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Journal of Ultrasound|February 12, 2013
Imaging spectrum of EBV-infection in a young patientP Pelliccia, A Savino, C Cecamore, et al.European Journal of Neurology|May 16, 2000
Acute axonal form of Guillain-Barré syndrome in a multiple sclerosis patient: chance association or linked disorders?E Capello, L Roccatagliata, A Schenone, et al.Journal of Chemotherapy (Florence, Italy)|December 1, 1994
Observations on the tolerance and the paradoxical effect in enterococciM Puntorieri, A Primavera, O Privitera, et al.Journal of Chemotherapy (Florence, Italy)|August 1, 1992
Microbiological considerations of the etiological agents of lower respiratory tract infectionsM B Pellegrino, A Privitera, A Primavera, et al.Neuroscience Letters|July 26, 1996
Use of cosH1 probe in hereditary neuropathy with liability to pressure palsies: a reliable genetic test for demonstration of identical size of 17p11.2 deletion in unrelated patientsE Bellone, A Schenone, G Mancardi, et al.Neuromuscular Disorders : NMD|March 11, 2000
An Italian family with Ala-47 transthyretin mutation associated with cardiomyopathy and polyneuropathyC Solaro, A Schenone, A Di Sapio, et al.Psychiatry Research|August 1, 1992
Increased right caudate nucleus size in obsessive-compulsive disorder: detection with magnetic resonance imagingS Scarone, C Colombo, S Livian, et al.Neurology|August 3, 1999
A SOD1 gene mutation in a patient with slowly progressing familial ALSS Penco, A Schenone, D Bordo, et al.Electroencephalography and Clinical Neurophysiology|October 1, 1993
Impairment of central motor conduction in diabetic patientsG Abbruzzese, A Schenone, G Scramuzza, et al.Journal of the Neurological Sciences|July 1, 1992
Hereditary motor and sensory neuropathy with deafness, mental retardation and absence of large myelinated fibersG L Mancardi, M Di Rocco, A Schenone, et al.Pageof 12