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Neuromuscular Disorders : NMD|August 21, 2014
Progression of muscle histopathology but not of spliceopathy in myotonic dystrophy type 2Rosanna Cardani, Marzia Giagnacovo, Giulia Rossi, et al.
Frontiers in Neurology|December 6, 2024
Cardiac risk and myocardial fibrosis assessment with cardiac magnetic resonance in patients with myotonic dystrophyElena Abati, Claudia Alberti, Valentina Tambè, et al.
Journal of the Neurological Sciences|January 16, 2002
Proximal myotonic myopathy: a syndrome with a favourable prognosis?Giovanni Meola, V Sansone, K Marinou, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 28, 2018
Incidence of amplification failure in DMPK allele due to allelic dropout event in a diagnostic laboratoryClaudia De Siena, Rosanna Cardani, Elisa Brigonzi, et al.
Frontiers in Neurology|October 10, 2018
Neuropsychological and Psychological Functioning Aspects in Myotonic Dystrophy Type 1 Patients in ItalyEdward Callus, Enrico G Bertoldo, Maria Beretta, et al.
Frontiers in Genetics|December 23, 2024
Case report: Multiple approach analysis in a case of clinically assessed myotonia congenitaSabrina Lucchiari, Francesco Fortunato, Giovanni Meola, et al.
Biomed Research International|June 14, 2013
Identification and characterization of DM1 patients by a new diagnostic certified assay: neuromuscular and cardiac assessmentsRea Valaperta, Valeria Sansone, Fortunata Lombardi, et al.
Neuromuscular Disorders : NMD|November 2, 2015
Electromechanical delay components during skeletal muscle contraction and relaxation in patients with myotonic dystrophy type 1Fabio Esposito, Emiliano Cè, Susanna Rampichini, et al.
Journal of Neuromuscular Diseases|February 12, 2026
Minute-by minute gait variations during the 6-Minute walk test in subjects with myotonic dystrophy type 1Fabio Alexander Storm, Eleonora Diella, Luca Emanuele Molteni, et al.
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