CIRCULATION

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Codice:

E037295

ISSN:

0009-7322

Dati Generali

Pubblicazioni (217)

2011 ACCF/AHA/HRS focused updates incorporated into the ACC/AHA/ESC 2006 guidelines for the management of patients with atrial fibrillation: a report of the American College of Cardiology Foundation/ American Heart Association Task Force on practice guidelines. American College of Cardiology Foundation/American Heart Association Task Force.

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25th anniversary of the International Long-QT Syndrome Registry: an ongoing quest to uncover the secrets of long-QT syndrome.

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A New Method for Quantification of Regurgitant Flow Rate Using Color Doppler Flow Imaging of the Flow Convergence RegionProximal to a Discrete Orifice - An In Vitro Study

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A Recessive Variant of the Romano-Ward Long QT Syndrome

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ACC/AHA/ESC 2006 Guidelines for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death: a report of the American College of Cardiology/American Heart Association Task Force and the European Society of Cardiology Committee for Practice Guidelines (writing committee to develop Guidelines for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death): developed in collaboration with the European Heart Rhythm Association and the Heart Rhythm Society

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ACC/AHA/ESC 2006 Guidelines for the Management of Patients with Atrial Fibrillation: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines and the European Society of Cardiology Committee for Practice Guidelines (Writing Committee to Revise the 2001 Guidelines for the Management of Patients With Atrial Fibrillation): developed in collaboration with the European Heart Rhythm Association and the Heart Rhythm Society.

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ACC/AHA/ESC guidelines for the management of patients with supraventricular arrhythmias¿executive summary: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines and the European Society of Cardiology Committee for Practice Guidelines (Writing Committee to Develop Guidelines for the Management of Patients With Supraventricular Arrhythmias).

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Abstract 12013: Nuclear Localization of PDGFRa Tyrosine Kinase Represents a Novel Mechanism Controlling the Fibrotic Response of Mesenchymal Stromal Cells to Myocardial Ischemia

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Abstract 9386: Attenuation of Post-infarct Cardiac Hypertrophy by Allogeneic Cell-mediated Supplemental Igf-1 Propeptide Delivery

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Age and sex-related differences in the clinical manifestations of congenital long QT syndrome: findings from the International Prospective LQTS Registry

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Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes.

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Ambulatory blood pressure is superior to clinic blood pressure in predicting treatment-induced regression of left ventricular hypertrophy. SAMPLE Study Group. Study on Ambulatory Monitoring of Blood Pressure and Lisinopril Evaluation

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An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of CASQ2 -Catecholaminergic Polymorphic Ventricular Tachycardia

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Arterial baroreflexes and ventricular tachycardia.

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Association of Hydroxychloroquine with QTc Interval in Patients with COVID-19

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Atherothrombotic Risk Stratification and the Efficacy and Safety of Vorapaxar in Patients with Stable Ischemic Heart Disease and Previous Myocardial Infarction

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Atorvastatin addition to losartan or to atenolol and recurrence of paroxysmal atrial fibrillation in hypertension

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Autonomic mechanisms and sudden death. New insights from analysis of baroreceptor reflexes in conscious dogs with and without a myocardial infarction.

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Autonomic mechanisms in ventricular fibrillation induced by myocardial ischemia during exercise in dogs with healed myocardial infarction. An experimental preparation for sudden cardiac death.

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Autonomic nervous system and sudden cardiac death. Experimental basis and clinical observations for post-myocardial infarction risk stratification.

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Baroreceptor reflex control of heart rate: a predictor of sudden cardiac death.

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Baroreflex sensitivity and heart rate variability in the identification of patients at risk for life-threatening arrhythmias: implications for clinical trials.

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Baroreflex sensitivity, clinical correlates, and cardiovascular mortality among patients with a first myocardial infarction. A prospective study.

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CAST and beyond. Implications of the Cardiac Arrhythmia Suppression Trial. Task Force of the Working Group on Arrhythmias of the European Society of Cardiology.

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CD34+ and endothelial progenitor cells in patients with various degrees of congestive heart failure.

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CONTROLLED TRIAL OF PHYSICAL TRAINING IN CHRONIC HEART FAILURE. EXERCISE PERFORMANCE, HEMODYNAMICS, VNTILATION AND AUTONOMIC FUNCTION

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Calmodulin mutations associated with recurrent cardiac arrest in infants.

