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Management, treatment, and clinical approach of Sydenham's chorea in children: Italian survey on expert-based experience.
Eur J Paediatr Neurol. 2024 Sep;52:103-108. doi: 10.1016/j.ejpn.2024.08.002. Epub 2024 Aug 20.
Eur J Paediatr Neurol. 2024.
PMID: 39226700
Free article.
Neuroinflammation and status epilepticus: a narrative review unraveling a complex interplay.
Foiadelli T, Santangelo A, Costagliola G, Costa E, Scacciati M, Riva A, Volpedo G, Smaldone M, Bonuccelli A, Clemente AM, Ferretti A, Savasta S, Striano P, Orsini A.
Foiadelli T, et al. Among authors: scacciati m.
Front Pediatr. 2023 Nov 21;11:1251914. doi: 10.3389/fped.2023.1251914. eCollection 2023.
Front Pediatr. 2023.
PMID: 38078329
Free PMC article.
Review.
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Congenital Myopathy as a Phenotypic Expression of CACNA1S Gene Mutation: Case Report and Systematic Review of the Literature.
Marinella G, Orsini A, Scacciati M, Costa E, Santangelo A, Astrea G, Frosini S, Pasquariello R, Rubegni A, Sgherri G, Corsi M, Bonuccelli A, Battini R.
Marinella G, et al. Among authors: scacciati m.
Genes (Basel). 2023 Jun 28;14(7):1363. doi: 10.3390/genes14071363.
Genes (Basel). 2023.
PMID: 37510268
Free PMC article.
Review.
Item in Clipboard
Phenotypic Spectrum of NFIA Haploinsufficiency: Two Additional Cases and Review of the Literature.
Bertini V, Cambi F, Orsini A, Bonuccelli A, Fiorini A, Santangelo A, Scacciati M, Elia M, Galesi O, Peroni D, Valetto A.
Bertini V, et al. Among authors: scacciati m.
Genes (Basel). 2022 Nov 30;13(12):2249. doi: 10.3390/genes13122249.
Genes (Basel). 2022.
PMID: 36553517
Free PMC article.
Review.
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