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2020

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
2019

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

2018
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

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 1 2018, In : Epigenomics. 10, 8, p. 1121-1130 10 p.

Research output: Contribution to journalArticle

2017

Tubulin-related cerebellar dysplasia: definition of a distinct pattern of cerebellar malformation

Romaniello, R., Arrigoni, F., Panzeri, E., Poretti, A., Micalizzi, A., Citterio, A., Bedeschi, M. F., Berardinelli, A., Cusmai, M., D’Arrigo, S., Ferraris, A., Hackenberg, A., Kuechler, A., Mancardi, M., Nuovo, S., Oehl-Jaschkowitz, B., Rossi, A., Signorini, S., Tüttelmann, F., Wahl, D. & 5 others, Hehr, U., Boltshauser, E., Bassi, M. T., Valente, E. M. & Borgatti, R., 2017, In : European Radiology. 27, 12, p. 5080-5092 13 p.

Research output: Contribution to journalArticle

Tubulin-related cerebellar dysplasia

Romaniello, R., Arrigoni, F., Panzeri, E., Poretti, A., Micalizzi, A., Citterio, A., Bedeschi, M. F., Berardinelli, A., Cusmai, R., D'Arrigo, S., Ferraris, A., Hackenberg, A., Kuechler, A., Mancardi, M. M., Nuovo, S., Oehl-Jaschkowitz, B., Rossi, A., Signorini, S., Tüttelmann, F., Wahl, D. & 5 others, Hehr, U., Boltshauser, E., Bassi, M. T., Valente, E. M. & Borgatti, R., Dec 2017, In : European Radiology. 27, 12, p. 5080-5092 13 p.

Research output: Contribution to journalArticle

Tubulin-related cerebellar dysplasia: definition of a distinct pattern of cerebellar malformation

Romaniello, R., Arrigoni, F., Panzeri, E., Poretti, A., Micalizzi, A., Citterio, A., Bedeschi, M. F., Berardinelli, A., Cusmai, M., D'Arrigo, S., Ferraris, A., Hackenberg, A., Kuechler, A., Mancardi, M., Nuovo, S., Oehl-Jaschkowitz, B., Rossi, A., Signorini, S., Tuettelmann, F., Wahl, D. & 5 others, Hehr, U., Boltshauser, E., Bassi, M. T., Valente, E. M. & Borgatti, R., Dec 1 2017, In : European Radiology. 27, 12, p. 5080-5092 13 p.

Research output: Contribution to journalArticle

Tubulin-related cerebellar dysplasia: definition of a distinct pattern of cerebellar malformation

Romaniello, R., Arrigoni, F., Panzeri, E., Poretti, A., Micalizzi, A., Citterio, A., Bedeschi, M. F., Berardinelli, A., Cusmai, R., D’Arrigo, S., Ferraris, A., Hackenberg, A., Kuechler, A., Mancardi, M., Nuovo, S., Oehl-Jaschkowitz, B., Rossi, A., Signorini, S., Tüttelmann, F., Wahl, D. & 5 others, Hehr, U., Boltshauser, E., Bassi, M. T., Valente, E. M. & Borgatti, R., 2017, In : European Radiology. 27, 12, p. 5080-5092 13 p.

Research output: Contribution to journalArticle

Tubulin-related cerebellar dysplasia: definition of a distinct pattern of cerebellar malformation

Romaniello, R., Arrigoni, F., Panzeri, E., Poretti, A., Micalizzi, A., Citterio, A., Bedeschi, M. F., Berardinelli, A., Cusmai, R., D’Arrigo, S., Ferraris, A., Hackenberg, A., Kuechler, A., Mancardi, M., Nuovo, S., Oehl-Jaschkowitz, B., Rossi, A., Signorini, S., Tüttelmann, F., Wahl, D. & 5 others, Hehr, U., Boltshauser, E., Bassi, M. T., Valente, E. M. & Borgatti, R., 2017, In : European Radiology. 27, 12, p. 5080-5092 13 p.

Research output: Contribution to journalArticle

2016

Clinical and paraclinical indicators of motor system impairment in hereditary spastic paraplegia: A pilot study

Martinuzzi, A., Montanaro, D., Vavla, M., Paparella, G., Bonanni, P., Musumeci, O., Brighina, E., Hlavata, H., Rossi, G., Aghakhanyan, G., Martino, N., Baratto, A., D'Angelo, M. G., Peruch, F., Fantin, M., Arnoldi, A., Citterio, A., Vantaggiato, C., Rizzo, V., Toscano, A. & 2 others, Bresolin, N. & Bassi, M. T., Apr 1 2016, In : PLoS One. 11, 4, e0153283.

Research output: Contribution to journalArticle