(Q52540375)

2 May 2018

title

Progressive atrioventricular conduction block in a mouse myotonic dystrophy model. (English)

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2 May 2018

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C I Berul

1

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2 May 2018

C T Maguire

series ordinal

2

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2 May 2018

J Gehrmann

series ordinal

3

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S Reddy

series ordinal

4

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2 May 2018

publication date

1 June 2000

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2 May 2018

Journal of Interventional Cardiac Electrophysiology

published in

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2 May 2018

volume

4

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2 May 2018

page(s)

351-358

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2 May 2018

issue

2

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2 May 2018

https://scigraph.springernature.com/pub.10.1023/a:1009842114968

exact match

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cites work

In vivo cardiac electrophysiology studies in the mouse

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12 December 2020

Systemic delivery of recombinant proteins by genetically modified myoblasts

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12 December 2020

Myoblast transfer in the treatment of Duchenne's muscular dystrophy

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12 December 2020

The fate of individual myoblasts after transplantation into muscles of DMD patients

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12 December 2020

Myotonia dystrophica: ventricular arrhythmias, intraventricular conduction abnormalities, atrioventricular block and Stokes-Adams attacks successfully treated with permanent transvenous pacemaker

1 reference

12 December 2020

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

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12 December 2020

Course, prognosis and complications of childhood-onset myotonic dystrophy

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12 December 2020

Electrophysiologic study of the condition system in normal children

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12 December 2020

Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice.

1 reference

12 December 2020

DMPK dosage alterations result in atrioventricular conduction abnormalities in a mouse myotonic dystrophy model

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12 December 2020

A family with myotonic dystrophy associated with diffuse cardiac conduction disturbances as demonstrated by His bundle electrocardiography

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12 December 2020

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

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12 December 2020

Cardiac involvement in myotonic dystrophy

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12 December 2020

Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathy

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12 December 2020

Localization of the sites of conduction abnormalities in a mouse model of myotonic dystrophy

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12 December 2020

The natural history of conduction system disease in myotonic muscular dystrophy as determined by serial electrophysiologic studies

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12 December 2020

An unstable triplet repeat in a gene related to myotonic muscular dystrophy

1 reference

12 December 2020

Value of the electrocardiogram in determining cardiac events and mortality in myotonic dystrophy

1 reference

12 December 2020

Normal dystrophin transcripts detected in Duchenne muscular dystrophy patients after myoblast transplantation

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12 December 2020

Cardiac involvement in myotonic muscular dystrophy (Steinert's disease): a prospective study of 25 patients

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12 December 2020

Familial hypertrophic cardiomyopathy mice display gender differences in electrophysiological abnormalities.

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12 December 2020

A-V dissociation in dystrophia myotonica

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12 December 2020

Identifiers

DOI

10.1023/A:1009842114968

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2 May 2018

Dimensions Publication ID

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2 May 2018