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Glia
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September 23, 2008
Molecular mechanisms of inherited demyelinating neuropathies
Steven S Scherer, Lawrence Wrabetz
Journal of Neuromuscular Diseases
|
August 20, 2019
A MT-ATP6 Mutation Causes a Slowly Progressive Myeloneuropathy
Tanya Bardakjian, Steven S Scherer
Neurology
|
June 13, 2014
Ranvier revisited: novel nodal antigens stimulate interest in GBS pathogenesis
Hugh Willison, Steven S Scherer
Neurobiology of Disease
|
June 9, 2015
Activated immune response in an inherited leukodystrophy disease caused by the loss of oligodendrocyte gap junctions
Sameh K Wasseff, Steven S Scherer
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 11, 2005
Altered ion channels in an animal model of Charcot-Marie-Tooth disease type IA
Jérôme J Devaux, Steven S Scherer
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
October 4, 2021
Axonal Charcot-Marie-Tooth Disease: from Common Pathogenic Mechanisms to Emerging Treatment Opportunities
Brett A McCray, Steven S Scherer
The Journal of Comparative Neurology
|
December 3, 2011
Kv7.5 is the primary Kv7 subunit expressed in C-fibers
Chih H King, Steven S Scherer
Journal of the Peripheral Nervous System : JPNS
|
April 10, 2002
Recent progress on the molecular organization of myelinated axons
Steven S Scherer, Edgardo J Arroyo
Journal of Neuroimmunology
|
March 4, 2014
Activated microglia do not form functional gap junctions in vivo
Sameh K Wasseff, Steven S Scherer
Journal of the Peripheral Nervous System : JPNS
|
January 3, 2013
X-linked Charcot-Marie-Tooth disease
Steven S Scherer, Kleopas A Kleopa
Page
of 16
Search research articles
Search
Showing results (11-20 of 159) with videos related to
Sort By:
Page
of 16
Glia
|
September 23, 2008
Molecular mechanisms of inherited demyelinating neuropathies
Steven S Scherer, Lawrence Wrabetz
Journal of Neuromuscular Diseases
|
August 20, 2019
A MT-ATP6 Mutation Causes a Slowly Progressive Myeloneuropathy
Tanya Bardakjian, Steven S Scherer
Neurology
|
June 13, 2014
Ranvier revisited: novel nodal antigens stimulate interest in GBS pathogenesis
Hugh Willison, Steven S Scherer
Neurobiology of Disease
|
June 9, 2015
Activated immune response in an inherited leukodystrophy disease caused by the loss of oligodendrocyte gap junctions
Sameh K Wasseff, Steven S Scherer
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 11, 2005
Altered ion channels in an animal model of Charcot-Marie-Tooth disease type IA
Jérôme J Devaux, Steven S Scherer
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
October 4, 2021
Axonal Charcot-Marie-Tooth Disease: from Common Pathogenic Mechanisms to Emerging Treatment Opportunities
Brett A McCray, Steven S Scherer
The Journal of Comparative Neurology
|
December 3, 2011
Kv7.5 is the primary Kv7 subunit expressed in C-fibers
Chih H King, Steven S Scherer
Journal of the Peripheral Nervous System : JPNS
|
April 10, 2002
Recent progress on the molecular organization of myelinated axons
Steven S Scherer, Edgardo J Arroyo
Journal of Neuroimmunology
|
March 4, 2014
Activated microglia do not form functional gap junctions in vivo
Sameh K Wasseff, Steven S Scherer
Journal of the Peripheral Nervous System : JPNS
|
January 3, 2013
X-linked Charcot-Marie-Tooth disease
Steven S Scherer, Kleopas A Kleopa
Page
of 16