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Journal of Clinical Neuromuscular Disease|February 17, 2021
Myotonic Muscular Dystrophy Type 2 in CT, USA: A Single-Center Experience With 50 PatientsBhaskar Roy, Qian Wu, Charles H Whitaker, et al.
Muscle & Nerve|January 6, 2015
Fulminant lipid storage myopathy due to multiple acyl-coenzyme a dehydrogenase deficiencyCharles H Whitaker, Kevin J Felice, David Silvers, et al.
Muscle & Nerve|August 29, 2025
Focal Neurogenic Muscle Hypertrophy and Focal Neurogenic MyositisKevin J Felice, Charles H Whitaker, William J Pesce, et al.
Journal of Clinical Neuromuscular Disease|August 25, 2020
Laing Myopathy: Report of 4 New Families With Novel MYH7 Mutations, Double Mutations, and Severe PhenotypeCatherine E Alessi, Qian Wu, Charles H Whitaker, et al.
Journal of Clinical Neuromuscular Disease|December 17, 2008
The Clinical Features of Facioscapulohumeral Muscular Dystrophy Associated With Borderline (>/=35 kb) 4q35 EcoRI FragmentsKevin J Felice, Charles H Whitaker
Muscle & Nerve|February 26, 2004
Biopsy-proven alpha-glucosidase deficiency with normal lymphocyte enzyme activityCharles H Whitaker, Kevin J Felice, Marvin Natowicz
Muscle & Nerve|July 7, 2021
Diagnostic yield of advanced genetic testing in patients with hereditary neuropathies: A retrospective single-site studyKevin J Felice, Charles H Whitaker, Sadaf Khorasanizadeh
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