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Iodine supplementation in the newborn.
Ghirri P, Lunardi S, Boldrini A. Ghirri P, et al. Among authors: lunardi s. Nutrients. 2014 Jan 20;6(1):382-90. doi: 10.3390/nu6010382. Nutrients. 2014. PMID: 24448111 Free PMC article. Review.
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: lunardi s. 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
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: lunardi s. Front Pediatr. 2017 Nov 7;5:236. doi: 10.3389/fped.2017.00236. eCollection 2017. Front Pediatr. 2017. PMID: 29164086 Free PMC article.