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Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|September 6, 2023
Evolving Therapeutic Options for the Treatment of Duchenne Muscular DystrophyEleonora S D'Ambrosio, Jerry R MendellJournal of Clinical Medicine|March 11, 2023
Cancer and Myotonic DystrophyEleonora S D'Ambrosio, Paloma Gonzalez-PerezNeuromuscular Disorders : NMD|November 3, 2024
Concurrent nodular lymphocytic myositis and myasthenia gravis. A case reportEleonora S D'Ambrosio, Matti D Allen, Burcak Ozes, et al.Genes|March 28, 2026
Adeno-Associated Virus Toxicity in Duchenne Muscular Dystrophy: Mechanisms and Clinical ConsiderationsEzgi Saylam, Eleonora S D'ambrosio, Maria Tozzo Pesco, et al.Muscle & Nerve|February 15, 2023
Frequency and type of cancers in myotonic dystrophy: A retrospective cross-sectional studyEleonora S D'Ambrosio, Kathy Chuang, William S David, et al.Case Reports in Infectious Diseases|July 17, 2023
Seizure as Presenting Symptom of Multisystem Inflammatory Syndrome in ChildrenEleonora S D'Ambrosio, Stefanie Gauguet, Christine Miller, et al.Neurology. Genetics|May 1, 2023
Parent-of-Origin Effect on the Age at Symptom Onset in Myotonic Dystrophy Type 2Paloma Gonzalez-Perez, Eleonora S D'Ambrosio, Vincent Picher-Martel, et al.Muscles (Basel, Switzerland)|March 27, 2026
Duchenne Muscular Dystrophy: Contemporary Therapeutic Options and Real-World Challenges in Treatment SelectionMaria Tozzo Pesco, Gülru Zeynep Öztürk, Shivkumar C Bhadola, et al.Annals of Clinical and Translational Neurology|April 28, 2025
Validity and Reliability of Clinical and Patient-Reported Outcomes in Multisystem Proteinopathy 1Lindsay N Alfano, Megan A Iammarino, Natalie F Reash, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|May 7, 2025
Current clinical applications of AAV-mediated gene therapyBarry J Byrne, Kevin M Flanigan, Susan E Matesanz, et al.Pageof 1