Myoclonus generators in sialidosis

OBJECTIVE: Sialidosis is an inborn error of metabolism. There is evidence that the myoclonic movements observed in this disorder have a cortical origin, but this mechanism does not fully explain the bilaterally synchronous myoclonus activity frequently observed in many patients. We present evidence...

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Detalles Bibliográficos
Autores principales: Vial, Felipe, McGurrin, Patrick, Attaripour, Sanaz, d'Azzo, Alesandra, Tifft, Cynthia J., Toro, Camilo, Hallett, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9253402/
https://www.ncbi.nlm.nih.gov/pubmed/35800887
http://dx.doi.org/10.1016/j.cnp.2022.05.004

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9253402/
https://www.ncbi.nlm.nih.gov/pubmed/35800887
http://dx.doi.org/10.1016/j.cnp.2022.05.004

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