Therapeutic Use of Cerebellar Intermittent Theta Burst Stimulation (iTBS) in a Sardinian Family Affected by Spinocerebellar Ataxia 38 (SCA 38)

Spinocerebellar ataxia 38 (SCA 38) is an autosomal dominant disorder caused by conventional mutations in the ELOVL5 gene which encodes an enzyme involved in the synthesis of very long fatty acids, with a specific expression in cerebellar Purkinje cells. Three Italian families carrying the mutation,...

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Detalles Bibliográficos
Autores principales: Sanna, Angela, Follesa, Paolo, Tacconi, Paolo, Serra, Mariangela, Pisu, Maria Giuseppina, Cocco, Viola, Figorilli, Michela, Defazio, Giovanni, Puligheddu, Monica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9325795/
https://www.ncbi.nlm.nih.gov/pubmed/34410614
http://dx.doi.org/10.1007/s12311-021-01313-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9325795/
https://www.ncbi.nlm.nih.gov/pubmed/34410614
http://dx.doi.org/10.1007/s12311-021-01313-z

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