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1 age: 68 +/- 12 years; 53.2% had a history of ischemic heart disease).
2 d cardiomyopathy and 21 patients (21.6%) had ischemic heart disease).
3 larizing damaged myocardium in patients with ischemic heart disease.
4 s with acute myocardial infarction or stable ischemic heart disease.
5  of cardiac stem/progenitor cell therapy for ischemic heart disease.
6 tion of PM2.5 with circulatory mortality and ischemic heart disease.
7 also be confirmed in patients suffering from ischemic heart disease.
8 y age, sex, time of symptom onset, and known ischemic heart disease.
9 novel diagnostic and therapeutic targets for ischemic heart disease.
10 lated with QTc prolongation in patients with ischemic heart disease.
11  reducing myocardial injury in subjects with ischemic heart disease.
12 2 could be a potential therapeutic target in ischemic heart disease.
13 onservative strategy in patients with stable ischemic heart disease.
14  clinical workup and therapeutic guidance in ischemic heart disease.
15  ejection fraction not caused by valvular or ischemic heart disease.
16 rophy, cardio-oncology, aortic stenosis, and ischemic heart disease.
17 y and the proportion of adults with baseline ischemic heart disease.
18 ding those presenting early or known to have ischemic heart disease.
19 1941-1994) for mortality from all causes and ischemic heart disease.
20 bral microbleeds, hypertension, diabetes and ischemic heart disease.
21 y for the management of patients with stable ischemic heart disease.
22 se affects almost one-third of patients with ischemic heart disease.
23 poptosis is a significant problem underlying ischemic heart disease.
24 ng the therapeutic potential of AC modRNA in ischemic heart disease.
25          Equal numbers in each group died of ischemic heart disease.
26  saved for each exposed worker who died from ischemic heart disease.
27 ing fluid was recently linked to deaths from ischemic heart disease.
28 -effectiveness of CABG versus PCI for stable ischemic heart disease.
29 0, 5,807) life-years among those who died of ischemic heart disease.
30 edical therapy alone in patients with stable ischemic heart disease.
31 ents who had both type 2 diabetes and stable ischemic heart disease.
32  and ameliorates remodeling in patients with ischemic heart disease.
33 ysis of preclinical data of cell therapy for ischemic heart disease.
34 ticularly high rates of premature death from ischemic heart disease.
35 scular disease but one only half as great on ischemic heart disease.
36 maging immune activity in organs involved in ischemic heart disease.
37 tion report of no association between SU and ischemic heart disease.
38 duced risks of ischemic vascular disease and ischemic heart disease.
39 ve coronary angiography for suspected stable ischemic heart disease.
40 nce on mitral valve geometry and function in ischemic heart disease.
41 ticipants undergoing evaluation for possible ischemic heart disease.
42 revalence/incidence data for each NCD except ischemic heart disease.
43 n is often performed in patients with stable ischemic heart disease.
44 evalence/incidence data for each NCD, except ischemic heart disease.
45 ng that is independent of clinically evident ischemic heart disease.
46  with neither personal nor family history of ischemic heart disease.
47 ally translatable therapeutic strategies for ischemic heart disease.
48 ociation was modified by age, sex, and prior ischemic heart disease.
49 e was 75 years, 73% were female, and 23% had ischemic heart disease.
50 cular contractions (>5000/24 h) and no known ischemic heart disease.
51 iding important diagnostic information about ischemic heart diseases.
52 agnoses (in months) was HF 11.7 (11.6-11.8), ischemic heart disease 1.6 (1.5-1.7), stroke 6.4 (6.3-6.
53         Five-year risk ratios were lower for ischemic heart disease (1.3 [1.3-1.4]), stroke (2.2 [2.1
54 9-1.6), 1.5 (1.2-2.0), and 2.0 (1.4-2.9) for ischemic heart disease; 1.4 (0.9-2.1), 1.2 (0.8-1.9), an
55  analyses revealed a significant increase in ischemic heart disease (10-year hazard ratio, 1.14; 95%
56 litus (+13.1% [95% CI, 10.1-16.0]) but lower ischemic heart disease (-10.6% [95% CI, -13.6 to -7.6])
57 ation was observed in 30.5% of patients with ischemic heart disease: 11.3% had mild airflow limitatio
58  at the 90th and 10th percentile was 2.0 for ischemic heart disease (119.1 vs 235.7 deaths per 100000
59 ercutaneous coronary intervention for stable ischemic heart disease, 1550, 2776, and 6661 received BM
60                        South Asians had more ischemic heart disease (+16.5% [95% CI, 14.3-18.6]), hyp
61 ulation, which ranked third in the US behind ischemic heart disease (2447) and low back and neck pain
62 riable odds ratio estimates were as follows: ischemic heart disease 3.30 (95% confidence interval, 2.
