Prion disease resembling frontotemporal dementia and parkinsonism linked to chromosome 17

OBJECTIVE: To compare the clinical features of a familial prion disease with those of frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17). BACKGROUND: Prion diseases are not usually considered in the differential diagnosis of FTDP-17, since familial Creutzfeldt-Jakob disease (...

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Autors principals:	Nitrini Ricardo, Silva Luís Sidônio Teixeira da, Rosemberg Sérgio, Caramelli Paulo, Carrilho Paulo Eduardo Mestrinelli, Iughetti Paula, Passos-Bueno Maria Rita, Zatz Mayana, Albrecht Stephen, LeBlanc Andrea
Format:	Artigo
Idioma:	Inglês
Publicat:	Thieme Revinter Publicações 2001-01-01
Col·lecció:	Arquivos de Neuro-Psiquiatria
Matèries:	prion protein mutation prion disease Creutzfeldt-Jakob disease frontotemporal dementia parkinsonism
Accés en línia:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2001000200001
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