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Emma Ciafaloni

Showing results (31-40 of 114) with videos related to

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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.
Neurology|November 13, 2013
Can outcomes in Duchenne muscular dystrophy be improved by public reporting of data?Holly L Peay, Michele A Scully, Valerie A Cwik, 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.
Annals of the New York Academy of Sciences|November 1, 2003
Antibodies in sera of patients with late-onset myasthenia gravis recognize the PEVK domain of titinMirta Mihovilovic, Emma Ciafaloni, Jennifer Butterworth-Robinette, 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.
Journal of Child Neurology|October 22, 2021
Health Profile of Preterm Males With Duchenne Muscular DystrophyAida Soim, Bailey Wallace, Nedra Whitehead, et al.
Journal of Neuromuscular Diseases|November 19, 2016
The Impact of Pregnancy on Myotonic Dystrophy: A Registry-Based StudyNicholas E Johnson, Man Hung, Eriko Nasser, et al.
Orphanet Journal of Rare Diseases|November 2, 2024
Latent factors underlying the symptoms of adult-onset myotonic dystrophy type 1 during the clinical courseYanan Zhang, Bailey Wallace, Bo Cai, et al.
Pageof 12

Showing results (31-40 of 114) with videos related to

Sort By:
Pageof 12
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.
Neurology|November 13, 2013
Can outcomes in Duchenne muscular dystrophy be improved by public reporting of data?Holly L Peay, Michele A Scully, Valerie A Cwik, 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.
Annals of the New York Academy of Sciences|November 1, 2003
Antibodies in sera of patients with late-onset myasthenia gravis recognize the PEVK domain of titinMirta Mihovilovic, Emma Ciafaloni, Jennifer Butterworth-Robinette, 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.
Journal of Child Neurology|October 22, 2021
Health Profile of Preterm Males With Duchenne Muscular DystrophyAida Soim, Bailey Wallace, Nedra Whitehead, et al.
Journal of Neuromuscular Diseases|November 19, 2016
The Impact of Pregnancy on Myotonic Dystrophy: A Registry-Based StudyNicholas E Johnson, Man Hung, Eriko Nasser, et al.
Orphanet Journal of Rare Diseases|November 2, 2024
Latent factors underlying the symptoms of adult-onset myotonic dystrophy type 1 during the clinical courseYanan Zhang, Bailey Wallace, Bo Cai, et al.
Pageof 12