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SATURN: assessing the feasibility of utilising existing registries for real-world evidence data collection to meet patients, regulatory, health technology assessment and payer requirements.
Sangiorgi L, Boarini M, Mordenti M, Wang V, Westerheim I, Skarberg RT, Cavaller-Bellaubi M, Clancy J, Pinedo-Villanueva R, Lente EJV, Marchetti M. Sangiorgi L, et al. Among authors: boarini m. Orphanet J Rare Dis. 2024 Sep 12;19(1):336. doi: 10.1186/s13023-024-03341-4. Orphanet J Rare Dis. 2024. PMID: 39267100 Free PMC article.
Genotype-phenotype correlation study in 364 osteogenesis imperfecta Italian patients.
Maioli M, Gnoli M, Boarini M, Tremosini M, Zambrano A, Pedrini E, Mordenti M, Corsini S, D'Eufemia P, Versacci P, Celli M, Sangiorgi L. Maioli M, et al. Among authors: boarini m. Eur J Hum Genet. 2019 Jul;27(7):1090-1100. doi: 10.1038/s41431-019-0373-x. Epub 2019 Mar 18. Eur J Hum Genet. 2019. PMID: 30886339 Free PMC article. Clinical Trial.
The Rizzoli Multiple Osteochondromas Classification revised: describing the phenotype to improve clinical practice.
Mordenti M, Gnoli M, Boarini M, Trisolino G, Evangelista A, Pedrini E, Corsini S, Tremosini M, Staals EL, Antonioli D, Stilli S, Donati DM, Sangiorgi L. Mordenti M, et al. Among authors: boarini m. Am J Med Genet A. 2021 Nov;185(11):3466-3475. doi: 10.1002/ajmg.a.62470. Epub 2021 Sep 3. Am J Med Genet A. 2021. PMID: 34477285 Free PMC article.
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