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Clinical and molecular description of the first Italian cohort of 33 subjects with hypophosphatasia.
Cinque L, Pugliese F, Salcuni AS, Trombetta D, Battista C, Biagini T, Augello B, Nardella G, Conti F, Corbetta S, Fischetto R, Foiadelli T, Gaudio A, Giannini C, Grosso E, Guabello G, Massuras S, Palermo A, Politano L, Pigliaru F, Ruggeri RM, Scarano E, Vicchio P, Cannavò S, Celli M, Petrizzelli F, Mastroianno M, Castori M, Scillitani A, Guarnieri V. Cinque L, et al. Among authors: celli m. Front Endocrinol (Lausanne). 2023 Aug 1;14:1205977. doi: 10.3389/fendo.2023.1205977. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37600704 Free PMC article.
Osteogenesis imperfecta and rapid maxillary expansion: Report of 3 patients.
Ierardo G, Calcagnile F, Luzzi V, Ladniak B, Bossu M, Celli M, Zambrano A, Franchi L, Polimeni A. Ierardo G, et al. Among authors: celli m. Am J Orthod Dentofacial Orthop. 2015 Jul;148(1):130-7. doi: 10.1016/j.ajodo.2015.01.029. Am J Orthod Dentofacial Orthop. 2015. PMID: 26124036
The line between COVID-19 pandemic and rare bone diseases.
Sangiorgi L, Brizola E; COVID-19 Helpline for Rare Bone Diseases Group. Sangiorgi L, et al. Ir J Med Sci. 2021 Aug;190(3):1243-1244. doi: 10.1007/s11845-020-02400-6. Epub 2020 Nov 2. Ir J Med Sci. 2021. PMID: 33140293 Free PMC article. No abstract available.
Osteogenesis Imperfecta: the audiological phenotype lacks correlation with the genotype.
Swinnen FK, Coucke PJ, De Paepe AM, Symoens S, Malfait F, Gentile FV, Sangiorgi L, D'Eufemia P, Celli M, Garretsen TJ, Cremers CW, Dhooge IJ, De Leenheer EM. Swinnen FK, et al. Among authors: celli m. Orphanet J Rare Dis. 2011 Dec 29;6:88. doi: 10.1186/1750-1172-6-88. Orphanet J Rare Dis. 2011. PMID: 22206639 Free PMC article.
154 results