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Neuromuscular Disorders : NMD|December 3, 2021
Diagnostic delay in patients with FKRP-related muscular dystrophyLauren N Coffey, Carrie M Stephan, M B Zimmerman, et al.Neurology|November 5, 2017
Illness-associated muscle weakness in dystroglycanopathiesCourtney R Carlson, Steven D McGaughey, Jamie M Eskuri, et al.Muscle & Nerve|January 27, 2021
The outcomes and experience of pregnancy in limb girdle muscular dystrophy type R9Eric M Libell, Noelle C Bowdler, Carrie M Stephan, et al.Neuromuscular Disorders : NMD|May 29, 2023
Pain interference and fatigue in limb-girdle muscular dystrophy R9Anna M Reelfs, Carrie M Stephan, Shelley R H Mockler, et al.Journal of Child Neurology|November 23, 2016
Childhood Activity on Progression in Limb Girdle Muscular Dystrophy 2IBrianna N Brun, Shelley R H Mockler, Katie M Laubscher, et al.Annals of Clinical and Translational Neurology|January 5, 2026
Predicting Loss of Ambulation in Limb Girdle Muscular Dystrophy R9Chandra L Miller, Lauren N Coffey, Shelley R H Mockler, et al.Neurology|August 9, 2020
Motor outcome measures in patients with FKRP mutations: A longitudinal follow-upAmber M Gedlinske, Carrie M Stephan, Shelley R H Mockler, et al.Annals of Clinical and Translational Neurology|April 17, 2025
UDP-glucose dehydrogenase variants cause dystroglycanopathyAnna M Reelfs, Carrie M Stephan, Theresa M Czech, et al.Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|July 22, 2010
Exercise-induced left ventricular systolic dysfunction in women heterozygous for dystrophinopathyRobert M Weiss, Richard E Kerber, Jane K Jones, et al.Neurology|January 15, 2017
Comparison of brain MRI findings with language and motor function in the dystroglycanopathiesBrianna N Brun, Shelley R H Mockler, Katie M Laubscher, et al.Pageof 2