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Frontiers in Pediatrics|November 29, 2023
Detecting early signs in Duchenne muscular dystrophy: comprehensive review and diagnostic implicationsEugenio Mercuri, Marika Pane, Gianpaolo Cicala, et al.Muscle & Nerve|May 7, 2021
Time is muscle: A recommendation for early treatment for preterm infants with spinal muscular atrophyBo Hoon Lee, Megan A Waldrop, Anne M Connolly, et al.Muscle & Nerve|April 23, 2015
The course and outcome of pregnancy in women with nondystrophic myotoniasYuliya Snyder, Colleen Donlin-Smith, Eric Snyder, et al.Neurology|August 10, 2000
Retrospective analysis of the use of cyclosporine in myasthenia gravisE Ciafaloni, N K Nikhar, J M Massey, et al.Neurology|January 10, 2001
Mycophenolate mofetil for myasthenia gravis: an open-label pilot studyE Ciafaloni, J M Massey, B Tucker-Lipscomb, et al.BMJ Case Reports|February 19, 2013
Double trouble in a patient with myotoniaMichael K Hehir, Eric Logigian, Dipa L Raja Rayan, et al.Journal of Child Neurology|June 29, 2010
Change in natural history of Duchenne muscular dystrophy with long-term corticosteroid treatment: implications for managementRichard T Moxley, Shree Pandya, Emma Ciafaloni, et al.American Journal of Medical Genetics. Part A|July 7, 2020
Spinal muscular atrophy and Farber disease due to ASAH1 variants: A case reportBo Hoon Lee, Phillip Mongiovi, Thierry Levade, et al.Journal of the Neurological Sciences|September 1, 1992
Use of single strand conformation polymorphism analysis to detect point mutations in human mitochondrial DNAA Suomalainen, E Ciafaloni, Y Koga, et al.Child Neurology Open|February 27, 2023
Epilepsy Characteristics in Duchenne and Becker Muscular DystrophiesPraveen Kumar Ramani, Kindann Fawcett, Debra Guntrum, et al.Pageof 13