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Right Ventricular DysplasiaCardiomyopathy; Exercise-Induced Right Ventricular Cardiomyopathy; Dilated Cardiomyopathy; Sarcoidosis; Amyloidosis;
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Edited and written by internationally recognized authorities, Current Concepts in Arrhythmogenic Right Ventricular CardiomyopathyDysplasia;
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Arrhythmogenic right ventricular dysplasia is an inherited heart muscle disorder that may cause abnormal electrical heart rhythms and;
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death. Some types of cardiomyopathy are dilated cardiomyopathy, hypertrophic cardiomyopathy, arrhythmogenic right ventricular dysplasia;
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cardiomyopathy, dilated cardiomyopathy, takotsubo cardiomyopathy and arrhythmogenic right ventricular dysplasia. Hypertrophic cardiomyopathy is usually;
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distinctive attention in recent years. This book covers the whole spectrum of arrhythmogenic right ventricular cardiomyopathies. The reader will find;
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cardiomyopathy, restricted cardiomyopathy, takotsubo cardiomyopathy and arrhythmogenic right ventricular dysplasia. Each of these affects the cardiac;
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therapies; Right Ventricular Function: Imaging Techniques; Arrhythmogenic Right Ventricular Cardiomyopayhy: An Update; Real-Time 3-D;
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Cardiac MRI in Diagnosis, Clinical Management and Prognosis of Arrhythmogenic Right Ventricular Cardiomyopathy / Dysplasia
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, arrhythmogenic right ventricular cardiomyopathy, and sick sinus syndrome. The issue concludes with a consideration of the potential for genetic testing;
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dilated cardiomyopathy, hypertrophic cardiomyopathy, restrictive cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy and infiltrative;
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, Epicardial Ablation of Non-ischemic Ventricular Tachycardia, Epicardial Ablation of Arrhythmogenic Right Ventricular Cardiomyopathy, Epicardial;
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- hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy (DCM) and arrhythmogenic right ventricular cardiomyopathy (ARVC). This book also details the;
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localized, a ventricular aneurysmforms. Whencomplicatedbyarrhythmias,myocarditispresentsas arrhythmogenic right ventricular cardiomyopathy. When;
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localized, a ventricular aneurysmforms. Whencomplicatedbyarrhythmias,myocarditispresentsas arrhythmogenic right ventricular cardiomyopathy. When;
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regurgitation, RV outflow tract tachycardia, pulmonary hypertension, arrhythmogenic right ventricular dysplasia, aortic stenosis, atrial myxoma, atrial;
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, ventricular tachycardia in CAD, ECG characteristics of outflow tract VT, fascicular tachycardias, VT in non-ischemic dilated cardiomyopathy, VT;
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fibrillation; ventricular tachycardia; hypertrophic cardiomyopathy, arrhythmogenic cardiomyopathy, and congenital heart disease.
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normal cardiac anatomy, Intracardiac echography to guide catheter ablation of ventricular arrhythmias in ischemic cardiomyopathy, Intracardiac;
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fibrosis and restrictive cardiomyopathy, severe unclassified cardiomyopathy, and severe arrhythmogenic right ventricular cardiomyopathy.
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causes of heart failure, such as right heart failure, valvular cardiomyopathy, molecular mechanisms of sarcomeric cardiomyopathies, and;
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/ Right Ventricular Infarction / Acute Left Ventricular Ischemia / Chronic Congestive Heart Failure / Pericardial Tamponade / Pericardial;
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Takotsubo cardiomyopathy (TC) is a relatively new pathological concept in cardiovascular disease, originally described in the Japanese;
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This issue of Heart Failure Clinics covers stress (takotsubo) cardiomyopathy. Expert authors review the most current information available;
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This issue of Cardiology Clinics, guest edited by Drs. Srihari S. Naidu and Julio A. Panza, will focus on Hypertrophic Cardiomyopathy;
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(Stress) Cardiomyopathy. Topics covered will include the influence of age and gender on TTS; current concepts in pathophysiology; the clinician's;
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in surgery and cardiac catheterization to treat. Right Ventricular Physiology, Adaptation and Failure in Congenital and Acquired Heart Disease;
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