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Jayakody H, Zarei S, Nguyen H, et al. (2020) Cobblestone Malformation in LAMA2 Congenital Muscular Dystrophy (MDC1A). Journal of Neuropathology and Experimental Neurology
Nix JS, Moore SA. (2020) What Every Neuropathologist Needs to Know: The Muscle Biopsy. Journal of Neuropathology and Experimental Neurology
Saylam E, Moore SA, Aravindhan A, et al. (2020) A novel noncoding mutation in early onset limb-girdle muscular dystrophy. Neurology. Genetics. 6: e388
Earle AJ, Kirby TJ, Fedorchak GR, et al. (2019) Mutant lamins cause nuclear envelope rupture and DNA damage in skeletal muscle cells. Nature Materials
Bhatia A, Mobley BC, Cogan J, et al. (2019) Magnetic Resonance Imaging characteristics in case of TOR1AIP1 muscular dystrophy. Clinical Imaging. 58: 108-113
Lee AJ, Jones KA, Butterfield RJ, et al. (2019) Clinical, genetic, and pathologic characterization of Mexican founder mutation c.1387A>G. Neurology. Genetics. 5: e315
Liewluck T, Niu Z, Moore SA, et al. (2019) ACTA1-myopathy with prominent finger flexor weakness and rimmed vacuoles. Neuromuscular Disorders : Nmd
Locht Mvd, Winter Jd, Conijn S, et al. (2019) P.163Mutations in fast skeletal troponin C (TNNC2) cause contractile dysfunction Neuromuscular Disorders. 29
Chandran S, Suggs JA, Wang BJ, et al. (2018) Suppression of myopathic lamin mutations by muscle-specific activation of AMPK and modulation of downstream signaling. Human Molecular Genetics
Aeffner F, Faelan C, Moore SA, et al. (2018) Validation of a Muscle-Specific Tissue Image-Analysis Tool for Quantitative Assessment of Dystrophin Staining in Frozen Muscle Biopsies. Archives of Pathology & Laboratory Medicine