Cardiomyopathies: a revolution in molecular medicine and cardiac imaging. - Wikidata - wikimedia - TriplyDB

Cardiomyopathies: a revolution in molecular medicine and cardiac imaging.

Cardiomyopathies: a revolution in molecular medicine and cardiac imaging.

http://www.wikidata.org/entity/Q33580865

about

Speckle tracking: distinction of physiologic from pathologic LVH?CMR-determined scar volume: predictive for ventricular tachycardias?Does heart rate influence CMR image quality of the coronary vessel wall?Evaluation of hypertrophic cardiomyopathy: new horizons for CMR?Left ventricular mass assessment by CMR; how to define the optimal index.Assessment of left ventricular volumes; reliable by gated SPECT?Assessment of left ventricular function: visual or quantitative?Aortic stiffness in type-1 diabetes mellitus; beware of hypertension

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Cardiomyopathies: a revolution in molecular medicine and cardiac imaging.

http://www.wikidata.org/entity/Q33580865

description

2009 nî lūn-bûn

@nan

2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年論文

@yue

2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

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2009年论文

@wuu

name

Cardiomyopathies: a revolution in molecular medicine and cardiac imaging.

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Cardiomyopathies: a revolution in molecular medicine and cardiac imaging.

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Cardiomyopathies: a revolution in molecular medicine and cardiac imaging.

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Cardiomyopathies: a revolution in molecular medicine and cardiac imaging.

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Cardiomyopathies: a revolution in molecular medicine and cardiac imaging.

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Cardiomyopathies: a revolution in molecular medicine and cardiac imaging.

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Cardiomyopathies: a revolution in molecular medicine and cardiac imaging.

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Cardiomyopathies: a revolution in molecular medicine and cardiac imaging.

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Cardiomyopathies: a revolution in molecular medicine and cardiac imaging.

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Netherlands Heart Journal

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Cardiomyopathies: a revolution in molecular medicine and cardiac imaging.

@en

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Ten Cate FJ

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P2860

Hypertrophic cardiomyopathy family with double-heterozygous mutations; does disease severity suggest doubleheterozygosity?

A Dutch case of a takotsubo cardiomyopathy after pacemaker implantation.

Unexpected massive myocardial calcification.

The importance of cardiac MRI as a diagnostic tool in viral myocarditis-induced cardiomyopathy.

Effect of successful alcohol septal ablation on microvascular function in patients with obstructive hypertrophic cardiomyopathy.

Reduced regional myocardial perfusion reserve is associated with impaired contractile performance in idiopathic dilated cardiomyopathy.

Left ventricular aneurysm in patients with idiopathic dilated cardiomyopathy: clinical analysis of six cases

Risk stratification for sudden cardiac death in hypertrophic cardiomyopathy: Dutch cardiologists and the care of mutation carriers.

Clinical profile and significance of delayed enhancement in hypertrophic cardiomyopathy.

Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases.

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456-457

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scholarly article

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10.1007/BF03086303

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12

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17

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2009-12-01T00:00:00Z

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1020841280

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20087447

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2804076

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