Biventricular noncompaction cardiomyopathy with malignant arrhythmia as a cause of sudden death.

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Biventricular noncompaction cardiomyopathy with malignant arrhythmia as a cause of sudden death.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Biventricular noncompaction ca ...... ia as a cause of sudden death.

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Biventricular noncompaction ca ...... ia as a cause of sudden death.

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Item

label

Biventricular noncompaction ca ...... ia as a cause of sudden death.

@en

Biventricular noncompaction ca ...... ia as a cause of sudden death.

@nl

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Biventricular noncompaction ca ...... ia as a cause of sudden death.

@en

Biventricular noncompaction ca ...... ia as a cause of sudden death.

@nl

P1476

Biventricular noncompaction ca ...... ia as a cause of sudden death.

@en

P2093

Klára Marecová

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Marie Staňková

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Petr Handlos

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Tomáš Gruszka

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P2860

Isolated noncompaction of left ventricular myocardium. A study of eight cases

Left ventricular hypertrabeculation/noncompaction and association with additional cardiac abnormalities and neuromuscular disorders.

Novel gene locus for autosomal dominant left ventricular noncompaction maps to chromosome 11p15.

Clinical features of isolated ventricular noncompaction in adults long-term clinical course, echocardiographic properties, and predictors of left ventricular failure.

Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome.

Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: a step towards classification as a distinct cardiomyopathy.

Noncompaction Cardiomyopathy: Case Presentation with Cardiac Magnetic Resonance Imaging Findings and Literature Review.

Isolated noncompaction of the myocardium in adults.

Sudden death due to biventricular non-compaction cardiomyopathy in a 14-year-old.

Isolated ventricular non-compaction in adults with idiopathic cardiomyopathy: cardiac magnetic resonance and pathologic characterization of the anomaly.

P2888

s12024-017-9889-y

P304

495-499

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scholarly article

P356

10.1007/S12024-017-9889-Y

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P433

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P478

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P50

Marek Joukal

P577

2017-06-15T00:00:00Z

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P698

28616812

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