Literature DB >> 3354423

Ventricular tachycardia and sudden death in myotonic dystrophy.

S Hiromasa1, T Ikeda, K Kubota, N Hattori, H Coto, C Maldonado, J Kupersmith.   

Abstract

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Year:  1988        PMID： 3354423     DOI： 10.1016/0002-8703(88)90901-5

Source DB:  PubMed          Journal:  Am Heart J        ISSN： 0002-8703            Impact factor:   4.749


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  7 in total

Review 1.  Arrhythmia and neuronal/endothelial myocyte uncoupling in hyperhomocysteinemia.

Authors:  Dorothea Rosenberger; Karni S Moshal; Ganesh K Kartha; Neetu Tyagi; Utpal Sen; David Lominadze; Claudio Maldonado; Andrew M Roberts; Suresh C Tyagi
Journal:  Arch Physiol Biochem       Date:  2006 Oct-Dec       Impact factor: 4.076

2.  Synergism between arrhythmia and hyperhomo-cysteinemia in structural heart disease.

Authors:  Srikanth Givvimani; Natia Qipshidze; Neetu Tyagi; Paras K Mishra; Utpal Sen; Suresh C Tyagi
Journal:  Int J Physiol Pathophysiol Pharmacol       Date:  2011-05-29

3.  Left ventricular diastolic function in congenital myotonic dystrophy.

Authors:  F A Bu'Lock; M Sood; J V De Giovanni; S H Green
Journal:  Arch Dis Child       Date:  1999-03       Impact factor: 3.791

4.  Heart-specific overexpression of CUGBP1 reproduces functional and molecular abnormalities of myotonic dystrophy type 1.

Authors:  Misha Koshelev; Satyam Sarma; Roger E Price; Xander H T Wehrens; Thomas A Cooper
Journal:  Hum Mol Genet       Date:  2010-01-05       Impact factor: 6.150

Review 5.  Usefulness of heart rate variability as a predictor of sudden cardiac death in muscular dystrophies.

Authors:  L Politano; A Palladino; G Nigro; M Scutifero; V Cozza
Journal:  Acta Myol       Date:  2008-12

6.  iPSC-derived cardiomyocytes from patients with myotonic dystrophy type 1 have abnormal ion channel functions and slower conduction velocities.

Authors:  Hugo Poulin; Aurélie Mercier; Mohammed Djemai; Valérie Pouliot; Isabelle Deschenes; Mohamed Boutjdir; Jack Puymirat; Mohamed Chahine
Journal:  Sci Rep       Date:  2021-01-28       Impact factor: 4.379

7.  CRISPR -Mediated Expression of the Fetal Scn5a Isoform in Adult Mice Causes Conduction Defects and Arrhythmias.

Authors:  Paul D Pang; Katherina M Alsina; Shuyi Cao; Amrita B Koushik; Xander H T Wehrens; Thomas A Cooper
Journal:  J Am Heart Assoc       Date:  2018-10-02       Impact factor: 5.501
  7 in total

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