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1 tervention (n=80) were randomized to receive intracoronary (10 mL) sodium nitrite (1.8 mumol) or NaCl
2                    Under control conditions (intracoronary 5% dextrose in water), atrial-pacing tachy
3                       Patients randomized to intracoronary abciximab also had a significant reduction
4 improve outcomes after primary PCI are bolus intracoronary abciximab and manual aspiration thrombecto
5                                          The intracoronary abciximab bolus did not reduce the primary
6                         Administration of an intracoronary abciximab bolus during primary percutaneou
7                       Patients randomized to intracoronary abciximab compared with no abciximab had a
8 y reduced in diabetic patients randomized to intracoronary abciximab compared with those randomized t
9  open-label, 2 x 2 factorial design to bolus intracoronary abciximab delivered locally at the infarct
10 t 30 days was significantly reduced by bolus intracoronary abciximab delivered to the infarct lesion
11 icantly less congestive heart failure in the intracoronary abciximab group.
12 c patients with STEMI, the administration of intracoronary abciximab improved the effectiveness of pr
13 resent in 181 and 172 patients randomized to intracoronary abciximab vs no abciximab, respectively, a
14 e epicardial vasoconstriction in response to intracoronary acetylcholine (-19+/-2% versus -14+/-1% ch
15 -four patients of the latter (86%) underwent intracoronary acetylcholine (ACH) testing, which elicite
16 cular resistance, and vasomotor responses to intracoronary acetylcholine (vasospasm provocation) was
17             However, provocation tests using intracoronary acetylcholine administration are rarely pe
18                                          The intracoronary acetylcholine provocation test is a safe t
19  angiographic characteristics, and safety of intracoronary acetylcholine provocation testing in white
20                                          The intracoronary acetylcholine provocation testing was perf
21 ACS patients without culprit lesion, in whom intracoronary acetylcholine provocation was performed, h
22 dial endothelial functional assessment using intracoronary acetylcholine; second, epicardial severity
23 mized (3:1 ratio) to receive 1 of 5 doses of intracoronary Ad5.hAC6 or placebo.
24                Thirty-nine patients received intracoronary adeno-associated virus type 1/sarcoplasmic
25 coronary flow reserve was examined by use of intracoronary adenosine and nitroglycerin.
26 d baseline coronary flow reserve (CFR) after intracoronary adenosine in 189 women referred to evaluat
27 endent) coronary flow reserve in response to intracoronary adenosine were evaluated.
28 y measurements were performed at rest, after intracoronary adenosine, and during increasing infusion
29 ty was not different between intravenous and intracoronary administration (1.47% versus 1.33%; P=0.5)
30                                              Intracoronary administration of Ad5.hAC6 (3.2 x 109 to 1
31                     Preclinical studies with intracoronary administration of Ad5FGF-4 (alferminogene
32 The modest effects of clinical studies using intracoronary administration of autologous bone marrow-d
33                                              Intracoronary administration of autologous bone marrow-d
34                                              Intracoronary administration of autologous CDCs did not
35 hronic heart failure, shock wave-facilitated intracoronary administration of BMCs vs shock wave treat
36                                              Intracoronary administration of CDCs has been demonstrat
37                                              Intracoronary administration of CPCs in the setting of a
38  model of AMI relevant to the human disease, intracoronary administration of IGF-1/HGF is a practical
39 day outcome in 775 consecutive procedures of intracoronary administration of progenitor cells using t
40 p, n=9) were compared with animals receiving intracoronary AdvEGFP (2x10(12) vp, n=6).
41 d regional function before and 30 days after intracoronary AdvFGF-5 (2x10(12) vp, n=9) were compared
42 hodology, we compared the efficacy of global intracoronary allogeneic MSCs (icMSCs, approximately 35x
43 4 to 6 h, adjunctive treatment with low-dose intracoronary alteplase during primary percutaneous coro
44 hin 6 hours of symptoms, adjunctive low-dose intracoronary alteplase given during the primary percuta
45 of a therapeutic strategy involving low-dose intracoronary alteplase infused early after coronary rep
46                                              Intracoronary alteplase may be harmful for this subgroup
47 tematically compared FFR measurements during intracoronary and intravenous application of adenosine a
48 52) did not differ significantly between the intracoronary and the intravenous abciximab groups.
