Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 78

1.

Expanding the spectrum of genes responsible for hereditary motor neuropathies.

Previtali SC, Zhao E, Lazarevic D, Pipitone GB, Fabrizi GM, Manganelli F, Mazzeo A, Pareyson D, Schenone A, Taroni F, Vita G, Bellone E, Ferrarini M, Garibaldi M, Magri S, Padua L, Pennisi E, Pisciotta C, Riva N, Scaioli V, Scarlato M, Tozza S, Geroldi A, Jordanova A, Ferrari M, Molineris I, Reilly MM, Comi G, Carrera P, Devoto M, Bolino A.

J Neurol Neurosurg Psychiatry. 2019 Oct;90(10):1171-1179. doi: 10.1136/jnnp-2019-320717. Epub 2019 Jun 5.

PMID:
31167812
2.

Progressive myoclonus epilepsy caused by a gain-of-function KCNA2 mutation.

Canafoglia L, Castellotti B, Ragona F, Freri E, Granata T, Chiapparini L, Gellera C, Scaioli V, Franceschetti S, DiFrancesco JC.

Seizure. 2019 Feb;65:106-108. doi: 10.1016/j.seizure.2019.01.005. Epub 2019 Jan 8. No abstract available.

PMID:
30660924
3.

Sensory trick in task-specific tremor.

Bagella CF, Romito LM, Scaioli V, Elia AE.

Neurol Sci. 2017 Jul;38(7):1341-1342. doi: 10.1007/s10072-017-2913-x. Epub 2017 Mar 18. No abstract available.

PMID:
28315971
4.

Movement-activated cortical myoclonus in Dravet syndrome.

Canafoglia L, Ragona F, Panzica F, Piazza E, Freri E, Binelli S, Scaioli V, Avanzini G, Granata T, Franceschetti S.

Epilepsy Res. 2017 Feb;130:47-52. doi: 10.1016/j.eplepsyres.2017.01.007. Epub 2017 Jan 19.

PMID:
28126647
5.

When it rains it pours: amyotrophic lateral sclerosis concealed with Isaac's syndrome.

Mantero V, Rigamonti A, Basso F, Stanzani L, Scaioli V, Salmaggi A.

Neurol Sci. 2016 Jul;37(7):1181-3. doi: 10.1007/s10072-016-2528-7. Epub 2016 Feb 25. No abstract available.

PMID:
26914588
6.

Spinal and bulbar muscular atrophy and Charcot-Marie-Tooth type 1A: Co-existence of two rare neuromuscular genetic diseases in the same patient.

Sagnelli A, Scaioli V, Piscosquito G, Salsano E, Dalla Bella E, Gellera C, Pareyson D.

Neuromuscul Disord. 2015 Oct;25(10):800-1. doi: 10.1016/j.nmd.2015.07.015. Epub 2015 Jul 29.

PMID:
26298608
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.

Neurology. 2015 Jul 28;85(4):316-24. doi: 10.1212/WNL.0000000000001784. Epub 2015 Jun 26.

8.

Significance of multiple neurophysiological measures in patients with chronic disorders of consciousness.

Rossi Sebastiano D, Panzica F, Visani E, Rotondi F, Scaioli V, Leonardi M, Sattin D, D'Incerti L, Parati E, Ferini Strambi L, Franceschetti S.

Clin Neurophysiol. 2015 Mar;126(3):558-64. doi: 10.1016/j.clinph.2014.07.004. Epub 2014 Jul 11.

PMID:
25082091
9.

A new mutation in GJC2 associated with subclinical leukodystrophy.

Abrams CK, Scherer SS, Flores-Obando R, Freidin MM, Wong S, Lamantea E, Farina L, Scaioli V, Pareyson D, Salsano E.

J Neurol. 2014 Oct;261(10):1929-38. doi: 10.1007/s00415-014-7429-1. Epub 2014 Jul 25.

10.

Recurrent generalized seizures, visual loss, and palinopsia as phenotypic features of neuronal ceroid lipofuscinosis due to progranulin gene mutation.

Canafoglia L, Morbin M, Scaioli V, Pareyson D, D'Incerti L, Fugnanesi V, Tagliavini F, Berkovic SF, Franceschetti S.

Epilepsia. 2014 Jun;55(6):e56-9. doi: 10.1111/epi.12632. Epub 2014 Apr 29.