63 aths globally between 1990 and 2017 were for ischemic heart disease (3.2 million) and stroke (2.2 mil
64 fold for myocardial infarction, 3.2-fold for ischemic heart disease, 3.2-fold for ischemic stroke, an
65  was responsible for 31% of all deaths, with ischemic heart disease (31%) and cerebrovascular disease
66 mated loss in life expectancy was related to ischemic heart disease (36% in men, 31% in women) but de
67 D as the underlying cause, including chronic ischemic heart disease (42% of CVD deaths), hypertensive
68 it, 1.15; 95% CI, 1.01-1.31; p = 0.041), and ischemic heart disease (7.39; 95% CI, 1.57-34.7; p = 0.0
69 5.6% were women, 23.4% were Black, 53.5% had ischemic heart disease, 87.7% had symptomatic heart fail
70 ary events (myocardial infarction plus fatal ischemic heart disease), 8849 and 10,922 ischemic stroke
71 ubstantial health care spending in 2016 were ischemic heart disease ($89.3 billion [95% CI, $81.1-$95
72 tion fraction who have a lower prevalence of ischemic heart disease, a less severe hemodynamic, bioma
73                                We found that ischemic heart disease accounted for only 12% of the com
74                                              Ischemic heart disease accounted for the second-highest
75 ulant rivaroxaban) for patients with chronic ischemic heart disease, acute coronary syndromes, and th
76                 In contrast to patients with ischemic heart disease, after ICD shock HCM patients rar
77 l PM2.5 was associated with a higher risk of ischemic heart disease among aluminum manufacturing work
78 y-related mortality, and higher incidence of ischemic heart disease among PLWHIV in cohort studies) o
79 nd mortality (all-cause, cardiovascular, and ischemic heart disease) among 835 white men in the Norma
80 d concordance statistic of 0.70 and 0.70 for ischemic heart disease and 0.63 and 0.66 for stroke, res
81 ance statistics ranged from 0.66 to 0.67 for ischemic heart disease and 0.68 to 0.72 for stroke.
82 were 0.87 (95% CI: 0.78, 0.97; P = 0.01) for ischemic heart disease and 0.80 (95% CI: 0.73, 0.88; P <
83  was 0.90 (95% CI: 0.75, 1.08; P = 0.27) for ischemic heart disease and 0.88 (0.72, 1.08; P = 0.22) f
84 he equation for prognostic information about ischemic heart disease and all-cause death was evaluated
85          Secondary outcomes included 10-year ischemic heart disease and all-cause death.
86 d vegetables was associated with low risk of ischemic heart disease and all-cause mortality.
87  vegetables, are associated with low risk of ischemic heart disease and all-cause mortality.
88 were 2.5 times and 5.9 times more at risk of ischemic heart disease and cardiomyopathy/heart failure
89                                              Ischemic heart disease and cerebrovascular disease age-s
90 o adjusted for competing risks of death from ischemic heart disease and death from any cancer], 3.45;
91                                              Ischemic heart disease and greater age, but not diabetes
92 in myocardium from patients with valvular or ischemic heart disease and heart failure with preserved
93 erapeutic armamentarium in the fight against ischemic heart disease and heart failure.
94 societies, the most common drivers of HF are ischemic heart disease and hypertension.
95                                              Ischemic heart disease and ischemic stroke comprise the
96 declines in the incidence and mortality from ischemic heart disease and ischemic stroke since the mid
97 e clinical events among patients with stable ischemic heart disease and moderate or severe ischemia.
98 onservative strategy in patients with stable ischemic heart disease and moderate/severe myocardial is
99 al population, mainly because of deaths from ischemic heart disease and other smoking-related disease
100                    However, mortality due to ischemic heart disease and other somatic diseases decrea
101 at road traffic noise increases the risk for ischemic heart disease and potentially other cardiometab
102                         Patients with stable ischemic heart disease and previous myocardial infarctio
103 risk of adverse outcome after adjustment for ischemic heart disease and QRS width (hazard ratio [HR]:
104 tment in improving survival in patients with ischemic heart disease and reduced ejection fraction.
