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

Year Number of Results
2002 3
2003 6
2004 1
2005 1
2006 1
2007 1
2008 7
2009 7
2010 4
2011 2
2012 9
2013 8
2014 10
2015 7
2016 13
2017 13
2018 6
2019 3
2020 8
2021 10
2022 11
2023 7
2024 5

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122 results

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Page 1
Consensus Paper: Revisiting the Symptoms and Signs of Cerebellar Syndrome.
Bodranghien F, Bastian A, Casali C, Hallett M, Louis ED, Manto M, Mariën P, Nowak DA, Schmahmann JD, Serrao M, Steiner KM, Strupp M, Tilikete C, Timmann D, van Dun K. Bodranghien F, et al. Among authors: casali c. Cerebellum. 2016 Jun;15(3):369-91. doi: 10.1007/s12311-015-0687-3. Cerebellum. 2016. PMID: 26105056 Free PMC article. Review.
NGS in Hereditary Ataxia: When Rare Becomes Frequent.
Galatolo D, De Michele G, Silvestri G, Leuzzi V, Casali C, Musumeci O, Antenora A, Astrea G, Barghigiani M, Battini R, Battisti C, Caputi C, Cioffi E, De Michele G, Dotti MT, Fico T, Fiorillo C, Galosi S, Lieto M, Malandrini A, Melone MAB, Mignarri A, Natale G, Pegoraro E, Petrucci A, Ricca I, Riso V, Rossi S, Rubegni A, Scarlatti A, Tinelli F, Trovato R, Tedeschi G, Tessa A, Filla A, Santorelli FM. Galatolo D, et al. Among authors: casali c. Int J Mol Sci. 2021 Aug 6;22(16):8490. doi: 10.3390/ijms22168490. Int J Mol Sci. 2021. PMID: 34445196 Free PMC article.
Neurophysiology of gait.
Serrao M, Ranavolo A, Casali C. Serrao M, et al. Among authors: casali c. Handb Clin Neurol. 2018;154:299-303. doi: 10.1016/B978-0-444-63956-1.00018-7. Handb Clin Neurol. 2018. PMID: 29903447 Review.
Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias.
Cunha P, Petit E, Coutelier M, Coarelli G, Mariotti C, Faber J, Van Gaalen J, Damasio J, Fleszar Z, Tosi M, Rocca C, De Michele G, Minnerop M, Ewenczyk C, Santorelli FM, Heinzmann A, Bird T, Amprosi M, Indelicato E, Benussi A, Charles P, Stendel C, Romano S, Scarlato M, Le Ber I, Bassi MT, Serrano M, Schmitz-Hübsch T, Doss S, Van Velzen GAJ, Thomas Q, Trabacca A, Ortigoza-Escobar JD, D'Arrigo S, Timmann D, Pantaleoni C, Martinuzzi A, Besse-Pinot E, Marsili L, Cioffi E, Nicita F, Giorgetti A, Moroni I, Romaniello R, Casali C, Ponger P, Casari G, De Bot ST, Ristori G, Blumkin L, Borroni B, Goizet C, Marelli C, Boesch S, Anheim M, Filla A, Houlden H, Bertini E, Klopstock T, Synofzik M, Riant F, Zanni G, Magri S, Di Bella D, Nanetti L, Sequeiros J, Oliveira J, Van de Warrenburg B, Schöls L, Taroni F, Brice A, Durr A. Cunha P, et al. Among authors: casali c. Am J Hum Genet. 2023 Jul 6;110(7):1098-1109. doi: 10.1016/j.ajhg.2023.05.009. Epub 2023 Jun 9. Am J Hum Genet. 2023. PMID: 37301203 Free PMC article.
Consensus Paper: Ataxic Gait.
Cabaraux P, Agrawal SK, Cai H, Calabro RS, Casali C, Damm L, Doss S, Habas C, Horn AKE, Ilg W, Louis ED, Mitoma H, Monaco V, Petracca M, Ranavolo A, Rao AK, Ruggieri S, Schirinzi T, Serrao M, Summa S, Strupp M, Surgent O, Synofzik M, Tao S, Terasi H, Torres-Russotto D, Travers B, Roper JA, Manto M. Cabaraux P, et al. Among authors: casali c. Cerebellum. 2023 Jun;22(3):394-430. doi: 10.1007/s12311-022-01373-9. Epub 2022 Apr 12. Cerebellum. 2023. PMID: 35414041
Correction to: Consensus Paper: Ataxic Gait.
Cabaraux P, Agrawal SK, Cai H, Calabro RS, Casali C, Damm L, Doss S, Habas C, Horn AKE, Ilg W, Louis ED, Mitoma H, Monaco V, Petracca M, Ranavolo A, Rao AK, Ruggieri S, Schirinzi T, Serrao M, Summa S, Strupp M, Surgent O, Synofzik M, Tao S, Terasi H, Torres-Russotto D, Travers B, Roper JA, Manto M. Cabaraux P, et al. Among authors: casali c. Cerebellum. 2023 Jun;22(3):431-432. doi: 10.1007/s12311-022-01413-4. Cerebellum. 2023. PMID: 35536510 No abstract available.
Roussy-Lévy syndrome: a case of genotype-phenotype correlation.
Cioffi E, Gioiosa V, Serrao M, Casali C. Cioffi E, et al. Among authors: casali c. Neurol Sci. 2021 Oct;42(10):4357-4358. doi: 10.1007/s10072-021-05451-4. Epub 2021 Jul 7. Neurol Sci. 2021. PMID: 34232402 No abstract available.
122 results