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Progress in Neuro-Psychopharmacology & Biological Psychiatry|January 1, 1989
One year treatment with lisuride delivery pump in Parkinson's diseaseS Ruggieri, F Stocchi, A Carta, et al.
Headache|June 1, 1991
Migraine and epilepsy with infantile onset and electroencephalographic findings of occipital spike-wave complexesF De Romanis, M G Buzzi, R Cerbo, et al.
Biochemical and Biophysical Research Communications|August 16, 1993
Molecular characteristics of a protease-resistant, amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion proteinC Selvaggini, L De Gioia, L Cantù, et al.
Brain Pathology (Zurich, Switzerland)|April 1, 1996
Prion protein amyloidosisB Ghetti, P Piccardo, B Frangione, et al.
Cephalalgia : an International Journal of Headache|January 1, 1988
Spectral EEG analysis and flunarizine treatment in migraine patientsR Formisano, N Martucci, G Fabbrini, et al.
Journal of Neuropathology and Experimental Neurology|November 1, 1996
Proteinase-K-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease (Indiana kindred)P Piccardo, C Seiler, S R Dlouhy, et al.
Cell|November 18, 1994
Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant alleleF Tagliavini, F Prelli, M Porro, et al.
Brain Pathology (Zurich, Switzerland)|July 1, 1995
Tissue handling in suspected Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases)H Budka, A Aguzzi, P Brown, et al.
Brain Research|July 9, 1993
A68 is a component of paired helical filaments of Gerstmann-Sträussler-Scheinker disease, Indiana kindredF Tagliavini, G Giaccone, F Prelli, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|March 29, 2005
FVEPs in Creutzfeldt-Jacob disease: waveforms and interaction with the periodic EEG pattern assessed by single sweep analysisE Visani, P Agazzi, V Scaioli, et al.
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