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Real-world Use of Deutetrabenazine Reduces Tardive Dyskinesia Severity and Improves Quality of Life: Patient-reported Outcomes in the IMPACT-TD Study

Author:Finkbeiner, Stacy   Konings, Martijn   Henegar, Mark   Klakotskaia, Diana   Yu, Daisy   Jackson, Richard   

Session Name:P7: Movement Disorders: Hyperkinetic Movement Disorders 2  

Topic:Movement Disorders  

Program Number:P7.004  

Author Institution:Teva Branded Pharmaceutical Products R&D LLC, Parsippany, NJ  University of Michigan School of Medicine, Ann Arbor, MI  

Multi-modality Evoked Potentials and Electroretinogram in Patients with Wilson's Disease

Author:Kolluru, Karthik   Radhakrishnan, Divya M   Srivastava, Achal Kumar   Pandit, Awadh Kishor   Rajan, Roopa   Das, Animesh   Varasi, Ela   Agarwal, Ayush   Garg, Divyani   Garg, Ajay   ., Shalimar   Dhiman, Rebika   

Session Name:P7: Movement Disorders: Spastic Paraplegias and Other Rare Movement Disorders 1  

Topic:Movement Disorders  

Program Number:P7.004  

Author Institution:All India institute of Medical Sciences New Delhi, New delhi, India  All India institute of Medical Sciences New Delhi, India  

Parkinsonism and Psychosis as the Only Initial Features of SLE in an Elderly Female - Case Report

Author:Shvueli, Ethan   Lam, Ming-Tuen   Scheers-Masters, Joshua   Amlang, Christian   Jacoby, Nuri   

Session Name:P7: Movement Disorders: Spastic Paraplegias and Other Rare Movement Disorders 1  

Topic:Movement Disorders  

Program Number:P7.005  

Author Institution:SUNY downstate, Brooklyn, NY  Maimonides Medical Center, NY  Maimonides Medical Center, Brooklyn, NY  

Real-world Persistence in Patients with Tardive Dyskinesia: A Comparative Study of Valbenazine and Deutetrabenazine XR

Author:Doshi, Riddhi   Pandya, Shivani   Zhou, Xiaoyu   Nedzesky, Justin   Tapp, Dwight   Serbin, Michael   

Session Name:P7: Movement Disorders: Hyperkinetic Movement Disorders 2  

Topic:Movement Disorders  

Program Number:P7.005  

Author Institution:IQVIA, NC  Neurocrine Biosciences, Inc., San Diego, CA  

A Genetic Triple Play: Adolescent-onset Hyperkinetic Syndrome with Multilocus KMT2B and FGF14 Variants and Familial Hunter Syndrome in One Pedigree

Author:Palakodeti, Sanjana   Khan, Hina Rmsha Alfia   Natteru, Prashant   

Session Name:P7: Movement Disorders: Hyperkinetic Movement Disorders 2  

Topic:Movement Disorders  

Program Number:P7.006  

Author Institution:Kamineni Institute of Medical Sciences, Hyderabad, India  Mayo Clinic Health System , la Crosse, WI  Mayo Clinic Health System, La Crosse, WI