20172019

Research output per year

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

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Research Output

  • Axonal peripheral neuropathy in propionic acidemia: A severe side effect of long-term metronidazole therapy

    Diodato, D., Olivieri, G., Pro, S., Maiorani, D., Martinelli, D., Deodato, F., Taurisano, R., Di Capua, M. & Dionisi-Vici, C., Sep 18 2018, In : Neurology. 91, 12, p. 565-567 3 p.

    Research output: Contribution to journalArticle

    Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy

    Parini, R., De Lorenzo, P., Dardis, A., Burlina, A., Cassio, A., Cavarzere, P., Concolino, D., Della Casa, R., Deodato, F., Donati, M. A., Fiumara, A., Gasperini, S., Menni, F., Pagliardini, V., Sacchini, M., Spada, M., Taurisano, R., Valsecchi, M. G., Di Rocco, M. & Bembi, B., Feb 8 2018, In : Orphanet Journal of Rare Diseases. 13, 1, 32.

    Research output: Contribution to journalArticle

  • Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy

    Parini, R., De Lorenzo, P., Dardis, A., Burlina, A., Cassio, A., Cavarzere, P., Concolino, D., Della Casa, R., Deodato, F., Donati, M. A., Fiumara, A., Gasperini, S., Menni, F., Pagliardini, V., Sacchini, M., Spada, M., Taurisano, R., Valsecchi, M. G., Di Rocco, M. & Bembi, B., Feb 8 2018, In : Orphanet Journal of Rare Diseases. 13, 1, 12 p., 32.

    Research output: Contribution to journalArticle

  • Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy

    Parini, R., De Lorenzo, P., Dardis, A., Burlina, A., Cassio, A., Cavarzere, P., Concolino, D., Della Casa, R., Deodato, F., Donati, M. A., Fiumara, A., Gasperini, S., Menni, F., Pagliardini, V., Sacchini, M., Spada, M., Taurisano, R., Valsecchi, M. G., Di Rocco, M. & Bembi, B., 2018, In : Orphanet Journal of Rare Diseases. 13, 1

    Research output: Contribution to journalArticle