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

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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Bibliographic Details
Main Authors: Stefano Zanigni, Stefania Evangelisti, Maria Pia Giannoccaro, Federico Oppi, Roberto Poda, Antonio Giorgio, Claudia Testa, David Neil Manners, Patrizia Avoni, Laura Ludovica Gramegna, Nicola De Stefano, Raffaele Lodi, Caterina Tonon, Rocco Liguori
Format: Article
Language:English
Published: Elsevier 2016-01-01
Series:NeuroImage: Clinical
Subjects:
myotonic dystrophy type 1
DTI
TBSS
VBM
cortical thickness
Online Access:http://www.sciencedirect.com/science/article/pii/S2213158216300766

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http://www.sciencedirect.com/science/article/pii/S2213158216300766

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