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Meghan Moore Burk

Observed names: M Moore Burk, M. Moore Burk, Meghan F. Moore Burk
ORCID: 0000-0002-4376-4567
Observed ORCID: 0000-0002-4376-4567
OpenAlex ID: A5113416918
ACAD9 treatment with bezafibrate and nicotinamide riboside temporarily stabilizes cardiomyopathy and lactic acidosis
2024 · Johan L.K. Van Hove, Marisa W. Friederich, et al. · Mitochondrion · 11
Letter to the editor: Mortenson et al. (2025) “rehabilitation practices for childhood Spinal Muscular Atrophy”
2025 · Meghan Moore Burk, Carolyn Kelley, et al. · Disability and Rehabilitation · 1
Letter to the editor: A case of spinal muscular atrophy type 0 treated with nusinersen without progression of early-onset scoliosis
2025 · Meghan Moore Burk, Carolyn Kelley, et al. · Brain and Development · 1
192P A community-based experience with the new 12-Tier functional ability scale for Evolving Spinal Muscular Atrophy (EVOLVE-SMA)
2024 · M. Moore Burk, K. Johnson, et al. · Neuromuscular Disorders · 1
4.60P Comprehensive natural history in children with myotonic dystrophy: a single-institution experience over 20 years
2026 · Meghan Moore Burk, Caroline Meyer, et al. · Neuromuscular Disorders
1.77P Beyond the clinic: multiday analysis of leg movement quantity and kinematic characteristics in infants with SMA and infants with typical development
2026 · Melissa McIntyre, Jinseok Oh, et al. · Neuromuscular Disorders
2.30eP Development and validation of a novel dystrophinopathy foot index (DFI) for comparison and surgical decision-making related foot contracture
2026 · Meghan Moore Burk, Amanda Appel, et al. · Neuromuscular Disorders
1.95eP Translation and cross-cultural adaption of the functional ability scale for evolving spinal muscular atrophy (EVOLVE-SMA) into Spanish– escala de capacidad funcional para atrofia muscular espinal evolutiva
2026 · Meghan Moore Burk, Magalí Squitin Tasende, et al. · Neuromuscular Disorders
4.57P Characterizing brain MRI finding in pediatric myotonic dystrophy: a single institution experience
2026 · Meghan Moore Burk, Caroline Meyer, et al. · Neuromuscular Disorders
Transcranial Motor-Evoked Potentials Provide More Reliable Intraoperative Neuromonitoring Than Somatosensory-Evoked Potentials in Charcot-Marie-Tooth Patients Undergoing Periacetabular Osteotomy for Hip Dysplasia
2026 · Michele L. Yang, Susan Apkon, et al. · Journal of the Pediatric Orthopaedic Society of North America
Navigating new motor function trajectories: Consensus recommendations for assessment in the era of newborn screening and early treatment in SMA
2026 · Kristin J Krosschell, Sally Dunaway Young, et al. · Journal of Neuromuscular Diseases
New SMA era: A broad-range tiered assessment of function for the evolving SMA phenotype (EVOLVE-SMA)
2025 · Meghan Moore Burk, Thomas O Crawford, et al. · Journal of Neuromuscular Diseases
A qualitative, mixed-method approach to reaching consensus on function, fatigue, and fatigability outcomes in teens and adults living with spinal muscular atrophy
2025 · Jacqueline Glascock, Lisa T. Belter, et al. · Orphanet Journal of Rare Diseases
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P80 Beyond the clinic: multiday analysis of leg movement quantity and kinematic characteristics in infants with SMA.
2023 · M. McIntyre, T. Duong, et al. · Neuromuscular Disorders
Works count: 14
Citation count: 14
H-index: 1
I10-index: 1
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