Gaetano Cantalupo
Affiliations: | University of Verona, Verona, WI, United States |
Area:
Neuroscience, Clinical Neurology, Neurophysiology, EpileptologyGoogle:
"Gaetano Cantalupo"Mean distance: 106866
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Publications
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| Proietti J, Fiorini E, Cantalupo G, et al. (2024) Refractory tonic-myoclonic status epilepticus with catamenial recurrence in epilepsy with myoclonic atonic seizures: A case report. Heliyon. 10: e24747 |
| Mirandola L, Cantalupo G, d'Orsi G, et al. (2023) Ictal semiology of gelastic seizures. Epilepsy & Behavior : E&B. 140: 109025 |
| Proietti J, Fiorini E, Meneghello L, et al. (2022) Non-convulsive febrile status epilepticus mimicking a postictal state after a febrile seizure: an ictal electroclinical and evolutive study. Epileptic Disorders : International Epilepsy Journal With Videotape |
| Proietti J, Amadori E, Striano P, et al. (2021) Epilepsy features in ARID1B-related Coffin-Siris syndrome. Epileptic Disorders : International Epilepsy Journal With Videotape. 23: 865-874 |
| Piffer S, Cantalupo G, Filipponi S, et al. (2021) Agrypnia excitata as the main feature in anti-leucine-rich glioma-inactivated 1 encephalitis: a detailed clinical and polysomnographic semiological analysis. European Journal of Neurology. 29: 890-894 |
| Bozzetti S, Rossini F, Ferrari S, et al. (2020) Epileptic seizures of suspected autoimmune origin: a multicentre retrospective study. Journal of Neurology, Neurosurgery, and Psychiatry |
| Maguolo A, Rodella G, Dianin A, et al. (2020) Diagnosis, genetic characterization and clinical follow up of mitochondrial fatty acid oxidation disorders in the new era of expanded newborn screening: A single centre experience. Molecular Genetics and Metabolism Reports. 24: 100632 |
| Gardella E, Cantalupo G, Larsson PG, et al. (2019) EEG features in Encephalopathy related to Status Epilepticus during slow Sleep. Epileptic Disorders. 21: 22-30 |
| Cantalupo G, Pavlidis E, Beniczky S, et al. (2019) Quantitative EEG analysis in Encephalopathy related to Status Epilepticus during slow Sleep Epileptic Disorders. 21: 31-40 |
| Bisulli F, Licchetta L, Baldassari S, et al. (2019) SCN1A mutations in focal epilepsy with auditory features: widening the spectrum of GEFS plus. Epileptic Disorders : International Epilepsy Journal With Videotape |