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Author: E. van der Wall
Publisher: Springer Science & Business Media
ISBN: 9400949944
Category : Medical
Languages : en
Pages : 151
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Book Description
In Groningen there has been a continuous investigation of hypertrophic cardio myopathy for almost twenty years. Members of this working-group have tried to study the many aspects of this intriguing disease, and it is in this volume that they present their recent results and current concepts (chapters 2, 3, 5 and 6). A contribution from the Dutch interuniversity Institute of Cardiology presenting a detailed account of evaluation by means of radionuclide techniques completes the non-invasive picture of cardiomyopathies (chapter 4). On July 6th, 1984, a symposium entitled 'Recent views on hypertrophic cardio myopathy' was held at the University Hospital Groningen. The main reason to organize this meeting was the retirement of one of our working-group members, namely E. van der Wall, as head of the cardiological department. The speakers at the symposium presented their lectures based on their contributions to this book. It is an honour for us to have obtained their full cooperation for this book and for the symposium. We are very grateful that this Groningen manifestation could include the outstanding contributions of several well-known experts from abroad. We there fore thank our colleagues Profs. Epstein, Goodwin, Kaltenbach and Schulte for their spontaneous and valuable cooperation (chapters 1, 7,8 and 9). Thanks to their efforts especially, this book has acquired the international character that the study of this subject deserves.
Author: E. van der Wall
Publisher: Springer Science & Business Media
ISBN: 9400949944
Category : Medical
Languages : en
Pages : 151
Get Book
Book Description
In Groningen there has been a continuous investigation of hypertrophic cardio myopathy for almost twenty years. Members of this working-group have tried to study the many aspects of this intriguing disease, and it is in this volume that they present their recent results and current concepts (chapters 2, 3, 5 and 6). A contribution from the Dutch interuniversity Institute of Cardiology presenting a detailed account of evaluation by means of radionuclide techniques completes the non-invasive picture of cardiomyopathies (chapter 4). On July 6th, 1984, a symposium entitled 'Recent views on hypertrophic cardio myopathy' was held at the University Hospital Groningen. The main reason to organize this meeting was the retirement of one of our working-group members, namely E. van der Wall, as head of the cardiological department. The speakers at the symposium presented their lectures based on their contributions to this book. It is an honour for us to have obtained their full cooperation for this book and for the symposium. We are very grateful that this Groningen manifestation could include the outstanding contributions of several well-known experts from abroad. We there fore thank our colleagues Profs. Epstein, Goodwin, Kaltenbach and Schulte for their spontaneous and valuable cooperation (chapters 1, 7,8 and 9). Thanks to their efforts especially, this book has acquired the international character that the study of this subject deserves.
Author: Barry J. Maron
Publisher: John Wiley & Sons
ISBN: 140514615X
Category : Medical
Languages : en
Pages : 527
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Book Description
Diagnosis and Management of Hypertrophic Cardiomyopathy is aunique, multi-authored compendium of information regarding thecomplexities of clinical and genetic diagnosis, natural history,and management of hypertrophic cardiomyopathy (HCM)—the mostcommon and important of the genetic cardiovasculardiseases—as well as related issues impacting the health oftrained athletes. Edited by Dr. Barry J. Maron, a world authority on HCM, and withmajor contributions from all of the international experts in thisfield, this book provides a single comprehensive source ofinformation concerning HCM. Recent advances in the field arediscussed, including the importance of left ventricular outflowtract obstruction, the use of implantable defibrillators for theprevention of sudden death in young people, definition of thegenetic basis for HCM and its role in clinical diagnosis and riskstratification, the development of more precise strategies forassessing the level of risk for sudden death among all patientswith HCM, and the evolution of invasive interventions for heartfailure symptoms, such as surgical management and its alternatives(alcohol septal ablation and dual-chamber pacing). Key Features: Contributions from all experts in the field,representing diverse viewpoints regarding this heterogeneousdisease and related issues in athletes Information to dispel misunderstandings regarding issuesassociated with HCM and cardiovascular disease in athletes The only comprehensive source of information available on thetopic
Author: Srihari S. Naidu
Publisher: Springer
ISBN: 3319924230
Category : Medical
Languages : en
Pages : 479
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Book Description
This extensively updated edition provides a comprehensive review of hypertrophic cardiomyopathy, the most common genetic disorder of the heart characterized by dysfunctional contractility at the sarcomere level. The disease produces abnormal and oftentimes focal hypertrophy on a macroscopic level that further impairs cardiac performance and may lead to life-threatening arrhythmias. This edition provides a practical approach, establishing evidence-based best practice for all scenarios. Hypertrophic Cardiomyopathy provides readers with key points and critical clinical pearls to assist them in managing patients. New chapters have been included on managing hypertension, sleep apnea, coronary artery disease, structural and congenital disease, nutrition and pharmacotherapies. All aspects of treatment are covered – medications, pacemakers and defibrillators, and invasive septal reduction therapy (both surgical myectomy and alcohol septal ablation) – in addition to genetics, family screening, lifestyle concerns, and athletic screening. The practical approach has been reinforced with an expanded emphasis on creating a Center of Excellence, how to facilitate the multi-disciplinary approach, and on case-based reviews and discussions, with each chapter ending with a post-test. This book is an essential text for cardiology professionals from trainee to board-certified physician, and includes important information for interventional cardiologists, cardiac surgeons, cardiac imagers, critical care physicians, sports medicine physicians, genetic counsellors, and electrophysiologists.
