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Altered body schema processing in frontotemporal dementia with C9ORF72 mutations

BACKGROUND: Mutations in C9ORF72 are an important cause of frontotemporal dementia (FTD) and motor neuron disease. Accumulating evidence suggests that FTD associated with C9ORF72 mutations (C9ORF72-FTD) is distinguished clinically by early prominent neuropsychiatric features that might collectively...

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Detalhes bibliográficos
Main Authors: Downey, Laura E, Fletcher, Phillip D, Golden, Hannah L, Mahoney, Colin J, Agustus, Jennifer L, Schott, Jonathan M, Rohrer, Jonathan D, Beck, Jonathan, Mead, Simon, Rossor, Martin N, Crutch, Sebastian J, Warren, Jason D
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Publishing Group 2014
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4145454/
https://ncbi.nlm.nih.gov/pubmed/24521566
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp-2013-306995
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