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Blurred Lines in Neurology: ATP1A1 Variant Redefines CMT Spectrum

Author:Alhallaq, Lamees   Williamson, Madeline   Avila, J. David   

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

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P12.020  

Author Institution:Geisinger Medical Center, Danville, PA  

Hereditary Motor Sensory Neuropathy: Case Report and Update Genetic Implications

Author:Ghani, Mohammad   Lightman, Rebecca   Brown, Martin   

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

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P12.021  

Author Institution:University of Louisville, Louisville, KY  

CMT1B Presenting with Hemifacial Spasm and Multiple Cranial Nerve Enhancement

Author:Bloom, Jessica   Ferrey, Dominic   

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

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P12.022  

Author Institution:University of California, San Diego, San Diego, CA  

Entire Sequence Deletion of PMP22 Presenting as a Length-dependent Peripheral Neuropathy

Author:Ilardi, Marissa   Kwon, Patrick   

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

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P12.023  

Author Institution:NYU Grossman School of Medicine , New York, NY  NYU Grossman School of Medicine , Brooklyn, NY  

Charcot-Marie-Tooth Disease and Parkinsonism in a 50 Year Old Patient with FIG4 Mutation

Author:Caillier, Rebecca   Sefain, Andrew   

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

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P12.024  

Author Institution:Sanford Health, Fargo, ND  University of North Dakota, Fargo, ND