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Journal of Inherited Metabolic Disease|October 11, 2011
Effects of enzyme replacement therapy on five patients with advanced late-onset glycogen storage disease type II: a 2-year follow-up studyYoshihiko Furusawa, Madoka Mori-Yoshimura, Toshiyuki Yamamoto, et al.
Muscle & Nerve|May 4, 2022
Comparison of strength testing modalities in dysferlinopathyNatalie F Reash, Meredith K James, Lindsay N Alfano, et al.
Neuromuscular Disorders : NMD|August 23, 2024
Performance of upper limb entry item to predict forced vital capacity in dysferlin-deficient limb girdle muscular dystrophyHolly Borland, Ursula Moore, Heather Gordish Dressman, et al.
Annals of Neurology|February 12, 2021
Assessing Dysferlinopathy Patients Over Three Years With a New Motor ScaleMarni B Jacobs, Meredoith K James, Linda P Lowes, et al.
Frontiers in Neurology|April 1, 2022
Assessing the Relationship of Patient Reported Outcome Measures With Functional Status in Dysferlinopathy: A Rasch Analysis ApproachAnna G Mayhew, Meredith K James, Ursula Moore, et al.
Neurology|January 11, 2019
Assessment of disease progression in dysferlinopathy: A 1-year cohort studyUrsula Moore, Marni Jacobs, Meredith K James, et al.
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