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Human Gene Therapy
|
September 1, 2010
Combination of SMN trans-splicing and a neurotrophic factor increases the life span and body mass in a severe model of spinal muscular atrophy
Monir Shababi, Jacqueline Glascock, Christian L Lorson
Contemporary Clinical Trials Communications
|
February 9, 2026
An updated review of the SMA clinical trial landscape in the United States: Findings from analysis of recruitment targets on ClinicalTrials.gov and a survey of SMA clinical trial sites on factors affecting site capacity and readiness
Fatou Sarr, Ilse Peterson, Jacqueline Glascock, et al.
Orphanet Journal of Rare Diseases
|
October 17, 2025
A qualitative, mixed-method approach to reaching consensus on function, fatigue, and fatigability outcomes in teens and adults living with spinal muscular atrophy
Jacqueline Glascock, Lisa T Belter, Meghan Moore Burk, et al.
JAMA Pediatrics
|
July 15, 2024
Newborn Screening and Birth Prevalence for Spinal Muscular Atrophy in the US
Lisa Belter, Jennifer L Taylor, Erica Jorgensen, 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.
Journal of Neuromuscular Diseases
|
April 5, 2018
Treatment Algorithm for Infants Diagnosed with Spinal Muscular Atrophy through Newborn Screening
Jacqueline Glascock, Jacinda Sampson, Amanda Haidet-Phillips, et al.
Journal of Neuromuscular Diseases
|
February 3, 2020
Revised Recommendations for the Treatment of Infants Diagnosed with Spinal Muscular Atrophy Via Newborn Screening Who Have 4 Copies of SMN2
Jacqueline Glascock, Jacinda Sampson, Anne M Connolly, et al.
Immunohorizons
|
July 24, 2018
The RNA-Binding Protein HuR Posttranscriptionally Regulates IL-2 Homeostasis and CD4<sup>+</sup> Th2 Differentiation
Patsharaporn Techasintana, Jason S Ellis, Jacqueline Glascock, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Human Gene Therapy
|
September 1, 2010
Combination of SMN trans-splicing and a neurotrophic factor increases the life span and body mass in a severe model of spinal muscular atrophy
Monir Shababi, Jacqueline Glascock, Christian L Lorson
Contemporary Clinical Trials Communications
|
February 9, 2026
An updated review of the SMA clinical trial landscape in the United States: Findings from analysis of recruitment targets on ClinicalTrials.gov and a survey of SMA clinical trial sites on factors affecting site capacity and readiness
Fatou Sarr, Ilse Peterson, Jacqueline Glascock, et al.
Orphanet Journal of Rare Diseases
|
October 17, 2025
A qualitative, mixed-method approach to reaching consensus on function, fatigue, and fatigability outcomes in teens and adults living with spinal muscular atrophy
Jacqueline Glascock, Lisa T Belter, Meghan Moore Burk, et al.
JAMA Pediatrics
|
July 15, 2024
Newborn Screening and Birth Prevalence for Spinal Muscular Atrophy in the US
Lisa Belter, Jennifer L Taylor, Erica Jorgensen, 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.
Journal of Neuromuscular Diseases
|
April 5, 2018
Treatment Algorithm for Infants Diagnosed with Spinal Muscular Atrophy through Newborn Screening
Jacqueline Glascock, Jacinda Sampson, Amanda Haidet-Phillips, et al.
Journal of Neuromuscular Diseases
|
February 3, 2020
Revised Recommendations for the Treatment of Infants Diagnosed with Spinal Muscular Atrophy Via Newborn Screening Who Have 4 Copies of SMN2
Jacqueline Glascock, Jacinda Sampson, Anne M Connolly, et al.
Immunohorizons
|
July 24, 2018
The RNA-Binding Protein HuR Posttranscriptionally Regulates IL-2 Homeostasis and CD4<sup>+</sup> Th2 Differentiation
Patsharaporn Techasintana, Jason S Ellis, Jacqueline Glascock, et al.
Page
of 1