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Role of OPRM1, clinical and anthropometric variants in neonatal pain reduction.
Erbi I, Ciantelli M, Farinella R, Tuoni C, Gentiluomo M, Moscuzza F, Rizzato C, Bedini A, Faraoni M, Giusfredi S, Tavanti A, Ghirri P, Campa D. Erbi I, et al. Among authors: moscuzza f. Sci Rep. 2020 Apr 27;10(1):7091. doi: 10.1038/s41598-020-63790-2. Sci Rep. 2020. PMID: 32341423 Free PMC article. Clinical Trial.
Polymorphic variants in Sweet and Umami taste receptor genes and birthweight.
Farinella R, Erbi I, Bedini A, Donato S, Gentiluomo M, Angelucci C, Lupetti A, Cuttano A, Moscuzza F, Tuoni C, Rizzato C, Ciantelli M, Campa D. Farinella R, et al. Among authors: moscuzza f. Sci Rep. 2021 Mar 2;11(1):4971. doi: 10.1038/s41598-021-84491-4. Sci Rep. 2021. PMID: 33654187 Free PMC article. Clinical Trial.
Maternal anthropometric variables and clinical factors shape neonatal microbiome.
Farinella R, Rizzato C, Bottai D, Bedini A, Gemignani F, Landi S, Peduzzi G, Rosati S, Lupetti A, Cuttano A, Moscuzza F, Tuoni C, Filippi L, Ciantelli M, Tavanti A, Campa D. Farinella R, et al. Among authors: moscuzza f. Sci Rep. 2022 Feb 21;12(1):2875. doi: 10.1038/s41598-022-06792-6. Sci Rep. 2022. PMID: 35190600 Free PMC article.
Lutein and Neurodevelopment in Preterm Infants.
Giampietri M, Lorenzoni F, Moscuzza F, Boldrini A, Ghirri P. Giampietri M, et al. Among authors: moscuzza f. Front Neurosci. 2016 Sep 7;10:411. doi: 10.3389/fnins.2016.00411. eCollection 2016. Front Neurosci. 2016. PMID: 27656124 Free PMC article. No abstract available.
Nutrition, epigenetic markers and growth in preterm infants.
Tozzi MG, Moscuzza F, Michelucci A, Scaramuzzo RT, Cosini C, Chesi F, Caligo MA, Ciantelli M, Ghirri P. Tozzi MG, et al. Among authors: moscuzza f. J Matern Fetal Neonatal Med. 2021 Dec;34(23):3963-3968. doi: 10.1080/14767058.2019.1702952. Epub 2019 Dec 16. J Matern Fetal Neonatal Med. 2021. PMID: 31842645
A Novel Missense Mutation of the NSD1 Gene Associated with Overgrowth in Three Generations of an Italian Family: Case Report, Differential Diagnosis, and Review of Mutations of NSD1 Gene in Familial Sotos Syndrome.
Laccetta G, Moscuzza F, Michelucci A, Guzzetta A, Lunardi S, Lorenzoni F, Ghirri P. Laccetta G, et al. Among authors: moscuzza f. Front Pediatr. 2017 Nov 7;5:236. doi: 10.3389/fped.2017.00236. eCollection 2017. Front Pediatr. 2017. PMID: 29164086 Free PMC article.
Neonatal outcome in newborns from mothers with endocrinopathies.
Betti M, Ceccatelli G, Belcari F, Moscuzza F, Cuttano A, Vuerich M, Boldrini A, Ghirri P. Betti M, et al. Among authors: moscuzza f. Gynecol Endocrinol. 2011 Apr;27(4):248-50. doi: 10.3109/09513590.2010.487618. Epub 2010 Jun 2. Gynecol Endocrinol. 2011. PMID: 20518638
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