• 498 Citations
  • 9 h-Index
20022018
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Fingerprint Dive into the research topics where Melania Giannotta is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 8 Similar Profiles
Rolandic Epilepsy Medicine & Life Sciences
Mutation Medicine & Life Sciences
Myoclonic Epilepsy Medicine & Life Sciences
Sleep Medicine & Life Sciences
etiracetam Medicine & Life Sciences
Acetazolamide Medicine & Life Sciences
Facilitative Glucose Transport Proteins Medicine & Life Sciences
Partial Epilepsy Medicine & Life Sciences

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Research Output 2002 2018

  • 498 Citations
  • 9 h-Index
  • 14 Article
2 Citations (Scopus)

Neurologic phenotypes associated with mutations in RTN4IP1 (OPA10) in children and young adults

Charif, M., Nasca, A., Thompson, K., Gerber, S., Makowski, C., Mazaheri, N., Bris, C., Goudenège, D., Legati, A., Maroofian, R., Shariati, G., Lamantea, E., Hopton, S., Ardissone, A., Moroni, I., Giannotta, M., Siegel, C., Strom, T. M., Prokisch, H., Vignal-Clermont, C. & 22 others, Derrien, S., Zanlonghi, X., Kaplan, J., Hamel, C. P., Leruez, S., Procaccio, V., Bonneau, D., Reynier, P., White, F. E., Hardy, S. A., Barbosa, I. A., Simpson, M. A., Vara, R., Trujillo, Y. P., Galehdari, H., Deshpande, C., Haack, T. B., Rozet, J. M., Taylor, R. W., Ghezzi, D., Amati-Bonneau, P. & Lenaers, G., Jan 1 2018, In : JAMA Neurology. 75, 1, p. 105-113 9 p.

Research output: Contribution to journalArticle

Optic Atrophy
Nervous System
Young Adult
Phenotype
Mutation
9 Citations (Scopus)

Alternating Hemiplegia of Childhood: Pharmacological treatment of 30 Italian patients

Pisciotta, L., Gherzi, M., Stagnaro, M., Calevo, M. G., Giannotta, M., Vavassori, M. R., Veneselli, E., I.B.AHC Consortium & De Grandis, E., Jun 1 2017, In : Brain and Development. 39, 6, p. 521-528 8 p.

Research output: Contribution to journalArticle

Pharmacology
Flunarizine
olanzapine
Therapeutics
Ketogenic Diet
55 Citations (Scopus)

Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood - A study of 155 patients

Panagiotakaki, E., De Grandis, E., Stagnaro, M., Heinzen, E. L., Fons, C., Sisodiya, S., De Vries, B., Goubau, C., Weckhuysen, S., Kemlink, D., Scheffer, I., Lesca, G., Rabilloud, M., Klich, A., Ramirez-Camacho, A., Ulate-Campos, A., Campistol, J., Giannotta, M., Moutard, M. L., Doummar, D. & 13 others, Hubsch-Bonneaud, C., Jaffer, F., Cross, H., Gurrieri, F., Tiziano, D., Nevsimalova, S., Nicole, S., Neville, B., Van Den Maagdenberg, A. M. J. M., Mikati, M., Goldstein, D. B., Vavassori, R. & Arzimanoglou, A., Sep 26 2015, In : Orphanet Journal of Rare Diseases. 10, 1, 123.

Research output: Contribution to journalArticle

Mutation
Phenotype
Alternating hemiplegia of childhood
Genes
Early Medical Intervention
9 Citations (Scopus)
Rolandic Epilepsy
Eye Movements
Sleep
Electroencephalography
Child Language
6 Citations (Scopus)

Lack of SLC2A1 (Glucose Transporter 1) mutations in 30 Italian patients with alternating hemiplegia of childhood

De Grandis, E., Stagnaro, M., Biancheri, R., Giannotta, M., Gobbi, G., Traverso, M., Veneselli, E. & Zara, F., Jul 2013, In : Journal of Child Neurology. 28, 7, p. 863-866 4 p.

Research output: Contribution to journalArticle

Facilitative Glucose Transport Proteins
Mutation
Ketogenic Diet
3-O-Methylglucose
Dystonia