49  In an open-label blinded study, we compared intracoronary and transendocardial CD34(+) cell transpla
50                                              Intracoronary angiotensin-converting enzyme inhibitors h
51 c reperfusion was performed for 90 min using intracoronary AO.
52                    Limited data validate the intracoronary application of adenosine against standard
53                    Reported discomfort after intracoronary application was significantly lower compar
54 ee cycles of 10/10 min r-I/R by percutaneous intracoronary balloon inflation/deflation in the mid lef
55 tions were by immunoblotting in systemic and intracoronary blood from independent cohorts of patients
56 ry cells in the infarct border zone, whereas intracoronary BM cell injection provided more homogeneou
57  of NT-proBNP serum levels at 4 months after intracoronary BMC administration in patients with ICM, s
58 ntial impairment of kidney function received intracoronary BMC administration.
59 cell retention and determine the response to intracoronary BMC application in patients with ICM.
60 istics than on whether the patient underwent intracoronary BMC transplantation.
61 ated with primary PCI, the administration of intracoronary BMCs at either 3 days or 7 days after the
62 ention, 120 patients were randomized to a 1) intracoronary BMMC injection; 2) mobilization with G-CSF
63  intravenous infusion versus 23 +/- 14 s for intracoronary bolus administration of adenosine (P < 0.0
64                                              Intracoronary bolus administration of eptifibatide durin
65                                              Intracoronary bolus administration of eptifibatide may r
66   Two FFR measurements were performed during intracoronary bolus injection (40 mug for the right and
67                                              Intracoronary bolus injection of adenosine (40 mug for t
68 aseline and maximal hyperemia, induced by an intracoronary bolus of adenosine (20-40 microg).
69                                              Intracoronary bolus of apelin-36 increased coronary bloo
70 ly assigned 40 patients to receive either an intracoronary bolus of enalaprilat (50 mug) or placebo b
71                                              Intracoronary cardiospheres are also remarkably effectiv
72                                 Importantly, intracoronary cardiospheres decreased left ventricular e
73         We investigated long-term effects of intracoronary CD34+ cell transplantation in dilated card
74 erform a meta-analysis of clinical trials on intracoronary cell therapy after acute myocardial infarc
75       We analyzed the safety and efficacy of intracoronary cell therapy after acute myocardial infarc
76                                              Intracoronary cell therapy continues to be evaluated in
77                                              Intracoronary cell therapy following percutaneous corona
78                       Subjects that received intracoronary cell therapy had a significant improvement
79 zed trials targeted to address the impact of intracoronary cell therapy on overall and event-free lon
80 databases for controlled trials reporting on intracoronary cell therapy performed in patients with a
81 ls in patients with recent AMI revealed that intracoronary cell therapy provided no benefit, in terms
82                                              Intracoronary cell therapy was also associated with a no
83 hearts of three different mammalian species, intracoronary chloroquine perfusion reduced fibrillatory
84 ased only in diabetic patients randomized to intracoronary compared with intravenous abciximab (54.4;
85 nt study was undertaken to determine whether intracoronary CSCs are beneficial in a porcine model of
86 farction, the dose-response relationship for intracoronary CSCs is flat.
87 etrospective multicentric registry and Mainz Intracoronary Database.
88                                   Initially, intracoronary delivery conditions were optimized in 20 s
89                                      Ex vivo intracoronary delivery of adenovirus-mediated gene trans
90 ate the safety, feasibility, and efficacy of intracoronary delivery of allogeneic human cardiac stem
91 sed the safety, feasibility, and efficacy of intracoronary delivery of allogeneic MPCs directly after
92 test, for the first time, the feasibility of intracoronary delivery of an innovative, injectable bioa
93          Clinical trial results suggest that intracoronary delivery of autologous bone marrow mononuc
94                  Harvesting, processing, and intracoronary delivery of BMCs in this setting was feasi
95                                              Intracoronary delivery of BNP116.I-1c was safe and impro
96                                              Intracoronary delivery of c-kit-positive human cardiac s
97 luating the safety and efficacy of optimized intracoronary delivery of cardiospheres in a porcine mod
98                                              Intracoronary delivery of cardiospheres is safe.
99                                              Intracoronary delivery of CDCs in a preclinical model of
100 rgitation induction, pigs were randomized to intracoronary delivery of either BNP116.I-1c (n = 6) or
101  after myocardial infarction, pigs underwent intracoronary delivery of either recombinant adeno-assoc
102                  At 2 months, pigs underwent intracoronary delivery of either recombinant adeno-assoc
103                                              Intracoronary delivery of endothelial progenitor cells (
104 rdial blood flow, to quantify the effects of intracoronary delivery of recombinant TIMP-3 (rTIMP-3) o
105 o evaluate therapeutic interventions such as intracoronary delivery of rTIMP-3 for reduction of I/R i
106     This first-in-man pilot study shows that intracoronary deployment of an IK-5001 scaffold is feasi
107                                              Intracoronary deployment of BCM 2 to 5 days after succes
108 efined as the successful manipulation of the intracoronary devices using the robotic system only.
