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Hip Displacement in Spinal Muscular Atrophy: The Influences of Genetic Severity, Functional Level, and Disease-modifying Treatments.
J Pediatr Orthop. 2024 Mar 1;44(3):e226-e231. doi: 10.1097/BPO.0000000000002595. Epub 2023 Dec 11.
J Pediatr Orthop. 2024.
PMID: 38073182
Diverse Cardiac Phenotype of Becker Muscular Dystrophy: Under-Recognized Subclinical Cardiomyopathy Due to Partial Dystrophin Deficiency in a Contemporary Era.
Nigam P, Fitzgerald KK, Scavina M, Tsuda T.
Nigam P, et al.
Pediatr Cardiol. 2024 Jan 19. doi: 10.1007/s00246-023-03382-9. Online ahead of print.
Pediatr Cardiol. 2024.
PMID: 38240762
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A Mixed-Method Study Exploring Patient-Experienced and Caregiver-Reported Benefits and Side Effects of Corticosteroid Use in Duchenne Muscular Dystrophy.
Fischer R, Porter K, Donovan JM, Scavina MT, Armstrong N, Denger B, Hasham S, Peay H.
Fischer R, et al. Among authors: scavina mt.
J Neuromuscul Dis. 2023;10(4):593-613. doi: 10.3233/JND-221617.
J Neuromuscul Dis. 2023.
PMID: 37182893
Free PMC article.
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The Early Care (0-3 Years) In Duchenne Muscular Dystrophy Meeting Report.
Armstrong N, Apkon S, Berggren KN, Braun C, Ciafaloni E, Connolly A, Kennedy A, Kuntz N, Mathews K, McGuire M, Parad R, Scavina M, Scharf RJ, Waldrop M.
Armstrong N, et al.
J Neuromuscul Dis. 2024;11(2):525-533. doi: 10.3233/JND-230180.
J Neuromuscul Dis. 2024.
PMID: 38189762
Free PMC article.
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Critical Airway Stenosis in an Adolescent Male With Pompe Disease and Thoracic Lordosis: A Case Report.
Brenn BR, Theroux MT, Shah SA, Mackenzie WG, Heinle R, Scavina MT.
Brenn BR, et al. Among authors: scavina mt.
A A Case Rep. 2017 Oct 1;9(7):199-203. doi: 10.1213/XAA.0000000000000564.
A A Case Rep. 2017.
PMID: 28542051
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Design and testing of a functional arm orthosis in patients with neuromuscular diseases.
Rahman T, Sample W, Seliktar R, Scavina MT, Clark AL, Moran K, Alexander MA.
Rahman T, et al. Among authors: scavina mt.
IEEE Trans Neural Syst Rehabil Eng. 2007 Jun;15(2):244-51. doi: 10.1109/TNSRE.2007.897026.
IEEE Trans Neural Syst Rehabil Eng. 2007.
PMID: 17601194
Free article.
Clinical Trial.
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T118M PMP22 mutation causes partial loss of function and HNPP-like neuropathy.
Shy ME, Scavina MT, Clark A, Krajewski KM, Li J, Kamholz J, Kolodny E, Szigeti K, Fischer RA, Saifi GM, Scherer SS, Lupski JR.
Shy ME, et al. Among authors: scavina mt.
Ann Neurol. 2006 Feb;59(2):358-64. doi: 10.1002/ana.20777.
Ann Neurol. 2006.
PMID: 16437560
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Krabbe's disease presenting as a peripheral neuropathy.
Marks HG, Scavina MT, Kolodny EH, Palmieri M, Childs J.
Marks HG, et al. Among authors: scavina mt.
Muscle Nerve. 1997 Aug;20(8):1024-8. doi: 10.1002/(sici)1097-4598(199708)20:8<1024::aid-mus13>3.0.co;2-v.
Muscle Nerve. 1997.
PMID: 9236794
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