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Alexander M Rossor

Showing results (61-70 of 97) with videos related to

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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.
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.
Journal of Neurology, Neurosurgery, and Psychiatry|September 18, 2020
Mutation in <i>RNF170</i> causes sensory ataxic neuropathy with vestibular areflexia: a CANVAS mimicAndrea Cortese, Ilaria Callegari, Riccardo Currò, et al.
Neurology|May 25, 2021
MicroRNAs as Biomarkers of Charcot-Marie-Tooth Disease Type 1AHongge Wang, Matthew Davison, Kathryn Wang, et al.
Neurology|August 4, 2017
Cross-sectional analysis of a large cohort with X-linked Charcot-Marie-Tooth disease (CMTX1)Francis B Panosyan, Matilde Laura, Alexander M Rossor, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 12, 2012
Charcot-Marie-Tooth disease: frequency of genetic subtypes and guidelines for genetic testingSinead M Murphy, Matilde Laura, Katherine Fawcett, et al.
Plos Genetics|November 9, 2022
A new mouse model of Charcot-Marie-Tooth 2J neuropathy replicates human axonopathy and suggest alteration in axo-glia communicationGhjuvan'Ghjacumu Shackleford, Leandro N Marziali, Yo Sasaki, et al.
Pageof 10

Showing results (61-70 of 97) with videos related to

Sort By:
Pageof 10
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.
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.
Journal of Neurology, Neurosurgery, and Psychiatry|September 18, 2020
Mutation in <i>RNF170</i> causes sensory ataxic neuropathy with vestibular areflexia: a CANVAS mimicAndrea Cortese, Ilaria Callegari, Riccardo Currò, et al.
Neurology|May 25, 2021
MicroRNAs as Biomarkers of Charcot-Marie-Tooth Disease Type 1AHongge Wang, Matthew Davison, Kathryn Wang, et al.
Neurology|August 4, 2017
Cross-sectional analysis of a large cohort with X-linked Charcot-Marie-Tooth disease (CMTX1)Francis B Panosyan, Matilde Laura, Alexander M Rossor, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 12, 2012
Charcot-Marie-Tooth disease: frequency of genetic subtypes and guidelines for genetic testingSinead M Murphy, Matilde Laura, Katherine Fawcett, et al.
Plos Genetics|November 9, 2022
A new mouse model of Charcot-Marie-Tooth 2J neuropathy replicates human axonopathy and suggest alteration in axo-glia communicationGhjuvan'Ghjacumu Shackleford, Leandro N Marziali, Yo Sasaki, et al.
Pageof 10