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Fingerprint Dive into the research topics where Maria Teresa Bassi 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
  • Autophagy controls neonatal myogenesis by regulating the GH-IGF1 system through a NFE2L2- and DDIT3-mediated mechanism

    Zecchini, S., Giovarelli, M., Perrotta, C., Morisi, F., Touvier, T., Di Renzo, I., Moscheni, C., Bassi, M. T., Cervia, D., Sandri, M., Clementi, E. & De Palma, C., 2019, In : Autophagy. 15, 1, p. 58-77 20 p.

    Research output: Contribution to journalArticle

  • Broadening the spectrum of adulthood X-linked adrenoleukodystrophy: A report of two atypical cases

    Foschi, M., Vacchiano, V., Avoni, P., Incensi, A., Battaglia, S., Donadio, V., Panzeri, E., Bassi, M. T., Liguori, R. & Rizzo, G., Jan 1 2019, In : Frontiers in Neurology. 10, FEB, 6 p., 70.

    Research output: Contribution to journalArticle

    Open Access
  • Charcot-Marie-Tooth disease with pyramidal features due to a new mutation of EGR2 gene

    Fusco, C., Spagnoli, C., Salerno, G. G., Pavlidis, E., Frattini, D., Pisani, F. & Bassi, M. T., Jan 24 2019, In : Acta bio-medica : Atenei Parmensis. 90, 1, p. 104-107 4 p.

    Research output: Contribution to journalArticle