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Page 1
Correction: Sciacca, F. L., et al. Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya Syndrome. Int. J. Mol. Sci. 2018, 19, 3675.
Sciacca FL, Rizzo A, Bedini G, Capone F, Di Lazzaro V, Nava S, Acerbi F, Rossi Sebastiano D, Binelli S, Faragò G, Gioppo A, Grisoli M, Bruzzone MG, Ferroli P, Pantaleoni C, Caputi L, Gomez JV, Parati EA, Bersano A. Sciacca FL, et al. Int J Mol Sci. 2019 Dec 18;21(1):20. doi: 10.3390/ijms21010020. Int J Mol Sci. 2019. PMID: 31861461 Free PMC article.
Neurological phenotype of Potocki-Lupski syndrome.
Ciaccio C, Pantaleoni C, Milani D, Alfei E, Sciacca FL, Canafoglia L, Erbetta A, D'Arrigo S. Ciaccio C, et al. Among authors: sciacca fl. Am J Med Genet A. 2020 Oct;182(10):2317-2324. doi: 10.1002/ajmg.a.61789. Epub 2020 Aug 15. Am J Med Genet A. 2020. PMID: 33043631
Rhythmic cortical myoclonus in patients with 6Q22.1 deletion.
Canafoglia L, Zibordi F, Deleo F, Strigaro G, Varrasi C, Ciaccio C, Nardocci N, Panzica F, Franceschetti S, Sciacca FL. Canafoglia L, et al. Among authors: sciacca fl. Eur J Paediatr Neurol. 2023 May;44:25-27. doi: 10.1016/j.ejpn.2023.03.001. Epub 2023 Mar 22. Eur J Paediatr Neurol. 2023. PMID: 36990055
The relevance of mitochondrial DNA variants fluctuation during reprogramming and neuronal differentiation of human iPSCs.
Palombo F, Peron C, Caporali L, Iannielli A, Maresca A, Di Meo I, Fiorini C, Segnali A, Sciacca FL, Rizzo A, Levi S, Suomalainen A, Prigione A, Broccoli V, Carelli V, Tiranti V. Palombo F, et al. Among authors: sciacca fl. Stem Cell Reports. 2021 Aug 10;16(8):1953-1967. doi: 10.1016/j.stemcr.2021.06.016. Epub 2021 Jul 29. Stem Cell Reports. 2021. PMID: 34329598 Free PMC article.
CGH Findings in Children with Complex and Essential Autistic Spectrum Disorder.
Annunziata S, Bulgheroni S, D'Arrigo S, Esposito S, Taddei M, Saletti V, Alfei E, Sciacca FL, Rizzo A, Pantaleoni C, Riva D. Annunziata S, et al. J Autism Dev Disord. 2023 Feb;53(2):615-623. doi: 10.1007/s10803-020-04833-5. Epub 2021 Jan 4. J Autism Dev Disord. 2023. PMID: 33394245
Cortical Myoclonus and Complex Paroxysmal Dyskinesias in a Patient with NAA15 Variant.
Freri E, Canafoglia L, Ciaccio C, Rossi Sebastiano D, Caputo D, Solazzi R, Sciacca FL, Iascone M, Panzica F, Granata T, Franceschetti S, Nardocci N. Freri E, et al. Among authors: sciacca fl. Mov Disord. 2024 Apr 21. doi: 10.1002/mds.29793. Online ahead of print. Mov Disord. 2024. PMID: 38643413 No abstract available.
The noncoding RNA AK127244 in 2p16.3 locus: A new susceptibility region for neuropsychiatric disorders.
Rizzo A, Alfei E, Zibordi F, Saletti V, Zorzi G, Freri E, Estienne M, Girgenti V, D'Arrigo S, Esposito S, Buldrini B, Moroni I, Milani D, Granata T, Ardissone A, Eoli M, Molteni B, Bigoni S, Pantaleoni C, Nardocci N, Sciacca FL. Rizzo A, et al. Am J Med Genet B Neuropsychiatr Genet. 2018 Sep;177(6):557-562. doi: 10.1002/ajmg.b.32649. Epub 2018 Aug 14. Am J Med Genet B Neuropsychiatr Genet. 2018. PMID: 30105822
25 results