20052019

Research output per year

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

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Research Output

Hereditary spastic paraplegia is a novel phenotype for germline de novo ATP1A1 mutation

Stregapede, F., Travaglini, L., Rebelo, A. P., Cintra, V. P., Bellacchio, E., Bosco, L., Alfieri, P., Pro, S., Zuchner, S., Bertini, E. & Nicita, F., 2019, In : Clinical Genetics. 97, 3, p. 521-526 6 p.

Research output: Contribution to journalArticle

  • Vipera aspis bite neurotoxicity: two pediatric cases in Central Italy

    Marano, M., Di Giuseppe, M., Pro, S., Pisani, M., Montibeller, M., Bottari, G., Nunziata, J. & Cecchetti, C., Nov 14 2019, In : Clinical Toxicology. p. 1-2 2 p.

    Research output: Contribution to journalArticle

    A cohort study on acute ocular motility disorders in pediatric emergency department

    Raucci, U., Parisi, P., Vanacore, N., Ferro, V., Garone, G., Sancetta, F., Petroni, S., Pro, S., Rossi, R., Reale, A. & Pirozzi, N., May 29 2018, In : Italian Journal of Pediatrics. 44, 1

    Research output: Contribution to journalArticle

  • A cohort study on acute ocular motility disorders in pediatric emergency department

    Raucci, U., Parisi, P., Vanacore, N., Ferro, V., Garone, G., Sancetta, F., Petroni, S., Pro, S., Rossi, R., Reale, A. & Pirozzi, N., May 29 2018, In : Italian Journal of Pediatrics. 44, 1, p. 62 18 p.

    Research output: Contribution to journalArticle

  • A novel KCTD17 mutation is associated with childhood early-onset hyperkinetic movement disorder

    Graziola, F., Stregapede, F., Travaglini, L., Garone, G., Verardo, M., Bosco, L., Pro, S., Bertini, E., Curatolo, P., Vigevano, F. & Capuano, A., Dec 7 2018, In : Parkinsonism and Related Disorders. 3 p.

    Research output: Contribution to journalArticle