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European Journal of Neurology|June 22, 2010
Occurrence and characterization of Pain in immune-mediated neuropathies: a multicentre prospective studyC Pazzaglia, C Briani, E Nobile-Orazio, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|August 22, 2001
Inhibition of motor system excitability at cortical and spinal level by tonic muscle painD Le Pera, T Graven-Nielsen, M Valeriani, et al.
Gait & Posture|January 25, 2011
Levodopa effect on electromyographic activation patterns of tibialis anterior muscle during walking in Parkinson's diseaseP Caliandro, M Ferrarin, M Cioni, et al.
Journal of Neurology|March 14, 2007
Functional involvement of cerebral cortex in adult sleepwalkingA Oliviero, G Della Marca, P A Tonali, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|August 22, 2007
Segregating two inhibitory circuits in human motor cortex at the level of GABAA receptor subtypes: a TMS studyV Di Lazzaro, F Pilato, M Dileone, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|October 3, 2008
In vivo functional evaluation of central cholinergic circuits in vascular dementiaV Di Lazzaro, F Pilato, M Dileone, et al.
Blood|June 20, 1998
Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patientsV De Stefano, P Chiusolo, K Paciaroni, et al.
Journal of Neurology|September 21, 2002
Functional involvement of central nervous system in acute exacerbation of chronic obstructive pulmonary disease A preliminary transcranial magnetic stimulation studyA Oliviero, G Corbo, P A Tonali, et al.
Experimental Brain Research|April 5, 2003
Direct demonstration of reduction of the output of the human motor cortex induced by a fatiguing muscle contractionV Di Lazzaro, A Oliviero, P A Tonali, et al.
Journal of the Neurological Sciences|January 7, 2010
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiencyM Luigetti, A Pizzuti, S Bartoletti, et al.
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