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Journal of Geophysical Research. Atmospheres : JGR
|
July 5, 2021
Transport of Nitric Oxide Via Lagrangian Coherent Structures Into the Top of the Polar Vortex
V Lynn Harvey, Seebany Datta-Barua, Nicholas M Pedatella, et al.
Brain : a Journal of Neurology
|
May 19, 2009
PMP22 expression in dermal nerve myelin from patients with CMT1A
Istvan Katona, Xingyao Wu, Shawna M E Feely, et al.
Muscle & Nerve
|
March 5, 2013
Anterior tibialis CMAP amplitude correlations with impairment in CMT1A
Kelsey Komyathy, Stephanie Neal, Shawna Feely, et al.
Neurology
|
April 22, 2011
MFN2 mutations cause severe phenotypes in most patients with CMT2A
S M E Feely, M Laura, C E Siskind, et al.
Annals of Neurology
|
November 22, 2020
Development and Validation of the Pediatric Charcot-Marie-Tooth Disease Quality of Life Outcome Measure
Sindhu Ramchandren, Tong Tong Wu, Richard S Finkel, et al.
Neurology. Genetics
|
April 12, 2016
Novel mutations highlight the key role of the ankyrin repeat domain in TRPV4-mediated neuropathy
Jeremy M Sullivan, Christina M Zimanyi, William Aisenberg, et al.
Journal of the Peripheral Nervous System : JPNS
|
February 7, 2023
Validation of the parent-proxy pediatric Charcot-Marie-Tooth disease quality of life outcome measure
Tong Tong Wu, Richard S Finkel, Carly E Siskind, et al.
Neuromuscular Disorders : NMD
|
April 10, 2012
X inactivation in females with X-linked Charcot-Marie-Tooth disease
Sinéad M Murphy, Richard Ovens, James Polke, et al.
Journal of the Peripheral Nervous System : JPNS
|
May 11, 2023
Validation of the parent-proxy version of the pediatric Charcot-Marie-Tooth disease quality of life instrument for children aged 0-7 years
Tong Tong Wu, Richard S Finkel, Carly E Siskind, et al.
Brain : a Journal of Neurology
|
August 28, 2015
Genotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene
Oranee Sanmaneechai, Shawna Feely, Steven S Scherer, et al.
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of 4
Search research articles
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Showing results (21-30 of 37) with videos related to
Sort By:
Page
of 4
Journal of Geophysical Research. Atmospheres : JGR
|
July 5, 2021
Transport of Nitric Oxide Via Lagrangian Coherent Structures Into the Top of the Polar Vortex
V Lynn Harvey, Seebany Datta-Barua, Nicholas M Pedatella, et al.
Brain : a Journal of Neurology
|
May 19, 2009
PMP22 expression in dermal nerve myelin from patients with CMT1A
Istvan Katona, Xingyao Wu, Shawna M E Feely, et al.
Muscle & Nerve
|
March 5, 2013
Anterior tibialis CMAP amplitude correlations with impairment in CMT1A
Kelsey Komyathy, Stephanie Neal, Shawna Feely, et al.
Neurology
|
April 22, 2011
MFN2 mutations cause severe phenotypes in most patients with CMT2A
S M E Feely, M Laura, C E Siskind, et al.
Annals of Neurology
|
November 22, 2020
Development and Validation of the Pediatric Charcot-Marie-Tooth Disease Quality of Life Outcome Measure
Sindhu Ramchandren, Tong Tong Wu, Richard S Finkel, et al.
Neurology. Genetics
|
April 12, 2016
Novel mutations highlight the key role of the ankyrin repeat domain in TRPV4-mediated neuropathy
Jeremy M Sullivan, Christina M Zimanyi, William Aisenberg, et al.
Journal of the Peripheral Nervous System : JPNS
|
February 7, 2023
Validation of the parent-proxy pediatric Charcot-Marie-Tooth disease quality of life outcome measure
Tong Tong Wu, Richard S Finkel, Carly E Siskind, et al.
Neuromuscular Disorders : NMD
|
April 10, 2012
X inactivation in females with X-linked Charcot-Marie-Tooth disease
Sinéad M Murphy, Richard Ovens, James Polke, et al.
Journal of the Peripheral Nervous System : JPNS
|
May 11, 2023
Validation of the parent-proxy version of the pediatric Charcot-Marie-Tooth disease quality of life instrument for children aged 0-7 years
Tong Tong Wu, Richard S Finkel, Carly E Siskind, et al.
Brain : a Journal of Neurology
|
August 28, 2015
Genotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene
Oranee Sanmaneechai, Shawna Feely, Steven S Scherer, et al.
Page
of 4