20022018

Research output per year

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

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Research Output

Neurologic phenotypes associated with mutations in RTN4IP1 (OPA10) in children and young adults

Charif, M., Nasca, A., Thompson, K., Gerber, S., Makowski, C., Mazaheri, N., Bris, C., Goudenège, D., Legati, A., Maroofian, R., Shariati, G., Lamantea, E., Hopton, S., Ardissone, A., Moroni, I., Giannotta, M., Siegel, C., Strom, T. M., Prokisch, H., Vignal-Clermont, C. & 22 others, Derrien, S., Zanlonghi, X., Kaplan, J., Hamel, C. P., Leruez, S., Procaccio, V., Bonneau, D., Reynier, P., White, F. E., Hardy, S. A., Barbosa, I. A., Simpson, M. A., Vara, R., Trujillo, Y. P., Galehdari, H., Deshpande, C., Haack, T. B., Rozet, J. M., Taylor, R. W., Ghezzi, D., Amati-Bonneau, P. & Lenaers, G., Jan 1 2018, In : JAMA Neurology. 75, 1, p. 105-113 9 p.

Research output: Contribution to journalArticle

  • Alternating Hemiplegia of Childhood: Pharmacological treatment of 30 Italian patients

    Pisciotta, L., Gherzi, M., Stagnaro, M., Calevo, M. G., Giannotta, M., Vavassori, M. R., Veneselli, E., I.B.AHC Consortium & De Grandis, E., Jun 1 2017, In : Brain and Development. 39, 6, p. 521-528 8 p.

    Research output: Contribution to journalArticle

  • Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood - A study of 155 patients

    Panagiotakaki, E., De Grandis, E., Stagnaro, M., Heinzen, E. L., Fons, C., Sisodiya, S., De Vries, B., Goubau, C., Weckhuysen, S., Kemlink, D., Scheffer, I., Lesca, G., Rabilloud, M., Klich, A., Ramirez-Camacho, A., Ulate-Campos, A., Campistol, J., Giannotta, M., Moutard, M. L., Doummar, D. & 13 others, Hubsch-Bonneaud, C., Jaffer, F., Cross, H., Gurrieri, F., Tiziano, D., Nevsimalova, S., Nicole, S., Neville, B., Van Den Maagdenberg, A. M. J. M., Mikati, M., Goldstein, D. B., Vavassori, R. & Arzimanoglou, A., Sep 26 2015, In : Orphanet Journal of Rare Diseases. 10, 1, 123.

    Research output: Contribution to journalArticle

  • Lack of SLC2A1 (Glucose Transporter 1) mutations in 30 Italian patients with alternating hemiplegia of childhood

    De Grandis, E., Stagnaro, M., Biancheri, R., Giannotta, M., Gobbi, G., Traverso, M., Veneselli, E. & Zara, F., Jul 2013, In : Journal of Child Neurology. 28, 7, p. 863-866 4 p.

    Research output: Contribution to journalArticle