Myotonic dystrophy type 1 (DM1) is a dominant genetic disease in which the expansion of
long CTG trinucleotides in the 3′ UTR of the myotonic dystrophy protein kinase (DMPK) …

Myotonic dystrophy is a hereditary disorder with systemic involvement. The Italian Neuro-
Cardiology Network-“Rete delle Neurocardiologie”(INCN-RNC) is a unique collaborative …

Myotonic dystrophy (DM) is caused by expansions of C (C) TG repeats in the non-coding
regions of the DMPK and CNBP genes, and DM patients often suffer from sudden cardiac …

Myotonic dystrophy type 1 (DM1) is a genetic disorder that causes muscle weakness and
myotonia. In DM1 patients, cardiac electrical manifestations include conduction defects and …

Introduction: Myotonic dystrophy type 1 (DM1) is a multisystemic genetic disorder caused by
the increased number of CTG repeats in 3′ UTR of Dystrophia Myotonia Protein Kinase …

Current studies concerning myotonic dystrophy type 1 (DM1) are in the process of
transitioning from molecular investigations to preclinical and clinical trials. Several papers …

Myotonic dystrophy type I (MDI) is the most common muscular dystrophy in adults. The main
objectives of this study were to determine the prevalence of MDI in the Community of Madrid …

Background Cardiac involvement represents a major cause of morbidity and mortality in
patients with myotonic dystrophy type 1 (DM1) and prevention of sudden cardiac death …

Cardiac implantable electronic devices (CIED) including pacemakers (PM), implantable
cardioverter defibrillators (ICD), and cardiac resynchronized therapy (CRT) have become …

Background: Myotonic dystrophy type 1 (MD1), which is characterized by decreased muscle
tone, progressive muscle weakness, and cardiac involvement, is an autosomal dominant …