Pubblicazioni di Neuropsichiatria Infantile

Filippini M, Boni A, Giannotta M, Pini A, Russo A, Musti MA, Guerra A, Lassonde M, Gobbi G.
Comparing cortical auditory processing in children with typical and atypical benign epilepsy with centrotemporal spikes: Electrophysiologic evidence of the role of non-rapid eye movement sleep abnormalities.
Epilepsia. 2015 May; 56(5):726-34. doi: 10.1111/epi.12959. Epub 2015 Mar 25. PMID: 25809446.

Russo A, Lallas M, Jayakar P, Miller I, Hyslop A, Dunoyer C, Resnick T, Duchowny M.
The diagnostic utility of 3D-ESI rotating and moving dipole methodology in the pre-surgical evaluation of MRI-negative childhood epilepsy due to focal cortical dysplasia. Epilepsia. 2016 Sep;57(9):1450-7. doi: 10.1111/epi.13454. Epub 2016 Jul 8. PMID: 27387565.

Filippini M, Guerra A, Negosanti A, Santi S, Sarajlija J, Musti MA, Gobbi G, Lassonde M, Pini A.
Mismatch Negativity Recording in Children With Duchenne Muscular Dystrophy: A Preliminary Study Integrating Neurophysiological and Neuropsychological Results.
Journal of Child Neurology. 2016 Nov; 31(13):1468-1474. doi: 10.1177/0883073816656404. Epub 2016 Jul 15. PMID: 27422795.

Giacometti G, Ferreri C, Sansone A, Chatgilialoglu C, Marzetti C, Spyratou E, Georgakilas AG, Marini M, Abruzzo PM, Bolotta A, Ghezzo A, Minguzzi R, Posar A, Visconti P.
High predictive values of RBC membrane-based diagnostics by biophotonics in an integrated approach for Autism Spectrum Disorders.
Scientific Reports 2017 Aug 29;7(1):9854. doi: 10.1038/s41598-017-10361-7. PMID: 28852136

D'Amico A, Catteruccia M, Baranello G, Politano L, Govoni A, Previtali SC, Pane M, D'Angelo MG, Bruno C, Messina S, Ricci F, Pegoraro E, Pini A, Berardinelli A, Gorni K, Battini R, Vita G, Trucco F, Scutifero M, Petillo R, D'Ambrosio P, Ardissone A, Pasanisi B, Vita G, Mongini T, Moggio M, Comi GP, Mercuri E, Bertini E.
Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements.
Neuromuscul Disord. 2017 May;27(5):447-451. doi: 10.1016/j.nmd.2017.02.006. Epub 2017 Feb 14. PMID: 28262469.

Messana T, Russo A, Vergaro R, Boni A, Santucci M, Pini A.
Glucose Transporter Type 1 Deficiency Syndrome: Developmental Delay and Early-Onset Ataxia in a Novel Mutation of the SLC2A1 Gene.
Journal of Pediatric Neurosciences. 2018 Oct-Dec;13(4):496-499. doi: 10.4103/JPN.JPN_169_17. PMID: 30937099

Posar A, Visconti P.
Sensory abnormalities in children with autism spectrum disorder.
Jornal de Pediatria (Rio J). 2018 Jul-Aug;94(4):342-350. doi:10.1016/j.jped.2017.08.008. Epub 2017 Nov 4. PMID: 29112858.

Pellino G, Chiavarino F, Fiumana E, Boni A, Russo A, Faggioli R.
Prognostic factors in epileptic encephalopathies at onset in the first 2 years of life: The experience of a tertiary healthcare center in Italy.
Epilepsy Behavior. 2019 Oct;99:106465. doi: 10.1016/j.yebeh.2019.106465. Epub 2019 Aug 14. PMID:31421519.

Posar A, Visconti P, Blunda V, Pizza F, Plazzi G.
Autism Spectrum Disorder and Narcolepsy: A Possible Connection That Deserves to Be Investigated.
Frontiers in Psychiatry. 2020 Apr 8;11:265. doi: 10.3389/fpsyt.2020.00265. PMID: 32322223; .

Neri M, Rossi R, Trabanelli C, Mauro A, Selvatici R, Falzarano MS, Spedicato N, Margutti A, Rimessi P, Fortunato F, Fabris M, Gualandi F, Comi G, Tedeschi S, Seia M, Fiorillo C, Traverso M, Bruno C, Giardina E, Piemontese MR, Merla G, Cau M, Marica M, Scuderi C, Borgione E, Tessa A, Astrea G, Santorelli FM, Merlini L, Mora M, Bernasconi P, Gibertini S, Sansone V, Mongini T, Berardinelli A, Pini A, Liguori R, Filosto M, Messina S, Vita G, Toscano A, Vita G, Pane M, Servidei S, Pegoraro E, Bello L, Travaglini L, Bertini E, D'Amico A, Ergoli M, Politano L, Torella A, Nigro V, Mercuri E, Ferlini A.
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study.
Front Genet. 2020 Mar 3;11:131. doi: 10.3389/fgene.2020.00131. PMID: 32194622