NR AOHO
AU Tabaka,J.; Nowacki,P.; Stankiewicz,J.; Wierzba-Bobrowicz,T.
TI Extreme loss of neurons in sporadic Creutzfeldt-Jakob disease with 14-3-3 protein in cerebrospinal fluid
QU Folia Neuropathologica 2003; 41(1): 47-50
PT journal article
AB Spongiform changes and astrogliosis predominantly represent the classical neuropathological features of sporadic Creutzfeldt-Jakob disease (CJD). They are accompanied by neuronal loss, which is usually of moderate intensity, and by PrPsc plaques. We present sporadic CJD lasting 12 months, confirmed by 14-3-3 P, with almost complete loss of neurones in many grey structures of the brain.
MH Aged; Astrocytes/pathology; Case Report; Cell Movement; Creutzfeldt-Jakob Syndrome/*cerebrospinal fluid/*pathology; Fatal Outcome; Female; Human; Nerve Degeneration/cerebrospinal fluid/pathology; Neurons/*pathology; Tyrosine 3-Monooxygenase/*cerebrospinal fluid
AD Department of Neurology, Pomeranian Medical University, Szczecin, Poland.
SP englisch
PO Polen