Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

E Siskind

Showing results (21-30 of 37) with videos related to

Pageof 4
Sort By:
Journal of Geophysical Research. Atmospheres : JGR|July 5, 2021
Transport of Nitric Oxide Via Lagrangian Coherent Structures Into the Top of the Polar VortexV 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 CMT1AIstvan Katona, Xingyao Wu, Shawna M E Feely, et al.
Muscle & Nerve|March 5, 2013
Anterior tibialis CMAP amplitude correlations with impairment in CMT1AKelsey Komyathy, Stephanie Neal, Shawna Feely, et al.
Neurology|April 22, 2011
MFN2 mutations cause severe phenotypes in most patients with CMT2AS 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 MeasureSindhu 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 neuropathyJeremy 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 measureTong 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 diseaseSinéad 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 yearsTong 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 geneOranee Sanmaneechai, Shawna Feely, Steven S Scherer, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Journal of Geophysical Research. Atmospheres : JGR|July 5, 2021
Transport of Nitric Oxide Via Lagrangian Coherent Structures Into the Top of the Polar VortexV 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 CMT1AIstvan Katona, Xingyao Wu, Shawna M E Feely, et al.
Muscle & Nerve|March 5, 2013
Anterior tibialis CMAP amplitude correlations with impairment in CMT1AKelsey Komyathy, Stephanie Neal, Shawna Feely, et al.
Neurology|April 22, 2011
MFN2 mutations cause severe phenotypes in most patients with CMT2AS 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 MeasureSindhu 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 neuropathyJeremy 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 measureTong 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 diseaseSinéad 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 yearsTong 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 geneOranee Sanmaneechai, Shawna Feely, Steven S Scherer, et al.
Pageof 4