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Characterization and Clinical Management of Dilated Cardiomyopathy

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Understanding Cardiomyopathy

cardiomyopathy, dilated cardiomyopathy, takotsubo cardiomyopathy and arrhythmogenic right ventricular dysplasia. Hypertrophic cardiomyopathy is usually;

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Clinical Echocardiography and Other Imaging Techniques in Cardiomyopathies

dilated cardiomyopathy, hypertrophic cardiomyopathy, restrictive cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy and infiltrative;

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Advances in Clinical Cardiovascular Imaging, Echocardiography & Interventions

, such as dilated, restrictive and hypertrophic cardiomyopathy, cardiac dyssynchrony, pericardial effusion, oncology, cardiac tamponade and;

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Cardiomyopathies

- hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy (DCM) and arrhythmogenic right ventricular cardiomyopathy (ARVC). This book also details the;

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Cardiomyopathy

muscle in a different way. The heart muscle enlarges and thickens in hypertrophic cardiomyopathy, while ventricles enlarge and weaken in dilated;

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Cardiomyopathies

, shortness of breath, fainting, irregular heartbeat and increased tiredness. Individuals with cardiomyopathy are at a higher risk of sudden cardiac;

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Arrhythmias in Cardiomyopathies, An Issue of Cardiac Electrophysiology Clinics

Arrhythmias in Hypertrophic Cardiomyopathy and Its Variants; Role of Cardiac MRI in Risk Stratification of Hypertrophic Cardiomyopathy; Arrhythmogenic;

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The Concise Manual of Apheresis Therapy

, dilated cardiomyopathy, and many other conditions. The books also reviews the growing trend towards adopting this unique therapy for a wide range;

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Takotsubo (Stress) Cardiomyopathy, An Issue of Heart Failure Clinics

about imaging modalities, clinical profile, natural history, management, and different types of stress cardiomyopathy. Keep up-to-the-minute;

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Manual of Canine and Feline Cardiology

The most effective, practical approach to the recognition and management of cardiovascular and cardiopulmonary medicine, Manual;

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Heart Transplantation

disease in younger age groups. Of the candidates, 54% have some form of dilated cardiomyopathy, which often has an unclear origin. The remaining 1;

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Peripartum and Dilated Cardiomyopathies

the mainstay of treatment for PPCM, and the management strategy is broadly aligned with established guidelines for cardiac failure;

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Cardiomyopathies and Heart Failure

Theclinicalpresentationofviralmyocarditisisvariable. Whenmyocardial necrosis is diffuse, congestive heart failure develops, and later, dilated cardiomyopathy. If the myocardial lesions are;

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Cardiomyopathies and Heart Failure

Theclinicalpresentationofviralmyocarditisisvariable. Whenmyocardial necrosis is diffuse, congestive heart failure develops, and later, dilated cardiomyopathy. If the myocardial lesions are;

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A handbook of Aortoarteritis And Ruptured sinus Of Valsalva

relatively common disease in Indian subcontinent. It is a common cause of dilated cardiomyopathy in this region. It has various presentations due to;

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Heart Disease in Men

, for example: Angina; Arrhythmia; Congenital heart disease; Coronary artery disease (CAD); Dilated cardiomyopathy; Heart attack (myocardial;

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Heart Disease in Women

, for example: Angina; Arrhythmia; Congenital heart disease; Coronary artery disease (CAD); Dilated cardiomyopathy; Heart attack (myocardial;

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Hypertrophic Cardiomyopathy

. Hypertrophic Cardiomyopathy: A Practical Guide to Diagnosis and Management describes the various sub-types of this condition, including its unique;

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Hypertrophic Cardiomyopathy

. Hypertrophic Cardiomyopathy: A Practical Guide to Diagnosis and Management describes the various sub-types of this condition, including its unique;

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Noncompaction Cardiomyopathy

modalities, such as contrast echocardiography and magnetic resonance imaging in relation to noncompaction cardiomyopathy treatment. Noncompaction;

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Cardiac Complications of Cancer Therapy

the management of cardiac problems, including both texts and journal articles, no other clinical reference book on the current market;

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Genetics of Cardiomyopathy and Heart Failure, An Issue of Heart Failure Clinics

This issue explores the genetic basis of specific cardiomyopathies and phenotypic components of heart failure with an eye to the clinical;

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Electrocardiography of Complex Arrhythmias, An Issue of Cardiac Electrophysiology Clinics

, ventricular tachycardia in CAD, ECG characteristics of outflow tract VT, fascicular tachycardias, VT in non-ischemic dilated cardiomyopathy, VT;

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Diagnosis and Management of Hypertrophic Cardiomyopathy

of clinical and genetic diagnosis, natural history, and management of hypertrophic cardiomyopathy (HCM) - the most common and important of the genetic;

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Clinical Arrhythmology and Electrophysiology

, offers complete coverage of the latest diagnosis and management options for patients with arrhythmias. Expanded clinical content, clear;

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T1-Mapping in Myocardial Disease

This book details the advances in cardiac MRI that have enabled quantitative tissue characterization of the myocardium using myocardial and;

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