Binelli S - Search Results

1

Infantile neuroaxonal dystrophy: clinical spectrum and diagnostic criteria.

Nardocci N, Zorzi G, Farina L, Binelli S, Scaioli W, Ciano C, Verga L, Angelini L, Savoiardo M, Bugiani O. Nardocci N, et al. Among authors: binelli s. Neurology. 1999 Apr 22;52(7):1472-8. doi: 10.1212/wnl.52.7.1472. Neurology. 1999. PMID: 10227637

2

Neuronal ceroid-lipofuscinosis: a clinical and morphological study of 19 patients.

Nardocci N, Verga ML, Binelli S, Zorzi G, Angelini L, Bugiani O. Nardocci N, et al. Among authors: binelli s. Am J Med Genet. 1995 Jun 5;57(2):137-41. doi: 10.1002/ajmg.1320570205. Am J Med Genet. 1995. PMID: 7668317

3

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: binelli s. Neurology. 2015 Jul 28;85(4):316-24. doi: 10.1212/WNL.0000000000001784. Epub 2015 Jun 26. Neurology. 2015. PMID: 26115733 Free PMC article.

4

Periodic electroencephalogram complexes in a patient with variant Creutzfeldt-Jakob disease.

Binelli S, Agazzi P, Giaccone G, Will RG, Bugiani O, Franceschetti S, Tagliavini F. Binelli S, et al. Ann Neurol. 2006 Feb;59(2):423-7. doi: 10.1002/ana.20768. Ann Neurol. 2006. PMID: 16437565

5

Paroxysmal non-epileptic motor events in childhood: a clinical and video-EEG-polymyographic study.

Canavese C, Canafoglia L, Costa C, Zibordi F, Zorzi G, Binelli S, Franceschetti S, Nardocci N. Canavese C, et al. Among authors: binelli s. Dev Med Child Neurol. 2012 Apr;54(4):334-8. doi: 10.1111/j.1469-8749.2011.04217.x. Epub 2012 Jan 28. Dev Med Child Neurol. 2012. PMID: 22283661 Free article.

6

Burst suppression and impairment of neocortical ontogenesis: electroclinical and neuropathologic findings in two infants with early myoclonic encephalopathy.

Spreafico R, Angelini L, Binelli S, Granata T, Rumi V, Rosti D, Runza L, Bugiani O. Spreafico R, et al. Among authors: binelli s. Epilepsia. 1993 Sep-Oct;34(5):800-8. doi: 10.1111/j.1528-1157.1993.tb02093.x. Epilepsia. 1993. PMID: 8404728

7

A novel phenotype of sporadic Creutzfeldt-Jakob disease.

Giaccone G, Di Fede G, Mangieri M, Limido L, Capobianco R, Suardi S, Grisoli M, Binelli S, Fociani P, Bugiani O, Tagliavini F. Giaccone G, et al. Among authors: binelli s. J Neurol Neurosurg Psychiatry. 2007 Dec;78(12):1379-82. doi: 10.1136/jnnp.2007.115444. J Neurol Neurosurg Psychiatry. 2007. PMID: 18024694 Free PMC article.

8

Progressive myoclonus epilepsies: an electroclinical, biochemical, morphological and molecular genetic study of 17 cases.

Franceschetti S, Antozzi C, Binelli S, Carrara F, Nardocci N, Zeviani M, Avanzini G. Franceschetti S, et al. Among authors: binelli s. Acta Neurol Scand. 1993 Mar;87(3):219-23. doi: 10.1111/j.1600-0404.1993.tb04105.x. Acta Neurol Scand. 1993. PMID: 8386419

9

Partial seizures associated with antiphospholipid antibodies in childhood.

Angelini L, Granata T, Zibordi F, Binelli S, Zorzi G, Besana C. Angelini L, et al. Among authors: binelli s. Neuropediatrics. 1998 Oct;29(5):249-53. doi: 10.1055/s-2007-973570. Neuropediatrics. 1998. PMID: 9810560 Clinical Trial.

10

Movement-activated myoclonus in genetically defined progressive myoclonic epilepsies: EEG-EMG relationship estimated using autoregressive models.

Panzica F, Canafoglia L, Franceschetti S, Binelli S, Ciano C, Visani E, Avanzini G. Panzica F, et al. Among authors: binelli s. Clin Neurophysiol. 2003 Jun;114(6):1041-52. doi: 10.1016/s1388-2457(03)00066-x. Clin Neurophysiol. 2003. PMID: 12804673

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