• 199 Citations
  • 7 h-Index
20002019
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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.

  • 2 Similar Profiles
Mutation Medicine & Life Sciences
Italy Medicine & Life Sciences
Prealbumin Medicine & Life Sciences
Multicenter Studies Medicine & Life Sciences
CADASIL Medicine & Life Sciences
Longitudinal Studies Medicine & Life Sciences
Safety Medicine & Life Sciences
Parkinson Disease Medicine & Life Sciences

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Research Output 2000 2019

  • 199 Citations
  • 7 h-Index
  • 26 Article

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

Cerebellar Ataxia
Homozygote
Ataxia
Heterozygote
Italy
4 Citations (Scopus)

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

Amyloidosis
Genetic Association Studies
Mutation
Transcriptome
Genes
3 Citations (Scopus)

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

Prealbumin
Population
Genetic Association Studies
Atrial Appendage
Inborn Genetic Diseases
4 Citations (Scopus)

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

Cerebellar Ataxia
Phenotype
Mutation
Genes
Missense Mutation

Erratum to: Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area (Journal of Neurology, DOI: 10.1007/s00415-016-8064-9)

Cortese, A., Vita, G., Luigetti, M., Russo, M., Bisogni, G., Sabatelli, M., Manganelli, F., Santoro, L., Cavallaro, T., Fabrizi, G. M., Schenone, A., Grandis, M., Gemelli, C., Mauro, A., Pradotto, L., Gentile, L., Stancanelli, C., Lozza, A., Perlini, S., Piscosquito, G. & 4 others, Calabrese, D., Mazzeo, A., Obici, L. P. & Pareyson, D., May 1 2016, In : Journal of Neurology. 263, 5, p. 925-926 2 p.

Research output: Contribution to journalArticle