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

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Research Output

Awareness of rare and genetic neurological diseases among italian neurologist. A national survey

Mancuso, M., Filosto, M., Lamperti, C., Musumeci, O., Santorelli, F. M., Servidei, S., Valente, E. M., Zeviani, M., Mancardi, G., Tedeschi, G. & Federico, A., Jan 1 2020, (Accepted/In press) In : Neurological Sciences.

Research output: Contribution to journalArticle

  • Awareness of rare and genetic neurological diseases among italian neurologist. A national survey

    Mancuso, M., Filosto, M., Lamperti, C., Musumeci, O., Santorelli, F. M., Servidei, S., Valente, E. M., Zeviani, M., Mancardi, G., Tedeschi, G. & Federico, A., 2020, In : Neurological Sciences. 41, 6, p. 1567-1570 4 p.

    Research output: Contribution to journalArticle

    Clinical-genetic features and peculiar muscle histopathology in infantile DNM1L-related mitochondrial epileptic encephalopathy

    Verrigni, D., Di Nottia, M., Ardissone, A., Baruffini, E., Nasca, A., Legati, A., Bellacchio, E., Fagiolari, G., Martinelli, D., Fusco, L., Battaglia, D., Trani, G., Versienti, G., Marchet, S., Torraco, A., Rizza, T., Verardo, M., D'Amico, A., Diodato, D., Moroni, I. & 7 others, Lamperti, C., Petrini, S., Moggio, M., Goffrini, P., Ghezzi, D., Carrozzo, R. & Bertini, E., May 1 2019, In : Human Mutation. 40, 5, p. 601-618 18 p.

    Research output: Contribution to journalArticle

  • Clinical-genetic features and peculiar muscle histopathology in infantile DNM1L-related mitochondrial epileptic encephalopathy

    Verrigni, D., Di Nottia, M., Ardissone, A., Baruffini, E., Nasca, A., Legati, A., Bellacchio, E., Fagiolari, G., Martinelli, D., Fusco, L., Battaglia, D., Trani, G., Versienti, G., Marchet, S., Torraco, A., Rizza, T., Verardo, M., D'Amico, A., Diodato, D., Moroni, I. & 7 others, Lamperti, C., Petrini, S., Moggio, M., Goffrini, P., Ghezzi, D., Carrozzo, R. & Bertini, E., May 2019, In : Human Mutation. 40, 5, p. 601-618 18 p.

    Research output: Contribution to journalArticle