105                                              Ischemic heart disease and stroke are the predominant ca
106 rpose We aimed to predict individual risk of ischemic heart disease and stroke in 5-year survivors of
107 Substantial differences exist between county ischemic heart disease and stroke mortality rates.
108                                      Results Ischemic heart disease and stroke occurred in 265 and 29
109                                              Ischemic heart disease and stroke remain the leading cau
110 y can predict individual risk for subsequent ischemic heart disease and stroke with reasonable accura
111  through age 50 years for the development of ischemic heart disease and stroke.
112 lence of airflow limitation in patients with ischemic heart disease and the effects on quality of lif
113 ents who had both type 2 diabetes and stable ischemic heart disease and were enrolled in the Bypass A
114 e pathogenesis of common maladies, including ischemic heart diseases and inflammation.
115 f noninvasive modalities in the detection of ischemic heart disease, and discuss nonischemic cardiomy
116 ies (diabetes, hypertension, hyperlipidemia, ischemic heart disease, and glaucoma).
117 y impairment, including sickle cell disease, ischemic heart disease, and heart failure.
118 additional adjustment for diabetes mellitus, ischemic heart disease, and hypertension.
119  hearts is the most comprehensive to date in ischemic heart disease, and its similarities to nonische
120 996 through 2013; with spending on diabetes, ischemic heart disease, and low back and neck pain accou
121     Mortality due to cardiovascular disease, ischemic heart disease, and myocardial infarction.
122 nosis and Management of Patients with Stable Ischemic Heart Disease, and the 2018 European Society of
123 ts with atrial fibrillation, cardiomyopathy, ischemic heart disease, and valvular heart disease.
124 rs, and comorbid conditions of HF (including ischemic heart disease, aortic valve disease, atrial fib
125                                              Ischemic heart diseases are leading causes of death and
126             Major depressive disorder topped ischemic heart disease as the number one cause of disabi
127 king fluids and mortality, particularly from ischemic heart disease, as well as an instructive exampl
128 ere 45 to 83 years of age and free of HF and ischemic heart disease at baseline.
129 d our ability to understand the pathology of ischemic heart disease, atherosclerosis, and heart failu
130 n the prevalence, symptoms, and prognosis of ischemic heart disease between men and women.
131 ts referred for cardiac CT for evaluation of ischemic heart disease between September 2014 and March
132 ontrol is the cornerstone of managing stable ischemic heart disease but is often not achieved.
133 PCI) relieves angina in patients with stable ischemic heart disease, but clinical trials have not sho
134 centrations are associated with high risk of ischemic heart disease, but whether this is also the cas
135  from all cardiovascular diseases, including ischemic heart disease, cerebrovascular disease, ischemi
136  mortality risks for cardiovascular disease, ischemic heart disease, cerebrovascular disease, or card
137 s, hypertension, dyslipidemia) and diseases (ischemic heart disease, cerebrovascular, and peripheral
138                               In addition to ischemic heart disease, certain nonischemic conditions m
139 tial hypertension, coronary atherosclerosis, ischemic heart disease, chronic ischemic heart disease,
140 ent comorbidities, including cardiomyopathy, ischemic heart disease; chronic renal failure, with and
141 zations, whereas 172 suffered from a chronic ischemic heart disease (CIHD), 126 of whom underwent cha
142    The methods are illustrated using data on ischemic heart disease classification, and data from the
143 n patients with hypertrophic cardiomyopathy, ischemic heart disease, diabetes mellitus, and more.
144 ased, including liver disease, hypertension, ischemic heart disease, disorders of lipid metabolism, a
145         Coronary arteries from patients with ischemic heart disease express large amounts of IL-1beta
146 United States who were followed for incident ischemic heart disease from 1998 to 2012, and we address
147                                              Ischemic heart disease has been relatively uncommon.
148 ic resonance strain imaging in patients with ischemic heart disease have been limited by sample size
149  last few decades, but mortality trends from ischemic heart disease have been more varied, with some
150 cardiac comorbidities in patients with COPD: ischemic heart disease, heart failure, and atrial fibril
151 xamination to identify signs and symptoms of ischemic heart disease, heart failure, and severe valvul
152 morbidity and mortality rates in adults with ischemic heart disease, heart failure, or cardiac surger
153      Among patients with diabetes and stable ischemic heart disease, higher SYNTAX scores predict hig
154 larization is an effective means of treating ischemic heart disease; however, current therapeutic rev
155  by national guidelines in the management of ischemic heart disease; however, few studies have examin
156 lung cancer (HR = 1.08, 95% CI: 1.02, 1.14), ischemic heart disease (HR = 1.09, 95% CI: 1.02, 1.16),
157 3; 95% confidence interval [CI], 1.01-1.06), ischemic heart disease (HR, 1.06; 95% CI, 1.02-1.09), re
158 (HR per 10 ppb, 1.06; 95% CI, 1.04-1.08) and ischemic heart disease (HR, 1.08; 95% CI, 1.05-1.11).
