Scaioli V - Search Results

1

Visual involvement in Friedreich's ataxia: PERG and VEP study.

Pinto F, Amantini A, de Scisciolo G, Scaioli V, Guidi L, Frosini R. Pinto F, et al. Among authors: scaioli v. Eur Neurol. 1988;28(5):246-51. doi: 10.1159/000116277. Eur Neurol. 1988. PMID: 3224618

2

Peripheral nerve involvement in Churg-Strauss syndrome.

Marazzi R, Pareyson D, Boiardi A, Corbo M, Scaioli V, Sghirlanzoni A. Marazzi R, et al. Among authors: scaioli v. J Neurol. 1992 Jul;239(6):317-21. doi: 10.1007/BF00867587. J Neurol. 1992. PMID: 1324984

3

Focal reflex myoclonus in corticobasal degeneration.

Carella F, Scaioli V, Franceschetti S, Girotti F, Giovannini P, Ciano C, Caraceni T. Carella F, et al. Among authors: scaioli v. Funct Neurol. 1991 Apr-Jun;6(2):165-70. Funct Neurol. 1991. PMID: 1916457

4

Double-blind randomized trial of ACTH versus dexamethasone versus methylprednisolone in multiple sclerosis bouts. Clinical, cerebrospinal fluid and neurophysiological results.

Milanese C, La Mantia L, Salmaggi A, Campi A, Eoli M, Scaioli V, Nespolo A, Corridori F. Milanese C, et al. Among authors: scaioli v. Eur Neurol. 1989;29(1):10-4. doi: 10.1159/000116368. Eur Neurol. 1989. PMID: 2540005 Clinical Trial.

5

Electrophysiological studies of the visual system in myotonic dystrophy.

Pinto F, Amantini A, de Scisciolo G, Scaioli V, Frosini R, Pizzi A, Marconi G. Pinto F, et al. Among authors: scaioli v. Acta Neurol Scand. 1987 Nov;76(5):351-8. doi: 10.1111/j.1600-0404.1987.tb03593.x. Acta Neurol Scand. 1987. PMID: 3425222

6

Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion.

Pareyson D, Scaioli V, Taroni F, Botti S, Lorenzetti D, Solari A, Ciano C, Sghirlanzoni A. Pareyson D, et al. Among authors: scaioli v. Neurology. 1996 Apr;46(4):1133-7. doi: 10.1212/wnl.46.4.1133. Neurology. 1996. PMID: 8780105

7

Electroclinical spectrum of the neuronal ceroid lipofuscinoses associated with CLN6 mutations.

Canafoglia L, Gilioli I, Invernizzi F, Sofia V, Fugnanesi V, Morbin M, Chiapparini L, Granata T, Binelli S, Scaioli V, Garavaglia B, Nardocci N, Berkovic SF, Franceschetti S. Canafoglia L, et al. Among authors: scaioli v. Neurology. 2015 Jul 28;85(4):316-24. doi: 10.1212/WNL.0000000000001784. Epub 2015 Jun 26. Neurology. 2015. PMID: 26115733 Free PMC article.

8

Nerve conduction velocity in CMT1A: what else can we tell?

Manganelli F, Pisciotta C, Reilly MM, Tozza S, Schenone A, Fabrizi GM, Cavallaro T, Vita G, Padua L, Gemignani F, Laurà M, Hughes RA, Solari A, Pareyson D, Santoro L; CMT-TRIAAL and CMT-TRAUK Group. Manganelli F, et al. Eur J Neurol. 2016 Oct;23(10):1566-71. doi: 10.1111/ene.13079. Epub 2016 Jul 14. Eur J Neurol. 2016. PMID: 27412484 Free PMC article. Clinical Trial.

9

Adult-onset leukodystrophy with vanishing white matter: a case series of 19 patients.

Benzoni C, Moscatelli M, Farina L, Magri S, Ciano C, Scaioli V, Alverà S, Cammarata G, Bianchi-Marzoli S, Castellani M, Zito FM, Marotta G, Piacentini S, Villacara A, Mantegazza R, Gellera C, Durães J, Gouveia A, Matos A, do Carmo Macário M, Pareyson D, Taroni F, Di Bella D, Salsano E. Benzoni C, et al. Among authors: scaioli v. J Neurol. 2023 Sep;270(9):4219-4234. doi: 10.1007/s00415-023-11762-7. Epub 2023 May 12. J Neurol. 2023. PMID: 37171481

10

F response and somatosensory and brainstem auditory evoked potential studies in HMSN type I and II.

Scaioli V, Pareyson D, Avanzini G, Sghirlanzoni A. Scaioli V, et al. J Neurol Neurosurg Psychiatry. 1992 Nov;55(11):1027-31. doi: 10.1136/jnnp.55.11.1027. J Neurol Neurosurg Psychiatry. 1992. PMID: 1469398 Free PMC article.

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