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Targeted re-sequencing for early diagnosis of genetic causes of childhood epilepsy: the Italian experience from the 'beyond epilepsy' project.
Amadori E, Scala M, Cereda GS, Vari MS, Marchese F, Di Pisa V, Mancardi MM, Giacomini T, Siri L, Vercellino F, Serino D, Orsini A, Bonuccelli A, Bagnasco I, Papa A, Minetti C, Cordelli DM, Striano P. Amadori E, et al. Among authors: siri l. Ital J Pediatr. 2020 Jul 6;46(1):92. doi: 10.1186/s13052-020-00860-1. Ital J Pediatr. 2020. PMID: 32631363 Free PMC article.
Focal status and acute encephalopathy in a 13-year-old boy with de novo DNM1L mutation: Video-polygraphic pattern and clues for differential diagnosis.
Mancardi MM, Nesti C, Febbo F, Cordani R, Siri L, Nobili L, Lampugnani E, Giacomini T, Granata T, Marucci G, Consales A, Rossi A, Luria G, Santorelli FM, Buratti S. Mancardi MM, et al. Among authors: siri l. Brain Dev. 2021 May;43(5):644-651. doi: 10.1016/j.braindev.2020.12.017. Epub 2021 Jan 21. Brain Dev. 2021. PMID: 33485697
Impact of the COVID-19 Outbreak on the Behavior of Families in Italy: A Focus on Children and Adolescents.
Uccella S, De Grandis E, De Carli F, D'Apruzzo M, Siri L, Preiti D, Di Profio S, Rebora S, Cimellaro P, Biolcati Rinaldi A, Venturino C, Petralia P, Ramenghi LA, Nobili L. Uccella S, et al. Among authors: siri l. Front Public Health. 2021 Feb 5;9:608358. doi: 10.3389/fpubh.2021.608358. eCollection 2021. Front Public Health. 2021. PMID: 33614580 Free PMC article.
47 results