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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

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
  • Very preterm birth is associated with PLAGL1 gene hypomethylation at birth and discharge

    Provenzi, L., Carli, P. D., Fumagalli, M., Giorda, R., Casavant, S., Beri, S., Citterio, A., D'Agata, A., Morandi, F., Mosca, F., Borgatti, R. & Montirosso, R., Aug 2018, In : Epigenomics. 10, 8, p. 1121-1130 10 p.

    Research output: Contribution to journalArticle