Istituto "Eugenio Medea" - Associazione La Nostra Famiglia

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    Projects

    Research Output

    Adaptor protein complex 4 deficiency: a paradigm of childhood-onset hereditary spastic paraplegia caused by defective protein trafficking: Human molecular genetics

    Behne, R., Teinert, J., Wimmer, M., D'Amore, A., Davies, A. K., Scarrott, J. M., Eberhardt, K., Brechmann, B., Chen, IP-F., Buttermore, E. D., Barrett, L., Dwyer, S., Chen, T., Hirst, J., Wiesener, A., Segal, D., Martinuzzi, A., Duarte, S. T., Bennett, J. T., Bourinaris, T. & 9 others, Houlden, H., Roubertie, A., Santorelli, F. M., Robinson, M., Azzouz, M., Lipton, J. O., Borner, G. H. H., Sahin, M. & Ebrahimi-Fakhari, D., 2020, In : Hum. Mol. Genet.. 29, 2, p. 320-334 15 p.

    Research output: Contribution to journalArticle

  • A focus on valproate and cognitive deficits in Bipolar Disorders: A mini-review

    Pigoni, A., Mandolini, G. M., Delvecchio, G., Bressi, C., Soares, J. C. & Brambilla, P., 2020, In : Journal of Affective Disorders. 261, p. 277-281

    Research output: Contribution to journalArticle

  • A multi-metric registration strategy for the alignment of longitudinal brain images in pediatric oncology

    Montin, E., Belfatto, A., Bologna, M., Meroni, S., Cavatorta, C., Pecori, E., Diletto, B., Massimino, M., Oprandi, M. C., Poggi, G., Arrigoni, F., Peruzzo, D., Pignoli, E., Gandola, L., Cerveri, P. & Mainardi, L., Jan 1 2020, (Accepted/In press) In : Medical and Biological Engineering and Computing.

    Research output: Contribution to journalArticle