109 onary pulse wave analysis, we calculated the intracoronary diastolic suction wave (the principal acce
110 d troponin, microemboli can be visualized by intracoronary Doppler and the resulting microinfarcts by
111 three patients were studied; in 24 patients, intracoronary Doppler flow velocity measurements were pe
112 y disease, and may be accurately assessed by intracoronary Doppler flow velocity measurements.
113  primary percutaneous coronary intervention, intracoronary Doppler flow velocity was measured in the
114 s calculated from flow velocity, measured by intracoronary Doppler, and luminal diameter, measured by
115              Of these, 5 received 5 biweekly intracoronary doxorubicin doses (0.45 mg/kg/injection) a
116 u) responses were assessed during continuous intracoronary drug infusion in sinus rhythm followed by
117                      There was a decrease in intracoronary ECG ST-elevation during RCA occlusion from
118 erve during vessel patency, the quantitative intracoronary ECG ST-segment elevation, and angina pecto
119  end point was the quantitatively determined intracoronary ECG ST-segment elevation.
120                                              Intracoronary ECG ST-segment elevations were significant
121 the second and third inflations, both on the intracoronary electrocardiogram (ECG) (21.0 +/- 2.8 mm v
122                                              Intracoronary enalaprilat improves coronary microvascula
123     This study investigated the influence of intracoronary enalaprilat on coronary microvascular func
124 l, or other adverse findings attributable to intracoronary eptifibatide.
125           This emphasizes the requirement of intracoronary flow assessment in addition to coronary pr
126 including quantitative coronary angiography, intracoronary flow velocity probes, and pharmacologic st
127 overexpression in pig hearts was achieved by intracoronary gene delivery of adenovirus in the 3 main
128 ression of SERCA2a by in vivo rAAV1-mediated intracoronary gene transfer preserved systolic function,
129 ndocardial group (+8.1 +/- 4.3%) than in the intracoronary group (+4.2 +/- 2.3%, P=0.03).
130 ndocardial group (19.2 +/- 4.8%) than in the intracoronary group (4.4 +/- 1.2%, P<0.01).
131                                       In the intracoronary group, cells were injected intracoronarily
132 endocardial group versus +86 +/- 13 m in the intracoronary group, P=0.03) and N-terminal pro-brain na
133 rdial group versus 103 +/- 27 x 10(6) in the intracoronary group, P=0.62).
134 e index, compared with established hyperemic intracoronary hemodynamic parameters, because achievemen
135                                              Intracoronary hyperoxemic reperfusion was safe and well
136  was tested by coronary dilation response to intracoronary (IC) acetylcholine and IC nitroglycerin.
137 rctions, few high-risk plaques identified by intracoronary imaging actually result in future major ad
138                                              Intracoronary imaging is critical to identify the mechan
139                       The highest-resolution intracoronary imaging modality, optical coherence tomogr
140                                              Intracoronary imaging provides unique insights to unrave
141  and coronary blood flow quantification, and intracoronary imaging to detect early changes in the ves
142 onsible for MACE and improves the ability of intracoronary imaging to predict events.
143 vention is also due to important advances in intracoronary imaging, and adjunct pharmacotherapy-each
144           An algorithmic approach, guided by intracoronary imaging, for the treatment of DES-ISR, is
145 ilability and application of high-resolution intracoronary imaging.
146                                              Intracoronary implantation of the EES is associated with
147  of heart failure, overexpression of I-1c by intracoronary in vivo gene transfer preserved cardiac fu
148 ogic analysis was used to confirm successful intracoronary infiltration of MGd and trypan blue within
149 million autologous CSCs were administered by intracoronary infusion at a mean of 113 days (SE 4) afte
150            AntimiR-21 (10 mg) was applied by intracoronary infusion at days 5 and 19 after the injury
151  injection and intravenous infusion, whereas intracoronary infusion demonstrated no improvement.
