22 in the jeopardized zone, and the duration of coronary occlusion.
23 mpared with reactive hyperemia after 45 s of coronary occlusion.
24 milieu, which fluctuates considerably after coronary occlusion.
25 ynamic status identifies patients with acute coronary occlusion.
26 with Smad7+ macrophages peaked 7 days after coronary occlusion.
27 nits; P=0.9181) that were not different from coronary occlusion.
28 (655 versus 422 woods units; P=0.0053) than coronary occlusion.
29 LO) myocardial phagocytes after experimental coronary occlusion.
30 primary outcome was the finding of a recent coronary occlusion.
31 rgoing angioplasty balloon-induced transient coronary occlusion.
32 asurement is modestly predictive of a recent coronary occlusion.
33 rotic coronary plaque, resulting in subtotal coronary occlusion.
34 e independent predictive factors of a recent coronary occlusion.
35 the optimum cutoff for identifying a recent coronary occlusion.
36 and angina pectoris during the same 1-minute coronary occlusion.
37 e a sensitive/specific marker for thrombotic coronary occlusion.
38 Src (p-cSrc) post-MI using a canine model of coronary occlusion.
39 diomyopathy (I/RC) arising from daily, brief coronary occlusion.
40 ague-Dawley rats were subjected to permanent coronary occlusion.
41 dministered at the time of reperfusion after coronary occlusion.
42 etector computed tomography during the index coronary occlusion.
43 al infarction in a porcine model of complete coronary occlusion.
44 (PDGF)-AB decreases myocardial injury after coronary occlusion.
45 h STEMI and mapped the location of the acute coronary occlusion.
46 ors are involved, then the benefits of brief coronary occlusion (1) should be manifested systemically
47 In protocol 1, dogs received 10 minutes of coronary occlusion + 10 minutes of reflow or a comparabl
48 clusion was preceded by brief I/R (10-minute coronary occlusion/10-minute reperfusion) versus 20-minu
50 us pigs underwent a sequence of ten 2-minute coronary occlusion/2-minute reperfusion cycles and then
52 te PC (one, three, or six cycles of 4-minute coronary occlusion [4'O]/4-minute reperfusion [4'R]; fou
54 tioned 24 h earlier with six cycles of 4-min coronary occlusion/4-min reperfusion exhibited a signifi
55 schemic PC (induced with six cycles of 4-min coronary occlusion/4-min reperfusion), immunoprecipitati
57 rabbits underwent a sequence of six 4-minute coronary occlusion/4-minute reperfusion cycles for 3 con
58 rabbits underwent a sequence of six 4-minute coronary occlusion/4-minute reperfusion cycles for 3 con
59 rabbits underwent a sequence of six 4-minute coronary occlusion/4-minute reperfusion cycles for 3 con
60 rabbits underwent a sequence of six 4-minute coronary occlusion/4-minute reperfusion cycles for 3 con
61 were subjected to ischemic PC (six 4-minute coronary occlusion/4-minute reperfusion cycles) and, 24
62 its were subjected to a sequence of 4-minute coronary occlusion/4-minute reperfusion cycles, myocardi
63 In mice preconditioned with six 4-minute coronary occlusion/4-minute reperfusion cycles, we found
69 ized rabbits received 5 minutes of transient coronary occlusion, 5 minutes of transient bilateral car
71 efractory OHCA patients frequently had acute coronary occlusion (64% versus 47%), especially left cir
72 usly in anesthetized, open-chest dogs before coronary occlusion (90 minutes) and reperfusion (120 min
73 In conscious swine subjected to a sustained coronary occlusion, a PC protocol that induces powerful
75 t administration of 99mTc-tetrofosmin during coronary occlusion accurately delineates the flow hetero
76 ion units (TPUs) and pH were measured before coronary occlusion, after occlusion, and after direct ex
78 en A3tg mice were subjected to 30 minutes of coronary occlusion and 24 hours of reperfusion, infarct
82 CaCl2 or saline before undergoing 1 hour of coronary occlusion and 4 hours of reperfusion (protocol
83 dence that ischemic PC (6 cycles of 4-minute coronary occlusion and 4-minute reperfusion) induces sel
88 s were observed in mouse models of permanent coronary occlusion and clinically relevant ischemia and
90 during this period of time, after prolonged coronary occlusion and complete reflow, the rate of myoc
92 of perfusion abnormalities that occur during coronary occlusion and may facilitate estimation of the
93 howing contrast enhancement on 3D MCE during coronary occlusion and postmortem risk volume (y = 1.2x
94 ntrast echocardiography were measured during coronary occlusion and reflow, using fundamental and har
97 finity (DuPont) at baseline and during brief coronary occlusion and reperfusion and were analyzed wit
100 ium where inflammation was induced by either coronary occlusion and reperfusion or tumor necrosis fac
101 the clinical scenario in which intermittent coronary occlusion and reperfusion superimposed on a cri
105 deduced that myocardial infarction is due to coronary occlusion and that subsequent death needs no ot
107 ld be produced in a porcine model of chronic coronary occlusion and to assess whether the adaptations
108 in L-NA-treated rabbits the sequence of six coronary occlusions and reperfusions performed on day 1
109 assessed for myocardial perfusion deficits, coronary occlusion, and abnormal myocardial wall motion.
