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Current Concepts in Arrhythmogenic Cardiomyopathy, Second Edition

Current Concepts in Arrhythmogenic Cardiomyopathy, Second Edition
Author: Prof. Dr. Corrinna Brunckhorst
Publisher: Cardiotext Publishing
Total Pages: 218
Release: 2021-03-01
Genre: Medical
ISBN: 1942909519
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Current Concepts in Arrhythmogenic Cardiomyopathy, Second Edition presents essential insights into all aspects of this complex disease and will serve as a valuable guide to help readers provide the best possible care for their patients. Discussion by internationally recognized authorities includes: -Increasing evidence that arrhythmogenic cardiomyopathy is not necessarily confined to the RV, but often involves both ventricles -Basic and clinical science of arrhythmogenic cardiomyopathy -Pathophysiology, molecular mechanisms, and genetic background -The mechanisms of disease progression leading to a diversity of diseasephenotypes -Guidance in the clinical setting for diagnosis, risk stratification, and therapy

Current Concepts in Arrhythmogenic Right Ventricular Cardiomyopathy / Dysplasia

Current Concepts in Arrhythmogenic Right Ventricular Cardiomyopathy / Dysplasia
Author: Corinna Brunckhorst
Publisher: Cardiotext Incorporated
Total Pages: 0
Release: 2014-08-15
Genre:
ISBN: 9781935395928
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Current Concepts in Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia (ARVC/D) presents important insights to all aspects of this disease. Discussion of ARVC/D by the experts includes: pathophysiology, molecular mechanisms, and genetic background; challenges in the clinical setting in regard to diagnosis, risk stratification, and therapy.

Current Concepts in Arrhytmmogenic Right Ventricular Cardiomyopathydyspiasia

Current Concepts in Arrhytmmogenic Right Ventricular Cardiomyopathydyspiasia
Author: Steven Finch
Publisher: Createspace Independent Publishing Platform
Total Pages: 158
Release: 2017-06
Genre:
ISBN: 9781547164134
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Edited and written by internationally recognized authorities, Current Concepts in Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia (ARVC/D) presents important insights to all aspects of this unique disease and will serve as a valuable guide to help readers provide the best possible care for their patients. Discussion of ARVC/D by the experts includes: Basic and clinical science. Pathophysiology, molecular mechanisms, and genetic background. The mechanisms of disease progression leading to a diversity of disease phenotypes. Challenges in the clinical setting with respect to diagnosis, risk stratification, and therapy.

Current Concepts in Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia

Current Concepts in Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia
Author: Corinna Brunckhorst, MD
Publisher: Cardiotext Publishing
Total Pages: 167
Release: 2014-08-01
Genre: Medical
ISBN: 193539519X
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Edited and written by internationally recognized authorities, Current Concepts in Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia (ARVC/D) presents important insights to all aspects of this unique disease and will serve as a valuable guide to help readers provide the best possible care for their patients. Discussion of ARVC/D by the experts includes: · Basic and clinical science. · Pathophysiology, molecular mechanisms, and genetic background. · The mechanisms of disease progression leading to a diversity of disease phenotypes. · Challenges in the clinical setting with respect to diagnosis, risk stratification, and therapy. “The editors…have enlisted as authors those who first recognized and named the disease, and most of those responsible for the recent advances in this fascinating area. The result is an excellent, comprehensive but very readable text dealing with this increasingly important spectrum of diseases. It is a unique book that should be found on the shelves of everyone who seeks to manage patients with cardiac arrhythmia because amongst those who seek advice there are sure to be patients with this challenging disease.” - From the foreword by A. John Camm, MD

Dilated Cardiomyopathy

Dilated Cardiomyopathy
Author: Gianfranco Sinagra
Publisher: Springer
Total Pages: 241
Release: 2019-05-17
Genre: Medical
ISBN: 303013864X
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This open access book presents a comprehensive overview of dilated cardiomyopathy, providing readers with practical guidelines for its clinical management. The first part of the book analyzes in detail the disease’s pathophysiology, its diagnostic work up as well as the prognostic stratification, and illustrates the role of genetics and gene-environment interaction. The second part presents current and future treatment options, highlighting the importance of long-term and individualized treatments and follow-up. Furthermore, it discusses open issues, such as the apparent healing phenomenon, the early prognosis of arrhythmic events or the use of genetic testing in clinical practice. Offering a multidisciplinary approach for optimizing the clinical management of DCM, this book is an invaluable aid not only for the clinical cardiologists, but for all physicians involved in the care of this challenging disease.

