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

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书目名称Dilated Cardiomyopathy影响因子(影响力)




书目名称Dilated Cardiomyopathy影响因子(影响力)学科排名




书目名称Dilated Cardiomyopathy网络公开度




书目名称Dilated Cardiomyopathy网络公开度学科排名




书目名称Dilated Cardiomyopathy被引频次




书目名称Dilated Cardiomyopathy被引频次学科排名




书目名称Dilated Cardiomyopathy年度引用




书目名称Dilated Cardiomyopathy年度引用学科排名




书目名称Dilated Cardiomyopathy读者反馈




书目名称Dilated Cardiomyopathy读者反馈学科排名

小鹿

Foolproof

Pathophysiology, include increased hemodynamic overload, ventricular remodeling, excessive neurohumoral stimulation, abnormal myocyte calcium cycling, excessive or inadequate proliferation of the extracellular matrix, accelerated apoptosis, and genetic mutations. Although beneficial in the early stages of heart fai

Neutropenia

Etiological Definition and Diagnostic Work-Up,ither pressure or volume overload or coronary artery disease sufficient to explain the dysfunction. It is pivotal to exclude possible removable causes of left ventricular dysfunction because this has prognostic implications. A comprehensive integrated approach, including third-level diagnostic tools

ARENA

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Role of Cardiac Imaging: Echocardiography,dilation and systolic dysfunction with impaired global contractility and normal LV wall thickness and LV diastolic dysfunction with elevation in LV filling pressure. Other frequent characteristics are LV dyssynchrony, right ventricular (RV) dysfunction, atrial dilation, functional mitral and tricusp

完整

N防腐剂

Endomyocardial Biopsy,ible because this technique is invariably characterized by a mild, but not negligible, rate of major complications (around 1%) even when performed by experienced operators. For these reasons, it is fundamental a correct selection of patients to undergo EMB. In addition to some particular clinical co

impaction

Arrhythmias in Dilated Cardiomyopathy: Diagnosis and Treatment,ntricular arrhythmias can frequently occur in some familial forms such as lamin A/C mutations. Nonsustained ventricular arrhythmias (VA) are observed in about 40% of patients with DCM, but their prognostic role is not clear, and conflicting data have been published in the last 30 years. Multiple mec