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Dilated Cardiomyopathy : From Genetics to Clinical Management / edited by Gianfranco Sinagra, Marco Merlo, Bruno Pinamonti

Contributor(s): SpringerLink (Online service) | Sinagra, Gianfranco., editor literario | Merlo, Marco., editor literario | Pinamonti, Bruno., editor literario
Material type: materialTypeLabelE-bookSeries: (Medicine (Springer-11650)).Publisher: Cham : Springer International Publishing : Imprint: Springer, 2019Description: 1 recurso en línea (IX, 241 páginas 55 ilustraciones, 45 ilustraciones a color).ISBN: 9783030138646.Subject: Miocardio -- EnfermedadesOnline resources: Acceso a este recurso digital (usuarios Universidad Europea de Madrid)Digital Resources
Contents:
1 Introduction -- 2 Epidemiology -- 3 Pathophysiology -- 4 Etiological definition and diagnostic work-up -- 5 Role of genetics and environmental factors -- 6 Clinical presentation, spectrum of disease, natural history -- 7 Role of cardiac imaging: echocardiography -- 8 Role of cardiac imaging: cardiac magnetic resonance and computed tomography -- 9 Endomyocardial biopsy -- 10 Arrhythmias in dilated cardiomyopathies -- 11 Regenerative Medicine and dilated cardiomyopathy -- 12 Prognostic stratification and importance of follow-up -- 14 Current management and treatment -- 14 Open issues and future perspectives -- 15 Dilated cardiomyopathy at the cross road: multidisciplinary approach.
Abstract: 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. .
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Holdings
Item type Current library Collection Call number Status Date due Barcode Item holds
LIBRO-E NO PRÉSTAMO LIBRO-E NO PRÉSTAMO Madrid Digital Acceso Electrónico (UEM) Ciencias de la Salud RC685 .M9 2019 EB (Browse shelf(Opens below)) Acceso electrónico eBook09072037
Total holds: 0

1 Introduction -- 2 Epidemiology -- 3 Pathophysiology -- 4 Etiological definition and diagnostic work-up -- 5 Role of genetics and environmental factors -- 6 Clinical presentation, spectrum of disease, natural history -- 7 Role of cardiac imaging: echocardiography -- 8 Role of cardiac imaging: cardiac magnetic resonance and computed tomography -- 9 Endomyocardial biopsy -- 10 Arrhythmias in dilated cardiomyopathies -- 11 Regenerative Medicine and dilated cardiomyopathy -- 12 Prognostic stratification and importance of follow-up -- 14 Current management and treatment -- 14 Open issues and future perspectives -- 15 Dilated cardiomyopathy at the cross road: multidisciplinary approach.

Open Access

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. .

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