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

Basil T Darras

Showing results (111-120 of 222) with videos related to

Pageof 23
Sort By:
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 9, 2016
Loss of electrical anisotropy is an unrecognized feature of dystrophic muscle that may serve as a convenient index of disease statusSeward B Rutkove, Jim S Wu, Craig Zaidman, et al.
Neuromuscular Disorders : NMD|July 16, 2023
Onasemnogene abeparvovec preserves bulbar function in infants with presymptomatic spinal muscular atrophy: a post-hoc analysis of the SPR1NT trialRichard D Shell, Katlyn E McGrattan, Rebecca Hurst-Davis, et al.
Pediatric Neurology|June 13, 2009
Congenital myasthenic syndrome with episodic apneaLeah A Mallory, James G Shaw, Stephanie L Burgess, et al.
Muscle & Nerve|October 11, 2019
Deflazacort vs prednisone treatment for Duchenne muscular dystrophy: A meta-analysis of disease progression rates in recent multicenter clinical trialsCraig M McDonald, Gautam Sajeev, Zhiwen Yao, et al.
Muscle & Nerve|June 18, 2014
Reply: To PMID 23893312Peter B Kang, Clifton L Gooch, Michael P McDermott, et al.
Neurology. Genetics|May 2, 2019
Homozygous <i>TRPV4</i> mutation causes congenital distal spinal muscular atrophy and arthrogryposisJose Velilla, Michael Mario Marchetti, Agnes Toth-Petroczy, et al.
Annals of Biomedical Engineering|May 22, 2026
Multifrequency Electrical Impedance Myography Enhanced with Machine Learning for Screening Patients with Neuromuscular DisordersBuket Sonbas-Cobb, Seward B Rutkove, Baoguo Wei, et al.
Muscle & Nerve|July 30, 2013
The motor neuron response to SMN1 deficiency in spinal muscular atrophyPeter B Kang, Clifton L Gooch, Michael P McDermott, et al.
Muscle & Nerve|September 27, 2016
Novel mutation in CNTNAP1 results in congenital hypomyelinating neuropathyPaulomi Mehta, Melanie Küspert, Tejus Bale, et al.
Journal of Neuromuscular Diseases|July 17, 2023
Identifying Biomarkers of Spinal Muscular Atrophy for Further DevelopmentJacqueline Glascock, Basil T Darras, Thomas O Crawford, et al.
Pageof 23

Showing results (111-120 of 222) with videos related to

Sort By:
Pageof 23
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 9, 2016
Loss of electrical anisotropy is an unrecognized feature of dystrophic muscle that may serve as a convenient index of disease statusSeward B Rutkove, Jim S Wu, Craig Zaidman, et al.
Neuromuscular Disorders : NMD|July 16, 2023
Onasemnogene abeparvovec preserves bulbar function in infants with presymptomatic spinal muscular atrophy: a post-hoc analysis of the SPR1NT trialRichard D Shell, Katlyn E McGrattan, Rebecca Hurst-Davis, et al.
Pediatric Neurology|June 13, 2009
Congenital myasthenic syndrome with episodic apneaLeah A Mallory, James G Shaw, Stephanie L Burgess, et al.
Muscle & Nerve|October 11, 2019
Deflazacort vs prednisone treatment for Duchenne muscular dystrophy: A meta-analysis of disease progression rates in recent multicenter clinical trialsCraig M McDonald, Gautam Sajeev, Zhiwen Yao, et al.
Muscle & Nerve|June 18, 2014
Reply: To PMID 23893312Peter B Kang, Clifton L Gooch, Michael P McDermott, et al.
Neurology. Genetics|May 2, 2019
Homozygous <i>TRPV4</i> mutation causes congenital distal spinal muscular atrophy and arthrogryposisJose Velilla, Michael Mario Marchetti, Agnes Toth-Petroczy, et al.
Annals of Biomedical Engineering|May 22, 2026
Multifrequency Electrical Impedance Myography Enhanced with Machine Learning for Screening Patients with Neuromuscular DisordersBuket Sonbas-Cobb, Seward B Rutkove, Baoguo Wei, et al.
Muscle & Nerve|July 30, 2013
The motor neuron response to SMN1 deficiency in spinal muscular atrophyPeter B Kang, Clifton L Gooch, Michael P McDermott, et al.
Muscle & Nerve|September 27, 2016
Novel mutation in CNTNAP1 results in congenital hypomyelinating neuropathyPaulomi Mehta, Melanie Küspert, Tejus Bale, et al.
Journal of Neuromuscular Diseases|July 17, 2023
Identifying Biomarkers of Spinal Muscular Atrophy for Further DevelopmentJacqueline Glascock, Basil T Darras, Thomas O Crawford, et al.
Pageof 23