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

復(fù)雜

書目名稱Dilated Cardiomyopathy影響因子(影響力)




書目名稱Dilated Cardiomyopathy影響因子(影響力)學科排名




書目名稱Dilated Cardiomyopathy網(wǎng)絡(luò)公開度




書目名稱Dilated Cardiomyopathy網(wǎng)絡(luò)公開度學科排名




書目名稱Dilated Cardiomyopathy被引頻次




書目名稱Dilated Cardiomyopathy被引頻次學科排名




書目名稱Dilated Cardiomyopathy年度引用




書目名稱Dilated Cardiomyopathy年度引用學科排名




書目名稱Dilated Cardiomyopathy讀者反饋




書目名稱Dilated Cardiomyopathy讀者反饋學科排名

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

ingestion

ingestion

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防腐劑

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