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Neuromuscular Disorders : NMD
|
September 1, 2004
Concerns about the design of clinical trials for spinal muscular atrophy
Thomas O Crawford
Annals of Neurology
|
November 26, 2002
The relationship of SMN to amyotrophic lateral sclerosis
Thomas O Crawford, Richard L Skolasky
The Journal of Clinical Investigation
|
August 2, 2021
Assuring long-term safety of highly effective gene-modulating therapeutics for rare diseases
Thomas O Crawford, Charlotte J Sumner
The Journal of Pediatrics
|
August 24, 2014
Motor and cognitive delay in Duchenne muscular dystrophy: implication for early diagnosis
Kara T Mirski, Thomas O Crawford
Investigative Ophthalmology & Visual Science
|
February 28, 2002
Slow target-directed eye movements in ataxia-telangiectasia
Richard F Lewis, Thomas O Crawford
Nature Medicine
|
July 15, 2022
Early treatment is a lifeline for infants with SMA
Charlotte J Sumner, Thomas O Crawford
The Journal of Clinical Investigation
|
July 10, 2018
Two breakthrough gene-targeted treatments for spinal muscular atrophy: challenges remain
Charlotte J Sumner, Thomas O Crawford
Pediatrics
|
July 19, 2006
The "slurp" test: bedside evaluation of bulbar muscle fatigue
Michelle P Hudspeth, Kenton R Holden, Thomas O Crawford
Journal of Pediatric Orthopedics
|
February 14, 2022
Hip Pain in Patients With Spinal Muscular Atrophy: Prevalence, Intensity, Interference, and Factors Associated With Moderate to Severe Pain
Amy L Xu, Thomas O Crawford, Paul D Sponseller
Current Treatment Options in Neurology
|
February 13, 2009
Emerging treatment options for spinal muscular atrophy
Barrington G Burnett, Thomas O Crawford, Charlotte J Sumner
Page
of 12
Search research articles
Search
Showing results (1-10 of 118) with videos related to
Sort By:
Page
of 12
Neuromuscular Disorders : NMD
|
September 1, 2004
Concerns about the design of clinical trials for spinal muscular atrophy
Thomas O Crawford
Annals of Neurology
|
November 26, 2002
The relationship of SMN to amyotrophic lateral sclerosis
Thomas O Crawford, Richard L Skolasky
The Journal of Clinical Investigation
|
August 2, 2021
Assuring long-term safety of highly effective gene-modulating therapeutics for rare diseases
Thomas O Crawford, Charlotte J Sumner
The Journal of Pediatrics
|
August 24, 2014
Motor and cognitive delay in Duchenne muscular dystrophy: implication for early diagnosis
Kara T Mirski, Thomas O Crawford
Investigative Ophthalmology & Visual Science
|
February 28, 2002
Slow target-directed eye movements in ataxia-telangiectasia
Richard F Lewis, Thomas O Crawford
Nature Medicine
|
July 15, 2022
Early treatment is a lifeline for infants with SMA
Charlotte J Sumner, Thomas O Crawford
The Journal of Clinical Investigation
|
July 10, 2018
Two breakthrough gene-targeted treatments for spinal muscular atrophy: challenges remain
Charlotte J Sumner, Thomas O Crawford
Pediatrics
|
July 19, 2006
The "slurp" test: bedside evaluation of bulbar muscle fatigue
Michelle P Hudspeth, Kenton R Holden, Thomas O Crawford
Journal of Pediatric Orthopedics
|
February 14, 2022
Hip Pain in Patients With Spinal Muscular Atrophy: Prevalence, Intensity, Interference, and Factors Associated With Moderate to Severe Pain
Amy L Xu, Thomas O Crawford, Paul D Sponseller
Current Treatment Options in Neurology
|
February 13, 2009
Emerging treatment options for spinal muscular atrophy
Barrington G Burnett, Thomas O Crawford, Charlotte J Sumner
Page
of 12