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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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Magazine 7.14

Doing without valproate in women of childbearing potential with idiopathic generalized epilepsy: Implications on seizure outcome.

Authors: Cerulli Irelli E, Morano A, Cocchi E, Casciato S, Fanella M, Albini M, Ivory F, Basili LM, Fisco G, Baron FA, Mascia A, D'Aniello A, Manfredi M, Fattouch J, Quarato P, Giallonardo AT, Di Gennaro G, Di Bonaventura C.

Date: 2019

Scope of interest: Epilepsy


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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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Capillary Leak Syndrome in haematological patients: management and treatment retrospective evaluation

Authors: Postorino M, Rossi R, Zizzari A, Marchesi F, Provenzano I, Franceschini L, Pupo L, Rizzo M, Giannì L, Gumenyuk S, De Santis G, Renzi D, Guiducci G, Fiorelli E, Coniglione F, Puliti R, Berrini A, Dauri M

Date: 2013

Scope of interest: Hematology/Transfusion Medicine


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