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Neurology and Therapy|October 19, 2023
Evaluating Perceived Fatigue within an Adult Spinal Muscular Atrophy PopulationLisa Belter, Ilse Peterson, Jill Jarecki
Orphanet Journal of Rare Diseases|August 26, 2020
Quality of life data for individuals affected by spinal muscular atrophy: a baseline dataset from the Cure SMA Community Update SurveyLisa Belter, Rosángel Cruz, Jill Jarecki
Plos One|November 8, 2022
Knowledge of genetic test results among caregivers and individuals with spinal muscular atrophyLisa Belter, Allison Mazzella, Shannon O'Brien, et al.
Orphanet Journal of Rare Diseases|February 23, 2021
"I have SMA, SMA doesn't have me": a qualitative snapshot into the challenges, successes, and quality of life of adolescents and young adults with SMAAllison Mazzella, Mary Curry, Lisa Belter, et al.
Neurology and Therapy|April 27, 2026
Impact of Early Intervention on Motor Milestone Achievement in Spinal Muscular Atrophy: Insights from Cure SMA Survey DataKendra A K Lawrence, Lisa Belter, Mary Curry, et al.
Journal of Market Access & Health Policy|November 23, 2020
Economic burden of spinal muscular atrophy: an analysis of claims dataLisa Belter, Rosángel Cruz, Sierra Kulas, et al.
Neurology and Therapy|June 22, 2023
Effects of the COVID-19 Pandemic on SMA Screening and Care: Physician and Community InsightsMary Curry, Ilse Peterson, Lisa Belter, et al.
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