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Dilated cardiomyopathy = from geneti...
~
Merlo, Marco.
Dilated cardiomyopathy = from genetics to clinical management /
Record Type:
Language materials, printed : Monograph/item
Title/Author:
Dilated cardiomyopathy/ edited by Gianfranco Sinagra, Marco Merlo, Bruno Pinamonti.
Reminder of title:
from genetics to clinical management /
other author:
Sinagra, Gianfranco.
Published:
Cham :Springer International Publishing : : 2019.,
Description:
ix, 241 p. :ill. (some col.), digital ; : 24 cm.;
Contained By:
Springer eBooks
Subject:
Myocardium - Diseases. -
Online resource:
https://doi.org/10.1007/978-3-030-13864-6
ISBN:
9783030138646
Dilated cardiomyopathy = from genetics to clinical management /
Dilated cardiomyopathy
from genetics to clinical management /[electronic resource] :edited by Gianfranco Sinagra, Marco Merlo, Bruno Pinamonti. - Cham :Springer International Publishing :2019. - ix, 241 p. :ill. (some col.), digital ;24 cm.
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.
ISBN: 9783030138646
Standard No.: 10.1007/978-3-030-13864-6doiSubjects--Topical Terms:
1227437
Myocardium
--Diseases.
LC Class. No.: RC685.M9 / D553 2019
Dewey Class. No.: 616.124
Dilated cardiomyopathy = from genetics to clinical management /
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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.
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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.
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Medicine (Springer-11650)
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