Ataxia with oculomotor apraxia type 2 (AOA2): an eye movement study of two siblings.

Bargagli, A; Rosini, F; Zanca, D; Serchi, V; Rufa, A

Bargagli, A; Rosini, F; Zanca, D; Serchi, V; Rufa, A.

Affiliation

Bargagli A; Department of Medicine Surgery and Neuroscience, Eye Tracking & Visual Application Lab EVALAB/NEUROSENSE, Neurology and Neurometabolic Unit, University of Siena, Siena, Italy.
Rosini F; Department of Medicine Surgery and Neuroscience, Eye Tracking & Visual Application Lab EVALAB/NEUROSENSE, Neurology and Neurometabolic Unit, University of Siena, Siena, Italy.
Zanca D; Department of Medicine Surgery and Neuroscience, Eye Tracking & Visual Application Lab EVALAB/NEUROSENSE, Neurology and Neurometabolic Unit, University of Siena, Siena, Italy.
Serchi V; Department of Artificial Intelligence in Biomedical Engineering, Machine Learning and Data Analytics Lab, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Rufa A; Department of Medicine Surgery and Neuroscience, Eye Tracking & Visual Application Lab EVALAB/NEUROSENSE, Neurology and Neurometabolic Unit, University of Siena, Siena, Italy.

Neurol Sci ; 42(7): 3039-3042, 2021 Jul.

Article in En | MEDLINE | ID: mdl-33770309

Subject(s)

Apraxias; Cogan Syndrome; Spinocerebellar Ataxias; Apraxias/complications; Apraxias/diagnostic imaging; Apraxias/genetics; Cogan Syndrome/complications; Cogan Syndrome/diagnostic imaging; Cogan Syndrome/genetics; Eye Movements; Humans; Mutation; Siblings; Spinocerebellar Ataxias/complications; Spinocerebellar Ataxias/congenital; Spinocerebellar Ataxias/diagnostic imaging; Spinocerebellar Ataxias/genetics

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Apraxias / Spinocerebellar Ataxias / Cogan Syndrome Limits: Humans Language: En Journal: Neurol Sci Year: 2021 Document type: Article

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