159 ] per 10 mug/m(3), 1.13; 95% CI, 1.08-1.18), ischemic heart disease (HR, 1.16; 95% CI, 1.10-1.23), an
160 ar intake was also inversely associated with ischemic heart disease (HR: 0.56; 95% CI: 0.35 to 0.87)
161 vement in clinical outcomes of patients with ischemic heart disease (IHD) after ventricular tachycard
162 ation to clarify the role of birth weight in ischemic heart disease (IHD) and lipids.
163  Cardiovascular diseases (CVDs), principally ischemic heart disease (IHD) and stroke, are the leading
164            However, their long-term risks of ischemic heart disease (IHD) and whether such risks are
165                                   Background Ischemic heart disease (IHD) has been considered the top
166                       The pathogenic role of ischemic heart disease (IHD) in heart failure (HF) with
167                               Recognition of ischemic heart disease (IHD) is often delayed or deferre
168 n to cardiovascular disease (CVD) mortality, ischemic heart disease (IHD) mortality, and all-cause mo
169 iations between long-term PM2.5 exposure and ischemic heart disease (IHD) mortality, as established i
170                                              Ischemic heart disease (IHD) occurred in 62% of patients
171 s in morbidity and mortality attributable to ischemic heart disease (IHD) require an understanding of
172 aise the impact of risk factor confluence on ischemic heart disease (IHD) risk by testing whether gen
173 etween saturated fatty acid (SFA) intake and ischemic heart disease (IHD) risk is debated.
174                   Obesity leads to increased ischemic heart disease (IHD) risk, but the risk is thoug
175 e of invasive coronary angiography in stable ischemic heart disease (IHD) varies widely.
176                                     Previous ischemic heart disease (IHD) was a predictor of in-hospi
177   To clarify the role of thyroid function in ischemic heart disease (IHD) we assessed IHD risk and ri
178 g 7,326 major coronary events (MCEs), 37,992 ischemic heart disease (IHD), and 42,951 strokes were re
179 he pollutants and all-cause, cardiovascular, ischemic heart disease (IHD), and respiratory mortality.
180                      Hospital admissions for ischemic heart disease (IHD), congestive heart failure (
181  including myocardial infarction (MI), other ischemic heart disease (IHD), congestive heart failure (
182 isease, previous myocardial infarction (MI), ischemic heart disease (IHD), heart failure (HF), atrial
183       COPD was independently associated with ischemic heart disease (IHD), heart failure (HF), atrial
184 ed estimates of the association of IDO1 with ischemic heart disease (IHD), ischemic stroke and their
185 l hypercholesterolemia (FH) in subjects with ischemic heart disease (IHD), premature IHD, and severe
186  cardiovascular outcomes were CVD [including ischemic heart disease (IHD), stroke, and vascular inter
187  rheumatoid arthritis (RA) is independent of ischemic heart disease (IHD).
188 acids (TFAs) are a well-known risk factor of ischemic heart disease (IHD).
189 s), has been associated with a lower risk of ischemic heart disease (IHD).
190  depression and Alzheimer's disease, but not ischemic heart disease (IHD).
191 red with that in nonstented patients without ischemic heart disease (IHD).
192 ejection fraction overall and in relation to ischemic heart disease (IHD).
193 the prevalence, presentation and outcomes of ischemic heart disease (IHD).
194 vance of animal foods to the pathogenesis of ischemic heart disease (IHD).
195                          Ischemic and/or non-ischemic heart diseases (IHD and/or NIHD) were detected
196 ques in coronary arteries from patients with ischemic heart disease implying a role in human arterial
197         Physicians have traditionally viewed ischemic heart disease in a cardiocentric manner: plaque
198 ost frequently identified cause of death was ischemic heart disease in both sexes: 71.7% among women
199  are associated with obesity and the risk of ischemic heart disease in men.
200 mained a significant predictor of asthma and ischemic heart disease in most bipollutant models.
201 sumption is associated with a higher risk of ischemic heart disease in patients with diabetes.
