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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 status
Seward 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 trial
Richard D Shell, Katlyn E McGrattan, Rebecca Hurst-Davis, et al.
Pediatric Neurology
|
June 13, 2009
Congenital myasthenic syndrome with episodic apnea
Leah 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 trials
Craig M McDonald, Gautam Sajeev, Zhiwen Yao, et al.
Muscle & Nerve
|
June 18, 2014
Reply: To PMID 23893312
Peter 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 arthrogryposis
Jose 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 Disorders
Buket Sonbas-Cobb, Seward B Rutkove, Baoguo Wei, et al.
Muscle & Nerve
|
July 30, 2013
The motor neuron response to SMN1 deficiency in spinal muscular atrophy
Peter B Kang, Clifton L Gooch, Michael P McDermott, et al.
Muscle & Nerve
|
September 27, 2016
Novel mutation in CNTNAP1 results in congenital hypomyelinating neuropathy
Paulomi Mehta, Melanie Küspert, Tejus Bale, et al.
Journal of Neuromuscular Diseases
|
July 17, 2023
Identifying Biomarkers of Spinal Muscular Atrophy for Further Development
Jacqueline Glascock, Basil T Darras, Thomas O Crawford, et al.
Page
of 23
Search research articles
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Showing results (111-120 of 222) with videos related to
Sort By:
Page
of 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 status
Seward 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 trial
Richard D Shell, Katlyn E McGrattan, Rebecca Hurst-Davis, et al.
Pediatric Neurology
|
June 13, 2009
Congenital myasthenic syndrome with episodic apnea
Leah 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 trials
Craig M McDonald, Gautam Sajeev, Zhiwen Yao, et al.
Muscle & Nerve
|
June 18, 2014
Reply: To PMID 23893312
Peter 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 arthrogryposis
Jose 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 Disorders
Buket Sonbas-Cobb, Seward B Rutkove, Baoguo Wei, et al.
Muscle & Nerve
|
July 30, 2013
The motor neuron response to SMN1 deficiency in spinal muscular atrophy
Peter B Kang, Clifton L Gooch, Michael P McDermott, et al.
Muscle & Nerve
|
September 27, 2016
Novel mutation in CNTNAP1 results in congenital hypomyelinating neuropathy
Paulomi Mehta, Melanie Küspert, Tejus Bale, et al.
Journal of Neuromuscular Diseases
|
July 17, 2023
Identifying Biomarkers of Spinal Muscular Atrophy for Further Development
Jacqueline Glascock, Basil T Darras, Thomas O Crawford, et al.
Page
of 23