Management of Cardiac Arrhythmias

Management of Cardiac Arrhythmias
Author: Gan-Xin Yan
Publisher: Springer Nature
Total Pages: 870
Release: 2020-07-27
Genre: Medical
ISBN: 3030419673
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A significantly expanded third edition, this book provides a comprehensive and concise overview of cardiac arrhythmias and their ECG/telemetry manifestations, including the principles of cardiac electrophysiology, current concepts of pharmacology, clinical features, diagnoses, and state-of-the-art treatments. Additionally, the book emphasizes decision-making strategies in approaching each individual patient and the application of technical innovations in specific clinical situations. Organized into eight parts, beginning chapters introduce the concepts and principles of cardiac electrophysiology, unique rhythms, and ECG waves/signs. These chapters are designed to integrate emerging knowledge in basic science and clinical medicine. Subsequent chapters focus on the diagnosis of a variety of cardiac arrhythmias using non-invasive methodology. Throughout the book, chapters continue to analyze pharmacological and other approaches to therapy of specific arrhythmias, including supraventricular tachycardias, atrial fibrillation and flutter, ventricular arrhythmias, and bradyarrhythmias. Finally, the book closes with coverage on inherited cardiac arrhythmia syndromes including the long, short QT, and J-wave syndromes, catecholaminergic polymorphic ventricular tachycardia, and arrhythmogenic right ventricular cardiomyopathy. The third edition of Management of Cardiac Arrhythmias, is an essential resource for physicians, residents, fellows, and medical students in cardiology, cardiac surgery, vascular surgery, cardiac electrophysiology, and cardiac radiology.

Cardiomyopathy

Cardiomyopathy
Author: Gustav Mattsson
Publisher:
Total Pages: 0
Release: 2021
Genre: Myocardium
ISBN: 9781789852240
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Cardiomyopathies are diseases of the heart muscle with diverse etiologies ranging from myocarditis to gene mutations. They are classified according to morphology and function, and then further categorized based on whether they are familial or non-familial and based on specific etiologies. This book examines the various cardiomyopathies, including arrhythmogenic cardiomyopathy, hypertrophic cardiomyopathy, and dilated cardiomyopathy, as well as their genetic basis.

Genetic Cardiomyopathies

Genetic Cardiomyopathies
Author: Gianfranco Sinagra
Publisher: Springer Science & Business Media
Total Pages: 170
Release: 2012-12-09
Genre: Medical
ISBN: 8847027578
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In the last decade, genetics has been emerging as a primary issue in the diagnosis and management of cardiomyopathies. This book is intended to be a state-of-the-art monograph on these diseases, describing their genetic causes, defining the molecular basis and presenting extensive descriptions of genotype–phenotype correlations. Other chapters are focused on the role of clinical observation, on ECG and echocardiography. With its highlight on the most recent discoveries in the field of molecular genetics as well as on the correct clinical approach to patients with heart muscle disease, the book is aimed at physicians and clinical cardiologists with a particular interest in myocardial diseases and in their genetic causes.

J Wave Syndromes

J Wave Syndromes
Author: Charles Antzelevitch
Publisher: Springer
Total Pages: 342
Release: 2016-06-27
Genre: Medical
ISBN: 3319315781
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This book delineates the state of the art of the diagnosis and treatment of J wave syndromes, as well as where future research needs to be directed. It covers basic science, translational and clinical aspects of these syndromes. The authors are leading experts in their respective fields, who have contributed prominently to the literature concerning these topics. J wave syndromes are one of the hottest topics in cardiology today. Cardiac arrhythmias associated with Brugada syndrome (BrS) or an early repolarization (ER) pattern in the inferior or infero-lateral ECG leads are thought to be mechanistically linked to accentuation of transient outward current (Ito)-mediated J waves. Although BrS and ER syndrome (ERS) differ with respect to magnitude and lead location of abnormal J waves, they are thought to represent a continuous spectrum of phenotypic expression termed J wave syndromes. ERS is divided into three subtypes with the most severe, Type 3, displaying an ER pattern globally in the inferior, lateral and right precordial leads. BrS has been linked to mutations in 19 different genes, whereas ERS has been associated with mutations in 7 different genes. There is a great deal of confusion as to how to properly diagnose and treat the J wave syndromes as well as confusion about the underlying mechanisms. The demonstration of successful epicardial ablation of BrS has provided new therapeutic options for the management of this syndrome for which treatment alternatives are currently very limited, particularly in the case of electrical storms caused by otherwise uncontrollable recurrent VT/VF. An early repolarization pattern is observed in 2-5% of the US population. While it is clear that the vast majority of individuals exhibiting an ER pattern are not at risk for sudden cardiac death, the challenge moving forward is to identify those individuals who truly are at risk and to design safe and effective treatments.