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Characterization of Peripheral Neuropathies in Spinocerebellar Ataxias: A Peruvian Cohort Study

Author:Gutierrez Arratia, Jesus Daniel   Arroyo Ramirez, Fitzgerald Aquiles   Abad, Alonso   Oporto, Brenda   Mattos Castillo, Jair   Galecio-Castillo, Milagros   Sarapura-Castro, Elison   Cornejo Olivas, Mario   

Session Name:P4: Movement Disorders: Ataxias 1  

Topic:Movement Disorders  

Program Number:P4.007  

Author Institution:Instituto Nacional de Ciencias Neurologicas, Lima, Peru  Instituto Nacional de Ciencias Neurologicas, Peru  University of Iowa Hospitals and Clinics, Iowa City, IA  

Onset of Bulbar Symptoms in Patients with Friedreich Ataxia: Analysis of U.S. Medicare Claims Data

Author:England, Sarah   Bian, Boyang   Gomes, Daniel   McKay, James   Avila, Robin   D’Alberto, Nicholas   

Session Name:P4: Movement Disorders: Ataxias 1  

Topic:Movement Disorders  

Program Number:P4.008  

Author Institution:Biogen Inc, Cambridge, MA  Voxanalytica, Pleasanton, CA  

Long Read Genome Sequencing for Cerebellar Ataxia

Author:Maki, Niki   Blanco, Kirsten   Barrick, Rebekah   Smith, Erica   de Dios, Ivan   Berger, Seth   Délot, Emmanuèle   Bluske, Krista   Pitsava, Greta   Das, Soma   Gomez, Christopher M.   Vilain, Eric   Xiao, Changrui   

Session Name:P4: Movement Disorders: Ataxias 1  

Topic:Movement Disorders  

Program Number:P4.009  

Author Institution:UC Irvine, CA  Children’s Hospital of Orange County (CHOC), CA  Ambry Genetics, CA  The University of Chicago, IL  UC Irvine, Orange, CA  

A Novel FA2H Variant with Cerebellar Hypometabolism: A Case Report of Suspected SPG35

Author:Talavera De la Esperanza, Blanca   Chinchihualpa Paredes, Nathaly   herrera, andrea   Collins-Ruff, Kathleen   Yu, Zheming   Lin, Amanda   Patino Murillas, Jorge   Espay, Alberto   Marsili, Luca   

Session Name:P4: Movement Disorders: Ataxias 1  

Topic:Movement Disorders  

Program Number:P4.010  

Author Institution:University of Cincinnati, Cincinnati, OH  University of Cincinnati, OH  University of Cincinnati Medical Center, Cincinnati, OH  

Ataxia and Azoospermia Caused by an MT-ATP6 Mutation with Apparent Anticipation due to Heteroplasmy in a Large Extended Kindred

Author:Zhu, David   Xiao, Changrui   Pryor, Jon   Frutiger, Sally   Clark, Brent   Casey, Hannah   Bower, Matthew   Yu, Guoyun   Du, Xiaofei   Toro, Camilo   Gomez, Christopher   

Session Name:P4: Movement Disorders: Ataxias 1  

Topic:Movement Disorders  

Program Number:P4.011  

Author Institution:University of Chicago, MA  UC Irvine, Orange, CA  University of Minnesota, MN  University of Chicago, IL  National Human Genome Research Institute, MD  NIH, Bethesda, MD  University of Chicago, Chicago, IL