Current Concepts In Arrhythmogenic Right Ventricular Cardiomyopathy Dysplasia
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Current Concepts in Arrhythmogenic Right Ventricular Cardiomyopathy / Dysplasia by Corinna Brunckhorst,Firat Duru,Ardan M. Saguner Pdf
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.
Prof. Dr. Corrinna Brunckhorst,PD Dr. Ardan M. Saguner,Prof. Dr. Firat Duru
Author : Prof. Dr. Corrinna Brunckhorst,PD Dr. Ardan M. Saguner,Prof. Dr. Firat Duru Publisher : Cardiotext Publishing Page : 218 pages File Size : 54,6 Mb Release : 2021-03-01 Category : Medical ISBN : 9781942909514
Current Concepts in Arrhythmogenic Cardiomyopathy, Second Edition by Prof. Dr. Corrinna Brunckhorst,PD Dr. Ardan M. Saguner,Prof. Dr. Firat Duru Pdf
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 disease phenotypes -Guidance in the clinical setting for diagnosis, risk strati fication, and therapy
Current Concepts in Arrhytmmogenic Right Ventricular Cardiomyopathydyspiasia by Steven Finch Pdf
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.
Arrhythmogenic RV Cardiomyopathy/Dysplasia by Frank I. Marcus,Andrea Nava,Gaetano Thiene Pdf
This book covers all aspects (biological, pathological, genetic, clinical and therapeutical) of arrhythmogenic right ventricular cardiomyopathy/dysplasia, a recent cardiomyopathy which represents a very high risk of sudden death in the young and in the athletes. This monograph gathers the results of a five-year research program on ARVC/D which allowed the discovery of 5 disease-causing genes, thus opening new avenues for the early identification of affected patients.
Current Concepts in Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia by Corinna Brunckhorst, MD,Firat Duru, MD,Ardan M. Saguner, MD Pdf
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 by Gianfranco Sinagra,Marco Merlo,Bruno Pinamonti Pdf
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.
Cardiomyopathy by Gustav Mattsson,Peter Magnusson Pdf
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.
Arrhythmogenic Right Ventricular Cardiomyopathy/dysplasia by Andrea Nava,Lino Rossi,Gaetano Thiene Pdf
Hardbound. In this book a complete overview of current knowledge is presented, running from pathology to recent progress in molecular biology and with special reference to diagnostic procedures and pharmacologic-non pharmacologic therapies. Incidence and natural history of the disease are addressed as well, stressing the occurrence of sudden death.The book, the first on the topic, is an updated survey on ARVC/D and includes 38 chapters with a worldwide authorship as a result of an international cooperative study.
Encyclopedia of Cardiovascular Research and Medicine by Anonim Pdf
Encyclopedia of Cardiovascular Research and Medicine offers researchers over 200 articles covering every aspect of cardiovascular research and medicine, including fully annotated figures, abundant color illustrations and links to supplementary datasets and references. With contributions from top experts in the field, this book is the most reputable and easily searchable resource of cardiovascular-focused basic and translational content for students, researchers, clinicians and teaching faculty across the biomedical and medical sciences. The panel of authors chosen from an international board of leading scholars renders the text trustworthy, contemporary and representative of the global scientific expertise in these domains. The book's thematic structuring of sections and in-depth breakdown of topics encourages user-friendly, easily searchable chapters. Cross-references to related articles and links to further reading and references will further guide readers to a full understanding of the topics under discussion. Readers will find an unparalleled, one-stop resource exploring all major aspects of cardiovascular research and medicine. Presents comprehensive coverage of every aspect of cardiovascular medicine and research Offers readers a broad, interdisciplinary overview of the concepts in cardiovascular research and medicine with applications across biomedical research Includes reputable, foundational content on genetics, cancer, immunology, cell biology and molecular biology Provides a multi-media enriched color-illustrated text with high quality images, graphs and tables.
J Wave Syndromes by Charles Antzelevitch,Gan-Xin Yan Pdf
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.
SIDS Sudden infant and early childhood death by Jhodie R. Duncan,Roger W. Byard Pdf
This volume covers aspects of sudden infant and early childhood death, ranging from issues with parental grief, to the most recent theories of brainstem neurotransmitters. It also deals with the changes that have occurred over time with the definitions of SIDS (sudden infant death syndrome), SUDI (sudden unexpected death in infancy) and SUDIC (sudden unexpected death in childhood). The text will be indispensable for SIDS researchers, SIDS organisations, paediatric pathologists, forensic pathologists, paediatricians and families, in addition to residents in training programs that involve paediatrics. It will also be of use to other physicians, lawyers and law enforcement officials who deal with these cases, and should be a useful addition to all medical examiner/forensic, paediatric and pathology departments, hospital and university libraries on a global scale. Given the marked changes that have occurred in the epidemiology and understanding of SIDS and sudden death in the very young over the past decade, a text such as this is very timely and is also urgently needed.
Author : Frank I. Marcus Publisher : Springer Science & Business Media Page : 221 pages File Size : 46,9 Mb Release : 2007-05-11 Category : Medical ISBN : 9788847004894
Arrhythmogenic RV Cardiomyopathy/Dysplasia by Frank I. Marcus Pdf
This book covers all aspects (biological, pathological, genetic, clinical and therapeutical) of arrhythmogenic right ventricular cardiomyopathy/dysplasia, a recent cardiomyopathy which represents a very high risk of sudden death in the young and in the athletes. This monograph gathers the results of a five-year research program on ARVC/D which allowed the discovery of 5 disease-causing genes, thus opening new avenues for the early identification of affected patients.
Clinical Cases in Right Heart Failure by Lana Tsao,Maxwell E. Afari Pdf
This book provides a practical clinical case-based review of right heart failure. Cases of common and rarely encountered presentations of right heart failure are covered. Featured cases include right heart failure due to pulmonary hypertension, pulmonary embolism, valvular heart disease, myocardial infarction and congenital heart disease as well as how to differentiate new onset right heart failure from left heart failure. The medical management and mechanical support of right ventricular failure utilizing percutaneous and surgical techniques is reviewed along with the latest palliative and rehabilitation strategies. Clinical Cases in Right Heart Failure features a wealth of common and unusual case presentations of right heart failure and its clinical management, providing an ideal resource for trainees and practicing clinicians who encounter these patients.
Until recently, the cellular basis for sudden death, the BrugadaSyndrome, has largely remained an unknown to modernarrhythmologists and cardiologists, particularly in the absence ofany structural heart disease. Detailed observations of age-groups,especially the young, families and populations where sudden deathfrequently occurs, and improved understanding of its contributoryfactors and mechanisms are, however, showing the way forward. This addition to the Clinical Approaches to Tachyarrhythmias(CATA) Series, written by the investigators who discovered andprobed the Brugada Syndrome, discusses the history, etiology,pathology and clinical manifestations of sudden death. Fromdiagnosis, prognosis, to therapeutic approaches using the latest incathater ablation techniques, electrophysiological surgery, andgenetic appraisal, the work is a testimony to the author'sinvestigation. Using clinical cases in Thailand and Laos, theyfurther unravel the syndrome's molecular mechanisms, studyingrelated syndromes, such as the long-QT syndrome, infant death, andarryhthmogenic right ventricular cardiomyopathy. By being informed of the electrophysiological abnormalities thatcontribute to familial and genetic diseases, physicians,cardiologists and all those who care for patients with cardiacarrhythmias will be better able to identify and treat patients inwhom the Brugada Syndrome may strike next.