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M E Shy

Showing results (21-30 of 50) with videos related to

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Neurology|October 13, 2006
Skin biopsies demonstrate MPZ splicing abnormalities in Charcot-Marie-Tooth neuropathy 1BA Sabet, J Li, K Ghandour, et al.
Neurology|October 1, 1984
Specificity of mouse and human monoclonal antibodies to myelin-associated glycoproteinE Nobile-Orazio, A P Hays, N Latov, et al.
Neurology|May 1, 1990
Lower motor neuron disease in a patient with autoantibodies against Gal(beta 1-3)GalNAc in gangliosides GM1 and GD1b: improvement following immunotherapyM E Shy, T Heiman-Patterson, G J Parry, et al.
Annals of Neurology|September 1, 1995
An adenoviral vector can transfer lacZ expression into Schwann cells in culture and in sciatic nerveM E Shy, M Tani, Y J Shi, et al.
Journal of Neuropathology and Experimental Neurology|July 1, 1997
Heterozygous P0 knockout mice develop a peripheral neuropathy that resembles chronic inflammatory demyelinating polyneuropathy (CIDP)M E Shy, E Arroyo, J Sladky, et al.
Annals of the New York Academy of Sciences|November 1, 2017
Heterozygous Null Mutation in the P<sub>0</sub> Gene Associated with Mild Charcot-Marie-Tooth DiseaseD Pareyson, D Menichella, S Botti, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Heterozygous null mutation in the P0 gene associated with mild Charcot-Marie-Tooth diseaseD Pareyson, D Menichella, S Botti, et al.
Archives of Neurology|March 1, 1987
An alert for motor neuron diseases and peripheral neuropathy: monoclonal paraproteinemia may be missed by routine electrophoresisS J Zuckerman, M A Pesce, L P Rowland, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 24, 2011
Strategy for genetic testing in Charcot-Marie-diseaseL J Miller, A S D Saporta, S L Sottile, et al.
Journal of Neuroscience Research|June 22, 2000
Absence of P0 leads to the dysregulation of myelin gene expression and myelin morphogenesisW Xu, D Manichella, H Jiang, et al.
Pageof 5

Showing results (21-30 of 50) with videos related to

Sort By:
Pageof 5
Neurology|October 13, 2006
Skin biopsies demonstrate MPZ splicing abnormalities in Charcot-Marie-Tooth neuropathy 1BA Sabet, J Li, K Ghandour, et al.
Neurology|October 1, 1984
Specificity of mouse and human monoclonal antibodies to myelin-associated glycoproteinE Nobile-Orazio, A P Hays, N Latov, et al.
Neurology|May 1, 1990
Lower motor neuron disease in a patient with autoantibodies against Gal(beta 1-3)GalNAc in gangliosides GM1 and GD1b: improvement following immunotherapyM E Shy, T Heiman-Patterson, G J Parry, et al.
Annals of Neurology|September 1, 1995
An adenoviral vector can transfer lacZ expression into Schwann cells in culture and in sciatic nerveM E Shy, M Tani, Y J Shi, et al.
Journal of Neuropathology and Experimental Neurology|July 1, 1997
Heterozygous P0 knockout mice develop a peripheral neuropathy that resembles chronic inflammatory demyelinating polyneuropathy (CIDP)M E Shy, E Arroyo, J Sladky, et al.
Annals of the New York Academy of Sciences|November 1, 2017
Heterozygous Null Mutation in the P<sub>0</sub> Gene Associated with Mild Charcot-Marie-Tooth DiseaseD Pareyson, D Menichella, S Botti, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Heterozygous null mutation in the P0 gene associated with mild Charcot-Marie-Tooth diseaseD Pareyson, D Menichella, S Botti, et al.
Archives of Neurology|March 1, 1987
An alert for motor neuron diseases and peripheral neuropathy: monoclonal paraproteinemia may be missed by routine electrophoresisS J Zuckerman, M A Pesce, L P Rowland, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 24, 2011
Strategy for genetic testing in Charcot-Marie-diseaseL J Miller, A S D Saporta, S L Sottile, et al.
Journal of Neuroscience Research|June 22, 2000
Absence of P0 leads to the dysregulation of myelin gene expression and myelin morphogenesisW Xu, D Manichella, H Jiang, et al.
Pageof 5