• 34 Citations
  • 4 h-Index
20172017
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Fingerprint Dive into the research topics where Elena Pasini is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

Myoclonus Medicine & Life Sciences
Mutation Medicine & Life Sciences
Unverricht-Lundborg Syndrome Medicine & Life Sciences
Myoclonic Epilepsy Medicine & Life Sciences
Amyotrophic Lateral Sclerosis Medicine & Life Sciences
Seizures Medicine & Life Sciences
Pedigree Medicine & Life Sciences
Fever Medicine & Life Sciences

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Research Output 2017 2017

  • 34 Citations
  • 4 h-Index
  • 4 Article
10 Citations (Scopus)

Multiple variants in families with amyotrophic lateral sclerosis and frontotemporal dementia related to C9orf72 repeat expansion: further observations on their oligogenic nature

Giannoccaro, M. P., Bartoletti-Stella, A., Piras, S., Pession, A., De Massis, P., Oppi, F., Stanzani-Maserati, M., Pasini, E., Baiardi, S., Avoni, P., Parchi, P., Liguori, R. & Capellari, S., Jul 1 2017, In : Journal of Neurology. 264, 7, p. 1426-1433 8 p.

Research output: Contribution to journalArticle

Amyotrophic Lateral Sclerosis
Mutation
Pedigree
Genes
Dementia
15 Citations (Scopus)

Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K+ channel properties

Oliver, K. L., Franceschetti, S., Milligan, C. J., Muona, M., Mandelstam, S. A., Canafoglia, L., Boguszewska-Chachulska, A. M., Korczyn, A. D., Bisulli, F., Di Bonaventura, C., Ragona, F., Michelucci, R., Ben-Zeev, B., Straussberg, R., Panzica, F., Massano, J., Friedman, D., Crespel, A., Engelsen, B. A., Andermann, F. & 20 others, Andermann, E., Spodar, K., Lasek-Bal, A., Riguzzi, P., Pasini, E., Tinuper, P., Licchetta, L., Gardella, E., Lindenau, M., Wulf, A., Møller, R. S., Benninger, F., Afawi, Z., Rubboli, G., Reid, C. A., Maljevic, S., Lerche, H., Lehesjoki, A. E., Petrou, S. & Berkovic, S. F., May 1 2017, In : Annals of Neurology. 81, 5, p. 677-689 13 p.

Research output: Contribution to journalArticle

Myoclonic Epilepsy
Myoclonus
Fever
Mutation
Temperature
5 Citations (Scopus)

The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations

Michelucci, R., Pulitano, P., Di Bonaventura, C., Binelli, S., Luisi, C., Pasini, E., Striano, S., Striano, P., Coppola, G., La Neve, A., Giallonardo, A. T., Mecarelli, O., Serioli, E., Dazzo, E., Fanciulli, M. & Nobile, C., Mar 1 2017, In : Epilepsy and Behavior. 68, p. 103-107 5 p.

Research output: Contribution to journalArticle

Phenotype
Mutation
Epilepsy
Seizures
Pedigree
4 Citations (Scopus)

Variable course of Unverricht-Lundborg disease: Early prognostic factors

Canafoglia, L., Ferlazzo, E., Michelucci, R., Striano, P., Magaudda, A., Gambardella, A., Pasini, E., Belcastro, V., Riguzzi, P., Fanella, M., Granata, T., Beccaria, F., Trentini, C., Bianchi, A., Aguglia, U., Panzica, F. & Franceschetti, S., 2017, In : Neurology.

Research output: Contribution to journalArticle

Unverricht-Lundborg Syndrome
Myoclonus
Seizures
Age of Onset
Cystatin B