Rapidly progressive atypical parkinsonism associated with frontotemporal lobar degeneration and motor neuron disease

OBJECTIVE: To report the rare but distinct clinical and neuropathological phenotype of non-familial, rapidly progressive parkinsonism and dementia associated with frontotemporal lobar degeneration with motor neuron disease (FTLD-MND). METHODS: Subjects included two 70-year-old women presenting with...

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Detalhes bibliográficos
Publicado no:J Neurol Neurosurg Psychiatry
Main Authors: Espay, Alberto J, Spina, Salvatore, Houghton, David J, Murrell, Jill R, de Courten-Myers, Gabrielle M, Ghetti, Bernardino, Litvan, Irene
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4449730/
https://ncbi.nlm.nih.gov/pubmed/20587488
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.2009.201608
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