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Journal of Neuromuscular Diseases
|
February 22, 2020
Scoliosis Surgery Significantly Impacts Motor Abilities in Higher-functioning Individuals with Spinal Muscular Atrophy1
Sally Dunaway Young, Jacqueline Montes, Rachel Salazar, et al.
Muscle & Nerve
|
April 6, 2022
Distribution of weight, stature, and growth status in children and adolescents with spinal muscular atrophy: An observational retrospective study in the United States
Basil T Darras, Sabrina Guye, Janine Hoffart, et al.
Plos One
|
March 15, 2019
Systemic nature of spinal muscular atrophy revealed by studying insurance claims
Scott L Lipnick, Denis M Agniel, Rahul Aggarwal, et al.
Annals of Neurology
|
February 28, 2017
Quantitative muscle ultrasound detects disease progression in Duchenne muscular dystrophy
Craig M Zaidman, Jim S Wu, Kush Kapur, et al.
Journal of Neuromuscular Diseases
|
September 4, 2023
Erratum to: Patients with Spinal Muscular Atrophy Type 1 Achieve and Maintain Bulbar Function Following Onasemnogene Abeparvovec Treatment
Katlyn E McGrattan, Richard D Shell, Rebecca Hurst-Davis, et al.
Journal of Neuromuscular Diseases
|
April 24, 2023
Patients with Spinal Muscular Atrophy Type 1 Achieve and Maintain Bulbar Function Following Onasemnogene Abeparvovec Treatment
Katlyn E McGrattan, Richard D Shell, Rebecca Hurst-Davis, et al.
Annals of Neurology
|
January 12, 2017
Electrical impedance myography for assessment of Duchenne muscular dystrophy
Seward 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 atrophy
Claudia 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 trials
Melanie L Leitner, Kush Kapur, Basil T Darras, 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 ataxia
Wendy K M Liew, Tawfeg Ben-Omran, Basil T Darras, et al.
Page
of 23
Search research articles
Search
Showing results (101-110 of 222) with videos related to
Sort By:
Page
of 23
Journal of Neuromuscular Diseases
|
February 22, 2020
Scoliosis Surgery Significantly Impacts Motor Abilities in Higher-functioning Individuals with Spinal Muscular Atrophy1
Sally Dunaway Young, Jacqueline Montes, Rachel Salazar, et al.
Muscle & Nerve
|
April 6, 2022
Distribution of weight, stature, and growth status in children and adolescents with spinal muscular atrophy: An observational retrospective study in the United States
Basil T Darras, Sabrina Guye, Janine Hoffart, et al.
Plos One
|
March 15, 2019
Systemic nature of spinal muscular atrophy revealed by studying insurance claims
Scott L Lipnick, Denis M Agniel, Rahul Aggarwal, et al.
Annals of Neurology
|
February 28, 2017
Quantitative muscle ultrasound detects disease progression in Duchenne muscular dystrophy
Craig M Zaidman, Jim S Wu, Kush Kapur, et al.
Journal of Neuromuscular Diseases
|
September 4, 2023
Erratum to: Patients with Spinal Muscular Atrophy Type 1 Achieve and Maintain Bulbar Function Following Onasemnogene Abeparvovec Treatment
Katlyn E McGrattan, Richard D Shell, Rebecca Hurst-Davis, et al.
Journal of Neuromuscular Diseases
|
April 24, 2023
Patients with Spinal Muscular Atrophy Type 1 Achieve and Maintain Bulbar Function Following Onasemnogene Abeparvovec Treatment
Katlyn E McGrattan, Richard D Shell, Rebecca Hurst-Davis, et al.
Annals of Neurology
|
January 12, 2017
Electrical impedance myography for assessment of Duchenne muscular dystrophy
Seward 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 atrophy
Claudia 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 trials
Melanie L Leitner, Kush Kapur, Basil T Darras, 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 ataxia
Wendy K M Liew, Tawfeg Ben-Omran, Basil T Darras, et al.
Page
of 23