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Italian Journal of Neurological Sciences|December 1, 1990
Amyotrophic lateral sclerosis: thyroid and prolactin hormone changes in thyrotropin-releasing hormone therapyD Testa, P G Chiodini, F Girotti, et al.
Journal of Neurology|May 1, 1996
Survival in multiple system atrophy: a study of prognostic factors in 59 casesD Testa, G Filippini, M Farinotti, et al.
Clinical Neuropathology|March 1, 1990
Cerebral multiple glio-vascular dysplasias--a case reportD Testa, M Savoiardo, R Fazio, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 1, 1995
Intrathecal immune activation in three patients with progressive myoclonic ataxiaA Salmaggi, F Carella, C Ciano, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 5, 2003
Progressive dysarthria: definition and clinical follow-upP Soliveri, S Piacentini, F Carella, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 4, 2001
Comparison of natural histories of progressive supranuclear palsy and multiple system atrophyD Testa, D Monza, M Ferrarini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 11, 2007
Progressive myoclonic ataxia with intrathecal immune activation in six patientsD Testa, E Ambrosoni, S Franceschetti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 5, 2003
Distal-proximal differences in limb apraxia in corticobasal degeneration but not progressive supranuclear palsyP Soliveri, S Piacentini, D Paridi, et al.
AJNR. American Journal of Neuroradiology|January 1, 1993
Hallervorden-Spatz disease: MR and pathologic findingsM Savoiardo, W C Halliday, N Nardocci, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 17, 2000
Neuropsychological follow up in patients with Parkinson's disease, striatonigral degeneration-type multisystem atrophy, and progressive supranuclear palsyP Soliveri, D Monza, D Paridi, et al.
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