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Visual Function in Children with GNAO1-Related Encephalopathy.
Gambardella ML, Pede E, Orazi L, Leone S, Quintiliani M, Amorelli GM, Petrianni M, Galanti M, Amore F, Musto E, Perulli M, Contaldo I, Veredice C, Mercuri EM, Battaglia DI, Ricci D. Gambardella ML, et al. Among authors: leone s. Genes (Basel). 2023 Feb 22;14(3):544. doi: 10.3390/genes14030544. Genes (Basel). 2023. PMID: 36980817 Free PMC article.
Cortical Visual Impairment in CDKL5 Deficiency Disorder.
Quintiliani M, Ricci D, Petrianni M, Leone S, Orazi L, Amore F, Gambardella ML, Contaldo I, Veredice C, Perulli M, Musto E, Mercuri EM, Battaglia DI. Quintiliani M, et al. Among authors: leone s. Front Neurol. 2022 Jan 26;12:805745. doi: 10.3389/fneur.2021.805745. eCollection 2021. Front Neurol. 2022. PMID: 35153983 Free PMC article.
[ANMCO Position paper: Amyloidosis for the clinical cardiologist. A "clinical primer" from the ANMCO Rare Disease Working Group].
Chimenti C, Grego S, Di Fusco S, De Luca L, Caldarola P, Cannillo M, Cipriani M, Di Lenarda A, Donato D, Leone S, Limongelli G, Navazio A, Riccio C, Valente S, Gulizia MM, Gabrielli D, Oliva F, Colivicchi F. Chimenti C, et al. Among authors: leone s. G Ital Cardiol (Rome). 2023 Feb;24(2):127-135. doi: 10.1714/3963.39421. G Ital Cardiol (Rome). 2023. PMID: 36735312 Italian.
Visual Function and Ophthalmological Findings in CHARGE Syndrome: Revision of Literature, Definition of a New Clinical Spectrum and Genotype Phenotype Correlation.
Onesimo R, Ricci D, Agazzi C, Leone S, Petrianni M, Orazi L, Amore F, Salerni A, Leoni C, Chieffo D, Tartaglia M, Mercuri E, Zampino G. Onesimo R, et al. Among authors: leone s. Genes (Basel). 2021 Jun 25;12(7):972. doi: 10.3390/genes12070972. Genes (Basel). 2021. PMID: 34202106 Free PMC article.