Search Results - "TOWBIN, Jeffrey"
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Inherited Cardiomyopathies
Published in Circulation Journal (2014)“…Cardiomyopathies (ie, diseases of the heart muscle) are major causes of morbidity and mortality. A significant percentage of patients with cardiomyopathies…”
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Left ventricular non-compaction cardiomyopathy
Published in The Lancet (British edition) (22-08-2015)“…Summary Left ventricular non-compaction, the most recently classified form of cardiomyopathy, is characterised by abnormal trabeculations in the left…”
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Cardiomyopathies Due to Left Ventricular Noncompaction, Mitochondrial and Storage Diseases, and Inborn Errors of Metabolism
Published in Circulation research (15-09-2017)“…The normal function of the human myocardium requires the proper generation and utilization of energy and relies on a series of complex metabolic processes to…”
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Left ventricular noncompaction cardiomyopathy: cardiac, neuromuscular, and genetic factors
Published in Nature reviews cardiology (01-04-2017)“…Key Points Patients with left ventricular hypertrabeculation (LVHT) should undergo evaluation for neuromuscular disorders, and patients with neuromuscular…”
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Dilated cardiomyopathy
Published in The Lancet (British edition) (27-02-2010)“…Summary Dilated cardiomyopathy is characterised by left ventricular dilation that is associated with systolic dysfunction. Diastolic dysfunction and impaired…”
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Diagnosis and Evaluation of Hypertrophic Cardiomyopathy: JACC State-of-the-Art Review
Published in Journal of the American College of Cardiology (01-02-2022)“…Hypertrophic cardiomyopathy (HCM) is a relatively common often inherited global heart disease, with complex phenotypic and genetic expression and natural…”
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Diagnosis and Management of Myocarditis in Children: A Scientific Statement From the American Heart Association
Published in Circulation (New York, N.Y.) (10-08-2021)“…Myocarditis remains a clinical challenge in pediatrics. Originally, it was recognized at autopsy before the application of endomyocardial biopsy, which led to…”
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Management of Hypertrophic Cardiomyopathy: JACC State-of-the-Art Review
Published in Journal of the American College of Cardiology (01-02-2022)“…Hypertrophic cardiomyopathy (HCM), a relatively common, globally distributed, and often inherited primary cardiac disease, has now transformed into a…”
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Genetics of Arrhythmogenic Right Ventricular Cardiomyopathy: A Practical Guide for Physicians
Published in Journal of the American College of Cardiology (14-05-2013)“…Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a genetically transmitted disease. However, the genetics are more complex than in other inherited…”
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Genetic arrhythmias complicating patients with dilated cardiomyopathy: How it happens
Published in Heart rhythm (01-02-2020)Get full text
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Left Ventricular Noncompaction and Vigorous Physical Activity: What Is the Connection?
Published in Journal of the American College of Cardiology (13-10-2020)Get full text
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Diagnostic, Prognostic, and Therapeutic Implications of Genetic Testing for Hypertrophic Cardiomyopathy
Published in Journal of the American College of Cardiology (14-07-2009)“…Over the last 2 decades, the pathogenic basis for the most common heritable cardiovascular disease, hypertrophic cardiomyopathy (HCM), has been investigated…”
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Cardiovascular Health Promotion in Children: Challenges and Opportunities for 2020 and Beyond: A Scientific Statement From the American Heart Association
Published in Circulation (New York, N.Y.) (20-09-2016)“…This document provides a pediatric-focused companion to “Defining and Setting National Goals for Cardiovascular Health Promotion and Disease ReductionThe…”
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Pediatric Cardiomyopathies
Published in Circulation research (15-09-2017)“…Pediatric cardiomyopathies are rare diseases with an annual incidence of 1.1 to 1.5 per 100 000. Dilated and hypertrophic cardiomyopathies are the most common;…”
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Association between diffuse myocardial fibrosis and diastolic dysfunction in sickle cell anemia
Published in Blood (13-07-2017)“…Sickle cell anemia (SCA)–related cardiomyopathy is characterized by diastolic dysfunction and hyperdynamic features. Diastolic dysfunction portends early…”
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Association of competitive and recreational sport participation with cardiac events in patients with arrhythmogenic right ventricular cardiomyopathy: results from the North American multidisciplinary study of arrhythmogenic right ventricular cardiomyopathy
Published in European heart journal (14-07-2015)“…It has been proposed that competitive sport increases the risk of ventricular tachyarrhythmias (VTA) and death in patients with arrhythmogenic…”
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Pediatric Primary Dilated Cardiomyopathy Gene Testing and Variant Reclassification: Does It Matter?
Published in Journal of the American Heart Association (02-06-2020)Get full text
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2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy
Published in Heart rhythm (01-11-2019)“…Arrhythmogenic cardiomyopathy (ACM) is an arrhythmogenic disorder of the myocardium not secondary to ischemic, hypertensive, or valvular heart disease. ACM…”
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