Prevalence and phenotype of the c.1529C>T SPG7 variant in adult‐onset cerebellar ataxia in Italy
Mancini, C., Giorgio, E., Rubegni, A., Pradotto, L., Bagnoli, S., Rubino, E., Prontera, P., Cavalieri, S., Di Gregorio, E., Ferrero, M., Pozzi, E., Riberi, E., Ferrero, P., Nigro, P., Mauro, A., Zibetti, M., Tessa, A., Barghigiani, M., Antenora, A., Sirchia, F., Piacentini, S., Silvestri, G., De Michele, G., Filla, A., Orsi, L., Santorelli, F. M., Brusco, A.
Published in European journal of neurology (01.01.2019)
Published in European journal of neurology (01.01.2019)
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60. The effect of cerebellar degeneration on human sensori-motor plasticity
Dubbioso, R, Pellegrino, G, Antenora, A, De Michele, G, Filla, A, Santoro, L, Manganelli, F
Published in Clinical neurophysiology (01.04.2016)
Published in Clinical neurophysiology (01.04.2016)
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Cognitive assessment in multiple system atrophy cerebellar type
Lieto, M, Saccà, F, Costabile, T, Antenora, A, Abate, F, Liguori, A, De Michele, G, Filla, A
Published in Journal of the neurological sciences (15.10.2015)
Published in Journal of the neurological sciences (15.10.2015)
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Intrafamilial phenotypic variability in Spinocerebellar ataxia type 8
Antenora, A, Peluso, S, Esposito, M, De Rosa, A, Brusco, A, Filla, A, De Michele, G
Published in Journal of the neurological sciences (15.10.2015)
Published in Journal of the neurological sciences (15.10.2015)
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Metabolic Ataxias in Adults
Antenora, A, Filla, A, Santorelli, F M, Peluso, S, Sacca, F, De Michele, G
Published in Current molecular medicine (01.01.2014)
Published in Current molecular medicine (01.01.2014)
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Hereditary spastic paraplegia type 5: natural history, biomarkers and a randomized controlled trial
Schöls, Ludger, Rattay, Tim W, Martus, Peter, Meisner, Christoph, Baets, Jonathan, Fischer, Imma, Jägle, Christine, Fraidakis, Matthew J, Martinuzzi, Andrea, Saute, Jonas Alex, Scarlato, Marina, Antenora, Antonella, Stendel, Claudia, Höflinger, Philip, Lourenco, Charles Marques, Abreu, Lisa, Smets, Katrien, Paucar, Martin, Deconinck, Tine, Bis, Dana M, Wiethoff, Sarah, Bauer, Peter, Arnoldi, Alessia, Marques, Wilson, Jardim, Laura Bannach, Hauser, Stefan, Criscuolo, Chiara, Filla, Alessandro, Züchner, Stephan, Bassi, Maria Teresa, Klopstock, Thomas, De Jonghe, Peter, Björkhem, Ingemar, Schüle, Rebecca
Published in Brain (London, England : 1878) (01.12.2017)
Published in Brain (London, England : 1878) (01.12.2017)
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The magnetic apraxia of Denny-Brown
Published in Neurology
(11.04.2017)
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Reversible valproate-induced subacute encephalopathy caused by a mitochondrial DNA variant
De Michele, G., Sorrentino, P., Ruggiero, L., De Michele, G., Peluso, S., Antenora, A., Nesti, C., Santorelli, F.M., Filla, A.
Published in Journal of the neurological sciences (15.10.2017)
Published in Journal of the neurological sciences (15.10.2017)
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Longitudinal study of a cohort of MSA-C patients in south Italy: Survival and clinical features
Lieto, M., Roca, A., Antenora, A., Peluso, S., Bellofatto, M., Bruzzese, D., De Michele, G., Filla, A.
Published in Journal of the neurological sciences (15.10.2017)
Published in Journal of the neurological sciences (15.10.2017)
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Journal Article
Prevalence and phenotype of the c.1529C>T SPG 7 variant in adult‐onset cerebellar ataxia in Italy
Mancini, C., Giorgio, E., Rubegni, A., Pradotto, L., Bagnoli, S., Rubino, E., Prontera, P., Cavalieri, S., Di Gregorio, E., Ferrero, M., Pozzi, E., Riberi, E., Ferrero, P., Nigro, P., Mauro, A., Zibetti, M., Tessa, A., Barghigiani, M., Antenora, A., Sirchia, F., Piacentini, S., Silvestri, G., De Michele, G., Filla, A., Orsi, L., Santorelli, F. M., Brusco, A.
Published in European journal of neurology (01.01.2019)
Published in European journal of neurology (01.01.2019)
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Parkinsonism may be part of the symptom complex of DOOR syndrome
Bilo, Leonilda, Peluso, Silvio, Antenora, Antonella, De Rosa, Anna, Auletta, Gennaro, Pappatà, Sabina, De Michele, Giuseppe
Published in Parkinsonism & related disorders (01.04.2014)
Published in Parkinsonism & related disorders (01.04.2014)
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