(Q36319453)

13 August 2017

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title

Is Wolff-Parkinson-White syndrome a genetic disease? (English)

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Wolff–Parkinson–White syndrome

13 August 2017

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Javed Ehtisham

1

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13 August 2017

Hugh Watkins

series ordinal

2

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13 August 2017

publication date

1 November 2005

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Journal of Cardiovascular Electrophysiology

13 August 2017

published in

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13 August 2017

volume

16

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13 August 2017

issue

11

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13 August 2017

page(s)

1258-1262

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Bundle-branch block with short P-R interval in healthy young people prone to paroxysmal tachycardia

13 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.50139.X

Identification of a gene responsible for familial Wolff-Parkinson-White syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.50139.X

Researches on the Structure and Function of the Mammalian Heart

21 January 2018

1 reference

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The syndrome of short P-R interval, normal QRS complex and paroxysmal rapid heart action

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.50139.X

The connecting pathways between the sinus node and A-V node and between the right and the left atrium in the human heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.50139.X

Familial Wolff-Parkinson-White syndrome with cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.50139.X

Canine tricuspid valve malformation, a model of human Ebstein anomaly, maps to dog chromosome 9.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.50139.X

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.50139.X

Pompe's disease presenting as hypertrophic myocardiopathy with Wolff-Parkinson-White syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.50139.X

Glycogen storage diseases presenting as hypertrophic cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.50139.X

Normal and abnormal consequences of apoptosis in the human heart. From postnatal morphogenesis to paroxysmal arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.50139.X

Hypertrophic cardiomyopathy:a paradigm for myocardial energy depletion

21 January 2018

1 reference

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Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis

21 January 2018

1 reference

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The AMP-activated protein kinase--fuel gauge of the mammalian cell?

21 January 2018

1 reference

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Characterization of AMP-activated protein kinase gamma-subunit isoforms and their role in AMP binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.50139.X

Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.50139.X

Electrophysiologic characterization and postnatal development of ventricular pre-excitation in a mouse model of cardiac hypertrophy and Wolff-Parkinson-White syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.50139.X

Transgenic mouse model of ventricular preexcitation and atrioventricular reentrant tachycardia induced by an AMP-activated protein kinase loss-of-function mutation responsible for Wolff-Parkinson-White syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2005.50139.X

Mutation analysis of AMP-activated protein kinase subunits in inherited cardiomyopathies: implications for kinase function and disease pathogenesis

21 January 2018

1 reference

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10.1111/J.1540-8167.2005.50139.X

21 January 2018

Identifiers

DOI

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13 August 2017

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