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Report/Poster of Convention/Congress Act

White matter abnormalities as endophenotypes of schizophrenia in 22q11 deletion syndrome

Authors: M. Frascarelli, N. Petsas, A. Buzzanca, M. Fanella, A.M. Monacelli, T. Accinni, G.M. Lattanzi, L. Carlone, C. Colonnese, P.Pantano, M. biondi, F. Di Fabio

Date: 2019

Scope of interest: Neuroimaging/rare diseases/psychiatric disorders




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Report/Poster of Convention/Congress Act

“Activation of the Therapeutic Apheresis clinic at the SIMT in Frosinone: the staff training course”

Authors: G.Guiducci – A.Di Folco – F.Docimo – M.Trimboli – C.Gargiulo

Date: 2022

Scope of interest: CLINICAL PATHOLOGY


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ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease.

Authors: Montecchiani C, Pedace L, Lo Giudice T, Casella A, Mearini M, Gaudiello F, Pedroso JL, Terracciano C, Caltagirone C, et al

Date: 2016

Scope of interest: Neurogenetics


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Cannabinoids in the Treatment of Epilepsy: Current Status and Future Prospects.

Authors: Morano A, Fanella M, Albini M, Cifelli P, Palma E, Giallonardo AT, Di Bonaventura C.

Date: 2020

Scope of interest: Epilepsy


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