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Rare Case of Hereditary Transthyretin Amyloidosis With a Val122Ile Mutation Presenting as Recurrent Foot Drop in a Young Woman

Author:Khan, Imran   Malik, Hanna   LaBoy, Shannon   

Session Name:P3: Neuromuscular and Clinical Neurophysiology (EMG): Case Studies in Neuromuscular Medicine 2  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P3.015  

Author Institution:University of Florida Jacksonville, FL  UF Health Neurology, Jacksonville, FL