11.

Marked phenotypic variability in two siblings with congenital myasthenic syndrome due to mutations in MUSK.

Maggi L, Brugnoni R, Scaioli V, Winden TL, Morandi L, Engel AG, Mantegazza R, Bernasconi P.

J Neurol. 2013 Oct 12. [Epub ahead of print] No abstract available.

12.

Giant SEPs and SEP-recovery function in Unverricht-Lundborg disease.

Visani E, Canafoglia L, Rossi Sebastiano D, Agazzi P, Panzica F, Scaioli V, Ciano C, Franceschetti S.

Clin Neurophysiol. 2013 May;124(5):1013-8. doi: 10.1016/j.clinph.2012.11.011. Epub 2012 Dec 29.

PMID:
23276489
13.

Tethered cord: natural history, surgical outcome and risk for Chiari malformation 1 (CM1): a review of 110 detethering.

Valentini LG, Selvaggio G, Visintini S, Erbetta A, Scaioli V, Solero CL.

Neurol Sci. 2011 Dec;32 Suppl 3:S353-6. doi: 10.1007/s10072-011-0745-7. Review.

14.

Characterization of severe action myoclonus in sialidoses.

Canafoglia L, Franceschetti S, Uziel G, Ciano C, Scaioli V, Guerrini R, Visani E, Panzica F.

Epilepsy Res. 2011 Mar;94(1-2):86-93. doi: 10.1016/j.eplepsyres.2011.01.013. Epub 2011 Feb 16.

PMID:
21330109
15.

Lower limb areflexia without central and peripheral conduction abnormalities is highly suggestive of Gerstmann-Sträussler-Scheinker disease Pro102Leu.

Salsano E, Fancellu R, Di Fede G, Ciano C, Scaioli V, Nanetti L, Politi LS, Tagliavini F, Mariotti C, Pareyson D.

J Neurol Sci. 2011 Mar 15;302(1-2):85-8. doi: 10.1016/j.jns.2010.11.019. Epub 2010 Dec 16.

PMID:
21167505
16.

Four novel cases of periaxin-related neuropathy and review of the literature.

Marchesi C, Milani M, Morbin M, Cesani M, Lauria G, Scaioli V, Piccolo G, Fabrizi GM, Cavallaro T, Taroni F, Pareyson D.

Neurology. 2010 Nov 16;75(20):1830-8. doi: 10.1212/WNL.0b013e3181fd6314. Review.

PMID:
21079185
17.

Myoclonus in Creutzfeldt-Jakob disease: polygraphic and video-electroencephalography assessment of 109 patients.

Binelli S, Agazzi P, Canafoglia L, Scaioli V, Panzica F, Visani E, Di Fede G, Giaccone G, Bizzi A, Bugiani O, Avanzini G, Tagliavini F, Franceschetti S.

Mov Disord. 2010 Dec 15;25(16):2818-27. doi: 10.1002/mds.23397.

PMID:
20939057
18.

Event-related potential (ERP) markers of melodic processing: The N2 component is modulated by structural complexity, not by melodic 'meaningfulness'.

Minati L, Salvatoni L, Rosazza C, Pietrocini E, Visani E, Panzica F, Scaioli V, Avanzini G, Franceschetti S.

Brain Res Bull. 2010 Aug 30;83(1-2):23-8. doi: 10.1016/j.brainresbull.2010.06.011. Epub 2010 Jun 30.

PMID:
20600678
19.

Slowly progressive sensory hemisyndrome: unusual presentation of paraneoplastic sensory neuronopathy.

Nanetti L, Lauria G, Scaioli V, Marchesi C, Salsano E, Lombardi R, Pareyson D.

J Peripher Nerv Syst. 2010 Mar;15(1):73-4. doi: 10.1111/j.1529-8027.2010.00254.x. No abstract available.

PMID:
20433608
20.

Vitamin E neuroprotection for cisplatin neuropathy: a randomized, placebo-controlled trial.

Pace A, Giannarelli D, Galiè E, Savarese A, Carpano S, Della Giulia M, Pozzi A, Silvani A, Gaviani P, Scaioli V, Jandolo B, Bove L, Cognetti F.

Neurology. 2010 Mar 2;74(9):762-6. doi: 10.1212/WNL.0b013e3181d5279e.

PMID:
20194916
21.