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Cangrelor, Tirofiban, and Chewed or Standard Prasugrel Regimens in Patients with ST-Segment-Elevation Myocardial Infarction: Primary Results of the FABOLUS-FASTER Trial

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Cardiac Histological Substrate in Patients With Clinical Phenotype of Brugada Syndrome

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Cardiac sodium channel dysfunction in sudden infant death syndrome.

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Chronic thromboembolic pulmonary hypertension (CTEPH): results from an international prospective registry

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Clinical Aspects of Type 3 Long-QT Syndrome: An International Multicenter Study.

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Clinical Benefit of Evolocumab by Severity and Extent of Coronary Artery Disease: An Analysis from FOURIER.

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Clinical Impact of Persistent Left Bundle-Branch Block After Transcatheter Aortic Valve Implantation With CoreValve Revalving System.

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Clinical Implications for affected parents and siblings of probands with Long QT Syndrome

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Clinical and Molecular Characterization of Patients with Catecholominergic Polymorphic Ventricular Tachycardia.

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Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families.

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Clinical implications for affected parents and siblings of probands with long-QT syndrome.

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Clinical management of catecholaminergic polymorphic ventricular tachycardia the role of left cardiac sympathetic denervation

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Clinical phenotype and functional characterization of CASQ2 mutations associated with Catecholaminergic Polymorphic Ventricular Tachycardia

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Consistent Reduction in Periprocedural Myocardial Infarction with Cangrelor as Assessed by Multiple Definitions: Findings from CHAMPION PHOENIX (Cangrelor Versus Standard Therapy to Achieve Optimal Management of Platelet Inhibition)

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Coronary arterial spasm as a cause of exercise-induced ST-segment elevation in patients with variant angina

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Cytokine-induced mobilization of circulating endothelial progenitor cells enhances repair of injured arteries

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DEMONSTRABLE CARDIAC REINNERVATION AFTER HUMAN HEART TRANSPLANTATION BY AROTID BAROREFLEX MODULATION OF RR INTERVAL

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Delayed after depolarizations elicited in vivo by left stellate ganglion stimulation.

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Delayed afterdepolarizations elicited in vivo by left stellate ganglion stimulation.

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Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects.

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Derivation and Validation of the PRECISE-HBR Score to Predict Bleeding After Percutaneous Coronary Intervention

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Desmoplakin cardiomyopathy, a fibrotic and inflammatory form of cardiomyopathy distinct from typical dilated or arrhythmogenic right ventricular cardiomyopathy

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Diagnostic criteria for the long QT syndrome. An update.

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Dispersion of the QT interval. A marker of therapeutic efficacy in the idiopathic long QT syndrome.

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Dispersion of the QT interval. A marker of therapeutic efficacy in the idiopathic long QT syndrome.

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Distinct patterns of calcium transients during early and delayed afterdepolarizations induced by isoproterenol in ventricular myocytes.

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Do increases in markers of vagal activity imply protection from sudden death? The case of scopolamine.

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Donor Age Negatively Influences Cytoprotective but Not Proangiogenic Paracrine Properties of Human Mesenchymal Stem Cells.

Contributo in Atti di convegno

Dynamic interactions between musical, cardiovascular, and cerebral rhythms in humans

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Dynamic interactions between musical, cardiovascular, and cerebral rhythms in humans

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ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome.

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Early afterdepolarizations induced in vivo by reperfusion of ischemic myocardium. A possible mechanism for reperfusion arrhythmias.

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Early afterdepolarizations induced in vivo by reperfusion of the ischemic myocardium. A possible mechanism for reperfusion arrhythmias.

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Effect of calcium channel block on the wall motion abnormality of the idiopathic long QT syndrome.

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Effect of telmisartan and ramipril on arial fibrillation episodes recurrence and severity in hypertensive patients with metabolic syndrome and lone paroxysmal atrial fibrillation

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Effect of telmisartan on paroxymal atrial fibrillation in hypertensive patients with different left atrial size

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Effect of transdermal nitroglycerin, oral N-acetylcysteine or both in the long term treatment of unstable angina pectoris

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Effect of valsartan and ramipril on P wave dispersion and prevention of atrial fibrillation recurrence in hypertensive patients with Ione paroxysmal atrial fibrillation

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Effect of valsartan on insulin sensitivity, leptin, and BMI in hypertensive obese patients

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Effectiveness and limitations of beta-blocker therapy in congenital Long QT Syndrome.

