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Evaluating the Genetic Subtypes and Phenotypic Features of Charcot-Marie-Tooth Disease in Türkiye

Author:Parman, Fatma Yesim   Cakar, Arman   Candayan, Ayse   Bagirova, Gulandam   Uyguner, Zehra Oya   Ceylaner, Serdar   Durmus, Hacer   Battaloglu, Esra   

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

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P12.025  

Author Institution:Neuromuscular Unit, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey  Molecular Genomics Group, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium and Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium, Antwerp, Belgium  Department of Molecular Biology and Genetics, Bogazici University, Istanbul, Türkiye, Istanbul, Turkey  

Motoneuron Involvement in CANVAS: A Case of ACAGG Expansions in a Guamanian Man

Author:Dufort, Gabrielle   Bonner, Devon   Anguiano, Beatriz   Bernstein, Jonathan   Wheeler, Matthew   Sampson, Jacinda   

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

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P12.026  

Author Institution:Stanford University, Stanford, CA  Stanford University, Palo Alto, CA  

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  

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