Alpha 2.0
Login Register
» Articles » PMID: 3354423

Ventricular Tachycardia and Sudden Death in Myotonic Dystrophy

Overview
Journal Am Heart J
Specialty Cardiology & Vascular Diseases
Date 1988 Apr 1
PMID 3354423
Citations 9
Authors
S Hiromasa
T Ikeda
K Kubota
N Hattori
H Coto
C Maldonado
J Kupersmith
Affiliations
Soon will be listed here.
Citing Articles

Pluripotent Stem Cells in Disease Modeling and Drug Discovery for Myotonic Dystrophy Type 1.

Berenger-Currias N, Martinat C, Baghdoyan S Cells. 2023; 12(4).

PMID: 36831237 PMC: 9954118. DOI: 10.3390/cells12040571.

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

Poulin H, Mercier A, Djemai M, Pouliot V, Deschenes I, Boutjdir M Sci Rep. 2021; 11(1):2500.

PMID: 33510259 PMC: 7844414. DOI: 10.1038/s41598-021-82007-8.

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

Pang P, Alsina K, Cao S, Koushik A, Wehrens X, Cooper T J Am Heart Assoc. 2018; 7(19):e010393.

PMID: 30371314 PMC: 6404881. DOI: 10.1161/JAHA.118.010393.

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

Givvimani S, Qipshidze N, Tyagi N, Mishra P, Sen U, Tyagi S Int J Physiol Pathophysiol Pharmacol. 2011; 3(2):107-19.

PMID: 21760969 PMC: 3134005.

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

Koshelev M, Sarma S, Price R, Wehrens X, Cooper T Hum Mol Genet. 2010; 19(6):1066-75.

PMID: 20051426 PMC: 2830830. DOI: 10.1093/hmg/ddp570.