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Effects of Intra-Aortic Balloon Pump on Markers of Right Ventricular Dysfunction Among End-Stage Heart Failure Patients Candidates to Cardiac Transplant or Ventricular Assist Device

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Effects of Patisiran, an RNA Interference Therapeutic, on Cardiac Parameters in Patients With Hereditary Transthyretin-Mediated Amyloidosis

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Effects of nifedipine on coronary hemodynamic findings during exercise in patients with stable exertional angina

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Effects of unilateral and bilateral carotid baroreflex stimulation on cardiac and neural sympathetic discharge oscillatory patterns.

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Effects of unilateral stellate ganglion stimulation and ablation on electrophysiologic changes induced by acute myocardial ischemia in dogs.

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Efficacy of permanent pacing in the management of high-risk patients with long QT syndrome.

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Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype.

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Enhancing the cardiomyogenic potential of human mesenchymal stem cells by modulation of miR expression.

Contributo in Atti di convegno

Evaluation of spatial aspects of T-wave complexity in the Long QT syndrome

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Evaluation of the spatial aspects of T-wave complexity in the long-QT syndrome.

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Evidence of genetic heterogeneity in Romano-Ward long QT syndrome. Analysis of 23 families.

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Exercise capacity before and after pulmonary thromboendoarterectomy in patients with chronic thromboembolic pulmonary hypertension

Contributo in Atti di convegno

Exercise training confers anticipatory protection from sudden death during acute myocardial ischemia

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Exercise training confers anticipatory protection from sudden death during acute myocardial ischemia.

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Exercise-induced increase in baroreflex sensitivity predicts improved prognosis after myocardial infarction.

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Exercise-induced increase in baroreflex sensitivity predicts improved prognosis after myocardial infarction.

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Factor V Leiden, But Not Prothrombin G20120A, Is Associated With Premature Myocardial Infarction

Contributo in Atti di convegno

Fibrinogen: a Circulating Factor in Search of Its Genetic Architecture

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From Vulnerable Plaque to Vulnerable Patient: A call for new definitions and risk assessment strategies: Part I

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From Vulnerable Plaque to Vulnerable Patient: A call for new definitions and risk assessment strategies: Part II.

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Gating Properties of SCN5A Mutations and the Response to Mexiletine in Long-QT Syndrome Type 3 Patients

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Genetic and molecular basis of cardiac arrhythmias: impact on clinical management. Part III.

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Genetic and molecular basis of cardiac arrhythmias: impact on clinical management.Parts I and II

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Genetically Akt modified mesenchymal stem cells secrete paracrine factors that increase cardiomyocyte contractility and improve ventricular function.

Contributo in Atti di convegno

Genetically engineered mesenchymal stem cells expressing Akt exhibit improved glucose metabolism, resistance to apoptosis and markedly improved performance of infarcted rat hearts.

Contributo in Atti di convegno

Genotype-Phenotype correlation in the Long QT Syndrome. Gene-specific triggers for life-threatening arrhythmias

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Heart Failure Resulting from Age-Related Cardiac Amyloid Disease Associated with Wild-Type Transthyretin: A Prospective, Observational Cohort Study

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Heart rate variability during specific sleep stages. A comparison of healthy subjects with patients after myocardial infarction.

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High efficacy of beta-blockers in Long QT Syndrome type 1: contribution of non-compliance and QT-prolonging drugs to the occurrence of beta-blocker treatment “failures”.

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Homozygous Deletion in KVLQT1 Associated With Jervell and Lange-Nielsen Syndrome.

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Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome.

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INFLUENCE OF TYPE OF SURGERY ON THE OCCURRENCE OF VAGAL REINNERVATION AFTER CARDIAC TRANSPLANTATION

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Identification of cardioprotective factors produced by fetal mesenchymal stem cells through a combined transcriptomic and proteomic approach.

