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Steven S Scherer

Showing results (81-90 of 159) with videos related to

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Neurobiology of Disease|March 21, 2008
Human oligodendrocytes express Cx31.3: function and interactions with Cx32 mutantsIrene Sargiannidou, Meejin Ahn, Alan D Enriquez, et al.
Neurogenetics|March 29, 2018
Genetic test utilization and diagnostic yield in adult patients with neurological disordersTanya M Bardakjian, Ingo Helbig, Colin Quinn, et al.
Nature Reviews. Disease Primers|January 22, 2026
Charcot-Marie-Tooth disease and related neuropathiesJoshua Burns, Vincent Timmerman, Matilde Laurá, et al.
Muscle & Nerve|July 11, 2017
Carpal tunnel syndrome in inherited neuropathies: A retrospective surveyFrancis B Panosyan, Callyn A Kirk, Devon Marking, et al.
Journal of Cellular and Molecular Medicine|November 21, 2007
Cell expression of GDAP1 in the nervous system and pathogenesis of Charcot-Marie-Tooth type 4A diseaseLaia Pedrola, Antonio Espert, Teresa Valdés-Sánchez, et al.
Journal of the Peripheral Nervous System : JPNS|October 19, 2011
Reliability of the CMT neuropathy score (second version) in Charcot-Marie-Tooth diseaseSinéad M Murphy, David N Herrmann, Michael P McDermott, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 7, 2002
Genetic dysmyelination alters the molecular architecture of the nodal regionEdgardo J Arroyo, Theodore Xu, Judith Grinspan, et al.
Annals of Neurology|March 9, 2023
Trials for Slowly Progressive Neurogenetic Diseases Need Surrogate EndpointsMary M Reilly, David N Herrmann, Davide Pareyson, et al.
The Journal of Cell Biology|August 21, 2002
Notch1 control of oligodendrocyte differentiation in the spinal cordStephane Genoud, Corinna Lappe-Siefke, Sandra Goebbels, et al.
Neurology. Genetics|October 6, 2025
Association of the Recurrent <i>ATP1</i> <i>A1</i> Variant p.Gly549Arg With Intermediate CMT and Loss of Na,K-ATPase FunctionKerri Spontarelli Fruit, J Fernando Olivera, Nicolas Colmano, et al.
Pageof 16

Showing results (81-90 of 159) with videos related to

Sort By:
Pageof 16
Neurobiology of Disease|March 21, 2008
Human oligodendrocytes express Cx31.3: function and interactions with Cx32 mutantsIrene Sargiannidou, Meejin Ahn, Alan D Enriquez, et al.
Neurogenetics|March 29, 2018
Genetic test utilization and diagnostic yield in adult patients with neurological disordersTanya M Bardakjian, Ingo Helbig, Colin Quinn, et al.
Nature Reviews. Disease Primers|January 22, 2026
Charcot-Marie-Tooth disease and related neuropathiesJoshua Burns, Vincent Timmerman, Matilde Laurá, et al.
Muscle & Nerve|July 11, 2017
Carpal tunnel syndrome in inherited neuropathies: A retrospective surveyFrancis B Panosyan, Callyn A Kirk, Devon Marking, et al.
Journal of Cellular and Molecular Medicine|November 21, 2007
Cell expression of GDAP1 in the nervous system and pathogenesis of Charcot-Marie-Tooth type 4A diseaseLaia Pedrola, Antonio Espert, Teresa Valdés-Sánchez, et al.
Journal of the Peripheral Nervous System : JPNS|October 19, 2011
Reliability of the CMT neuropathy score (second version) in Charcot-Marie-Tooth diseaseSinéad M Murphy, David N Herrmann, Michael P McDermott, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 7, 2002
Genetic dysmyelination alters the molecular architecture of the nodal regionEdgardo J Arroyo, Theodore Xu, Judith Grinspan, et al.
Annals of Neurology|March 9, 2023
Trials for Slowly Progressive Neurogenetic Diseases Need Surrogate EndpointsMary M Reilly, David N Herrmann, Davide Pareyson, et al.
The Journal of Cell Biology|August 21, 2002
Notch1 control of oligodendrocyte differentiation in the spinal cordStephane Genoud, Corinna Lappe-Siefke, Sandra Goebbels, et al.
Neurology. Genetics|October 6, 2025
Association of the Recurrent <i>ATP1</i> <i>A1</i> Variant p.Gly549Arg With Intermediate CMT and Loss of Na,K-ATPase FunctionKerri Spontarelli Fruit, J Fernando Olivera, Nicolas Colmano, et al.
Pageof 16