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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Detalhes bibliográficos
Publicado no:Neuroimage Clin
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Elsevier 2016
Assuntos:
Regular Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4900512/
https://ncbi.nlm.nih.gov/pubmed/27330968
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nicl.2016.04.012
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