Scaioli V - Search Results

1

A neurophysiological study of myoclonus in patients with DYT11 myoclonus-dystonia syndrome.

Marelli C, Canafoglia L, Zibordi F, Ciano C, Visani E, Zorzi G, Garavaglia B, Barzaghi C, Albanese A, Soliveri P, Leone M, Panzica F, Scaioli V, Pincherle A, Nardocci N, Franceschetti S. Marelli C, et al. Among authors: scaioli v. Mov Disord. 2008 Oct 30;23(14):2041-8. doi: 10.1002/mds.22256. Mov Disord. 2008. PMID: 18759336

2

Short-term neurophysiological monitoring in multiple sclerosis bouts. Evaluation of steroid treatment.

Scaioli V, Milanese C, Salmaggi A, LaMantia L, Campi A, Eoli M, Panzica F. Scaioli V, et al. Ital J Neurol Sci. 1992 Mar;13(2):107-12. doi: 10.1007/BF02226957. Ital J Neurol Sci. 1992. PMID: 1592569

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

Exteroceptive reflexes in dystonia: a study of the recovery cycle of the R2 component of the blink reflex and of the exteroceptive suppression of the contracting sternocleidomastoid muscle in blepharospasm and torticollis.

Carella F, Ciano C, Musicco M, Scaioli V. Carella F, et al. Among authors: scaioli v. Mov Disord. 1994 Mar;9(2):183-7. doi: 10.1002/mds.870090210. Mov Disord. 1994. PMID: 8196680

5

Adult onset myoclonic Huntington's disease.

Carella F, Scaioli V, Ciano C, Binelli S, Oliva D, Girotti F. Carella F, et al. Among authors: scaioli v. Mov Disord. 1993 Apr;8(2):201-5. doi: 10.1002/mds.870080216. Mov Disord. 1993. PMID: 8474490

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

Myoclonus in corticobasal degeneration.

Carella F, Ciano C, Panzica F, Scaioli V. Carella F, et al. Among authors: scaioli v. Mov Disord. 1997 Jul;12(4):598-603. doi: 10.1002/mds.870120419. Mov Disord. 1997. PMID: 9251081

8

Detection of hereditary neuropathy with liability to pressure palsies among patients with acute painless mononeuropathy or plexopathy.

Pareyson D, Solari A, Taroni F, Botti S, Fallica E, Scaioli V, Ciano C, Sghirlanzoni A. Pareyson D, et al. Among authors: scaioli v. Muscle Nerve. 1998 Dec;21(12):1686-91. doi: 10.1002/(sici)1097-4598(199812)21:12<1686::aid-mus10>3.0.co;2-z. Muscle Nerve. 1998. PMID: 9843070

9

Utility of multimodal evoked potential study and electroencephalography in mitochondrial encephalomyopathy.

Scaioli V, Antozzi C, Villani F, Rimoldi M, Zeviani M, Panzica F, Avanzini G. Scaioli V, et al. Ital J Neurol Sci. 1998 Oct;19(5):291-300. doi: 10.1007/BF00713855. Ital J Neurol Sci. 1998. PMID: 10933449

10

A pathophysiological study of neuronal ceroid lipofuscinoses in 17 patients: critical review and methodological proposal.

Scaioli V, Nardocci N. Scaioli V, et al. Neurol Sci. 2000;21(3 Suppl):S89-92. doi: 10.1007/s100720070046. Neurol Sci. 2000. PMID: 11073234

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