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

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Research Output

Loss of ap4s1 in zebrafish leads to neurodevelopmental defects resembling spastic paraplegia 52

D’Amore, A., Tessa, A., Naef, V., Bassi, M. T., Citterio, A., Romaniello, R., Fichi, G., Galatolo, D., Mero, S., Battini, R., Bertocci, G., Baldacci, J., Sicca, F., Gemignani, F., Ricca, I., Rubegni, A., Hirst, J., Marchese, M., Sahin, M., Ebrahimi-Fakhari, D. & 1 others, Santorelli, F. M., 2020, (Accepted/In press) In : Annals of Clinical and Translational Neurology.

Research output: Contribution to journalArticle

Open Access
  • A novel CAPN1 mutation causes a pure hereditary spastic paraplegia in an Italian family

    Cotti Piccinelli, S., Bassi, M. T., Citterio, A., Manganelli, F., Tozza, S., Santorelli, F. M., Cassarino, S. G., Caria, F., Baldelli, E., Galvagni, A., Santoro, L., Padovani, A. & Filosto, M., Jan 1 2019, In : Frontiers in Neurology. 10, 5 p., 580.

    Research output: Contribution to journalArticle

    Open Access
  • ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis

    Vantaggiato, C., Panzeri, E., Castelli, M., Citterio, A., Arnoldi, A., Santorelli, F. M., Liguori, R., Scarlato, M., Musumeci, O., Toscano, A., Clementi, E. & Bassi, M. T., 2019, In : Autophagy. 15, 1, p. 34-57 24 p.

    Research output: Contribution to journalArticle

  • Open Access