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PedAM

Pediatric Disease Annotations & Medicines




Disease myocardial infarction
Symptom C0151814|coronary occlusion
Sentences 7
PubMedID- 21764664 The aim of this study was to decipher the angiogenic, atherosclerotic, and inflammatory mrna profiles in whole blood samples collected at the site of coronary occlusion in patients with st-elevation myocardial infarction (stemi).
PubMedID- 25713468 Aims: the aim of this study was to report the association between episodes of anger and acute myocardial infarction (mi) in patients with angiographically confirmed coronary occlusion.
PubMedID- 22691691 Brain tissue samples from normal (n = 7; 2 females and 5 males) and alzheimer’s patients (n = 11; 6 females and 5 males) were used, with agonal states including: bronchopneumonia, cardiac failure, hypertension, pulmonary embolus, sideroblastic anaemia, coronary occlusion, carcinoma of left kidney, myocardial infarction and ischemic heart disease.
PubMedID- 20433716 The aim of the present study was to evaluate whether mar can be determined from the contrast enhanced myocardium using steady-state free precession (ssfp) cine cardiovascular magnetic resonance (cmr) performed one week after the acute event in st-elevation myocardial infarction (stemi) patients with total coronary occlusion.
PubMedID- 20435184 Collateral pressure and flow in acute myocardial infarction with total coronary occlusion correlate with angiographic collateral grade and creatine kinase levels.
PubMedID- 23976860 Nstemi was identified by st-segment depression or t-wave inversion, a positive serum troponin biomarker, absence of st-segment elevation, and chest pain or equivalent angina symptoms.1 unstable angina was defined as “evidence of coronary occlusion without myocardial infarction,” in accordance with the diagnosis related group criteria for “angina pectoris, intermediate coronary syndrome.” recordings were automatically scanned, manually edited, and annotated.
PubMedID- 23815556 We studied coronary occlusion/reperfusion-induced myocardial infarction (mi) in rabbits during a 9-months follow-up using 3.0 t magnetic resonance scanner, and confirmed the presence of mi in acute phase and lm in chronic phase using histopathology.

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