202 ations have been associated with low risk of ischemic heart disease in prospective studies, but resul
203        We will thoroughly review the role of ischemic heart disease in the pathogenesis of HF with re
204 d into 2 documents addressing ACS and stable ischemic heart disease individually.
205 l incidence rate (IR) for each condition are ischemic heart disease, IR=1518.7; myocardial infarction
206                                              Ischemic heart disease is a complex disease process caus
207                                              Ischemic heart disease is a leading cause of heart failu
208                                              Ischemic heart disease is a major cause of out-of-hospit
209 ure with reduced ejection fraction caused by ischemic heart disease is associated with increased morb
210 vascularization improves prognosis in stable ischemic heart disease is controversial.
211  Risk stratification in patients with stable ischemic heart disease is essential to guide treatment d
212  the prevalence of angina and mortality from ischemic heart disease is higher for women than men.
213                                              Ischemic heart disease is the leading cause of heart fai
214                                              Ischemic heart disease is the number one cause of death
215 OPD) exacerbations, pneumonias, lung cancer, ischemic heart disease, ischemic stroke, and all-cause m
216    Its major clinical manifestations include ischemic heart disease, ischemic stroke, and peripheral
217 e risk of first fatal or nonfatal CVD event (ischemic heart disease, ischemic stroke, heart failure,
218                           Heart samples from ischemic heart disease (ISHD) patients served as heart f
219 dalities for the diagnosis and management of ischemic heart disease, it is important for radiologists
220 condition categories (eg, diabetes mellitus, ischemic heart disease, liver disease).
221  to be younger, men, have diabetes mellitus, ischemic heart disease, lower left ventricular ejection
222 ed cardiovascular care for the management of ischemic heart disease may not be infected with this nov
223 roups including patients with versus without ischemic heart disease, men versus women, those aged <75
224 vative strategy) in participants with stable ischemic heart disease, moderate or severe ischemia, and
225                     Participants with stable ischemic heart disease, moderate or severe ischemia, and
226  1.1%-3.6%) and 6.9% (95% CI, 4.0%-9.9%) for ischemic heart disease mortality among adults 65 years a
227                                              Ischemic heart disease mortality and long-term exposure
228         The association between coal use and ischemic heart disease mortality diminished with increas
229            An overall trend for reduction in ischemic heart disease mortality was observed, most pron
230 86, 4.68) for all-cause, cardiovascular, and ischemic heart disease mortality, respectively.
231 men compared with men, with similar risk for ischemic heart disease mortality.
232 Mortality rates (MRs) for each condition are ischemic heart disease, MR=105.5; ischemic stroke, MR=42
233 rosclerosis, ischemic heart disease, chronic ischemic heart disease, myocardial infarction, and hyper
234                   Twenty sepsis patients, 11 ischemic heart disease, nine dilated cardiomyopathy, and
235 s between ingestion of inorganic arsenic and ischemic heart disease, nonmalignant respiratory disease
236                                              Ischemic heart disease (odds ratio [OR], 7.21; P < 0.001
237  HF was higher in patients with a history of ischemic heart disease or atrial fibrillation.
238 age, 67+/-11.6 years; 88 men) with suspected ischemic heart disease or known coronary disease who had
239  altered abundance in septic cardiomyopathy, ischemic heart disease, or dilated cardiomyopathy, in co
240 did not differ according to age, race, prior ischemic heart disease, or ejection fraction (all intera
241  and the coexistence of atrial fibrillation, ischemic heart disease, or hypertensive cardiopathy.
242 defined as a history of atrial fibrillation, ischemic heart diseases, or congestive heart failure.
243  cancer (HR = 1.14; 95% CI: 1.03, 1.27), and ischemic heart disease (overall HR = 1.61; 95% CI: 1.14,
244                   EBW occurred most often in ischemic heart disease patients (N=114, 49%) compared wi
245 R 0.33, 95% CI 0.14 to 0.80, p = 0.010), and ischemic heart disease (POR 0.46, 95% CI 0.29 to 0.73, p
246 e for HIV and the presence of a cough, COPD, ischemic heart disease, pregnancy-related mortality, mat
247                                              Ischemic heart disease prevalence increased for all to 2
248 genetic variants near IRF2BP2 associate with ischemic heart disease progression in humans.
