Browse All

Current Filters

CLEAR FILTER x

TITLE

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  

Disparities in Detection and Care of Parkinson’s Disease Among Hispanic Patients in South Texas

Author:Nguyen, Nicholas   Liu, Terri-Jeanne   Isaac, Patrick   Agis, Chloe   Petrosyan, Diana   Bhaya, Paro   Bitar, Sabrina   Adlis, Rachel   Khan, Imran   Klein, Preston   Privitt, Kayla   Himali, Jayanda   Horn, Sarah   

Session Name:P10: Movement Disorders: Care Models and Patient Perceptions in Movement Disorders 3  

Topic:Movement Disorders  

Program Number:P10.007  

Author Institution:UT Health San Antonio, TX  UT Health San Antonio, San Antonio, TX  UT Health Houston, Houston, TX  UT Health Austin, Austin, TX  UF Health Jacksonville, Jacksonville, FL  University of Virginia School of Medicine, Charlottesville, VA  UT Health Nashville, TN