I read the letter by Dr. Finsterer with a great interest [1], but I must say I am pretty much
concerned about wrong messages this letter sends to the readership and the way it was …

With interest we read the article by Peric et al. about a retrospective study by means of
clinical exam, ECG and echocardiography in 62 patients with myotonic dystrophy type 2 …

Cardiac involveent in type 1 myotonic dystrophy. - Abstract - Europe PMC Sign in | Create an
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Abstract Background and aim Myotonic Dystrophy (MD) is the most common inherited
muscular dystrophy of the adult. Cardiac manifestation, including arrhythmias and …

Abstract Myotonic dystrophy type 1 (DM1) is the commonest muscular dystrophy in adults,
affecting multiple organs in addition to skeletal muscles. Cardiac conduction system …

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 …

We do not agree with the conclusion that MD1 patient should receive prophylactic
implantation of a paemkaer (1). MD1 patients may not only experience supra-ventricular but …

Abstract Myotonic dystrophy type 2 (DM2) is a slowly progressive, autosomal-dominant
disease. This is a multisystemic disorder that affects the heart, which is one of the main …

Objective: To describe clinical and electrophysiological characteristics of patients with
myotonic dystrophy type I (DM1) and type II (DM2). Background: Myotonic dystrophy is …

Myotonic Dystrophy type 1 (DM1) is an autosomal dominant neuromuscular disorder
characterized by progressive muscle weakness and cardiac involvement. Routine cardiac …