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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:Epilepsy/Clinical Neurophysiology (EEG)  

Program Number:P5.001  

Author Institution:

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:

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:Cerebrovascular Disease and Interventional Neurology  

Program Number:P5.003  

Author Institution:

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:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P5.004  

Author Institution:

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:Epilepsy/Clinical Neurophysiology (EEG)  

Program Number:P5.005  

Author Institution: