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T Darras

Showing results (181-190 of 303) with videos related to

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Annals of Neurology|January 12, 2017
Electrical impedance myography for assessment of Duchenne muscular dystrophySeward B Rutkove, Kush Kapur, Craig M Zaidman, et al.
Neurology|February 12, 2016
Results from a phase 1 study of nusinersen (ISIS-SMN(Rx)) in children with spinal muscular atrophyClaudia A Chiriboga, Kathryn J Swoboda, Basil T Darras, et al.
Annals of Clinical and Translational Neurology|December 27, 2019
Electrical impedance myography for reducing sample size in Duchenne muscular dystrophy trialsMelanie L Leitner, Kush Kapur, Basil T Darras, et al.
Neurology|April 18, 2007
Steroid-responsive neurologic relapses in a child with a proteolipid protein-1 mutationM P Gorman, M R Golomb, L E Walsh, et al.
JAMA Neurology|May 24, 2013
Clinical application of whole-exome sequencing: a novel autosomal recessive spastic ataxia of Charlevoix-Saguenay sequence variation in a child with ataxiaWendy K M Liew, Tawfeg Ben-Omran, Basil T Darras, et al.
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.
Proceedings of the National Academy of Sciences of the United States of America|February 3, 2000
A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathyC G Bönnemann, G F Cox, F Shapiro, et al.
Pageof 31

Showing results (181-190 of 303) with videos related to

Sort By:
Pageof 31
Annals of Neurology|January 12, 2017
Electrical impedance myography for assessment of Duchenne muscular dystrophySeward B Rutkove, Kush Kapur, Craig M Zaidman, et al.
Neurology|February 12, 2016
Results from a phase 1 study of nusinersen (ISIS-SMN(Rx)) in children with spinal muscular atrophyClaudia A Chiriboga, Kathryn J Swoboda, Basil T Darras, et al.
Annals of Clinical and Translational Neurology|December 27, 2019
Electrical impedance myography for reducing sample size in Duchenne muscular dystrophy trialsMelanie L Leitner, Kush Kapur, Basil T Darras, et al.
Neurology|April 18, 2007
Steroid-responsive neurologic relapses in a child with a proteolipid protein-1 mutationM P Gorman, M R Golomb, L E Walsh, et al.
JAMA Neurology|May 24, 2013
Clinical application of whole-exome sequencing: a novel autosomal recessive spastic ataxia of Charlevoix-Saguenay sequence variation in a child with ataxiaWendy K M Liew, Tawfeg Ben-Omran, Basil T Darras, et al.
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.
Proceedings of the National Academy of Sciences of the United States of America|February 3, 2000
A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathyC G Bönnemann, G F Cox, F Shapiro, et al.
Pageof 31