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

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