• 469 Citations
  • 12 h-Index
1982 …2015
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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.

  • 23 Similar Profiles
Seizures Medicine & Life Sciences
Epilepsy Medicine & Life Sciences
Electroencephalography Medicine & Life Sciences
Infantile Spasms Medicine & Life Sciences
Neuronal Ceroid-Lipofuscinoses Medicine & Life Sciences
Status Epilepticus Medicine & Life Sciences
Myoclonic Epilepsy Medicine & Life Sciences
Brain Diseases Medicine & Life Sciences

Research Output 1982 2015

  • 469 Citations
  • 12 h-Index
  • 25 Article
  • 1 Conference contribution
13 Citations (Scopus)

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

Myoclonic Epilepsy
Generalized Epilepsy
Intellectual Disability
10 Citations (Scopus)

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

Chromosomes, Human, Pair 14
Forkhead Transcription Factors
21 Citations (Scopus)

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

Neuronal Ceroid-Lipofuscinoses
Molecular Epidemiology
15 Citations (Scopus)
6 Citations (Scopus)

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

Homovanillic Acid
Tyrosine 3-Monooxygenase
Brain Diseases
Missense Mutation