Sporadic Creutzfeldt-Jakob disease: a clinico-neuropathological analysis of nine definite cases

The authors have analyzed clinico-neuropathologically nine cases of the definite sporadic form of Creutzfeldt-Jakob disease (CJD). All cases were female, with mean age of 62.7 years. Eighty-nine percent of the patients exhibited prodromal and initial psychiatric symptoms; definite signs of dementia,...

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Principais autores:	CARLOS M. DE CASTRO COSTA, JEAN MARIE BRUCHER, CHRISTIAN LATERRE
Format:	Artigo
Jezik:	Inglês
Izdano:	Thieme Revinter Publicações 1998-09-01
Serija:	Arquivos de Neuro-Psiquiatria
Teme:	sporadic Creutzfeldt-Jakob disease dementia periodic EEG neuropathology prion protein (PrP) amyloid plaque prion disease
Online dostop:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X1998000300003&tlng=en
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