Contributo in Atti di convegno

Identification of upregulated microRNAs in the plasma of patients with acute myocardial infarction

Contributo in Atti di convegno

Images in cardiovascular medicine. Endocardial implantation of a cardioverter-defibrillator in a 13-month-old child affected by long-QT syndrome and syndactyly.

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Impaired circadian modulation of sympathovagal activity in diabetes. A possible explanation for altered temporal onset of cardiovascular disease.

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Increased risk of arrhythmic events in Long-QT Syndrome with mutations in the Pore Region of the human Ether-a-go-go-Related gene potassium channel.

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Influence of hypoxia on adrenergic modulation of triggered activity in isolated adult canine myocytes

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Influence of pregnancy on the risk for cardiac events in patients with hereditary long QT syndrome. LQTS Investigators.

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Initiative: Setting Up a Basic Science Lab to Investigate Stem Cell Therapy in Italy

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Insights into the Pathogenesis of Catecholaminergic Polymorphic Ventricular Tachycardia from Engineered Human Heart Tissue

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Interplay between Mitral Regurgitation and Transcatheter Aortic Valve Replacement with the CoreValve Revalving System: A Multicenter Registry.

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Interplay between mitral regurgitation and transcatheter aortic valve replacement with the CoreValve Revalving System: a multicenter registry.

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KCNH2-K897T Is a Genetic Modifier of Latent Congenital Long-QT Syndrome.

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KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome.

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KCNJ2-Specific ECG abnormalities in Type 1 Andersen-Tawil Syndrome: the enlarged U wave, prolonged QU interval and left ventricular arrhythmias.

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Left cardiac sympathetic denervation in the management of high-risk patients affected by the long-QT syndrome.

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Left cardiac sympathetic denervation in the therapy of congenital long QT syndrome. A worldwide report.

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Left stellectomy in the prevention of ventricular fibrillation caused by acute myocardial ischemia in conscious dogs with anterior myocardial infarction.

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Letter by De Ferrari and Verrier regarding article, "Role of microvolt T-wave alternans in assessment of arrhythmia vulnerability among patients with heart failure and systolic dysfunction: primary results from the T-wave alternans sudden cardiac death in heart failure trial substudy"

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Letter by Ferrari et al regarding article, "long-term arrhythmia-free survival in patients with severe left ventricular dysfunction and no inducible ventricular tachycardia after myocardial infarction"

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Letter regarding article by Coronel et al, ''right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and computational study''

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Letter regarding article by Wichterle et al. Prevalent low-frequency oscillation of heart rate: novel predictor of mortality after myocardial infarction¿

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Long QT syndrome patients with mutations on the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.

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Long-QT syndrome after age 40

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Long-Term Outcome of Patients With Chronic Thromboembolic Pulmonary Hypertension: Results From an International Prospective Registry

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Losartan and prevention of atrial fibril1ation recurrence in hypertensive patients

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Low penetrance in the Long QT Syndrome. Clinical Impact.

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Low penetrance in the long-QT syndrome: clinical impact.

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Mapping of body surface potentials in patients with the idiopathic long QT syndrome.

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Meandering Pathway Leading From Genotyping to Personalized Management of Long-QT Syndrome

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Mental stress as a provocative test in patients with various clinical syndromes of coronary heart disease.

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Mesenchymal stem cells overesxpressing Akt prevent cardiac metabolic remodelling after infarction.

Contributo in Atti di convegno

Midwall mechanics is improved following regression of hypertensive left ventricular hypertrophy and normalization of chamber geometry

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Missense mutations in plakophilin-2 cause sodium current deficit and associate with a brugada syndrome phenotype

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Molecular and cell based therapies for protection, rescue and repair of ischemic myocardium: reasons for cautious optimism

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Molecular underpinning of ''good luck''

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Mortality in patients after a recent myocardial infarction: a randomized, placebo-controlled trial of azimilide using heart rate variability for risk stratification.

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Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS.

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Music and the heart. Interview by Emma Baines

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Mutations in the Cardiac Ryanodine Receptor Gene (hRyR2) Underlie Catecholaminergic Polymorphic Ventricular Tachycardia

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NOS1AP Is a Genetic Modifier of the Long-QT Syndrome

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Natural History of Brugada Syndrome: Insights for risk stratification and management

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New approaches to antiarrhythmic therapy, Part I. Emerging therapeutic applications of the cell biology of cardiac arrhythmias.

