Relationship of white and gray matter abnormalities to clinical and genetic features in myotonic dystrophy type 1

BACKGROUND: Myotonic dystrophy type 1 (DM1) represents a multisystemic disorder in which diffuse brain white and gray matter alterations related to clinical and genetic features have been described. We aimed to evaluate in the brain of adult patients with DM1 (i) white and gray matter differences, i...

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Detalles Bibliográficos
Autores principales: Zanigni, Stefano, Evangelisti, Stefania, Giannoccaro, Maria Pia, Oppi, Federico, Poda, Roberto, Giorgio, Antonio, Testa, Claudia, Manners, David Neil, Avoni, Patrizia, Gramegna, Laura Ludovica, De Stefano, Nicola, Lodi, Raffaele, Tonon, Caterina, Liguori, Rocco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Regular Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4900512/
https://www.ncbi.nlm.nih.gov/pubmed/27330968
http://dx.doi.org/10.1016/j.nicl.2016.04.012

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4900512/
https://www.ncbi.nlm.nih.gov/pubmed/27330968
http://dx.doi.org/10.1016/j.nicl.2016.04.012

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