20192019

Research output per year

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

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Research Output

Dystonia-Ataxia with early handwriting deterioration in COQ8A mutation carriers: A case series and literature review

Galosi, S., Barca, E., Carrozzo, R., Schirinzi, T., Quinzii, C. M., Lieto, M., Vasco, G., Zanni, G., Di Nottia, M., Galatolo, D., Filla, A., Bertini, E., Santorelli, F. M., Leuzzi, V., Haas, R., Hirano, M. & Friedman, J., Nov 2019, In : Parkinsonism and Related Disorders. 68, p. 8-16 9 p.

Research output: Contribution to journalReview article

  • Dystonia-Ataxia with early handwriting deterioration in COQ8A mutation carriers: A case series and literature review

    Galosi, S., Barca, E., Carrozzo, R., Schirinzi, T., Quinzii, C. M., Lieto, M., Vasco, G., Zanni, G., Di Nottia, M., Galatolo, D., Filla, A., Bertini, E., Santorelli, F. M., Leuzzi, V., Haas, R., Hirano, M. & Friedman, J., Nov 1 2019, In : Parkinsonism and Related Disorders. 68, p. 8-16 9 p.

    Research output: Contribution to journalArticle

  • Overt Hypogonadism May Not Be a Sentinel Sign of RING Finger Protein 216: Two Novel Mutations Associated with Ataxia, Chorea, and Fertility

    Lieto, M., Galatolo, D., Roca, A., Cocozza, S., Pontillo, G., Fico, T., Pane, C., Saccà, F., De Michele, G., Santorelli, F. M. & Filla, A., Nov 1 2019, In : Movement Disorders Clinical Practice. 6, 8, p. 724-726 3 p.

    Research output: Contribution to journalLetter

    Spinocerebellar ataxia 48 presenting with ataxia associated with cognitive, psychiatric, and extrapyramidal features: A report of two Italian families

    De Michele, G., Lieto, M., Galatolo, D., Salvatore, E., Cocozza, S., Barghigiani, M., Tessa, A., Baldacci, J., Pappatà, S., Filla, A., De Michele, G. & Santorelli, F. M., Aug 2019, In : Parkinsonism and Related Disorders. 65, p. 91-96 6 p.

    Research output: Contribution to journalArticle

  • The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian families

    Lieto, M., Riso, V., Galatolo, D., De Michele, G., Rossi, S., Barghigiani, M., Cocozza, S., Pontillo, G., Trovato, R., Saccà, F., Salvatore, E., Tessa, A., Filla, A., Santorelli, F. M., De Michele, G. & Silvestri, G., Jan 1 2019, (Accepted/In press) In : European Journal of Neurology.

    Research output: Contribution to journalArticle