20002019

Research output per year

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Fingerprint Dive into the research topics where Luca Pradotto is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

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Research Output

Early weight loss in amyotrophic lateral sclerosis: Outcome relevance and clinical correlates in a population-based cohort

Piemonte and Valle d’Aosta Register for ALS (PARALS), Jun 1 2019, In : Journal of Neurology, Neurosurgery and Psychiatry. 90, 6, p. 666-673 8 p.

Research output: Contribution to journalArticle

  • 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. & 7 others, Piacentini, S., Silvestri, G., De Michele, G., Filla, A., Orsi, L., Santorelli, F. M. & Brusco, A., Jan 2019, In : European Journal of Neurology. 26, 1, p. 80-86 7 p.

    Research output: Contribution to journalArticle

  • Non-coding variants contribute to the clinical heterogeneity of TTR amyloidosis

    Iorio, A., De Lillo, A., De Angelis, F., Di Girolamo, M., Luigetti, M., Sabatelli, M., Pradotto, L., Mauro, A., Mazzeo, A., Stancanelli, C., Perfetto, F., Frusconi, S., My, F., Manfellotto, D., Fuciarelli, M. & Polimanti, R., Sep 1 2017, In : European Journal of Human Genetics. 25, 9, p. 1055-1060 6 p.

    Research output: Contribution to journalArticle

  • Population diversity of the genetically determined TTR expression in human tissues and its implications in TTR amyloidosis

    Iorio, A., De Angelis, F., Di Girolamo, M., Luigetti, M., Pradotto, L. G., Mazzeo, A., Frusconi, S., My, F., Manfellotto, D., Fuciarelli, M. & Polimanti, R., Mar 23 2017, In : BMC Genomics. 18, 1, p. 254

    Research output: Contribution to journalArticle

  • Episodic ataxia and SCA6 within the same family due to the D302N CACNA1A gene mutation

    Pradotto, L., Mencarelli, M., Bigoni, M., Milesi, A., Di Blasio, A. & Mauro, A., Dec 15 2016, In : Journal of the Neurological Sciences. 371, p. 81-84 4 p.

    Research output: Contribution to journalArticle