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ISSN 1932-6203, 2018
Individuals with spinal muscular atrophy (SMA) type 3 are able to walk but they have weakness, gait impairments and fatigue. Our primary study objective was to... 
Walking | Neurology | Aging | Spinal muscular atrophy
Journal Article
Pediatric Neurology, ISSN 0887-8994, 2017, Volume 70, pp. 5 - 6
Journal Article
American Journal of Occupational Therapy, ISSN 0272-9490, 03/2018, Volume 72, Issue 2, pp. 7202345010p1 - 5
Patients with Duchenne muscular dystrophy in their second decade of life present with decreased upper extremity strength and active range of motion (AROM) that... 
MOBILE ARM SUPPORTS | REHABILITATION | Design | Neuromuscular diseases | Activities of daily living | Archives & records | Disease | Research & development--R&D | Duchenne muscular dystrophy | Rehabilitation | Muscular dystrophy | Robotics | Gravity | Upper limbs
Journal Article
ISSN 1932-6203, 2017
Recent translational research developments in Spinal Muscular Atrophy (SMA), outcome measure design and demands from regulatory authorities require that... 
Medicine | Neurosciences | Psychometrics | Spinal muscular atrophy
Journal Article
Annals of Neurology, ISSN 0364-5134, 10/2014, Volume 76, Issue 4, pp. 541 - 549
Journal Article
JAMA Neurology, ISSN 2168-6149, 06/2015, Volume 72, Issue 6, pp. 689 - 689
New genomic strategies can now be applied to identify a diagnosis in patients and families with previously undiagnosed rare genetic conditions. The large... 
Journal Article
PloS one, ISSN 1932-6203, 2014, Volume 9, Issue 9, p. e106435
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2018, Volume 13, Issue 3, p. e0194283
Journal Article
Neurology, ISSN 0028-3878, 09/2014, Volume 83, Issue 11, pp. 974 - 980
Journal Article
Journal Article
Muscle & Nerve, ISSN 0148-639X, 12/2015, Volume 52, Issue 6, pp. 942 - 947
Journal Article