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Annals of Neurology|March 28, 2012
Gain of glycosylation: a new pathomechanism of myelin protein zero mutationsValeria Prada, Mario Passalacqua, Maria Bono, et al.
Neuromuscular Disorders : NMD|July 30, 2013
Influence of comorbidities on the phenotype of patients affected by Charcot-Marie-Tooth neuropathy type 1AGiulia Ursino, M Antonia Alberti, Marina Grandis, et al.
Journal of the Neurological Sciences|January 28, 2019
A novel mutation in the N-terminal acting-binding domain of Filamin C protein causing a distal myofibrillar myopathyChiara Gemelli, Valeria Prada, Chiara Fiorillo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 18, 2025
Is gaitrite system sensitive in discriminating gait pattern of subjects affected by Charcot Marie tooth? A pilot studyCristina Schenone, Maria Lagostina, Marta Ponzano, et al.
Frontiers in Neurology|November 15, 2023
Case report: Episodic ataxia without ataxia?Andrea Gaudio, Fabio Gotta, Clarissa Ponti, et al.
Brain : a Journal of Neurology|March 19, 2005
Skin biopsies in myelin-related neuropathies: bringing molecular pathology to the bedsideJun Li, Yunhong Bai, Khaled Ghandour, et al.
American Journal of Physical Medicine & Rehabilitation|June 18, 2011
Outcome measures and rehabilitation treatment in patients affected by Charcot-Marie-Tooth neuropathy: a pilot studyGiovanni Maggi, Margherita Monti Bragadin, Luca Padua, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 20, 2010
The spectrum of GNE mutations: allelic heterogeneity for a common phenotypeMarina Grandis, Rossella Gulli, Denise Cassandrini, et al.
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