A Multicentre Database for Normative Brainstem Auditory Evoked Potentials (BAEPs) in Children: Methodology for Data Collection and Evaluation.

Scaioli V, Brinciotti M, Di Capua M, Lori S, Janes A, Pastorino G, Peruzzi C, Sergi P, Suppiej A.

Open Neurol J. 2009 Oct 9;3:72-84. doi: 10.2174/1874205X00903010072.

22.

Systemic sagopilone (ZK-EPO) treatment of patients with recurrent malignant gliomas.

Silvani A, Gaviani P, Fiumani A, Scaioli V, Lamperti E, Eoli M, Botturi A, Salmaggi A.

J Neurooncol. 2009 Oct;95(1):61-64. doi: 10.1007/s11060-009-9890-8. Epub 2009 Apr 21.

PMID:
19381446
23.

Functional MRI/event-related potential study of sensory consonance and dissonance in musicians and nonmusicians.

Minati L, Rosazza C, D'Incerti L, Pietrocini E, Valentini L, Scaioli V, Loveday C, Bruzzone MG.

Neuroreport. 2009 Jan 7;20(1):87-92. doi: 10.1097/WNR.0b013e32831af235.

PMID:
19033878
24.

FMRI/ERP of musical syntax: comparison of melodies and unstructured note sequences.

Minati L, Rosazza C, D'Incerti L, Pietrocini E, Valentini L, Scaioli V, Loveday C, Bruzzone MG.

Neuroreport. 2008 Sep 17;19(14):1381-5. doi: 10.1097/WNR.0b013e32830c694b.

PMID:
18766016
25.

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.

Mov Disord. 2008 Oct 30;23(14):2041-8. doi: 10.1002/mds.22256.

PMID:
18759336
26.

Spatial correspondence between functional MRI (fMRI) activations and cortical current density maps of event-related potentials (ERP): a study with four tasks.

Minati L, Rosazza C, Zucca I, D'Incerti L, Scaioli V, Bruzzone MG.

Brain Topogr. 2008 Dec;21(2):112-27. doi: 10.1007/s10548-008-0064-3. Epub 2008 Aug 29.

PMID:
18758934
27.

Two cases of thymoma-associated myasthenia gravis without antibodies to the acetylcholine receptor.

Maggi L, Andreetta F, Antozzi C, Confalonieri P, Cornelio F, Scaioli V, Mantegazza R.

Neuromuscul Disord. 2008 Aug;18(8):678-80. doi: 10.1016/j.nmd.2008.06.368. Epub 2008 Jul 25.

PMID:
18657424
28.

High-frequency rhythmic cortical myoclonus in a long-surviving patient with nonketotic hypergylcemia.

Mastrangelo M, Canafoglia L, Franceschetti S, Oppezzo C, Mosca F, Menni F, Parini R, Ciano C, Scaioli V, Panzica F.

J Child Neurol. 2008 Mar;23(3):321-4. doi: 10.1177/0883073807308699. Epub 2008 Jan 8.

PMID:
18182648
29.

Rapid progression of late onset axonal Charcot-Marie-Tooth disease associated with a novel MPZ mutation in the extracellular domain.

Laurà M, Milani M, Morbin M, Moggio M, Ripolone M, Jann S, Scaioli V, Taroni F, Pareyson D.

J Neurol Neurosurg Psychiatry. 2007 Nov;78(11):1263-6.

30.
31.

Movement-related desynchronization-synchronization (ERD/ERS) in patients with Unverricht-Lundborg disease.

Visani E, Agazzi P, Canafoglia L, Panzica F, Ciano C, Scaioli V, Avanzini G, Franceschetti S.

Neuroimage. 2006 Oct 15;33(1):161-8. Epub 2006 Aug 10.

PMID:
16904345
32.

Clinical and electrophysiological aspects of Charcot-Marie-Tooth disease.

Pareyson D, Scaioli V, Laurà M.

Neuromolecular Med. 2006;8(1-2):3-22. Review.

PMID:
16775364
33.

Rhythmic cortical myoclonus in Niemann-Pick disease type C.

Canafoglia L, Bugiani M, Uziel G, Dalla Bernardina B, Ciano C, Scaioli V, Avanzini G, Franceschetti S, Panzica F.

Mov Disord. 2006 Sep;21(9):1453-6.

PMID:
16755579
34.

