Rhythm management in myotonic dystrophy: Progress has been made, but unsettled issues remain
Author:
Publisher
Elsevier BV
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine
Reference14 articles.
1. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member;Brook;Cell,1992
2. Loss of muscleblind-like 1 results in cardiac pathology and persistence of embryonic splice isoforms;Dixon;Sci Rep,2015
3. Pathology of the cardiac conduction system in myotonic dystrophy: a study of 12 cases;Nguyen;J Am Coll Cardiol,1988
4. Electrocardiographic abnormalities and risk of sudden death in myotonic dystrophy type 1;Groh;N Engl J Med,2008
5. Value of the electrocardiogram in determining cardiac events and mortality in myotonic dystrophy;Colleran;Am J Cardiol,1997
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2. Cardiac magnetic resonance findings and prognosis in type 1 myotonic dystrophy;Journal of Cardiovascular Medicine;2023-04-27
3. Cardiac Magnetic Resonance Findings and Prognosis in Type 1 Myotonic Dystrophy;SSRN Electronic Journal;2022
4. A Normal Electrocardiogram Does Not Exclude Infra-Hisian Conduction Disease in Patients With Myotonic Dystrophy Type 1;JACC: Clinical Electrophysiology;2021-08
5. The myotonic dystrophies;Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease;2020
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