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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: mordenti 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.
Outcomes of Temporary Hemiepiphyseal Stapling for Correcting Genu Valgum in Children with Multiple Osteochondromas: A Single Institution Study.
Trisolino G, Boarini M, Mordenti M, Evangelista A, Gallone G, Stallone S, Zarantonello P, Antonioli D, Di Gennaro GL, Stilli S, Sangiorgi L. Trisolino G, et al. Among authors: mordenti m. Children (Basel). 2021 Apr 8;8(4):287. doi: 10.3390/children8040287. Children (Basel). 2021. PMID: 33917765 Free PMC article.
Opportunities and Challenges for Machine Learning in Rare Diseases.
Decherchi S, Pedrini E, Mordenti M, Cavalli A, Sangiorgi L. Decherchi S, et al. Among authors: mordenti m. Front Med (Lausanne). 2021 Oct 5;8:747612. doi: 10.3389/fmed.2021.747612. eCollection 2021. Front Med (Lausanne). 2021. PMID: 34676229 Free PMC article. Review.
Secondary peripheral chondrosarcoma arising in solitary osteochondroma: variables influencing prognosis and survival.
Righi A, Pacheco M, Cocchi S, Asioli S, Gambarotti M, Donati DM, Evangelista A, Gnoli M, Locatelli M, Mordenti M, Boarini M, Brizola E, Pedrini E, Sangiorgi L. Righi A, et al. Among authors: mordenti m. Orphanet J Rare Dis. 2022 Feb 22;17(1):74. doi: 10.1186/s13023-022-02210-2. Orphanet J Rare Dis. 2022. PMID: 35193636 Free PMC article.
50 results