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Feeding and Nutritional Key Features of Crisponi/Cold-Induced Sweating Syndrome.
Onesimo R, Sforza E, Palermo F, Giorgio V, Leoni C, Rigante D, Trevisan V, Agazzi C, Limongelli D, Proli F, Kuczynska EM, Crisponi L, Crisponi G, Zampino G. Onesimo R, et al. Genes (Basel). 2024 Aug 23;15(9):1109. doi: 10.3390/genes15091109. Genes (Basel). 2024. PMID: 39336700 Free PMC article.
What to Expect of Feeding Abilities and Nutritional Aspects in Achondroplasia Patients: A Narrative Review.
Sforza E, Margiotta G, Giorgio V, Limongelli D, Proli F, Kuczynska EM, Leoni C, De Rose C, Trevisan V, Romeo DM, Calandrelli R, De Corso E, Massimi L, Palmacci O, Rigante D, Zampino G, Onesimo R. Sforza E, et al. Among authors: onesimo r. Genes (Basel). 2023 Jan 12;14(1):199. doi: 10.3390/genes14010199. Genes (Basel). 2023. PMID: 36672940 Free PMC article. Review.
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. Genes (Basel). 2023 Sep 22;14(10):1843. doi: 10.3390/genes14101843. Genes (Basel). 2023. PMID: 37895192 Free PMC article.
Trisomy 22 Mosaicism from Prenatal to Postnatal Findings: A Case Series and Systematic Review of the Literature.
Trevisan V, Meroni A, Leoni C, Sirchia F, Politano D, Fiandrino G, Giorgio V, Rigante D, Limongelli D, Perri L, Sforza E, Leonardi F, Viscogliosi G, Contaldo I, Orteschi D, Proietti L, Zampino G, Onesimo R. Trevisan V, et al. Among authors: onesimo r. Genes (Basel). 2024 Mar 8;15(3):346. doi: 10.3390/genes15030346. Genes (Basel). 2024. PMID: 38540405 Free PMC article. Review.
Impact of Costello syndrome on growth patterns.
Leoni C, Giorgio V, Onesimo R, Kuczynska E, Zampino G. Leoni C, et al. Among authors: onesimo r. Am J Med Genet A. 2020 Nov;182(11):2797-2799. doi: 10.1002/ajmg.a.61812. Epub 2020 Aug 26. Am J Med Genet A. 2020. PMID: 32845069 No abstract available.
Epilepsy and BRAF Mutations: Phenotypes, Natural History and Genotype-Phenotype Correlations.
Battaglia DI, Gambardella ML, Veltri S, Contaldo I, Chillemi G, Veredice C, Quintiliani M, Leoni C, Onesimo R, Verdolotti T, Radio FC, Martinelli D, Trivisano M, Specchio N, Dravet C, Tartaglia M, Zampino G. Battaglia DI, et al. Among authors: onesimo r. Genes (Basel). 2021 Aug 26;12(9):1316. doi: 10.3390/genes12091316. Genes (Basel). 2021. PMID: 34573299 Free PMC article.
123 results