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Magazine 7.33

Oxcarbazepine-induced myoclonic status epilepticus in juvenile myoclonic epilepsy

Authors: Fanella M, Aegean G, Fattouch J, Casciato S, Lapenta L, Morano A, Giallonardo AT, Di Bonaventura C

Date: 2013

Scope of interest: Epilepsy




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Report/Poster of Convention/Congress Act

Hereditary Spastic Paraplegia: a novel mutation and expansion of the phenotype variability in SPG10.

Authors: Judge T, Carosi L, , Di Lullo M, Lombardi F, Babalini C, Gaudiello F, Marfia GA, Massa R, Kawarai T, Orlacchio A

Date: 2014

Scope of interest: Neurogenetics


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Report/Poster of Convention/Congress Act

Outpatient Management of Secondary Epistaxis Anemia in Patients with Rendu-Osler Disease: The Role of Intravenous Martial Therapy

Authors: Trimboli M. et. al. D’Amico C. et al.

Date: 2022

Scope of interest: Transfusion Medicine


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22q11.2 deletion and epilepsy: syndromic contexts and neurophysiological aspects

Authors: M. Fanella, A. Morano, J. Fattouch, S. Casciato, M. Albini, L.M. Basili, M. Frascarelli, T. Accinni, A. Buzzanca, A.T. Giallonardo, M. Biondi, F. Di Fabio, C. Di Bonaventura

Date: 2018

Scope of interest: Rare diseases/epilepsy


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