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Neurobiology of Disease
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March 21, 2008
Human oligodendrocytes express Cx31.3: function and interactions with Cx32 mutants
Irene Sargiannidou, Meejin Ahn, Alan D Enriquez, et al.
Neurogenetics
|
March 29, 2018
Genetic test utilization and diagnostic yield in adult patients with neurological disorders
Tanya M Bardakjian, Ingo Helbig, Colin Quinn, et al.
Nature Reviews. Disease Primers
|
January 22, 2026
Charcot-Marie-Tooth disease and related neuropathies
Joshua Burns, Vincent Timmerman, Matilde Laurá, et al.
Muscle & Nerve
|
July 11, 2017
Carpal tunnel syndrome in inherited neuropathies: A retrospective survey
Francis 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 disease
Laia 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 disease
Sinéad 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 region
Edgardo J Arroyo, Theodore Xu, Judith Grinspan, et al.
Annals of Neurology
|
March 9, 2023
Trials for Slowly Progressive Neurogenetic Diseases Need Surrogate Endpoints
Mary 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 cord
Stephane 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 Function
Kerri Spontarelli Fruit, J Fernando Olivera, Nicolas Colmano, et al.
Page
of 16
Search research articles
Search
Showing results (81-90 of 159) with videos related to
Sort By:
Page
of 16
Neurobiology of Disease
|
March 21, 2008
Human oligodendrocytes express Cx31.3: function and interactions with Cx32 mutants
Irene Sargiannidou, Meejin Ahn, Alan D Enriquez, et al.
Neurogenetics
|
March 29, 2018
Genetic test utilization and diagnostic yield in adult patients with neurological disorders
Tanya M Bardakjian, Ingo Helbig, Colin Quinn, et al.
Nature Reviews. Disease Primers
|
January 22, 2026
Charcot-Marie-Tooth disease and related neuropathies
Joshua Burns, Vincent Timmerman, Matilde Laurá, et al.
Muscle & Nerve
|
July 11, 2017
Carpal tunnel syndrome in inherited neuropathies: A retrospective survey
Francis 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 disease
Laia 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 disease
Sinéad 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 region
Edgardo J Arroyo, Theodore Xu, Judith Grinspan, et al.
Annals of Neurology
|
March 9, 2023
Trials for Slowly Progressive Neurogenetic Diseases Need Surrogate Endpoints
Mary 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 cord
Stephane 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 Function
Kerri Spontarelli Fruit, J Fernando Olivera, Nicolas Colmano, et al.
Page
of 16