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Neurology|December 13, 2019
Targeted next-generation sequencing panels in the diagnosis of Charcot-Marie-Tooth diseaseAndrea Cortese, Janel E Wilcox, James M Polke, et al.
Journal of the Neurological Sciences|November 3, 2019
Routine blood monitoring in maintenance immunoglobulin treatment of inflammatory neuropathy: Is it clinically relevant?R Keh, A Kahlil, L Nihoyannopoulos, et al.
Neuromuscular Disorders : NMD|March 16, 2013
Rapidly progressive asymmetrical weakness in Charcot-Marie-Tooth disease type 4J resembles chronic inflammatory demyelinating polyneuropathyEllen Cottenie, Manoj P Menezes, Alexander M Rossor, et al.
Brain : a Journal of Neurology|June 20, 2023
Post-transcriptional microRNA repression of PMP22 dose in severe Charcot-Marie-Tooth disease type 1Menelaos Pipis, Seongsik Won, Roy Poh, et al.
Brain : a Journal of Neurology|March 14, 2024
Whole genome sequencing increases the diagnostic rate in Charcot-Marie-Tooth diseaseChristopher J Record, Menelaos Pipis, Mariola Skorupinska, et al.
Neurology|March 12, 2017
Mutations in noncoding regions of <i>GJB1</i> are a major cause of X-linked CMTPedro J Tomaselli, Alexander M Rossor, Alejandro Horga, et al.
Neurology|November 27, 2002
Chromosome 3 linked frontotemporal dementia (FTD-3)S Gydesen, J M Brown, A Brun, et al.
Brain : a Journal of Neurology|March 26, 2019
Gene replacement therapy in a model of Charcot-Marie-Tooth 4C neuropathyNatasa Schiza, Elena Georgiou, Alexia Kagiava, et al.
Annals of the New York Academy of Sciences|May 20, 2000
Hereditary vascular dementia linked to notch 3 mutations. CADASIL in British familiesN J Thomas, C M Morris, F Scaravilli, et al.
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