249                         Patients with stable ischemic heart disease remain at substantial risk for lo
250                                              Ischemic heart disease remains rare in most countries.
251                                              Ischemic heart disease remains the foremost cause of dea
252 y syndrome (ACS), the acute manifestation of ischemic heart disease, remains a major cause of morbidi
253                                              Ischemic heart disease resulting from myocardial infarct
254                      In patients with stable ischemic heart disease, routine revascularization was no
255  (rate ratio [RR], 1.14; 95% CI, 1.13-1.14), ischemic heart disease (RR, 1.11; 95% CI, 1.10-1.11), ma
256  (rate ratio [RR], 1.62; 95% CI, 1.20-21.8), ischemic heart disease (RR, 4.31; 95% CI, 3.38-5.49), an
257 ), asthma (RR=1.12, 95% CI: 1.03, 1.22), and ischemic heart disease (RR=1.19, 95% CI: 1.03, 1.38).
258   Autologous and allogeneic cell therapy for ischemic heart disease show a similar improvement in lef
259  prediction model including QRS duration and ischemic heart disease significantly improved the net re
260 -world population among subjects with stable ischemic heart disease (SIHD) and acute coronary syndrom
261 sk factor management in patients with stable ischemic heart disease (SIHD) and diabetes mellitus (DM)
262 ve (FFR) measurement in patients with stable ischemic heart disease (SIHD) are uncertain, as prior st
263                                       Stable ischemic heart disease (SIHD) is a leading cause of deat
264                     All patients with stable ischemic heart disease (SIHD) should be managed with gui
265 ularization strategy in patients with stable ischemic heart disease (SIHD) who have type 2 diabetes (
266  long-term prognosis in patients with stable ischemic heart disease (SIHD).
267 atures such as age, history of arrhythmia or ischemic heart disease, size of goiter, and severity of
268    Cardiovascular diseases (CVDs), including ischemic heart disease, stroke, and heart failure, are w
269 10 dietary factors accounts for 18.2% of all ischemic heart disease, stroke, and type 2 diabetes cost
270 years associated with the development of HF, ischemic heart disease, stroke, peripheral artery diseas
271 rtension, diabetes mellitus, hyperlipidemia, ischemic heart disease, stroke, total cholesterol level,
272 ween acute myocardial Infarction and chronic ischemic heart disease subgroups.
273              More people die every year from ischemic heart disease than any other disease.
274 in patients with congestive heart failure or ischemic heart disease than in those without (P = 0.021
275 nosis and Management of Patients with Stable Ischemic Heart Disease, the 2014 Focused Update of the A
276 ts with systolic heart failure not caused by ischemic heart disease, the association between the ICD
277 TSD) is associated with an increased risk of ischemic heart disease, though the pathophysiologic mech
278 ogenic precursors link coronary anomalies to ischemic heart disease.Though coronary arteries are cruc
279  randomly assigned 2287 patients with stable ischemic heart disease to an initial management strategy
280  phases of the disease, potentially allowing ischemic heart disease to be tracked during a patient's
281 t they might be used in patients with stable ischemic heart disease to identify those at high risk fo
282 , including individual data of patients with ischemic heart disease treated with cell therapy.
283 ty of mitral regurgitation, 67 patients with ischemic heart disease underwent cardiac magnetic resona
284 med stress score <3 and without a history of ischemic heart disease), valvular, and end-organ disease
285 rtality ratios and absolute excess risks for ischemic heart disease, valvular heart disease, and card
286 ar disease such as congestive heart failure, ischemic heart disease, valvular heart disease, pulmonar
287                               Mortality from ischemic heart disease was lower among former players th
288                                              Ischemic heart disease was present in 72% of patients.
289 ntative sample of 50 patients with suspected ischemic heart disease was retrospectively selected from
290 cells in immunosuppressed animals with acute ischemic heart disease, we previously showed that these
291 y, peripheral neuropathy, diabetic foot, and ischemic heart disease were 21.9%, 17.6%, 28.0%, 6.2%, a
292 creatinine level, black race, older age, and ischemic heart disease were associated with troponin ele
293 in acute coronary syndromes (ACS) and stable ischemic heart disease were combined into 1 document.
294 , nonshockable rhythm, arterial lactate, and ischemic heart disease were identified as independent pr
295  tissue samples from patients suffering from ischemic heart disease were used to validate our finding
296 d exertional E/e' >13), excluding those with ischemic heart disease, were recruited in a tertiary car
297                Among the 3,103 patients with ischemic heart disease who were recruited, lung function
298  significant in the pathophysiology of human ischemic heart disease with a preservative role in maint
299 ted myocardium, even in patients with stable ischemic heart disease with preserved LV ejection fracti
300 dox is an observation of a low prevalence of ischemic heart disease, with high intakes of saturated f

 
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