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Stroke|May 1, 1992
Transcranial Doppler in spontaneous attacks of migraineE M Zanette, A Agnoli, C Roberti, et al.
The EMBO Journal|March 1, 1991
Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58F Tagliavini, F Prelli, J Ghiso, et al.
Neurology|May 5, 1999
Infantile neuroaxonal dystrophy: clinical spectrum and diagnostic criteriaN Nardocci, G Zorzi, L Farina, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1992
Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindredG Giaccone, L Verga, O Bugiani, et al.
Cancer Genetics and Cytogenetics|July 15, 1994
Increasing complexity of the karyotype in 50 human gliomas. Progressive evolution and de novo occurrence of cytogenetic alterationsI Magnani, S Guerneri, B Pollo, et al.
Functional Neurology|April 1, 1987
Spasmophilia: a clinical neurophysiopathological and biochemical studyF de Romanis, M Feliciani, M V Rosati, et al.
Clinical Neuropharmacology|October 1, 1991
Antagonist effect of terguride in Parkinson's diseaseS Ruggieri, F Stocchi, F Baronti, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1988
Comparison between L-dopa and lisuride intravenous infusions: a clinical studyS Ruggieri, F Stocchi, A Carta, et al.
Functional Neurology|January 1, 1987
Neurophysiological and magnetic resonance studies in a patient with hemiballismusA Berardelli, F Stocchi, M Gallucci, et al.
Clinical Neuropharmacology|October 1, 1989
Effects of terguride in patients with Huntington's diseaseF Stocchi, A Carta, A Berardelli, et al.
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