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From Feeding Challenges to Oral-Motor Dyspraxia: A Comprehensive Description of 10 New Cases with CTNNB1 Syndrome.
Onesimo R, Sforza E, Trevisan V, Leoni C, Giorgio V, Rigante D, Kuczynska EM, Proli F, Agazzi C, Limongelli D, Digilio MC, Dentici ML, Macchiaiolo M, Novelli A, Bartuli A, Sinibaldi L, Tartaglia M, Zampino G. Onesimo R, et al. Among authors: agazzi c. Genes (Basel). 2023 Sep 22;14(10):1843. doi: 10.3390/genes14101843. Genes (Basel). 2023. PMID: 37895192 Free PMC article.
Ligamentous laxity in children with achondroplasia: Prevalence, joint involvement, and implications for early intervention strategies.
Romeo DM, Pironi V, Velli C, Sforza E, Rigante D, Giorgio V, Leoni C, De Rose C, Kuczynska EM, Limongelli D, Ruiz R, Agazzi C, Mercuri E, Zampino G, Onesimo R. Romeo DM, et al. Among authors: agazzi c. Eur J Med Genet. 2024 Apr;68:104930. doi: 10.1016/j.ejmg.2024.104930. Epub 2024 Feb 28. Eur J Med Genet. 2024. PMID: 38428804 Free article.
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: agazzi c. Genes (Basel). 2021 Jun 25;12(7):972. doi: 10.3390/genes12070972. Genes (Basel). 2021. PMID: 34202106 Free PMC article.