Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

19 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
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.
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.
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.
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.
Identification of three novel mutations in the CHD7 gene in patients with clinical signs of typical or atypical CHARGE syndrome.
Michelucci A, Ghirri P, Iacopetti P, Conidi ME, Fogli A, Baldinotti F, Lunardi S, Forli F, Moscuzza F, Berrettini S, Boldrini A, Simi P, Pellegrini S. Michelucci A, et al. Among authors: moscuzza f. Int J Pediatr Otorhinolaryngol. 2010 Dec;74(12):1441-4. doi: 10.1016/j.ijporl.2010.09.006. Epub 2010 Oct 12. Int J Pediatr Otorhinolaryngol. 2010. PMID: 20943277
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.
19 results