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2007 1
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2019 11
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Page 1
Early-onset Dopamine Transporter Deficiency Syndrome: Long-term Follow-up.
Baga M, Spagnoli C, Soliani L, Salerno GG, Rizzi S, Frattini D, Pisani F, Fusco C. Baga M, et al. Among authors: salerno gg. Can J Neurol Sci. 2021 Mar;48(2):285-286. doi: 10.1017/cjn.2020.144. Epub 2020 Jul 10. Can J Neurol Sci. 2021. PMID: 32646530 No abstract available.
Refining the mutational spectrum and gene-phenotype correlates in pontocerebellar hypoplasia: results of a multicentric study.
Nuovo S, Micalizzi A, Romaniello R, Arrigoni F, Ginevrino M, Casella A, Serpieri V, D'Arrigo S, Briguglio M, Salerno GG, Rossato S, Sartori S, Leuzzi V, Battini R, Ben-Zeev B, Graziano C, Mirabelli Badenier M, Brankovic V, Nardocci N, Spiegel R, Petković Ramadža D, Vento G, Marti I, Simonati A, Dipresa S, Freri E, Mazza T, Bassi MT, Bosco L, Travaglini L, Zanni G, Bertini ES, Vanacore N, Borgatti R, Valente EM. Nuovo S, et al. Among authors: salerno gg. J Med Genet. 2022 Apr;59(4):399-409. doi: 10.1136/jmedgenet-2020-107497. Epub 2021 Mar 5. J Med Genet. 2022. PMID: 34085948
IRF2BPL gene variants: One new case.
Spagnoli C, Rizzi S, Salerno GG, Frattini D, Fusco C. Spagnoli C, et al. Among authors: salerno gg. Am J Med Genet A. 2020 Jan;182(1):255-256. doi: 10.1002/ajmg.a.61401. Epub 2019 Nov 15. Am J Med Genet A. 2020. PMID: 31729144 No abstract available.
Long-term follow-up in infantile-onset SCAR18: A case report.
Iodice A, Spagnoli C, Cangini M, Soliani L, Rizzi S, Salerno GG, Frattini D, Pisani F, Fusco C. Iodice A, et al. Among authors: salerno gg. J Clin Neurosci. 2020 Jul;77:232-234. doi: 10.1016/j.jocn.2020.05.008. Epub 2020 May 6. J Clin Neurosci. 2020. PMID: 32387255
42 results