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Journal of the Peripheral Nervous System : JPNS|May 13, 2020
Validation of the Italian version of the Charcot-Marie-Tooth disease Pediatric ScaleRiccardo Zuccarino, Valeria Prada, Isabella Moroni, et al.Neurology|April 26, 2020
Attracting neurology's next generation: A qualitative study of specialty choice and perceptionsJustin T Jordan, Carolyn Cahill, Tasha Ostendorf, et al.Annals of Neurology|March 28, 2012
Gain of glycosylation: a new pathomechanism of myelin protein zero mutationsValeria Prada, Mario Passalacqua, Maria Bono, et al.Journal of the Peripheral Nervous System : JPNS|August 5, 2026
Clinical Development of Therapies for Charcot-Marie-Tooth Disease: Recommendations for Trial Design, Endpoints, and Regulatory PathwaysCharles K Abrams, Sue Bruhn, Joshua Burns, et al.Journal of Neuromuscular Diseases|July 16, 2019
Brain Structural Features of Myotonic Dystrophy Type 1 and their Relationship with CTG RepeatsEllen van der Plas, Mark J Hamilton, Jacob N Miller, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|November 12, 2013
C-reactive protein and long-term ischemic stroke prognosisReyna L VanGilder, Danielle M Davidov, Kyle R Stinehart, et al.Neurology|May 25, 2021
MicroRNAs as Biomarkers of Charcot-Marie-Tooth Disease Type 1AHongge Wang, Matthew Davison, Kathryn Wang, et al.JCI Insight|April 4, 2023
Sorbitol reduction via govorestat ameliorates synaptic dysfunction and neurodegeneration in sorbitol dehydrogenase deficiencyYi Zhu, Amanda G Lobato, Adriana P Rebelo, et al.Annals of the New York Academy of Sciences|November 1, 2017
Peripheral Neuropathy Caused by Proteolipid Protein Gene MutationsJames Y Garbern, Franca Cambi, Richard Lewis, et al.Annals of Neurology|March 9, 2018
Myelin abnormality in Charcot-Marie-Tooth type 4J recapitulates features of acquired demyelinationBo Hu, Megan McCollum, Vignesh Ravi, et al.Pageof 9