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Lead Poisoning mimicking Chronic Inflammatory Axonal Polyneuropathy

Author:Jacob, Shireen   Li, Xiangping   Wu, Laura   McHenry, James   Koleti, Meghana   Ramesh, Malvika   Abdul-Baki, Kian   

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

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P12.016  

Author Institution:University of Texas Medical Branch at Galveston , Gavleston, TX  University of Texas Medical Branch (UTMB), Galveston, TX  UTMB , Gavleston, TX  UTMB, Gavleston, TX  

Translating IGHMBP2 Variants with a CMT2S Patient-specific Organ-on-a-chip Model: Personalized Medicine ASO-based Therapeutic Rescue

Author:Smieszek, Sandra   Przychodzen, Bart   Tyner, Christina   Johnson, Caroline   Polymeropoulos, Christos   Birznieks, Gunther   Hagan, Walker   Lenkiu, Leticia   Niccum, Caitlyn   Cannon-Patron, Heather   Brighton, Rocky   Guo, Xiufang   Hawkins, Kenneth   Akanda, Nesar   Hickman, Jam   

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

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P12.017  

Author Institution:

Case Study on ALS Reversal: An Integrative Medicine Approach to Sporadic Limb-Onset ALS

Author:Noland, Diana   Bergeron, Rhett   Syrow, Larisa   

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

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P12.018  

Author Institution:Noland Nutrition, Coeur d Alene, ID  Real Health Medical, Roswell, GA  Cooper University Healthcare, Camden, NJ  

Homozygous Deletions in AHNAK2 as an Unexpected Genetic Cause of Polyneuropathy

Author:Mallett, Nicholas   Green, Rachel   Lee, Christopher   

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

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P12.019  

Author Institution:Vanderbilt University Medical Center, Nashville, TN  

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