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34 results

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Page 1
Congenital heart defects in CTNNB1 syndrome: Raising clinical awareness.
Sinibaldi L, Garone G, Mandarino A, Iarossi G, Chioma L, Dentici ML, Merla G, Agolini E, Micalizzi A, Mancini C, Niceta M, Macchiaiolo M, Diodato D, Onesimo R, Blandino R, Delogu AB, De Rosa G, Trevisan V, Iademarco M, Zampino G, Tartaglia M, Novelli A, Bartuli A, Digilio MC, Calcagni G. Sinibaldi L, et al. Among authors: trevisan v. Clin Genet. 2023 Nov;104(5):528-541. doi: 10.1111/cge.14404. Epub 2023 Jul 17. Clin Genet. 2023. PMID: 37455656
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: trevisan v. Genes (Basel). 2023 Jan 12;14(1):199. doi: 10.3390/genes14010199. Genes (Basel). 2023. PMID: 36672940 Free PMC article. Review.
Further case of enlarged spinal nerve roots in KRAS-related Noonan syndrome.
Leoni C, Viscogliosi G, Onesimo R, Verdolotti T, Biagini T, Mazza T, De Luca A, Perri L, Trevisan V, Flex E, Tartaglia M, Zampino G. Leoni C, et al. Among authors: trevisan v. Clin Genet. 2023 Jul;104(1):136-138. doi: 10.1111/cge.14308. Epub 2023 Feb 21. Clin Genet. 2023. PMID: 36757675
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: trevisan v. Genes (Basel). 2023 Sep 22;14(10):1843. doi: 10.3390/genes14101843. Genes (Basel). 2023. PMID: 37895192 Free PMC article.
Validation and cross-cultural adaptation of the Italian version of the paediatric eating assessment tool (I-PEDI-EAT-10) in genetic syndromes.
Onesimo R, Sforza E, Triumbari EKA, Proli F, Leoni C, Giorgio V, Rigante D, Trevisan V, De Rose C, Kuczynska EM, Cerchiari A, Pane M, Mercuri E, Belafsky P, Zampino G. Onesimo R, et al. Among authors: trevisan v. Int J Lang Commun Disord. 2024 May-Jun;59(3):1152-1162. doi: 10.1111/1460-6984.12986. Epub 2023 Nov 19. Int J Lang Commun Disord. 2024. PMID: 37982346
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. Genes (Basel). 2024 Mar 8;15(3):346. doi: 10.3390/genes15030346. Genes (Basel). 2024. PMID: 38540405 Free PMC article. Review.
34 results