110 fluorescent microspheres at baseline, during coronary occlusion, and at 5, 30, 90, and 180 min during
111 tensive resuscitation, higher rates of acute coronary occlusion, and poorer in-hospital outcomes, und
112 hyperemia, the size of the risk area during coronary occlusion, and the extent of myocardial salvage
113 hyperemia, the size of the risk area during coronary occlusion, and the extent of myocardial salvage
114 baseline; at reperfusion after 15 minutes of coronary occlusion; and at 30 minutes, 60 minutes, and 1
116 ent necrosis could be identified early after coronary occlusion as having the lowest microvascular fl
117 nt improvement in gene uptake with temporary coronary occlusions assisted by mechanical circulatory s
119 as injected before a brief (6 min) period of coronary occlusion at the following times: 15 min (n = 2
122 ents cardiac dysfunction and ischemia due to coronary occlusion by tightening the link between cardia
123 nfarct size was assessed at 24 h after acute coronary occlusion by triphenyltetrazolium chloride (TTC
124 aration of proteins from hearts subjected to coronary occlusion by two-dimensional electrophoresis an
125 decreases in coronary flow or repeated brief coronary occlusions can be followed by proportionate rev
126 te study of LV remodeling, after a 60-minute coronary occlusion, cardiac magnetic resonance imaging r
130 The presence of a concomitant chronic total coronary occlusion (CTO) and a large collateral contribu
131 nificant coronary disease have chronic total coronary occlusion (CTO), which is associated with long-
133 functional in the RI group because complete coronary occlusion did not induce any untoward effects o
135 on period (baseline 2) and a during a second coronary occlusion during bypass anastomosis (occlusion
136 aemic postconditioning uses repetitive brief coronary occlusion during early reperfusion of myocardia
137 transcatheter heart valves (THVs) may cause coronary occlusion during transcatheter aortic valve rep
138 t transcatheter aortic valve replacement, or coronary occlusion during transcatheter aortic valve rep
139 scious pigs underwent a sequence of 10 2-min coronary occlusions, each separated by 2 min of reperfus
140 ing), rabbits were subjected to six 4-minute coronary occlusions, each separated by 4-minute reperfus
141 he size of the infarcts produced by a 30-min coronary occlusion followed by 24 h of reperfusion was r
142 in rats was produced by using 30 minutes of coronary occlusion followed by 24 hours reperfusion.
143 on), conscious rabbits underwent a 30-minute coronary occlusion followed by 3 days of reperfusion.
145 tion), rabbits were subjected to a 30-minute coronary occlusion followed by 3 days of reperfusion.
146 groups of pigs were subjected to a 40-minute coronary occlusion followed by 3 days of reperfusion.
149 istration of SDF-1alpha before 30 minutes of coronary occlusion followed by 4 hours of reperfusion de
150 rdial infarction was produced by a 30-minute coronary occlusion followed by 4 hours of reperfusion.
151 low coronary flow (protocol 1) and transient coronary occlusion followed by reflow (protocol 2).
152 male Fischer 344 rats underwent a 30-minute coronary occlusion followed by reperfusion and 48 hours
153 Wild-type (WT) mice underwent a 30-minute coronary occlusion followed by reperfusion and received
154 open-chest dogs, which then underwent 2 h of coronary occlusion followed by reperfusion through the s
159 nt 90 or 180 min of left anterior descending coronary occlusion, followed by 180 min of reperfusion.
162 were assessed serially in dogs subjected to coronary occlusion for 45 min, 90 min, or permanently.
164 ed to collect data before, during, and after coronary occlusion from which percent systolic shortenin
165 r example, at matched ESVs before and during coronary occlusion, FRP was -1.1+/-1.1 (+/-SD) mm Hg bef
166 39 patients with successful angioplasty of a coronary occlusion (Group 1) and compared the frequency
167 ollBF were measured in 18 dogs: at 6 h after coronary occlusion (Group 1, n = 6), and during 40 micro
170 ral development after experimentally induced coronary occlusion; however, methods of bFGF delivery th
173 and maintenance of function during complete coronary occlusion in 3 groups of animals: sham (receive
175 n system to detect ST-segment elevation from coronary occlusion in a porcine model of ST-segment elev
177 cy, predictors, and clinical impact of acute coronary occlusion in hemodynamically stable and unstabl
178 rdiac troponin I can help to detect a recent coronary occlusion in out-of-hospital cardiac arrest.