152 1.3), as did intravenous infusion, but again intracoronary infusion demonstrating no improvement.
153 IE) was delivered into cardiac allografts by intracoronary infusion ex vivo.
154 ioactivity of autologous CD34+ cell (CLBS10) intracoronary infusion in patients with left ventricular
155 res may be viable therapeutic candidates for intracoronary infusion in selected myocardial disorders.
156 cardial injection, intravenous infusion, and intracoronary infusion indicated no improvement.
157 and web-response system, to receive a single intracoronary infusion of 1 x 10(13) DNase-resistant par
158 d 2-3 weeks later were randomized to receive intracoronary infusion of 12.5x10(6) mismatched allogene
159                                              Intracoronary infusion of 150 x 10(6) autologous BMCs (t
160                                              Intracoronary infusion of 150 x 106 BMCs or placebo (ran
161 33 severe) were randomized to receive either intracoronary infusion of 3 incremental doses of eMSC or
162 t failure therapy were randomized to receive intracoronary infusion of AAV1/SERCA2a in 1 of 3 doses (
163                               After a single intracoronary infusion of AAV1/SERCA2a in patients with
164                                              Intracoronary infusion of allogeneic MPCs is safe, feasi
165  dysfunction following reperfusion with PCI, intracoronary infusion of autologous BMCs vs intracorona
166                 However, the responses after intracoronary infusion of autologous bone marrow-derived
167                      INTERPRETATION: We show intracoronary infusion of autologous CDCs after myocardi
168                                              Intracoronary infusion of autologous CSCs improves regio
169                            They suggest that intracoronary infusion of autologous CSCs is effective i
170 LV dysfunction after successful reperfusion, intracoronary infusion of BM-MNC at either 5 to 7 days o
171 might be recommended as an anticoagulant for intracoronary infusion of BMCs for cell therapy after ca
172 ment were randomized to receive double-blind intracoronary infusion of BMCs or placebo, and patients
173 tients receiving placebo shock wave received intracoronary infusion of BMCs.
174                                              Intracoronary infusion of BMMNC is safe, but does not en
175                                   RATIONALE: Intracoronary infusion of bone marrow (BM) mononuclear c
176 ction induced by ischemia/reperfusion before intracoronary infusion of CDCexo, inert fibroblast exoso
177                                          The intracoronary infusion of cells imposes the potential ri
178 vestigate the efficacy of different doses of intracoronary infusion of eMSC in a porcine model of acu
179 g coronary angioplasty were randomized to an intracoronary infusion of enalaprilat or placebo, follow
180                  In an isolated heart model, intracoronary infusion of IL-18BP MSCs before ischemia i
181 sel stenosis were studied at rest and during intracoronary infusion of nitroglycerin (0.3 to 0.6 micr
182                                              Intracoronary infusion of progenitor cells can be perfor
183 ion, pigs with I/R were randomly assigned to intracoronary infusion of rTIMP-3 (1.0 mg/kg; n=5) or sa
184 sine-induced maximal hyperemia as reference, intracoronary infusion of saline at rates of 5, 10, 15,
185                                              Intracoronary infusion of saline at room temperature thr
186 metric coronary blood flow, we observed that intracoronary infusion of saline increased coronary flow
187 h angiographically normal coronary arteries, intracoronary infusion of SMTC (0.625 micromol/min) redu
188 nary occlusion/reperfusion, rats received an intracoronary infusion of vehicle or enhanced green fluo
189 796863), the authors assessed the effects of intracoronary infusion with bone marrow-derived mononucl
190 al in the setting of an old MI when given by intracoronary infusion, the most widely applicable thera
191 , have been associated with infarction after intracoronary infusion.
192 ells; N=78) or (2) diluent alone (N=83), via intracoronary infusion.
193 ing was performed after consecutive 5-minute intracoronary infusions (vehicle solution, 0.30 mug/min
194 change in coronary blood flow in response to intracoronary infusions of acetylcholine during diagnost
195 ardiomyopathy, 20 were randomized to receive intracoronary injection and 20 received transendocardial
196                      Dynamic tracking during intracoronary injection of (18)F-FDG-labeled CPC is feas
197                                              Intracoronary injection of AAV9.I-1c prevented further d
198                                              Intracoronary injection of autologous BMNCs does not imp
199 35, and optimized therapy were randomized to intracoronary injection of autologous BMNCs or placebo.
