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Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|June 27, 2009
Long-term follow-up free of ventricular fibrillation recurrence after resuscitated cardiac arrest in a myotonic dystrophy type 1 patientValeria A Sansone, Guido De Ambroggi, Alice Zanolini, et al.Neuromuscular Disorders : NMD|October 23, 2025
288<sup>th</sup> ENMC International Workshop. Towards better diagnosing, understanding and treating gastrointestinal symptoms in myotonic dystrophy: extended insights and practical recommendations. 16-18 May 2025, Hoofddorp, the NetherlandsSaskia Scholten, Janel A M Peterson, Lynn B Orriëns, et al.Plos One|December 31, 2013
Overexpression of CUGBP1 in skeletal muscle from adult classic myotonic dystrophy type 1 but not from myotonic dystrophy type 2Rosanna Cardani, Enrico Bugiardini, Laura V Renna, et al.Biomedicines|April 29, 2025
Evaluation of Sleep-Disordered Breathing and Respiratory Dysfunction in Children with Myotonic Dystrophy Type 1-A Retrospective Cross-Sectional StudyMihail Basa, Jovan Pesovic, Dusanka Savic-Pavicevic, et al.Plos One|September 16, 2017
Receptor and post-receptor abnormalities contribute to insulin resistance in myotonic dystrophy type 1 and type 2 skeletal muscleLaura Valentina Renna, Francesca Bosè, Sara Iachettini, et al.Muscle & Nerve|September 26, 2008
Preferential central nucleation of type 2 myofibers is an invariable feature of myotonic dystrophy type 2Valerio Pisani, Maria Beatrice Panico, Chiara Terracciano, et al.Scientific Reports|December 2, 2025
Characterizing white matter hyperintensities in myotonic dystrophy type 1 through IVIM derived metricsMarina Di Stefano, Nivedita Agarwal, Giulia Canella, et al.Frontiers in Neurology|March 1, 2024
Case report: Dihydropyridine receptor (<i>CACNA1S</i>) congenital myopathy, a novel phenotype with early onset periodic paralysisSamah K Aburahma, Liqa A Rousan, Mohammad Shboul, et al.Heliyon|March 4, 2024
Transcranial brain parenchyma sonographic findings in patients with myotonic dystrophy type 1 and 2Milija Mijajlovic, Ivo Bozovic, Aleksandra Pavlovic, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 13, 2021
Co-occurrence of DMPK expansion and CLCN1 mutation in a patient with myotoniaSara Locci, Rosanna Cardani, Paola Brunori, et al.Pageof 11