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Grey and white matter loss along cerebral midline structures in myotonic dystrophy type 2
Myotonic dystrophy type 2 (DM2) is an autosomal dominantly inherited multisystemic disorder and a common cause of muscular dystrophy in adults. Although neuromuscular symptoms predominate, there is clinical and imaging evidence of cerebral involvement. We used voxel-based morphometry (VBM) based on...
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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2770432/ https://ncbi.nlm.nih.gov/pubmed/19224318 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00415-008-0997-1 |
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