179 phy and to determine the prevalence of acute coronary occlusion in resuscitated patients with out-of-
182 of ischemia/reperfusion in a model of brief coronary occlusion in which no necrosis or inflammatory
183 r dysfunction was created by repetitive left coronary occlusions in 7 pigs (7 healthy pigs also inclu
184 ium-regulatory genes (after repetitive total coronary occlusions in swine) have given rise to the hyp
185 termine early predictive factors of a recent coronary occlusion (including cardiac troponin I) and th
187 human hearts and in murine hearts following coronary occlusion increased in endothelial lining of so
189 d in conscious pigs that a sequence of brief coronary occlusions induces severe myocardial stunning,
191 stered to isolated hearts before a 30-minute coronary occlusion, infarct size (15.6 +/- 2.0% of the r
193 uroprotections through cooling rapidity when coronary occlusion is complicated by cardiac arrest.
198 nt of microvascular obstruction during acute coronary occlusion may determine the eventual magnitude
201 e MRI scans followed by either 60 minutes of coronary occlusion (MI group, n=15) or thoracotomy witho
203 ental analysis with the use of larger animal coronary occlusion models should help determine the futu
204 endent LCx arterioles isolated after chronic coronary occlusion, most likely because of effects on ec
210 us rabbits underwent a sequence of six 4-min coronary occlusion (O)/4-min reperfusion (R) cycles for
211 les at baseline (baseline 1), during a 5-min coronary occlusion (occlusion 1), after a 5-min reperfus
213 of 53 mongrel dogs in an open chest model of coronary occlusion of various durations followed by repe
214 fter 10 min (Group 1) or 60 (Group 2) min of coronary occlusion or after 10 min of a fixed coronary o
216 recorded during 60 s of anterior descending coronary occlusion or local epicardial application of br
218 nfarction without reperfusion (chronic 7-day coronary occlusion) or receiving post-I/R high-dose ster
219 early after reperfusion following prolonged coronary occlusion overestimates the degree of viability
221 vs. 0.93 +/- 0.41 mm Hg.ml(-1) during acute coronary occlusion [p < 0.05] and 7.9 +/- 3.1 m.s(-2) be
223 (LV) structure and function after permanent coronary occlusion (PCO) and the potential involvement o
224 d in an ambulatory porcine model, with acute coronary occlusion precipitated by stent thrombosis.
228 est dogs were subjected to a 10-minute acute coronary occlusion (proximal left anterior descending co
229 its have demonstrated that a series of brief coronary occlusions renders the heart relatively resista
232 r repetitive ischemia differs in response to coronary occlusion-reperfusion versus supply-demand isch
235 rdioprotection, insofar as brief episodes of coronary occlusion/reperfusion preceding (ischemic preco
236 inhibition (GPI) on microvascular flow after coronary occlusion/reperfusion using quantitative myocar
237 nts undergoing CABG and from pigs undergoing coronary occlusion/reperfusion without (sham) and with R
238 ular flow and reduces the infarct area after coronary occlusion/reperfusion, independent of epicardia
244 kg) was infused 5 minutes after the onset of coronary occlusion (sCR1), 10 received HB-CPB only (HB-C
246 about symptoms that they might have during a coronary occlusion, steps that they should take, the imp
247 other cytokine combinations, at the time of coronary occlusion suppressed acute myocardial cell deat
248 three days and four to eight weeks following coronary occlusion; terminal values averaged 24 +/- 3% o
249 echocardiographic definition of the level of coronary occlusion, the left anterior descending artery
255 ythmias (VAs) were subjected to percutaneous coronary occlusion to induce myocardial infarction.
257 d a spatial map of the distribution of acute coronary occlusions to test our hypothesis that plaque r
258 fluid (MIF) from dogs undergoing repetitive coronary occlusions under control conditions or during a
260 e subjected to gradually developing regional coronary occlusion using an ameroid occluder placed arou
261 on was 4.1%, conversion to surgery was 0.6%, coronary occlusion was 0.8%, and new pacemaker insertion
263 , improvement in carotid patency after brief coronary occlusion was corroborated in anesthetized dogs
264 size in a model of acute infarction in which coronary occlusion was followed by prolonged reperfusion
266 stance from the ostium, the risk of an acute coronary occlusion was significantly decreased by 13% in
268 of scar, but infarct size at 10 weeks after coronary occlusion was still smaller (by 50%) in Cx43(+/
271 ion starting 30 s after release of the index coronary occlusion were added in the presence or absence
273 ST-segment shift, associated with thrombotic coronary occlusion, were 100% and 100%, respectively.
274 lateral development in dogs with progressive coronary occlusion when given during the period of natur
275 ification of these high-risk zones for acute coronary occlusions will lead to future advances in vuln
278 and reperfusion before a sustained period of coronary occlusion with reperfusion delays infarct devel
279 ions in regional function: dobutamine, 5-min coronary occlusion with reperfusion up to 1 h, followed
283 id not alter the hemodynamic response to the coronary occlusion, yet it prevented VF in 10 of 11 anim
284 nosine for both CFR and FFR; and 3) complete coronary occlusion yielded a better hyperemic response t