1982 …2015

Research output per year

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

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Research Output

  • 25 Article
  • 1 Conference contribution

CHD2 mutations are a rare cause of generalized epilepsy with myoclonic-atonic seizures

Trivisano, M., Striano, P., Sartorelli, J., Giordano, L., Traverso, M., Accorsi, P., Cappelletti, S., Claps, D. J., Vigevano, F., Zara, F. & Specchio, N., Oct 1 2015, In : Epilepsy and Behavior. 51, p. 53-56 4 p.

Research output: Contribution to journalArticle

  • Epilepsy in patients with duplications of chromosome 14 harboring FOXG1

    Pontrelli, G., Cappelletti, S., Claps, D., Sirleto, P., Ciocca, L., Petrocchi, S., Terracciano, A., Serino, D., Fusco, L., Vigevano, F. & Specchio, N., 2014, In : Pediatric Neurology. 50, 5, p. 530-535 6 p.

    Research output: Contribution to journalArticle

  • Molecular epidemiology of childhood neuronal ceroid-lipofuscinosis in Italy

    Santorelli, F. M., Garavaglia, B., Cardona, F., Nardocci, N., Bernardina, B. D., Sartori, S., Suppiej, A., Bertini, E., Claps, D., Battini, R., Biancheri, R., Filocamo, M., Pezzini, F. & Simonati, A., 2013, In : Orphanet Journal of Rare Diseases. 8, 1, 19.

    Research output: Contribution to journalArticle

  • A new tyrosine hydroxylase genotype associated with early-onset severe encephalopathy

    Giovanniello, T., Claps, D., Carducci, C., Carducci, C., Blau, N., Vigevano, F., Antonozzi, I. & Leuzzi, V., Apr 2012, In : Journal of Child Neurology. 27, 4, p. 523-525 3 p.

    Research output: Contribution to journalArticle