Novel mutations in the HSN2 gene causing hereditary sensory and autonomic neuropathy type II.

Coen K, Pareyson D, Auer-Grumbach M, Buyse G, Goemans N, Claeys KG, Verpoorten N, Laurà M, Scaioli V, Salmhofer W, Pieber TR, Nelis E, De Jonghe P, Timmerman V.

Neurology. 2006 Mar 14;66(5):748-51.

PMID:
16534117
35.

Electrophysiological evaluation of visual pathways in paclitaxel-treated patients.

Scaioli V, Caraceni A, Martini C, Curzi S, Capri G, Luca G.

J Neurooncol. 2006 Mar;77(1):79-87. Epub 2005 Aug 25.

PMID:
16132528
36.

FVEPs in Creutzfeldt-Jacob disease: waveforms and interaction with the periodic EEG pattern assessed by single sweep analysis.

Visani E, Agazzi P, Scaioli V, Giaccone G, Binelli S, Canafoglia L, Panzica F, Tagliavini F, Bugiani O, Avanzini G, Franceschetti S.

Clin Neurophysiol. 2005 Apr;116(4):895-904. Epub 2005 Jan 13.

PMID:
15792899
37.

Sensorimotor cortex excitability in Unverricht-Lundborg disease and Lafora body disease.

Canafoglia L, Ciano C, Panzica F, Scaioli V, Zucca C, Agazzi P, Visani E, Avanzini G, Franceschetti S.

Neurology. 2004 Dec 28;63(12):2309-15.

PMID:
15623692
38.

Enigmatic osteomyelitis and bilateral upper limb palsy in a neonate.

Estienne M, Scaioli V, Zibordi F, Angelini L.

Pediatr Neurol. 2005 Jan;32(1):56-9.

PMID:
15607607
39.

Neurovascular decompression in trigeminal neuralgia: role of intraoperative neurophysiological monitoring in the learning period.

Brock S, Scaioli V, Ferroli P, Broggi G.

Stereotact Funct Neurosurg. 2004;82(5-6):199-206. Epub 2004 Nov 30.

PMID:
15583464
40.

Subcortical nodular heterotopia: a functional MRI and somatosensory evoked potentials study.

Villani F, Vitali P, Scaioli V, Rodriguez G, Rosa M, Granata T, Avanzini G, Spreafico R, Angelini L.

Neurol Sci. 2004 Oct;25(4):225-9.

PMID:
15549509
41.
42.

Unusual neurophysiological and immunological findings in myasthenia gravis: a case report.

Scaioli V, Andreetta F, Mantegazza R.

J Peripher Nerv Syst. 2004 Jun;9(2):92-7.

PMID:
15104696
43.

Rhythmic cortical myoclonus in a case of HIV-related encephalopathy.

Canafoglia L, Panzica F, Franceschetti S, Carriero MR, Ciano C, Scaioli V, Chiapparini L, Visani E, Avanzini G.

Mov Disord. 2003 Dec;18(12):1533-8.

PMID:
14673894
44.

Neurophysiological features in relation to clinical signs in clinically diagnosed corticobasal degeneration.

Monza D, Ciano C, Scaioli V, Soliveri P, Carella F, Avanzini G, Girotti F.

Neurol Sci. 2003 Apr;24(1):16-23.

PMID:
12754652
45.

Repetitive nerve stimulation and muscle membrane excitability: case report and review.

Scaioli V, Morandi L.

Electromyogr Clin Neurophysiol. 2002 Sep;42(6):333-6.

PMID:
12224470
46.

Papillitis as an onset sign of Leber's hereditary optic neuropathy: a case report.

Pantaleoni C, D'Arrigo S, Bagnasco I, Piozzi E, Carrara F, Scaioli V, Riva D.

Brain Dev. 2001 Mar;23(2):125-7.

PMID:
11248462
47.

Cortical reorganization and seizure generation in dysplastic cortex.

Avanzini G, Spreafico R, Franceschetti S, Sancini G, Battaglia G, Scaioli V.

Int Rev Neurobiol. 2001;45:159-72. Review. No abstract available.

PMID:
11130897
48.
49.

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.

Ital J Neurol Sci. 1998 Oct;19(5):291-300.

PMID:
10933449
50.

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.

Muscle Nerve. 1998 Dec;21(12):1686-91.

PMID:
9843070

Supplemental Content

Loading ...
Support Center