200 ricular tachycardia for the initial 14 days; intracoronary injection of BM cells and intramyocardial
201                     Both intramyocardial and intracoronary injection of BM cells demonstrated similar
202 though various approaches have been studied, intracoronary injection of bone marrow autologous mononu
203                      We investigated whether intracoronary injection of nitrite during primary percut
204 rdial repair through a clinically applicable intracoronary injection protocol in a pig model of myoca
205 ulating progenitor cell (CPC) therapy during intracoronary injection, using a porcine model of acute
206 udy has shown that liposome-mediated ex vivo intracoronary interleukin (IL)-4 and IL-10 combined gene
207  cell delivery have been reported, including intracoronary, intramyocardial, intravenous, and epicard
208                                              Intracoronary levosimendan (3.75 and 12.5 microg/min for
209 bing findings suggestive of angiographic and intracoronary manifestations of coronary FMD.
210                                        Using intracoronary measurements, 91 coronaries (78 patients)
211 n emission tomography and its interplay with intracoronary measurements.
212                      In one study, dogs with intracoronary microembolization-induced HF were randomiz
213 rcts were created in Yorkshire pigs (n=6) by intracoronary microsphere injection.
214 c hibernating myocardium received autologous intracoronary MSCs (icMSCs; approximately 44 x10(6) cell
215 uvastatin 40 mg for 8-12 weeks and underwent intracoronary multimodality imaging of an obstructive no
216 tervention for a culprit lesion, followed by intracoronary multimodality imaging, including optical c
217                               In this study, intracoronary near-infrared spectroscopy (NIRS) was used
218  determine the long-term prognostic value of intracoronary NIRS as assessed in a nonculprit vessel in
219 vasomotor reactivity after administration of intracoronary nitrate.
220 he stenosis were measured at baseline, after intracoronary nitrates, and after stent PCI.
221 ng that a phase III clinical trial assessing intracoronary nitrite administration as an adjunct to pe
222                      In this phase II study, intracoronary nitrite infusion did not alter infarct siz
223 nderwent coronary diameter measurement after intracoronary nitroglycerin injection 5, 20, and 35 mm d
224  pacing for endothelium-dependent cases; and intracoronary nitroglycerin injection for endothelium-in
225    However, administration of cells requires intracoronary or intracardiac instrumentation, which is
226 IDA STEMI trial randomized 2,065 patients to intracoronary or intravenous abciximab and found similar
227 ents with and without diabetes randomized to intracoronary or intravenous abciximab bolus at the time
228  coronary syndrome were randomized to either intracoronary or intravenous bolus administration of ept
229 egment shift during inflations on either the intracoronary or the surface ECG.
230 ing utilized to further our understanding of intracoronary pathology and the effects of therapies bot
231 s performed to calculate aortic (Pa), distal intracoronary (Pd), and reservoir (Pr) pressure at basel
232 stable coronary artery disease who underwent intracoronary physiological evaluation of >/= 1 coronary
233 of functional coronary lesion severity using intracoronary physiological parameters such as coronary
234 intracoronary infusion of autologous BMCs vs intracoronary placebo infusion, 2 to 3 weeks after PCI,
235 ct of short-term intensive statin therapy on intracoronary plaque lipid content.
236 mbus aspirate analysis showed persistence of intracoronary polymer fragments in case 1.
237 l to the stenosis; in part 2 (118 stenoses), intracoronary pressure alone was measured.
238                                 Simultaneous intracoronary pressure and flow velocity recordings were
239                               In 51 vessels, intracoronary pressure and flow velocity was measured di
240                                              Intracoronary pressure and flow velocity were measured a
241                     In part 1 (39 stenoses), intracoronary pressure and flow velocity were measured d
242                                              Intracoronary pressure and flow velocity were measured i
243                                              Intracoronary pressure and flow velocity were simultaneo
244                              Small drifts in intracoronary pressure measurements (+/-2 mm Hg) can aff
245 for the use of FFR during PCI and shows that intracoronary pressure wire guidance confers prognostic
246                                              Intracoronary pressure wire measurement of fractional fl
247            Immediately after successful PCI, intracoronary pressure-flow measurements were performed
248 lysis identified a wave-free period in which intracoronary resistance at rest is similar in variabili
249                                              Intracoronary resistance is naturally constant and minim
250 f animals were not transplanted but received intracoronary rIFN-gamma infusion into the native heart.