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New mutations in the KVLQT1 potassium channel that cause long QT Syndrome.

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No evidence of Association between Prothrombotic Gene Polimorphisms and the Development of Acute Myocardial Infarction at a Young Age

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No evidence of association between prothrombotic gene polymorphisms and the development of acute myocardial infarction at a young age

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Nonbiopsy Diagnosis of Cardiac Transthyretin Amyloidosis

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Nonbiopsy diagnosis of cardiac transthyretin amyloidosis

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Origin of respiratory sinus arrhythmia in conscious humans. An important role for arterial carotid baroreceptors.

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Overexpression of Akt in mesenchymal stem cells improves ATP production under hypoxia by increasing glucose uptake and mitochondrial enzymes activity: a possible explanation for increased resistence to apoptosis.

Contributo in Atti di convegno

Paradoxical Effect of Increased Diastolic Ca2+ Release and Decreased Sinoatrial Node Activity in a Mouse Model of Catecholaminergic Polymorphic Ventricular Tachycardia.

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Partial reversal of asymmetry in microvessel neurochemical changes after ischemia by corpus callosum section.

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Patency of infarct-related artery. Effect of restoration of anterograde flow on vagal reflexes. ATRAMI (Automatic Tone and Reflexes After Myocardial Infarction) Investigators.

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Pathophysiology and prevention of atrial fibrillation.

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Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder population.

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Predictors of long-term recurrent vascular events after ischemic stroke at young age: the Italian Project on Stroke in Young Adults

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Preservation of the baroreceptor heart rate reflex by chemical sympathectomy in experimental heart failure

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Prevalence of long-QT syndrome gene variants in sudden infant death syndrome.

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Prevalence of the congenital long-QT syndrome.

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Prevalent low-frequency oscillation of heart rate: novel predictor of mortality after myocardial infarction.

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Programmed ventricular stimulation for risk stratification in the Brugada syndrome: A pooled analysis

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Proposed diagnostic criteria for the Brugada syndrome: consensus report

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QT interval prolongation as predictor of sudden death in patients with myocardial infarction.

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QTc behavior during exercise and genetic testing for the long-QT syndrome.

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Rapid heart rate increase at onset of exercise predicts adverse cardiac events in patients with coronary artery disease.

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Rapid heart rate increase at onset of exercise predicts adverse cardiac events in patients with coronary artery disease.

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Reflex versus tonic vagal activity as a prognostic parameter in patients with sustained ventricular tachycardia or ventricular fibrillation.

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Relationship between erectile dysfunction and silent myocardial ischemia in apparently uncomplicated type 2 diabetic patients

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Reply to letters regarding article, "risk of assessing mortality risk in elective cardiac operations: Age, creatinine, ejection fraction, and the law of parsimony"

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Response to Letters Regarding Article, "Clinical Management of Catecholaminergic Polymorphic Ventricular Tachycardia: The Role of Left Cardiac Sympathetic Denervation"

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Risk factors for aborted cardiac arrest and sudden cardiac death in children with the congenital long-QT syndrome

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Risk of assessing mortality risk in elective cardiac operations. Age, creatinine, ejection fraction, and law of parsimony.

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Role of genetic analyses in cardiology: part I: mendelian diseases: cardiac channelopathies

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Role of hypocapnic alkalosis in hyperventilation-induced coronary artery spasm in variant angina.

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Screening for sudden cardiac death in the young: report from a national heart, lung, and blood institute working group

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Serum N-terminal pro-brain natriuretic peptide is a sensitive marker of myocardial dysfunction in AL amyloidosis

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Should patients with an asymptomatic Brugada electrocardiogram undergo pharmacological and electrophysiological testing?

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Significance of exercise-induced ST- segment elevation in patients without myocardial infarction.

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Single delivery of an adeno-associated viral construct to transfer the CASQ2 gene to knock-in mice affected by catecholaminergic polymorphic ventricular tachycardia is able to cure the disease from birth to advanced age

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Slow breathing increases arterial baroreflex sensitivity in patients with chronic heart failure.

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Spectrum of mutations in long QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1 and KCNE2.

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Spectrum of ST-T-Wave Patterns and Repolarization Parameters in Congenital Long-QT Syndrome. ECG Findings Identify Genotypes.

