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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1987 1
1988 3
1989 3
1990 1
1991 4
1992 4
1993 2
1994 2
1995 5
1996 2
1997 1
1998 2
2000 1
2001 2
2002 1
2003 2
2004 5
2005 3
2006 5
2007 2
2008 6
2009 3
2010 6
2011 3
2012 1
2013 2
2014 3
2015 3
2016 1
2017 2
2019 3
2020 3
2022 0
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Article attribute
Article type
Publication date

Search Results

81 results
Results by year
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Page 1
Guillain-Barré Syndrome After Exposure to Mercury.
Pigatto PD, Scaioli V, Guzzi G. Pigatto PD, et al. Among authors: scaioli v. J Child Neurol. 2020 Jan;35(1):84-85. doi: 10.1177/0883073819872913. Epub 2019 Sep 27. J Child Neurol. 2020. PMID: 31559911 No abstract available.
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. Canafoglia L, et al. Among authors: scaioli v. Epilepsy Res. 2017 Feb;130:47-52. doi: 10.1016/j.eplepsyres.2017.01.007. Epub 2017 Jan 19. Epilepsy Res. 2017. PMID: 28126647
Sensory trick in task-specific tremor.
Bagella CF, Romito LM, Scaioli V, Elia AE. Bagella CF, et al. Among authors: scaioli v. Neurol Sci. 2017 Jul;38(7):1341-1342. doi: 10.1007/s10072-017-2913-x. Epub 2017 Mar 18. Neurol Sci. 2017. PMID: 28315971 No abstract available.
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
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. Previtali SC, et al. Among authors: scaioli v. J Neurol Neurosurg Psychiatry. 2019 Oct;90(10):1171-1179. doi: 10.1136/jnnp-2019-320717. Epub 2019 Jun 5. J Neurol Neurosurg Psychiatry. 2019. PMID: 31167812 Free article.
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. Canafoglia L, et al. Among authors: scaioli v. Seizure. 2019 Feb;65:106-108. doi: 10.1016/j.seizure.2019.01.005. Epub 2019 Jan 8. Seizure. 2019. PMID: 30660924 Free article. No abstract available.
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. Marchesi C, et al. Among authors: scaioli v. Neurology. 2010 Nov 16;75(20):1830-8. doi: 10.1212/WNL.0b013e3181fd6314. Neurology. 2010. PMID: 21079185 Review.
Early Parkinsonism in a Senegalese girl with Lafora disease.
Ragona F, Canafoglia L, Castellotti B, Solazzi R, Gabbiadini S, Freri E, Scaioli V, DiFrancesco JC, Gellera C, Granata T. Ragona F, et al. Among authors: scaioli v. Epileptic Disord. 2020 Apr 1;22(2):233-236. doi: 10.1684/epd.2020.1150. Epileptic Disord. 2020. PMID: 32301727 Free article.
81 results