Author: M. Kaltenbach
Publisher: Springer Science & Business Media
ISBN: 3642853692
Category : Medical
Languages : en
Pages : 282
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Book Description
Author: Eckhard Alt
Publisher: Springer Science & Business Media
ISBN: 3642765750
Category : Medical
Languages : en
Pages : 312
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Book Description
This monograph presents the most recent experience and in- formation concerning ICD-Therapy: indications, technical as- pects of this new pacemaker generation problems/side- effects, surgical implications; cost-effectiveness- discussion is included.
Author: Gustav Mattsson
Publisher:
ISBN: 9781789852240
Category : Myocardium
Languages : en
Pages : 0
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Book Description
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.
Author: John Lynn Jefferies
Publisher: Academic Press
ISBN: 0128005807
Category : Medical
Languages : en
Pages : 418
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Book Description
Cardioskeletal Myopathies in Children and Young Adults focuses on plaques that kill people in their 40’s-50’s and the way they start to form in young adulthood. The Annals of Family Medicine report that approximately half of young adults have at least one cardiovascular disease risk factor (Mar 2010), and an increase in cardiovascular mortality rates in young adults was substantiated in a study at Northwestern Medicine (Nov 2011). Given the increasing recognition of genetic triggers behind all types of cardiovascular disease, and the growing population of young adults with primary or acquired myocardial disease, the need has arisen for a reference that offers a comprehensive approach to the understanding of basic, translational, and clinical aspects of specific muscle diseases while making the link between young adult and adult health. Reveals the link between cardiac muscle disease and skeletal muscle disease Explains how genetics and environmental factors effect muscle function of diverse origins Designates current and novel therapeutic strategies that target both cardiac and skeletal muscle systems
Author: Narasimha Reddy Parine
Publisher: BoD – Books on Demand
ISBN: 9535135155
Category : Medical
Languages : en
Pages : 282
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Book Description
The objective of this Genetic Polymorphisms book is to rehighlight and provide few updates on the role of genetic polymorphisms in medicine and agriculture, which void emerging opinion on "full death" of genetic polymorphisms as useful genetic markers. Chapters presented here demonstrate the future benefit of SNPs in many genetic studies as well as prognosis disease and diagnosis.
Author: Umashankar Lakshmanadoss
Publisher: BoD – Books on Demand
ISBN: 9535127381
Category : Medical
Languages : en
Pages : 220
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Book Description
The world of echocardiography continues to be full of exciting new technological developments with an ultimate goal of better patient care. In this book, titled "Echocardiography in Heart Failure and Cardiac Electrophysiology", authors from various parts of the world contributed to the advancement of the field. We have included various chapters about the use of echocardiography and modalities of imaging in various common clinical scenarios - ranging from evaluation of commonly ignored right ventricle, imaging in congestive heart failure, to echocardiographic evaluation of critically ill patients. We have also included topics describing the use of echocardiography in cardiac electrophysiology with special interest to cardiac resynchronization therapy and atrial fibrillation ablation. These topics would be of great interest to the clinicians whether they are trainees, physicians, advanced care providers, or anyone involved in the patient care.
Author: Barry J. Maron
Publisher: John Wiley & Sons
ISBN: 1405172568
Category : Medical
Languages : en
Pages : 128
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Book Description
When there is a diagnosis of HCM in a family, this complete,easy-to-read guide is your essential resource for finding theanswers to your many questions. In clear and straightforwardlanguage, it explains what hypertrophic cardiomyopathy is, what thesymptoms are, and how it can be treated, as well as reviewing thegenetic implications and offering candid lifestyle advice. Drawing on the expertise of Dr. Barry Maron, an internationallyrecognized authority on HCM, the book addresses major questions andconcerns of both patients and families. Fully revised to reflectthe latest developments, Hypertrophic Cardiomyopathy: Forpatients, their families and interested physicians, SecondEdition, is a valuable source of straightforward advice anddependable information for everyone who is affected by HCM.
