Titlebook: Dilated Cardiomyopathy; From Genetics to Cli Gianfranco Sinagra,Marco Merlo,Bruno Pinamonti Book‘‘‘‘‘‘‘‘ 2019 The Editor(s) (if applicable)

Cougar

桉樹

Book‘‘‘‘‘‘‘‘ 2019ment. 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 i

Resection

Fecal-Impaction

https://doi.org/10.1007/978-3-322-99789-0logic basis of many so-called idiopathic heart muscle disease. A step toward a comprehensive DCM classification and an attempt to reconcile clinic with genetic in the complexity of the disease is genotype-phenotype correlation, with its prognostic implication in clinical practice. In this chapter wi

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Tremor

endure

Caroline Rozynek,Moritz Engbers radiation doses. The primary diagnostic application is in differentiation of ischemic from nonischemic etiology of left ventricular dysfunction. Its role in tissue characterization shows promise and is increasingly being studied.

LEVY

Caroline Rozynek,Moritz Engberssk is still a major issue. Despite its limitations, left ventricular (LV) dysfunction is still pivotal for the identification of patients who should be treated with ICD according to current guidelines, while the role of all other invasive and noninvasive parameters is still debated. Cardiac magnetic

具體

Franziska Henkel,Carsten Sommerdiomyopathy are generally young subjects. Therefore, the assessment of prognosis is essential. Biomarkers are nowadays widely available and are useful tools for risk stratification..Besides HF-dedicated biomarkers, such as natriuretic peptides, galectin-3, soluble ST2 and troponins, also the evaluat

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