Eye-tracking-aided characterization of saccades and antisaccades in SYNE1 ataxia patients: a pilot study

BACKGROUND: SYNE1 ataxia is an autosomal recessive hereditary condition, the main characteristic features of which are gait and limb ataxia and cerebellar dysarthria. Reports have revealed that the clinical phenotype of SYNE1 ataxia is more complex than the first published cases with pure cerebellar...

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Detalles Bibliográficos
Autores principales: Szpisjak, Laszlo, Szaraz, Gabor, Salamon, Andras, Nemeth, Viola L., Szepfalusi, Noemi, Veres, Gabor, Kincses, Balint, Maroti, Zoltan, Kalmar, Tibor, Rydzanicz, Malgorzata, Ploski, Rafal, Klivenyi, Peter, Zadori, Denes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7852103/
https://www.ncbi.nlm.nih.gov/pubmed/33526008
http://dx.doi.org/10.1186/s12868-021-00612-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7852103/
https://www.ncbi.nlm.nih.gov/pubmed/33526008
http://dx.doi.org/10.1186/s12868-021-00612-9

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