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From Unknown to Pathogenic: A Case of Cerebellar Ataxia due to RAB3A Variant

Author:Dyer, Kalyn   Shah-Zamora, Deepal   Harmon, Jennifer   Hite, Aubrey   

Session Name:P5: Movement Disorders: Ataxias 2  

Topic:Movement Disorders  

Program Number:P5.001  

Author Institution:Atrium Health Wake Forest Baptist, Winston-Salem, NC  Atrium Health Wake Forest Baptist, Washington, DC  Atrium Health Wake Forest Baptist, Winston Salem, NC  

A Tale of Two Inheritances: Possible Dual STUB1-linked Ataxias in One Family

Author:Palat Chirakkara, Sudhir Kumar   Zhang, Qiang   

Session Name:P5: Movement Disorders: Ataxias 2  

Topic:Movement Disorders  

Program Number:P5.002  

Author Institution:University of Iowa Healthcare, Iowa, IA  University of Iowa, Hospitals and Clinics, Iowa City, IA  

Cortical Atrophy Mediates the Link Between Clinical Severity and Retinal Neurodegeneration in Spinocerebellar Ataxia Type Three

Author:li, chuyi   

Session Name:P5: Movement Disorders: Ataxias 2  

Topic:Movement Disorders  

Program Number:P5.003  

Author Institution:The First Affiliated Hospital of Fujian Medical University, Fuzhou, China, People's Republic of  

AP3B2 Antibody Positive Cerebellar Ataxia With Parkinsonism: A Case Report

Author:Duncan, Irma   Khilan, Muhammad Haroon   Kass, Joseph   Bellows, Steven   

Session Name:P5: Movement Disorders: Ataxias 2  

Topic:Movement Disorders  

Program Number:P5.004  

Author Institution:Baylor College of Medicine, Houston, TX  

Report of a Novel Likely Pathogenic TGM6 c.538G>A (p.Gly180Arg) Variant Causing Familial SCA35

Author:Micci, Luca   Kidd, Charles   Schacht, John   Horvat, David   

Session Name:P5: Movement Disorders: Ataxias 2  

Topic:Movement Disorders  

Program Number:P5.005  

Author Institution:Walter Reed National Military Medical Center, Bethesda, MD  Alexander T. Augusta Military Medical Center, Fort Belvoir, VA