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Frontiers in Neurology|June 15, 2018
Flecainide-Induced Brugada Syndrome in a Patient With Skeletal Muscle Sodium Channelopathy: A Case Report With Critical Therapeutical Implications and Review of the LiteratureMichele Cavalli, Barbara Fossati, Raffaele Vitale, et al.Journal of Cardiovascular Medicine (Hagerstown, Md.)|May 19, 2009
Is it too early to recommend patent foramen ovale closure for all patients who suffer from migraine? A single-centre studyMassimo Chessa, Chiara Colombo, Gianfranco Butera, et al.Frontiers in Neurology|April 9, 2020
Rare Disease: Cardiac Risk Assessment With MRI in Patients With Myotonic Dystrophy Type 1Marco Alì, Caterina Beatrice Monti, Luca Melazzini, et al.Frontiers in Endocrinology|November 30, 2017
Circulating Irisin Is Reduced in Male Patients with Type 1 and Type 2 Myotonic DystrophiesElena Dozio, Elena Passeri, Rosanna Cardani, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 8, 2023
Myotonic dystrophy type 1 in the COVID-19 eraJelena Ilic Zivojinovic, Katarina Djurdjevic, Ivo Bozovic, et al.Scientific Reports|July 25, 2018
SCN4A as modifier gene in patients with myotonic dystrophy type 2Anna Binda, Laura V Renna, Francesca Bosè, et al.Frontiers in Neurology|October 16, 2019
<i>TNNT2</i> Missplicing in Skeletal Muscle as a Cardiac Biomarker in Myotonic Dystrophy Type 1 but Not in Myotonic Dystrophy Type 2Francesca Bosè, Laura Valentina Renna, Barbara Fossati, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 19, 2022
Clinical score for early diagnosis of myotonic dystrophy type 2Vukan Ivanovic, Stojan Peric, Jovan Pesovic, et al.Genetic Testing and Molecular Biomarkers|October 28, 2015
Development and Validation of a New Molecular Diagnostic Assay for Detection of Myotonic Dystrophy Type 2Rea Valaperta, Fortunata Lombardi, Rosanna Cardani, et al.Neuroimage. Clinical|January 31, 2021
Lesion distribution and substrate of white matter damage in myotonic dystrophy type 1: Comparison with multiple sclerosisSara Leddy, Laura Serra, Davide Esposito, et al.Pageof 11