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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|January 20, 2022
How to define and enhance diagnostic and assistance pathways in neuromuscular diseases during the COVID-19 pandemic: the concept of networkGuja Astrea, Gemma Marinella, Caterina Agosto, et al.Journal of the Peripheral Nervous System : JPNS|November 12, 2021
Techniques for the standard histological and ultrastructural assessment of nerve biopsiesJoachim Weis, Istvan Katona, Stefan Nikolin, et al.Journal of Ultrasonography|December 7, 2019
The primary role of radiological imaging in the diagnosis of rare musculoskeletal diseases. Emphasis on ultrasoundFederica Rossi, Carlo Martinoli, Giovanni Murialdo, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 6, 2021
Charcot-Marie-Tooth neuropathy score and ambulation index are both predictors of orthotic need for patients with CMTValeria Prada, Riccardo Zuccarino, Cristina Schenone, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 26, 2010
A novel mutation in KIF5A gene causing hereditary spastic paraplegia with axonal neuropathyOlimpia Musumeci, Maria Teresa Bassi, Anna Mazzeo, et al.Journal of Medical Case Reports|December 14, 2021
Parsonage-Turner syndrome following coronavirus disease 2019 immunization with ChAdOx1-S vaccine: a case report and review of the literatureBruno Kusznir Vitturi, Marina Grandis, Sabrina Beltramini, et al.Best Practice & Research. Clinical Rheumatology|May 3, 2025
Imaging for inflammatory neuropathiesFederico Zaottini, Federico Pistoia, Riccardo Picasso, et al.Journal of the Peripheral Nervous System : JPNS|November 3, 2020
Validation of a new hand function outcome measure in individuals with Charcot-Marie-Tooth diseaseValeria Prada, Giulia Robbiano, Giulia Mennella, et al.Frontiers in Pediatrics|August 25, 2025
Case Report: Parsonage-Turner syndrome due to SEPTIN9 mutation: report of an Italian family with childhood onset and review of the literatureLuca Bosisio, Matteo Cataldi, Marina Grandis, et al.Journal of Human Genetics|April 2, 2008
Gap junction beta 1 (GJB1) gene mutations in Italian patients with X-linked Charcot-Marie-Tooth diseasePaola Mandich, Marina Grandis, Alessandro Geroldi, et al.Pageof 10