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Natalie F Reash

Showing results (1-10 of 20) with videos related to

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Frontiers in Genetics|November 18, 2021
Remote Delivery of Motor Function Assessment and Training for Clinical Trials in Neuromuscular Disease: A Response to the COVID-19 Global PandemicMeredith K James, Kristy Rose, Lindsay N Alfano, et al.
Plos One|March 19, 2024
Feasibility and utility of in-home body weight support harness system use in young children treated for spinal muscular atrophy: A single-arm prospective cohort studyMegan A Iammarino, Lindsay N Alfano, Natalie F Reash, et al.
Developmental Medicine and Child Neurology|December 19, 2024
Psychometric evaluation of the PROMIS parent proxy mobility item bank for use in Duchenne muscular dystrophyLinda Pax Lowes, Corinne M Le Reun, Lindsay N Alfano, et al.
Journal of Neuromuscular Diseases|May 13, 2025
A prospective observational study assessing the functional disease progression of LGMDR4, betasarcoglycan-related limb girdle muscular dystrophyMegan A Iammarino, Natalie F Reash, Kiana Shannon, et al.
Frontiers in Neurology|June 10, 2025
Psychometric analysis of the patient-reported outcomes measurement information system parent proxy physical function-upper extremity item bank for children with Duchenne muscular dystrophyLinda Pax Lowes, Corinne M Le Reun, Teofil Ciobanu, et al.
Plos One|May 16, 2024
Validity of remote live stream video evaluation of the North Star Ambulatory Assessment in patients with Duchenne muscular dystrophyLinda P Lowes, Lindsay N Alfano, Megan A Iammarino, et al.
JAMA Neurology|May 17, 2021
Five-Year Extension Results of the Phase 1 START Trial of Onasemnogene Abeparvovec in Spinal Muscular AtrophyJerry R Mendell, Samiah A Al-Zaidy, Kelly J Lehman, et al.
Journal of Neuromuscular Diseases|March 10, 2024
Increase in Full-Length Dystrophin by Exon Skipping in Duchenne Muscular Dystrophy Patients with Single Exon Duplications: An Open-label StudyStefan Nicolau, Jyoti Malhotra, Maryann Kaler, et al.
Pediatric Neurology|July 16, 2021
Validity and Reliability of the Neuromuscular Gross Motor OutcomeLindsay N Alfano, Megan A Iammarino, Natalie F Reash, et al.
Physical Therapy|August 6, 2022
Validation of the North Star Assessment for Limb-Girdle Type Muscular DystrophiesMeredith K James, Lindsay N Alfano, Robert Muni-Lofra, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Frontiers in Genetics|November 18, 2021
Remote Delivery of Motor Function Assessment and Training for Clinical Trials in Neuromuscular Disease: A Response to the COVID-19 Global PandemicMeredith K James, Kristy Rose, Lindsay N Alfano, et al.
Plos One|March 19, 2024
Feasibility and utility of in-home body weight support harness system use in young children treated for spinal muscular atrophy: A single-arm prospective cohort studyMegan A Iammarino, Lindsay N Alfano, Natalie F Reash, et al.
Developmental Medicine and Child Neurology|December 19, 2024
Psychometric evaluation of the PROMIS parent proxy mobility item bank for use in Duchenne muscular dystrophyLinda Pax Lowes, Corinne M Le Reun, Lindsay N Alfano, et al.
Journal of Neuromuscular Diseases|May 13, 2025
A prospective observational study assessing the functional disease progression of LGMDR4, betasarcoglycan-related limb girdle muscular dystrophyMegan A Iammarino, Natalie F Reash, Kiana Shannon, et al.
Frontiers in Neurology|June 10, 2025
Psychometric analysis of the patient-reported outcomes measurement information system parent proxy physical function-upper extremity item bank for children with Duchenne muscular dystrophyLinda Pax Lowes, Corinne M Le Reun, Teofil Ciobanu, et al.
Plos One|May 16, 2024
Validity of remote live stream video evaluation of the North Star Ambulatory Assessment in patients with Duchenne muscular dystrophyLinda P Lowes, Lindsay N Alfano, Megan A Iammarino, et al.
JAMA Neurology|May 17, 2021
Five-Year Extension Results of the Phase 1 START Trial of Onasemnogene Abeparvovec in Spinal Muscular AtrophyJerry R Mendell, Samiah A Al-Zaidy, Kelly J Lehman, et al.
Journal of Neuromuscular Diseases|March 10, 2024
Increase in Full-Length Dystrophin by Exon Skipping in Duchenne Muscular Dystrophy Patients with Single Exon Duplications: An Open-label StudyStefan Nicolau, Jyoti Malhotra, Maryann Kaler, et al.
Pediatric Neurology|July 16, 2021
Validity and Reliability of the Neuromuscular Gross Motor OutcomeLindsay N Alfano, Megan A Iammarino, Natalie F Reash, et al.
Physical Therapy|August 6, 2022
Validation of the North Star Assessment for Limb-Girdle Type Muscular DystrophiesMeredith K James, Lindsay N Alfano, Robert Muni-Lofra, et al.
Pageof 2