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Spectrum of ST-T-wave patterns and repolarization parameters in congenital long-QT syndrome: ECG findings identify genotypes

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Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.

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Stent thrombosis in patients with atrial fibrillation undergoing coronary stenting in the augustus trial

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Stillbirths, sudden infant deaths, and long QT syndrome. Puzzle or mosaic, the pieces of the jigsaw are being fitted together

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Stillbirths, sudden infant deaths, and long-QT syndrome: puzzle or mosaic, the pieces of the Jigsaw are being fitted together.

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Stress and sudden death. The case of the long QT syndrome.

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Sudden Cardiac Death and Genetic Ion Channelopathies: Long QT, Brugada, Short QT, Catecholaminergic Polymorphic Ventricular Tachycardia, and Idiopathic Ventricular Fibrillation

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Sudden cardiac death, genes, and arrhythmogenesis : consideration of new population and mechanistic approaches from a national heart, lung, and blood institute workshop, part I.

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Sudden cardiac death, genes, and arrhythmogenesis: consideration of new population and mechanistic approaches from a National Heart, Lung, and Blood Institute workshop, Part II.

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Sudden cardiac death. Nonpharmacologic interventions.

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Survivors of out-of-hospital cardiac arrest with apparently normal heart: need for definition and standardized clinical evaluation . Consensus statement of the Joint Steering Committees of Unexpleined Cardiac Arrest Registry of Europe and of Idiophatic Ventricular Fibrillation Registry of the United States

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Sympathovagal balance.

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Systemic cardiac amyloidoses: disease profiles and clinical courses of the 3 main types

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Targeting of mitogen-activated protein kinases and phosphatidylinositol 3 kinase inhibits hepatocyte growth factor/scatter factor-induced angiogenesis.

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The Brugada numbers (correspondence)

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The Common Long QT Syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification.

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The Common Variant Rs9939609 In The FTO Gene Is Associated With Early-onset Myocardial Infarction

Contributo in Atti di convegno

The Jervell and Lange-Nielsen syndrome: natural history, molecular basis, and clinical outcome.

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The QT interval throughout the first 6 months of life: a prospective study.

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The effects of daily exercise on susceptibility to sudden cardiac death.

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The elusive link between LQT3 and Brugada syndrome: the role of flecainide challenge.

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The exercise test in variant angina: results in 114 patients

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The long QT syndrome. Prospective longitudinal study of 328 families.

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The long QT syndrome: a prospective international study.

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The quest for the mechanism of the sudden infant death syndrome. Doubts and progress

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The quest for the mechanisms of the sudden infant death syndrome: doubts and progress.

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Therapeutic Efficacy of Mexiletine for Long QT Syndrome Type 2: Evidence From Human Induced Pluripotent Stem Cell–Derived Cardiomyocytes, Transgenic Rabbits, and Patients

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Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome

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Transplantation of Mesenchymal stem cells overexpressing Akt limits infarct size and prevents cardiac dysfunction as early as 3 days after infarction: evidence suggesting paracrine action rather than regeneration.

Contributo in Atti di convegno

Transplantation of bone marrow-derived cells expressing Akt into infarcted murine heart produces dramatic improvement in cardiac function despite infrequent cellular fusion.

Contributo in Atti di convegno

Unexpected interaction between beta-adrenergic blockade and heart rate variability before and after myocardial infarction. A longitudinal study in dogs at high and low risk for sudden death.

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Universal definition of myocardial infarction.

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Unsuspected echocardiographic abnormality in the long QT syndrome. Diagnostic, prognostic, and pathogenetic implications.

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Use of biomarkers to predict specific causes of death in patients with Atrial fibrillation: Insights from the Aristotle Trial

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Valsartan amlodipine combination and prevention of atrial fibrillation recurrence in hypertensive diabetic patients.

Abstract

Who are the long-QT syndrome patients who receive an implantable cardioverter-defibrillator and what happens to them?: data from the European Long-QT Syndrome Implantable Cardioverter-Defibrillator (LQTS ICD) Registry.

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the procardiomyogenic effect of miR499 is sinergistically enhanced by miR133.

Contributo in Atti di convegno

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CIRCULATION

Dati Generali

Pubblicazioni (217)