High prevalence of cardiac involvement in patients with myotonic dystrophy type 1: A cross-sectional study-Reference-Cited by-同舟云学术

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High prevalence of cardiac involvement in patients with myotonic dystrophy type 1: A cross-sectional study

Published:2014-06 Issue:1 Volume:174 Page:31-36
ISSN:0167-5273
Container-title:International Journal of Cardiology
language:en
Short-container-title:International Journal of Cardiology

Author:

Petri Helle,Witting Nanna,Ersbøll Mads Kristian,Sajadieh Ahmad,Dunø Morten,Helweg-Larsen Susanne,Vissing John,Køber Lars,Bundgaard Henning

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference50 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

2. Electrocardiographic Abnormalities and Sudden Death in Myotonic Dystrophy Type 1

3. Cardiac manifestations of myotonic dystrophy type 1

4. Increased mortality with left ventricular systolic dysfunction and heart failure in adults with myotonic dystrophy type 1

5. Structural myocardial involvement in adult patients with type 1 myotonic dystrophy

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1. Living with adult-onset myotonic dystrophy type 1: a scoping review;Disability and Rehabilitation;2024-08-30

2. Rescue of Scn5a mis-splicing does not improve the structural and functional heart defects of a DM1 heart mouse model;Human Molecular Genetics;2024-08-11

3. Natural history of cardiac involvement in myotonic dystrophy type 1 – Emphasis on the need for lifelong follow-up;International Journal of Cardiology;2024-07

4. Clinical features and genetic spectrum of a multicenter Chinese cohort with myotonic dystrophy type 1;Orphanet Journal of Rare Diseases;2024-03-07

5. Electrophysiological basis of cardiac arrhythmia in a mouse model of myotonic dystrophy type 1;Frontiers in Physiology;2023-09-21

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