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Deep neurological phenotyping in oculo-dento-digital syndrome.
Lopriore P, Vista M, Maritato P, Caldarazzo Ienco E, Bassani L, Natale G, Tessa A, Santorelli FM, Orsucci D. Lopriore P, et al. Among authors: orsucci d. Neurol Sci. 2024 Jan 23. doi: 10.1007/s10072-024-07331-z. Online ahead of print. Neurol Sci. 2024. PMID: 38253744
Primary Coenzyme Q10 Deficiency-Related Ataxias.
Lopriore P, Vista M, Tessa A, Giuntini M, Caldarazzo Ienco E, Mancuso M, Siciliano G, Santorelli FM, Orsucci D. Lopriore P, et al. Among authors: orsucci d. J Clin Med. 2024 Apr 19;13(8):2391. doi: 10.3390/jcm13082391. J Clin Med. 2024. PMID: 38673663 Free PMC article. Review.
Mitochondrial Syndromes Revisited.
Orsucci D, Caldarazzo Ienco E, Rossi A, Siciliano G, Mancuso M. Orsucci D, et al. J Clin Med. 2021 Mar 17;10(6):1249. doi: 10.3390/jcm10061249. J Clin Med. 2021. PMID: 33802970 Free PMC article. Review.
Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia.
Lyu H, Boßelmann CM, Johannesen KM, Koko M, Ortigoza-Escobar JD, Aguilera-Albesa S, Garcia-Navas Núñez D, Linnankivi T, Gaily E, van Ruiten HJA, Richardson R, Betzler C, Horvath G, Brilstra E, Geerdink N, Orsucci D, Tessa A, Gardella E, Fleszar Z, Schöls L, Lerche H, Møller RS, Liu Y. Lyu H, et al. Among authors: orsucci d. EBioMedicine. 2023 Dec;98:104855. doi: 10.1016/j.ebiom.2023.104855. Epub 2023 Oct 28. EBioMedicine. 2023. PMID: 38251463 Free PMC article.
93 results