251 of autologous CD34(+) cells delivered via an intracoronary route after recent myocardial infarction i
252 oth P-selectin and ICAM-1 via the retrograde intracoronary route could be a promising new strategy fo
253                  However, the more desirable intracoronary route has been assumed to be unsafe for ca
254 ardial biopsy specimens were infused via the intracoronary route in 17 patients with left ventricular
255 peptide, and exercise capacity compared with intracoronary route.
256 ch arrhythmias may be prevented by using the intracoronary route.
257 her a direct intramyocardial or a retrograde intracoronary route.
258 icle solution, 0.30 mug/min and 0.60 mug/min intracoronary salbutamol) to measure changes in segmenta
259                                              Intracoronary saline given on top of an intravenous infu
260                                              Intracoronary saline infusion did not affect blood press
261 thoracic echocardiography during a prolonged intracoronary saline infusion.
262 ngle vessel coronary artery disease and mean intracoronary shear estimates at 2935 seconds(-1) (peak
263 mic minipigs (n=5) were instrumented with an intracoronary shear-modifying stent (SMS).
264                                              Intracoronary stem cell transplantation may be associate
265 ificant coronary artery disease receiving an intracoronary stent between April 2004 and December 2007
266 onary syndromes, 11 289 (61%) had at least 1 intracoronary stent.
267                    The aim of the ISAR-ASPI (Intracoronary Stenting and Antithrombotic Regimen-ASpiri
268 el in the setting of the ISAR REACT-5 trial (Intracoronary Stenting and Antithrombotic Regimen: Rapid
269 nt Intervention Triage Strategy (ACUITY) and Intracoronary Stenting and Antithrombotic Regimen: Rapid
270                            The ISAR-REACT 4 (Intracoronary Stenting and Antithrombotic Regimen: Rapid
271  being challenged by recent clinical trials (Intracoronary Stenting and Antithrombotic Regimen: Rapid
272 : Rapid Early Action for Coronary Treatment, Intracoronary Stenting and Antithrombotic Regimen: Rapid
273                                              Intracoronary stenting can improve procedural success an
274 atients with atrial fibrillation who undergo intracoronary stenting traditionally are treated with a
275 l methodologies confirmed the finding of the Intracoronary Stenting With Antithrombotic Regimen Cooli
276  only, small, randomized clinical trial, the Intracoronary Stenting With Antithrombotic Regimen Cooli
277 patients with atrial fibrillation undergoing intracoronary stenting, administration of either rivarox
278 ervention (PCI), which involves placement of intracoronary stents in most patients, is a less invasiv
279               Recent studies of drug-eluting intracoronary stents suggest that current antiplatelet r
280 tensive platelet inhibition in patients with intracoronary stents.
281 idly become a preferred modality for imaging intracoronary structures such as coronary plaques and co
282 had no effect on increases in flow evoked by intracoronary substance P (20 pmol/min).
283 ents who might benefit from further adjuvant intracoronary therapies, such as thrombolysis, vasodilat
284 r development of molecular MR imaging-guided intracoronary therapy.
285  elements in patients who succumbed to fatal intracoronary thrombosis.
286 atient population with a high probability of intracoronary thrombosis.
287                                   Persistent intracoronary thrombus after plaque rupture is associate
288                                      Routine intracoronary thrombus aspiration before primary percuta
289               The clinical effect of routine intracoronary thrombus aspiration before primary percuta
290              Ten patients were found to have intracoronary thrombus on x-ray coronary angiography (le
291 tery disease (atherosclerotic plaques and/or intracoronary thrombus).
292 motor tone after CTO reopening suggests that intracoronary ultrasound assessment is of paramount impo
293                                              Intracoronary ultrasounds failed to show changes of the
294 13 patients, distal vessels were assessed by intracoronary ultrasounds.
295 ular tachycardia, which was only resolved by intracoronary vasodilator injection.
296  patients to date demonstrates no benefit of intracoronary versus intravenous abciximab administratio
297 udy was to investigate potential benefits of intracoronary versus intravenous abciximab bolus adminis
298                     Among diabetic patients, intracoronary versus intravenous abciximab bolus was ass
299 tor occupancy was significantly greater with intracoronary versus intravenous administration: first b
300 yocardial infarction frame count (cTFC) with intracoronary versus intravenous administration: pre-PCI

 
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