• 2197 Citations
  • 27 h-Index
1985 …2019
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Fingerprint Dive into the research topics where Lucia Fusco is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 38 Similar Profiles
Seizures Medicine & Life Sciences
Epilepsy Medicine & Life Sciences
Electroencephalography Medicine & Life Sciences
Partial Epilepsy Medicine & Life Sciences
Status Epilepticus Medicine & Life Sciences
Brain Diseases Medicine & Life Sciences
Infantile Spasms Medicine & Life Sciences
Myoclonic Epilepsy Medicine & Life Sciences

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Research Output 1985 2019

  • 2197 Citations
  • 27 h-Index
  • 116 Article
  • 5 Chapter
  • 3 Conference contribution

Abnormal circadian rhythm in patients with GRIN1-related developmental epileptic encephalopathy

Scala, M., Amadori, E., Fusco, L., Marchese, F., Capra, V., Minetti, C., Vari, M. S. & Striano, P., May 24 2019, In : European Journal of Paediatric Neurology.

Research output: Contribution to journalArticle

Brain Diseases
Circadian Rhythm
Sleep
Crying
Inborn Genetic Diseases
1 Citation (Scopus)

Clinical-genetic features and peculiar muscle histopathology in infantile DNM1L-related mitochondrial epileptic encephalopathy

Verrigni, D., Di Nottia, M., Ardissone, A., Baruffini, E., Nasca, A., Legati, A., Bellacchio, E., Fagiolari, G., Martinelli, D., Fusco, L., Battaglia, D., Trani, G., Versienti, G., Marchet, S., Torraco, A., Rizza, T., Verardo, M., D'Amico, A., Diodato, D., Moroni, I. & 7 others, Lamperti, C., Petrini, S., Moggio, M., Goffrini, P., Ghezzi, D., Carrozzo, R. & Bertini, E., May 1 2019, In : Human Mutation. 40, 5, p. 601-618 18 p.

Research output: Contribution to journalArticle

Dynamin I
Mitochondria
Muscles
Peroxisomes
Organelles

Clinical-genetic features and peculiar muscle histopathology in infantile DNM1L-related mitochondrial epileptic encephalopathy

Verrigni, D., Di Nottia, M., Ardissone, A., Baruffini, E., Nasca, A., Legati, A., Bellacchio, E., Fagiolari, G., Martinelli, D., Fusco, L., Battaglia, D., Trani, G., Versienti, G., Marchet, S., Torraco, A., Rizza, T., Verardo, M., D'Amico, A., Diodato, D., Moroni, I. & 7 others, Lamperti, C., Petrini, S., Moggio, M., Goffrini, P., Ghezzi, D., Carrozzo, R. & Bertini, E., May 2019, In : Human Mutation. 40, 5, p. 601-618 18 p.

Research output: Contribution to journalArticle

Dynamin I
Mitochondria
Muscles
Peroxisomes
Organelles

Generalized tonic seizures with autonomic signs are the hallmark of SCN8A developmental and epileptic encephalopathy

Trivisano, M., Pavia, G. C., Ferretti, A., Fusco, L., Vigevano, F. & Specchio, N., Jul 2019, In : Epilepsy and Behavior. 96, p. 219-223 5 p.

Research output: Contribution to journalArticle

Brain Diseases
Seizures
Cyanosis
Tachycardia
Epilepsy

ATP1A3-related epileptic encephalopathy responding to ketogenic diet

Schirinzi, T., Graziola, F., Cusmai, R., Fusco, L., Nicita, F., Elia, M., Travaglini, L., Bertini, E., Curatolo, P., Vigevano, F. & Capuano, A., May 2018, In : Brain and Development. 40, 5, p. 433-438 6 p.

Research output: Contribution to journalArticle

Ketogenic Diet
Brain Diseases
Epilepsy
Mutation
Hemiplegia