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Neuromuscular Disorders : NMD|November 28, 2017
Identification and characterization of the novel m.8305C>T MTTK and m.4440G>A MTTM gene mutations causing mitochondrial myopathiesMauro Scarpelli, Lidia Carreño-Gago, Anna Russignan, et al.Neuromuscular Disorders : NMD|February 12, 2021
Next-generation sequencing application to investigate skeletal muscle channelopathies in a large cohort of Italian patientsRaffaella Brugnoni, Lorenzo Maggi, Eleonora Canioni, et al.Journal of Cardiovascular Medicine (Hagerstown, Md.)|July 31, 2024
Temporal implementation of a regional referral pathway in transthyretin cardiac amyloidosis: Emilia-Romagna experienceSimone Longhi, Elena Biagini, Pietro Guaraldi, et al.Frontiers in Neurology|September 15, 2025
Monitoring patients and asymptomatic carriers with hereditary transthyretin amyloidosis: regional protocol of Emilia-Romagna ATTR working groupPietro Guaraldi, Isabella Allegri, Alessandra Ariatti, et al.Neurology|August 5, 2024
Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies: Experience From the Italian NetworkSara Bortolani, Marco Savarese, Gaetano Vattemi, et al.Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|September 9, 2020
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phaseEleonora Mauri, Elena Abati, Olimpia Musumeci, et al.Pageof 3