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Steven S Scherer

Showing results (111-120 of 159) with videos related to

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Journal of the Peripheral Nervous System : JPNS|August 14, 2024
Diagnostic and clinical utility of comprehensive multigene panel testing for patients with neuropathyJennifer Roggenbuck, Ana Morales, Colin A Ellis, et al.
Scientific Reports|April 30, 2021
Inducible knockout of Clec16a in mice results in sensory neurodegenerationHeather S Hain, Rahul Pandey, Marina Bakay, et al.
Annals of Neurology|January 27, 2006
T118M PMP22 mutation causes partial loss of function and HNPP-like neuropathyMichael E Shy, Mena T Scavina, Alisa Clark, et al.
Neurology|May 11, 2016
Target-enrichment sequencing and copy number evaluation in inherited polyneuropathyWei Wang, Chen Wang, D Brian Dawson, et al.
The Journal of Clinical Investigation|December 5, 2017
PMP22 antisense oligonucleotides reverse Charcot-Marie-Tooth disease type 1A features in rodent modelsHien Tran Zhao, Sagar Damle, Karli Ikeda-Lee, et al.
Biorxiv : the Preprint Server for Biology|December 18, 2023
Sord deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insightsAdriana P Rebelo, Clemer Abad, Maike F Dohrn, et al.
Glia|April 15, 2011
Central nervous system dysfunction in a mouse model of FA2H deficiencyKathleen A Potter, Michael J Kern, George Fullbright, et al.
Brain : a Journal of Neurology|March 27, 2024
SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insightsAdriana P Rebelo, Clemer Abad, Maike F Dohrn, et al.
Journal of Neurology|January 4, 2016
Clinical, neurophysiological and morphological study of dominant intermediate Charcot-Marie-Tooth type C neuropathyFlorian P Thomas, Velina Guergueltcheva, Francisco A A Gondim, et al.
Human Molecular Genetics|June 19, 2013
Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1)Melody Caramins, James G Colebatch, Matthew N Bainbridge, et al.
Pageof 16

Showing results (111-120 of 159) with videos related to

Sort By:
Pageof 16
Journal of the Peripheral Nervous System : JPNS|August 14, 2024
Diagnostic and clinical utility of comprehensive multigene panel testing for patients with neuropathyJennifer Roggenbuck, Ana Morales, Colin A Ellis, et al.
Scientific Reports|April 30, 2021
Inducible knockout of Clec16a in mice results in sensory neurodegenerationHeather S Hain, Rahul Pandey, Marina Bakay, et al.
Annals of Neurology|January 27, 2006
T118M PMP22 mutation causes partial loss of function and HNPP-like neuropathyMichael E Shy, Mena T Scavina, Alisa Clark, et al.
Neurology|May 11, 2016
Target-enrichment sequencing and copy number evaluation in inherited polyneuropathyWei Wang, Chen Wang, D Brian Dawson, et al.
The Journal of Clinical Investigation|December 5, 2017
PMP22 antisense oligonucleotides reverse Charcot-Marie-Tooth disease type 1A features in rodent modelsHien Tran Zhao, Sagar Damle, Karli Ikeda-Lee, et al.
Biorxiv : the Preprint Server for Biology|December 18, 2023
Sord deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insightsAdriana P Rebelo, Clemer Abad, Maike F Dohrn, et al.
Glia|April 15, 2011
Central nervous system dysfunction in a mouse model of FA2H deficiencyKathleen A Potter, Michael J Kern, George Fullbright, et al.
Brain : a Journal of Neurology|March 27, 2024
SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insightsAdriana P Rebelo, Clemer Abad, Maike F Dohrn, et al.
Journal of Neurology|January 4, 2016
Clinical, neurophysiological and morphological study of dominant intermediate Charcot-Marie-Tooth type C neuropathyFlorian P Thomas, Velina Guergueltcheva, Francisco A A Gondim, et al.
Human Molecular Genetics|June 19, 2013
Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1)Melody Caramins, James G Colebatch, Matthew N Bainbridge, et al.
Pageof 16