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Deficits in social cognition and genetic predisposition to schizophrenia: a comparison between patients with 22q11.2 deletion syndrome, schizophrenic patients and healthy controls

Authors: M. Frascarelli, A. Buzzanca, G. Padovani, T. Acinni, L. Carlone, F. Ghezzi, G. Lattanzi, M. Fanella, C. Lambiase, B. marina, M. Biondi, F. di Fabio

Date: 2019

Scope of interest: Rare diseases/psychiatric disorders




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Ictal EEG/fMRI study of vertiginous seizures.

Authors: Morano A, Carnì M, Casciato S, Vaudano AE, Fattouch J, Fanella M, Albini M, Basili LM, Lucignani G, Scapeccia M, Tomassi R, Di Castro E, Colonnese C, Giallonardo AT, Di Bonaventura C.

Date: 2017

Scope of interest: Epilepsy


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Pulmonary embolism with minimal d-dimer increase – disagreement between clinic and laboratory: case report.

Authors: Ripa C, De Tommaso G, Lisa R, Lorenzi M, Melatini MC, Mazzanti I, Abbatecola A, Antonicelli R

Date: 2010

Scope of interest: gerontology, geriatrics


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Hereditary spastic paraplegia: Clinical-genetic characteristics and evolving molecular mechanisms.

Authors: Judge T, Lombardi F, Santorelli FM, Kawarai T, Orlacchio A.

Date: 2014

Scope of interest: Neurogetics


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