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Annals of Neurology|November 27, 2014
Cystic fibrosis newborn screening: a model for neuromuscular disease screening?Michele A Scully, Philip M Farrell, Emma Ciafaloni, et al.Muscle & Nerve|June 6, 2015
Health services received by individuals with duchenne/becker muscular dystrophyShree K Pandya, Kim A Campbell, Jennifer G Andrews, et al.Journal of Clinical Rheumatology : Practical Reports on Rheumatic & Musculoskeletal Diseases|January 7, 2010
Hydroxychloroquine-induced myopathyJun-Beom Kwon, Anatole Kleiner, Koto Ishida, et al.American Journal of Medical Genetics. Part A|August 16, 2014
Diagnostic and clinical characteristics of early-manifesting females with Duchenne or Becker muscular dystrophyLauren Imbornoni, Elinora T Price, Jennifer Andrews, et al.Muscle & Nerve|November 28, 2019
Nusinersen for older patients with spinal muscular atrophy: A real-world clinical setting experienceAravindhan Veerapandiyan, Katy Eichinger, Debra Guntrum, et al.Journal of Child Neurology|May 16, 2018
Is There a Delay in Diagnosis of Duchenne Muscular Dystrophy Among Preterm-Born Males?Aida Soim, Michael G Smith, Jennifer M Kwon, et al.Neurology|October 14, 2018
Evidence in focus: Nusinersen use in spinal muscular atrophy [RETIRED]: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of NeurologyDavid Michelson, Emma Ciafaloni, Stephen Ashwal, et al.Disability and Rehabilitation|April 12, 2017
Application of the International Classification of Functioning, Disability and Health system to symptoms of the Duchenne and Becker muscular dystrophiesKristin M Conway, Emma Ciafaloni, Dennis Matthews, et al.Annals of Neurology|June 1, 1991
Deletion of mitochondrial DNA in patients with combined features of Kearns-Sayre and MELAS syndromesM L Zupanc, C T Moraes, S Shanske, et al.The Journal of Pediatrics|March 1, 1993
Maternally inherited Leigh syndromeE Ciafaloni, F M Santorelli, S Shanske, et al.Pageof 13