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Could Droxidopa Become the First Symptomatic Therapy for Charcot-Marie-Tooth Disease? A Case Series

Author:Stoilova, Juliana   Martinez, Kenneth   

Session Name:P12: Neuromuscular and Clinical Neurophysiology (EMG): Hereditary Neuropathies  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P12.027  

Author Institution:Neurology & Pain Specialty Center, Aliso Viejo, CA  

Large Language Model-Supported Interactive Case-Based Learning: A Pilot Study

Author:Gim, Haelynn   Cook, Benjamin   Le, Jasmin   Guo, Christina   Arnold, Matthew   Stretton, Brandon   Gheihman, Galina   Bacchi, Stephen   

Session Name:P12: Education, Research, and Methodology: Using Technology in Neurology Education  

Topic:Education, Research, and Methodology  

Program Number:P12.027  

Author Institution:

Incorporating Patient Perspectives into a Composite Score for Measuring Disease Progression in Spinocerebellar Ataxia (SCA)

Author:Potashman, Michele   Rogula, Basia   Powell, Lauren   Korol, Ellen   Dickson, Samuel   Hendrix, Suzanne   Heinrich, Maggie   Rudell, Katja   Abetz Webb, Linda   Beiner, Melissa   Coric, Vlad   Rosenthal, Liana   Perlman, Susan   Schmahmann, Jeremy   L'Italien, Gilbert   

Session Name:P12: Movement Disorders: Ataxia 2  

Topic:Movement Disorders  

Program Number:P12.028  

Author Institution:Biohaven Pharmaceuticals, New Haven, CT  Broadstreet HEOR, Vancouver, BC, Canada  Pentara Corporation, Millcreek, UT  Parexel International, London, United Kingdom  Patient-Centered Outcomes Assessments, Bollington, United Kingdom  Johns Hopkins School of Medicine, Lutherville, MD  UCLA School of Medicine, Los Angeles, CA  Massachusettes General Hospital, Boston, MA  

Expanding the Clinical, Pathological, and Molecular Spectrum of HSPB8-Neuromuscular Disorder

Author:Putko, Brendan   Sorenson, Eric   Liewluck, Teerin   Milone, Margherita   

Session Name:P12: Neuromuscular and Clinical Neurophysiology (EMG): Hereditary Neuropathies  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P12.028  

Author Institution:Mayo Clinic, Rochester, MN  

Clinical and Genetic Profiles of Congenital Myasthenic Syndromes: A Single Tertiary Care Center Experience from Saudi Arabia

Author:Bahanan, Fahad   Aldawsari, Muteb   Bin Manea, Sara   alsagheir, Afaf   Alyahya, Mossaed   Alsolaihim, Alanoud   Alshehri, Ali Mohammed   

Session Name:P12: Neuromuscular and Clinical Neurophysiology (EMG): Neuromuscular Junction Disorders 2  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P12.029  

Author Institution:King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia