In Vivo Parieto-Occipital White Matter Metabolism Is Correlated with Visuospatial Deficits in Adult DM1 Patients

Myotonic dystrophy type 1 (DM1) is a genetic disorder caused by a (CTG) expansion in the DM protein kinase (DMPK) gene, representing the most common adult muscular dystrophy, characterized by a multisystem involvement with predominantly skeletal muscle and brain affection. Neuroimaging studies showe...

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Detalles Bibliográficos
Autores principales: Evangelisti, Stefania, Gramegna, Laura Ludovica, De Pasqua, Silvia, Rochat, Magali Jane, Morandi, Luca, Mitolo, Micaela, Bianchini, Claudio, Vornetti, Gianfranco, Testa, Claudia, Avoni, Patrizia, Liguori, Rocco, Lodi, Raffaele, Tonon, Caterina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9600392/
https://www.ncbi.nlm.nih.gov/pubmed/36291994
http://dx.doi.org/10.3390/diagnostics12102305

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9600392/
https://www.ncbi.nlm.nih.gov/pubmed/36291994
http://dx.doi.org/10.3390/diagnostics12102305

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