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Patients with NOTCH2NLC GGC Repeat Expansion Presenting with Vascular Leukoencephalopathy

Author:Liao, Yi-Chu   Chung, Chih-Ping   Lee, Yi-Chung   

Session Name:S36: Cerebrovascular Disease and Interventional Neurology: Basic and Translational Science  

Topic:Cerebrovascular Disease and Interventional Neurology  

Program Number:S36.003  

Author Institution:Taipei Veterans General Hospital, Taipei City, Taiwan  

Racial and Ethnic Disparities in Access to Huntington’s Disease (HD) care in North America: Analysis using the ENROLL-HD dataset

Author:Mendizabal, Adys   Perlman, Susan   Bordelon, Yvette   

Session Name:P1: Movement Disorders: Huntington's Disease and Chorea 1  

Topic:Movement Disorders  

Program Number:P1.009  

Author Institution:UCLA Dept. of Neurology, Los Angeles, CA  

Telehealth Utilization in a Comprehensive Multiple Sclerosis Clinic During the COVID-19 Pandemic: Single Center Experience

Author:Francis, Trieste   Noroozi Gilandehi, Sama   Shapiro, Sarah   Sun, Yiren   Wright, Melissa   Germaine, Sarah   Galli, Jonathan   Kadish, Robert   Klein, Julia   DeWitt, L   Smith, Tammy   Paz Soldan, M.   Clardy, Stacey   Wong, Ka-Ho   Rose, John   

Session Name:P3: MS Technology, Digital Tools and Artificial Intelligence  

Topic:MS and Inflammatory Disease  

Program Number:P3.005  

Author Institution:University of Utah, Salt Lake City, UT  Kansas City University College of Osteopathic Medicine, Kansas City, MO  3. BIPOC+ Next Generation Neuroscience Research Initiative, Salt Lake City, UT  University of Utah , Salt Lake City, UT  

From WEMINO To WEBINO With Unilateral LMN Facial Palsy

Author:Senthamarai Siddharthan, Yasodara Priyadharsi   Witt, Michael   Kini, Tonse Ashwini   Vasireddy, Rani Priyanka   Mathur Kumaraswamy, Vishakhadatta   

Session Name:P5: General Neurology: Case Reports 2  

Topic:General Neurology  

Program Number:P5.002  

Author Institution:university of Kentucky, Lexington, KY  

Myalgia in a Patient with Adult-Onset Asthma with Periocular Xanthogranuloma (AAPOX) due to Myotonic Dystrophy type 2

Author:Skolka, Michael   Amin, Shreyasee   Liewluck, Teerin   

Session Name:P6: Neuromuscular Disease: Inherited Muscle Disorders 3  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P6.013  

Author Institution:Department of Neurology, Mayo Clinic, Rochester, MN  Department of Rheumatology, Mayo Clinic, Rochester, MN